Item | Value |
---|---|
geneid | 92797 |
ensemblid | ENSG00000127311.10 |
hgncid | 17196 |
symbol | HELB |
name | DNA helicase B |
refseq_nuc | NM_001370285.1 |
refseq_prot | NP_001357214.1 |
ensembl_nuc | ENST00000247815.9 |
ensembl_prot | ENSP00000247815.5 |
mane_status | MANE Select |
chr | chr12 |
start | 66302493 |
end | 66338199 |
strand | + |
ver | v1.2 |
region | chr12:66302493-66338199 |
region5000 | chr12:66297493-66343199 |
regionname0 | HELB_chr12_66302493_66338199 |
regionname5000 | HELB_chr12_66297493_66343199 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1087 | 101 | 19 | 17 | 50 | 2 | 13 | 38 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0002 | 0/0 | 1087 | 95 | 7 | 23 | 56 | 3 | 6 | 44 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0003 | 0/1 | 1087 | 51 | 2 | 11 | 29 | 1 | 7 | 22 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0004 | 1/0 | 1087 | 48 | 12 | 5 | 21 | 2 | 7 | 13 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0005 | 0/0 | 1087 | 20 | 9 | 3 | 6 | 0 | 2 | 6 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0006 | 0/0 | 1087 | 16 | 16 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0007 | 0/0 | 1087 | 8 | 7 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0008 | 0/0 | 1087 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0009 | 0/0 | 1087 | 5 | 1 | 2 | 2 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0010 | 0/0 | 1087 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0011 | 0/0 | 1087 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0012 | 0/0 | 1087 | 4 | 0 | 1 | 0 | 0 | 3 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0013 | 0/0 | 1087 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0014 | 0/0 | 1087 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0015 | 0/0 | 1087 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0016 | 0/0 | 1087 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0017 | 0/0 | 739 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(734): Show |
chr12 | 66297493 | 66343199 |
a0018 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0019 | 0/0 | 1087 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0020 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0021 | 0/0 | 1087 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0022 | 0/0 | 830 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | MARSS others(825): Show |
chr12 | 66297493 | 66343199 |
a0023 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0024 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0025 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0026 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
a0027 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | MARSS others(1082): Show |
chr12 | 66297493 | 66343199 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 3261 | 61 | 6 | 16 | 29 | 2 | 8 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0001c0005 | 0/0 | 3261 | 19 | 0 | 0 | 16 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0001c0012 | 0/0 | 3261 | 5 | 0 | 0 | 5 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0001c0018 | 0/0 | 3261 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0001c0022 | 0/0 | 3261 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0001c0024 | 0/0 | 3261 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0001c0029 | 0/0 | 3261 | 2 | 1 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0001c0030 | 0/0 | 3261 | 2 | 1 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0001c0046 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0001c0050 | 0/0 | 3261 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0002c0001 | 0/0 | 3261 | 90 | 7 | 22 | 52 | 3 | 6 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0002c0017 | 0/0 | 3261 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0002c0037 | 0/0 | 3261 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0003c0003 | 0/1 | 3261 | 51 | 2 | 11 | 29 | 1 | 7 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0004c0004 | 1/0 | 3261 | 38 | 4 | 3 | 21 | 2 | 7 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0004c0008 | 0/0 | 3261 | 8 | 6 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0004c0034 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0004c0035 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0005c0006 | 0/0 | 3261 | 11 | 0 | 3 | 6 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0005c0015 | 0/0 | 3261 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0005c0023 | 0/0 | 3261 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0005c0033 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0005c0044 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0006c0007 | 0/0 | 3261 | 10 | 10 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0006c0010 | 0/0 | 3261 | 6 | 6 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0007c0009 | 0/0 | 3261 | 7 | 7 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0007c0043 | 0/0 | 3261 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0008c0011 | 0/0 | 3261 | 6 | 5 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0009c0014 | 0/0 | 3261 | 4 | 1 | 2 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0009c0047 | 0/0 | 3261 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0010c0020 | 0/0 | 3261 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0010c0027 | 0/0 | 3261 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0011c0013 | 0/0 | 3261 | 5 | 5 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0012c0025 | 0/0 | 3261 | 3 | 0 | 0 | 0 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0012c0048 | 0/0 | 3261 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0013c0019 | 0/0 | 3261 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0014c0016 | 0/0 | 3261 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0015c0026 | 0/0 | 3261 | 3 | 0 | 3 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0016c0021 | 0/0 | 3261 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0017c0028 | 0/0 | 3261 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0018c0039 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0019c0036 | 0/0 | 3261 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0020c0032 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0021c0049 | 0/0 | 3261 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0022c0038 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0023c0041 | 0/0 | 3261 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0024c0040 | 0/0 | 3261 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0025c0031 | 0/0 | 3261 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0026c0042 | 0/0 | 3261 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 | ||
a0027c0045 | 0/0 | 3261 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | ATGGC others(3256): Show |
chr12 | 66297493 | 66343199 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 3472 | 61 | 6 | 16 | 29 | 2 | 8 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0001c0005t0001 | 0/0 | 3472 | 19 | 0 | 0 | 16 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0001c0012t0001 | 0/0 | 3472 | 5 | 0 | 0 | 5 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0001c0018t0001 | 0/0 | 3472 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0001c0022t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0001c0024t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0001c0029t0001 | 0/0 | 3472 | 2 | 1 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0001c0030t0001 | 0/0 | 3472 | 2 | 1 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0001c0046t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0001c0050t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0002c0001t0001 | 0/0 | 3472 | 61 | 6 | 14 | 34 | 3 | 4 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0002c0001t0002 | 0/0 | 3471 | 29 | 1 | 8 | 18 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3466): Show |
chr12 | 66297493 | 66343199 |
a0002c0017t0001 | 0/0 | 3472 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0002c0037t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0003c0003t0001 | 0/1 | 3472 | 50 | 2 | 11 | 28 | 1 | 7 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0003c0003t0002 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3466): Show |
chr12 | 66297493 | 66343199 |
a0004c0004t0001 | 1/0 | 3472 | 38 | 4 | 3 | 21 | 2 | 7 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0004c0008t0001 | 0/0 | 3472 | 8 | 6 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0004c0034t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0004c0035t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0005c0006t0001 | 0/0 | 3472 | 7 | 0 | 3 | 2 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0005c0006t0002 | 0/0 | 3471 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3466): Show |
chr12 | 66297493 | 66343199 |
a0005c0015t0001 | 0/0 | 3472 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0005c0023t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0005c0033t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0005c0044t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0006c0007t0001 | 0/0 | 3472 | 10 | 10 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0006c0010t0001 | 0/0 | 3472 | 6 | 6 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0007c0009t0001 | 0/0 | 3472 | 7 | 7 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0007c0043t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0008c0011t0001 | 0/0 | 3472 | 6 | 5 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0009c0014t0001 | 0/0 | 3472 | 4 | 1 | 2 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0009c0047t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0010c0020t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0010c0027t0001 | 0/0 | 3472 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0011c0013t0001 | 0/0 | 3472 | 5 | 5 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0012c0025t0001 | 0/0 | 3472 | 3 | 0 | 0 | 0 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0012c0048t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0013c0019t0001 | 0/0 | 3472 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0014c0016t0001 | 0/0 | 3472 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0015c0026t0001 | 0/0 | 3472 | 3 | 0 | 3 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0016c0021t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0017c0028t0001 | 0/0 | 3472 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0018c0039t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0019c0036t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0020c0032t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0021c0049t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0022c0038t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0023c0041t0002 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3466): Show |
chr12 | 66297493 | 66343199 |
a0024c0040t0002 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3466): Show |
chr12 | 66297493 | 66343199 |
a0025c0031t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
a0026c0042t0002 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3466): Show |
chr12 | 66297493 | 66343199 |
a0027c0045t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | AGGCC others(3467): Show |
chr12 | 66297493 | 66343199 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0002 | 0/0 | 9 | 1 | 4 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0003 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0012t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0012t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0012t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0012t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0018t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0018t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0018t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0022t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0022t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0022t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0024t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0024t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0024t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0029t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0029t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0030t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0030t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0046t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0001c0050t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0007 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0017t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0017t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0017t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0002c0037t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0001 | 0/1 | 10 | 0 | 4 | 2 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0010 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0003c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0035 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0008t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0008t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0008t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0008t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0008t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0008t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0008t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0008t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0034t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0004c0035t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0006t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0006t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0006t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0006t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0006t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0006t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0006t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0006t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0006t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0006t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0006t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0015t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0015t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0015t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0015t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0023t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0023t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0023t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0033t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0005c0044t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0007t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0007t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0007t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0007t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0007t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0007t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0007t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0007t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0007t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0007t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0010t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0010t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0010t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0010t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0006c0010t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0007c0009t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0007c0009t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0007c0009t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0007c0009t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0007c0009t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0007c0009t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0007c0043t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0008c0011t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0008c0011t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0008c0011t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0008c0011t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0008c0011t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0009c0014t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0009c0014t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0009c0014t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0009c0014t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0009c0047t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0010c0020t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0010c0020t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0010c0020t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0010c0027t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0010c0027t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0011c0013t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0011c0013t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0011c0013t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0011c0013t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0011c0013t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0012c0025t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0012c0025t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0012c0025t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0012c0048t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0013c0019t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0013c0019t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0013c0019t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0014c0016t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0014c0016t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0014c0016t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0014c0016t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0015c0026t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0015c0026t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0016c0021t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0016c0021t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0016c0021t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0017c0028t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0018c0039t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0019c0036t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0020c0032t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0021c0049t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0022c0038t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0023c0041t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0024c0040t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0025c0031t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0026c0042t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
