Item | Value |
---|---|
geneid | 64919 |
ensemblid | ENSG00000127152.18 |
hgncid | 13222 |
symbol | BCL11B |
name | BCL11 transcription factor B |
refseq_nuc | NM_138576.4 |
refseq_prot | NP_612808.1 |
ensembl_nuc | ENST00000357195.8 |
ensembl_prot | ENSP00000349723.3 |
mane_status | MANE Select |
chr | chr14 |
start | 99169287 |
end | 99272197 |
strand | - |
ver | v1.2 |
region | chr14:99169287-99272197 |
region5000 | chr14:99164287-99277197 |
regionname0 | BCL11B_chr14_99169287_99272197 |
regionname5000 | BCL11B_chr14_99164287_99277197 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 894 | 347 | 94 | 70 | 124 | 12 | 45 | 94 | BCL11B_chr14_99164287_99277197 | BCL11B | MSRRK others(889): Show |
chr14 | 99164287 | 99277197 |
a0002 | 0/0 | 894 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | MSRRK others(889): Show |
chr14 | 99164287 | 99277197 |
a0003 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | MSRRK others(889): Show |
chr14 | 99164287 | 99277197 |
a0004 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | MSRRK others(889): Show |
chr14 | 99164287 | 99277197 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2682 | 249 | 66 | 50 | 88 | 8 | 35 | BCL11B_chr14_99164287_99277197 | BCL11B | ATGTC others(2677): Show |
chr14 | 99164287 | 99277197 | ||
a0001c0002 | 0/0 | 2682 | 84 | 20 | 17 | 35 | 4 | 8 | BCL11B_chr14_99164287_99277197 | BCL11B | ATGTC others(2677): Show |
chr14 | 99164287 | 99277197 | ||
a0001c0003 | 0/0 | 2682 | 6 | 1 | 3 | 0 | 0 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | ATGTC others(2677): Show |
chr14 | 99164287 | 99277197 | ||
a0001c0004 | 0/0 | 2682 | 3 | 3 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | ATGTC others(2677): Show |
chr14 | 99164287 | 99277197 | ||
a0001c0005 | 0/0 | 2682 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | ATGTC others(2677): Show |
chr14 | 99164287 | 99277197 | ||
a0001c0006 | 0/0 | 2682 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | ATGTC others(2677): Show |
chr14 | 99164287 | 99277197 | ||
a0001c0008 | 0/0 | 2682 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | ATGTC others(2677): Show |
chr14 | 99164287 | 99277197 | ||
a0002c0007 | 0/0 | 2682 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | ATGTC others(2677): Show |
chr14 | 99164287 | 99277197 | ||
a0003c0009 | 0/0 | 2682 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | ATGTC others(2677): Show |
chr14 | 99164287 | 99277197 | ||
a0004c0010 | 0/0 | 2682 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | ATGTC others(2677): Show |
chr14 | 99164287 | 99277197 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 8529 | 58 | 3 | 8 | 36 | 2 | 8 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0002 | 1/0 | 8528 | 38 | 9 | 7 | 15 | 2 | 4 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8523): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0003 | 0/0 | 8530 | 5 | 1 | 1 | 0 | 0 | 3 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0004 | 0/0 | 8529 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0005 | 0/0 | 8530 | 24 | 1 | 10 | 3 | 3 | 7 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0006 | 0/0 | 8530 | 19 | 1 | 6 | 7 | 0 | 5 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0007 | 0/0 | 8531 | 11 | 0 | 4 | 5 | 0 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0009 | 0/0 | 8527 | 9 | 9 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8522): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0010 | 0/0 | 8529 | 7 | 7 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0011 | 0/0 | 8532 | 7 | 0 | 5 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8527): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0012 | 0/0 | 8534 | 5 | 0 | 0 | 5 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8529): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0013 | 0/0 | 8528 | 4 | 4 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8523): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0014 | 0/0 | 8530 | 3 | 3 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0015 | 0/0 | 8529 | 3 | 3 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0018 | 0/0 | 8529 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0020 | 0/0 | 8536 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8531): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0021 | 0/0 | 8531 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0022 | 0/0 | 8530 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0024 | 0/0 | 8531 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0025 | 0/0 | 8532 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8527): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0026 | 0/0 | 8531 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0027 | 0/0 | 8531 | 2 | 0 | 1 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0028 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0029 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0030 | 0/0 | 8526 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8521): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0032 | 0/0 | 8528 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8523): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0033 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0034 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0035 | 0/0 | 8528 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8523): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0036 | 0/0 | 8528 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8523): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0037 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0038 | 0/0 | 8486 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8481): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0039 | 0/0 | 8528 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8523): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0040 | 0/0 | 8528 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8523): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0041 | 0/0 | 8528 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8523): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0042 | 0/0 | 8528 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8523): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0047 | 0/0 | 8528 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8523): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0049 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0050 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0051 | 0/0 | 8531 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0053 | 0/0 | 8535 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8530): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0054 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0055 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0056 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0057 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0062 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0063 | 0/0 | 8531 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0064 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0065 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0067 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0068 | 0/0 | 8550 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8545): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0069 | 0/0 | 8551 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8546): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0070 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0071 | 0/0 | 8531 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0073 | 0/0 | 8531 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0074 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0077 | 0/0 | 8532 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8527): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0078 | 0/0 | 8551 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8546): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0081 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0082 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0001t0083 | 0/0 | 8518 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8513): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0001 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0003 | 0/0 | 8530 | 27 | 5 | 5 | 15 | 0 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0004 | 0/0 | 8529 | 21 | 5 | 4 | 9 | 1 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0006 | 0/0 | 8530 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0007 | 0/0 | 8531 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0008 | 0/0 | 8531 | 9 | 0 | 3 | 3 | 1 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0011 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8527): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0016 | 0/0 | 8515 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8510): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0017 | 0/0 | 8529 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0019 | 0/0 | 8521 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8516): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0031 | 0/0 | 8528 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8523): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0043 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0045 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0046 | 0/0 | 8529 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0048 | 0/0 | 8529 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0052 | 0/0 | 8520 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8515): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0058 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0059 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0060 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0061 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0066 | 0/0 | 8531 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0072 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0075 | 0/0 | 8531 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0076 | 0/0 | 8531 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0079 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0002t0080 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0003t0003 | 0/0 | 8530 | 2 | 0 | 0 | 0 | 0 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0003t0004 | 0/0 | 8529 | 2 | 1 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0003t0008 | 0/0 | 8531 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0001c0004t0001 | 0/0 | 8529 | 3 | 3 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0005t0010 | 0/0 | 8529 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0001c0006t0023 | 0/0 | 8530 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0001c0008t0044 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8524): Show |
chr14 | 99164287 | 99277197 |
a0002c0007t0007 | 0/0 | 8531 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
a0003c0009t0003 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8525): Show |
chr14 | 99164287 | 99277197 |
a0004c0010t0007 | 0/0 | 8531 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | AGCCA others(8526): Show |
chr14 | 99164287 | 99277197 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0002g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0007g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0007g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0007g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0007g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0007g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0007g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0007g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0009g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0010g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0010g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0011g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0011g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0011g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0011g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0011g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0011g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0011g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0012g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0012g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0012g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0012g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0012g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0013g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0013g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0014g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0014g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0015g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0015g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0015g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0018g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0018g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0020g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0020g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0021g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0021g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0022g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0022g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0024g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0024g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0025g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0025g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0026g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0026g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0027g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0027g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0028g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0029g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0030g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0032g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0033g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0034g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0035g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0036g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0037g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0038g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0039g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0040g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0041g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0042g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0047g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0049g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0050g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0051g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0053g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0054g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0055g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0056g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0057g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0062g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0063g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0064g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0065g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0067g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0068g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0069g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0070g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0071g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0073g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0074g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0077g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0078g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0081g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0082g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0001t0083g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0006g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0007g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0007g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0008g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0008g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0008g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0008g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0008g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0008g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0008g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0008g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0008g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0011g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0016g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0016g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0017g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0019g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0019g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0031g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0043g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0045g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0046g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0048g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0052g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0058g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0059g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0060g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0061g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0066g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0072g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0075g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0076g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0079g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0002t0080g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0003t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0003t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0003t0008g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0003t0008g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0004t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0005t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0005t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0006t0023g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0006t0023g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0001c0008t0044g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0002c0007t0007g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0003c0009t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
a0004c0010t0007g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0027 | g0297 | EUR | GBR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0310 | EUR | GBR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0299 | EUR | GBR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | GBR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0002 | EUR | FIN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00280 | hp2 | a0001 | c0002 | t0006 | g0108 | EUR | FIN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00423 | hp1 | a0001 | c0001 | t0007 | g0196 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00438 | hp2 | a0001 | c0001 | t0041 | g0076 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00597 | hp2 | a0001 | c0002 | t0004 | g0125 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00609 | hp1 | a0001 | c0002 | t0003 | g0249 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00621 | hp1 | a0001 | c0001 | t0011 | g0341 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00621 | hp2 | a0001 | c0001 | t0074 | g0340 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00639 | hp1 | a0001 | c0002 | t0016 | g0011 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00639 | hp2 | a0001 | c0002 | t0048 | g0057 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00642 | hp2 | a0001 | c0002 | t0016 | g0012 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00673 | hp2 | a0001 | c0002 | t0003 | g0201 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00733 | hp1 | a0001 | c0001 | t0038 | g0038 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0331 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00735 | hp1 | a0001 | c0001 | t0005 | g0305 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00738 | hp1 | a0001 | c0001 | t0024 | g0250 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00738 | hp2 | a0001 | c0002 | t0004 | g0037 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0327 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0306 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01070 | hp1 | a0001 | c0002 | t0008 | g0314 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01070 | hp2 | a0001 | c0001 | t0026 | g0311 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0321 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01071 | hp2 | a0001 | c0001 | t0026 | g0303 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0070 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01081 | hp1 | a0001 | c0001 | t0011 | g0318 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01081 | hp2 | a0001 | c0001 | t0007 | g0268 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01099 | hp1 | a0001 | c0001 | t0042 | g0124 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0324 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01109 | hp2 | a0001 | c0002 | t0003 | g0151 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01168 | hp1 | a0001 | c0002 | t0008 | g0322 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01168 | hp2 | a0001 | c0002 | t0007 | g0255 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01169 | hp1 | a0001 | c0002 | t0007 | g0254 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0078 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0115 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01175 | hp2 | a0001 | c0001 | t0006 | g0062 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01192 | hp1 | a0001 | c0001 | t0024 | g0277 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0308 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0028 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0238 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01256 | hp2 | a0001 | c0001 | t0007 | g0256 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01257 | hp1 | a0001 | c0003 | t0008 | g0298 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0301 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01261 | hp1 | a0001 | c0001 | t0011 | g0328 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01261 | hp2 | a0001 | c0002 | t0004 | g0031 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01433 | hp1 | a0001 | c0002 | t0004 | g0033 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01433 | hp2 | a0001 | c0003 | t0004 | g0061 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0218 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01496 | hp2 | a0001 | c0001 | t0011 | g0323 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | IBS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | IBS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01517 | hp1 | a0001 | c0002 | t0046 | g0015 | EUR | IBS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0052 | EUR | IBS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01884 | hp1 | a0001 | c0002 | t0060 | g0176 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01884 | hp2 | a0001 | c0001 | t0063 | g0170 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01891 | hp1 | a0001 | c0002 | t0045 | g0014 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01891 | hp2 | a0001 | c0001 | t0032 | g0005 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01934 | hp2 | a0001 | c0002 | t0004 | g0079 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01943 | hp1 | a0001 | c0001 | t0007 | g0200 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01943 | hp2 | a0001 | c0003 | t0008 | g0302 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01952 | hp1 | a0001 | c0001 | t0027 | g0329 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01952 | hp2 | a0001 | c0002 | t0003 | g0213 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0205 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01975 | hp2 | a0001 | c0001 | t0073 | g0300 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01978 | hp2 | a0001 | c0002 | t0003 | g0153 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02004 | hp2 | a0001 | c0002 | t0008 | g0307 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0248 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02027 | hp1 | a0001 | c0002 | t0004 | g0034 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0334 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02055 | hp1 | a0001 | c0002 | t0079 | g0344 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02055 | hp2 | a0001 | c0002 | t0003 | g0264 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02056 | hp1 | a0001 | c0002 | t0008 | g0295 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02056 | hp2 | a0001 | c0001 | t0057 | g0152 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02071 | hp2 | a0001 | c0002 | t0008 | g0333 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02145 | hp2 | a0001 | c0001 | t0047 | g0101 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02148 | hp1 | a0001 | c0001 | t0011 | g0320 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CDX | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02257 | hp1 | a0001 | c0001 | t0081 | g0346 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02257 | hp2 | a0001 | c0002 | t0011 | g0338 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02258 | hp1 | a0001 | c0002 | t0003 | g0174 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02258 | hp2 | a0001 | c0001 | t0025 | g0228 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02280 | hp1 | a0001 | c0001 | t0009 | g0053 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0123 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02451 | hp1 | a0001 | c0001 | t0034 | g0007 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0054 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02572 | hp2 | a0001 | c0001 | t0010 | g0068 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02602 | hp1 | a0001 | c0002 | t0004 | g0050 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02602 | hp2 | a0001 | c0001 | t0069 | g0289 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02615 | hp1 | a0001 | c0001 | t0014 | g0083 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02615 | hp2 | a0001 | c0001 | t0015 | g0077 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02622 | hp1 | a0001 | c0001 | t0010 | g0132 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0286 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02630 | hp1 | a0001 | c0002 | t0080 | g0345 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02630 | hp2 | a0001 | c0002 | t0061 | g0169 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02647 | hp1 | a0001 | c0002 | t0004 | g0036 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02647 | hp2 | a0001 | c0001 | t0013 | g0259 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02683 | hp1 | a0001 | c0001 | t0068 | g0288 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02683 | hp2 | a0001 | c0001 | t0006 | g0082 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0080 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02698 | hp2 | a0001 | c0002 | t0075 | g0325 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02723 | hp1 | a0001 | c0001 | t0015 | g0030 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0127 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0168 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0047 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02809 | hp1 | a0001 | c0001 | t0022 | g0224 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02818 | hp2 | a0001 | c0001 | t0010 | g0043 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0339 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02886 | hp2 | a0001 | c0005 | t0010 | g0029 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02895 | hp2 | a0001 | c0004 | t0001 | g0001 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02896 | hp1 | a0001 | c0004 | t0001 | g0001 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02896 | hp2 | a0001 | c0006 | t0023 | g0191 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0178 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02897 | hp2 | a0001 | c0006 | t0023 | g0190 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02922 | hp2 | a0001 | c0001 | t0070 | g0290 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02965 | hp1 | a0001 | c0001 | t0049 | g0113 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0060 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02976 | hp1 | a0001 | c0001 | t0050 | g0086 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0135 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03017 | hp2 | a0001 | c0002 | t0008 | g0309 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03041 | hp1 | a0001 | c0001 | t0065 | g0165 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03041 | hp2 | a0001 | c0001 | t0071 | g0291 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03098 | hp1 | a0001 | c0001 | t0025 | g0164 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0094 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03130 | hp1 | a0001 | c0002 | t0072 | g0292 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03130 | hp2 | a0001 | c0001 | t0064 | g0186 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03139 | hp1 | a0001 | c0001 | t0014 | g0104 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03139 | hp2 | a0001 | c0001 | t0033 | g0008 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0173 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03195 | hp2 | a0001 | c0001 | t0013 | g0181 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03225 | hp1 | a0001 | c0002 | t0004 | g0092 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03225 | hp2 | a0001 | c0001 | t0010 | g0084 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03453 | hp1 | a0001 | c0001 | t0014 | g0087 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03453 | hp2 | a0001 | c0001 | t0028 | g0003 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03486 | hp1 | a0001 | c0001 | t0009 | g0091 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03486 | hp2 | a0001 | c0002 | t0017 | g0134 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03490 | hp1 | a0001 | c0001 | t0040 | g0110 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0304 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0294 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0313 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0293 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03516 | hp1 | a0001 | c0001 | t0029 | g0004 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03516 | hp2 | a0001 | c0002 | t0031 | g0006 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03540 | hp2 | a0001 | c0001 | t0030 | g0009 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0046 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0096 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0330 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03669 | hp2 | a0001 | c0003 | t0003 | g0262 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03688 | hp1 | a0001 | c0001 | t0006 | g0075 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03688 | hp2 | a0001 | c0003 | t0003 | g0270 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03710 | hp1 | a0001 | c0001 | t0077 | g0342 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03710 | hp2 | a0001 | c0001 | t0078 | g0343 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03831 | hp1 | a0001 | c0002 | t0003 | g0167 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03831 | hp2 | a0001 | c0002 | t0003 | g0261 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03834 | hp1 | a0001 | c0002 | t0008 | g0319 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0332 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03927 | hp2 | a0001 | c0001 | t0006 | g0109 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0275 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG04115 | hp1 | a0001 | c0001 | t0036 | g0063 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG04115 | hp2 | a0001 | c0002 | t0004 | g0041 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG04184 | hp2 | a0001 | c0002 | t0066 | g0281 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0285 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0315 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG04204 | hp2 | a0002 | c0007 | t0007 | g0283 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18522 | hp1 | a0001 | c0001 | t0010 | g0067 | AFR | YRI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | YRI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18942 | hp1 | a0001 | c0002 | t0003 | g0208 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18942 | hp2 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18947 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18947 | hp2 | a0001 | c0002 | t0004 | g0137 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18948 | hp2 | a0001 | c0002 | t0019 | g0139 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18950 | hp1 | a0001 | c0002 | t0076 | g0317 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18950 | hp2 | a0001 | c0002 | t0059 | g0244 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18951 | hp1 | a0001 | c0002 | t0003 | g0274 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18953 | hp2 | a0001 | c0002 | t0004 | g0018 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18960 | hp1 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18960 | hp2 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18962 | hp1 | a0001 | c0001 | t0083 | g0348 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18965 | hp2 | a0001 | c0001 | t0067 | g0258 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18966 | hp2 | a0001 | c0001 | t0012 | g0149 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18968 | hp1 | a0001 | c0001 | t0053 | g0145 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18968 | hp2 | a0001 | c0002 | t0008 | g0312 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18969 | hp1 | a0001 | c0001 | t0012 | g0143 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18969 | hp2 | a0001 | c0001 | t0021 | g0214 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18970 | hp2 | a0001 | c0001 | t0011 | g0316 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18971 | hp1 | a0001 | c0002 | t0004 | g0085 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18977 | hp1 | a0003 | c0009 | t0003 | g0263 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18978 | hp1 | a0001 | c0001 | t0055 | g0195 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18978 | hp2 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18979 | hp1 | a0001 | c0002 | t0004 | g0023 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18979 | hp2 | a0001 | c0002 | t0043 | g0111 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18981 | hp2 | a0001 | c0002 | t0003 | g0225 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18983 | hp1 | a0001 | c0002 | t0003 | g0180 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18995 | hp1 | a0001 | c0001 | t0020 | g0144 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18998 | hp2 | a0004 | c0010 | t0007 | g0287 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18999 | hp1 | a0001 | c0002 | t0003 | g0215 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA18999 | hp2 | a0001 | c0001 | t0007 | g0203 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19002 | hp1 | a0001 | c0001 | t0021 | g0280 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19002 | hp2 | a0001 | c0002 | t0004 | g0095 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19003 | hp1 | a0001 | c0008 | t0044 | g0089 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19004 | hp1 | a0001 | c0001 | t0006 | g0106 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19007 | hp1 | a0001 | c0001 | t0056 | g0273 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19007 | hp2 | a0001 | c0002 | t0058 | g0269 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19009 | hp2 | a0001 | c0001 | t0039 | g0138 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19010 | hp2 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19012 | hp2 | a0001 | c0001 | t0012 | g0147 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19030 | hp1 | a0001 | c0002 | t0004 | g0121 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19030 | hp2 | a0001 | c0001 | t0013 | g0175 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19043 | hp1 | a0001 | c0001 | t0022 | g0210 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19043 | hp2 | a0001 | c0001 | t0035 | g0010 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19057 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19057 | hp2 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19058 | hp1 | a0001 | c0002 | t0052 | g0141 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0337 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19063 | hp1 | a0001 | c0001 | t0005 | g0336 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19064 | hp1 | a0001 | c0001 | t0007 | g0257 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19064 | hp2 | a0001 | c0001 | t0037 | g0100 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19065 | hp1 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19065 | hp2 | a0001 | c0001 | t0012 | g0142 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19068 | hp1 | a0001 | c0002 | t0003 | g0253 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19068 | hp2 | a0001 | c0001 | t0007 | g0154 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19074 | hp1 | a0001 | c0001 | t0012 | g0148 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19074 | hp2 | a0001 | c0001 | t0054 | g0160 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19079 | hp2 | a0001 | c0002 | t0003 | g0265 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19080 | hp2 | a0001 | c0002 | t0003 | g0246 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19082 | hp1 | a0001 | c0002 | t0004 | g0136 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19082 | hp2 | a0001 | c0001 | t0020 | g0146 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19088 | hp2 | a0001 | c0002 | t0019 | g0140 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19090 | hp1 | a0001 | c0002 | t0004 | g0130 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19240 | hp1 | a0001 | c0001 | t0015 | g0093 | AFR | YRI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | YRI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA20129 | hp1 | a0001 | c0002 | t0004 | g0049 | AFR | ASW | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA20129 | hp2 | a0001 | c0001 | t0051 | g0128 | AFR | ASW | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA20752 | hp1 | a0001 | c0002 | t0008 | g0296 | EUR | TSI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA20752 | hp2 | a0001 | c0002 | t0004 | g0074 | EUR | TSI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | GIH | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0278 | SAS | GIH | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0326 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG01123 | hp2 | a0001 | c0001 | t0011 | g0335 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02109 | hp1 | a0001 | c0002 | t0017 | g0066 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0088 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02486 | hp1 | a0001 | c0001 | t0082 | g0347 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02486 | hp2 | a0001 | c0003 | t0004 | g0114 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02559 | hp1 | a0001 | c0005 | t0010 | g0013 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG02559 | hp2 | a0001 | c0001 | t0018 | g0021 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03471 | hp1 | a0001 | c0002 | t0003 | g0182 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG03471 | hp2 | a0001 | c0001 | t0018 | g0090 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | USA | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
