Item | Value |
---|---|
geneid | 10053 |
ensemblid | ENSG00000129354.12 |
hgncid | 558 |
symbol | AP1M2 |
name | adaptor related protein complex 1 subunit mu 2 |
refseq_nuc | NM_005498.5 |
refseq_prot | NP_005489.2 |
ensembl_nuc | ENST00000250244.11 |
ensembl_prot | ENSP00000250244.5 |
mane_status | MANE Select |
chr | chr19 |
start | 10572671 |
end | 10587312 |
strand | - |
ver | v1.2 |
region | chr19:10572671-10587312 |
region5000 | chr19:10567671-10592312 |
regionname0 | AP1M2_chr19_10572671_10587312 |
regionname5000 | AP1M2_chr19_10567671_10592312 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 423 | 393 | 88 | 69 | 174 | 16 | 44 | 132 | AP1M2_chr19_10567671_10592312 | AP1M2 | MSASA others(418): Show |
chr19 | 10567671 | 10592312 |
a0002 | 0/0 | 26 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | MSASA others(21): Show |
chr19 | 10567671 | 10592312 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1269 | 196 | 59 | 42 | 43 | 15 | 35 | AP1M2_chr19_10567671_10592312 | AP1M2 | ATGTC others(1264): Show |
chr19 | 10567671 | 10592312 | ||
a0001c0002 | 0/0 | 1269 | 177 | 28 | 27 | 112 | 1 | 9 | AP1M2_chr19_10567671_10592312 | AP1M2 | ATGTC others(1264): Show |
chr19 | 10567671 | 10592312 | ||
a0001c0003 | 0/0 | 1269 | 18 | 0 | 0 | 18 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | ATGTC others(1264): Show |
chr19 | 10567671 | 10592312 | ||
a0001c0004 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | ATGTC others(1264): Show |
chr19 | 10567671 | 10592312 | ||
a0001c0005 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | ATGTC others(1264): Show |
chr19 | 10567671 | 10592312 | ||
a0002c0006 | 0/0 | 1258 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | ATGTC others(1253): Show |
chr19 | 10567671 | 10592312 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1748 | 186 | 58 | 37 | 42 | 14 | 34 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0001t0002 | 0/0 | 1748 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0001t0005 | 1/0 | 1748 | 7 | 0 | 5 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0001t0009 | 0/0 | 1748 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0001t0011 | 0/0 | 1748 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0002t0001 | 0/0 | 1748 | 21 | 15 | 3 | 3 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0002t0002 | 0/0 | 1748 | 93 | 5 | 9 | 79 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0002t0003 | 0/0 | 1746 | 47 | 8 | 15 | 15 | 1 | 8 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1741): Show |
chr19 | 10567671 | 10592312 |
a0001c0002t0004 | 0/0 | 1748 | 10 | 0 | 0 | 10 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0002t0006 | 0/0 | 1748 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0002t0007 | 0/0 | 1748 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0002t0008 | 0/0 | 1748 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0002t0010 | 0/0 | 1746 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1741): Show |
chr19 | 10567671 | 10592312 |
a0001c0002t0012 | 0/0 | 1748 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0003t0001 | 0/0 | 1748 | 18 | 0 | 0 | 18 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0004t0001 | 0/0 | 1748 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0001c0005t0002 | 0/0 | 1748 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1743): Show |
chr19 | 10567671 | 10592312 |
a0002c0006t0003 | 0/0 | 1735 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | GCTTC others(1730): Show |
chr19 | 10567671 | 10592312 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0008 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0016 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0005g0007 | 1/0 | 4 | 0 | 2 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0009g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0001t0011g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0002 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0005 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0010g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0002t0012g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0004t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0001c0005t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
a0002c0006t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0152 | EUR | GBR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0311 | EUR | GBR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | FIN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0326 | EUR | FIN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00438 | hp2 | a0001 | c0003 | t0001 | g0225 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00597 | hp1 | a0001 | c0005 | t0002 | g0110 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0091 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00639 | hp2 | a0001 | c0002 | t0003 | g0124 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00673 | hp1 | a0001 | c0002 | t0003 | g0167 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | CHS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00735 | hp1 | a0002 | c0006 | t0003 | g0157 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0230 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0256 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01069 | hp1 | a0001 | c0002 | t0003 | g0006 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0136 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0322 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0160 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0127 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01167 | hp2 | a0001 | c0002 | t0003 | g0143 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0089 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0228 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01255 | hp2 | a0001 | c0002 | t0003 | g0150 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0006 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01346 | hp2 | a0001 | c0002 | t0003 | g0162 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01433 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01496 | hp2 | a0001 | c0002 | t0003 | g0006 | AMR | CLM | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01975 | hp2 | a0001 | c0002 | t0003 | g0151 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG01981 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02004 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02015 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0083 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02080 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0332 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0253 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | CDX | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02165 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | CDX | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0227 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0129 | AMR | PEL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02523 | hp2 | a0001 | c0002 | t0004 | g0041 | EAS | KHV | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02615 | hp2 | a0001 | c0002 | t0003 | g0104 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0116 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02698 | hp2 | a0001 | c0002 | t0003 | g0166 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02818 | hp1 | a0001 | c0002 | t0003 | g0005 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02922 | hp2 | a0001 | c0002 | t0003 | g0145 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03139 | hp1 | a0001 | c0002 | t0003 | g0260 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0115 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03239 | hp2 | a0001 | c0002 | t0003 | g0101 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03490 | hp1 | a0001 | c0002 | t0010 | g0153 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03491 | hp1 | a0001 | c0002 | t0003 | g0186 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03516 | hp1 | a0001 | c0002 | t0003 | g0023 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0109 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03669 | hp2 | a0001 | c0002 | t0003 | g0182 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | STU | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | STU | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | BEB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03834 | hp2 | a0001 | c0002 | t0003 | g0002 | SAS | BEB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03942 | hp2 | a0001 | c0002 | t0003 | g0024 | SAS | BEB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG04184 | hp2 | a0001 | c0001 | t0009 | g0214 | SAS | BEB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG04199 | hp1 | a0001 | c0002 | t0003 | g0266 | SAS | STU | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | STU | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | STU | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | STU | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | STU | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | YRI | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | CHB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0156 | EAS | CHB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | YRI | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | YRI | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18942 | hp2 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18946 | hp1 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18952 | hp2 | a0001 | c0002 | t0003 | g0132 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0196 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18963 | hp2 | a0001 | c0003 | t0001 | g0208 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18967 | hp1 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18968 | hp1 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18970 | hp1 | a0001 | c0002 | t0004 | g0017 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18970 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18971 | hp2 | a0001 | c0003 | t0001 | g0243 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18974 | hp1 | a0001 | c0002 | t0012 | g0334 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0219 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18977 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18979 | hp2 | a0001 | c0003 | t0001 | g0188 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18980 | hp2 | a0001 | c0002 | t0006 | g0142 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18981 | hp1 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18982 | hp1 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18985 | hp2 | a0001 | c0002 | t0004 | g0042 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18992 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18992 | hp2 | a0001 | c0003 | t0001 | g0240 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18995 | hp2 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18997 | hp1 | a0001 | c0002 | t0008 | g0045 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18998 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19002 | hp2 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19005 | hp2 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19010 | hp2 | a0001 | c0002 | t0007 | g0037 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19012 | hp2 | a0001 | c0002 | t0006 | g0141 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | LWK | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | LWK | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19064 | hp1 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19068 | hp2 | a0001 | c0002 | t0004 | g0017 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19070 | hp2 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19076 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19076 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19082 | hp2 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19084 | hp1 | a0001 | c0002 | t0004 | g0036 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19088 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | YRI | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ASW | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA20129 | hp2 | a0001 | c0001 | t0011 | g0333 | AFR | ASW | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0007 | EUR | TSI | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0321 | EUR | TSI | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | GIH | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0140 | SAS | GIH | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02109 | hp1 | a0001 | c0004 | t0001 | g0201 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03471 | hp1 | a0001 | c0002 | t0003 | g0114 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | USA | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0112 | AFR | USA | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | USA | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | LWK | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0058 | REF | REF | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0007 | REF | REF | AP1M2_chr19_10567671_10592312 | AP1M2 | chr19 | 10567671 | 10592312 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:10584037 | CCACATCG others(4): Show |
C | 1 | a0002 | 1 | HG00735.hp1 | frameshift_variant | HIGH | c.65_75delAGGGCGATGT others(1): Show |
p.Lys22fs | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 2/12 | 156/1748 | 65/1272 | 22/423 | chr19 | 10584037 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:10575018 | C | T | 1 | a0001c0004 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1059G>A | p.Glu353Glu | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 10/12 | 1140/1748 | 1059/1272 | 353/423 | chr19 | 10575018 | |||
chr19:10581324 | T | C | 3 | a0001c0002 a0001c0005 a0002c0006 |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
synonymous_variant | LOW | c.615A>G | p.Ser205Ser | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/12 | 696/1748 | 615/1272 | 205/423 | chr19 | 10581324 | |||
chr19:10581375 | G | A | 1 | a0001c0003 | 18 | HG00438.hp2 NA18942.hp2 NA18948.hp2 others(15): Show |
synonymous_variant | LOW | c.564C>T | p.Ser188Ser | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/12 | 645/1748 | 564/1272 | 188/423 | chr19 | 10581375 | |||
chr19:10583941 | G | A | 1 | a0001c0005 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.172C>T | p.Leu58Leu | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 2/12 | 253/1748 | 172/1272 | 58/423 | chr19 | 10583941 | |||
chr19:10584044 | G | A | 1 | a0001c0001 | 4 | HG00099.hp2 HG01074.hp1 HG01257.hp2 others(1): Show |
synonymous_variant | LOW | c.69C>T | p.Gly23Gly | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 2/12 | 150/1748 | 69/1272 | 23/423 | chr19 | 10584044 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:10572693 | T | A | 1 | a0001c0002t0006 | 2 | NA18980.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*373A>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 12/12 | 373 | chr19 | 10572693 | ||||||
chr19:10572714 | C | T | 1 | a0001c0002t0010 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 12/12 | 352 | chr19 | 10572714 | ||||||
chr19:10572801 | A | G | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(14): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*265T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 12/12 | 265 | chr19 | 10572801 | ||||||
chr19:10572874 | CAG | C | 3 | a0001c0002t0003 a0001c0002t0010 a0002c0006t0003 |
49 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*190_*191delCT | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 12/12 | 190 | chr19 | 10572874 | ||||||
chr19:10572898 | A | G | 1 | a0001c0001t0009 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 12/12 | 168 | chr19 | 10572898 | ||||||
chr19:10572926 | C | T | 7 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0006 others(4): Show |
100 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*140G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 12/12 | 140 | chr19 | 10572926 | ||||||
chr19:10587232 | G | T | 1 | a0001c0002t0008 | 1 | NA18997.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1C>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/12 | 1 | chr19 | 10587232 | ||||||
chr19:10587259 | G | A | 1 | a0001c0001t0011 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-28C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/12 | 28 | chr19 | 10587259 | ||||||
chr19:10587262 | A | G | 1 | a0001c0002t0012 | 1 | NA18974.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/12 | 31 | chr19 | 10587262 | ||||||
chr19:10587263 | G | A | 1 | a0001c0002t0012 | 1 | NA18974.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/12 | 32 | chr19 | 10587263 | ||||||
chr19:10587268 | C | G | 2 | a0001c0002t0004 a0001c0002t0007 |
11 | HG02523.hp2 NA18946.hp1 NA18968.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-37G>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/12 | 37 | chr19 | 10587268 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:10573148 | G | A | 5 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250-60C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573148 | |||||||
chr19:10573301 | C | A | 1 | a0001c0001t0001g0313 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1250-213G>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573301 | |||||||
chr19:10573365 | GCTGAGAT others(35): Show |
G | 1 | a0001c0002t0002g0265 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1250-319_1250-278d others(44): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573365 | |||||||
chr19:10573373 | T | C | 324 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(321): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1250-285A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573373 | |||||||
chr19:10573493 | C | G | 12 | a0001c0001t0001g0035 a0001c0001t0001g0320 a0001c0001t0001g0321 others(9): Show |
13 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1250-405G>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573493 | |||||||
chr19:10573659 | C | T | 1 | a0001c0002t0002g0107 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1250-571G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573659 | |||||||
chr19:10573660 | C | CT | 18 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0064 others(15): Show |
18 | HG00735.hp2 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.1250-573dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573660 | |||||||
chr19:10573660 | C | CTT | 48 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0187 others(45): Show |
54 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1250-574_1250-573d others(4): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573660 | |||||||
chr19:10573660 | C | CTTT | 10 | a0001c0001t0001g0093 a0001c0001t0001g0193 a0001c0001t0001g0202 others(7): Show |
10 | HG00438.hp2 HG01952.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250-575_1250-573d others(5): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573660 | |||||||
chr19:10573660 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1250-572G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573660 | |||||||
chr19:10573660 | CT | C | 86 | a0001c0001t0002g0238 a0001c0002t0001g0020 a0001c0002t0001g0084 others(83): Show |
107 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1250-573delA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573660 | |||||||
chr19:10573660 | CTT | C | 36 | a0001c0002t0001g0118 a0001c0002t0001g0119 a0001c0002t0002g0136 others(33): Show |
48 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.1250-574_1250-573d others(4): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573660 | |||||||
chr19:10573661 | T | C | 1 | a0001c0002t0002g0107 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1250-573A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573661 | |||||||
chr19:10573731 | A | G | 6 | a0001c0002t0002g0012 a0001c0002t0002g0088 a0001c0002t0002g0091 others(3): Show |
8 | HG00639.hp1 HG01081.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1250-643T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573731 | |||||||
chr19:10573918 | C | G | 132 | a0001c0001t0002g0238 a0001c0002t0001g0020 a0001c0002t0001g0084 others(129): Show |
165 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.1249+499G>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10573918 | |||||||
chr19:10574030 | T | G | 2 | a0001c0002t0002g0122 a0001c0002t0002g0165 |
2 | NA18943.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1249+387A>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10574030 | |||||||
chr19:10574108 | C | T | 3 | a0001c0002t0001g0117 a0001c0002t0001g0118 a0001c0002t0001g0119 |
3 | HG02559.hp1 HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1249+309G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10574108 | |||||||
chr19:10574118 | G | C | 5 | a0001c0002t0004g0017 a0001c0002t0004g0038 a0001c0002t0004g0040 others(2): Show |
6 | HG02523.hp2 NA18970.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1249+299C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10574118 | |||||||
chr19:10574173 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1249+244G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10574173 | |||||||
chr19:10574358 | G | A | 3 | a0001c0002t0001g0117 a0001c0002t0001g0118 a0001c0002t0001g0119 |
3 | HG02559.hp1 HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1249+59C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10574358 | |||||||
chr19:10574380 | C | T | 1 | a0001c0002t0002g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1249+37G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 11/11 | chr19 | 10574380 | |||||||
chr19:10574514 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1174-22A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 10/11 | chr19 | 10574514 | |||||||