a0027c0045t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0001 | t0001 | g0159 | EUR | GBR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00140 | hp2 | a0004 | c0004 | t0001 | g0009 | EUR | GBR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00280 | hp1 | a0003 | c0003 | t0001 | g0150 | EUR | FIN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0046 | EUR | FIN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00438 | hp1 | a0004 | c0004 | t0001 | g0126 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00438 | hp2 | a0001 | c0005 | t0001 | g0059 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00544 | hp1 | a0004 | c0004 | t0001 | g0113 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00544 | hp2 | a0004 | c0004 | t0001 | g0145 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00558 | hp2 | a0003 | c0003 | t0001 | g0030 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00597 | hp1 | a0004 | c0004 | t0001 | g0119 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00597 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00621 | hp1 | a0004 | c0004 | t0001 | g0127 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00621 | hp2 | a0001 | c0012 | t0001 | g0017 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00639 | hp2 | a0015 | c0026 | t0001 | g0005 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00642 | hp1 | a0004 | c0004 | t0001 | g0080 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00642 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00738 | hp2 | a0002 | c0037 | t0001 | g0158 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01069 | hp1 | a0004 | c0008 | t0001 | g0161 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0252 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01070 | hp1 | a0015 | c0026 | t0001 | g0241 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01070 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01071 | hp1 | a0015 | c0026 | t0001 | g0005 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01071 | hp2 | a0004 | c0008 | t0001 | g0160 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01074 | hp2 | a0002 | c0001 | t0001 | g0054 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01081 | hp1 | a0005 | c0006 | t0001 | g0274 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01099 | hp1 | a0002 | c0001 | t0001 | g0095 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01099 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0298 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01109 | hp2 | a0008 | c0011 | t0001 | g0123 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01167 | hp1 | a0003 | c0003 | t0001 | g0082 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01167 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01168 | hp1 | a0003 | c0003 | t0001 | g0132 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01168 | hp2 | a0005 | c0006 | t0001 | g0285 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01175 | hp1 | a0003 | c0003 | t0001 | g0122 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01175 | hp2 | a0005 | c0006 | t0001 | g0273 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01192 | hp1 | a0004 | c0004 | t0001 | g0129 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01192 | hp2 | a0002 | c0001 | t0001 | g0153 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01243 | hp1 | a0002 | c0001 | t0001 | g0032 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01243 | hp2 | a0009 | c0014 | t0001 | g0066 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0286 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01255 | hp2 | a0002 | c0001 | t0002 | g0039 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01257 | hp2 | a0002 | c0001 | t0001 | g0036 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01258 | hp1 | a0002 | c0001 | t0001 | g0027 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01258 | hp2 | a0002 | c0001 | t0001 | g0036 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01261 | hp1 | a0004 | c0004 | t0001 | g0169 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0289 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01346 | hp2 | a0012 | c0048 | t0001 | g0255 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01358 | hp1 | a0002 | c0001 | t0002 | g0039 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01358 | hp2 | a0003 | c0003 | t0001 | g0010 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01361 | hp1 | a0001 | c0029 | t0001 | g0214 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01361 | hp2 | a0002 | c0001 | t0002 | g0037 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01496 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01496 | hp2 | a0002 | c0001 | t0002 | g0208 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01515 | hp1 | a0002 | c0001 | t0001 | g0171 | EUR | IBS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0283 | EUR | IBS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01884 | hp1 | a0006 | c0007 | t0001 | g0226 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01884 | hp2 | a0007 | c0009 | t0001 | g0243 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01891 | hp1 | a0004 | c0008 | t0001 | g0109 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01891 | hp2 | a0004 | c0004 | t0001 | g0154 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01934 | hp1 | a0002 | c0001 | t0002 | g0207 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01934 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01952 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01952 | hp2 | a0002 | c0001 | t0002 | g0206 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01978 | hp1 | a0009 | c0014 | t0001 | g0062 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01978 | hp2 | a0002 | c0001 | t0001 | g0168 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01993 | hp2 | a0002 | c0001 | t0002 | g0211 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02015 | hp1 | a0003 | c0003 | t0001 | g0143 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02027 | hp1 | a0002 | c0001 | t0001 | g0152 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02027 | hp2 | a0002 | c0001 | t0001 | g0100 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02040 | hp1 | a0001 | c0005 | t0001 | g0057 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02040 | hp2 | a0004 | c0004 | t0001 | g0074 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02055 | hp1 | a0001 | c0022 | t0001 | g0174 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02055 | hp2 | a0001 | c0030 | t0001 | g0244 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02056 | hp1 | a0009 | c0014 | t0001 | g0060 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02071 | hp1 | a0002 | c0001 | t0002 | g0197 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02071 | hp2 | a0017 | c0028 | t0001 | g0003 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02074 | hp1 | a0017 | c0028 | t0001 | g0003 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02074 | hp2 | a0004 | c0004 | t0001 | g0144 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02080 | hp1 | a0002 | c0001 | t0001 | g0117 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02080 | hp2 | a0001 | c0005 | t0001 | g0063 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02083 | hp1 | a0002 | c0001 | t0001 | g0167 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02083 | hp2 | a0002 | c0001 | t0001 | g0114 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02129 | hp1 | a0003 | c0003 | t0001 | g0131 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02129 | hp2 | a0002 | c0001 | t0001 | g0170 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02132 | hp1 | a0001 | c0012 | t0001 | g0172 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0120 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0110 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02135 | hp2 | a0004 | c0004 | t0001 | g0094 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02145 | hp1 | a0006 | c0007 | t0001 | g0293 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02145 | hp2 | a0010 | c0020 | t0001 | g0228 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02155 | hp1 | a0003 | c0003 | t0001 | g0084 | EAS | CDX | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02155 | hp2 | a0001 | c0012 | t0001 | g0017 | EAS | CDX | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02165 | hp1 | a0001 | c0012 | t0001 | g0018 | EAS | CDX | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CDX | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02257 | hp1 | a0007 | c0009 | t0001 | g0248 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02257 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02258 | hp1 | a0002 | c0001 | t0001 | g0029 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02258 | hp2 | a0002 | c0001 | t0001 | g0007 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02273 | hp1 | a0002 | c0001 | t0002 | g0185 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02273 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02280 | hp1 | a0004 | c0008 | t0001 | g0151 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02280 | hp2 | a0004 | c0004 | t0001 | g0022 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02293 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02300 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02451 | hp1 | a0006 | c0007 | t0001 | g0229 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02451 | hp2 | a0007 | c0009 | t0001 | g0245 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02523 | hp1 | a0001 | c0012 | t0001 | g0056 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02523 | hp2 | a0002 | c0001 | t0001 | g0015 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02572 | hp1 | a0011 | c0013 | t0001 | g0238 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02572 | hp2 | a0007 | c0009 | t0001 | g0246 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02602 | hp1 | a0001 | c0005 | t0001 | g0018 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02615 | hp1 | a0001 | c0024 | t0001 | g0182 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02615 | hp2 | a0011 | c0013 | t0001 | g0237 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02622 | hp1 | a0007 | c0009 | t0001 | g0042 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02622 | hp2 | a0011 | c0013 | t0001 | g0235 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02630 | hp1 | a0006 | c0007 | t0001 | g0225 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02630 | hp2 | a0018 | c0039 | t0001 | g0107 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02647 | hp1 | a0004 | c0034 | t0001 | g0149 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02647 | hp2 | a0013 | c0019 | t0001 | g0047 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02683 | hp1 | a0001 | c0005 | t0001 | g0003 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02683 | hp2 | a0004 | c0004 | t0001 | g0088 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02698 | hp1 | a0001 | c0030 | t0001 | g0089 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02698 | hp2 | a0019 | c0036 | t0001 | g0004 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02717 | hp1 | a0007 | c0009 | t0001 | g0042 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02717 | hp2 | a0004 | c0008 | t0001 | g0093 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02723 | hp1 | a0007 | c0009 | t0001 | g0247 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02723 | hp2 | a0013 | c0019 | t0001 | g0279 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02735 | hp1 | a0002 | c0001 | t0001 | g0079 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02735 | hp2 | a0004 | c0004 | t0001 | g0009 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02738 | hp1 | a0012 | c0025 | t0001 | g0291 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02738 | hp2 | a0002 | c0001 | t0001 | g0072 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02809 | hp1 | a0016 | c0021 | t0001 | g0224 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02809 | hp2 | a0006 | c0010 | t0001 | g0041 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02818 | hp1 | a0001 | c0024 | t0001 | g0181 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02818 | hp2 | a0005 | c0015 | t0001 | g0179 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02886 | hp1 | a0005 | c0023 | t0001 | g0069 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02886 | hp2 | a0011 | c0013 | t0001 | g0234 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02895 | hp1 | a0010 | c0020 | t0001 | g0230 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02895 | hp2 | a0006 | c0010 | t0001 | g0040 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02896 | hp1 | a0006 | c0007 | t0001 | g0041 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02896 | hp2 | a0010 | c0027 | t0001 | g0220 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02897 | hp1 | a0006 | c0010 | t0001 | g0250 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02897 | hp2 | a0010 | c0027 | t0001 | g0223 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02922 | hp1 | a0010 | c0020 | t0001 | g0292 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02922 | hp2 | a0004 | c0008 | t0001 | g0108 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02965 | hp2 | a0008 | c0011 | t0001 | g0033 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02970 | hp1 | a0001 | c0022 | t0001 | g0070 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02970 | hp2 | a0002 | c0001 | t0001 | g0078 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02976 | hp1 | a0004 | c0004 | t0001 | g0073 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02976 | hp2 | a0001 | c0022 | t0001 | g0071 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03041 | hp1 | a0001 | c0024 | t0001 | g0180 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03041 | hp2 | a0006 | c0007 | t0001 | g0218 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03098 | hp1 | a0006 | c0010 | t0001 | g0040 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03098 | hp2 | a0004 | c0004 | t0001 | g0035 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03130 | hp1 | a0001 | c0018 | t0001 | g0281 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03130 | hp2 | a0006 | c0007 | t0001 | g0213 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03139 | hp1 | a0005 | c0015 | t0001 | g0299 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03139 | hp2 | a0001 | c0029 | t0001 | g0178 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03209 | hp1 | a0006 | c0007 | t0001 | g0216 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03209 | hp2 | a0005 | c0015 | t0001 | g0050 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03225 | hp1 | a0001 | c0018 | t0001 | g0043 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03225 | hp2 | a0003 | c0003 | t0001 | g0028 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03239 | hp1 | a0005 | c0006 | t0001 | g0267 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03453 | hp1 | a0005 | c0023 | t0001 | g0067 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03486 | hp1 | a0016 | c0021 | t0001 | g0222 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03486 | hp2 | a0005 | c0033 | t0001 | g0236 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0277 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03491 | hp2 | a0003 | c0003 | t0001 | g0010 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0275 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03492 | hp2 | a0003 | c0003 | t0001 | g0010 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03516 | hp1 | a0008 | c0011 | t0001 | g0166 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03516 | hp2 | a0020 | c0032 | t0001 | g0249 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03540 | hp1 | a0005 | c0044 | t0001 | g0242 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03540 | hp2 | a0001 | c0018 | t0001 | g0043 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03579 | hp1 | a0011 | c0013 | t0001 | g0239 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03579 | hp2 | a0005 | c0023 | t0001 | g0068 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03688 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03688 | hp2 | a0002 | c0001 | t0002 | g0199 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03704 | hp2 | a0002 | c0001 | t0002 | g0200 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03710 | hp1 | a0012 | c0025 | t0001 | g0002 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03710 | hp2 | a0002 | c0001 | t0001 | g0118 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03831 | hp1 | a0001 | c0005 | t0001 | g0003 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03831 | hp2 | a0004 | c0004 | t0001 | g0031 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03834 | hp2 | a0004 | c0004 | t0001 | g0128 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03942 | hp1 | a0012 | c0025 | t0001 | g0272 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0013 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG04115 | hp1 | a0004 | c0004 | t0001 | g0115 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG04115 | hp2 | a0021 | c0049 | t0001 | g0257 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG04184 | hp1 | a0005 | c0006 | t0001 | g0258 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG04184 | hp2 | a0003 | c0003 | t0001 | g0157 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG04199 | hp1 | a0002 | c0001 | t0001 | g0007 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG04199 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG04204 | hp1 | a0004 | c0004 | t0001 | g0105 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG04204 | hp2 | a0001 | c0050 | t0001 | g0013 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0276 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG04228 | hp2 | a0004 | c0004 | t0001 | g0102 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18522 | hp1 | a0004 | c0008 | t0001 | g0091 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18522 | hp2 | a0002 | c0001 | t0001 | g0121 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18612 | hp1 | a0002 | c0001 | t0001 | g0096 | EAS | CHB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18612 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | CHB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0087 | EAS | CHB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18747 | hp2 | a0002 | c0001 | t0001 | g0090 | EAS | CHB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18906 | hp2 | a0022 | c0038 | t0001 | g0022 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18939 | hp1 | a0002 | c0001 | t0001 | g0081 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18939 | hp2 | a0002 | c0017 | t0001 | g0016 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18941 | hp1 | a0003 | c0003 | t0001 | g0133 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18941 | hp2 | a0005 | c0006 | t0002 | g0262 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18942 | hp1 | a0002 | c0001 | t0002 | g0205 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18942 | hp2 | a0002 | c0001 | t0001 | g0086 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18948 | hp1 | a0001 | c0005 | t0001 | g0020 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18950 | hp1 | a0002 | c0001 | t0002 | g0196 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18950 | hp2 | a0023 | c0041 | t0002 | g0188 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18952 | hp1 | a0004 | c0004 | t0001 | g0097 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18952 | hp2 | a0002 | c0001 | t0001 | g0098 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18953 | hp1 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18953 | hp2 | a0002 | c0001 | t0002 | g0202 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18954 | hp2 | a0002 | c0017 | t0001 | g0138 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18957 | hp1 | a0002 | c0001 | t0001 | g0165 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18963 | hp2 | a0002 | c0001 | t0002 | g0204 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18965 | hp2 | a0004 | c0004 | t0001 | g0175 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18966 | hp1 | a0001 | c0005 | t0001 | g0019 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18967 | hp1 | a0001 | c0005 | t0001 | g0058 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18967 | hp2 | a0002 | c0001 | t0002 | g0101 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18968 | hp1 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18968 | hp2 | a0004 | c0004 | t0001 | g0190 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18969 | hp1 | a0004 | c0004 | t0001 | g0189 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18969 | hp2 | a0002 | c0001 | t0001 | g0034 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18970 | hp1 | a0009 | c0047 | t0001 | g0266 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18970 | hp2 | a0004 | c0004 | t0001 | g0187 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18971 | hp1 | a0002 | c0001 | t0002 | g0038 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18971 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18975 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18978 | hp1 | a0005 | c0006 | t0001 | g0290 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18978 | hp2 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18979 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18979 | hp2 | a0001 | c0005 | t0001 | g0019 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18980 | hp2 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18982 | hp1 | a0001 | c0005 | t0001 | g0065 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18982 | hp2 | a0004 | c0004 | t0001 | g0051 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18983 | hp1 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18983 | hp2 | a0004 | c0004 | t0001 | g0031 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18984 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18986 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18986 | hp2 | a0002 | c0001 | t0001 | g0116 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18987 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18990 | hp2 | a0002 | c0001 | t0001 | g0099 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18991 | hp1 | a0002 | c0001 | t0001 | g0164 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18991 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18992 | hp1 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18993 | hp1 | a0024 | c0040 | t0002 | g0193 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18993 | hp2 | a0001 | c0005 | t0001 | g0021 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18995 | hp1 | a0002 | c0001 | t0002 | g0210 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18995 | hp2 | a0002 | c0001 | t0002 | g0186 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18999 | hp1 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18999 | hp2 | a0014 | c0016 | t0001 | g0139 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19000 | hp1 | a0005 | c0006 | t0002 | g0240 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19000 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19004 | hp1 | a0002 | c0001 | t0002 | g0201 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19004 | hp2 | a0004 | c0004 | t0001 | g0111 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19005 | hp1 | a0001 | c0005 | t0001 | g0020 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19005 | hp2 | a0002 | c0017 | t0001 | g0016 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19006 | hp1 | a0005 | c0006 | t0002 | g0268 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19006 | hp2 | a0001 | c0005 | t0001 | g0173 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19007 | hp1 | a0025 | c0031 | t0001 | g0142 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19007 | hp2 | a0004 | c0004 | t0001 | g0141 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19009 | hp1 | a0005 | c0006 | t0002 | g0261 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19009 | hp2 | a0003 | c0003 | t0001 | g0163 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19011 | hp2 | a0001 | c0005 | t0001 | g0061 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19012 | hp1 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19012 | hp2 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19030 | hp1 | a0004 | c0035 | t0001 | g0183 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19030 | hp2 | a0008 | c0011 | t0001 | g0001 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19043 | hp1 | a0006 | c0007 | t0001 | g0219 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19043 | hp2 | a0008 | c0011 | t0001 | g0033 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19054 | hp1 | a0026 | c0042 | t0002 | g0195 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19054 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19055 | hp1 | a0002 | c0001 | t0001 | g0034 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19055 | hp2 | a0003 | c0003 | t0001 | g0112 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19056 | hp1 | a0003 | c0003 | t0001 | g0212 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19056 | hp2 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19057 | hp1 | a0002 | c0001 | t0002 | g0038 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19057 | hp2 | a0003 | c0003 | t0001 | g0085 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19058 | hp1 | a0005 | c0006 | t0001 | g0265 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19058 | hp2 | a0002 | c0001 | t0002 | g0198 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19060 | hp2 | a0003 | c0003 | t0001 | g0124 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19062 | hp1 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19062 | hp2 | a0002 | c0001 | t0001 | g0053 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19063 | hp2 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19064 | hp1 | a0007 | c0043 | t0001 | g0012 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19066 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19067 | hp1 | a0002 | c0017 | t0001 | g0055 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19068 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19068 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19072 | hp2 | a0003 | c0003 | t0001 | g0147 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19074 | hp1 | a0003 | c0003 | t0002 | g0130 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19074 | hp2 | a0002 | c0001 | t0002 | g0209 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19075 | hp1 | a0002 | c0001 | t0002 | g0194 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19075 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19076 | hp1 | a0004 | c0004 | t0001 | g0176 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19077 | hp1 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19077 | hp2 | a0002 | c0001 | t0002 | g0192 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19078 | hp1 | a0004 | c0004 | t0001 | g0106 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19080 | hp1 | a0003 | c0003 | t0001 | g0125 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19082 | hp1 | a0002 | c0001 | t0002 | g0191 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19082 | hp2 | a0004 | c0004 | t0001 | g0135 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19083 | hp2 | a0002 | c0001 | t0002 | g0052 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19084 | hp1 | a0002 | c0001 | t0002 | g0184 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19085 | hp1 | a0014 | c0016 | t0001 | g0137 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19087 | hp1 | a0014 | c0016 | t0001 | g0136 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19087 | hp2 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19090 | hp1 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19090 | hp2 | a0001 | c0005 | t0001 | g0021 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19091 | hp1 | a0014 | c0016 | t0001 | g0140 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19091 | hp2 | a0027 | c0045 | t0001 | g0045 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19240 | hp1 | a0006 | c0007 | t0001 | g0217 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA19240 | hp2 | a0013 | c0019 | t0001 | g0280 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | ASW | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA20129 | hp2 | a0016 | c0021 | t0001 | g0221 | AFR | ASW | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA20805 | hp1 | a0004 | c0004 | t0001 | g0009 | EUR | TSI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA20805 | hp2 | a0002 | c0001 | t0001 | g0032 | EUR | TSI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA20905 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | GIH | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0296 | SAS | GIH | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02109 | hp1 | a0009 | c0014 | t0001 | g0064 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02109 | hp2 | a0001 | c0018 | t0001 | g0259 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02486 | hp1 | a0003 | c0003 | t0001 | g0028 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02486 | hp2 | a0005 | c0015 | t0001 | g0177 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02559 | hp1 | a0001 | c0046 | t0001 | g0288 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG02559 | hp2 | a0006 | c0010 | t0001 | g0227 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03471 | hp1 | a0013 | c0019 | t0001 | g0047 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG03471 | hp2 | a0006 | c0010 | t0001 | g0215 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG06807 | hp1 | a0004 | c0008 | t0001 | g0092 | AFR | USA | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | USA | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18955 | hp1 | a0004 | c0004 | t0001 | g0203 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA20300 | hp1 | a0002 | c0001 | t0001 | g0077 | AFR | USA | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA20300 | hp2 | a0002 | c0001 | t0002 | g0037 | AFR | USA | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA21309 | hp1 | a0008 | c0011 | t0001 | g0076 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0001 | REF | REF | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
homoSapiens | grch38p0 | a0004 | c0004 | t0001 | g0035 | REF | REF | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:66302684 | C | A | 1 | a0025 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.81C>A | p.Asp27Glu | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/13 | 192/3472 | 81/3264 | 27/1087 | chr12 | 66302684 | |||
chr12:66304989 | A | G | 1 | a0026 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.446A>G | p.Lys149Arg | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/13 | 557/3472 | 446/3264 | 149/1087 | chr12 | 66304989 | |||
chr12:66305057 | G | A | 3 | a0006 a0010 a0016 |
24 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(21): Show |
missense_variant | MODERATE | c.514G>A | p.Glu172Lys | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/13 | 625/3472 | 514/3264 | 172/1087 | chr12 | 66305057 | |||
chr12:66305115 | T | C | 15 | a0001 a0005 a0006 others(12): Show |
179 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(176): Show |
missense_variant | MODERATE | c.572T>C | p.Leu191Pro | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/13 | 683/3472 | 572/3264 | 191/1087 | chr12 | 66305115 | |||
chr12:66309727 | C | T | 1 | a0008 | 6 | HG01109.hp2 HG02965.hp2 HG03516.hp1 others(3): Show |
missense_variant | MODERATE | c.799C>T | p.Leu267Phe | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/13 | 910/3472 | 799/3264 | 267/1087 | chr12 | 66309727 | |||
chr12:66310388 | G | A | 2 | a0007 a0020 |
9 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.1460G>A | p.Arg487His | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/13 | 1571/3472 | 1460/3264 | 487/1087 | chr12 | 66310388 | |||
chr12:66310445 | A | G | 3 | a0012 a0015 a0021 |
8 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
missense_variant | MODERATE | c.1517A>G | p.Asp506Gly | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/13 | 1628/3472 | 1517/3264 | 506/1087 | chr12 | 66310445 | |||
chr12:66310496 | A | C | 1 | a0015 | 3 | HG00639.hp2 HG01070.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.1568A>C | p.Gln523Pro | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/13 | 1679/3472 | 1568/3264 | 523/1087 | chr12 | 66310496 | |||
chr12:66314028 | A | G | 1 | a0013 | 4 | HG02647.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.1723A>G | p.Thr575Ala | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/13 | 1834/3472 | 1723/3264 | 575/1087 | chr12 | 66314028 | |||
chr12:66315325 | A | G | 4 | a0011 a0016 a0023 others(1): Show |
10 | HG02572.hp1 HG02615.hp2 HG02622.hp2 others(7): Show |
missense_variant | MODERATE | c.1942A>G | p.Ile648Val | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/13 | 2053/3472 | 1942/3264 | 648/1087 | chr12 | 66315325 | |||