HG06807 | hp2 | a0001 | c0001 | t0013 | g0189 | AFR | USA | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA20300 | hp1 | a0001 | c0002 | t0004 | g0081 | AFR | USA | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA20300 | hp2 | a0001 | c0001 | t0062 | g0219 | AFR | USA | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0194 | REF | REF | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0131 | REF | REF | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:99174951 | C | A | 1 | a0003 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.1885G>T | p.Gly629Cys | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2864/8528 | 1885/2685 | 629/894 | chr14 | 99174951 | |||
chr14:99257616 | G | T | 1 | a0002 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.282C>A | p.Asp94Glu | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/4 | 1261/8528 | 282/2685 | 94/894 | chr14 | 99257616 | |||
chr14:99257827 | T | A | 1 | a0004 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.71A>T | p.His24Leu | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/4 | 1050/8528 | 71/2685 | 24/894 | chr14 | 99257827 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:99174568 | G | A | 1 | a0001c0003 | 6 | HG01257.hp1 HG01433.hp2 HG01943.hp2 others(3): Show |
synonymous_variant | LOW | c.2268C>T | p.Pro756Pro | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3247/8528 | 2268/2685 | 756/894 | chr14 | 99174568 | |||
chr14:99174601 | G | T | 1 | a0001c0004 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.2235C>A | p.Ser745Ser | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3214/8528 | 2235/2685 | 745/894 | chr14 | 99174601 | |||
chr14:99174931 | G | A | 1 | a0001c0005 | 2 | HG02559.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.1905C>T | p.Asp635Asp | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2884/8528 | 1905/2685 | 635/894 | chr14 | 99174931 | |||
chr14:99174934 | G | A | 1 | a0001c0008 | 1 | NA19003.hp1 | synonymous_variant | LOW | c.1902C>T | p.Gly634Gly | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2881/8528 | 1902/2685 | 634/894 | chr14 | 99174934 | |||
chr14:99175399 | G | A | 1 | a0001c0006 | 2 | HG02896.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.1437C>T | p.His479His | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2416/8528 | 1437/2685 | 479/894 | chr14 | 99175399 | |||
chr14:99176023 | C | G | 4 | a0001c0002 a0001c0003 a0001c0008 others(1): Show |
92 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(89): Show |
synonymous_variant | LOW | c.813G>C | p.Pro271Pro | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1792/8528 | 813/2685 | 271/894 | chr14 | 99176023 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:99169889 | A | T | 1 | a0001c0006t0023 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4262T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 4262 | chr14 | 99169889 | ||||||
chr14:99169996 | G | A | 4 | a0001c0002t0017 a0001c0002t0060 a0001c0002t0072 others(1): Show |
5 | HG01884.hp1 HG02109.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4155C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 4155 | chr14 | 99169996 | ||||||
chr14:99170058 | T | C | 2 | a0001c0001t0057 a0001c0001t0074 |
2 | HG00621.hp2 HG02056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4093A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 4093 | chr14 | 99170058 | ||||||
chr14:99170262 | T | G | 1 | a0001c0001t0027 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3889A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3889 | chr14 | 99170262 | ||||||
chr14:99170310 | G | A | 1 | a0001c0001t0040 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3841C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3841 | chr14 | 99170310 | ||||||
chr14:99170353 | A | T | 1 | a0001c0001t0024 | 2 | HG00738.hp1 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3798T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3798 | chr14 | 99170353 | ||||||
chr14:99170552 | A | G | 2 | a0001c0001t0039 a0001c0001t0056 |
2 | NA19007.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3599T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3599 | chr14 | 99170552 | ||||||
chr14:99170997 | TCTCTCGC others(35): Show |
T | 1 | a0001c0001t0038 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3112_*3153delGCCA others(38): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3112 | chr14 | 99170997 | ||||||
chr14:99170998 | C | G | 1 | a0001c0002t0003 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3153G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3153 | chr14 | 99170998 | ||||||
chr14:99171171 | G | A | 1 | a0001c0001t0064 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2980C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2980 | chr14 | 99171171 | ||||||
chr14:99171314 | C | T | 5 | a0001c0001t0027 a0001c0001t0032 a0001c0001t0064 others(2): Show |
6 | HG00099.hp1 HG00639.hp2 HG01891.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2837G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2837 | chr14 | 99171314 | ||||||
chr14:99171334 | G | A | 2 | a0001c0002t0045 a0001c0002t0061 |
2 | HG01891.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2817C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2817 | chr14 | 99171334 | ||||||
chr14:99171639 | A | C | 1 | a0001c0001t0063 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2512T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2512 | chr14 | 99171639 | ||||||
chr14:99171760 | A | G | 1 | a0001c0008t0044 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2391T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2391 | chr14 | 99171760 | ||||||
chr14:99172013 | T | G | 1 | a0001c0001t0073 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2138A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2138 | chr14 | 99172013 | ||||||
chr14:99172159 | T | C | 1 | a0001c0001t0029 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1992A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1992 | chr14 | 99172159 | ||||||
chr14:99172399 | A | AT | 11 | a0001c0001t0014 a0001c0001t0025 a0001c0001t0033 others(8): Show |
14 | HG01884.hp2 HG01975.hp2 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1751dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1751 | chr14 | 99172399 | ||||||
chr14:99172409 | T | C | 3 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0030 |
14 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1742A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1742 | chr14 | 99172409 | ||||||
chr14:99172529 | A | G | 3 | a0001c0002t0043 a0001c0002t0059 a0001c0002t0076 |
3 | NA18950.hp1 NA18950.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1622T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1622 | chr14 | 99172529 | ||||||
chr14:99172681 | C | T | 1 | a0001c0002t0058 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1470G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1470 | chr14 | 99172681 | ||||||
chr14:99172706 | G | C | 1 | a0001c0001t0041 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1445C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1445 | chr14 | 99172706 | ||||||
chr14:99172845 | GA | G | 4 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0030 others(1): Show |
15 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1305delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1305 | chr14 | 99172845 | ||||||
chr14:99172913 | C | T | 1 | a0001c0001t0047 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1238G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1238 | chr14 | 99172913 | ||||||
chr14:99172933 | T | G | 25 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0010 others(22): Show |
74 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1218A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1218 | chr14 | 99172933 | ||||||
chr14:99173019 | C | G | 1 | a0001c0001t0054 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1132G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1132 | chr14 | 99173019 | ||||||
chr14:99173063 | A | G | 1 | a0001c0002t0075 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1088T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1088 | chr14 | 99173063 | ||||||
chr14:99173552 | A | G | 1 | a0001c0001t0062 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*599T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 599 | chr14 | 99173552 | ||||||
chr14:99173554 | C | A | 1 | a0001c0001t0047 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*597G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 597 | chr14 | 99173554 | ||||||
chr14:99173554 | C | CA | 43 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(40): Show |
146 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*596dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 596 | chr14 | 99173554 | ||||||
chr14:99173575 | A | AT | 2 | a0001c0001t0021 a0001c0001t0037 |
3 | NA18969.hp2 NA19002.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*575dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 575 | chr14 | 99173575 | ||||||
chr14:99173577 | T | TA | 36 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0010 others(33): Show |
88 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*573dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 573 | chr14 | 99173577 | ||||||
chr14:99173805 | T | TA | 9 | a0001c0001t0015 a0001c0001t0025 a0001c0001t0033 others(6): Show |
12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*345dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 345 | chr14 | 99173805 | ||||||
chr14:99173963 | C | G | 1 | a0001c0001t0036 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 188 | chr14 | 99173963 | ||||||
chr14:99271290 | CCGCCGCC others(1): Show |
C | 2 | a0001c0002t0019 a0001c0002t0052 |
3 | NA18948.hp2 NA19058.hp1 NA19088.hp2 |
5_prime_UTR_variant | MODIFIER | c.-80_-73delCGGCGGCG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 73 | chr14 | 99271290 | ||||||
chr14:99271298 | G | GCGCCGCT others(2): Show |
13 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(10): Show |
43 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(40): Show |
5_prime_UTR_variant | MODIFIER | c.-89_-81dupGCAGCGGC others(1): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 81 | chr14 | 99271298 | ||||||
chr14:99271298 | G | GCGCGCTG others(13): Show |
1 | a0001c0001t0077 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-81_-80insGCGGCAGC others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 81 | chr14 | 99271298 | ||||||
chr14:99271298 | GCGCCGCT others(23): Show |
G | 1 | a0001c0001t0007 | 1 | NA18960.hp2 | 5_prime_UTR_variant | MODIFIER | c.-110_-81delGCGGCGG others(23): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 81 | chr14 | 99271298 | ||||||
chr14:99271305 | T | C | 1 | a0001c0001t0077 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-87A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 87 | chr14 | 99271305 | ||||||
chr14:99271305 | T | TGCCGCCG others(14): Show |
3 | a0001c0001t0068 a0001c0001t0069 a0001c0001t0078 |
3 | HG02602.hp2 HG02683.hp1 HG03710.hp2 |
5_prime_UTR_variant | MODIFIER | c.-108_-88dupGGCGGCG others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 88 | chr14 | 99271305 | ||||||
chr14:99271314 | T | C | 4 | a0001c0001t0028 a0001c0001t0029 a0001c0001t0070 others(1): Show |
4 | HG02922.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-96A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 96 | chr14 | 99271314 | ||||||
chr14:99271314 | T | TGCCGCC | 3 | a0001c0001t0012 a0001c0001t0020 a0001c0001t0053 |
8 | NA18966.hp2 NA18968.hp1 NA18969.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-102_-97dupGGCGGC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 97 | chr14 | 99271314 | ||||||
chr14:99271314 | TGCCGCCG others(8): Show |
T | 1 | a0001c0002t0016 | 2 | HG00639.hp1 HG00642.hp2 |
5_prime_UTR_variant | MODIFIER | c.-111_-97delGGCGGCG others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 97 | chr14 | 99271314 | ||||||
chr14:99271384 | T | G | 1 | a0001c0001t0035 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-166A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 166 | chr14 | 99271384 | ||||||
chr14:99271467 | G | A | 4 | a0001c0001t0081 a0001c0001t0082 a0001c0002t0072 others(1): Show |
4 | HG02257.hp1 HG02486.hp1 HG02630.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-249C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 249 | chr14 | 99271467 | ||||||
chr14:99271515 | C | CA | 41 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(38): Show |
149 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(146): Show |
5_prime_UTR_variant | MODIFIER | c.-298dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 298 | chr14 | 99271515 | ||||||
chr14:99271515 | C | CAA | 14 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0026 others(11): Show |
54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-299_-298dupTT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 298 | chr14 | 99271515 | ||||||
chr14:99271515 | CA | C | 6 | a0001c0001t0030 a0001c0001t0032 a0001c0001t0033 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG03139.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-298delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 298 | chr14 | 99271515 | ||||||
chr14:99271656 | C | T | 2 | a0001c0001t0028 a0001c0001t0029 |
2 | HG03453.hp2 HG03516.hp1 |
5_prime_UTR_variant | MODIFIER | c.-438G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 438 | chr14 | 99271656 | ||||||
chr14:99271755 | AT | A | 4 | a0001c0001t0081 a0001c0001t0082 a0001c0002t0079 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-538delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 538 | chr14 | 99271755 | ||||||
chr14:99271899 | CTGTTTTT others(5): Show |
C | 1 | a0001c0001t0083 | 1 | NA18962.hp1 | 5_prime_UTR_variant | MODIFIER | c.-693_-682delAAAACA others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 682 | chr14 | 99271899 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:99176310 | T | A | 146 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(143): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.641-115A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176310 | |||||||
chr14:99176377 | G | C | 1 | a0001c0001t0077g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.641-182C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176377 | |||||||
chr14:99176430 | G | A | 3 | a0001c0001t0001g0162 a0001c0001t0012g0147 a0001c0001t0012g0148 |
3 | NA18953.hp1 NA19012.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.641-235C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176430 | |||||||
chr14:99176467 | C | A | 1 | a0001c0001t0042g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.641-272G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176467 | |||||||
chr14:99176472 | A | G | 11 | a0001c0001t0002g0071 a0001c0001t0010g0043 a0001c0001t0010g0067 others(8): Show |
11 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.641-277T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176472 | |||||||
chr14:99176507 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.641-312G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176507 | |||||||
chr14:99176577 | C | T | 1 | a0001c0002t0066g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.641-382G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176577 | |||||||
chr14:99176632 | C | T | 1 | a0001c0001t0074g0340 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.641-437G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176632 | |||||||
chr14:99176635 | C | T | 72 | a0001c0001t0009g0046 a0001c0001t0009g0053 a0001c0001t0009g0088 others(69): Show |
72 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.641-440G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176635 | |||||||
chr14:99176684 | G | T | 1 | a0001c0001t0050g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.641-489C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176684 | |||||||
chr14:99176844 | A | G | 3 | a0001c0001t0018g0090 a0001c0001t0029g0004 a0001c0001t0034g0007 |
3 | HG02451.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.641-649T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176844 | |||||||
chr14:99176873 | C | T | 2 | a0001c0001t0026g0303 a0001c0001t0026g0311 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.641-678G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176873 | |||||||
chr14:99176920 | C | CT | 12 | a0001c0001t0001g0188 a0001c0001t0002g0056 a0001c0001t0003g0267 others(9): Show |
12 | HG01175.hp1 HG01884.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-726dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176920 | |||||||
chr14:99176920 | CT | C | 13 | a0001c0001t0001g0171 a0001c0001t0005g0301 a0001c0001t0026g0303 others(10): Show |
13 | HG01071.hp2 HG01169.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-726delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176920 | |||||||
chr14:99177462 | C | G | 7 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0129 others(4): Show |
7 | HG00099.hp1 HG01952.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-1267G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177462 | |||||||
chr14:99177481 | T | A | 1 | a0001c0002t0008g0312 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.641-1286A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177481 | |||||||
chr14:99177517 | A | G | 261 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(258): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.641-1322T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177517 | |||||||
chr14:99177598 | T | C | 82 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0166 others(79): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.641-1403A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177598 | |||||||
chr14:99177623 | C | G | 3 | a0001c0001t0018g0090 a0001c0001t0029g0004 a0001c0001t0034g0007 |
3 | HG02451.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.641-1428G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177623 | |||||||
chr14:99177715 | A | C | 7 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0129 others(4): Show |
7 | HG00099.hp1 HG01952.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-1520T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177715 | |||||||
chr14:99177818 | T | C | 3 | a0001c0001t0018g0090 a0001c0001t0029g0004 a0001c0001t0034g0007 |
3 | HG02451.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.641-1623A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177818 | |||||||
chr14:99177950 | T | C | 26 | a0001c0001t0001g0188 a0001c0001t0002g0071 a0001c0001t0002g0072 others(23): Show |
26 | HG00099.hp1 HG01099.hp1 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.641-1755A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177950 | |||||||
chr14:99178152 | C | T | 1 | a0001c0002t0008g0322 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.641-1957G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178152 | |||||||
chr14:99178236 | G | A | 1 | a0001c0001t0012g0142 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.641-2041C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178236 | |||||||
chr14:99178252 | G | A | 1 | a0001c0001t0014g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.641-2057C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178252 | |||||||
chr14:99178275 | T | G | 4 | a0001c0001t0013g0189 a0001c0002t0045g0014 a0001c0002t0048g0057 others(1): Show |
4 | HG00639.hp2 HG01891.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-2080A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178275 | |||||||
chr14:99178385 | T | C | 232 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(229): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.641-2190A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178385 | |||||||
chr14:99178480 | G | A | 1 | a0001c0002t0072g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.641-2285C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178480 | |||||||
chr14:99178492 | C | CCA | 3 | a0001c0001t0018g0090 a0001c0001t0029g0004 a0001c0001t0034g0007 |
3 | HG02451.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.641-2299_641-2298d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178492 | |||||||
chr14:99178500 | C | G | 138 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(135): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.641-2305G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178500 | |||||||
chr14:99178617 | G | A | 232 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(229): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.641-2422C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178617 | |||||||
chr14:99178675 | C | G | 80 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0166 others(77): Show |
80 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.641-2480G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178675 | |||||||
chr14:99178756 | C | T | 25 | a0001c0001t0005g0331 a0001c0001t0006g0024 a0001c0001t0006g0028 others(22): Show |
25 | HG00733.hp2 HG00738.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.641-2561G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178756 | |||||||
chr14:99178823 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-2628A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178823 | |||||||
chr14:99178849 | G | A | 1 | a0001c0001t0009g0088 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.641-2654C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178849 | |||||||
chr14:99178851 | C | T | 1 | a0001c0001t0051g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.641-2656G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178851 | |||||||
chr14:99178895 | C | T | 1 | a0001c0001t0051g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.641-2700G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178895 | |||||||
chr14:99179043 | G | A | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.641-2848C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179043 | |||||||
chr14:99179083 | A | C | 136 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(133): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.641-2888T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179083 | |||||||
chr14:99179240 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.641-3045C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179240 | |||||||
chr14:99179330 | C | T | 3 | a0001c0001t0009g0054 a0001c0001t0010g0043 a0001c0001t0014g0087 |
3 | HG02572.hp1 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.641-3135G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179330 | |||||||
chr14:99179341 | G | T | 1 | a0001c0003t0003g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.641-3146C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179341 | |||||||
chr14:99179473 | T | TA | 64 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0172 others(61): Show |
64 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.641-3279dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | |||||||
chr14:99179473 | T | TAA | 8 | a0001c0001t0001g0202 a0001c0001t0002g0105 a0001c0001t0006g0028 others(5): Show |
8 | HG00423.hp1 HG00438.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-3280_641-3279d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | |||||||
chr14:99179473 | TA | T | 143 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(140): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.641-3279delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | |||||||
chr14:99179473 | TAA | T | 19 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0216 others(16): Show |
19 | HG01069.hp2 HG01099.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.641-3280_641-3279d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | |||||||
chr14:99179473 | TAAA | T | 10 | a0001c0001t0010g0068 a0001c0001t0010g0084 a0001c0001t0010g0127 others(7): Show |
10 | HG01884.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.641-3281_641-3279d others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | |||||||
chr14:99179473 | TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0025g0164 a0001c0001t0025g0228 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.641-3288_641-3279d others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | |||||||
chr14:99179500 | GCTT | G | 6 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0129 others(3): Show |
6 | HG01952.hp1 HG02602.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-3308_641-3306d others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179500 | |||||||
chr14:99179609 | G | A | 5 | a0001c0001t0013g0175 a0001c0001t0015g0030 a0001c0001t0015g0077 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-3414C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179609 | |||||||
chr14:99179716 | C | T | 1 | a0001c0001t0051g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.641-3521G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179716 | |||||||
chr14:99179767 | C | T | 2 | a0001c0001t0002g0055 a0001c0001t0051g0128 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.641-3572G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179767 | |||||||
chr14:99179796 | A | C | 131 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0166 others(128): Show |
131 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.641-3601T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179796 | |||||||
chr14:99179803 | T | C | 4 | a0001c0001t0001g0226 a0001c0001t0001g0237 a0001c0001t0001g0252 others(1): Show |
4 | HG00609.hp2 NA18981.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-3608A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179803 | |||||||
chr14:99180162 | G | A | 1 | a0001c0001t0005g0327 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.641-3967C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180162 | |||||||
chr14:99180229 | C | T | 263 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(260): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.641-4034G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180229 | |||||||
chr14:99180504 | T | C | 1 | a0001c0002t0003g0193 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.641-4309A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180504 | |||||||
chr14:99180562 | A | C | 1 | a0001c0002t0076g0317 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.641-4367T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180562 | |||||||
chr14:99180691 | C | T | 5 | a0001c0002t0004g0036 a0001c0002t0004g0049 a0001c0002t0031g0006 others(2): Show |
5 | HG02055.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-4496G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180691 | |||||||
chr14:99180711 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0005g0326 |
2 | HG01106.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.641-4516C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180711 | |||||||
chr14:99180718 | T | C | 3 | a0001c0002t0008g0309 a0001c0003t0003g0262 a0001c0003t0004g0114 |
3 | HG02486.hp2 HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.641-4523A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180718 | |||||||
chr14:99180724 | A | C | 1 | a0001c0001t0009g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.641-4529T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180724 | |||||||
chr14:99180877 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.641-4682C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180877 | |||||||
chr14:99180992 | T | G | 88 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0166 others(85): Show |
88 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.641-4797A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180992 | |||||||
chr14:99181049 | C | T | 113 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(110): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.641-4854G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181049 | |||||||
chr14:99181191 | G | A | 4 | a0001c0001t0002g0040 a0001c0001t0003g0232 a0001c0001t0025g0164 others(1): Show |
4 | HG00733.hp1 HG02145.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-4996C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181191 | |||||||
chr14:99181202 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0279 |
2 | HG00558.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.641-5007C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181202 | |||||||
chr14:99181218 | G | A | 1 | a0001c0002t0004g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.641-5023C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181218 | |||||||
chr14:99181427 | C | T | 98 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(95): Show |
98 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.641-5232G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181427 | |||||||
chr14:99181553 | C | A | 305 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(302): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.641-5358G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181553 | |||||||
chr14:99181709 | C | T | 2 | a0001c0001t0015g0093 a0001c0001t0062g0219 |
2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.641-5514G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181709 | |||||||
chr14:99181881 | G | A | 88 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(85): Show |
88 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.641-5686C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181881 | |||||||
chr14:99181891 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-5696A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181891 | |||||||
chr14:99181917 | C | T | 1 | a0001c0001t0018g0021 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.641-5722G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181917 | |||||||
chr14:99181919 | G | A | 91 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(88): Show |
91 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.641-5724C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181919 | |||||||
chr14:99181975 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.641-5780G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181975 | |||||||
chr14:99181988 | T | C | 1 | a0001c0002t0031g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.641-5793A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181988 | |||||||
chr14:99182051 | G | A | 1 | a0001c0001t0025g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.641-5856C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182051 | |||||||
chr14:99182157 | C | A | 101 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(98): Show |
102 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.641-5962G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182157 | |||||||
chr14:99182428 | C | T | 221 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(218): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.641-6233G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182428 | |||||||
chr14:99182443 | C | T | 16 | a0001c0001t0001g0183 a0001c0001t0001g0266 a0001c0001t0002g0129 others(13): Show |
16 | HG00597.hp2 HG01884.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.641-6248G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182443 | |||||||
chr14:99182505 | A | T | 1 | a0001c0001t0009g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.641-6310T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182505 | |||||||
chr14:99182689 | G | A | 2 | a0001c0001t0032g0005 a0001c0002t0031g0006 |
2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.641-6494C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182689 | |||||||
chr14:99182693 | A | G | 102 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(99): Show |
102 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.641-6498T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182693 | |||||||
chr14:99182727 | T | C | 88 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0001g0199 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.641-6532A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182727 | |||||||
chr14:99182731 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.641-6536G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182731 | |||||||
chr14:99183057 | AG | A | 127 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(124): Show |
127 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.641-6863delC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183057 | |||||||
chr14:99183059 | G | C | 2 | a0001c0001t0003g0232 a0001c0001t0009g0123 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.641-6864C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183059 | |||||||
chr14:99183170 | C | A | 256 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(253): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.641-6975G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183170 | |||||||
chr14:99183226 | C | A | 60 | a0001c0001t0001g0204 a0001c0001t0001g0209 a0001c0001t0001g0211 others(57): Show |
60 | HG00621.hp1 HG00621.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.641-7031G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183226 | |||||||
chr14:99183243 | C | T | 34 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(31): Show |
34 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.641-7048G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183243 | |||||||
chr14:99183260 | G | A | 17 | a0001c0001t0001g0177 a0001c0001t0001g0272 a0001c0001t0002g0042 others(14): Show |
17 | HG00738.hp2 HG01069.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.641-7065C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183260 | |||||||
chr14:99183337 | A | G | 1 | a0001c0001t0007g0203 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.641-7142T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183337 | |||||||
chr14:99183376 | T | C | 154 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0161 others(151): Show |
154 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.641-7181A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183376 | |||||||
chr14:99183575 | C | T | 1 | a0001c0001t0007g0196 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.641-7380G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183575 | |||||||
chr14:99183644 | G | A | 1 | a0001c0001t0070g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.641-7449C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183644 | |||||||
chr14:99183665 | T | C | 1 | a0001c0001t0006g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.641-7470A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183665 | |||||||
chr14:99183673 | CACATACA others(5): Show |
C | 1 | a0001c0001t0042g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.641-7490_641-7479d others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183673 | |||||||
chr14:99183728 | T | G | 1 | a0001c0001t0010g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.641-7533A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183728 | |||||||
chr14:99183770 | A | G | 17 | a0001c0001t0001g0177 a0001c0001t0002g0042 a0001c0001t0010g0043 others(14): Show |
17 | HG00738.hp2 HG01069.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.641-7575T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183770 | |||||||
chr14:99183797 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.641-7602G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183797 | |||||||
chr14:99183890 | C | A | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-7695G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183890 | |||||||
chr14:99183958 | C | A | 93 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(90): Show |
93 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.641-7763G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183958 | |||||||
chr14:99184251 | C | T | 18 | a0001c0001t0001g0177 a0001c0001t0002g0042 a0001c0001t0010g0043 others(15): Show |
18 | HG00738.hp2 HG01069.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.641-8056G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184251 | |||||||