chr19:10574609 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1174-117C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 10/11 | chr19 | 10574609 | |||||||
chr19:10574753 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1173+151C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 10/11 | chr19 | 10574753 | |||||||
chr19:10574754 | A | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+150T>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 10/11 | chr19 | 10574754 | |||||||
chr19:10574833 | G | A | 56 | a0001c0002t0002g0004 a0001c0002t0002g0011 a0001c0002t0002g0012 others(53): Show |
69 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1173+71C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 10/11 | chr19 | 10574833 | |||||||
chr19:10575183 | G | C | 325 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.1048-154C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575183 | |||||||
chr19:10575377 | G | GT | 9 | a0001c0002t0004g0017 a0001c0002t0004g0036 a0001c0002t0004g0038 others(6): Show |
10 | HG02523.hp2 NA18946.hp1 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1048-349dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575377 | |||||||
chr19:10575447 | G | A | 47 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0093 others(44): Show |
53 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1048-418C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575447 | |||||||
chr19:10575750 | T | C | 1 | a0001c0002t0002g0107 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1048-721A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575750 | |||||||
chr19:10575759 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0244 a0001c0001t0001g0247 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048-741_1048-731d others(13): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575759 | |||||||
chr19:10575769 | CT | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(173): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1048-741delA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575769 | |||||||
chr19:10575769 | CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0001g0174 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1048-751_1048-741d others(13): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575769 | |||||||
chr19:10575887 | C | T | 1 | a0001c0002t0003g0132 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1048-858G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575887 | |||||||
chr19:10575911 | G | C | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG01934.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048-882C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575911 | |||||||
chr19:10575932 | A | AT | 12 | a0001c0001t0001g0079 a0001c0001t0001g0187 a0001c0001t0001g0216 others(9): Show |
12 | HG01934.hp2 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1048-904dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575932 | |||||||
chr19:10575932 | AT | A | 141 | a0001c0001t0002g0238 a0001c0002t0001g0020 a0001c0002t0001g0084 others(138): Show |
175 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.1048-904delA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575932 | |||||||
chr19:10575963 | C | T | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0320 others(10): Show |
15 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1048-934G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10575963 | |||||||
chr19:10576027 | C | T | 1 | a0001c0002t0003g0182 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1048-998G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576027 | |||||||
chr19:10576093 | G | GT | 207 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0031 others(204): Show |
247 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1048-1065dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576093 | |||||||
chr19:10576093 | GT | G | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG01934.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048-1065delA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576093 | |||||||
chr19:10576196 | A | C | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG01934.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1047+1002T>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576196 | |||||||
chr19:10576252 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1047+946G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576252 | |||||||
chr19:10576258 | A | AT | 128 | a0001c0001t0001g0028 a0001c0001t0001g0050 a0001c0001t0001g0051 others(125): Show |
162 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.1047+939dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576258 | |||||||
chr19:10576258 | A | ATT | 7 | a0001c0002t0002g0113 a0001c0002t0002g0148 a0001c0002t0002g0176 others(4): Show |
7 | HG01255.hp2 NA18939.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1047+938_1047+939d others(4): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576258 | |||||||
chr19:10576258 | AT | A | 45 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0048 others(42): Show |
47 | HG00558.hp2 HG00621.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1047+939delA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576258 | |||||||
chr19:10576323 | C | T | 3 | a0001c0002t0002g0026 a0001c0002t0002g0164 a0001c0002t0007g0037 |
4 | NA18990.hp2 NA19003.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047+875G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576323 | |||||||
chr19:10576408 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1047+790C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576408 | |||||||
chr19:10576483 | C | T | 68 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0031 others(65): Show |
74 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1047+715G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576483 | |||||||
chr19:10576505 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1047+693C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576505 | |||||||
chr19:10576507 | C | T | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0320 others(10): Show |
15 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1047+691G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576507 | |||||||
chr19:10576513 | C | G | 51 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0093 others(48): Show |
57 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.1047+685G>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576513 | |||||||
chr19:10576622 | C | T | 1 | a0001c0002t0002g0133 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1047+576G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576622 | |||||||
chr19:10576703 | A | T | 1 | a0001c0002t0004g0044 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1047+495T>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576703 | |||||||
chr19:10576706 | C | CT | 14 | a0001c0001t0001g0072 a0001c0001t0001g0245 a0001c0001t0001g0246 others(11): Show |
14 | HG00741.hp1 HG01934.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1047+491dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576706 | |||||||
chr19:10576706 | CT | C | 13 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0001g0306 others(10): Show |
13 | HG00738.hp2 HG01069.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1047+491delA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576706 | |||||||
chr19:10576727 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1047+471G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576727 | |||||||
chr19:10576816 | C | T | 41 | a0001c0002t0001g0099 a0001c0002t0001g0117 a0001c0002t0001g0118 others(38): Show |
53 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1047+382G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576816 | |||||||
chr19:10576836 | G | A | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG01934.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1047+362C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576836 | |||||||
chr19:10576891 | G | C | 1 | a0001c0002t0002g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1047+307C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576891 | |||||||
chr19:10576945 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1047+253G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10576945 | |||||||
chr19:10577031 | G | A | 1 | a0001c0002t0001g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1047+167C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10577031 | |||||||
chr19:10577081 | T | C | 312 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(309): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1047+117A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 9/11 | chr19 | 10577081 | |||||||
chr19:10577400 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0286 |
3 | HG01515.hp2 HG01517.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.889-44T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577400 | |||||||
chr19:10577423 | C | CT | 45 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0031 others(42): Show |
50 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.889-68dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577423 | |||||||
chr19:10577423 | C | CTT | 26 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(23): Show |
28 | HG00323.hp1 HG00544.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.889-69_889-68dupAA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577423 | |||||||
chr19:10577423 | C | CTTT | 54 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0029 others(51): Show |
64 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.889-70_889-68dupAA others(1): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577423 | |||||||
chr19:10577423 | C | CTTTT | 33 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(30): Show |
37 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.889-71_889-68dupAA others(2): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577423 | |||||||
chr19:10577423 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01934.hp2 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-77_889-68dupAA others(8): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577423 | |||||||
chr19:10577423 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.889-78_889-68dupAA others(9): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577423 | |||||||
chr19:10577423 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0248 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.889-79_889-68dupAA others(10): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577423 | |||||||
chr19:10577423 | CTTTT | C | 18 | a0001c0002t0001g0117 a0001c0002t0002g0083 a0001c0002t0002g0105 others(15): Show |
19 | HG00741.hp2 HG01346.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.889-71_889-68delAA others(2): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577423 | |||||||
chr19:10577423 | CTTTTT | C | 98 | a0001c0002t0001g0020 a0001c0002t0001g0096 a0001c0002t0001g0097 others(95): Show |