chr12:66318648 | C | T | 1 | a0018 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.2011C>T | p.Arg671Cys | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/13 | 2122/3472 | 2011/3264 | 671/1087 | chr12 | 66318648 | |||
chr12:66322010 | C | T | 1 | a0017 | 2 | HG02071.hp2 HG02074.hp1 |
stop_gained | HIGH | c.2218C>T | p.Gln740* | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/13 | 2329/3472 | 2218/3264 | 740/1087 | chr12 | 66322010 | |||
chr12:66322762 | A | T | 1 | a0023 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.2276A>T | p.His759Leu | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/13 | 2387/3472 | 2276/3264 | 759/1087 | chr12 | 66322762 | |||
chr12:66324176 | C | T | 1 | a0022 | 1 | NA18906.hp2 | stop_gained | HIGH | c.2491C>T | p.Arg831* | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/13 | 2602/3472 | 2491/3264 | 831/1087 | chr12 | 66324176 | |||
chr12:66331160 | G | A | 1 | a0027 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.2677G>A | p.Glu893Lys | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 2788/3472 | 2677/3264 | 893/1087 | chr12 | 66331160 | |||
chr12:66331320 | G | A | 1 | a0014 | 4 | NA18999.hp2 NA19085.hp1 NA19087.hp1 others(1): Show |
missense_variant | MODERATE | c.2837G>A | p.Arg946His | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 2948/3472 | 2837/3264 | 946/1087 | chr12 | 66331320 | |||
chr12:66331373 | G | T | 1 | a0019 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.2890G>T | p.Asp964Tyr | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3001/3472 | 2890/3264 | 964/1087 | chr12 | 66331373 | |||
chr12:66331380 | C | T | 17 | a0002 a0003 a0005 others(14): Show |
200 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(197): Show |
missense_variant | MODERATE | c.2897C>T | p.Pro966Leu | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3008/3472 | 2897/3264 | 966/1087 | chr12 | 66331380 | |||
chr12:66331422 | C | T | 8 | a0003 a0009 a0014 others(5): Show |
64 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(61): Show |
missense_variant | MODERATE | c.2939C>T | p.Thr980Ile | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3050/3472 | 2939/3264 | 980/1087 | chr12 | 66331422 | |||
chr12:66331521 | T | C | 1 | a0013 | 4 | HG02647.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.3038T>C | p.Phe1013Ser | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3149/3472 | 3038/3264 | 1013/1087 | chr12 | 66331521 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:66302630 | C | T | 14 | a0001c0002 a0001c0018 a0001c0046 others(11): Show |
94 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(91): Show |
synonymous_variant | LOW | c.27C>T | p.Arg9Arg | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/13 | 138/3472 | 27/3264 | 9/1087 | chr12 | 66302630 | |||
chr12:66306493 | G | A | 6 | a0001c0005 a0001c0012 a0001c0022 others(3): Show |
36 | HG00438.hp2 HG00621.hp2 HG01243.hp2 others(33): Show |
synonymous_variant | LOW | c.756G>A | p.Pro252Pro | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/13 | 867/3472 | 756/3264 | 252/1087 | chr12 | 66306493 | |||
chr12:66309963 | A | T | 1 | a0001c0050 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.1035A>T | p.Thr345Thr | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/13 | 1146/3472 | 1035/3264 | 345/1087 | chr12 | 66309963 | |||
chr12:66324004 | T | A | 12 | a0001c0005 a0001c0012 a0001c0022 others(9): Show |
54 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(51): Show |
synonymous_variant | LOW | c.2319T>A | p.Val773Val | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/13 | 2430/3472 | 2319/3264 | 773/1087 | chr12 | 66324004 | |||
chr12:66324130 | G | A | 1 | a0012c0048 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.2445G>A | p.Thr815Thr | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/13 | 2556/3472 | 2445/3264 | 815/1087 | chr12 | 66324130 | |||
chr12:66324130 | G | T | 12 | a0001c0005 a0001c0012 a0001c0022 others(9): Show |
54 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(51): Show |
synonymous_variant | LOW | c.2445G>T | p.Thr815Thr | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/13 | 2556/3472 | 2445/3264 | 815/1087 | chr12 | 66324130 | |||
chr12:66331336 | G | A | 1 | a0001c0012 | 5 | HG00621.hp2 HG02132.hp1 HG02155.hp2 others(2): Show |
synonymous_variant | LOW | c.2853G>A | p.Leu951Leu | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 2964/3472 | 2853/3264 | 951/1087 | chr12 | 66331336 | |||
chr12:66331357 | C | T | 1 | a0002c0037 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.2874C>T | p.Ser958Ser | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 2985/3472 | 2874/3264 | 958/1087 | chr12 | 66331357 | |||
chr12:66331426 | G | A | 1 | a0002c0017 | 4 | NA18939.hp2 NA18954.hp2 NA19005.hp2 others(1): Show |
synonymous_variant | LOW | c.2943G>A | p.Pro981Pro | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3054/3472 | 2943/3264 | 981/1087 | chr12 | 66331426 | |||
chr12:66331486 | C | T | 1 | a0004c0035 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.3003C>T | p.Ser1001Ser | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3114/3472 | 3003/3264 | 1001/1087 | chr12 | 66331486 | |||
chr12:66331612 | G | A | 1 | a0001c0018 | 4 | HG02109.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.3129G>A | p.Val1043Val | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3240/3472 | 3129/3264 | 1043/1087 | chr12 | 66331612 | |||
chr12:66338084 | C | A | 32 | a0001c0022 a0001c0024 a0001c0046 others(29): Show |
226 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(223): Show |
synonymous_variant | LOW | c.3246C>A | p.Thr1082Thr | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 13/13 | 3357/3472 | 3246/3264 | 1082/1087 | chr12 | 66338084 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:66338132 | GT | G | 6 | a0002c0001t0002 a0003c0003t0002 a0005c0006t0002 others(3): Show |
37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*35delT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 13/13 | 35 | INFO_REALIGN_3_PRIME | chr12 | 66338132 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:66302902 | A | G | 1 | a0005c0015t0001g0299 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.187+112A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66302902 | |||||||
chr12:66302903 | G | A | 1 | a0005c0015t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+113G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66302903 | |||||||
chr12:66302926 | C | T | 149 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(146): Show |
178 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(175): Show |
intron_variant | MODIFIER | c.187+136C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66302926 | |||||||
chr12:66302985 | G | GT | 13 | a0001c0002t0001g0049 a0001c0002t0001g0294 a0001c0002t0001g0295 others(10): Show |
14 | HG00741.hp1 HG01109.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.187+210dupT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66302985 | ||||||
chr12:66302985 | GT | G | 16 | a0001c0024t0001g0180 a0001c0024t0001g0181 a0001c0024t0001g0182 others(13): Show |
18 | HG01074.hp2 HG02486.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.187+210delT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66302985 | ||||||
chr12:66302989 | T | G | 9 | a0001c0024t0001g0180 a0001c0024t0001g0181 a0001c0024t0001g0182 others(6): Show |
9 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.187+199T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66302989 | |||||||
chr12:66303086 | CT | C | 45 | a0001c0029t0001g0178 a0002c0001t0001g0081 a0002c0001t0001g0086 others(42): Show |
48 | HG01167.hp1 HG01255.hp2 HG01358.hp1 others(45): Show |
intron_variant | MODIFIER | c.187+317delT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66303086 | ||||||
chr12:66303086 | CTT | C | 12 | a0001c0029t0001g0214 a0006c0007t0001g0213 a0006c0007t0001g0216 others(9): Show |
12 | HG01361.hp1 HG02809.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.187+316_187+317del others(2): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66303086 | ||||||
chr12:66303101 | T | A | 3 | a0001c0012t0001g0017 a0001c0012t0001g0056 a0001c0012t0001g0172 |
4 | HG00621.hp2 HG02132.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+311T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303101 | |||||||
chr12:66303102 | T | A | 12 | a0001c0005t0001g0018 a0001c0012t0001g0017 a0001c0012t0001g0018 others(9): Show |
13 | HG00621.hp2 HG02132.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+312T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303102 | |||||||
chr12:66303103 | T | A | 61 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(58): Show |
73 | HG00438.hp2 HG00621.hp2 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.187+313T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303103 | |||||||
chr12:66303104 | T | A | 67 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(64): Show |
79 | HG00438.hp2 HG00621.hp2 HG01243.hp2 others(76): Show |
intron_variant | MODIFIER | c.187+314T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303104 | |||||||
chr12:66303105 | T | A | 69 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(66): Show |
81 | HG00438.hp2 HG00621.hp2 HG01243.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+315T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303105 | |||||||
chr12:66303105 | TTTA | T | 6 | a0006c0007t0001g0041 a0006c0007t0001g0225 a0006c0007t0001g0226 others(3): Show |
7 | HG01884.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+316_187+318del others(3): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303105 | |||||||
chr12:66303106 | T | A | 80 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(77): Show |
92 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.187+316T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303106 | |||||||
chr12:66303106 | TTA | T | 20 | a0001c0002t0001g0231 a0001c0002t0001g0232 a0001c0002t0001g0233 others(17): Show |
21 | HG01070.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.187+317_187+318del others(2): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303106 | |||||||
chr12:66303107 | T | A | 205 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(202): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.187+317T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303107 | |||||||
chr12:66303107 | T | TA | 3 | a0002c0017t0001g0055 a0003c0003t0001g0162 a0003c0003t0001g0163 |
3 | NA18978.hp2 NA19009.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.187+321dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66303107 | ||||||
chr12:66303107 | TA | T | 60 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(57): Show |
84 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.187+321delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66303107 | ||||||
chr12:66303108 | A | T | 4 | a0001c0002t0001g0289 a0001c0002t0001g0298 a0005c0006t0001g0290 others(1): Show |
4 | HG01109.hp1 HG01261.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+318A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303108 | |||||||
chr12:66303620 | T | C | 176 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(173): Show |
214 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.187+830T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303620 | |||||||
chr12:66303889 | T | C | 1 | a0002c0001t0001g0090 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.188-842T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303889 | |||||||
chr12:66303900 | T | C | 5 | a0006c0007t0001g0229 a0006c0007t0001g0293 a0010c0020t0001g0228 others(2): Show |
5 | HG02145.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-831T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303900 | |||||||
chr12:66304008 | A | G | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.188-723A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304008 | |||||||
chr12:66304024 | C | T | 3 | a0001c0024t0001g0180 a0001c0024t0001g0181 a0001c0024t0001g0182 |
3 | HG02615.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.188-707C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304024 | |||||||
chr12:66304065 | A | G | 1 | a0001c0002t0001g0049 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.188-666A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304065 | |||||||
chr12:66304295 | T | G | 2 | a0001c0002t0001g0251 a0001c0002t0001g0252 |
2 | HG01069.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.188-436T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304295 | |||||||
chr12:66304296 | GAT | G | 86 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(83): Show |
111 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.188-433_188-432del others(2): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66304296 | ||||||
chr12:66304364 | A | G | 136 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(133): Show |
171 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.188-367A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304364 | |||||||
chr12:66304658 | G | A | 176 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(173): Show |
214 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.188-73G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304658 | |||||||
chr12:66304681 | A | G | 136 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(133): Show |
171 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.188-50A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304681 | |||||||
chr12:66304700 | C | T | 1 | a0002c0001t0002g0039 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.188-31C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304700 | |||||||
chr12:66304719 | GT | G | 8 | a0001c0024t0001g0180 a0001c0024t0001g0181 a0001c0024t0001g0182 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.188-3delT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66304719 | ||||||
chr12:66305174 | C | G | 201 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(198): Show |
247 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.607+24C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305174 | |||||||
chr12:66305314 | T | C | 1 | a0006c0010t0001g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.607+164T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305314 | |||||||
chr12:66305380 | C | T | 176 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(173): Show |
214 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.607+230C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305380 | |||||||
chr12:66305511 | G | A | 32 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(29): Show |
35 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.607+361G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305511 | |||||||
chr12:66305746 | TA | T | 160 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(157): Show |
203 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.608-584delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 66305746 | ||||||
chr12:66305782 | T | A | 4 | a0004c0008t0001g0091 a0004c0008t0001g0092 a0004c0008t0001g0093 others(1): Show |
4 | HG02280.hp1 HG02717.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-563T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305782 | |||||||
chr12:66305790 | G | A | 1 | a0002c0001t0001g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.608-555G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305790 | |||||||
chr12:66305974 | G | A | 1 | a0006c0007t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.608-371G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305974 | |||||||
chr12:66306087 | A | C | 8 | a0001c0030t0001g0244 a0007c0009t0001g0042 a0007c0009t0001g0243 others(5): Show |
9 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.608-258A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66306087 | |||||||
chr12:66306142 | G | T | 160 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(157): Show |
203 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.608-203G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66306142 | |||||||
chr12:66306324 | T | C | 7 | a0002c0001t0001g0023 a0002c0001t0001g0024 a0002c0001t0001g0025 others(4): Show |
10 | HG01099.hp1 HG02135.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.608-21T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66306324 | |||||||
chr12:66306592 | T | C | 3 | a0004c0004t0001g0022 a0004c0004t0001g0073 a0022c0038t0001g0022 |
3 | HG02280.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.777+78T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66306592 | |||||||
chr12:66306928 | C | T | 1 | a0001c0002t0001g0287 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.777+414C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66306928 | |||||||
chr12:66306942 | C | T | 1 | a0001c0002t0001g0286 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.777+428C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66306942 | |||||||
chr12:66306950 | A | G | 1 | a0003c0003t0001g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.777+436A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66306950 | |||||||
chr12:66307221 | A | G | 134 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(131): Show |
168 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.777+707A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307221 | |||||||
chr12:66307300 | A | G | 1 | a0001c0029t0001g0214 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.777+786A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307300 | |||||||