chr14:99184582 | G | A | 6 | a0001c0001t0014g0087 a0001c0001t0022g0210 a0001c0001t0022g0224 others(3): Show |
7 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-8387C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184582 | |||||||
chr14:99184596 | C | T | 13 | a0001c0001t0001g0183 a0001c0001t0001g0266 a0001c0002t0001g0236 others(10): Show |
13 | HG00597.hp2 HG02056.hp1 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-8401G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184596 | |||||||
chr14:99184597 | G | C | 256 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(253): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.641-8402C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184597 | |||||||
chr14:99184603 | TG | T | 67 | a0001c0001t0001g0177 a0001c0001t0001g0183 a0001c0001t0001g0266 others(64): Show |
67 | HG00597.hp2 HG00738.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.641-8409delC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184603 | |||||||
chr14:99184681 | G | A | 4 | a0001c0001t0001g0222 a0001c0001t0002g0058 a0001c0001t0002g0117 others(1): Show |
4 | HG02071.hp1 HG02523.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-8486C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184681 | |||||||
chr14:99184714 | T | C | 68 | a0001c0001t0001g0177 a0001c0001t0001g0183 a0001c0001t0001g0266 others(65): Show |
68 | HG00597.hp2 HG00738.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.641-8519A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184714 | |||||||
chr14:99184793 | C | T | 1 | a0001c0001t0005g0331 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.641-8598G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184793 | |||||||
chr14:99184812 | G | A | 1 | a0001c0001t0077g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.641-8617C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184812 | |||||||
chr14:99184828 | T | C | 1 | a0001c0001t0011g0335 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.641-8633A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184828 | |||||||
chr14:99185378 | G | A | 1 | a0001c0001t0070g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.641-9183C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185378 | |||||||
chr14:99185446 | G | A | 1 | a0001c0001t0025g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.641-9251C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185446 | |||||||
chr14:99185446 | GA | G | 228 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.641-9252delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185446 | |||||||
chr14:99185446 | GAA | G | 12 | a0001c0001t0002g0056 a0001c0001t0013g0175 a0001c0001t0014g0083 others(9): Show |
13 | HG02615.hp1 HG02809.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-9253_641-9252d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185446 | |||||||
chr14:99185447 | A | G | 2 | a0001c0001t0025g0164 a0001c0002t0008g0314 |
2 | HG01070.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.641-9252T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185447 | |||||||
chr14:99185456 | A | G | 6 | a0001c0001t0014g0087 a0001c0001t0022g0210 a0001c0001t0022g0224 others(3): Show |
7 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-9261T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185456 | |||||||
chr14:99185459 | A | C | 155 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(152): Show |
155 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.641-9264T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185459 | |||||||
chr14:99185466 | T | C | 44 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0001g0185 others(41): Show |
44 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.641-9271A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185466 | |||||||
chr14:99185473 | AGTAATGT others(298): Show |
A | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.641-9583_641-9279d others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185473 | |||||||
chr14:99185532 | C | A | 1 | a0001c0001t0042g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.641-9337G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185532 | |||||||
chr14:99185564 | G | C | 3 | a0001c0002t0007g0254 a0001c0002t0007g0255 a0001c0002t0011g0338 |
3 | HG01168.hp2 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.641-9369C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185564 | |||||||
chr14:99185586 | G | A | 1 | a0001c0002t0003g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.641-9391C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185586 | |||||||
chr14:99185601 | T | C | 1 | a0001c0003t0003g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.641-9406A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185601 | |||||||
chr14:99185632 | G | A | 1 | a0001c0001t0010g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.641-9437C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185632 | |||||||
chr14:99185734 | T | C | 170 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(167): Show |
170 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.641-9539A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185734 | |||||||
chr14:99185740 | C | T | 2 | a0001c0001t0010g0068 a0001c0001t0010g0127 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.641-9545G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185740 | |||||||
chr14:99185772 | T | C | 2 | a0001c0001t0009g0135 a0001c0001t0010g0060 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.641-9577A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185772 | |||||||
chr14:99185856 | G | A | 2 | a0001c0001t0010g0068 a0001c0001t0010g0127 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.641-9661C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185856 | |||||||
chr14:99185913 | C | T | 1 | a0001c0002t0008g0295 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.641-9718G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185913 | |||||||
chr14:99185973 | G | A | 1 | a0001c0001t0006g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.641-9778C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185973 | |||||||
chr14:99186031 | G | T | 1 | a0001c0001t0070g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.641-9836C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186031 | |||||||
chr14:99186153 | A | T | 1 | a0001c0001t0042g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.641-9958T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186153 | |||||||
chr14:99186224 | T | G | 267 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(264): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.641-10029A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186224 | |||||||
chr14:99186376 | C | A | 1 | a0001c0003t0003g0262 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.641-10181G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186376 | |||||||
chr14:99186399 | A | G | 13 | a0001c0001t0001g0183 a0001c0001t0001g0266 a0001c0002t0001g0236 others(10): Show |
13 | HG00597.hp2 HG02056.hp1 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-10204T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186399 | |||||||
chr14:99186445 | T | G | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.641-10250A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186445 | |||||||
chr14:99186475 | G | A | 1 | a0001c0001t0041g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.641-10280C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186475 | |||||||
chr14:99186736 | C | T | 344 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(341): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.641-10541G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186736 | |||||||
chr14:99186769 | C | T | 3 | a0001c0001t0009g0091 a0001c0001t0009g0094 a0001c0001t0010g0084 |
3 | HG03098.hp2 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.641-10574G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186769 | |||||||
chr14:99186786 | C | T | 16 | a0001c0001t0001g0177 a0001c0001t0002g0042 a0001c0001t0006g0047 others(13): Show |
16 | HG00738.hp1 HG01069.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.641-10591G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186786 | |||||||
chr14:99186863 | CTTTCCAT others(6): Show |
C | 1 | a0001c0002t0003g0225 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.641-10681_641-1066 others(17): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186863 | |||||||
chr14:99187104 | T | G | 2 | a0001c0001t0010g0068 a0001c0001t0010g0127 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.641-10909A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187104 | |||||||
chr14:99187412 | G | A | 1 | a0001c0002t0080g0345 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.641-11217C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187412 | |||||||
chr14:99187588 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-11393A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187588 | |||||||
chr14:99187662 | C | CA | 234 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0163 others(231): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.641-11468dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187662 | |||||||
chr14:99187662 | C | CAA | 8 | a0001c0001t0001g0227 a0001c0001t0001g0260 a0001c0001t0005g0334 others(5): Show |
8 | HG00673.hp2 HG01109.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-11469_641-1146 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187662 | |||||||
chr14:99187739 | G | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0044 a0001c0001t0038g0038 others(1): Show |
4 | HG00639.hp2 HG00733.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-11544C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187739 | |||||||
chr14:99187758 | A | C | 3 | a0001c0001t0005g0326 a0001c0001t0006g0047 a0001c0001t0011g0323 |
3 | HG01123.hp1 HG01496.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.641-11563T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187758 | |||||||
chr14:99187778 | T | TTCCTCCT others(2): Show |
265 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0163 others(262): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.641-11592_641-1158 others(13): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187778 | |||||||
chr14:99187870 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-11675T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187870 | |||||||
chr14:99187886 | G | A | 20 | a0001c0001t0002g0065 a0001c0001t0006g0133 a0001c0001t0009g0046 others(17): Show |
20 | HG01099.hp1 HG02258.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.641-11691C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187886 | |||||||
chr14:99187886 | G | T | 1 | a0001c0001t0037g0100 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.641-11691C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187886 | |||||||
chr14:99187985 | T | C | 263 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0163 others(260): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.641-11790A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187985 | |||||||
chr14:99187989 | G | A | 1 | a0001c0001t0035g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.641-11794C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187989 | |||||||
chr14:99188058 | T | C | 1 | a0001c0001t0009g0135 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.641-11863A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188058 | |||||||
chr14:99188095 | G | A | 8 | a0001c0001t0001g0163 a0001c0001t0001g0266 a0001c0001t0002g0058 others(5): Show |
8 | HG00423.hp2 HG02523.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-11900C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188095 | |||||||
chr14:99188099 | T | C | 260 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0163 others(257): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.641-11904A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188099 | |||||||
chr14:99188176 | T | C | 1 | a0001c0003t0003g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.641-11981A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188176 | |||||||
chr14:99188293 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-12098T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188293 | |||||||
chr14:99188386 | C | A | 3 | a0001c0001t0025g0228 a0001c0001t0071g0291 a0001c0002t0017g0066 |
3 | HG02109.hp1 HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.641-12191G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188386 | |||||||
chr14:99188437 | C | T | 2 | a0001c0001t0014g0083 a0001c0001t0062g0219 |
2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.641-12242G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188437 | |||||||
chr14:99188440 | G | A | 1 | a0001c0001t0006g0048 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.641-12245C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188440 | |||||||
chr14:99188537 | C | CCTGGGG | 60 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0177 others(57): Show |
61 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.641-12348_641-1234 others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188537 | |||||||
chr14:99188537 | C | CCTGGGGC others(5): Show |
2 | a0001c0001t0001g0179 a0001c0002t0003g0193 |
2 | HG02451.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.641-12354_641-1234 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188537 | |||||||
chr14:99188537 | CCTGGGG | C | 60 | a0001c0001t0001g0163 a0001c0001t0001g0209 a0001c0001t0001g0216 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.641-12348_641-1234 others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188537 | |||||||
chr14:99188537 | CCTGGGGC others(5): Show |
C | 5 | a0001c0001t0001g0226 a0001c0001t0001g0252 a0001c0001t0005g0336 others(2): Show |
5 | HG00609.hp2 HG03831.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-12354_641-1234 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188537 | |||||||
chr14:99188537 | CCTGGGGC others(11): Show |
C | 1 | a0001c0001t0002g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.641-12360_641-1234 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188537 | |||||||
chr14:99188866 | T | G | 1 | a0001c0002t0008g0319 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.641-12671A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188866 | |||||||
chr14:99189011 | G | A | 1 | a0001c0001t0002g0027 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.641-12816C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189011 | |||||||
chr14:99189433 | T | G | 1 | a0001c0001t0005g0332 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.641-13238A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189433 | |||||||
chr14:99189622 | G | A | 1 | a0001c0002t0072g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.641-13427C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189622 | |||||||
chr14:99189689 | GAGGGCAG others(5): Show |
G | 2 | a0001c0001t0012g0148 a0001c0002t0003g0208 |
2 | NA18942.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.641-13506_641-1349 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189689 | |||||||
chr14:99189883 | T | C | 1 | a0001c0002t0008g0322 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.641-13688A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189883 | |||||||
chr14:99189901 | G | T | 3 | a0001c0001t0006g0062 a0001c0001t0011g0318 a0001c0001t0011g0320 |
3 | HG01081.hp1 HG01175.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.641-13706C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189901 | |||||||
chr14:99189908 | G | C | 39 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0216 others(36): Show |
40 | HG00673.hp1 HG01070.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.641-13713C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189908 | |||||||
chr14:99189942 | G | A | 39 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0216 others(36): Show |
40 | HG00673.hp1 HG01070.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.641-13747C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189942 | |||||||
chr14:99190111 | C | T | 8 | a0001c0001t0001g0163 a0001c0001t0001g0266 a0001c0001t0002g0058 others(5): Show |
8 | HG00423.hp2 HG02523.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-13916G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190111 | |||||||
chr14:99190219 | TG | T | 121 | a0001c0001t0001g0184 a0001c0001t0001g0209 a0001c0001t0001g0212 others(118): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.641-14025delC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190219 | |||||||
chr14:99190315 | C | T | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.641-14120G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190315 | |||||||
chr14:99190350 | G | A | 1 | a0001c0002t0003g0246 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.641-14155C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190350 | |||||||
chr14:99190482 | C | T | 5 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0005g0334 others(2): Show |
5 | HG02027.hp2 HG02056.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-14287G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190482 | |||||||
chr14:99190517 | T | A | 40 | a0001c0001t0001g0212 a0001c0001t0002g0056 a0001c0001t0002g0065 others(37): Show |
40 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.641-14322A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190517 | |||||||
chr14:99190541 | T | A | 1 | a0001c0002t0003g0265 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.641-14346A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190541 | |||||||
chr14:99190550 | T | C | 41 | a0001c0001t0001g0212 a0001c0001t0002g0056 a0001c0001t0002g0065 others(38): Show |
41 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.641-14355A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190550 | |||||||
chr14:99190600 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-14405T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190600 | |||||||
chr14:99190855 | G | A | 39 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0179 others(36): Show |
40 | HG00673.hp1 HG01070.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.641-14660C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190855 | |||||||
chr14:99190890 | C | T | 25 | a0001c0001t0001g0209 a0001c0001t0001g0226 a0001c0001t0001g0239 others(22): Show |
25 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.641-14695G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190890 | |||||||
chr14:99190907 | C | CG | 228 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0163 others(225): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.641-14713dupC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190907 | |||||||
chr14:99191169 | G | A | 21 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0001t0001g0235 others(18): Show |
21 | HG00609.hp1 HG00673.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.641-14974C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191169 | |||||||
chr14:99191174 | T | C | 1 | a0001c0001t0064g0186 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.641-14979A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191174 | |||||||
chr14:99191217 | CT | C | 281 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0163 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.641-15023delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191217 | |||||||
chr14:99191221 | G | C | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.641-15026C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191221 | |||||||
chr14:99191291 | C | T | 1 | a0001c0001t0015g0093 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.641-15096G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191291 | |||||||
chr14:99191402 | T | TA | 8 | a0001c0001t0001g0163 a0001c0001t0001g0266 a0001c0001t0002g0058 others(5): Show |
8 | HG00423.hp2 HG02523.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-15208dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191402 | |||||||
chr14:99191402 | TA | T | 180 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0166 others(177): Show |
181 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.641-15208delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191402 | |||||||
chr14:99191520 | C | T | 8 | a0001c0001t0001g0163 a0001c0001t0001g0266 a0001c0001t0002g0058 others(5): Show |
8 | HG00423.hp2 HG02523.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-15325G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191520 | |||||||
chr14:99191708 | G | A | 8 | a0001c0001t0001g0163 a0001c0001t0001g0266 a0001c0001t0002g0058 others(5): Show |
8 | HG00423.hp2 HG02523.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-15513C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191708 | |||||||
chr14:99191720 | C | CA | 30 | a0001c0001t0001g0209 a0001c0001t0001g0211 a0001c0001t0001g0226 others(27): Show |
30 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.641-15526dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191720 | |||||||
chr14:99192395 | G | A | 1 | a0001c0002t0003g0215 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.641-16200C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192395 | |||||||
chr14:99192400 | A | G | 1 | a0001c0001t0063g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.641-16205T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192400 | |||||||
chr14:99192480 | G | A | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.641-16285C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192480 | |||||||
chr14:99192550 | G | A | 1 | a0001c0001t0071g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.641-16355C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192550 | |||||||
chr14:99192673 | G | T | 1 | a0001c0001t0005g0327 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.641-16478C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192673 | |||||||
chr14:99192869 | GTGAA | G | 208 | a0001c0001t0001g0150 a0001c0001t0001g0163 a0001c0001t0001g0166 others(205): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.641-16678_641-1667 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192869 | |||||||
chr14:99192885 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.641-16690T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192885 | |||||||
chr14:99192905 | A | G | 211 | a0001c0001t0001g0150 a0001c0001t0001g0163 a0001c0001t0001g0166 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.641-16710T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192905 | |||||||
chr14:99192935 | A | T | 9 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(6): Show |
9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-16740T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192935 | |||||||
chr14:99192939 | TAGTGAAT others(1): Show |
T | 111 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0171 others(108): Show |
111 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.641-16752_641-1674 others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192939 | |||||||
chr14:99193034 | G | A | 111 | a0001c0001t0001g0184 a0001c0001t0001g0209 a0001c0001t0001g0212 others(108): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.641-16839C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193034 | |||||||
chr14:99193185 | C | G | 2 | a0001c0001t0006g0133 a0001c0001t0010g0132 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.641-16990G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193185 | |||||||
chr14:99193327 | T | C | 9 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(6): Show |
9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-17132A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193327 | |||||||
chr14:99193372 | A | C | 1 | a0001c0001t0001g0155 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.641-17177T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193372 | |||||||
chr14:99193413 | G | A | 1 | a0001c0001t0011g0323 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.641-17218C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193413 | |||||||
chr14:99193546 | G | A | 5 | a0001c0001t0001g0220 a0001c0001t0001g0284 a0001c0001t0005g0337 others(2): Show |
5 | HG00597.hp1 NA18969.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.641-17351C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193546 | |||||||
chr14:99193645 | G | A | 2 | a0001c0001t0001g0202 a0001c0002t0008g0307 |
2 | HG00438.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.641-17450C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193645 | |||||||
chr14:99194122 | C | T | 2 | a0001c0006t0023g0190 a0001c0006t0023g0191 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.641-17927G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194122 | |||||||
chr14:99194152 | C | T | 1 | a0001c0001t0011g0328 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.641-17957G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194152 | |||||||
chr14:99194314 | G | A | 2 | a0001c0001t0002g0051 a0001c0001t0002g0052 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.641-18119C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194314 | |||||||
chr14:99194546 | G | A | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.641-18351C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194546 | |||||||
chr14:99194697 | C | T | 2 | a0001c0001t0006g0133 a0001c0001t0010g0132 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.641-18502G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194697 | |||||||
chr14:99194805 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.641-18610C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194805 | |||||||
chr14:99194830 | G | C | 1 | a0001c0001t0009g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.641-18635C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194830 | |||||||
chr14:99194924 | C | T | 2 | a0001c0001t0064g0186 a0001c0002t0003g0151 |
2 | HG01109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.641-18729G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194924 | |||||||
chr14:99194965 | A | C | 1 | a0001c0001t0001g0155 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.641-18770T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194965 | |||||||
chr14:99195089 | A | C | 1 | a0001c0001t0025g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.641-18894T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99195089 | |||||||
chr14:99195313 | G | C | 1 | a0001c0002t0004g0050 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.641-19118C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99195313 | |||||||
chr14:99195567 | C | G | 1 | a0001c0001t0007g0268 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.641-19372G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99195567 | |||||||
chr14:99195752 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.641-19557G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99195752 | |||||||
chr14:99195952 | T | C | 5 | a0001c0001t0002g0065 a0001c0001t0009g0046 a0001c0001t0022g0210 others(2): Show |
5 | HG02809.hp1 HG02922.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-19757A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99195952 | |||||||
chr14:99196164 | A | C | 237 | a0001c0001t0001g0150 a0001c0001t0001g0163 a0001c0001t0001g0166 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.641-19969T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196164 | |||||||
chr14:99196394 | G | A | 1 | a0001c0002t0072g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.641-20199C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196394 | |||||||
chr14:99196531 | GA | G | 93 | a0001c0001t0001g0184 a0001c0001t0001g0212 a0001c0001t0001g0221 others(90): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.641-20337delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196531 | |||||||
chr14:99196639 | G | A | 1 | a0001c0001t0007g0256 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.641-20444C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196639 | |||||||
chr14:99196768 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.641-20573C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196768 | |||||||
chr14:99196864 | C | A | 1 | a0001c0001t0002g0098 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.641-20669G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196864 | |||||||
chr14:99197124 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.641-20929A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197124 | |||||||
chr14:99197214 | C | T | 2 | a0001c0002t0043g0111 a0001c0002t0059g0244 |
2 | NA18950.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.641-21019G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197214 | |||||||
chr14:99197379 | A | G | 4 | a0001c0001t0002g0129 a0001c0001t0081g0346 a0001c0002t0003g0286 others(1): Show |
4 | HG02257.hp1 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-21184T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197379 | |||||||
chr14:99197464 | A | G | 2 | a0001c0001t0006g0133 a0001c0001t0010g0132 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.641-21269T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197464 | |||||||
chr14:99197510 | A | G | 282 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0163 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.641-21315T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197510 | |||||||
chr14:99197551 | G | T | 10 | a0001c0001t0001g0212 a0001c0001t0001g0242 a0001c0001t0002g0098 others(7): Show |
10 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.641-21356C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197551 | |||||||
chr14:99197588 | G | C | 1 | a0001c0001t0071g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.641-21393C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197588 | |||||||
chr14:99197651 | C | T | 1 | a0001c0002t0003g0218 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.641-21456G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197651 | |||||||
chr14:99197747 | C | T | 3 | a0001c0001t0009g0094 a0001c0001t0010g0084 a0001c0001t0015g0093 |
3 | HG03098.hp2 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.641-21552G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197747 | |||||||
chr14:99197865 | G | A | 5 | a0001c0001t0002g0129 a0001c0001t0030g0009 a0001c0001t0081g0346 others(2): Show |
5 | HG02257.hp1 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-21670C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197865 | |||||||
chr14:99197919 | T | C | 1 | a0001c0001t0002g0126 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.641-21724A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197919 | |||||||
chr14:99198227 | C | T | 9 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(6): Show |
9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-22032G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198227 | |||||||
chr14:99198321 | T | C | 3 | a0001c0001t0039g0138 a0001c0002t0003g0274 a0001c0002t0004g0136 |
3 | NA18951.hp1 NA19009.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.641-22126A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198321 | |||||||
chr14:99198333 | G | C | 3 | a0001c0001t0001g0234 a0001c0001t0002g0051 a0001c0001t0002g0052 |
3 | HG01516.hp1 HG01517.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.641-22138C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198333 | |||||||
chr14:99198646 | C | T | 9 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(6): Show |
9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-22451G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198646 | |||||||
chr14:99198647 | G | A | 136 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0184 others(133): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.641-22452C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198647 | |||||||
chr14:99198679 | A | G | 1 | a0001c0001t0007g0256 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.641-22484T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198679 | |||||||
chr14:99198686 | TGCACCTT others(2): Show |
T | 7 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0005g0339 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-22500_641-2249 others(13): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198686 | |||||||
chr14:99198705 | G | A | 98 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0185 others(95): Show |
98 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.641-22510C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198705 | |||||||
chr14:99198858 | G | C | 1 | a0001c0002t0008g0319 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.641-22663C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198858 | |||||||
chr14:99198994 | G | A | 245 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0166 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.641-22799C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198994 | |||||||
chr14:99199003 | G | A | 1 | a0001c0001t0015g0093 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.641-22808C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199003 | |||||||
chr14:99199423 | T | C | 1 | a0001c0001t0006g0120 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.641-23228A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199423 | |||||||
chr14:99199462 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.641-23267C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199462 | |||||||
chr14:99199639 | G | GCT | 20 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0260 others(17): Show |
20 | HG00438.hp1 HG00738.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.641-23446_641-2344 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199639 | |||||||
chr14:99199640 | C | CTCTG | 16 | a0001c0001t0001g0185 a0001c0001t0001g0223 a0001c0001t0001g0235 others(13): Show |
16 | HG01257.hp1 HG01934.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.641-23446_641-2344 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | |||||||
chr14:99199640 | C | CTCTGTG | 8 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0006g0106 others(5): Show |
8 | HG00609.hp1 HG00673.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-23446_641-2344 others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | |||||||
chr14:99199640 | C | CTCTGTGT others(3): Show |
1 | a0001c0001t0002g0102 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.641-23446_641-2344 others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | |||||||
chr14:99199640 | C | CTG | 14 | a0001c0001t0001g0220 a0001c0001t0001g0226 a0001c0001t0001g0237 others(11): Show |
14 | HG00609.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.641-23447_641-2344 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | |||||||
chr14:99199640 | CTG | C | 27 | a0001c0001t0001g0172 a0001c0001t0001g0183 a0001c0001t0001g0206 others(24): Show |
27 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.641-23447_641-2344 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | |||||||
chr14:99199640 | CTGTG | C | 25 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(22): Show |
25 | HG01433.hp1 HG01975.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.641-23449_641-2344 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | |||||||
chr14:99199640 | CTGTGTG | C | 7 | a0001c0001t0004g0115 a0001c0001t0007g0196 a0001c0002t0003g0208 others(4): Show |
7 | HG00423.hp1 HG01175.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-23451_641-2344 others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | |||||||
chr14:99199640 | CTGTGTGT others(1): Show |
C | 3 | a0001c0001t0006g0062 a0001c0001t0011g0318 a0001c0001t0011g0320 |
3 | HG01081.hp1 HG01175.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.641-23453_641-2344 others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | |||||||
chr14:99199642 | G | C | 185 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0166 others(182): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.641-23447C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199642 | |||||||
chr14:99199644 | G | C | 2 | a0001c0002t0007g0254 a0001c0002t0011g0338 |
2 | HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.641-23449C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199644 | |||||||
chr14:99199646 | G | C | 1 | a0001c0006t0023g0191 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.641-23451C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199646 | |||||||
chr14:99199648 | G | C | 1 | a0001c0006t0023g0190 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.641-23453C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199648 | |||||||
chr14:99199650 | G | C | 3 | a0001c0001t0006g0062 a0001c0001t0011g0318 a0001c0001t0011g0320 |
3 | HG01081.hp1 HG01175.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.641-23455C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199650 | |||||||
chr14:99199661 | TGTGTGTG others(37): Show |
T | 1 | a0001c0002t0080g0345 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.641-23510_641-2346 others(48): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199661 | |||||||
chr14:99199669 | TGTGTGTG others(29): Show |
T | 8 | a0001c0001t0001g0216 a0001c0001t0001g0227 a0001c0001t0009g0054 others(5): Show |
8 | HG02572.hp1 NA18948.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-23510_641-2347 others(40): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199669 | |||||||
chr14:99199670 | GTGTGTGT others(51): Show |
G | 2 | a0001c0001t0005g0324 a0001c0001t0007g0238 |
2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.641-23533_641-2347 others(62): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199670 | |||||||
chr14:99199671 | TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0011g0341 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.641-23490_641-2347 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199671 | |||||||
chr14:99199671 | TGTGTGTG others(27): Show |
T | 12 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(9): Show |
12 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-23510_641-2347 others(38): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199671 | |||||||
chr14:99199672 | GTGTGTGT others(49): Show |
G | 2 | a0001c0001t0024g0250 a0001c0001t0024g0277 |