130 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.889-72_889-68delAA others(3): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577423 | |||||||
chr19:10577423 | CTTTTTT | C | 24 | a0001c0002t0001g0084 a0001c0002t0001g0085 a0001c0002t0001g0086 others(21): Show |
25 | HG01109.hp2 HG01975.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.889-73_889-68delAA others(4): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577423 | |||||||
chr19:10577423 | CTTTTTTT others(3): Show |
C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0323 others(7): Show |
12 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.889-77_889-68delAA others(8): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577423 | |||||||
chr19:10577430 | T | C | 9 | a0001c0002t0004g0017 a0001c0002t0004g0036 a0001c0002t0004g0038 others(6): Show |
10 | HG02523.hp2 NA18946.hp1 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.889-74A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577430 | |||||||
chr19:10577457 | G | A | 1 | a0001c0001t0011g0333 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.889-101C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577457 | |||||||
chr19:10577477 | A | G | 5 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0213 others(2): Show |
5 | HG00140.hp2 HG01261.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.889-121T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577477 | |||||||
chr19:10577724 | C | A | 1 | a0001c0002t0001g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.889-368G>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577724 | |||||||
chr19:10577734 | C | CT | 22 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0064 others(19): Show |
23 | HG00735.hp2 HG00741.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.889-379dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577734 | |||||||
chr19:10577734 | CTTTTT | C | 138 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(135): Show |
172 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.889-383_889-379del others(5): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577734 | |||||||
chr19:10577786 | G | C | 1 | a0001c0002t0003g0104 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.889-430C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577786 | |||||||
chr19:10577926 | G | C | 131 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(128): Show |
164 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.889-570C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10577926 | |||||||
chr19:10578109 | C | T | 140 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(137): Show |
174 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.889-753G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578109 | |||||||
chr19:10578154 | G | C | 1 | a0001c0002t0002g0154 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.888+738C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578154 | |||||||
chr19:10578199 | C | T | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG01934.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.888+693G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578199 | |||||||
chr19:10578260 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0329 |
3 | HG02572.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.888+632C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578260 | |||||||
chr19:10578263 | C | T | 140 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(137): Show |
174 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.888+629G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578263 | |||||||
chr19:10578293 | G | C | 140 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(137): Show |
174 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.888+599C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578293 | |||||||
chr19:10578339 | A | C | 140 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(137): Show |
174 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.888+553T>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578339 | |||||||
chr19:10578342 | C | T | 2 | a0001c0001t0001g0326 a0001c0001t0001g0327 |
2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.888+550G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578342 | |||||||
chr19:10578347 | C | T | 140 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(137): Show |
174 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.888+545G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578347 | |||||||
chr19:10578351 | A | G | 140 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(137): Show |
174 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.888+541T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578351 | |||||||
chr19:10578375 | G | A | 1 | a0001c0002t0003g0143 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.888+517C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578375 | |||||||
chr19:10578422 | C | T | 140 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(137): Show |
174 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.888+470G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578422 | |||||||
chr19:10578437 | A | G | 141 | a0001c0001t0001g0325 a0001c0002t0001g0020 a0001c0002t0001g0084 others(138): Show |
175 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.888+455T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578437 | |||||||
chr19:10578489 | AAACG | A | 140 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(137): Show |
174 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.888+399_888+402del others(4): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578489 | |||||||
chr19:10578508 | A | C | 140 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(137): Show |
174 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.888+384T>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578508 | |||||||
chr19:10578580 | T | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(42): Show |
54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.888+312A>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578580 | |||||||
chr19:10578815 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.888+77C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578815 | |||||||
chr19:10578841 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.888+51G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578841 | |||||||
chr19:10578842 | G | A | 141 | a0001c0001t0001g0226 a0001c0002t0001g0020 a0001c0002t0001g0084 others(138): Show |
175 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.888+50C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578842 | |||||||
chr19:10578865 | G | A | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0307 others(1): Show |
4 | HG01952.hp1 HG02109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.888+27C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 8/11 | chr19 | 10578865 | |||||||
chr19:10578981 | G | C | 1 | a0001c0002t0003g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.817-18C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10578981 | |||||||
chr19:10578987 | T | A | 1 | a0001c0001t0011g0333 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.817-24A>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10578987 | |||||||
chr19:10579015 | C | CT | 6 | a0001c0001t0001g0079 a0001c0001t0001g0221 a0001c0001t0001g0232 others(3): Show |
6 | HG01175.hp1 HG02055.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-53dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579015 | |||||||
chr19:10579015 | CT | C | 143 | a0001c0001t0001g0199 a0001c0001t0001g0211 a0001c0001t0001g0280 others(140): Show |
177 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.817-53delA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579015 | |||||||
chr19:10579034 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0068 |
2 | HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.817-71A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579034 | |||||||
chr19:10579121 | C | T | 140 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(137): Show |
174 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.817-158G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579121 | |||||||
chr19:10579185 | G | C | 1 | a0001c0001t0001g0318 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.817-222C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579185 | |||||||
chr19:10579191 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.817-228G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579191 | |||||||
chr19:10579235 | C | T | 3 | a0001c0002t0003g0092 a0001c0002t0003g0183 a0001c0002t0003g0184 |
3 | HG02165.hp1 NA18967.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.817-272G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579235 | |||||||
chr19:10579259 | G | A | 3 | a0001c0002t0003g0092 a0001c0002t0003g0183 a0001c0002t0003g0184 |
3 | HG02165.hp1 NA18967.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.817-296C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579259 | |||||||
chr19:10579279 | G | A | 139 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(136): Show |
173 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.817-316C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579279 | |||||||
chr19:10579333 | G | A | 31 | a0001c0002t0003g0002 a0001c0002t0003g0005 a0001c0002t0003g0006 others(28): Show |
43 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.817-370C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579333 | |||||||
chr19:10579365 | G | A | 11 | a0001c0002t0002g0130 a0001c0002t0002g0138 a0001c0002t0002g0149 others(8): Show |
11 | NA18944.hp2 NA18945.hp2 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+351C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579365 | |||||||
chr19:10579437 | A | T | 205 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0031 others(202): Show |
245 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.816+279T>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579437 | |||||||
chr19:10579440 | A | T | 1 | a0001c0002t0003g0092 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.816+276T>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579440 | |||||||
chr19:10579447 | A | G | 94 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(91): Show |
115 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.816+269T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579447 | |||||||
chr19:10579456 | GCAATTCT others(18): Show |
G | 1 | a0001c0002t0002g0163 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.816+235_816+259del others(25): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579456 | |||||||
chr19:10579511 | G | A | 4 | a0001c0002t0002g0130 a0001c0002t0002g0171 a0001c0002t0006g0141 others(1): Show |
4 | NA18944.hp2 NA18980.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+205C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579511 | |||||||
chr19:10579533 | TA | T | 135 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(132): Show |