chr12:66307376 | T | TA | 19 | a0002c0001t0001g0015 a0002c0001t0001g0027 a0002c0001t0001g0053 others(16): Show |
23 | HG01258.hp1 HG02027.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.777+869dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 66307376 | ||||||
chr12:66307767 | T | C | 111 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(108): Show |
144 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.777+1253T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307767 | |||||||
chr12:66307797 | G | T | 168 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(165): Show |
211 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.777+1283G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307797 | |||||||
chr12:66307844 | G | A | 1 | a0002c0001t0001g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.777+1330G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307844 | |||||||
chr12:66307948 | A | C | 201 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(198): Show |
247 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.777+1434A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307948 | |||||||
chr12:66308043 | T | TA | 30 | a0001c0002t0001g0252 a0001c0002t0001g0283 a0001c0002t0001g0284 others(27): Show |
32 | HG00140.hp2 HG01069.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.777+1551dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 66308043 | ||||||
chr12:66308043 | T | TAA | 127 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(124): Show |
169 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.777+1550_777+1551d others(4): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 66308043 | ||||||
chr12:66308043 | T | TAAA | 10 | a0001c0002t0001g0254 a0002c0001t0001g0034 a0002c0001t0001g0087 others(7): Show |
11 | HG01192.hp2 HG01346.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.777+1549_777+1551d others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 66308043 | ||||||
chr12:66308043 | TA | T | 13 | a0001c0024t0001g0180 a0001c0024t0001g0181 a0001c0024t0001g0182 others(10): Show |
14 | HG02486.hp2 HG02615.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.777+1551delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 66308043 | ||||||
chr12:66308070 | A | G | 1 | a0001c0002t0001g0048 | 2 | HG02293.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.777+1556A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308070 | |||||||
chr12:66308102 | T | A | 1 | a0003c0003t0001g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.777+1588T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308102 | |||||||
chr12:66308102 | T | G | 160 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(157): Show |
203 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.777+1588T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308102 | |||||||
chr12:66308183 | C | T | 1 | a0001c0024t0001g0182 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.778-1523C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308183 | |||||||
chr12:66308203 | A | T | 6 | a0006c0007t0001g0041 a0006c0007t0001g0225 a0006c0010t0001g0040 others(3): Show |
7 | HG02559.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-1503A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308203 | |||||||
chr12:66308296 | T | A | 1 | a0001c0002t0001g0256 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.778-1410T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308296 | |||||||
chr12:66308348 | G | A | 1 | a0003c0003t0001g0010 | 3 | HG01358.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.778-1358G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308348 | |||||||
chr12:66308378 | A | T | 201 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(198): Show |
247 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.778-1328A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308378 | |||||||
chr12:66308647 | G | C | 1 | a0021c0049t0001g0257 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.778-1059G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308647 | |||||||
chr12:66309060 | G | T | 1 | a0001c0002t0001g0282 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.778-646G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66309060 | |||||||
chr12:66309204 | C | T | 1 | a0001c0022t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.778-502C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66309204 | |||||||
chr12:66310621 | A | G | 3 | a0010c0020t0001g0228 a0010c0020t0001g0230 a0010c0020t0001g0292 |
3 | HG02145.hp2 HG02895.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1680+13A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310621 | |||||||
chr12:66310727 | T | C | 1 | a0007c0009t0001g0243 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1680+119T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310727 | |||||||
chr12:66310811 | A | G | 205 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(202): Show |
251 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.1680+203A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310811 | |||||||
chr12:66310818 | C | G | 1 | a0001c0018t0001g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1680+210C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310818 | |||||||
chr12:66310828 | G | A | 1 | a0001c0005t0001g0019 | 2 | NA18966.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1680+220G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310828 | |||||||
chr12:66310846 | A | G | 34 | a0001c0029t0001g0178 a0002c0001t0002g0037 a0002c0001t0002g0038 others(31): Show |
37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.1680+238A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310846 | |||||||
chr12:66310916 | C | T | 1 | a0002c0001t0002g0186 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1680+308C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310916 | |||||||
chr12:66310917 | G | A | 124 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(121): Show |
156 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.1680+309G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310917 | |||||||
chr12:66311036 | G | A | 157 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(154): Show |
193 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.1680+428G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311036 | |||||||
chr12:66311086 | G | C | 2 | a0001c0002t0001g0251 a0001c0002t0001g0252 |
2 | HG01069.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1680+478G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311086 | |||||||
chr12:66311088 | T | A | 7 | a0001c0029t0001g0214 a0004c0008t0001g0091 a0004c0008t0001g0092 others(4): Show |
7 | HG01361.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1680+480T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311088 | |||||||
chr12:66311149 | G | A | 3 | a0001c0024t0001g0180 a0001c0024t0001g0181 a0001c0024t0001g0182 |
3 | HG02615.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1680+541G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311149 | |||||||
chr12:66311157 | G | GA | 140 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(137): Show |
175 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.1680+563dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 66311157 | ||||||
chr12:66311202 | T | G | 6 | a0004c0008t0001g0091 a0004c0008t0001g0092 a0004c0008t0001g0093 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1680+594T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311202 | |||||||
chr12:66311332 | T | C | 5 | a0006c0007t0001g0229 a0006c0007t0001g0293 a0010c0020t0001g0228 others(2): Show |
5 | HG02145.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1680+724T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311332 | |||||||
chr12:66311817 | G | C | 7 | a0001c0029t0001g0214 a0004c0008t0001g0091 a0004c0008t0001g0092 others(4): Show |
7 | HG01361.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1680+1209G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311817 | |||||||
chr12:66311860 | A | C | 2 | a0001c0002t0001g0276 a0001c0002t0001g0277 |
2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1680+1252A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311860 | |||||||
chr12:66312028 | G | T | 34 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(31): Show |
43 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1680+1420G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312028 | |||||||
chr12:66312144 | A | G | 1 | a0001c0005t0001g0063 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1680+1536A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312144 | |||||||
chr12:66312173 | AG | A | 15 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(12): Show |
18 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.1680+1566delG | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312173 | |||||||
chr12:66312203 | A | G | 1 | a0002c0001t0001g0032 | 2 | HG01243.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1680+1595A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312203 | |||||||
chr12:66312246 | G | A | 199 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(196): Show |
244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.1680+1638G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312246 | |||||||
chr12:66312306 | G | T | 145 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(142): Show |
180 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(177): Show |
intron_variant | MODIFIER | c.1681-1680G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312306 | |||||||
chr12:66312779 | T | G | 309 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(306): Show |
387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1681-1207T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312779 | |||||||
chr12:66312968 | T | G | 198 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(195): Show |
243 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.1681-1018T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312968 | |||||||
chr12:66312990 | T | C | 8 | a0001c0029t0001g0214 a0004c0008t0001g0091 a0004c0008t0001g0092 others(5): Show |
8 | HG01361.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1681-996T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312990 | |||||||
chr12:66313114 | C | A | 2 | a0003c0003t0001g0112 a0004c0004t0001g0111 |
2 | NA19004.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1681-872C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313114 | |||||||
chr12:66313200 | T | TAGAAAAA others(3): Show |
116 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(113): Show |
148 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.1681-779_1681-778i others(12): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 66313200 | ||||||
chr12:66313380 | C | T | 3 | a0001c0012t0001g0017 a0001c0012t0001g0056 a0001c0012t0001g0172 |
4 | HG00621.hp2 HG02132.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.1681-606C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313380 | |||||||
chr12:66313543 | C | T | 7 | a0002c0001t0001g0023 a0002c0001t0001g0024 a0002c0001t0001g0025 others(4): Show |
10 | HG01099.hp1 HG02135.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1681-443C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313543 | |||||||
chr12:66313619 | G | A | 2 | a0003c0003t0001g0028 a0003c0003t0001g0082 |
3 | HG01167.hp1 HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1681-367G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313619 | |||||||
chr12:66313864 | G | T | 47 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(44): Show |
56 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1681-122G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313864 | |||||||
chr12:66313949 | A | T | 2 | a0002c0001t0002g0184 a0002c0001t0002g0201 |
2 | NA19004.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1681-37A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313949 | |||||||
chr12:66313973 | A | G | 5 | a0006c0007t0001g0229 a0006c0007t0001g0293 a0010c0020t0001g0228 others(2): Show |
5 | HG02145.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1681-13A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313973 | |||||||
chr12:66314213 | GTTAGTTG others(14): Show |
G | 29 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(26): Show |
32 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.1858+71_1858+91del others(21): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 66314213 | ||||||
chr12:66314284 | C | T | 7 | a0001c0046t0001g0288 a0007c0009t0001g0042 a0007c0009t0001g0243 others(4): Show |
8 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1858+121C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | chr12 | 66314284 | |||||||
chr12:66314358 | T | A | 199 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(196): Show |
244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.1858+195T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | chr12 | 66314358 | |||||||
chr12:66314727 | G | C | 48 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(45): Show |
57 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.1859-515G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | chr12 | 66314727 | |||||||
chr12:66314976 | A | G | 1 | a0003c0003t0001g0146 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1859-266A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | chr12 | 66314976 | |||||||
chr12:66315004 | C | T | 289 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(286): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.1859-238C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | chr12 | 66315004 | |||||||
chr12:66315573 | T | C | 199 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(196): Show |
244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.2000+190T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315573 | |||||||
chr12:66315654 | T | A | 6 | a0007c0009t0001g0042 a0007c0009t0001g0243 a0007c0009t0001g0245 others(3): Show |
7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2000+271T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315654 | |||||||
chr12:66315708 | C | T | 40 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(37): Show |
49 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2000+325C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315708 | |||||||
chr12:66315751 | G | T | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2000+368G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315751 | |||||||
chr12:66315792 | C | T | 65 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(62): Show |
88 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.2000+409C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315792 | |||||||
chr12:66315904 | C | T | 7 | a0001c0046t0001g0288 a0007c0009t0001g0042 a0007c0009t0001g0243 others(4): Show |
8 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2000+521C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315904 | |||||||
chr12:66315968 | T | C | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2000+585T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315968 | |||||||
chr12:66315987 | G | A | 1 | a0001c0002t0001g0260 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2000+604G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315987 | |||||||
chr12:66316183 | C | T | 8 | a0001c0029t0001g0214 a0004c0008t0001g0091 a0004c0008t0001g0092 others(5): Show |
8 | HG01361.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2000+800C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316183 | |||||||
chr12:66316258 | G | A | 1 | a0009c0014t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2000+875G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316258 | |||||||
chr12:66316330 | A | G | 1 | a0006c0007t0001g0293 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2000+947A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316330 | |||||||
chr12:66316344 | T | A | 1 | a0006c0007t0001g0293 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2000+961T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316344 | |||||||
chr12:66316421 | G | A | 5 | a0006c0007t0001g0229 a0006c0007t0001g0293 a0010c0020t0001g0228 others(2): Show |
5 | HG02145.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2000+1038G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316421 | |||||||
chr12:66316567 | A | AAAT | 8 | a0001c0005t0001g0020 a0002c0001t0001g0025 a0003c0003t0001g0085 others(5): Show |
10 | HG00544.hp2 HG02015.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2000+1217_2000+121 others(7): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | ||||||
chr12:66316567 | A | AAATAAT | 72 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(69): Show |
83 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.2000+1214_2000+121 others(10): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | ||||||
chr12:66316567 | A | AAATAATA others(2): Show |
20 | a0001c0029t0001g0178 a0001c0029t0001g0214 a0004c0034t0001g0149 others(17): Show |
22 | HG01361.hp1 HG01884.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2000+1211_2000+121 others(13): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | ||||||
chr12:66316567 | A | AAATAATA others(5): Show |
12 | a0001c0022t0001g0070 a0001c0022t0001g0174 a0001c0030t0001g0244 others(9): Show |
12 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2000+1208_2000+121 others(16): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | ||||||
chr12:66316567 | A | AAATAATA others(8): Show |
3 | a0001c0022t0001g0071 a0001c0046t0001g0288 a0011c0013t0001g0238 |