2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.641-23533_641-2347 others(60): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199672 | |||||||
chr14:99199673 | TGTGTGTG others(25): Show |
T | 8 | a0001c0001t0005g0315 a0001c0001t0005g0327 a0001c0001t0005g0334 others(5): Show |
8 | HG00099.hp1 HG00741.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.641-23510_641-2347 others(36): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199673 | |||||||
chr14:99199673 | TGTGTGTG others(33): Show |
T | 1 | a0001c0001t0035g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.641-23518_641-2347 others(44): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199673 | |||||||
chr14:99199675 | T | TGCGC | 4 | a0001c0001t0001g0177 a0001c0001t0002g0045 a0001c0001t0068g0288 others(1): Show |
4 | HG00673.hp1 HG02683.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-23481_641-2348 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199675 | |||||||
chr14:99199675 | TGTGTGTG others(23): Show |
T | 4 | a0001c0001t0001g0230 a0001c0001t0002g0055 a0001c0001t0006g0082 others(1): Show |
4 | HG02015.hp1 HG02683.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-23510_641-2348 others(34): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199675 | |||||||
chr14:99199677 | T | C | 10 | a0001c0001t0001g0177 a0001c0001t0002g0045 a0001c0001t0005g0326 others(7): Show |
10 | HG00673.hp1 HG01074.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.641-23482A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199677 | |||||||
chr14:99199677 | TGTGTGTG others(15): Show |
T | 5 | a0001c0001t0009g0088 a0001c0001t0013g0181 a0001c0001t0013g0259 others(2): Show |
5 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-23504_641-2348 others(26): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199677 | |||||||
chr14:99199677 | TGTGTGTG others(21): Show |
T | 29 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0279 others(26): Show |
30 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.641-23510_641-2348 others(32): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199677 | |||||||
chr14:99199679 | T | C | 17 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0002g0045 others(14): Show |
17 | HG00673.hp1 HG01070.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.641-23484A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199679 | |||||||
chr14:99199679 | TGTGTGCG others(19): Show |
T | 8 | a0001c0001t0001g0282 a0001c0001t0002g0016 a0001c0001t0002g0040 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.641-23510_641-2348 others(30): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199679 | |||||||
chr14:99199681 | T | C | 34 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0212 others(31): Show |
34 | HG00642.hp1 HG00673.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.641-23486A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | |||||||
chr14:99199681 | T | TGCGCGCG others(4): Show |
1 | a0001c0002t0004g0074 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.641-23487_641-2348 others(15): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | |||||||
chr14:99199681 | T | TGCGCGCG others(5): Show |
1 | a0001c0002t0008g0322 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.641-23487_641-2348 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | |||||||
chr14:99199681 | TGTGC | T | 5 | a0001c0001t0001g0162 a0001c0001t0005g0326 a0001c0001t0006g0047 others(2): Show |
5 | HG01123.hp1 HG01496.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.641-23490_641-2348 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | |||||||
chr14:99199681 | TGTGCGCG others(11): Show |
T | 1 | a0001c0002t0008g0319 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.641-23504_641-2348 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | |||||||
chr14:99199681 | TGTGCGCG others(17): Show |
T | 2 | a0001c0001t0001g0188 a0001c0001t0028g0003 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.641-23510_641-2348 others(28): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | |||||||
chr14:99199683 | T | C | 70 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0177 others(67): Show |
70 | HG00597.hp2 HG00621.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.641-23488A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGCGCGCG others(11): Show |
1 | a0001c0001t0001g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGCG others(7): Show |
1 | a0001c0005t0010g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.641-23489_641-2348 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0243 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0009g0135 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.641-23489_641-2348 others(20): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGTG others(11): Show |
2 | a0001c0001t0003g0275 a0001c0001t0003g0285 |
2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.641-23489_641-2348 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGTG others(3): Show |
1 | a0001c0002t0060g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGTG others(5): Show |
1 | a0001c0001t0003g0247 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0025g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0198 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.641-23489_641-2348 others(24): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0034g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGTG others(19): Show |
1 | a0001c0001t0001g0150 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(30): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGTG others(13): Show |
1 | a0001c0002t0004g0137 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.641-23489_641-2348 others(24): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | T | TGTGTGTG others(21): Show |
3 | a0001c0002t0061g0169 a0001c0004t0001g0001 a0001c0004t0001g0178 |
4 | HG02630.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-23489_641-2348 others(32): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | TGCGCGCG others(9): Show |
T | 5 | a0001c0001t0001g0166 a0001c0001t0003g0232 a0001c0001t0007g0154 others(2): Show |
5 | HG01978.hp2 HG02559.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.641-23504_641-2348 others(20): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199683 | TGCGCGCG others(15): Show |
T | 2 | a0001c0002t0003g0180 a0001c0002t0004g0121 |
2 | NA18983.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.641-23510_641-2348 others(26): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | |||||||
chr14:99199684 | GCGCGCGC others(7): Show |
G | 5 | a0001c0001t0002g0071 a0001c0001t0002g0073 a0001c0001t0012g0147 others(2): Show |
5 | HG02004.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-23503_641-2349 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199684 | |||||||
chr14:99199684 | GCGCGCGC others(13): Show |
G | 8 | a0001c0001t0001g0234 a0001c0001t0002g0051 a0001c0001t0002g0052 others(5): Show |
8 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.641-23509_641-2349 others(24): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199684 | |||||||
chr14:99199685 | C | CGCGT | 8 | a0001c0001t0002g0065 a0001c0001t0006g0120 a0001c0001t0009g0046 others(5): Show |
8 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.641-23491_641-2349 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199685 | |||||||
chr14:99199685 | C | CGT | 14 | a0001c0001t0001g0212 a0001c0001t0002g0056 a0001c0001t0002g0119 others(11): Show |
14 | HG00597.hp2 HG00639.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.641-23491_641-2349 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199685 | |||||||
chr14:99199685 | C | T | 29 | a0001c0001t0001g0171 a0001c0001t0001g0185 a0001c0001t0001g0242 others(26): Show |
29 | HG01074.hp1 HG01943.hp1 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.641-23490G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199685 | |||||||
chr14:99199686 | GCGCGCGC others(5): Show |
G | 4 | a0001c0001t0002g0072 a0001c0001t0029g0004 a0001c0002t0003g0215 others(1): Show |
4 | HG03516.hp1 NA18999.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-23503_641-2349 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199686 | |||||||
chr14:99199686 | GCGCGCGC others(11): Show |
G | 5 | a0001c0001t0001g0171 a0001c0001t0006g0070 a0001c0001t0007g0200 others(2): Show |
5 | HG01074.hp1 HG01943.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-23509_641-2349 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199686 | |||||||
chr14:99199687 | C | T | 2 | a0001c0001t0005g0339 a0001c0001t0049g0113 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.641-23492G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199687 | |||||||
chr14:99199689 | C | CGCGCGCG others(10): Show |
1 | a0001c0001t0013g0189 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.641-23495_641-2349 others(21): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199689 | |||||||
chr14:99199689 | C | T | 3 | a0001c0001t0002g0126 a0001c0001t0005g0339 a0001c0001t0049g0113 |
3 | HG02886.hp1 HG02965.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.641-23494G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199689 | |||||||
chr14:99199693 | CGCGCACG others(11): Show |
C | 2 | a0001c0001t0005g0339 a0001c0001t0049g0113 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.641-23516_641-2349 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199693 | |||||||
chr14:99199696 | G | A | 28 | a0001c0001t0001g0187 a0001c0001t0001g0220 a0001c0001t0001g0226 others(25): Show |
28 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.641-23501C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199696 | |||||||
chr14:99199696 | G | C | 1 | a0001c0001t0005g0337 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.641-23501C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199696 | |||||||
chr14:99199696 | G | GCA | 4 | a0001c0001t0001g0209 a0001c0001t0018g0021 a0001c0001t0063g0170 others(1): Show |
4 | HG01496.hp1 HG01516.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-23503_641-2350 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199696 | |||||||
chr14:99199697 | C | G | 1 | a0001c0001t0005g0337 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.641-23502G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199697 | |||||||
chr14:99199699 | C | T | 9 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(6): Show |
9 | HG02004.hp2 HG02809.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.641-23504G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199699 | |||||||
chr14:99199703 | C | T | 12 | a0001c0001t0001g0166 a0001c0001t0002g0071 a0001c0001t0002g0072 others(9): Show |
12 | HG01978.hp2 HG02559.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-23508G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199703 | |||||||
chr14:99199704 | A | G | 12 | a0001c0001t0001g0166 a0001c0001t0002g0071 a0001c0001t0002g0072 others(9): Show |
12 | HG01978.hp2 HG02559.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-23509T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199704 | |||||||
chr14:99199705 | C | T | 25 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0234 others(22): Show |
25 | HG01074.hp1 HG01516.hp1 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.641-23510G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199705 | |||||||
chr14:99199711 | T | C | 13 | a0001c0001t0001g0163 a0001c0001t0001g0171 a0001c0001t0001g0188 others(10): Show |
13 | HG00423.hp2 HG01261.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.641-23516A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199711 | |||||||
chr14:99199713 | C | T | 2 | a0001c0001t0001g0177 a0001c0002t0004g0074 |
2 | HG03669.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.641-23518G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199713 | |||||||
chr14:99199733 | T | G | 7 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0005g0339 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-23538A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199733 | |||||||
chr14:99200063 | C | T | 147 | a0001c0001t0001g0158 a0001c0001t0001g0171 a0001c0001t0001g0177 others(144): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.641-23868G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200063 | |||||||
chr14:99200108 | CT | C | 11 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0222 others(8): Show |
11 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.641-23914delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200108 | |||||||
chr14:99200120 | T | A | 1 | a0001c0001t0005g0310 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.641-23925A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200120 | |||||||
chr14:99200142 | T | A | 1 | a0001c0001t0002g0039 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.641-23947A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200142 | |||||||
chr14:99200234 | T | C | 4 | a0001c0001t0002g0040 a0001c0001t0002g0044 a0001c0001t0038g0038 others(1): Show |
4 | HG00639.hp2 HG00733.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-24039A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200234 | |||||||
chr14:99200329 | C | G | 7 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0005g0339 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-24134G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200329 | |||||||
chr14:99200329 | C | T | 1 | a0001c0001t0002g0126 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.641-24134G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200329 | |||||||
chr14:99200382 | C | T | 200 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0171 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.641-24187G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200382 | |||||||
chr14:99200411 | G | A | 9 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(6): Show |
9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-24216C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200411 | |||||||
chr14:99200451 | G | A | 2 | a0001c0001t0055g0195 a0001c0002t0058g0269 |
2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.641-24256C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200451 | |||||||
chr14:99200507 | G | A | 1 | a0001c0001t0004g0115 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.641-24312C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200507 | |||||||
chr14:99200594 | C | A | 7 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0005g0339 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-24399G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200594 | |||||||
chr14:99200598 | G | A | 2 | a0001c0001t0024g0250 a0001c0001t0024g0277 |
2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.641-24403C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200598 | |||||||
chr14:99200603 | G | A | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.641-24408C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200603 | |||||||
chr14:99200709 | G | A | 99 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0185 others(96): Show |
99 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.641-24514C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200709 | |||||||
chr14:99200781 | G | A | 1 | a0001c0001t0006g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.641-24586C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200781 | |||||||
chr14:99200842 | G | A | 45 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(42): Show |
46 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(43): Show |
intron_variant | MODIFIER | c.641-24647C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200842 | |||||||
chr14:99200882 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.641-24687G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200882 | |||||||
chr14:99201016 | G | C | 1 | a0001c0001t0001g0243 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.641-24821C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201016 | |||||||
chr14:99201127 | G | A | 1 | a0001c0001t0009g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.641-24932C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201127 | |||||||
chr14:99201137 | G | C | 102 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0179 others(99): Show |
102 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.641-24942C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201137 | |||||||
chr14:99201179 | C | T | 7 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0005g0339 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-24984G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201179 | |||||||
chr14:99201288 | T | G | 1 | a0001c0001t0014g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.641-25093A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201288 | |||||||
chr14:99201316 | C | T | 5 | a0001c0001t0001g0177 a0001c0001t0006g0062 a0001c0001t0011g0318 others(2): Show |
5 | HG01081.hp1 HG01175.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-25121G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201316 | |||||||
chr14:99201347 | G | C | 1 | a0001c0001t0025g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.641-25152C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201347 | |||||||
chr14:99201349 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.641-25154G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201349 | |||||||
chr14:99201350 | G | A | 102 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0179 others(99): Show |
102 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.641-25155C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201350 | |||||||
chr14:99201506 | G | A | 1 | a0001c0001t0006g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.641-25311C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201506 | |||||||
chr14:99201514 | C | T | 1 | a0001c0002t0008g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.641-25319G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201514 | |||||||
chr14:99201536 | T | G | 2 | a0001c0001t0039g0138 a0001c0002t0004g0136 |
2 | NA19009.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.641-25341A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201536 | |||||||
chr14:99202304 | G | A | 7 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0005g0339 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-26109C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202304 | |||||||
chr14:99202333 | C | T | 107 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(104): Show |
107 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.641-26138G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202333 | |||||||
chr14:99202368 | C | T | 5 | a0001c0001t0073g0300 a0001c0002t0004g0037 a0001c0002t0008g0296 others(2): Show |
5 | HG00738.hp2 HG01975.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.641-26173G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202368 | |||||||
chr14:99202614 | A | G | 98 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(95): Show |
98 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.641-26419T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202614 | |||||||
chr14:99202668 | G | C | 76 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0209 others(73): Show |
77 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.641-26473C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202668 | |||||||
chr14:99202683 | T | C | 107 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(104): Show |
107 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.641-26488A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202683 | |||||||
chr14:99202774 | G | A | 1 | a0001c0003t0003g0262 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.641-26579C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202774 | |||||||
chr14:99202806 | G | T | 9 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(6): Show |
9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-26611C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202806 | |||||||
chr14:99202862 | G | A | 1 | a0001c0001t0037g0100 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.641-26667C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202862 | |||||||
chr14:99203016 | G | A | 6 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0252 others(3): Show |
6 | HG00609.hp2 HG03831.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-26821C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203016 | |||||||
chr14:99203167 | T | C | 252 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(249): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.641-26972A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203167 | |||||||
chr14:99203194 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.641-26999G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203194 | |||||||
chr14:99203199 | G | T | 105 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(102): Show |
105 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.641-27004C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203199 | |||||||
chr14:99203530 | C | T | 9 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(6): Show |
9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-27335G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203530 | |||||||
chr14:99203604 | G | T | 1 | a0001c0002t0003g0248 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.641-27409C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203604 | |||||||
chr14:99203631 | T | C | 3 | a0001c0001t0002g0129 a0001c0001t0081g0346 a0001c0002t0003g0286 |
3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.641-27436A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203631 | |||||||
chr14:99203668 | A | C | 103 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(100): Show |
103 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.641-27473T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203668 | |||||||
chr14:99203695 | A | G | 266 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(263): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.641-27500T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203695 | |||||||
chr14:99203705 | C | G | 1 | a0001c0001t0050g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.641-27510G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203705 | |||||||
chr14:99203754 | C | A | 1 | a0001c0002t0004g0074 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.641-27559G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203754 | |||||||
chr14:99203791 | C | G | 2 | a0001c0001t0013g0181 a0001c0001t0014g0104 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.640+27554G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203791 | |||||||
chr14:99203827 | G | A | 2 | a0001c0001t0006g0047 a0001c0001t0011g0323 |
2 | HG01496.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.640+27518C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203827 | |||||||
chr14:99203891 | G | A | 5 | a0001c0001t0013g0175 a0001c0001t0015g0030 a0001c0001t0018g0090 others(2): Show |
5 | HG02723.hp1 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.640+27454C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203891 | |||||||
chr14:99203895 | C | T | 1 | a0001c0002t0003g0193 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.640+27450G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203895 | |||||||
chr14:99203913 | A | AC | 99 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(96): Show |
99 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.640+27431dupG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203913 | |||||||
chr14:99204019 | A | G | 57 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(54): Show |
57 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.640+27326T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204019 | |||||||
chr14:99204037 | C | T | 1 | a0001c0002t0017g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.640+27308G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204037 | |||||||
chr14:99204108 | G | A | 50 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0001g0212 others(47): Show |
50 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.640+27237C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204108 | |||||||
chr14:99204190 | A | C | 50 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0001g0212 others(47): Show |
50 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.640+27155T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204190 | |||||||
chr14:99204198 | T | A | 114 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(111): Show |
114 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.640+27147A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204198 | |||||||
chr14:99204302 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.640+27043G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204302 | |||||||
chr14:99204408 | C | G | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+26937G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204408 | |||||||
chr14:99204454 | G | A | 52 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(49): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.640+26891C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204454 | |||||||
chr14:99204572 | T | C | 50 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0001g0212 others(47): Show |
50 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.640+26773A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204572 | |||||||
chr14:99204639 | G | A | 54 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(51): Show |
54 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.640+26706C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204639 | |||||||
chr14:99204674 | A | G | 10 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(7): Show |
10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+26671T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204674 | |||||||
chr14:99204828 | G | A | 53 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(50): Show |
53 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.640+26517C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204828 | |||||||
chr14:99205108 | G | A | 4 | a0001c0001t0025g0164 a0001c0001t0032g0005 a0001c0001t0070g0290 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+26237C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205108 | |||||||
chr14:99205238 | G | A | 10 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(7): Show |
10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+26107C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205238 | |||||||
chr14:99205252 | C | T | 1 | a0001c0001t0009g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.640+26093G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205252 | |||||||
chr14:99205350 | C | A | 45 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0001g0212 others(42): Show |
45 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.640+25995G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205350 | |||||||
chr14:99205392 | C | T | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+25953G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205392 | |||||||
chr14:99205451 | G | A | 51 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(48): Show |
52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.640+25894C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205451 | |||||||
chr14:99205456 | A | T | 14 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(11): Show |
14 | HG00423.hp2 HG01884.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.640+25889T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205456 | |||||||
chr14:99205811 | C | T | 1 | a0001c0002t0003g0246 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.640+25534G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205811 | |||||||
chr14:99205995 | G | C | 1 | a0001c0001t0001g0271 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.640+25350C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205995 | |||||||
chr14:99206068 | T | C | 2 | a0001c0001t0009g0096 a0001c0002t0045g0014 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.640+25277A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206068 | |||||||
chr14:99206201 | C | T | 246 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.640+25144G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206201 | |||||||
chr14:99206460 | C | G | 130 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0171 others(127): Show |
131 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.640+24885G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206460 | |||||||
chr14:99206572 | A | G | 1 | a0001c0001t0007g0238 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.640+24773T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206572 | |||||||
chr14:99206580 | C | T | 132 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0171 others(129): Show |
133 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.640+24765G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206580 | |||||||
chr14:99206591 | G | A | 50 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0001g0212 others(47): Show |
50 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.640+24754C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206591 | |||||||
chr14:99206611 | G | A | 1 | a0001c0002t0011g0338 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.640+24734C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206611 | |||||||
chr14:99206629 | C | T | 251 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.640+24716G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206629 | |||||||
chr14:99206718 | T | C | 2 | a0001c0001t0034g0007 a0001c0001t0082g0347 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+24627A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206718 | |||||||
chr14:99206937 | G | C | 1 | a0001c0001t0073g0300 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.640+24408C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206937 | |||||||
chr14:99206941 | T | C | 191 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(188): Show |
192 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.640+24404A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206941 | |||||||
chr14:99206987 | A | C | 80 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0177 others(77): Show |
81 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.640+24358T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206987 | |||||||
chr14:99206997 | A | G | 80 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0177 others(77): Show |
81 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.640+24348T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206997 | |||||||
chr14:99207185 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.640+24160T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207185 | |||||||
chr14:99207369 | G | A | 41 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0216 others(38): Show |
42 | HG00621.hp1 HG00673.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.640+23976C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207369 | |||||||
chr14:99207466 | T | C | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+23879A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207466 | |||||||
chr14:99207520 | A | G | 67 | a0001c0001t0001g0163 a0001c0001t0001g0171 a0001c0001t0001g0188 others(64): Show |
67 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.640+23825T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207520 | |||||||
chr14:99207658 | C | A | 2 | a0001c0001t0025g0228 a0001c0001t0064g0186 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.640+23687G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207658 | |||||||
chr14:99207669 | C | T | 2 | a0001c0001t0005g0293 a0001c0001t0005g0294 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.640+23676G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207669 | |||||||
chr14:99207742 | C | G | 42 | a0001c0001t0001g0212 a0001c0001t0001g0242 a0001c0001t0002g0056 others(39): Show |
42 | HG00639.hp1 HG00642.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.640+23603G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207742 | |||||||
chr14:99207778 | G | A | 2 | a0001c0001t0034g0007 a0001c0001t0082g0347 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+23567C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207778 | |||||||
chr14:99207863 | C | G | 1 | a0001c0001t0005g0337 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.640+23482G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207863 | |||||||
chr14:99207967 | G | A | 39 | a0001c0001t0001g0212 a0001c0001t0001g0242 a0001c0001t0002g0056 others(36): Show |
39 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.640+23378C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207967 | |||||||
chr14:99208159 | T | C | 33 | a0001c0001t0001g0212 a0001c0001t0001g0242 a0001c0001t0002g0056 others(30): Show |
33 | HG01099.hp1 HG01496.hp2 HG01952.hp2 others(30): Show |
intron_variant | MODIFIER | c.640+23186A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99208159 | |||||||
chr14:99208336 | C | T | 55 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(52): Show |
55 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.640+23009G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99208336 | |||||||
chr14:99208574 | G | A | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+22771C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99208574 | |||||||
chr14:99209096 | C | T | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+22249G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209096 | |||||||
chr14:99209242 | G | A | 58 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(55): Show |
59 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(56): Show |
intron_variant | MODIFIER | c.640+22103C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209242 | |||||||
chr14:99209244 | T | C | 1 | a0001c0002t0004g0079 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.640+22101A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209244 | |||||||
chr14:99209287 | A | G | 11 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(8): Show |
11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+22058T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209287 | |||||||
chr14:99209313 | G | A | 1 | a0001c0001t0010g0067 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.640+22032C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209313 | |||||||
chr14:99209369 | C | T | 1 | a0001c0001t0013g0259 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.640+21976G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209369 | |||||||
chr14:99209611 | C | G | 87 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(84): Show |
87 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.640+21734G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209611 | |||||||
chr14:99209632 | T | C | 1 | a0001c0002t0004g0137 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.640+21713A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209632 | |||||||
chr14:99209678 | A | T | 1 | a0001c0001t0007g0154 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.640+21667T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209678 | |||||||
chr14:99209696 | G | A | 2 | a0001c0001t0034g0007 a0001c0001t0082g0347 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+21649C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209696 | |||||||
chr14:99209711 | G | A | 184 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(181): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.640+21634C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209711 | |||||||
chr14:99209849 | G | A | 35 | a0001c0001t0001g0212 a0001c0001t0001g0242 a0001c0001t0002g0056 others(32): Show |
35 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.640+21496C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209849 | |||||||
chr14:99210269 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.640+21076C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210269 | |||||||
chr14:99210286 | T | C | 184 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(181): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.640+21059A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210286 | |||||||
chr14:99210392 | C | T | 1 | a0001c0002t0003g0151 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.640+20953G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210392 | |||||||
chr14:99210418 | C | A | 1 | a0001c0001t0006g0120 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.640+20927G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210418 | |||||||
chr14:99210467 | T | C | 3 | a0001c0001t0007g0168 a0001c0002t0003g0167 a0001c0002t0075g0325 |
3 | HG02698.hp2 HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.640+20878A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210467 | |||||||
chr14:99210470 | A | G | 184 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(181): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.640+20875T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210470 | |||||||
chr14:99210613 | C | T | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+20732G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210613 | |||||||
chr14:99210708 | G | A | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+20637C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210708 | |||||||
chr14:99210791 | C | T | 24 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0226 others(21): Show |
24 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.640+20554G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210791 | |||||||
chr14:99210867 | A | T | 64 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0217 others(61): Show |
64 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.640+20478T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210867 | |||||||
chr14:99210887 | A | AAGACACC others(42): Show |
1 | a0001c0001t0001g0237 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.640+20409_640+2045 others(53): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210887 | |||||||
chr14:99211017 | G | A | 2 | a0001c0001t0028g0003 a0001c0001t0029g0004 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.640+20328C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211017 | |||||||