168 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.816+182delT | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579533 | |||||||
chr19:10579645 | C | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(41): Show |
53 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.816+71G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 7/11 | chr19 | 10579645 | |||||||
chr19:10579881 | G | C | 325 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.674-23C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10579881 | |||||||
chr19:10579918 | C | T | 1 | a0001c0002t0002g0332 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.674-60G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10579918 | |||||||
chr19:10580044 | G | GT | 26 | a0001c0001t0001g0229 a0001c0001t0001g0241 a0001c0001t0005g0228 others(23): Show |
26 | HG00621.hp2 HG00741.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.674-187dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580044 | |||||||
chr19:10580044 | G | GTT | 8 | a0001c0002t0004g0017 a0001c0002t0004g0036 a0001c0002t0004g0039 others(5): Show |
9 | HG02523.hp2 NA18946.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.674-188_674-187dup others(2): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580044 | |||||||
chr19:10580044 | GT | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(116): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.674-187delA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580044 | |||||||
chr19:10580044 | GTT | G | 59 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0031 others(56): Show |
64 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.674-188_674-187del others(2): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580044 | |||||||
chr19:10580047 | T | G | 1 | a0001c0002t0002g0154 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.674-189A>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580047 | |||||||
chr19:10580129 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0075 a0001c0001t0001g0082 |
3 | HG00733.hp2 HG01243.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.674-271C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580129 | |||||||
chr19:10580150 | C | G | 5 | a0001c0002t0003g0104 a0001c0002t0003g0112 a0001c0002t0003g0114 others(2): Show |
5 | HG02615.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.674-292G>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580150 | |||||||
chr19:10580239 | C | T | 1 | a0001c0001t0005g0227 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.674-381G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580239 | |||||||
chr19:10580349 | G | A | 1 | a0001c0001t0011g0333 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.674-491C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580349 | |||||||
chr19:10580387 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.674-529G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580387 | |||||||
chr19:10580487 | T | C | 312 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(309): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.674-629A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580487 | |||||||
chr19:10580508 | A | C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0320 a0001c0001t0001g0321 others(7): Show |
11 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.674-650T>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580508 | |||||||
chr19:10580595 | G | A | 1 | a0001c0002t0003g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.673+671C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580595 | |||||||
chr19:10580631 | C | T | 61 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0031 others(58): Show |
67 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.673+635G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580631 | |||||||
chr19:10580647 | G | T | 124 | a0001c0002t0001g0099 a0001c0002t0001g0117 a0001c0002t0001g0118 others(121): Show |
156 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.673+619C>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580647 | |||||||
chr19:10580665 | T | C | 1 | a0001c0002t0003g0124 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.673+601A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580665 | |||||||
chr19:10580709 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.673+557C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580709 | |||||||
chr19:10580769 | A | C | 145 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.673+497T>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580769 | |||||||
chr19:10580822 | G | T | 1 | a0001c0002t0002g0103 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.673+444C>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580822 | |||||||
chr19:10580881 | G | A | 145 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.673+385C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580881 | |||||||
chr19:10580930 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.673+336C>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580930 | |||||||
chr19:10580942 | G | A | 145 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.673+324C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10580942 | |||||||
chr19:10581025 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.673+241C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10581025 | |||||||
chr19:10581077 | G | A | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0307 others(1): Show |
4 | HG01952.hp1 HG02109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+189C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 6/11 | chr19 | 10581077 | |||||||
chr19:10581441 | T | C | 144 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(141): Show |
178 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.546+46A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 5/11 | chr19 | 10581441 | |||||||
chr19:10581453 | G | A | 145 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.546+34C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 5/11 | chr19 | 10581453 | |||||||
chr19:10582038 | G | T | 144 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(141): Show |
178 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.268-160C>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582038 | |||||||
chr19:10582044 | T | C | 144 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(141): Show |
178 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.268-166A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582044 | |||||||
chr19:10582064 | G | A | 1 | a0001c0002t0001g0253 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.268-186C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582064 | |||||||
chr19:10582184 | C | T | 144 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(141): Show |
178 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.268-306G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582184 | |||||||
chr19:10582287 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.268-409G>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582287 | |||||||
chr19:10582317 | T | TG | 145 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.268-440dupC | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582317 | |||||||
chr19:10582331 | G | A | 135 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(132): Show |
168 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.268-453C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582331 | |||||||
chr19:10582332 | G | C | 145 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.268-454C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582332 | |||||||
chr19:10582410 | G | A | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG01934.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.268-532C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582410 | |||||||
chr19:10582450 | C | T | 1 | a0001c0002t0002g0088 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.268-572G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582450 | |||||||
chr19:10582577 | G | A | 7 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.268-699C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582577 | |||||||
chr19:10582619 | C | T | 10 | a0001c0002t0004g0017 a0001c0002t0004g0036 a0001c0002t0004g0038 others(7): Show |
11 | HG02523.hp2 NA18946.hp1 NA18968.hp1 others(8): Show |
intron_variant | MODIFIER | c.268-741G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582619 | |||||||
chr19:10582823 | G | C | 1 | a0001c0002t0001g0253 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.267+783C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582823 | |||||||
chr19:10582830 | C | CT | 137 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(134): Show |
171 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.267+775dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582830 | |||||||
chr19:10582830 | C | CTT | 6 | a0001c0002t0001g0117 a0001c0002t0001g0118 a0001c0002t0001g0119 others(3): Show |
6 | HG02559.hp1 HG02630.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.267+774_267+775dup others(2): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582830 | |||||||
chr19:10582830 | CT | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(173): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.267+775delA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582830 | |||||||
chr19:10582891 | TCTTGGCT others(3): Show |
T | 5 | a0001c0002t0001g0084 a0001c0002t0001g0085 a0001c0002t0001g0086 others(2): Show |
5 | HG01109.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+705_267+714del others(10): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582891 | |||||||
chr19:10582948 | T | C | 145 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.267+658A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582948 | |||||||
chr19:10582952 | C | A | 145 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.267+654G>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10582952 | |||||||
chr19:10583077 | T | C | 145 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.267+529A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10583077 | |||||||
chr19:10583088 | A | C | 145 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.267+518T>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10583088 | |||||||
chr19:10583131 | C | CT | 144 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(141): Show |
178 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.267+474dupA | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10583131 | |||||||
chr19:10583160 | G | T | 145 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.267+446C>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10583160 | |||||||
chr19:10583267 | T | C | 325 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.267+339A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10583267 | |||||||
chr19:10583346 | C | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0059 others(5): Show |
10 | HG02056.hp2 HG02071.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.267+260G>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10583346 | |||||||