3 | HG02559.hp1 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2000+1205_2000+121 others(19): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | ||||||
chr12:66316567 | A | AAATAATA others(11): Show |
1 | a0011c0013t0001g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2000+1202_2000+121 others(22): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | ||||||
chr12:66316567 | AAAT | A | 60 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(57): Show |
83 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.2000+1217_2000+121 others(7): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | ||||||
chr12:66316567 | AAATAAT | A | 32 | a0001c0002t0001g0231 a0001c0002t0001g0232 a0001c0002t0001g0233 others(29): Show |
41 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2000+1214_2000+121 others(10): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | ||||||
chr12:66316567 | AAATAATA others(5): Show |
A | 5 | a0001c0002t0001g0289 a0001c0002t0001g0294 a0001c0002t0001g0295 others(2): Show |
5 | HG00741.hp1 HG01109.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.2000+1208_2000+121 others(16): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | ||||||
chr12:66316619 | C | T | 1 | a0025c0031t0001g0142 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2000+1236C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316619 | |||||||
chr12:66316741 | C | T | 6 | a0006c0007t0001g0041 a0006c0007t0001g0225 a0006c0010t0001g0040 others(3): Show |
7 | HG02559.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2000+1358C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316741 | |||||||
chr12:66316748 | G | A | 7 | a0001c0046t0001g0288 a0007c0009t0001g0042 a0007c0009t0001g0243 others(4): Show |
8 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2000+1365G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316748 | |||||||
chr12:66316757 | T | G | 2 | a0001c0029t0001g0178 a0005c0015t0001g0177 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2000+1374T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316757 | |||||||
chr12:66316816 | G | A | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2000+1433G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316816 | |||||||
chr12:66316887 | C | T | 1 | a0001c0002t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2000+1504C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316887 | |||||||
chr12:66316892 | G | A | 48 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(45): Show |
57 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2000+1509G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316892 | |||||||
chr12:66316897 | T | C | 29 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(26): Show |
32 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.2000+1514T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316897 | |||||||
chr12:66316950 | C | T | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2000+1567C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316950 | |||||||
chr12:66316967 | C | T | 2 | a0002c0001t0001g0024 a0002c0001t0001g0081 |
3 | NA18939.hp1 NA19063.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2000+1584C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316967 | |||||||
chr12:66317018 | C | CA | 10 | a0003c0003t0001g0030 a0003c0003t0001g0110 a0003c0003t0001g0122 others(7): Show |
12 | HG00558.hp2 HG01175.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.2001-1599dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66317018 | ||||||
chr12:66317018 | CA | C | 141 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(138): Show |
173 | HG00140.hp1 HG00558.hp1 HG00639.hp1 others(170): Show |
intron_variant | MODIFIER | c.2001-1599delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66317018 | ||||||
chr12:66317018 | CAA | C | 52 | a0001c0002t0001g0046 a0001c0002t0001g0277 a0001c0002t0001g0278 others(49): Show |
64 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.2001-1600_2001-159 others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66317018 | ||||||
chr12:66317101 | A | G | 199 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(196): Show |
244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.2001-1537A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317101 | |||||||
chr12:66317111 | C | T | 28 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(25): Show |
31 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2001-1527C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317111 | |||||||
chr12:66317185 | C | T | 2 | a0005c0015t0001g0050 a0005c0015t0001g0299 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2001-1453C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317185 | |||||||
chr12:66317196 | C | CA | 29 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0034 others(26): Show |
38 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2001-1430dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66317196 | ||||||
chr12:66317196 | CA | C | 10 | a0003c0003t0001g0147 a0004c0004t0001g0176 a0006c0007t0001g0041 others(7): Show |
11 | HG01884.hp1 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2001-1430delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66317196 | ||||||
chr12:66317311 | A | G | 2 | a0001c0022t0001g0070 a0001c0022t0001g0071 |
2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2001-1327A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317311 | |||||||
chr12:66317455 | A | T | 199 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(196): Show |
244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.2001-1183A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317455 | |||||||
chr12:66317562 | C | T | 1 | a0005c0033t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2001-1076C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317562 | |||||||
chr12:66317677 | G | A | 206 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(203): Show |
252 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.2001-961G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317677 | |||||||
chr12:66317720 | C | T | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2001-918C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317720 | |||||||
chr12:66317721 | G | T | 2 | a0002c0001t0002g0199 a0002c0001t0002g0200 |
2 | HG03688.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2001-917G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317721 | |||||||
chr12:66317814 | C | A | 1 | a0008c0011t0001g0123 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2001-824C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317814 | |||||||
chr12:66317933 | G | A | 1 | a0002c0001t0001g0168 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2001-705G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317933 | |||||||
chr12:66318096 | C | T | 22 | a0001c0024t0001g0180 a0001c0024t0001g0181 a0001c0024t0001g0182 others(19): Show |
22 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2001-542C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66318096 | |||||||
chr12:66318097 | A | G | 3 | a0002c0001t0001g0029 a0002c0001t0001g0054 a0002c0001t0001g0121 |
4 | HG01074.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001-541A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66318097 | |||||||
chr12:66318115 | A | G | 48 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(45): Show |
57 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2001-523A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66318115 | |||||||
chr12:66318564 | A | T | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2001-74A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66318564 | |||||||
chr12:66318872 | C | T | 48 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(45): Show |
57 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2155+80C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66318872 | |||||||
chr12:66318940 | G | T | 90 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(87): Show |
121 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.2155+148G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66318940 | |||||||
chr12:66319101 | C | A | 1 | a0007c0009t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2155+309C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319101 | |||||||
chr12:66319110 | T | C | 6 | a0007c0009t0001g0042 a0007c0009t0001g0243 a0007c0009t0001g0245 others(3): Show |
7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2155+318T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319110 | |||||||
chr12:66319167 | A | T | 1 | a0006c0007t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2155+375A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319167 | |||||||
chr12:66319280 | C | A | 199 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(196): Show |
244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.2155+488C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319280 | |||||||
chr12:66319280 | C | T | 1 | a0002c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2155+488C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319280 | |||||||
chr12:66319605 | G | A | 1 | a0009c0014t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2155+813G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319605 | |||||||
chr12:66319880 | G | GT | 125 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(122): Show |
158 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.2155+1088_2155+108 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319880 | |||||||
chr12:66319880 | G | GTT | 28 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(25): Show |
31 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2155+1088_2155+108 others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319880 | |||||||
chr12:66319881 | G | T | 195 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
240 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.2155+1089G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319881 | |||||||
chr12:66320080 | C | T | 6 | a0007c0009t0001g0042 a0007c0009t0001g0243 a0007c0009t0001g0245 others(3): Show |
7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2155+1288C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320080 | |||||||
chr12:66320113 | A | G | 1 | a0001c0002t0001g0275 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2155+1321A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320113 | |||||||
chr12:66320122 | C | G | 2 | a0014c0016t0001g0139 a0014c0016t0001g0140 |
2 | NA18999.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2155+1330C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320122 | |||||||
chr12:66320198 | T | C | 32 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(29): Show |
41 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2155+1406T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320198 | |||||||
chr12:66320430 | A | C | 115 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(112): Show |
147 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.2156-1518A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320430 | |||||||
chr12:66320513 | A | G | 6 | a0007c0009t0001g0042 a0007c0009t0001g0243 a0007c0009t0001g0245 others(3): Show |
7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2156-1435A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320513 | |||||||
chr12:66320728 | G | GA | 195 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
240 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.2156-1220_2156-121 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320728 | |||||||
chr12:66320812 | G | A | 2 | a0003c0003t0001g0124 a0003c0003t0001g0125 |
2 | NA19060.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2156-1136G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320812 | |||||||
chr12:66320854 | G | GA | 6 | a0007c0009t0001g0042 a0007c0009t0001g0243 a0007c0009t0001g0245 others(3): Show |
7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2156-1089dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 66320854 | ||||||
chr12:66320916 | A | G | 29 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(26): Show |
32 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.2156-1032A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320916 | |||||||
chr12:66320975 | G | A | 29 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(26): Show |
32 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.2156-973G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320975 | |||||||
chr12:66320997 | T | C | 195 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
240 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.2156-951T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320997 | |||||||
chr12:66321000 | C | T | 7 | a0001c0030t0001g0244 a0005c0033t0001g0236 a0011c0013t0001g0234 others(4): Show |
7 | HG02055.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2156-948C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321000 | |||||||
chr12:66321001 | G | A | 1 | a0002c0001t0001g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2156-947G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321001 | |||||||
chr12:66321050 | C | T | 1 | a0002c0001t0001g0103 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2156-898C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321050 | |||||||
chr12:66321102 | T | A | 2 | a0001c0029t0001g0178 a0005c0015t0001g0177 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2156-846T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321102 | |||||||
chr12:66321103 | G | T | 2 | a0001c0029t0001g0178 a0005c0015t0001g0177 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2156-845G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321103 | |||||||
chr12:66321174 | A | G | 3 | a0001c0002t0001g0231 a0001c0002t0001g0232 a0001c0002t0001g0233 |
3 | HG02965.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2156-774A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321174 | |||||||
chr12:66321240 | C | T | 1 | a0002c0001t0001g0170 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2156-708C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321240 | |||||||
chr12:66321419 | T | C | 6 | a0007c0009t0001g0042 a0007c0009t0001g0243 a0007c0009t0001g0245 others(3): Show |
7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2156-529T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321419 | |||||||
chr12:66321539 | A | G | 1 | a0002c0001t0001g0156 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2156-409A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321539 | |||||||
chr12:66321631 | T | C | 3 | a0004c0008t0001g0091 a0004c0008t0001g0092 a0004c0008t0001g0151 |
3 | HG02280.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2156-317T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321631 | |||||||
chr12:66321633 | G | A | 2 | a0002c0001t0001g0029 a0002c0001t0001g0121 |
3 | HG02257.hp2 HG02258.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2156-315G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321633 | |||||||
chr12:66321708 | T | A | 150 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(147): Show |
186 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.2156-240T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321708 | |||||||
chr12:66321793 | G | A | 1 | a0001c0002t0001g0263 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2156-155G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321793 | |||||||
chr12:66322038 | T | C | 4 | a0006c0007t0001g0293 a0010c0020t0001g0228 a0010c0020t0001g0230 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2237+9T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | chr12 | 66322038 | |||||||
chr12:66322089 | A | G | 29 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(26): Show |
32 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.2237+60A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | chr12 | 66322089 | |||||||
chr12:66322222 | T | A | 3 | a0001c0018t0001g0043 a0001c0018t0001g0259 a0001c0018t0001g0281 |
4 | HG02109.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2237+193T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | chr12 | 66322222 | |||||||
chr12:66322271 | A | G | 115 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(112): Show |
147 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.2237+242A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | chr12 | 66322271 | |||||||
chr12:66322285 | G | T | 5 | a0002c0017t0001g0138 a0014c0016t0001g0136 a0014c0016t0001g0137 others(2): Show |
5 | NA18954.hp2 NA18999.hp2 NA19085.hp1 others(2): Show |
intron_variant | MODIFIER | c.2237+256G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | chr12 | 66322285 | |||||||
chr12:66322565 | CA | C | 85 | a0001c0046t0001g0288 a0002c0001t0001g0015 a0002c0001t0001g0027 others(82): Show |
114 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.2238-142delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 66322565 | ||||||
chr12:66322565 | CAAA | C | 93 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(90): Show |
125 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.2238-144_2238-142d others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 66322565 | ||||||
chr12:66322565 | CAAAA | C | 101 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(98): Show |
114 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(111): Show |
intron_variant | MODIFIER | c.2238-145_2238-142d others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 66322565 | ||||||