chr14:99211098 | G | A | 4 | a0001c0001t0025g0164 a0001c0001t0032g0005 a0001c0001t0070g0290 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+20247C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211098 | |||||||
chr14:99211225 | C | T | 1 | a0001c0001t0011g0323 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.640+20120G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211225 | |||||||
chr14:99211339 | A | G | 11 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(8): Show |
11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+20006T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211339 | |||||||
chr14:99211355 | G | A | 1 | a0001c0001t0010g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.640+19990C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211355 | |||||||
chr14:99211396 | C | G | 20 | a0001c0001t0002g0065 a0001c0001t0009g0046 a0001c0001t0009g0091 others(17): Show |
20 | HG01099.hp1 HG02258.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.640+19949G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211396 | |||||||
chr14:99211531 | T | C | 1 | a0001c0001t0009g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.640+19814A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211531 | |||||||
chr14:99211569 | T | C | 55 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(52): Show |
55 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.640+19776A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211569 | |||||||
chr14:99211628 | C | T | 2 | a0001c0001t0034g0007 a0001c0001t0082g0347 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+19717G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211628 | |||||||
chr14:99211713 | C | T | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+19632G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211713 | |||||||
chr14:99212179 | G | A | 2 | a0001c0001t0034g0007 a0001c0001t0082g0347 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+19166C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212179 | |||||||
chr14:99212282 | A | C | 190 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.640+19063T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212282 | |||||||
chr14:99212308 | G | A | 32 | a0001c0001t0001g0212 a0001c0001t0001g0242 a0001c0001t0002g0056 others(29): Show |
32 | HG01099.hp1 HG01496.hp2 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.640+19037C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212308 | |||||||
chr14:99212335 | TGCA | T | 50 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(47): Show |
51 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(48): Show |
intron_variant | MODIFIER | c.640+19007_640+1900 others(7): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212335 | |||||||
chr14:99212343 | C | T | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+19002G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212343 | |||||||
chr14:99212450 | C | T | 1 | a0001c0001t0068g0288 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.640+18895G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212450 | |||||||
chr14:99212612 | A | C | 1 | a0001c0001t0042g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.640+18733T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212612 | |||||||
chr14:99212706 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.640+18639C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212706 | |||||||
chr14:99212721 | G | A | 3 | a0001c0001t0068g0288 a0001c0001t0069g0289 a0001c0001t0078g0343 |
3 | HG02602.hp2 HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.640+18624C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212721 | |||||||
chr14:99212773 | C | T | 1 | a0001c0002t0004g0033 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.640+18572G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212773 | |||||||
chr14:99212825 | G | C | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+18520C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212825 | |||||||
chr14:99212844 | C | A | 7 | a0001c0001t0009g0054 a0001c0001t0025g0228 a0001c0001t0064g0186 others(4): Show |
7 | HG00639.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.640+18501G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212844 | |||||||
chr14:99212911 | C | T | 3 | a0001c0001t0002g0129 a0001c0001t0081g0346 a0001c0002t0003g0286 |
3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.640+18434G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212911 | |||||||
chr14:99212912 | C | T | 3 | a0001c0001t0002g0129 a0001c0001t0081g0346 a0001c0002t0003g0286 |
3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.640+18433G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212912 | |||||||
chr14:99213170 | C | T | 48 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+18175G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213170 | |||||||
chr14:99213248 | G | A | 1 | a0001c0001t0047g0101 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.640+18097C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213248 | |||||||
chr14:99213276 | T | C | 1 | a0001c0001t0006g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.640+18069A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213276 | |||||||
chr14:99213411 | C | T | 2 | a0001c0001t0024g0250 a0001c0001t0024g0277 |
2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.640+17934G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213411 | |||||||
chr14:99213438 | A | G | 130 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(127): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.640+17907T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213438 | |||||||
chr14:99213459 | A | G | 189 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.640+17886T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213459 | |||||||
chr14:99213700 | C | T | 1 | a0001c0001t0002g0126 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.640+17645G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213700 | |||||||
chr14:99213921 | G | A | 1 | a0001c0003t0004g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.640+17424C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213921 | |||||||
chr14:99214266 | G | T | 23 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0226 others(20): Show |
23 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.640+17079C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214266 | |||||||
chr14:99214671 | A | T | 4 | a0001c0001t0002g0071 a0001c0003t0004g0061 a0001c0003t0008g0298 others(1): Show |
4 | HG01257.hp1 HG01433.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+16674T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214671 | |||||||
chr14:99214674 | AT | A | 3 | a0001c0001t0001g0279 a0001c0001t0021g0214 a0001c0001t0021g0280 |
3 | NA18969.hp2 NA19002.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.640+16670delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214674 | |||||||
chr14:99214675 | T | A | 42 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(39): Show |
43 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(40): Show |
intron_variant | MODIFIER | c.640+16670A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214675 | |||||||
chr14:99214787 | T | G | 2 | a0001c0001t0007g0203 a0001c0002t0004g0125 |
2 | HG00597.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.640+16558A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214787 | |||||||
chr14:99214889 | C | T | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+16456G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214889 | |||||||
chr14:99214913 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.640+16432G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214913 | |||||||
chr14:99214914 | G | A | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+16431C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214914 | |||||||
chr14:99214952 | G | A | 1 | a0001c0002t0004g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.640+16393C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214952 | |||||||
chr14:99215348 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.640+15997G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99215348 | |||||||
chr14:99215446 | G | C | 11 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(8): Show |
11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+15899C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99215446 | |||||||
chr14:99215812 | A | G | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+15533T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99215812 | |||||||
chr14:99215959 | G | A | 1 | a0001c0001t0005g0315 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.640+15386C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99215959 | |||||||
chr14:99216318 | G | T | 2 | a0001c0001t0002g0065 a0001c0001t0009g0046 |
2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.640+15027C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216318 | |||||||
chr14:99216319 | C | T | 2 | a0001c0001t0002g0065 a0001c0001t0009g0046 |
2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.640+15026G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216319 | |||||||
chr14:99216419 | A | G | 1 | a0001c0002t0003g0151 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.640+14926T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216419 | |||||||
chr14:99216573 | C | T | 41 | a0001c0001t0001g0185 a0001c0001t0001g0212 a0001c0001t0001g0242 others(38): Show |
41 | HG01074.hp1 HG01099.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.640+14772G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216573 | |||||||
chr14:99216580 | T | C | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+14765A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216580 | |||||||
chr14:99216852 | C | T | 47 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(44): Show |
48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.640+14493G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216852 | |||||||
chr14:99216859 | A | G | 1 | a0001c0002t0004g0023 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.640+14486T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216859 | |||||||
chr14:99216863 | G | A | 1 | a0001c0002t0003g0249 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.640+14482C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216863 | |||||||
chr14:99216874 | C | T | 2 | a0001c0001t0006g0133 a0001c0001t0010g0132 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.640+14471G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216874 | |||||||
chr14:99216909 | T | C | 48 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14436A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216909 | |||||||
chr14:99216923 | C | CAT | 48 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14420_640+1442 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216923 | |||||||
chr14:99216954 | C | A | 48 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14391G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216954 | |||||||
chr14:99216960 | A | C | 48 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14385T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216960 | |||||||
chr14:99216965 | T | A | 48 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14380A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216965 | |||||||
chr14:99217018 | T | G | 1 | a0001c0002t0043g0111 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.640+14327A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217018 | |||||||
chr14:99217084 | C | T | 10 | a0001c0001t0009g0088 a0001c0001t0013g0181 a0001c0001t0013g0189 others(7): Show |
11 | HG02109.hp2 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.640+14261G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217084 | |||||||
chr14:99217281 | TACAA | T | 11 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(8): Show |
11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+14060_640+1406 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217281 | |||||||
chr14:99217301 | CAT | C | 48 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14042_640+1404 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217301 | |||||||
chr14:99217363 | T | C | 47 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(44): Show |
48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.640+13982A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217363 | |||||||
chr14:99217371 | T | TACACACA others(11): Show |
9 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0005g0326 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+13956_640+1397 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217371 | |||||||
chr14:99217381 | T | TACAGACA others(17): Show |
1 | a0001c0001t0009g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.640+13963_640+1396 others(28): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217381 | |||||||
chr14:99217385 | G | GAC | 15 | a0001c0001t0001g0199 a0001c0001t0001g0272 a0001c0001t0002g0107 others(12): Show |
15 | HG00558.hp1 HG01169.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.640+13958_640+1395 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | |||||||
chr14:99217385 | G | GACAC | 13 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0002g0040 others(10): Show |
13 | HG00733.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.640+13956_640+1395 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | |||||||
chr14:99217385 | G | GACACACA others(17): Show |
1 | a0001c0002t0004g0079 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.640+13959_640+1396 others(28): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | |||||||
chr14:99217385 | G | GACACACA others(13): Show |
52 | a0001c0001t0001g0185 a0001c0001t0001g0212 a0001c0001t0001g0217 others(49): Show |
52 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.640+13959_640+1396 others(24): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | |||||||
chr14:99217385 | G | GACACACA others(15): Show |
65 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(62): Show |
65 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.640+13959_640+1396 others(26): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | |||||||
chr14:99217385 | G | GACACACA others(17): Show |
3 | a0001c0001t0009g0096 a0001c0002t0003g0248 a0001c0002t0045g0014 |
3 | HG01891.hp1 HG02015.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.640+13959_640+1396 others(28): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | |||||||
chr14:99217385 | G | GACACACA others(19): Show |
2 | a0001c0001t0001g0237 a0001c0001t0001g0271 |
2 | NA19004.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.640+13959_640+1396 others(30): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | |||||||
chr14:99217385 | G | GACACACA others(21): Show |
10 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(7): Show |
10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+13959_640+1396 others(32): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | |||||||
chr14:99217385 | G | GACACACA others(19): Show |
1 | a0001c0002t0060g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.640+13959_640+1396 others(30): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | |||||||
chr14:99217385 | GACACACA others(11): Show |
G | 1 | a0001c0001t0001g0204 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.640+13942_640+1395 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | |||||||
chr14:99217387 | C | CACACACA others(9): Show |
1 | a0001c0001t0006g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.640+13957_640+1395 others(20): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217387 | |||||||
chr14:99217389 | C | CACACACA others(7): Show |
1 | a0001c0001t0007g0229 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.640+13955_640+1395 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217389 | |||||||
chr14:99217391 | C | CACACACA others(5): Show |
7 | a0001c0001t0001g0279 a0001c0001t0007g0257 a0001c0001t0021g0214 others(4): Show |
7 | HG03139.hp2 NA18969.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+13953_640+1395 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217391 | |||||||
chr14:99217393 | C | CACACATA others(3): Show |
40 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(37): Show |
41 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(38): Show |
intron_variant | MODIFIER | c.640+13951_640+1395 others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217393 | |||||||
chr14:99217418 | G | A | 49 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(46): Show |
50 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(47): Show |
intron_variant | MODIFIER | c.640+13927C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217418 | |||||||
chr14:99217453 | C | A | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+13892G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217453 | |||||||
chr14:99217632 | G | A | 192 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.640+13713C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217632 | |||||||
chr14:99217932 | T | C | 197 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.640+13413A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217932 | |||||||
chr14:99217997 | A | G | 1 | a0001c0001t0067g0258 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.640+13348T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217997 | |||||||
chr14:99218061 | G | GT | 40 | a0001c0001t0001g0161 a0001c0001t0001g0172 a0001c0001t0001g0202 others(37): Show |
40 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.640+13283dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218061 | |||||||
chr14:99218061 | GT | G | 24 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0226 others(21): Show |
24 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.640+13283delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218061 | |||||||
chr14:99218084 | G | A | 2 | a0001c0001t0006g0133 a0001c0001t0010g0132 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.640+13261C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218084 | |||||||
chr14:99218114 | A | G | 4 | a0001c0001t0001g0187 a0001c0001t0001g0231 a0001c0001t0001g0271 others(1): Show |
4 | NA19004.hp2 NA19063.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+13231T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218114 | |||||||
chr14:99218152 | G | A | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+13193C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218152 | |||||||
chr14:99218232 | A | AT | 99 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0161 others(96): Show |
99 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.640+13112dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218232 | |||||||
chr14:99218232 | A | ATT | 17 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(14): Show |
17 | HG00423.hp1 HG00423.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.640+13111_640+1311 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218232 | |||||||
chr14:99218232 | A | ATTTTT | 20 | a0001c0001t0001g0209 a0001c0001t0001g0226 a0001c0001t0001g0239 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.640+13108_640+1311 others(9): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218232 | |||||||
chr14:99218232 | AT | A | 11 | a0001c0001t0003g0232 a0001c0001t0003g0275 a0001c0001t0003g0285 others(8): Show |
11 | HG01168.hp2 HG01257.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.640+13112delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218232 | |||||||
chr14:99218325 | C | T | 1 | a0001c0001t0005g0336 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.640+13020G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218325 | |||||||
chr14:99218332 | G | A | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+13013C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218332 | |||||||
chr14:99218375 | C | T | 190 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.640+12970G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218375 | |||||||
chr14:99218540 | C | T | 1 | a0001c0002t0004g0018 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.640+12805G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218540 | |||||||
chr14:99218669 | T | C | 11 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0002g0040 others(8): Show |
11 | HG00733.hp1 HG02145.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.640+12676A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218669 | |||||||
chr14:99218764 | G | A | 3 | a0001c0001t0009g0096 a0001c0001t0051g0128 a0001c0002t0045g0014 |
3 | HG01891.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.640+12581C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218764 | |||||||
chr14:99218796 | G | A | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+12549C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218796 | |||||||
chr14:99218833 | G | C | 27 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0161 others(24): Show |
27 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.640+12512C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218833 | |||||||
chr14:99218855 | G | A | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.640+12490C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218855 | |||||||
chr14:99218971 | C | T | 1 | a0001c0001t0004g0115 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.640+12374G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218971 | |||||||
chr14:99219045 | CT | C | 166 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.640+12299delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219045 | |||||||
chr14:99219049 | T | C | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+12296A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219049 | |||||||
chr14:99219094 | T | C | 15 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(12): Show |
15 | HG00423.hp2 HG01884.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.640+12251A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219094 | |||||||
chr14:99219095 | G | A | 15 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(12): Show |
15 | HG00423.hp2 HG01884.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.640+12250C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219095 | |||||||
chr14:99219291 | CCCAAAGT others(10): Show |
C | 1 | a0001c0001t0005g0336 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.640+12037_640+1205 others(21): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219291 | |||||||
chr14:99219314 | G | A | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+12031C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219314 | |||||||
chr14:99219411 | G | A | 1 | a0001c0001t0006g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.640+11934C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219411 | |||||||
chr14:99219692 | C | T | 1 | a0001c0001t0028g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.640+11653G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219692 | |||||||
chr14:99219811 | A | T | 1 | a0001c0001t0067g0258 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.640+11534T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219811 | |||||||
chr14:99219813 | T | A | 1 | a0001c0001t0067g0258 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.640+11532A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219813 | |||||||
chr14:99219813 | T | TA | 55 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0204 others(52): Show |
56 | HG00621.hp1 HG00673.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.640+11531dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219813 | |||||||
chr14:99219813 | T | TAA | 36 | a0001c0001t0001g0212 a0001c0001t0001g0242 a0001c0001t0002g0065 others(33): Show |
36 | HG01099.hp1 HG01168.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.640+11530_640+1153 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219813 | |||||||
chr14:99219813 | TA | T | 13 | a0001c0001t0001g0171 a0001c0001t0001g0188 a0001c0001t0002g0040 others(10): Show |
13 | HG00733.hp1 HG01256.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.640+11531delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219813 | |||||||
chr14:99219928 | A | G | 138 | a0001c0001t0001g0163 a0001c0001t0001g0184 a0001c0001t0001g0185 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.640+11417T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219928 | |||||||
chr14:99220035 | C | G | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+11310G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220035 | |||||||
chr14:99220051 | T | G | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+11294A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220051 | |||||||
chr14:99220071 | T | C | 2 | a0001c0001t0002g0025 a0001c0001t0002g0026 |
2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.640+11274A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220071 | |||||||
chr14:99220107 | G | A | 2 | a0001c0001t0010g0068 a0001c0001t0010g0127 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.640+11238C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220107 | |||||||
chr14:99220170 | T | C | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+11175A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220170 | |||||||
chr14:99220178 | G | A | 1 | a0001c0001t0070g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.640+11167C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220178 | |||||||
chr14:99220196 | A | G | 95 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0212 others(92): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.640+11149T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220196 | |||||||
chr14:99220199 | A | G | 97 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0212 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.640+11146T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220199 | |||||||
chr14:99220207 | T | C | 26 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0226 others(23): Show |
26 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.640+11138A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220207 | |||||||
chr14:99220241 | G | A | 1 | a0001c0002t0008g0319 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.640+11104C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220241 | |||||||
chr14:99220277 | A | G | 95 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0212 others(92): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.640+11068T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220277 | |||||||
chr14:99220278 | C | T | 196 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.640+11067G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220278 | |||||||
chr14:99220281 | A | G | 1 | a0001c0003t0004g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.640+11064T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220281 | |||||||
chr14:99220285 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.640+11060A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220285 | |||||||
chr14:99220297 | G | A | 1 | a0001c0002t0019g0140 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.640+11048C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220297 | |||||||
chr14:99220556 | C | T | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+10789G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220556 | |||||||
chr14:99220565 | G | T | 7 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0161 others(4): Show |
7 | HG02083.hp1 NA18953.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+10780C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220565 | |||||||
chr14:99220566 | G | A | 7 | a0001c0001t0009g0054 a0001c0001t0025g0228 a0001c0001t0064g0186 others(4): Show |
7 | HG00639.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.640+10779C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220566 | |||||||
chr14:99220633 | A | T | 101 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0212 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.640+10712T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220633 | |||||||
chr14:99220665 | G | A | 8 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.640+10680C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220665 | |||||||
chr14:99220835 | T | C | 2 | a0001c0002t0003g0167 a0001c0002t0075g0325 |
2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.640+10510A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220835 | |||||||
chr14:99220874 | A | G | 165 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(162): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.640+10471T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220874 | |||||||
chr14:99220919 | C | T | 1 | a0001c0002t0048g0057 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.640+10426G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220919 | |||||||
chr14:99221103 | G | A | 3 | a0001c0001t0009g0054 a0001c0002t0003g0264 a0001c0002t0017g0134 |
3 | HG02055.hp2 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.640+10242C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221103 | |||||||
chr14:99221136 | G | A | 1 | a0001c0002t0003g0253 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.640+10209C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221136 | |||||||
chr14:99221193 | C | G | 1 | a0001c0001t0002g0039 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.640+10152G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221193 | |||||||
chr14:99221436 | C | T | 191 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.640+9909G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221436 | |||||||
chr14:99221559 | G | C | 3 | a0001c0002t0080g0345 a0001c0006t0023g0190 a0001c0006t0023g0191 |
3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.640+9786C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221559 | |||||||
chr14:99221560 | C | T | 3 | a0001c0002t0080g0345 a0001c0006t0023g0190 a0001c0006t0023g0191 |
3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.640+9785G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221560 | |||||||
chr14:99221642 | G | A | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+9703C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221642 | |||||||
chr14:99221745 | G | A | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+9600C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221745 | |||||||
chr14:99221810 | G | A | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+9535C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221810 | |||||||
chr14:99221856 | C | T | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+9489G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221856 | |||||||
chr14:99221924 | G | C | 200 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.640+9421C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221924 | |||||||
chr14:99222072 | G | A | 176 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.640+9273C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222072 | |||||||
chr14:99222097 | G | A | 1 | a0001c0001t0042g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.640+9248C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222097 | |||||||
chr14:99222261 | GA | G | 178 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.640+9083delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222261 | |||||||
chr14:99222333 | G | A | 176 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.640+9012C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222333 | |||||||
chr14:99222406 | T | C | 67 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(64): Show |
67 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.640+8939A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222406 | |||||||
chr14:99222434 | G | A | 6 | a0001c0001t0009g0088 a0001c0001t0013g0181 a0001c0001t0013g0259 others(3): Show |
6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+8911C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222434 | |||||||
chr14:99222561 | G | A | 45 | a0001c0001t0001g0185 a0001c0001t0001g0212 a0001c0001t0001g0242 others(42): Show |
45 | HG01074.hp1 HG01099.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.640+8784C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222561 | |||||||
chr14:99222587 | G | T | 10 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(7): Show |
10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+8758C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222587 | |||||||
chr14:99222731 | C | G | 64 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(61): Show |
64 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.640+8614G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222731 | |||||||
chr14:99222836 | C | CCTTT | 45 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0204 others(42): Show |
46 | HG00621.hp1 HG00673.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.640+8505_640+8508d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222836 | |||||||
chr14:99222836 | C | CCTTTCTT others(5): Show |
1 | a0001c0001t0009g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.640+8497_640+8508d others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222836 | |||||||
chr14:99222836 | C | CCTTTCTT others(21): Show |
1 | a0001c0002t0060g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.640+8508_640+8509i others(30): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222836 | |||||||
chr14:99222836 | CCTTT | C | 30 | a0001c0001t0001g0150 a0001c0001t0001g0163 a0001c0001t0001g0166 others(27): Show |
30 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.640+8505_640+8508d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222836 | |||||||
chr14:99222897 | CTT | C | 3 | a0001c0001t0009g0054 a0001c0002t0003g0264 a0001c0002t0017g0134 |
3 | HG02055.hp2 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.640+8446_640+8447d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222897 | |||||||
chr14:99223550 | C | T | 3 | a0001c0002t0080g0345 a0001c0006t0023g0190 a0001c0006t0023g0191 |
3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.640+7795G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99223550 | |||||||
chr14:99223654 | G | T | 4 | a0001c0001t0025g0228 a0001c0001t0064g0186 a0001c0002t0048g0057 others(1): Show |
4 | HG00639.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+7691C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99223654 | |||||||
chr14:99223944 | G | A | 1 | a0001c0002t0046g0015 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.640+7401C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99223944 | |||||||
chr14:99223960 | T | C | 1 | a0001c0001t0009g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.640+7385A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99223960 | |||||||
chr14:99224048 | C | T | 2 | a0001c0001t0002g0105 a0001c0001t0005g0327 |
2 | HG00741.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.640+7297G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224048 | |||||||
chr14:99224049 | G | A | 1 | a0001c0001t0007g0154 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.640+7296C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224049 | |||||||
chr14:99224129 | A | G | 28 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0226 others(25): Show |
28 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.640+7216T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224129 | |||||||
chr14:99224190 | G | A | 46 | a0001c0001t0001g0163 a0001c0001t0001g0209 a0001c0001t0001g0217 others(43): Show |
46 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.640+7155C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224190 | |||||||
chr14:99224532 | C | T | 5 | a0001c0001t0001g0185 a0001c0001t0006g0070 a0001c0001t0006g0080 others(2): Show |
5 | HG00639.hp2 HG01074.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.640+6813G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224532 | |||||||
chr14:99224533 | G | A | 2 | a0001c0001t0002g0097 a0001c0001t0006g0017 |
2 | NA18964.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.640+6812C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224533 | |||||||
chr14:99224570 | C | A | 251 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.640+6775G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224570 | |||||||
chr14:99224598 | C | T | 10 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(7): Show |
10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+6747G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224598 | |||||||
chr14:99224616 | G | A | 2 | a0001c0001t0034g0007 a0001c0001t0082g0347 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+6729C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224616 | |||||||
chr14:99224648 | T | C | 10 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(7): Show |
10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+6697A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224648 | |||||||
chr14:99224696 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.640+6649T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224696 | |||||||
chr14:99224753 | A | G | 6 | a0001c0001t0012g0147 a0001c0001t0012g0148 a0001c0001t0020g0144 others(3): Show |
6 | NA18968.hp1 NA18983.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+6592T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224753 | |||||||
chr14:99224843 | G | T | 199 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.640+6502C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224843 | |||||||
chr14:99224992 | G | T | 110 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(107): Show |
110 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.640+6353C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224992 | |||||||
chr14:99225086 | G | C | 3 | a0001c0001t0009g0094 a0001c0001t0015g0093 a0001c0002t0004g0092 |
3 | HG03098.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.640+6259C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225086 | |||||||
chr14:99225129 | T | C | 2 | a0001c0001t0064g0186 a0001c0002t0072g0292 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.640+6216A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225129 | |||||||
chr14:99225266 | T | G | 7 | a0001c0001t0025g0228 a0001c0001t0064g0186 a0001c0002t0048g0057 others(4): Show |