chr19:10583439 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.267+167T>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10583439 | |||||||
chr19:10583563 | A | G | 145 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.267+43T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10583563 | |||||||
chr19:10583568 | C | T | 145 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(142): Show |
179 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.267+38G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 3/11 | chr19 | 10583568 | |||||||
chr19:10583687 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.200-14C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 2/11 | chr19 | 10583687 | |||||||
chr19:10583861 | C | T | 1 | a0001c0002t0001g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.199+53G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 2/11 | chr19 | 10583861 | |||||||
chr19:10583892 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.199+22C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 2/11 | chr19 | 10583892 | |||||||
chr19:10584306 | C | T | 1 | a0001c0002t0002g0264 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.43-236G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10584306 | |||||||
chr19:10584311 | TGGCTCAC others(21): Show |
T | 1 | a0001c0002t0002g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-269_43-242delCA others(26): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10584311 | |||||||
chr19:10584449 | G | A | 1 | a0001c0002t0003g0162 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.43-379C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10584449 | |||||||
chr19:10584598 | G | T | 1 | a0001c0002t0003g0023 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.43-528C>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10584598 | |||||||
chr19:10584614 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG01175.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.43-544C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10584614 | |||||||
chr19:10584673 | AAGGAAGG others(1): Show |
A | 144 | a0001c0001t0001g0259 a0001c0002t0001g0020 a0001c0002t0001g0084 others(141): Show |
178 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.43-611_43-604delAC others(6): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10584673 | |||||||
chr19:10584832 | T | G | 1 | a0001c0001t0001g0315 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43-762A>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10584832 | |||||||
chr19:10584928 | C | A | 12 | a0001c0001t0001g0280 a0001c0001t0001g0318 a0001c0002t0004g0017 others(9): Show |
13 | HG02257.hp1 HG02523.hp2 HG03209.hp1 others(10): Show |
intron_variant | MODIFIER | c.43-858G>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10584928 | |||||||
chr19:10584928 | C | CA | 8 | a0001c0001t0001g0187 a0001c0001t0001g0198 a0001c0001t0001g0199 others(5): Show |
8 | HG00099.hp2 HG01074.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.43-859dupT | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10584928 | |||||||
chr19:10584931 | A | C | 17 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0281 others(14): Show |
19 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.43-861T>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10584931 | |||||||
chr19:10584934 | A | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0320 others(11): Show |
16 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.43-864T>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10584934 | |||||||
chr19:10585017 | C | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.43-947G>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585017 | |||||||
chr19:10585136 | G | C | 1 | a0001c0002t0002g0163 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.43-1066C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585136 | |||||||
chr19:10585137 | C | G | 1 | a0001c0002t0002g0163 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.43-1067G>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585137 | |||||||
chr19:10585148 | G | A | 146 | a0001c0001t0001g0102 a0001c0001t0001g0259 a0001c0002t0001g0020 others(143): Show |
180 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.43-1078C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585148 | |||||||
chr19:10585218 | A | G | 1 | a0001c0002t0002g0191 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.43-1148T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585218 | |||||||
chr19:10585220 | G | A | 1 | a0001c0002t0002g0191 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.43-1150C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585220 | |||||||
chr19:10585221 | A | G | 1 | a0001c0002t0002g0191 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.43-1151T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585221 | |||||||
chr19:10585228 | A | G | 1 | a0001c0002t0002g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-1158T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585228 | |||||||
chr19:10585239 | A | G | 1 | a0001c0002t0002g0163 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.43-1169T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585239 | |||||||
chr19:10585239 | AGAAAGAA others(1): Show |
A | 23 | a0001c0001t0001g0102 a0001c0001t0001g0330 a0001c0001t0001g0331 others(20): Show |
30 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.43-1177_43-1170del others(8): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585239 | |||||||
chr19:10585241 | A | G | 1 | a0001c0002t0002g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.43-1171T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585241 | |||||||
chr19:10585243 | A | G | 1 | a0002c0006t0003g0157 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.43-1173T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585243 | |||||||
chr19:10585247 | G | A | 2 | a0001c0002t0002g0012 a0001c0002t0002g0083 |
2 | HG02055.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.43-1177C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585247 | |||||||
chr19:10585255 | G | A | 2 | a0001c0002t0002g0012 a0001c0002t0002g0090 |
2 | NA18946.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.43-1185C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585255 | |||||||
chr19:10585255 | G | GGAAAGAA others(20): Show |
1 | a0001c0002t0004g0041 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.43-1186_43-1185ins others(27): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585255 | |||||||
chr19:10585257 | A | AAAGAAAG others(4): Show |
11 | a0001c0002t0001g0158 a0001c0002t0002g0025 a0001c0002t0002g0159 others(8): Show |
12 | HG00673.hp1 HG01099.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.43-1188_43-1187ins others(11): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585257 | |||||||
chr19:10585259 | AGAAG | A | 16 | a0001c0001t0001g0259 a0001c0002t0001g0084 a0001c0002t0001g0117 others(13): Show |
18 | HG00621.hp2 HG00639.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-1193_43-1190del others(4): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585259 | |||||||
chr19:10585261 | A | AAAGAAAG | 26 | a0001c0002t0001g0172 a0001c0002t0001g0173 a0001c0002t0001g0174 others(23): Show |
30 | HG00099.hp1 HG00408.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.43-1192_43-1191ins others(7): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585261 | |||||||
chr19:10585262 | AG | A | 3 | a0001c0002t0002g0083 a0001c0002t0002g0090 a0001c0002t0002g0100 |
3 | HG02055.hp1 NA18947.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.43-1193delC | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585262 | |||||||
chr19:10585263 | G | A | 99 | a0001c0001t0001g0268 a0001c0001t0001g0320 a0001c0001t0001g0321 others(96): Show |
123 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.43-1193C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585263 | |||||||
chr19:10585263 | G | GAAAGAAG others(9): Show |
1 | a0001c0002t0002g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-1194_43-1193ins others(16): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585263 | |||||||
chr19:10585265 | A | AAAG | 27 | a0001c0002t0001g0086 a0001c0002t0001g0094 a0001c0002t0001g0095 others(24): Show |
38 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.43-1198_43-1196dup others(3): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585265 | |||||||
chr19:10585265 | A | AAAGAAAG others(3): Show |
1 | a0001c0001t0001g0314 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.43-1196_43-1195ins others(10): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585265 | |||||||
chr19:10585268 | GA | G | 29 | a0001c0002t0001g0020 a0001c0002t0001g0085 a0001c0002t0001g0099 others(26): Show |
35 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.43-1199delT | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585268 | |||||||
chr19:10585268 | GAAAGAAA others(13): Show |
G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0324 |
2 | HG01358.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43-1218_43-1199del others(20): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585268 | |||||||
chr19:10585268 | GAAAGAAA others(17): Show |
G | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.43-1222_43-1199del others(24): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585268 | |||||||
chr19:10585268 | GAAAGAAA others(21): Show |
G | 3 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0002t0003g0322 |
3 | HG01081.hp2 HG01168.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.43-1226_43-1199del others(28): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585268 | |||||||
chr19:10585275 | A | G | 16 | a0001c0001t0001g0259 a0001c0002t0001g0084 a0001c0002t0001g0117 others(13): Show |
18 | HG00621.hp2 HG00639.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-1205T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585275 | |||||||
chr19:10585276 | G | A | 16 | a0001c0001t0001g0259 a0001c0002t0001g0084 a0001c0002t0001g0117 others(13): Show |
18 | HG00621.hp2 HG00639.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-1206C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585276 | |||||||
chr19:10585276 | G | GA | 81 | a0001c0001t0001g0314 a0001c0002t0001g0020 a0001c0002t0001g0085 others(78): Show |
104 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.43-1207dupT | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585276 | |||||||
chr19:10585276 | G | GAAAAGAA others(3): Show |
1 | a0001c0002t0002g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-1207_43-1206ins others(10): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585276 | |||||||
chr19:10585276 | G | GAAGAAAG others(21): Show |
1 | a0001c0003t0001g0243 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.43-1207_43-1206ins others(28): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585276 | |||||||
chr19:10585276 | G | GAAGAAAG others(29): Show |