chr12:66323039 | A | G | 6 | a0006c0007t0001g0041 a0006c0007t0001g0225 a0006c0010t0001g0040 others(3): Show |
7 | HG02559.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2297+256A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323039 | |||||||
chr12:66323064 | G | A | 150 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(147): Show |
186 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.2297+281G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323064 | |||||||
chr12:66323246 | A | T | 1 | a0002c0001t0001g0053 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2297+463A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323246 | |||||||
chr12:66323333 | C | G | 1 | a0004c0004t0001g0102 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2297+550C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323333 | |||||||
chr12:66323422 | C | T | 45 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(42): Show |
54 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2298-561C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323422 | |||||||
chr12:66323423 | G | A | 7 | a0006c0007t0001g0041 a0006c0007t0001g0225 a0006c0007t0001g0226 others(4): Show |
8 | HG01884.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2298-560G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323423 | |||||||
chr12:66323680 | G | A | 1 | a0001c0002t0001g0264 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2298-303G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323680 | |||||||
chr12:66323912 | T | G | 195 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
240 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.2298-71T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323912 | |||||||
chr12:66323916 | T | C | 1 | a0003c0003t0001g0124 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2298-67T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323916 | |||||||
chr12:66323936 | C | T | 195 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
240 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.2298-47C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323936 | |||||||
chr12:66324218 | GA | G | 45 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(42): Show |
54 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2526+11delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 66324218 | ||||||
chr12:66324230 | T | G | 1 | a0009c0014t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2526+19T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324230 | |||||||
chr12:66324427 | G | T | 45 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(42): Show |
54 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2526+216G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324427 | |||||||
chr12:66324499 | G | A | 1 | a0006c0007t0001g0229 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2526+288G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324499 | |||||||
chr12:66324590 | T | C | 1 | a0001c0030t0001g0244 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2526+379T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324590 | |||||||
chr12:66324885 | A | G | 2 | a0001c0002t0001g0276 a0001c0002t0001g0277 |
2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2527-98A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324885 | |||||||
chr12:66324953 | A | G | 1 | a0006c0007t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2527-30A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324953 | |||||||
chr12:66325177 | C | T | 4 | a0001c0022t0001g0174 a0004c0008t0001g0160 a0004c0008t0001g0161 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+51C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325177 | |||||||
chr12:66325193 | C | G | 36 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(33): Show |
45 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.2670+67C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325193 | |||||||
chr12:66325272 | C | T | 105 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(102): Show |
136 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2670+146C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325272 | |||||||
chr12:66325297 | C | G | 1 | a0002c0001t0001g0155 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2670+171C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325297 | |||||||
chr12:66325370 | C | T | 1 | a0002c0001t0001g0165 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2670+244C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325370 | |||||||
chr12:66325445 | A | G | 1 | a0002c0001t0002g0198 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2670+319A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325445 | |||||||
chr12:66325496 | G | A | 1 | a0002c0037t0001g0158 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2670+370G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325496 | |||||||
chr12:66325545 | G | C | 7 | a0006c0007t0001g0041 a0006c0007t0001g0225 a0006c0007t0001g0226 others(4): Show |
8 | HG01884.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2670+419G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325545 | |||||||
chr12:66325572 | T | C | 1 | a0001c0024t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2670+446T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325572 | |||||||
chr12:66325598 | G | A | 1 | a0005c0015t0001g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2670+472G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325598 | |||||||
chr12:66325873 | C | A | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2670+747C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325873 | |||||||
chr12:66326015 | T | C | 78 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(75): Show |
105 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.2670+889T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66326015 | |||||||
chr12:66326195 | A | C | 1 | a0001c0002t0001g0271 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2670+1069A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66326195 | |||||||
chr12:66326537 | G | A | 4 | a0014c0016t0001g0136 a0014c0016t0001g0137 a0014c0016t0001g0139 others(1): Show |
4 | NA18999.hp2 NA19085.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+1411G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66326537 | |||||||
chr12:66326724 | AT | A | 167 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(164): Show |
213 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.2670+1610delT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66326724 | ||||||
chr12:66326797 | C | T | 2 | a0002c0001t0001g0053 a0009c0014t0001g0064 |
2 | HG02109.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2670+1671C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66326797 | |||||||
chr12:66327028 | T | C | 4 | a0005c0015t0001g0050 a0005c0015t0001g0177 a0005c0015t0001g0179 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+1902T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327028 | |||||||
chr12:66327035 | C | CA | 5 | a0001c0002t0001g0044 a0004c0004t0001g0080 a0004c0004t0001g0127 others(2): Show |
6 | HG00621.hp1 HG00642.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.2670+1941dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327035 | ||||||
chr12:66327035 | CA | C | 119 | a0001c0002t0001g0008 a0001c0002t0001g0045 a0001c0002t0001g0049 others(116): Show |
166 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.2670+1941delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327035 | ||||||
chr12:66327035 | CAA | C | 23 | a0001c0002t0001g0270 a0001c0005t0001g0061 a0001c0005t0001g0173 others(20): Show |
24 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327035 | ||||||
chr12:66327054 | A | ATATATAT others(16): Show |
1 | a0004c0035t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2670+1928_2670+192 others(27): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327054 | |||||||
chr12:66327054 | A | T | 1 | a0006c0007t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2670+1928A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327054 | |||||||
chr12:66327056 | A | T | 2 | a0004c0035t0001g0183 a0006c0007t0001g0226 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2670+1930A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327056 | |||||||
chr12:66327058 | A | T | 16 | a0002c0001t0001g0027 a0002c0001t0001g0053 a0002c0001t0001g0099 others(13): Show |
17 | HG01168.hp2 HG01258.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2670+1932A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327058 | |||||||
chr12:66327060 | A | AATATATA others(5): Show |
2 | a0006c0007t0001g0213 a0006c0007t0001g0229 |
2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2670+1935_2670+193 others(16): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327060 | ||||||
chr12:66327060 | A | AATATATA others(7): Show |
1 | a0005c0033t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2670+1935_2670+193 others(18): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327060 | ||||||
chr12:66327060 | A | AT | 3 | a0003c0003t0001g0082 a0009c0014t0001g0062 a0009c0014t0001g0066 |
3 | HG01167.hp1 HG01243.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2670+1934_2670+193 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327060 | |||||||
chr12:66327060 | A | T | 50 | a0001c0002t0001g0232 a0001c0005t0001g0020 a0001c0005t0001g0021 others(47): Show |
60 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.2670+1934A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327060 | |||||||
chr12:66327062 | A | AATATATA others(3): Show |
1 | a0001c0022t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2670+1937_2670+193 others(14): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327062 | ||||||
chr12:66327062 | A | AT | 3 | a0001c0002t0001g0231 a0001c0002t0001g0289 a0006c0010t0001g0250 |
3 | HG01261.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2670+1936_2670+193 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327062 | |||||||
chr12:66327062 | A | T | 167 | a0001c0002t0001g0232 a0001c0005t0001g0003 a0001c0005t0001g0018 others(164): Show |
210 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.2670+1936A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327062 | |||||||
chr12:66327064 | A | AATATATA others(17): Show |
1 | a0010c0027t0001g0223 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2670+1939_2670+194 others(28): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327064 | ||||||
chr12:66327064 | A | AATATATA others(21): Show |
2 | a0002c0001t0002g0186 a0002c0001t0002g0200 |
2 | HG03704.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.2670+1939_2670+194 others(32): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327064 | ||||||
chr12:66327064 | A | AATATATA others(23): Show |
3 | a0002c0001t0002g0038 a0002c0001t0002g0208 a0005c0006t0002g0268 |
4 | HG01496.hp2 NA18971.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+1939_2670+194 others(34): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327064 | ||||||
chr12:66327064 | A | AATATATA others(27): Show |
1 | a0005c0006t0002g0262 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2670+1939_2670+194 others(38): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327064 | ||||||
chr12:66327064 | A | AATATATA others(45): Show |
1 | a0023c0041t0002g0188 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2670+1939_2670+194 others(56): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327064 | ||||||
chr12:66327064 | A | AT | 4 | a0001c0002t0001g0233 a0001c0002t0001g0269 a0001c0002t0001g0295 others(1): Show |
4 | HG01346.hp1 NA18906.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.2670+1938_2670+193 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327064 | |||||||
chr12:66327064 | A | ATATATAT others(22): Show |
1 | a0002c0001t0002g0211 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2670+1938_2670+193 others(33): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327064 | |||||||
chr12:66327064 | A | ATATATAT others(28): Show |
1 | a0002c0001t0002g0210 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2670+1938_2670+193 others(39): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327064 | |||||||
chr12:66327064 | A | T | 188 | a0001c0002t0001g0014 a0001c0002t0001g0231 a0001c0002t0001g0232 others(185): Show |
238 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.2670+1938A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327064 | |||||||
chr12:66327066 | A | AAAAAAAA others(19): Show |
1 | a0005c0015t0001g0299 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(30): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AAAAAATA others(31): Show |
1 | a0002c0001t0002g0192 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(42): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AAAAATAT others(26): Show |
1 | a0024c0040t0002g0193 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(37): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AAAATATA others(21): Show |
1 | a0005c0015t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(32): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AAAATATA others(25): Show |
2 | a0002c0001t0002g0198 a0002c0001t0002g0201 |
2 | NA19004.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2670+1941_2670+194 others(36): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AAAATATA others(27): Show |
1 | a0002c0001t0002g0184 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(38): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AAAATATA others(29): Show |
1 | a0005c0006t0002g0240 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(40): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AAATATAT others(30): Show |
1 | a0002c0001t0002g0194 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(41): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AATATATA others(11): Show |
1 | a0005c0015t0001g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2670+1956_2670+195 others(22): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AATATATA others(19): Show |
2 | a0002c0001t0002g0206 a0016c0021t0001g0221 |
2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2670+1956_2670+195 others(30): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AATATATA others(23): Show |
3 | a0002c0001t0002g0202 a0002c0001t0002g0204 a0002c0001t0002g0205 |
3 | NA18942.hp1 NA18953.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2670+1956_2670+195 others(34): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AATATATA others(25): Show |
1 | a0002c0001t0002g0052 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2670+1956_2670+195 others(36): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AATATATA others(29): Show |
1 | a0026c0042t0002g0195 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2670+1956_2670+195 others(40): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | ||||||
chr12:66327066 | A | AT | 3 | a0001c0002t0001g0013 a0001c0050t0001g0013 a0004c0004t0001g0105 |
4 | HG03942.hp2 HG04204.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | |||||||
chr12:66327066 | A | ATATATAT others(10): Show |
1 | a0005c0015t0001g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2670+1940_2670+194 others(21): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | |||||||
chr12:66327066 | A | ATATATAT others(18): Show |
1 | a0010c0027t0001g0220 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2670+1940_2670+194 others(29): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | |||||||
chr12:66327066 | A | ATATATAT others(20): Show |
2 | a0002c0001t0002g0037 a0002c0001t0002g0185 |
3 | HG01361.hp2 HG02273.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(31): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | |||||||
chr12:66327066 | A | ATATATAT others(22): Show |
3 | a0002c0001t0002g0039 a0002c0001t0002g0207 a0016c0021t0001g0222 |
4 | HG01255.hp2 HG01358.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(33): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | |||||||
chr12:66327066 | A | ATATATAT others(24): Show |
2 | a0004c0004t0001g0190 a0016c0021t0001g0224 |
2 | HG02809.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(35): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | |||||||
chr12:66327066 | A | ATATATAT others(26): Show |
1 | a0002c0001t0002g0199 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2670+1940_2670+194 others(37): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | |||||||
chr12:66327066 | A | ATATATAT others(28): Show |
5 | a0002c0001t0002g0101 a0002c0001t0002g0191 a0002c0001t0002g0196 others(2): Show |
5 | HG02071.hp1 NA18950.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(39): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | |||||||
chr12:66327066 | A | T | 234 | a0001c0002t0001g0005 a0001c0002t0001g0014 a0001c0002t0001g0045 others(231): Show |
291 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(288): Show |
intron_variant | MODIFIER | c.2670+1940A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | |||||||
chr12:66327321 | C | G | 167 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(164): Show |
213 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.2670+2195C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327321 | |||||||
chr12:66327342 | T | C | 1 | a0006c0007t0001g0216 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2670+2216T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327342 | |||||||
chr12:66327566 | G | GT | 25 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0032 others(22): Show |