7 | HG00639.hp2 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+6079A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225266 | |||||||
chr14:99225364 | G | A | 2 | a0001c0001t0003g0247 a0001c0001t0077g0342 |
2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.640+5981C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225364 | |||||||
chr14:99225406 | C | T | 1 | a0001c0001t0037g0100 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.640+5939G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225406 | |||||||
chr14:99225456 | G | C | 28 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0226 others(25): Show |
28 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.640+5889C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225456 | |||||||
chr14:99225642 | A | T | 6 | a0001c0001t0009g0088 a0001c0001t0013g0181 a0001c0001t0013g0259 others(3): Show |
6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+5703T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225642 | |||||||
chr14:99225651 | G | A | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+5694C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225651 | |||||||
chr14:99225657 | A | AAAAG | 4 | a0001c0001t0003g0267 a0001c0001t0036g0063 a0001c0002t0003g0151 others(1): Show |
4 | HG01109.hp2 HG01981.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+5684_640+5687d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225657 | |||||||
chr14:99225883 | GCCCCAAC others(11): Show |
G | 1 | a0001c0001t0025g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.640+5444_640+5461d others(20): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225883 | |||||||
chr14:99225917 | T | C | 48 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+5428A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225917 | |||||||
chr14:99225934 | T | C | 47 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(44): Show |
48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.640+5411A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225934 | |||||||
chr14:99225988 | T | G | 11 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(8): Show |
11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+5357A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225988 | |||||||
chr14:99226057 | C | T | 1 | a0001c0002t0003g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.640+5288G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226057 | |||||||
chr14:99226093 | G | A | 148 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.640+5252C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226093 | |||||||
chr14:99226318 | G | A | 30 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0161 others(27): Show |
30 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.640+5027C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226318 | |||||||
chr14:99226350 | C | T | 3 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0002t0004g0049 |
3 | HG02922.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.640+4995G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226350 | |||||||
chr14:99226351 | G | A | 2 | a0001c0001t0034g0007 a0001c0001t0082g0347 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+4994C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226351 | |||||||
chr14:99226402 | G | A | 47 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(44): Show |
48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.640+4943C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226402 | |||||||
chr14:99227097 | A | T | 10 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(7): Show |
10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+4248T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227097 | |||||||
chr14:99227211 | T | A | 1 | a0001c0002t0003g0207 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.640+4134A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227211 | |||||||
chr14:99227250 | G | A | 58 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(55): Show |
58 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.640+4095C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227250 | |||||||
chr14:99227298 | T | C | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+4047A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227298 | |||||||
chr14:99227375 | C | T | 3 | a0001c0001t0002g0129 a0001c0001t0081g0346 a0001c0002t0003g0286 |
3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.640+3970G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227375 | |||||||
chr14:99227482 | C | T | 6 | a0001c0001t0009g0088 a0001c0001t0013g0181 a0001c0001t0013g0259 others(3): Show |
6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+3863G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227482 | |||||||
chr14:99227506 | G | T | 27 | a0001c0001t0001g0209 a0001c0001t0001g0217 a0001c0001t0001g0226 others(24): Show |
27 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.640+3839C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227506 | |||||||
chr14:99227565 | C | T | 3 | a0001c0002t0007g0254 a0001c0002t0007g0255 a0001c0002t0011g0338 |
3 | HG01168.hp2 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.640+3780G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227565 | |||||||
chr14:99227576 | G | A | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.640+3769C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227576 | |||||||
chr14:99227654 | G | A | 3 | a0001c0001t0001g0220 a0001c0001t0012g0142 a0001c0001t0012g0143 |
3 | NA18969.hp1 NA18977.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.640+3691C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227654 | |||||||
chr14:99227676 | C | T | 3 | a0001c0001t0009g0096 a0001c0001t0051g0128 a0001c0002t0045g0014 |
3 | HG01891.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.640+3669G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227676 | |||||||
chr14:99227855 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.640+3490G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227855 | |||||||
chr14:99227881 | T | G | 6 | a0001c0001t0009g0054 a0001c0001t0009g0123 a0001c0001t0070g0290 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+3464A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227881 | |||||||
chr14:99228112 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.640+3233A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228112 | |||||||
chr14:99228379 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.640+2966A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228379 | |||||||
chr14:99228423 | C | A | 17 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(14): Show |
17 | HG00423.hp2 HG00639.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.640+2922G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228423 | |||||||
chr14:99228537 | A | C | 2 | a0001c0002t0004g0095 a0001c0002t0004g0130 |
2 | NA19002.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.640+2808T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228537 | |||||||
chr14:99228714 | G | A | 2 | a0001c0001t0055g0195 a0001c0002t0058g0269 |
2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.640+2631C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228714 | |||||||
chr14:99228931 | G | A | 57 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(54): Show |
57 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.640+2414C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228931 | |||||||
chr14:99228976 | A | C | 1 | a0001c0002t0003g0215 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.640+2369T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228976 | |||||||
chr14:99229003 | A | AATGG | 15 | a0001c0001t0001g0204 a0001c0001t0001g0216 a0001c0001t0001g0227 others(12): Show |
15 | HG01074.hp2 HG01934.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.640+2338_640+2341d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | |||||||
chr14:99229003 | A | AATGGAGG others(5): Show |
4 | a0001c0001t0009g0088 a0001c0001t0013g0259 a0001c0001t0014g0087 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+2341_640+2342i others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | |||||||
chr14:99229003 | A | AATGGATG others(1): Show |
11 | a0001c0001t0001g0187 a0001c0001t0001g0206 a0001c0001t0001g0233 others(8): Show |
12 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.640+2334_640+2341d others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | |||||||
chr14:99229003 | A | AATGGATG others(5): Show |
5 | a0001c0001t0034g0007 a0001c0001t0035g0010 a0001c0002t0001g0236 others(2): Show |
5 | HG02056.hp1 HG02451.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.640+2330_640+2341d others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | |||||||
chr14:99229003 | A | G | 1 | a0001c0001t0011g0323 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.640+2342T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | |||||||
chr14:99229003 | AATGG | A | 3 | a0001c0001t0001g0272 a0001c0002t0003g0151 a0001c0002t0004g0050 |
3 | HG01109.hp2 HG01981.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.640+2338_640+2341d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | |||||||
chr14:99229003 | AATGGATG others(33): Show |
A | 1 | a0001c0002t0048g0057 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.640+2302_640+2341d others(42): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | |||||||
chr14:99229007 | GATGGATG others(29): Show |
G | 5 | a0001c0001t0025g0228 a0001c0001t0064g0186 a0001c0002t0080g0345 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.640+2302_640+2337d others(38): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229007 | |||||||
chr14:99229011 | GATGGATG others(25): Show |
G | 1 | a0001c0002t0072g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.640+2302_640+2333d others(34): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229011 | |||||||
chr14:99229031 | G | GATGGATG others(9): Show |
2 | a0001c0001t0002g0056 a0001c0001t0005g0308 |
2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.640+2313_640+2314i others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229031 | |||||||
chr14:99229031 | G | GATGGATG others(13): Show |
4 | a0001c0001t0001g0192 a0001c0001t0001g0241 a0001c0001t0055g0195 others(1): Show |
4 | HG01109.hp1 HG02293.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+2313_640+2314i others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229031 | |||||||
chr14:99229035 | G | C | 1 | a0001c0002t0017g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.640+2310C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229035 | |||||||
chr14:99229035 | G | GATGGATG others(9): Show |
6 | a0001c0001t0002g0058 a0001c0001t0082g0347 a0001c0002t0003g0173 others(3): Show |
6 | HG02258.hp1 HG02486.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2309_640+2310i others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229035 | |||||||
chr14:99229039 | G | GATGGATG others(1): Show |
4 | a0001c0001t0001g0202 a0001c0001t0001g0271 a0001c0001t0070g0290 others(1): Show |
4 | HG00438.hp1 HG00609.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+2305_640+2306i others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229039 | |||||||
chr14:99229039 | G | GATGGATG others(5): Show |
33 | a0001c0001t0001g0156 a0001c0001t0001g0161 a0001c0001t0001g0162 others(30): Show |
33 | HG00621.hp2 HG01261.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.640+2305_640+2306i others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229039 | |||||||
chr14:99229039 | G | GATGGATG others(9): Show |
8 | a0001c0001t0001g0157 a0001c0001t0002g0102 a0001c0001t0004g0115 others(5): Show |
8 | HG00423.hp1 HG01175.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+2305_640+2306i others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229039 | |||||||
chr14:99229039 | GATGC | G | 6 | a0001c0001t0009g0096 a0001c0001t0051g0128 a0001c0002t0003g0201 others(3): Show |
6 | HG00673.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+2302_640+2305d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229039 | |||||||
chr14:99229043 | C | CATGG | 46 | a0001c0001t0001g0188 a0001c0001t0001g0199 a0001c0001t0001g0212 others(43): Show |
46 | HG00558.hp1 HG00597.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.640+2298_640+2301d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | |||||||
chr14:99229043 | C | CATGGATG others(1): Show |
12 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0171 others(9): Show |
12 | HG01099.hp1 HG02615.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.640+2294_640+2301d others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | |||||||
chr14:99229043 | C | CATGGATG others(5): Show |
6 | a0001c0001t0005g0339 a0001c0001t0006g0120 a0001c0001t0015g0077 others(3): Show |
6 | HG02257.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2290_640+2301d others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | |||||||
chr14:99229043 | C | CATGGATG others(9): Show |
1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.640+2286_640+2301d others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | |||||||
chr14:99229043 | C | CATGGATG others(13): Show |
1 | a0001c0001t0001g0260 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.640+2282_640+2301d others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | |||||||
chr14:99229043 | C | G | 140 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.640+2302G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | |||||||
chr14:99229043 | CATGG | C | 4 | a0001c0001t0011g0323 a0001c0001t0018g0090 a0001c0002t0016g0011 others(1): Show |
4 | HG00639.hp1 HG00642.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+2298_640+2301d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | |||||||
chr14:99229047 | G | C | 6 | a0001c0001t0002g0117 a0001c0001t0012g0148 a0001c0001t0013g0181 others(3): Show |
6 | HG01884.hp1 HG02015.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2298C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229047 | |||||||
chr14:99229047 | G | GATGC | 37 | a0001c0001t0001g0155 a0001c0001t0001g0184 a0001c0001t0001g0221 others(34): Show |
37 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.640+2297_640+2298i others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229047 | |||||||
chr14:99229047 | G | GATGGATG others(1): Show |
7 | a0001c0001t0001g0185 a0001c0001t0003g0267 a0001c0001t0006g0080 others(4): Show |
7 | HG01981.hp2 HG02698.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.640+2297_640+2298i others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229047 | |||||||
chr14:99229047 | G | GATGGATG others(5): Show |
3 | a0001c0001t0002g0016 a0001c0001t0005g0330 a0001c0001t0006g0028 |
3 | HG01243.hp1 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.640+2297_640+2298i others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229047 | |||||||
chr14:99229051 | G | C | 5 | a0001c0001t0001g0252 a0001c0001t0001g0276 a0001c0001t0057g0152 others(2): Show |
5 | HG00140.hp2 HG00609.hp2 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.640+2294C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229051 | |||||||
chr14:99229051 | G | GATGC | 15 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0239 others(12): Show |
15 | HG00438.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.640+2293_640+2294i others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229051 | |||||||
chr14:99229055 | G | C | 7 | a0001c0001t0002g0042 a0001c0001t0009g0096 a0001c0001t0051g0128 others(4): Show |
7 | HG00280.hp2 HG01069.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+2290C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229055 | |||||||
chr14:99229055 | G | GATGA | 4 | a0001c0001t0001g0237 a0001c0002t0001g0236 a0001c0002t0003g0265 others(1): Show |
4 | HG02056.hp1 NA18952.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+2289_640+2290i others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229055 | |||||||
chr14:99229055 | G | GATGCATG others(13): Show |
6 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0266 others(3): Show |
6 | HG00423.hp2 HG02071.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2289_640+2290i others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229055 | |||||||
chr14:99229059 | G | A | 1 | a0001c0002t0004g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.640+2286C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229059 | |||||||
chr14:99229059 | G | C | 4 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0005g0332 others(1): Show |
4 | HG01099.hp2 HG01516.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+2286C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229059 | |||||||
chr14:99229090 | A | G | 7 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0002g0042 others(4): Show |
7 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.640+2255T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229090 | |||||||
chr14:99229094 | G | A | 1 | a0001c0002t0003g0215 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.640+2251C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229094 | |||||||
chr14:99229098 | G | A | 6 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0002g0042 others(3): Show |
6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2247C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229098 | |||||||
chr14:99229110 | A | G | 6 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0002g0042 others(3): Show |
6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2235T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229110 | |||||||
chr14:99229111 | C | G | 6 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0002g0042 others(3): Show |
6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2234G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229111 | |||||||
chr14:99229113 | G | T | 6 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0002g0042 others(3): Show |
6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2232C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229113 | |||||||
chr14:99229113 | GGGATGAA others(5): Show |
G | 4 | a0001c0002t0072g0292 a0001c0002t0080g0345 a0001c0006t0023g0190 others(1): Show |
4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+2220_640+2231d others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229113 | |||||||
chr14:99229115 | GATGA | G | 11 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(8): Show |
11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+2226_640+2229d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229115 | |||||||
chr14:99229118 | G | A | 6 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0002g0042 others(3): Show |
6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2227C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229118 | |||||||
chr14:99229119 | A | AATGG | 102 | a0001c0001t0001g0179 a0001c0001t0001g0188 a0001c0001t0001g0198 others(99): Show |
103 | HG00558.hp1 HG00597.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.640+2222_640+2225d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229119 | |||||||
chr14:99229119 | A | AATGGATG others(1): Show |
13 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0097 others(10): Show |
13 | HG01074.hp1 HG01099.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.640+2218_640+2225d others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229119 | |||||||
chr14:99229119 | A | C | 6 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0002g0042 others(3): Show |
6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2226T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229119 | |||||||
chr14:99229119 | AATGG | A | 27 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0019 others(24): Show |
28 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.640+2222_640+2225d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229119 | |||||||
chr14:99229119 | AATGGATG others(1): Show |
A | 22 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0239 others(19): Show |
22 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.640+2218_640+2225d others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229119 | |||||||
chr14:99229121 | T | G | 6 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0002g0042 others(3): Show |
6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2224A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229121 | |||||||
chr14:99229127 | G | A | 6 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0002g0042 others(3): Show |
6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2218C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229127 | |||||||
chr14:99229153 | T | C | 63 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(60): Show |
63 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.640+2192A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229153 | |||||||
chr14:99229167 | G | A | 1 | a0001c0002t0058g0269 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.640+2178C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229167 | |||||||
chr14:99229337 | G | A | 2 | a0001c0001t0005g0293 a0001c0001t0005g0294 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.640+2008C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229337 | |||||||
chr14:99229360 | GGCAGA | G | 4 | a0001c0001t0025g0228 a0001c0001t0064g0186 a0001c0002t0048g0057 others(1): Show |
4 | HG00639.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+1980_640+1984d others(7): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229360 | |||||||
chr14:99229367 | C | A | 4 | a0001c0001t0025g0228 a0001c0001t0064g0186 a0001c0002t0048g0057 others(1): Show |
4 | HG00639.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+1978G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229367 | |||||||
chr14:99229369 | C | T | 4 | a0001c0001t0025g0228 a0001c0001t0064g0186 a0001c0002t0048g0057 others(1): Show |
4 | HG00639.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+1976G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229369 | |||||||
chr14:99229370 | C | T | 4 | a0001c0001t0025g0228 a0001c0001t0064g0186 a0001c0002t0048g0057 others(1): Show |
4 | HG00639.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+1975G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229370 | |||||||
chr14:99229432 | G | T | 1 | a0001c0001t0006g0024 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.640+1913C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229432 | |||||||
chr14:99229504 | C | T | 2 | a0001c0001t0003g0247 a0001c0001t0077g0342 |
2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.640+1841G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229504 | |||||||
chr14:99229543 | A | G | 10 | a0001c0001t0009g0054 a0001c0001t0009g0123 a0001c0001t0009g0135 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.640+1802T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229543 | |||||||
chr14:99229604 | T | C | 2 | a0001c0001t0034g0007 a0001c0001t0082g0347 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+1741A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229604 | |||||||
chr14:99229732 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0002g0107 |
2 | HG01981.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.640+1613C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229732 | |||||||
chr14:99229767 | C | T | 198 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(195): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.640+1578G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229767 | |||||||
chr14:99229801 | G | A | 1 | a0001c0001t0025g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.640+1544C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229801 | |||||||
chr14:99230265 | A | G | 6 | a0001c0001t0009g0088 a0001c0001t0013g0181 a0001c0001t0013g0259 others(3): Show |
6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+1080T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230265 | |||||||
chr14:99230371 | C | T | 1 | a0001c0001t0006g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.640+974G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230371 | |||||||
chr14:99230439 | A | G | 1 | a0001c0002t0017g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.640+906T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230439 | |||||||
chr14:99230774 | C | T | 2 | a0001c0001t0067g0258 a0001c0002t0003g0225 |
2 | NA18965.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.640+571G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230774 | |||||||
chr14:99230820 | G | A | 4 | a0001c0001t0005g0306 a0001c0001t0005g0321 a0001c0001t0005g0327 others(1): Show |
4 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+525C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230820 | |||||||
chr14:99230973 | G | A | 6 | a0001c0001t0009g0088 a0001c0001t0013g0181 a0001c0001t0013g0259 others(3): Show |
6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+372C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230973 | |||||||
chr14:99230995 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.640+350C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230995 | |||||||
chr14:99231000 | A | AG | 9 | a0001c0001t0001g0223 a0001c0001t0001g0251 a0001c0001t0002g0098 others(6): Show |
9 | HG00438.hp2 HG01099.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.640+344dupC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99231000 | |||||||
chr14:99231082 | A | G | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+263T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99231082 | |||||||
chr14:99231248 | T | C | 1 | a0001c0001t0015g0030 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.640+97A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99231248 | |||||||
chr14:99231328 | G | A | 2 | a0001c0001t0002g0051 a0001c0001t0002g0052 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.640+17C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99231328 | |||||||
chr14:99231638 | C | T | 1 | a0001c0001t0025g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.428-81G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231638 | |||||||
chr14:99231648 | T | G | 7 | a0001c0001t0001g0185 a0001c0001t0006g0070 a0001c0001t0006g0080 others(4): Show |
7 | HG01074.hp1 HG02015.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-91A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231648 | |||||||
chr14:99231653 | A | G | 7 | a0001c0001t0001g0185 a0001c0001t0006g0070 a0001c0001t0006g0080 others(4): Show |
7 | HG01074.hp1 HG02015.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-96T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231653 | |||||||
chr14:99231664 | C | T | 6 | a0001c0001t0009g0088 a0001c0001t0013g0181 a0001c0001t0013g0259 others(3): Show |
6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-107G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231664 | |||||||
chr14:99231815 | G | A | 1 | a0001c0002t0011g0338 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.428-258C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231815 | |||||||
chr14:99231867 | A | C | 1 | a0001c0002t0003g0253 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.428-310T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231867 | |||||||
chr14:99231874 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.428-317C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231874 | |||||||
chr14:99231932 | T | G | 1 | a0001c0001t0009g0135 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.428-375A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231932 | |||||||
chr14:99231976 | G | A | 3 | a0001c0001t0015g0030 a0001c0001t0018g0090 a0001c0005t0010g0029 |
3 | HG02723.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.428-419C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231976 | |||||||
chr14:99232158 | C | T | 6 | a0001c0001t0009g0088 a0001c0001t0013g0181 a0001c0001t0013g0259 others(3): Show |
6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-601G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232158 | |||||||
chr14:99232198 | C | A | 2 | a0001c0001t0034g0007 a0001c0001t0082g0347 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.428-641G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232198 | |||||||
chr14:99232454 | T | C | 5 | a0001c0001t0001g0185 a0001c0001t0006g0070 a0001c0001t0006g0080 others(2): Show |
5 | HG01074.hp1 HG02015.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-897A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232454 | |||||||
chr14:99232505 | G | C | 4 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0005g0324 others(1): Show |
4 | HG01106.hp2 HG01243.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-948C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232505 | |||||||
chr14:99232594 | C | A | 82 | a0001c0001t0001g0163 a0001c0001t0001g0184 a0001c0001t0001g0212 others(79): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.428-1037G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232594 | |||||||
chr14:99232595 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.428-1038C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232595 | |||||||
chr14:99232740 | T | C | 5 | a0001c0001t0001g0185 a0001c0001t0006g0070 a0001c0001t0006g0080 others(2): Show |
5 | HG01074.hp1 HG02015.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-1183A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232740 | |||||||
chr14:99232776 | C | T | 7 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0005g0002 others(4): Show |
8 | HG00140.hp1 HG00280.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-1219G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232776 | |||||||
chr14:99232866 | C | T | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.428-1309G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232866 | |||||||
chr14:99233025 | T | C | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.428-1468A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233025 | |||||||
chr14:99233033 | G | A | 1 | a0001c0001t0035g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.428-1476C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233033 | |||||||
chr14:99233359 | C | T | 11 | a0001c0001t0001g0209 a0001c0001t0001g0251 a0001c0001t0001g0276 others(8): Show |
11 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.428-1802G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233359 | |||||||
chr14:99233682 | T | A | 47 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(44): Show |
47 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.428-2125A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233682 | |||||||
chr14:99233743 | C | T | 43 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0001g0230 others(40): Show |
44 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.428-2186G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233743 | |||||||
chr14:99233778 | G | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0285 |
2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.428-2221C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233778 | |||||||
chr14:99233794 | G | A | 10 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(7): Show |
10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.428-2237C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233794 | |||||||
chr14:99234117 | C | T | 133 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.428-2560G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234117 | |||||||
chr14:99234205 | G | A | 1 | a0001c0001t0007g0196 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.428-2648C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234205 | |||||||
chr14:99234482 | C | G | 1 | a0001c0001t0041g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.428-2925G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234482 | |||||||
chr14:99234657 | A | G | 2 | a0001c0001t0034g0007 a0001c0001t0082g0347 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.428-3100T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234657 | |||||||
chr14:99234677 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0006g0082 |
2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.428-3120C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234677 | |||||||
chr14:99234759 | G | T | 29 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0161 others(26): Show |
29 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.428-3202C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234759 | |||||||
chr14:99234855 | C | CA | 48 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0001t0001g0202 others(45): Show |
48 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.428-3299dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234855 | |||||||
chr14:99234855 | CA | C | 33 | a0001c0001t0001g0230 a0001c0001t0002g0016 a0001c0001t0002g0064 others(30): Show |
34 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.428-3299delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234855 | |||||||
chr14:99234855 | CAA | C | 34 | a0001c0001t0002g0065 a0001c0001t0002g0071 a0001c0001t0002g0072 others(31): Show |
35 | HG01099.hp1 HG01109.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.428-3300_428-3299d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234855 | |||||||
chr14:99234880 | A | AAAAG | 6 | a0001c0001t0005g0332 a0001c0001t0005g0336 a0001c0001t0007g0238 others(3): Show |
6 | HG00673.hp2 HG01192.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-3324_428-3323i others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234880 | |||||||
chr14:99234880 | A | AAAG | 25 | a0001c0001t0001g0163 a0001c0001t0001g0209 a0001c0001t0001g0217 others(22): Show |
25 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.428-3324_428-3323i others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234880 | |||||||
chr14:99234880 | A | AAG | 18 | a0001c0001t0001g0222 a0001c0001t0001g0237 a0001c0001t0001g0266 others(15): Show |
18 | HG00621.hp1 HG01433.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.428-3324_428-3323i others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234880 | |||||||
chr14:99234880 | A | AG | 23 | a0001c0001t0001g0156 a0001c0001t0001g0212 a0001c0001t0001g0245 others(20): Show |
23 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.428-3324dupC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234880 | |||||||
chr14:99234880 | A | G | 44 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0161 others(41): Show |
44 | HG00558.hp2 HG00733.hp2 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.428-3323T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234880 | |||||||
chr14:99235038 | T | C | 1 | a0001c0001t0002g0112 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.428-3481A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235038 | |||||||
chr14:99235044 | C | T | 1 | a0001c0002t0004g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.428-3487G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235044 | |||||||
chr14:99235122 | G | C | 198 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.428-3565C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235122 | |||||||
chr14:99235171 | G | A | 13 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(10): Show |
13 | HG00423.hp2 HG00621.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.428-3614C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235171 | |||||||
chr14:99235238 | C | T | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.428-3681G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235238 | |||||||
chr14:99235344 | G | A | 1 | a0001c0002t0003g0208 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.428-3787C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235344 | |||||||
chr14:99235644 | TC | T | 40 | a0001c0001t0002g0065 a0001c0001t0002g0071 a0001c0001t0002g0072 others(37): Show |
41 | HG00639.hp2 HG01099.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.428-4088delG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235644 | |||||||
chr14:99235746 | G | T | 1 | a0001c0002t0017g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.428-4189C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235746 | |||||||
chr14:99235831 | A | AT | 13 | a0001c0001t0001g0163 a0001c0001t0001g0222 a0001c0001t0001g0237 others(10): Show |
13 | HG00423.hp2 HG00621.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.428-4275dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235831 | |||||||
chr14:99235898 | A | T | 1 | a0001c0001t0001g0231 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.428-4341T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235898 | |||||||
chr14:99235906 | TA | T | 194 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(191): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.428-4350delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235906 | |||||||
chr14:99235953 | T | A | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.428-4396A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235953 | |||||||
chr14:99235961 | G | C | 1 | a0001c0001t0002g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.428-4404C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235961 | |||||||
chr14:99236171 | G | A | 1 | a0001c0002t0004g0137 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.428-4614C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99236171 | |||||||
chr14:99236253 | A | T | 2 | a0001c0001t0007g0203 a0001c0002t0004g0125 |
2 | HG00597.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.428-4696T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99236253 | |||||||
chr14:99237041 | C | T | 1 | a0001c0002t0004g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.428-5484G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237041 | |||||||
chr14:99237137 | G | A | 31 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(28): Show |
32 | HG01099.hp1 HG01109.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.428-5580C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237137 | |||||||
chr14:99237236 | CT | C | 43 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(40): Show |
44 | HG00639.hp2 HG00673.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.428-5680delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237236 | |||||||
chr14:99237621 | C | G | 14 | a0001c0001t0001g0163 a0001c0001t0001g0198 a0001c0001t0001g0222 others(11): Show |
14 | HG00423.hp2 HG00621.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.428-6064G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237621 | |||||||