1 | a0001c0002t0004g0039 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.43-1207_43-1206ins others(36): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585276 | |||||||
chr19:10585276 | GAAGAAAA others(1): Show |
G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0294 a0001c0001t0001g0295 others(3): Show |
8 | HG02071.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.43-1214_43-1207del others(8): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585276 | |||||||
chr19:10585276 | GAAGAAAA others(5): Show |
G | 21 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0033 others(18): Show |
24 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-1218_43-1207del others(12): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585276 | |||||||
chr19:10585276 | GAAGAAAA others(9): Show |
G | 7 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0200 others(4): Show |
9 | HG00558.hp2 HG02109.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.43-1222_43-1207del others(16): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585276 | |||||||
chr19:10585276 | GAAGAAAA others(13): Show |
G | 11 | a0001c0001t0001g0034 a0001c0001t0001g0192 a0001c0001t0001g0193 others(8): Show |
12 | HG01175.hp2 HG01255.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-1226_43-1207del others(20): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585276 | |||||||
chr19:10585276 | GAAGAAAA others(17): Show |
G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.43-1230_43-1207del others(24): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585276 | |||||||
chr19:10585276 | GAAGAAAA others(25): Show |
G | 1 | a0001c0001t0001g0318 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.43-1238_43-1207del others(32): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585276 | |||||||
chr19:10585278 | A | AG | 7 | a0001c0002t0001g0158 a0001c0002t0002g0025 a0001c0002t0002g0159 others(4): Show |
8 | HG01099.hp2 HG01346.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.43-1209dupC | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585278 | |||||||
chr19:10585278 | A | AGAAAGAA others(21): Show |
1 | a0001c0001t0001g0247 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.43-1209_43-1208ins others(28): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585278 | |||||||
chr19:10585278 | A | AGAAAGAA others(17): Show |
6 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(3): Show |
6 | HG00140.hp2 HG00438.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-1209_43-1208ins others(24): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585278 | |||||||
chr19:10585279 | G | A | 2 | a0001c0002t0002g0100 a0001c0002t0003g0156 |
2 | NA18747.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.43-1209C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585279 | |||||||
chr19:10585279 | GAAAA | G | 28 | a0001c0001t0001g0102 a0001c0001t0001g0221 a0001c0001t0001g0297 others(25): Show |
31 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.43-1213_43-1210del others(4): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585279 | |||||||
chr19:10585280 | A | AAAGAAAG others(16): Show |
1 | a0001c0001t0001g0250 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.43-1211_43-1210ins others(23): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585280 | |||||||
chr19:10585280 | A | G | 4 | a0001c0002t0002g0100 a0001c0002t0003g0156 a0001c0002t0012g0334 others(1): Show |
4 | HG00735.hp1 NA18747.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-1210T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585280 | |||||||
chr19:10585281 | A | AAGAAAGA others(31): Show |
4 | a0001c0002t0004g0017 a0001c0002t0004g0036 a0001c0002t0004g0038 others(1): Show |
5 | NA18970.hp1 NA19002.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-1212_43-1211ins others(38): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585281 | |||||||
chr19:10585281 | A | G | 1 | a0001c0002t0004g0041 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.43-1211T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585281 | |||||||
chr19:10585282 | A | AGAAAGAA others(13): Show |
11 | a0001c0001t0001g0226 a0001c0001t0001g0232 a0001c0001t0001g0233 others(8): Show |
13 | HG01978.hp1 HG02300.hp1 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.43-1213_43-1212ins others(20): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585282 | |||||||
chr19:10585282 | A | AGAAAGAA others(21): Show |
1 | a0001c0001t0001g0312 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43-1213_43-1212ins others(28): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585282 | |||||||
chr19:10585282 | A | AGAAAGAA others(21): Show |
3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0077 |
3 | HG02145.hp2 HG03453.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.43-1213_43-1212ins others(28): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585282 | |||||||
chr19:10585282 | A | G | 24 | a0001c0002t0001g0172 a0001c0002t0001g0173 a0001c0002t0001g0174 others(21): Show |
29 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.43-1212T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585282 | |||||||
chr19:10585283 | A | G | 233 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(230): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.43-1213T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585283 | |||||||
chr19:10585283 | AAAAGAAA others(5): Show |
A | 1 | a0001c0001t0005g0007 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.43-1225_43-1214del others(12): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585283 | |||||||
chr19:10585283 | AAAAGAAA others(9): Show |
A | 1 | a0001c0001t0005g0007 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.43-1229_43-1214del others(16): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585283 | |||||||
chr19:10585284 | A | G | 3 | a0001c0002t0003g0156 a0001c0002t0012g0334 a0002c0006t0003g0157 |
3 | HG00735.hp1 NA18747.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.43-1214T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585284 | |||||||
chr19:10585285 | A | G | 2 | a0001c0002t0002g0155 a0001c0002t0004g0041 |
2 | HG02523.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.43-1215T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585285 | |||||||
chr19:10585286 | A | AGAAAGAA others(13): Show |
1 | a0001c0001t0001g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.43-1217_43-1216ins others(20): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585286 | |||||||
chr19:10585286 | A | AGAAAGAA others(9): Show |
11 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0093 others(8): Show |
15 | HG00408.hp1 HG02165.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.43-1217_43-1216ins others(16): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585286 | |||||||
chr19:10585286 | A | AGAAAGAA others(17): Show |
1 | a0001c0001t0001g0293 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.43-1217_43-1216ins others(24): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585286 | |||||||
chr19:10585286 | A | AGAAAGAA others(17): Show |
10 | a0001c0001t0001g0009 a0001c0001t0001g0046 a0001c0001t0001g0050 others(7): Show |
12 | HG00733.hp2 HG01433.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.43-1217_43-1216ins others(24): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585286 | |||||||
chr19:10585286 | A | AGAAAGAA others(13): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0076 |
3 | HG00558.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.43-1217_43-1216ins others(20): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585286 | |||||||
chr19:10585286 | A | G | 25 | a0001c0002t0001g0086 a0001c0002t0001g0094 a0001c0002t0001g0095 others(22): Show |
37 | HG00099.hp1 HG01081.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.43-1216T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585286 | |||||||
chr19:10585287 | G | A | 1 | a0001c0002t0004g0041 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.43-1217C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585287 | |||||||
chr19:10585287 | G | GAAAGAAA others(27): Show |
1 | a0001c0002t0004g0040 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.43-1218_43-1217ins others(34): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585287 | |||||||
chr19:10585288 | A | AAAGAAAG others(8): Show |
1 | a0001c0001t0001g0213 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.43-1233_43-1219dup others(15): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585288 | |||||||
chr19:10585290 | A | AGAAAGAA others(9): Show |
1 | a0001c0001t0001g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.43-1221_43-1220ins others(16): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585290 | |||||||
chr19:10585290 | A | AGAAAGAA others(5): Show |
11 | a0001c0001t0001g0187 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG00099.hp2 HG00280.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.43-1221_43-1220ins others(12): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585290 | |||||||
chr19:10585290 | A | AGAAAGAA others(13): Show |
12 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0049 others(9): Show |
15 | HG00735.hp2 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.43-1221_43-1220ins others(20): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585290 | |||||||
chr19:10585290 | A | AGAAAGAA others(9): Show |
1 | a0001c0001t0001g0070 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.43-1221_43-1220ins others(16): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585290 | |||||||
chr19:10585290 | A | G | 28 | a0001c0002t0001g0020 a0001c0002t0001g0085 a0001c0002t0001g0099 others(25): Show |
34 | HG00438.hp1 HG00544.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.43-1220T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585290 | |||||||
chr19:10585291 | G | GAAAGAAG others(23): Show |
1 | a0001c0002t0004g0042 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.43-1222_43-1221ins others(30): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585291 | |||||||
chr19:10585294 | A | AGAAAGAA others(1): Show |
6 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0198 others(3): Show |
6 | HG01074.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-1225_43-1224ins others(8): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585294 | |||||||
chr19:10585294 | A | AGAAAGAA others(9): Show |
9 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0047 others(6): Show |
12 | HG00323.hp1 HG00733.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-1225_43-1224ins others(16): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585294 | |||||||
chr19:10585294 | A | G | 17 | a0001c0001t0001g0259 a0001c0002t0001g0084 a0001c0002t0001g0117 others(14): Show |
19 | HG00621.hp2 HG00639.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.43-1224T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585294 | |||||||
chr19:10585295 | G | GAAGGAAA others(19): Show |
1 | a0001c0002t0004g0043 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.43-1226_43-1225ins others(26): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585295 | |||||||
chr19:10585297 | A | AGGAAAGA others(15): Show |
1 | a0001c0002t0004g0044 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.43-1228_43-1227ins others(22): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585297 | |||||||
chr19:10585298 | A | AGAAGGAA others(5): Show |
4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG00280.hp2 HG01346.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-1229_43-1228ins others(12): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585298 | |||||||
chr19:10585298 | A | G | 12 | a0001c0002t0001g0253 a0001c0002t0002g0021 a0001c0002t0002g0111 others(9): Show |
16 | HG00597.hp2 HG00741.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.43-1228T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585298 | |||||||
chr19:10585299 | G | A | 1 | a0001c0002t0004g0044 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.43-1229C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585299 | |||||||
chr19:10585302 | A | G | 16 | a0001c0001t0001g0053 a0001c0001t0001g0102 a0001c0001t0001g0189 others(13): Show |
19 | HG00597.hp1 HG00673.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.43-1232T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585302 | |||||||
chr19:10585306 | A | G | 2 | a0001c0001t0001g0053 a0001c0002t0002g0100 |
2 | HG00738.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.43-1236T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585306 | |||||||
chr19:10585307 | G | A | 1 | a0001c0002t0002g0100 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.43-1237C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585307 | |||||||
chr19:10585313 | AAGAAAGA others(7): Show |
A | 1 | a0001c0001t0001g0315 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43-1257_43-1244del others(14): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585313 | |||||||
chr19:10585320 | A | AAAAGAAA others(4): Show |
1 | a0001c0002t0008g0045 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.43-1251_43-1250ins others(11): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585320 | |||||||
chr19:10585331 | G | GAAAGAAA others(3): Show |
1 | a0001c0001t0001g0316 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.43-1271_43-1262dup others(10): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585331 | |||||||
chr19:10585353 | A | AAGAAAGA others(7): Show |
1 | a0001c0003t0001g0188 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.43-1284_43-1283ins others(14): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585353 | |||||||
chr19:10585396 | C | T | 2 | a0001c0002t0003g0101 a0001c0002t0003g0186 |
2 | HG03239.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.43-1326G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585396 | |||||||
chr19:10585405 | G | C | 1 | a0001c0001t0001g0317 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.43-1335C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585405 | |||||||
chr19:10585421 | G | A | 10 | a0001c0002t0004g0017 a0001c0002t0004g0036 a0001c0002t0004g0038 others(7): Show |
11 | HG02523.hp2 NA18946.hp1 NA18968.hp1 others(8): Show |
intron_variant | MODIFIER | c.43-1351C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585421 | |||||||
chr19:10585459 | G | A | 1 | a0001c0002t0002g0100 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.43-1389C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585459 | |||||||
chr19:10585460 | A | G | 1 | a0001c0002t0002g0100 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.43-1390T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585460 | |||||||
chr19:10585466 | A | C | 1 | a0001c0002t0012g0334 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.43-1396T>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585466 | |||||||
chr19:10585479 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.43-1409T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585479 | |||||||
chr19:10585584 | C | T | 1 | a0001c0002t0003g0186 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.43-1514G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585584 | |||||||
chr19:10585629 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.43-1559C>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585629 | |||||||
chr19:10585732 | C | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+1458G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585732 | |||||||
chr19:10585918 | G | A | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG01934.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.42+1272C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585918 | |||||||
chr19:10585965 | T | C | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG01934.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.42+1225A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10585965 | |||||||
chr19:10586001 | C | G | 1 | a0001c0002t0003g0092 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.42+1189G>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586001 | |||||||
chr19:10586002 | G | C | 1 | a0001c0002t0003g0092 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.42+1188C>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586002 | |||||||
chr19:10586010 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.42+1180C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586010 | |||||||
chr19:10586015 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0320 others(11): Show |
16 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.42+1175C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586015 | |||||||
chr19:10586218 | G | T | 1 | a0001c0002t0012g0334 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.42+972C>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586218 | |||||||
chr19:10586269 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.42+921G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586269 | |||||||
chr19:10586270 | G | A | 11 | a0001c0002t0003g0186 a0001c0002t0004g0017 a0001c0002t0004g0036 others(8): Show |
12 | HG02523.hp2 HG03491.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+920C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586270 | |||||||
chr19:10586283 | GA | G | 144 | a0001c0001t0001g0102 a0001c0001t0001g0258 a0001c0001t0001g0259 others(141): Show |
178 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.42+906delT | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586283 | |||||||
chr19:10586331 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.42+859A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586331 | |||||||
chr19:10586399 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(38): Show |
50 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.42+791C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586399 | |||||||
chr19:10586442 | A | G | 22 | a0001c0002t0001g0020 a0001c0002t0001g0084 a0001c0002t0001g0085 others(19): Show |
24 | HG01109.hp2 HG02145.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+748T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586442 | |||||||
chr19:10586445 | ACT | A | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG01934.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.42+743_42+744delAG | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586445 | |||||||
chr19:10586453 | T | TA | 90 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0032 others(87): Show |
97 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.42+736dupT | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586453 | |||||||
chr19:10586453 | TA | T | 12 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0093 others(9): Show |
12 | HG00639.hp1 HG01169.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+736delT | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586453 | |||||||
chr19:10586453 | TAAAAAAA | T | 10 | a0001c0002t0004g0017 a0001c0002t0004g0036 a0001c0002t0004g0038 others(7): Show |
11 | HG02523.hp2 NA18946.hp1 NA18968.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+730_42+736delTT others(5): Show |
AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586453 | |||||||
chr19:10586477 | A | T | 1 | a0001c0002t0002g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42+713T>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586477 | |||||||
chr19:10586528 | T | G | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(38): Show |
50 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.42+662A>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586528 | |||||||
chr19:10586607 | C | A | 1 | a0001c0002t0008g0045 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.42+583G>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586607 | |||||||
chr19:10586608 | T | C | 1 | a0001c0002t0008g0045 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.42+582A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586608 | |||||||
chr19:10586611 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.42+579C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586611 | |||||||
chr19:10586625 | T | C | 1 | a0001c0002t0002g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42+565A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586625 | |||||||
chr19:10586626 | C | T | 1 | a0001c0002t0002g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42+564G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586626 | |||||||
chr19:10586658 | C | A | 1 | a0001c0002t0008g0045 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.42+532G>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586658 | |||||||
chr19:10586684 | T | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0320 others(11): Show |
16 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.42+506A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586684 | |||||||
chr19:10586896 | T | C | 1 | a0001c0002t0002g0332 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.42+294A>G | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586896 | |||||||
chr19:10586930 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.42+260G>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10586930 | |||||||
chr19:10587097 | A | G | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(38): Show |
50 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.42+93T>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10587097 | |||||||
chr19:10587120 | G | T | 1 | a0001c0002t0008g0045 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.42+70C>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10587120 | |||||||
chr19:10587125 | G | A | 1 | a0001c0002t0012g0334 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.42+65C>T | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10587125 | |||||||
chr19:10587125 | G | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
51 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.42+65C>A | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10587125 | |||||||
chr19:10587126 | C | G | 1 | a0001c0002t0012g0334 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.42+64G>C | AP1M2 | ENSG00000129354.12 | transcript | ENST00000250244.11 | protein_coding | 1/11 | chr19 | 10587126 |