chr14:99237631 | C | T | 44 | a0001c0001t0001g0184 a0001c0001t0001g0230 a0001c0001t0001g0282 others(41): Show |
45 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.428-6074G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237631 | |||||||
chr14:99237844 | C | A | 159 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(156): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.428-6287G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237844 | |||||||
chr14:99237860 | C | A | 1 | a0001c0001t0010g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.428-6303G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237860 | |||||||
chr14:99237907 | G | A | 31 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(28): Show |
32 | HG01099.hp1 HG01109.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.428-6350C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237907 | |||||||
chr14:99238090 | A | G | 44 | a0001c0001t0001g0184 a0001c0001t0001g0230 a0001c0001t0001g0282 others(41): Show |
45 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.428-6533T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238090 | |||||||
chr14:99238113 | G | A | 1 | a0003c0009t0003g0263 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.428-6556C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238113 | |||||||
chr14:99238115 | G | A | 44 | a0001c0001t0001g0184 a0001c0001t0001g0230 a0001c0001t0001g0282 others(41): Show |
45 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.428-6558C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238115 | |||||||
chr14:99238195 | G | A | 1 | a0001c0002t0003g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.428-6638C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238195 | |||||||
chr14:99238344 | G | A | 1 | a0001c0001t0051g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.428-6787C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238344 | |||||||
chr14:99238432 | C | T | 1 | a0001c0002t0072g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.428-6875G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238432 | |||||||
chr14:99238954 | T | A | 148 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(145): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.428-7397A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238954 | |||||||
chr14:99238989 | A | ACATATG | 14 | a0001c0001t0001g0163 a0001c0001t0001g0198 a0001c0001t0001g0222 others(11): Show |
14 | HG00423.hp2 HG00621.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.428-7438_428-7433d others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238989 | |||||||
chr14:99238994 | T | C | 45 | a0001c0001t0001g0184 a0001c0001t0001g0230 a0001c0001t0001g0282 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.428-7437A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238994 | |||||||
chr14:99238999 | G | A | 200 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.428-7442C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238999 | |||||||
chr14:99239420 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.428-7863C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239420 | |||||||
chr14:99239488 | G | C | 5 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0252 others(2): Show |
5 | HG00609.hp2 HG03831.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-7931C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239488 | |||||||
chr14:99239617 | G | A | 149 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(146): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.428-8060C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239617 | |||||||
chr14:99239625 | T | A | 2 | a0001c0001t0025g0228 a0001c0001t0070g0290 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.428-8068A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239625 | |||||||
chr14:99239785 | A | G | 1 | a0001c0002t0003g0248 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.428-8228T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239785 | |||||||
chr14:99239875 | G | A | 7 | a0001c0001t0002g0039 a0001c0001t0034g0007 a0001c0001t0082g0347 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-8318C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239875 | |||||||
chr14:99240137 | G | A | 45 | a0001c0001t0001g0184 a0001c0001t0001g0230 a0001c0001t0001g0282 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.428-8580C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240137 | |||||||
chr14:99240283 | G | A | 149 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(146): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.428-8726C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240283 | |||||||
chr14:99240297 | C | T | 4 | a0001c0001t0009g0123 a0001c0001t0025g0228 a0001c0001t0070g0290 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-8740G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240297 | |||||||
chr14:99240369 | T | C | 1 | a0001c0001t0005g0310 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.428-8812A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240369 | |||||||
chr14:99240500 | A | T | 24 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0239 others(21): Show |
24 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.428-8943T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240500 | |||||||
chr14:99240691 | C | T | 1 | a0001c0001t0006g0082 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.428-9134G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240691 | |||||||
chr14:99240774 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.428-9217G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240774 | |||||||
chr14:99240849 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0063g0170 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.428-9292G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240849 | |||||||
chr14:99240854 | C | T | 1 | a0001c0001t0014g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.428-9297G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240854 | |||||||
chr14:99240880 | G | A | 198 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.428-9323C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240880 | |||||||
chr14:99240991 | T | C | 4 | a0001c0001t0010g0068 a0001c0001t0010g0127 a0001c0001t0032g0005 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-9434A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240991 | |||||||
chr14:99241018 | AT | A | 61 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(58): Show |
61 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.428-9462delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241018 | |||||||
chr14:99241487 | A | G | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.428-9930T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241487 | |||||||
chr14:99241492 | C | T | 3 | a0001c0001t0010g0084 a0001c0001t0014g0083 a0001c0001t0062g0219 |
3 | HG02615.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.428-9935G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241492 | |||||||
chr14:99241596 | C | T | 53 | a0001c0001t0001g0184 a0001c0001t0001g0230 a0001c0001t0001g0282 others(50): Show |
54 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.428-10039G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241596 | |||||||
chr14:99241677 | C | T | 3 | a0001c0001t0001g0202 a0001c0002t0003g0249 a0001c0002t0008g0307 |
3 | HG00438.hp1 HG00609.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.428-10120G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241677 | |||||||
chr14:99241936 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.428-10379G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241936 | |||||||
chr14:99241992 | C | T | 1 | a0001c0001t0034g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.428-10435G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241992 | |||||||
chr14:99241997 | G | A | 3 | a0001c0002t0003g0173 a0001c0002t0003g0174 a0001c0002t0003g0182 |
3 | HG02258.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.428-10440C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241997 | |||||||
chr14:99242028 | G | A | 15 | a0001c0001t0001g0198 a0001c0001t0001g0222 a0001c0001t0001g0237 others(12): Show |
15 | HG00621.hp1 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.428-10471C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242028 | |||||||
chr14:99242310 | G | A | 8 | a0001c0001t0001g0276 a0001c0001t0003g0267 a0001c0001t0005g0326 others(5): Show |
8 | HG00140.hp2 HG00738.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.428-10753C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242310 | |||||||
chr14:99242334 | C | T | 1 | a0001c0001t0049g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.428-10777G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242334 | |||||||
chr14:99242400 | G | A | 4 | a0001c0001t0010g0127 a0001c0001t0032g0005 a0001c0001t0050g0086 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-10843C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242400 | |||||||
chr14:99242466 | A | G | 2 | a0001c0001t0002g0019 a0001c0002t0004g0034 |
2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.428-10909T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242466 | |||||||
chr14:99242494 | A | C | 1 | a0001c0001t0034g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.428-10937T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242494 | |||||||
chr14:99242539 | G | A | 116 | a0001c0001t0001g0158 a0001c0001t0001g0171 a0001c0001t0001g0177 others(113): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.428-10982C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242539 | |||||||
chr14:99242598 | C | T | 2 | a0001c0001t0009g0096 a0001c0001t0035g0010 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.428-11041G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242598 | |||||||
chr14:99243099 | G | A | 58 | a0001c0001t0001g0158 a0001c0001t0001g0171 a0001c0001t0001g0177 others(55): Show |
58 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.428-11542C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243099 | |||||||
chr14:99243139 | C | A | 3 | a0001c0001t0015g0030 a0001c0001t0018g0090 a0001c0005t0010g0029 |
3 | HG02723.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.428-11582G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243139 | |||||||
chr14:99243281 | C | T | 34 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0239 others(31): Show |
34 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.428-11724G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243281 | |||||||
chr14:99243365 | A | C | 90 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0198 others(87): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.428-11808T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243365 | |||||||
chr14:99243424 | A | G | 30 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0239 others(27): Show |
30 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.428-11867T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243424 | |||||||
chr14:99243533 | G | A | 1 | a0001c0001t0006g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.428-11976C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243533 | |||||||
chr14:99243693 | A | G | 3 | a0001c0001t0009g0096 a0001c0001t0010g0060 a0001c0001t0035g0010 |
3 | HG02970.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.428-12136T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243693 | |||||||
chr14:99243837 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.428-12280C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243837 | |||||||
chr14:99243918 | TAAAAA | T | 6 | a0001c0001t0001g0198 a0001c0001t0011g0341 a0001c0001t0039g0138 others(3): Show |
6 | HG00621.hp1 HG02055.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-12366_428-1236 others(9): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243918 | |||||||
chr14:99243918 | TAAAAAA | T | 19 | a0001c0001t0001g0184 a0001c0001t0001g0222 a0001c0001t0001g0230 others(16): Show |
19 | HG01074.hp1 HG01106.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.428-12367_428-1236 others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243918 | |||||||
chr14:99243918 | TAAAAAAA | T | 43 | a0001c0001t0002g0016 a0001c0001t0002g0055 a0001c0001t0002g0064 others(40): Show |
44 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.428-12368_428-1236 others(11): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243918 | |||||||
chr14:99243918 | TAAAAAAA others(11): Show |
T | 3 | a0001c0001t0009g0096 a0001c0001t0010g0060 a0001c0001t0035g0010 |
3 | HG02970.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.428-12379_428-1236 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243918 | |||||||
chr14:99243918 | TAAAAAAA others(13): Show |
T | 2 | a0001c0001t0025g0228 a0001c0001t0064g0186 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.428-12381_428-1236 others(24): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243918 | |||||||
chr14:99243942 | A | T | 1 | a0001c0002t0080g0345 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.428-12385T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243942 | |||||||
chr14:99243964 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.428-12407C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243964 | |||||||
chr14:99243988 | C | G | 1 | a0001c0001t0035g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.428-12431G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243988 | |||||||
chr14:99243989 | G | T | 1 | a0001c0001t0020g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.428-12432C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243989 | |||||||
chr14:99244009 | A | T | 1 | a0001c0001t0074g0340 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.428-12452T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244009 | |||||||
chr14:99244109 | C | T | 1 | a0001c0001t0006g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.428-12552G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244109 | |||||||
chr14:99244121 | T | C | 3 | a0001c0001t0009g0054 a0001c0002t0003g0264 a0001c0002t0017g0134 |
3 | HG02055.hp2 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.428-12564A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244121 | |||||||
chr14:99244295 | C | A | 1 | a0001c0002t0004g0137 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.428-12738G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244295 | |||||||
chr14:99244296 | C | T | 1 | a0001c0002t0004g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.428-12739G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244296 | |||||||
chr14:99244300 | CT | C | 4 | a0001c0001t0001g0171 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-12744delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244300 | |||||||
chr14:99244301 | T | A | 3 | a0001c0002t0080g0345 a0001c0006t0023g0190 a0001c0006t0023g0191 |
3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.428-12744A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244301 | |||||||
chr14:99244301 | T | C | 6 | a0001c0001t0001g0157 a0001c0001t0009g0096 a0001c0001t0010g0060 others(3): Show |
6 | HG02970.hp2 HG03579.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-12744A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244301 | |||||||
chr14:99244303 | A | C | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.428-12746T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244303 | |||||||
chr14:99244303 | A | T | 3 | a0001c0001t0001g0157 a0001c0002t0003g0159 a0004c0010t0007g0287 |
3 | NA18971.hp2 NA18998.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.428-12746T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244303 | |||||||
chr14:99244350 | C | T | 34 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(31): Show |
35 | HG01099.hp1 HG01109.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.428-12793G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244350 | |||||||
chr14:99244506 | C | T | 257 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(254): Show |
258 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.428-12949G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244506 | |||||||
chr14:99244634 | A | G | 1 | a0001c0001t0009g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427+12837T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244634 | |||||||
chr14:99244994 | G | A | 257 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(254): Show |
258 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.427+12477C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244994 | |||||||
chr14:99245057 | T | C | 110 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0179 others(107): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.427+12414A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245057 | |||||||
chr14:99245415 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.427+12056G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245415 | |||||||
chr14:99245544 | C | A | 1 | a0001c0001t0015g0077 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427+11927G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245544 | |||||||
chr14:99245545 | C | A | 1 | a0001c0001t0015g0077 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427+11926G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245545 | |||||||
chr14:99245581 | C | A | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.427+11890G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245581 | |||||||
chr14:99245616 | A | G | 110 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0179 others(107): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.427+11855T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245616 | |||||||
chr14:99245695 | G | A | 56 | a0001c0001t0001g0184 a0001c0001t0001g0230 a0001c0001t0001g0282 others(53): Show |
57 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.427+11776C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245695 | |||||||
chr14:99245957 | G | A | 1 | a0001c0001t0005g0330 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.427+11514C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245957 | |||||||
chr14:99245964 | G | A | 83 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0179 others(80): Show |
83 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.427+11507C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245964 | |||||||
chr14:99246032 | C | G | 46 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(43): Show |
46 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.427+11439G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246032 | |||||||
chr14:99246069 | G | A | 6 | a0001c0001t0007g0256 a0001c0001t0007g0278 a0001c0002t0007g0254 others(3): Show |
6 | HG01168.hp2 HG01169.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+11402C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246069 | |||||||
chr14:99246112 | T | C | 32 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0239 others(29): Show |
32 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.427+11359A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246112 | |||||||
chr14:99246276 | A | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0241 a0001c0001t0005g0308 |
3 | HG01109.hp1 HG01192.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.427+11195T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246276 | |||||||
chr14:99246283 | T | G | 1 | a0001c0001t0002g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.427+11188A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246283 | |||||||
chr14:99246360 | T | C | 15 | a0001c0001t0001g0198 a0001c0001t0001g0222 a0001c0001t0001g0237 others(12): Show |
15 | HG00621.hp1 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.427+11111A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246360 | |||||||
chr14:99246457 | C | T | 42 | a0001c0001t0001g0184 a0001c0001t0001g0230 a0001c0001t0001g0282 others(39): Show |
43 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.427+11014G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246457 | |||||||
chr14:99246483 | C | G | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427+10988G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246483 | |||||||
chr14:99246485 | A | G | 2 | a0001c0001t0055g0195 a0001c0002t0058g0269 |
2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.427+10986T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246485 | |||||||
chr14:99246556 | T | C | 15 | a0001c0001t0001g0185 a0001c0001t0001g0209 a0001c0001t0001g0251 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.427+10915A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246556 | |||||||
chr14:99246608 | A | G | 54 | a0001c0001t0001g0184 a0001c0001t0001g0230 a0001c0001t0001g0282 others(51): Show |
55 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.427+10863T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246608 | |||||||
chr14:99246911 | A | G | 1 | a0001c0002t0003g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.427+10560T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246911 | |||||||
chr14:99246946 | C | T | 2 | a0001c0001t0011g0316 a0001c0002t0076g0317 |
2 | NA18950.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.427+10525G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246946 | |||||||
chr14:99247662 | C | T | 1 | a0001c0001t0035g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.427+9809G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99247662 | |||||||
chr14:99247694 | C | T | 1 | a0001c0002t0008g0319 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.427+9777G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99247694 | |||||||
chr14:99247827 | G | C | 1 | a0001c0001t0035g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.427+9644C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99247827 | |||||||
chr14:99248096 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.427+9375C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99248096 | |||||||
chr14:99248269 | A | G | 2 | a0001c0001t0009g0123 a0001c0002t0060g0176 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.427+9202T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99248269 | |||||||
chr14:99248420 | G | A | 260 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(257): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.427+9051C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99248420 | |||||||
chr14:99248795 | C | T | 1 | a0001c0001t0034g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.427+8676G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99248795 | |||||||
chr14:99249062 | A | C | 1 | a0001c0001t0002g0032 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.427+8409T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249062 | |||||||
chr14:99249070 | G | A | 31 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0239 others(28): Show |
31 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.427+8401C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249070 | |||||||
chr14:99249237 | A | G | 2 | a0001c0001t0009g0096 a0001c0001t0010g0060 |
2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.427+8234T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249237 | |||||||
chr14:99249495 | A | G | 4 | a0001c0001t0013g0189 a0001c0002t0061g0169 a0001c0004t0001g0001 others(1): Show |
5 | HG02630.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+7976T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249495 | |||||||
chr14:99249587 | T | G | 69 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0209 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.427+7884A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249587 | |||||||
chr14:99249594 | T | G | 1 | a0001c0002t0004g0136 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.427+7877A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249594 | |||||||
chr14:99249631 | C | T | 2 | a0001c0001t0002g0019 a0001c0002t0004g0034 |
2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.427+7840G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249631 | |||||||
chr14:99249690 | A | ATCTCTGG others(3): Show |
1 | a0001c0001t0035g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.427+7771_427+7780d others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249690 | |||||||
chr14:99249789 | T | C | 17 | a0001c0001t0001g0192 a0001c0001t0001g0241 a0001c0001t0001g0243 others(14): Show |
17 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.427+7682A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249789 | |||||||
chr14:99250026 | G | A | 1 | a0001c0002t0004g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.427+7445C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250026 | |||||||
chr14:99250033 | C | CT | 37 | a0001c0001t0001g0217 a0001c0001t0002g0071 a0001c0001t0002g0072 others(34): Show |
38 | HG01099.hp1 HG01175.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.427+7437dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250033 | |||||||
chr14:99250033 | CT | C | 136 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0179 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.427+7437delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250033 | |||||||
chr14:99250075 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.427+7396C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250075 | |||||||
chr14:99250225 | C | T | 47 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(44): Show |
47 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.427+7246G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250225 | |||||||
chr14:99250241 | T | C | 33 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0239 others(30): Show |
33 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.427+7230A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250241 | |||||||
chr14:99250413 | G | A | 1 | a0001c0001t0034g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.427+7058C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250413 | |||||||
chr14:99250438 | A | T | 1 | a0001c0002t0004g0136 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.427+7033T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250438 | |||||||
chr14:99250481 | C | T | 2 | a0001c0001t0001g0177 a0001c0002t0004g0074 |
2 | HG03669.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.427+6990G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250481 | |||||||
chr14:99250501 | C | T | 1 | a0001c0001t0035g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.427+6970G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250501 | |||||||
chr14:99250571 | T | C | 71 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0209 others(68): Show |
72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.427+6900A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250571 | |||||||
chr14:99250818 | G | A | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.427+6653C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250818 | |||||||
chr14:99250867 | G | GA | 341 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(338): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.427+6603dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250867 | |||||||
chr14:99250905 | G | C | 331 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(328): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.427+6566C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250905 | |||||||
chr14:99251570 | G | A | 331 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(328): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.427+5901C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99251570 | |||||||
chr14:99251768 | T | C | 70 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0209 others(67): Show |
71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.427+5703A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99251768 | |||||||
chr14:99251836 | G | A | 56 | a0001c0001t0001g0158 a0001c0001t0001g0171 a0001c0001t0001g0177 others(53): Show |
56 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.427+5635C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99251836 | |||||||
chr14:99252179 | G | A | 1 | a0001c0002t0072g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.427+5292C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252179 | |||||||
chr14:99252261 | G | A | 4 | a0001c0001t0009g0054 a0001c0002t0003g0264 a0001c0002t0004g0079 others(1): Show |
4 | HG01934.hp2 HG02055.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.427+5210C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252261 | |||||||
chr14:99252408 | G | A | 1 | a0001c0002t0003g0193 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.427+5063C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252408 | |||||||
chr14:99252526 | G | C | 1 | a0001c0002t0004g0136 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.427+4945C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252526 | |||||||
chr14:99252586 | G | A | 244 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0166 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.427+4885C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252586 | |||||||
chr14:99252588 | G | A | 47 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(44): Show |
47 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.427+4883C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252588 | |||||||
chr14:99252685 | C | T | 1 | a0001c0002t0001g0236 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.427+4786G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252685 | |||||||
chr14:99252695 | C | G | 1 | a0001c0001t0001g0279 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.427+4776G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252695 | |||||||
chr14:99252807 | G | A | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.427+4664C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252807 | |||||||
chr14:99252882 | A | G | 267 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(264): Show |
268 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.427+4589T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252882 | |||||||
chr14:99253055 | C | T | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427+4416G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253055 | |||||||
chr14:99253131 | A | G | 9 | a0001c0001t0001g0227 a0001c0001t0003g0275 a0001c0001t0003g0285 others(6): Show |
9 | HG00639.hp1 HG00642.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.427+4340T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253131 | |||||||
chr14:99253343 | T | C | 132 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0177 others(129): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.427+4128A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253343 | |||||||
chr14:99253362 | A | G | 4 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0252 others(1): Show |
4 | HG00609.hp2 NA18948.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.427+4109T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253362 | |||||||
chr14:99253391 | A | G | 21 | a0001c0001t0001g0185 a0001c0001t0001g0209 a0001c0001t0006g0080 others(18): Show |
21 | HG01496.hp1 HG01516.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.427+4080T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253391 | |||||||
chr14:99253465 | C | T | 2 | a0001c0001t0010g0067 a0001c0002t0017g0066 |
2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.427+4006G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253465 | |||||||
chr14:99253536 | A | G | 167 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(164): Show |
167 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.427+3935T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253536 | |||||||
chr14:99253537 | T | G | 1 | a0001c0001t0006g0017 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.427+3934A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253537 | |||||||
chr14:99253858 | A | G | 4 | a0001c0001t0009g0135 a0001c0001t0010g0084 a0001c0001t0014g0083 others(1): Show |
4 | HG02615.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.427+3613T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253858 | |||||||
chr14:99254233 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.427+3238G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254233 | |||||||
chr14:99254271 | A | C | 1 | a0001c0002t0072g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.427+3200T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254271 | |||||||
chr14:99254313 | A | T | 2 | a0001c0001t0039g0138 a0001c0002t0004g0136 |
2 | NA19009.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.427+3158T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254313 | |||||||
chr14:99254414 | G | A | 1 | a0001c0002t0003g0248 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.427+3057C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254414 | |||||||
chr14:99254501 | C | T | 1 | a0001c0001t0007g0256 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.427+2970G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254501 | |||||||
chr14:99254583 | G | C | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427+2888C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254583 | |||||||
chr14:99254642 | G | A | 128 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0177 others(125): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.427+2829C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254642 | |||||||
chr14:99254738 | G | A | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427+2733C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254738 | |||||||
chr14:99254871 | C | CA | 7 | a0001c0001t0001g0188 a0001c0001t0010g0127 a0001c0001t0025g0164 others(4): Show |
7 | HG01891.hp2 HG02723.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.427+2599dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254871 | |||||||
chr14:99254890 | A | G | 1 | a0001c0001t0034g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.427+2581T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254890 | |||||||
chr14:99255038 | T | C | 1 | a0001c0001t0006g0082 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.427+2433A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255038 | |||||||
chr14:99255154 | G | A | 1 | a0001c0002t0003g0246 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.427+2317C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255154 | |||||||
chr14:99255178 | G | A | 1 | a0001c0001t0009g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.427+2293C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255178 | |||||||
chr14:99255405 | G | GAAAAAAA others(3): Show |
2 | a0001c0001t0001g0252 a0001c0001t0005g0336 |
2 | HG00609.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.427+2056_427+2065d others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | |||||||
chr14:99255405 | G | GAAAAAAA others(6): Show |
1 | a0001c0002t0003g0253 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.427+2053_427+2065d others(15): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | |||||||
chr14:99255405 | GA | G | 179 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(176): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.427+2065delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | |||||||
chr14:99255405 | GAAA | G | 26 | a0001c0001t0001g0177 a0001c0001t0001g0212 a0001c0001t0002g0019 others(23): Show |
26 | HG00423.hp1 HG01517.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.427+2063_427+2065d others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | |||||||
chr14:99255405 | GAAAA | G | 68 | a0001c0001t0001g0179 a0001c0001t0001g0184 a0001c0001t0001g0188 others(65): Show |
69 | HG00438.hp2 HG00597.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.427+2062_427+2065d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | |||||||
chr14:99255405 | GAAAAA | G | 11 | a0001c0001t0001g0187 a0001c0001t0002g0025 a0001c0001t0002g0026 others(8): Show |
11 | HG00099.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.427+2061_427+2065d others(7): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | |||||||
chr14:99255405 | GAAAAAA | G | 7 | a0001c0001t0009g0135 a0001c0001t0010g0084 a0001c0001t0014g0083 others(4): Show |
7 | HG02055.hp2 HG02615.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+2060_427+2065d others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | |||||||
chr14:99255405 | GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0005g0334 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.427+2056_427+2065d others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | |||||||
chr14:99255405 | GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0006g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.427+2055_427+2065d others(13): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | |||||||
chr14:99255405 | GAAAAAAA others(6): Show |
G | 2 | a0001c0001t0007g0168 a0001c0002t0046g0015 |
2 | HG01517.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.427+2053_427+2065d others(15): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | |||||||
chr14:99255419 | A | G | 1 | a0001c0001t0012g0148 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.427+2052T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255419 | |||||||
chr14:99255424 | A | C | 1 | a0001c0001t0001g0284 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.427+2047T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255424 | |||||||
chr14:99255431 | A | C | 220 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(217): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.427+2040T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255431 | |||||||
chr14:99255542 | G | C | 4 | a0001c0001t0009g0054 a0001c0001t0035g0010 a0001c0002t0003g0264 others(1): Show |
4 | HG02055.hp2 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.427+1929C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255542 | |||||||
chr14:99255629 | A | G | 1 | a0001c0001t0012g0147 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.427+1842T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255629 | |||||||
chr14:99255678 | C | T | 1 | a0001c0001t0002g0122 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.427+1793G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255678 | |||||||
chr14:99255795 | G | C | 1 | a0001c0002t0003g0193 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.427+1676C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255795 | |||||||
chr14:99255943 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.427+1528G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255943 | |||||||
chr14:99255953 | G | C | 36 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0282 others(33): Show |
37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.427+1518C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255953 | |||||||
chr14:99255963 | C | T | 1 | a0001c0001t0009g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.427+1508G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255963 | |||||||
chr14:99256068 | A | G | 345 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(342): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.427+1403T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256068 | |||||||
chr14:99256108 | C | T | 2 | a0001c0002t0007g0254 a0001c0002t0007g0255 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.427+1363G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256108 | |||||||
chr14:99256299 | A | G | 345 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(342): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.427+1172T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256299 | |||||||
chr14:99256418 | C | T | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.427+1053G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256418 | |||||||
chr14:99256712 | G | A | 6 | a0001c0001t0009g0091 a0001c0001t0009g0094 a0001c0001t0010g0068 others(3): Show |
6 | HG02572.hp2 HG03098.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.427+759C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256712 | |||||||
chr14:99256791 | G | A | 1 | a0001c0002t0075g0325 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.427+680C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256791 | |||||||
chr14:99256867 | C | G | 2 | a0001c0001t0003g0247 a0001c0001t0077g0342 |
2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.427+604G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256867 | |||||||
chr14:99256960 | G | C | 85 | a0001c0001t0001g0177 a0001c0001t0001g0184 a0001c0001t0001g0187 others(82): Show |
86 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.427+511C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256960 | |||||||
chr14:99257124 | G | A | 345 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(342): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.427+347C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99257124 | |||||||
chr14:99257216 | G | A | 4 | a0001c0001t0013g0189 a0001c0002t0061g0169 a0001c0004t0001g0001 others(1): Show |
5 | HG02630.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+255C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99257216 | |||||||
chr14:99257346 | G | A | 7 | a0001c0001t0001g0171 a0001c0001t0002g0040 a0001c0001t0002g0044 others(4): Show |
7 | HG00733.hp1 HG02145.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+125C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99257346 | |||||||
chr14:99258196 | C | G | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.59-357G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258196 | |||||||
chr14:99258264 | A | G | 2 | a0001c0001t0002g0025 a0001c0001t0002g0026 |
2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.59-425T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258264 | |||||||
chr14:99258351 | C | G | 2 | a0001c0001t0001g0179 a0001c0001t0063g0170 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.59-512G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258351 | |||||||
chr14:99258446 | G | A | 2 | a0001c0001t0005g0310 a0001c0001t0006g0047 |
2 | HG00099.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.59-607C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258446 | |||||||
chr14:99258796 | C | T | 41 | a0001c0001t0001g0222 a0001c0001t0001g0234 a0001c0001t0001g0237 others(38): Show |
41 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.59-957G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258796 | |||||||
chr14:99258894 | G | GT | 217 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(214): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.59-1056dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258894 | |||||||
chr14:99258894 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.59-1055C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258894 | |||||||
chr14:99258912 | A | G | 345 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(342): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.59-1073T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258912 | |||||||
chr14:99259005 | C | CG | 209 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(206): Show |
209 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.59-1167_59-1166ins others(1): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259005 | |||||||
chr14:99259006 | A | G | 8 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0233 others(5): Show |
8 | HG00609.hp2 HG03239.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-1167T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259006 | |||||||
chr14:99259076 | C | T | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.59-1237G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259076 | |||||||
chr14:99259214 | G | A | 8 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0233 others(5): Show |
8 | HG00609.hp2 HG03239.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-1375C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259214 | |||||||
chr14:99259394 | A | G | 2 | a0001c0001t0003g0247 a0001c0001t0077g0342 |
2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.59-1555T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259394 | |||||||
chr14:99259589 | G | A | 1 | a0001c0001t0071g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.59-1750C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259589 | |||||||
chr14:99259663 | G | C | 215 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(212): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.59-1824C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259663 | |||||||
chr14:99259668 | A | G | 8 | a0001c0001t0001g0220 a0001c0001t0012g0142 a0001c0001t0012g0143 others(5): Show |
8 | NA18968.hp1 NA18969.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-1829T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259668 | |||||||
chr14:99259704 | C | T | 2 | a0001c0001t0001g0157 a0004c0010t0007g0287 |
2 | NA18971.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.59-1865G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259704 | |||||||
chr14:99259793 | C | T | 2 | a0001c0001t0006g0133 a0001c0001t0010g0132 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.59-1954G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259793 | |||||||
chr14:99259881 | C | T | 3 | a0001c0001t0009g0054 a0001c0002t0003g0264 a0001c0002t0017g0134 |
3 | HG02055.hp2 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.59-2042G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259881 | |||||||
chr14:99259981 | G | A | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.59-2142C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259981 | |||||||
chr14:99260072 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.59-2233C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260072 | |||||||
chr14:99260220 | G | A | 1 | a0001c0002t0045g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.59-2381C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260220 | |||||||
chr14:99260311 | G | A | 1 | a0001c0002t0003g0246 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59-2472C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260311 | |||||||
chr14:99260382 | T | C | 181 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(178): Show |
181 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.59-2543A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260382 | |||||||
chr14:99260430 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0002g0069 a0001c0001t0010g0084 others(1): Show |
4 | HG01934.hp1 HG01978.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-2591C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260430 | |||||||
chr14:99260584 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.59-2745G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260584 | |||||||
chr14:99260627 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.59-2788G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260627 | |||||||
chr14:99260748 | C | T | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.59-2909G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260748 | |||||||
chr14:99260749 | G | A | 39 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0282 others(36): Show |
40 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.59-2910C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260749 | |||||||
chr14:99260777 | G | A | 181 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(178): Show |
181 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.59-2938C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260777 | |||||||
chr14:99261254 | A | G | 183 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(180): Show |
183 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.59-3415T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261254 | |||||||
chr14:99261255 | A | G | 82 | a0001c0001t0001g0177 a0001c0001t0001g0184 a0001c0001t0001g0187 others(79): Show |
83 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.59-3416T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261255 | |||||||
chr14:99261283 | G | A | 6 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0233 others(3): Show |
6 | HG00609.hp2 HG03239.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3444C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261283 | |||||||
chr14:99261452 | A | G | 1 | a0001c0001t0033g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.59-3613T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261452 | |||||||
chr14:99261478 | T | C | 1 | a0001c0001t0007g0278 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.59-3639A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261478 | |||||||
chr14:99261513 | C | T | 1 | a0001c0001t0009g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.59-3674G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261513 | |||||||
chr14:99261805 | G | A | 1 | a0001c0002t0004g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-3966C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261805 | |||||||
chr14:99261832 | G | A | 2 | a0001c0001t0011g0316 a0001c0002t0076g0317 |
2 | NA18950.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.59-3993C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261832 | |||||||
chr14:99261878 | T | TAC | 28 | a0001c0001t0001g0179 a0001c0001t0001g0212 a0001c0001t0002g0019 others(25): Show |
28 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.59-4041_59-4040dup others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261878 | |||||||
chr14:99261903 | G | A | 1 | a0001c0002t0072g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.59-4064C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261903 | |||||||
chr14:99262111 | C | T | 11 | a0001c0001t0002g0019 a0001c0001t0002g0035 a0001c0001t0004g0115 others(8): Show |
11 | HG01109.hp2 HG01175.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-4272G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262111 | |||||||
chr14:99262112 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0063g0170 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.59-4273C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262112 | |||||||
chr14:99262172 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.59-4333C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262172 | |||||||
chr14:99262192 | C | A | 1 | a0001c0001t0005g0336 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.59-4353G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262192 | |||||||
chr14:99262219 | C | T | 3 | a0001c0001t0002g0129 a0001c0001t0081g0346 a0001c0002t0003g0286 |
3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.59-4380G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262219 | |||||||
chr14:99262280 | G | A | 1 | a0001c0001t0049g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.59-4441C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262280 | |||||||
chr14:99262456 | C | T | 77 | a0001c0001t0001g0177 a0001c0001t0001g0184 a0001c0001t0001g0187 others(74): Show |
78 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.59-4617G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262456 | |||||||
chr14:99262465 | T | C | 1 | a0001c0001t0002g0098 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.59-4626A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262465 | |||||||
chr14:99262479 | C | T | 1 | a0001c0001t0003g0267 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.59-4640G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262479 | |||||||
chr14:99262549 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.59-4710G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262549 | |||||||
chr14:99262571 | G | A | 1 | a0001c0001t0007g0168 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.59-4732C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262571 | |||||||
chr14:99262693 | C | T | 1 | a0001c0002t0004g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-4854G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262693 | |||||||
chr14:99262708 | A | G | 8 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(5): Show |
8 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-4869T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262708 | |||||||
chr14:99262740 | G | A | 1 | a0001c0002t0003g0246 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59-4901C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262740 | |||||||
chr14:99262756 | C | T | 1 | a0001c0001t0005g0334 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.59-4917G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262756 | |||||||
chr14:99262768 | C | T | 1 | a0002c0007t0007g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.59-4929G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262768 | |||||||
chr14:99262783 | C | T | 8 | a0001c0001t0002g0064 a0001c0001t0005g0330 a0001c0001t0006g0022 others(5): Show |
8 | HG00735.hp2 HG00741.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-4944G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262783 | |||||||
chr14:99262967 | C | G | 2 | a0001c0001t0009g0096 a0001c0001t0049g0113 |
2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.59-5128G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262967 | |||||||
chr14:99262973 | C | A | 2 | a0001c0001t0006g0133 a0001c0001t0010g0132 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.59-5134G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262973 | |||||||
chr14:99263050 | G | A | 7 | a0001c0001t0001g0177 a0001c0001t0001g0184 a0001c0001t0001g0230 others(4): Show |
7 | HG01074.hp1 HG01106.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-5211C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263050 | |||||||
chr14:99263212 | A | G | 28 | a0001c0001t0001g0179 a0001c0001t0001g0212 a0001c0001t0002g0019 others(25): Show |
28 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.59-5373T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263212 | |||||||
chr14:99263390 | C | G | 1 | a0001c0001t0010g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.59-5551G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263390 | |||||||
chr14:99263436 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.59-5597C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263436 | |||||||
chr14:99263470 | C | A | 21 | a0001c0001t0001g0212 a0001c0001t0002g0019 a0001c0001t0002g0035 others(18): Show |
21 | HG00099.hp2 HG00597.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-5631G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263470 | |||||||
chr14:99263480 | G | C | 1 | a0001c0002t0045g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.59-5641C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263480 | |||||||
chr14:99263626 | A | G | 210 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(207): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.59-5787T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263626 | |||||||
chr14:99263874 | C | T | 6 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0233 others(3): Show |
6 | HG00609.hp2 HG03239.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-6035G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263874 | |||||||
chr14:99264141 | CG | C | 38 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0282 others(35): Show |
39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.59-6303delC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264141 | |||||||
chr14:99264288 | G | GC | 73 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0221 others(70): Show |
74 | HG00438.hp2 HG00639.hp1 HG01106.hp2 others(71): Show |
intron_variant | MODIFIER | c.59-6450dupG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264288 | |||||||
chr14:99264288 | G | GCC | 14 | a0001c0001t0002g0026 a0001c0001t0002g0107 a0001c0001t0004g0115 others(11): Show |
14 | HG00423.hp1 HG00642.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-6451_59-6450dup others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264288 | |||||||
chr14:99264288 | GC | G | 15 | a0001c0001t0001g0156 a0001c0001t0001g0222 a0001c0001t0001g0266 others(12): Show |
15 | HG02071.hp1 HG02486.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-6450delG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264288 | |||||||
chr14:99264295 | C | CG | 11 | a0001c0001t0001g0177 a0001c0001t0001g0184 a0001c0001t0001g0230 others(8): Show |
11 | HG01074.hp1 HG01106.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-6457_59-6456ins others(1): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264295 | |||||||
chr14:99264339 | T | A | 1 | a0001c0002t0072g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.59-6500A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264339 | |||||||
chr14:99264497 | A | AT | 211 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(208): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.59-6659dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264497 | |||||||
chr14:99264538 | T | A | 7 | a0001c0001t0001g0171 a0001c0001t0002g0040 a0001c0001t0002g0044 others(4): Show |
7 | HG00733.hp1 HG02145.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+6623A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264538 | |||||||
chr14:99264546 | G | A | 4 | a0001c0001t0009g0054 a0001c0001t0035g0010 a0001c0002t0003g0264 others(1): Show |
4 | HG02055.hp2 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+6615C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264546 | |||||||
chr14:99264683 | C | G | 1 | a0001c0001t0050g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58+6478G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264683 | |||||||
chr14:99264698 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.58+6463C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264698 | |||||||
chr14:99264703 | T | C | 10 | a0001c0001t0001g0251 a0001c0001t0001g0276 a0001c0001t0005g0326 others(7): Show |
10 | HG00140.hp2 HG00738.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+6458A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264703 | |||||||
chr14:99264827 | C | T | 1 | a0001c0002t0003g0218 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.58+6334G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264827 | |||||||
chr14:99264934 | G | C | 215 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(212): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.58+6227C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264934 | |||||||
chr14:99265070 | C | T | 1 | a0001c0001t0064g0186 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.58+6091G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265070 | |||||||
chr14:99265097 | G | A | 1 | a0001c0002t0008g0296 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.58+6064C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265097 | |||||||
chr14:99265112 | C | G | 1 | a0001c0001t0001g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.58+6049G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265112 | |||||||
chr14:99265330 | C | A | 8 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(5): Show |
8 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+5831G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265330 | |||||||
chr14:99265394 | A | C | 38 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0001g0282 others(35): Show |
39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.58+5767T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265394 | |||||||
chr14:99265443 | C | T | 1 | a0001c0001t0009g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58+5718G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265443 | |||||||
chr14:99265483 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.58+5678T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265483 | |||||||
chr14:99265508 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.58+5653A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265508 | |||||||
chr14:99265625 | G | T | 1 | a0001c0001t0020g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.58+5536C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265625 | |||||||
chr14:99265789 | G | A | 4 | a0001c0001t0009g0135 a0001c0001t0010g0084 a0001c0001t0014g0083 others(1): Show |
4 | HG02615.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+5372C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265789 | |||||||
chr14:99265804 | T | C | 5 | a0001c0001t0001g0179 a0001c0001t0009g0053 a0001c0001t0063g0170 others(2): Show |
5 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+5357A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265804 | |||||||
chr14:99265824 | C | A | 5 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0252 others(2): Show |
5 | HG00609.hp2 NA18948.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+5337G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265824 | |||||||
chr14:99266079 | G | C | 214 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(211): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.58+5082C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266079 | |||||||
chr14:99266155 | G | T | 4 | a0001c0001t0009g0135 a0001c0001t0010g0084 a0001c0001t0014g0083 others(1): Show |
4 | HG02615.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+5006C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266155 | |||||||
chr14:99266159 | C | T | 5 | a0001c0001t0001g0279 a0001c0001t0007g0229 a0001c0001t0007g0257 others(2): Show |
5 | NA18960.hp2 NA18969.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+5002G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266159 | |||||||
chr14:99266543 | G | A | 4 | a0001c0001t0009g0135 a0001c0001t0010g0084 a0001c0001t0014g0083 others(1): Show |
4 | HG02615.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+4618C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266543 | |||||||
chr14:99266605 | G | A | 2 | a0001c0001t0082g0347 a0001c0002t0004g0036 |
2 | HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.58+4556C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266605 | |||||||
chr14:99266660 | C | T | 5 | a0001c0001t0007g0256 a0001c0001t0007g0278 a0001c0002t0007g0254 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+4501G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266660 | |||||||
chr14:99267047 | G | C | 57 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0226 others(54): Show |
58 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.58+4114C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267047 | |||||||
chr14:99267270 | CA | C | 8 | a0001c0001t0005g0336 a0001c0001t0010g0060 a0001c0001t0013g0181 others(5): Show |
8 | HG02258.hp1 HG02970.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+3890delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267270 | |||||||
chr14:99267271 | A | C | 3 | a0001c0001t0009g0054 a0001c0002t0003g0264 a0001c0002t0017g0134 |
3 | HG02055.hp2 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.58+3890T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267271 | |||||||
chr14:99267327 | T | A | 1 | a0001c0001t0005g0326 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.58+3834A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267327 | |||||||
chr14:99267544 | A | ACC | 31 | a0001c0001t0001g0166 a0001c0001t0002g0064 a0001c0001t0005g0002 others(28): Show |
32 | HG00099.hp1 HG00280.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+3615_58+3616dup others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267544 | |||||||
chr14:99267544 | AC | A | 19 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0002g0065 others(16): Show |
19 | HG01074.hp1 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.58+3616delG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267544 | |||||||
chr14:99267544 | ACC | A | 267 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(264): Show |
268 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.58+3615_58+3616del others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267544 | |||||||
chr14:99267552 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.58+3609G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267552 | |||||||
chr14:99267554 | C | A | 2 | a0001c0001t0009g0053 a0001c0002t0048g0057 |
2 | HG00639.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.58+3607G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267554 | |||||||
chr14:99267554 | C | CA | 4 | a0001c0001t0002g0056 a0001c0001t0009g0054 a0001c0002t0003g0264 others(1): Show |
4 | HG02055.hp2 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3606dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267554 | |||||||
chr14:99267565 | C | CA | 8 | a0001c0001t0002g0056 a0001c0001t0009g0053 a0001c0001t0009g0054 others(5): Show |
8 | HG00639.hp2 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+3595dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267565 | |||||||
chr14:99267617 | C | T | 295 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(292): Show |
296 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.58+3544G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267617 | |||||||
chr14:99267649 | C | T | 1 | a0001c0001t0042g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.58+3512G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267649 | |||||||
chr14:99268020 | C | T | 1 | a0001c0001t0013g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.58+3141G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268020 | |||||||
chr14:99268102 | C | G | 1 | a0001c0002t0045g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58+3059G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268102 | |||||||
chr14:99268262 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.58+2899C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268262 | |||||||
chr14:99268274 | C | T | 325 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(322): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.58+2887G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268274 | |||||||
chr14:99268320 | T | C | 48 | a0001c0001t0001g0150 a0001c0001t0001g0179 a0001c0001t0002g0016 others(45): Show |
48 | HG00642.hp1 HG00673.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.58+2841A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268320 | |||||||
chr14:99268390 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.58+2771C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268390 | |||||||
chr14:99268547 | G | A | 9 | a0001c0001t0001g0220 a0001c0001t0012g0142 a0001c0001t0012g0143 others(6): Show |
9 | NA18966.hp2 NA18968.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+2614C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268547 | |||||||
chr14:99268647 | A | G | 285 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0156 others(282): Show |
286 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.58+2514T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268647 | |||||||
chr14:99268794 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.58+2367G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268794 | |||||||
chr14:99268896 | T | C | 59 | a0001c0001t0001g0166 a0001c0001t0001g0220 a0001c0001t0002g0055 others(56): Show |
60 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(57): Show |
intron_variant | MODIFIER | c.58+2265A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268896 | |||||||
chr14:99269143 | T | C | 50 | a0001c0001t0001g0166 a0001c0001t0002g0055 a0001c0001t0002g0056 others(47): Show |
51 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(48): Show |
intron_variant | MODIFIER | c.58+2018A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269143 | |||||||
chr14:99269156 | A | AC | 37 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(34): Show |
37 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.58+2004dupG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269156 | |||||||
chr14:99269205 | G | A | 6 | a0001c0001t0001g0171 a0001c0001t0005g0339 a0001c0001t0013g0175 others(3): Show |
6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+1956C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269205 | |||||||
chr14:99269515 | T | TC | 103 | a0001c0001t0001g0177 a0001c0001t0001g0184 a0001c0001t0001g0185 others(100): Show |
103 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.58+1645dupG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269515 | |||||||
chr14:99269515 | T | TCC | 35 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0187 others(32): Show |
36 | HG00733.hp1 HG01109.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.58+1644_58+1645dup others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269515 | |||||||
chr14:99269515 | T | TTC | 4 | a0001c0001t0013g0181 a0001c0002t0003g0173 a0001c0002t0003g0174 others(1): Show |
4 | HG02258.hp1 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1645_58+1646ins others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269515 | |||||||
chr14:99269518 | C | G | 4 | a0001c0001t0013g0181 a0001c0002t0003g0173 a0001c0002t0003g0174 others(1): Show |
4 | HG02258.hp1 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1643G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269518 | |||||||
chr14:99269524 | C | CG | 37 | a0001c0001t0001g0166 a0001c0001t0005g0002 a0001c0001t0005g0299 others(34): Show |
38 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(35): Show |
intron_variant | MODIFIER | c.58+1636_58+1637ins others(1): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269524 | |||||||
chr14:99269526 | C | A | 7 | a0001c0001t0002g0064 a0001c0001t0005g0330 a0001c0001t0009g0096 others(4): Show |
7 | HG00741.hp1 HG01123.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+1635G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269526 | |||||||
chr14:99269527 | A | C | 12 | a0001c0001t0001g0220 a0001c0001t0002g0065 a0001c0001t0010g0067 others(9): Show |
12 | HG02109.hp1 NA18522.hp1 NA18522.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+1634T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269527 | |||||||
chr14:99269651 | A | C | 10 | a0001c0001t0001g0220 a0001c0001t0012g0142 a0001c0001t0012g0143 others(7): Show |
10 | NA18966.hp2 NA18968.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+1510T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269651 | |||||||
chr14:99269658 | A | ATATT | 8 | a0001c0001t0005g0002 a0001c0001t0005g0299 a0001c0001t0005g0301 others(5): Show |
9 | HG00140.hp1 HG00280.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+1499_58+1502dup others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269658 | |||||||
chr14:99269875 | T | TA | 34 | a0001c0001t0001g0266 a0001c0001t0001g0271 a0001c0001t0001g0272 others(31): Show |
34 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.58+1285dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TA | T | 42 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0202 others(39): Show |
42 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.58+1285delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAA | T | 11 | a0001c0001t0001g0192 a0001c0001t0002g0119 a0001c0001t0002g0122 others(8): Show |
11 | HG02293.hp1 HG02293.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+1284_58+1285del others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAA | T | 40 | a0001c0001t0001g0172 a0001c0001t0001g0183 a0001c0001t0001g0184 others(37): Show |
40 | HG00280.hp2 HG01106.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.58+1283_58+1285del others(3): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAAA | T | 45 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0002g0051 others(42): Show |
46 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.58+1282_58+1285del others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAAAA | T | 16 | a0001c0001t0001g0171 a0001c0001t0002g0039 a0001c0001t0002g0040 others(13): Show |
16 | HG00673.hp1 HG01069.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.58+1281_58+1285del others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAAAAA | T | 29 | a0001c0001t0001g0150 a0001c0001t0002g0016 a0001c0001t0002g0019 others(26): Show |
29 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.58+1280_58+1285del others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAAAAAA others(2): Show |
T | 9 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0064 others(6): Show |
9 | HG00639.hp2 HG00741.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+1277_58+1285del others(9): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAAAAAA others(3): Show |
T | 37 | a0001c0001t0001g0166 a0001c0001t0005g0002 a0001c0001t0005g0299 others(34): Show |
38 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.58+1276_58+1285del others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0027g0297 a0001c0002t0008g0296 |
2 | HG00099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.58+1275_58+1285del others(11): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAAAAAA others(5): Show |
T | 1 | a0001c0005t0010g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58+1274_58+1285del others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAAAAAA others(6): Show |
T | 12 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(9): Show |
12 | HG00423.hp2 HG02056.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+1273_58+1285del others(13): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0001g0155 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.58+1272_58+1285del others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0006g0059 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.58+1271_58+1285del others(15): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269875 | TAAAAAAA others(12): Show |
T | 1 | a0001c0001t0070g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.58+1267_58+1285del others(19): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | |||||||
chr14:99269876 | A | T | 2 | a0001c0001t0005g0337 a0003c0009t0003g0263 |
2 | NA18977.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.58+1285T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269876 | |||||||
chr14:99269878 | A | T | 1 | a0001c0002t0003g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.58+1283T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269878 | |||||||
chr14:99269879 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.58+1282T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269879 | |||||||
chr14:99270091 | G | T | 1 | a0001c0001t0002g0058 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.58+1070C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270091 | |||||||
chr14:99270521 | G | A | 1 | a0004c0010t0007g0287 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.58+640C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270521 | |||||||
chr14:99270635 | AG | A | 8 | a0001c0001t0012g0142 a0001c0001t0012g0143 a0001c0001t0012g0147 others(5): Show |
8 | NA18966.hp2 NA18968.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+525delC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270635 | |||||||
chr14:99270647 | C | T | 5 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0009g0053 others(2): Show |
5 | HG00639.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+514G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270647 | |||||||
chr14:99270664 | C | A | 1 | a0001c0005t0010g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58+497G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270664 | |||||||
chr14:99270672 | C | G | 1 | a0001c0001t0035g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.58+489G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270672 | |||||||
chr14:99270706 | C | T | 1 | a0001c0001t0007g0154 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.58+455G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270706 | |||||||
chr14:99270792 | C | G | 1 | a0001c0001t0082g0347 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58+369G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270792 | |||||||
chr14:99270812 | C | T | 2 | a0001c0001t0002g0051 a0001c0001t0002g0052 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.58+349G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270812 | |||||||
chr14:99270868 | A | G | 43 | a0001c0001t0001g0150 a0001c0001t0002g0016 a0001c0001t0002g0019 others(40): Show |
43 | HG00642.hp1 HG00673.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.58+293T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270868 | |||||||
chr14:99270942 | G | C | 3 | a0001c0001t0032g0005 a0001c0002t0031g0006 a0001c0005t0010g0013 |
3 | HG01891.hp2 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+219C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270942 | |||||||
chr14:99271072 | A | C | 12 | a0001c0001t0012g0142 a0001c0001t0012g0143 a0001c0001t0012g0147 others(9): Show |
12 | HG01891.hp2 HG02559.hp1 HG03516.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+89T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99271072 |