34 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.2670+2440_2670+244 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327566 | |||||||
chr12:66327567 | G | C | 25 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0032 others(22): Show |
34 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.2670+2441G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327567 | |||||||
chr12:66327567 | G | GTTC | 142 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(139): Show |
179 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.2670+2443_2670+244 others(7): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327567 | ||||||
chr12:66327761 | A | G | 167 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(164): Show |
213 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.2670+2635A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327761 | |||||||
chr12:66327793 | T | TA | 34 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(31): Show |
37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.2670+2675dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327793 | ||||||
chr12:66327949 | G | A | 2 | a0004c0008t0001g0160 a0004c0008t0001g0161 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2670+2823G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327949 | |||||||
chr12:66328011 | G | A | 1 | a0006c0007t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2670+2885G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328011 | |||||||
chr12:66328011 | G | C | 2 | a0002c0001t0002g0196 a0024c0040t0002g0193 |
2 | NA18950.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2670+2885G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328011 | |||||||
chr12:66328056 | A | G | 4 | a0001c0002t0001g0012 a0001c0002t0001g0253 a0001c0002t0001g0282 others(1): Show |
5 | NA18984.hp1 NA19011.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.2670+2930A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328056 | |||||||
chr12:66328079 | G | A | 1 | a0006c0010t0001g0227 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2670+2953G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328079 | |||||||
chr12:66328172 | G | C | 1 | a0006c0007t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2671-2982G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328172 | |||||||
chr12:66328337 | A | G | 164 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(161): Show |
210 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.2671-2817A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328337 | |||||||
chr12:66328455 | C | T | 1 | a0004c0004t0001g0176 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2671-2699C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328455 | |||||||
chr12:66328498 | G | T | 2 | a0010c0027t0001g0220 a0010c0027t0001g0223 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2671-2656G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328498 | |||||||
chr12:66328578 | C | G | 1 | a0004c0008t0001g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2671-2576C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328578 | |||||||
chr12:66328665 | A | C | 1 | a0001c0022t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2671-2489A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328665 | |||||||
chr12:66328803 | AATG | A | 33 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(30): Show |
36 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.2671-2345_2671-234 others(7): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66328803 | ||||||
chr12:66328811 | T | G | 1 | a0005c0006t0001g0273 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2671-2343T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328811 | |||||||
chr12:66328886 | G | T | 1 | a0004c0008t0001g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2671-2268G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328886 | |||||||
chr12:66329160 | A | G | 2 | a0002c0001t0001g0099 a0002c0001t0001g0165 |
2 | NA18957.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2671-1994A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329160 | |||||||
chr12:66329336 | G | A | 1 | a0012c0025t0001g0291 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2671-1818G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329336 | |||||||
chr12:66329513 | A | G | 3 | a0002c0001t0001g0029 a0002c0001t0001g0054 a0002c0001t0001g0121 |
4 | HG01074.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2671-1641A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329513 | |||||||
chr12:66329538 | G | A | 2 | a0010c0027t0001g0220 a0010c0027t0001g0223 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2671-1616G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329538 | |||||||
chr12:66329736 | G | A | 34 | a0001c0005t0001g0003 a0001c0005t0001g0018 a0001c0005t0001g0019 others(31): Show |
43 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.2671-1418G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329736 | |||||||
chr12:66329768 | A | G | 1 | a0002c0001t0002g0210 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2671-1386A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329768 | |||||||
chr12:66330166 | A | G | 1 | a0003c0003t0001g0146 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2671-988A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66330166 | |||||||
chr12:66330691 | G | A | 4 | a0005c0015t0001g0050 a0005c0015t0001g0177 a0005c0015t0001g0179 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2671-463G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66330691 | |||||||
chr12:66330760 | C | A | 1 | a0002c0001t0001g0153 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2671-394C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66330760 | |||||||
chr12:66331790 | C | A | 1 | a0004c0035t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3162+145C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66331790 | |||||||
chr12:66332116 | A | G | 1 | a0003c0003t0001g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3162+471A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66332116 | |||||||
chr12:66332132 | C | A | 159 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0015 others(156): Show |
200 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.3162+487C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66332132 | |||||||
chr12:66332421 | G | C | 1 | a0003c0003t0001g0148 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3162+776G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66332421 | |||||||
chr12:66332575 | G | A | 115 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0015 others(112): Show |
153 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.3162+930G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66332575 | |||||||
chr12:66332659 | C | T | 180 | a0001c0022t0001g0174 a0001c0024t0001g0180 a0001c0024t0001g0181 others(177): Show |
222 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(219): Show |
intron_variant | MODIFIER | c.3162+1014C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66332659 | |||||||
chr12:66333239 | T | C | 1 | a0001c0018t0001g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3162+1594T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333239 | |||||||
chr12:66333571 | C | T | 1 | a0003c0003t0001g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3162+1926C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333571 | |||||||
chr12:66333599 | G | C | 1 | a0005c0015t0001g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3162+1954G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333599 | |||||||
chr12:66333615 | T | C | 4 | a0005c0015t0001g0050 a0005c0015t0001g0177 a0005c0015t0001g0179 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3162+1970T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333615 | |||||||
chr12:66333628 | A | G | 159 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0015 others(156): Show |
200 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.3162+1983A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333628 | |||||||
chr12:66333788 | A | G | 159 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0015 others(156): Show |
200 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.3162+2143A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333788 | |||||||
chr12:66333823 | T | C | 1 | a0002c0001t0001g0153 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3162+2178T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333823 | |||||||
chr12:66333862 | T | C | 1 | a0001c0022t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3162+2217T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333862 | |||||||
chr12:66333864 | C | T | 1 | a0003c0003t0001g0011 | 3 | HG01123.hp2 HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.3162+2219C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333864 | |||||||
chr12:66333965 | G | T | 4 | a0005c0015t0001g0050 a0005c0015t0001g0177 a0005c0015t0001g0179 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3162+2320G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333965 | |||||||
chr12:66334029 | A | G | 1 | a0006c0007t0001g0225 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3162+2384A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334029 | |||||||
chr12:66334051 | G | T | 309 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(306): Show |
387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.3162+2406G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334051 | |||||||
chr12:66334052 | C | T | 1 | a0004c0035t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3162+2407C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334052 | |||||||
chr12:66334053 | G | T | 155 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0015 others(152): Show |
196 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(193): Show |
intron_variant | MODIFIER | c.3162+2408G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334053 | |||||||
chr12:66334092 | C | T | 1 | a0003c0003t0001g0112 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3162+2447C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334092 | |||||||
chr12:66334170 | C | A | 6 | a0007c0009t0001g0042 a0007c0009t0001g0243 a0007c0009t0001g0245 others(3): Show |
7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3162+2525C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334170 | |||||||
chr12:66334275 | A | G | 1 | a0012c0048t0001g0255 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3162+2630A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334275 | |||||||
chr12:66334422 | G | A | 34 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(31): Show |
37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.3162+2777G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334422 | |||||||
chr12:66334454 | C | G | 159 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0015 others(156): Show |
200 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.3162+2809C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334454 | |||||||
chr12:66334471 | GA | G | 125 | a0001c0022t0001g0174 a0001c0024t0001g0180 a0001c0024t0001g0181 others(122): Show |
160 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.3162+2843delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66334471 | ||||||
chr12:66334471 | GAA | G | 35 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(32): Show |
38 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.3162+2842_3162+284 others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66334471 | ||||||
chr12:66334501 | A | C | 1 | a0005c0044t0001g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3162+2856A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334501 | |||||||
chr12:66334524 | T | C | 1 | a0005c0015t0001g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3162+2879T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334524 | |||||||
chr12:66334549 | C | T | 12 | a0005c0023t0001g0067 a0005c0023t0001g0068 a0005c0023t0001g0069 others(9): Show |
13 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3162+2904C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334549 | |||||||
chr12:66334550 | G | A | 1 | a0004c0004t0001g0190 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3162+2905G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334550 | |||||||
chr12:66334752 | C | A | 2 | a0001c0002t0001g0263 a0001c0002t0001g0298 |
2 | HG00738.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.3162+3107C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334752 | |||||||
chr12:66334780 | A | AAAAT | 19 | a0001c0024t0001g0180 a0001c0024t0001g0181 a0001c0024t0001g0182 others(16): Show |
20 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.3162+3153_3162+315 others(8): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66334780 | ||||||
chr12:66334780 | AAAAT | A | 114 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0015 others(111): Show |
152 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.3162+3153_3162+315 others(8): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66334780 | ||||||
chr12:66334798 | A | C | 120 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0015 others(117): Show |
158 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.3162+3153A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334798 | |||||||
chr12:66334920 | G | T | 1 | a0002c0001t0001g0117 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3163-3081G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334920 | |||||||
chr12:66334962 | G | C | 3 | a0010c0020t0001g0228 a0010c0020t0001g0230 a0010c0020t0001g0292 |
3 | HG02145.hp2 HG02895.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3163-3039G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334962 | |||||||
chr12:66334990 | G | C | 1 | a0001c0002t0001g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3163-3011G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334990 | |||||||
chr12:66335010 | A | T | 2 | a0001c0005t0001g0058 a0001c0005t0001g0059 |
2 | HG00438.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.3163-2991A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335010 | |||||||
chr12:66335062 | G | A | 159 | a0002c0001t0001g0006 a0002c0001t0001g0007 a0002c0001t0001g0015 others(156): Show |
200 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.3163-2939G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335062 | |||||||
chr12:66335140 | T | C | 34 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(31): Show |
37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.3163-2861T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335140 | |||||||
chr12:66335420 | G | C | 1 | a0005c0044t0001g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3163-2581G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335420 | |||||||
chr12:66335457 | A | G | 3 | a0001c0018t0001g0043 a0001c0018t0001g0259 a0001c0018t0001g0281 |
4 | HG02109.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3163-2544A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335457 | |||||||
chr12:66335470 | T | C | 180 | a0001c0022t0001g0174 a0001c0024t0001g0180 a0001c0024t0001g0181 others(177): Show |
222 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(219): Show |
intron_variant | MODIFIER | c.3163-2531T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335470 | |||||||
chr12:66335535 | G | T | 1 | a0001c0022t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3163-2466G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335535 | |||||||
chr12:66335536 | G | C | 1 | a0003c0003t0001g0030 | 2 | HG00558.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3163-2465G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335536 | |||||||
chr12:66335603 | A | C | 34 | a0002c0001t0002g0037 a0002c0001t0002g0038 a0002c0001t0002g0039 others(31): Show |
37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.3163-2398A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335603 | |||||||
chr12:66336088 | T | G | 1 | a0004c0004t0001g0190 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3163-1913T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336088 | |||||||
chr12:66336211 | T | C | 13 | a0001c0024t0001g0180 a0001c0024t0001g0181 a0001c0024t0001g0182 others(10): Show |
13 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3163-1790T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336211 | |||||||
chr12:66336617 | G | T | 4 | a0002c0001t0001g0098 a0002c0017t0001g0016 a0002c0017t0001g0055 others(1): Show |
5 | NA18939.hp2 NA18952.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.3163-1384G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336617 | |||||||
chr12:66336760 | T | C | 14 | a0001c0022t0001g0174 a0001c0024t0001g0180 a0001c0024t0001g0181 others(11): Show |
14 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3163-1241T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336760 | |||||||
chr12:66336813 | G | A | 1 | a0004c0035t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3163-1188G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336813 | |||||||
chr12:66336833 | C | T | 13 | a0001c0024t0001g0180 a0001c0024t0001g0181 a0001c0024t0001g0182 others(10): Show |
13 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3163-1168C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336833 | |||||||
chr12:66336840 | C | T | 1 | a0001c0002t0001g0276 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3163-1161C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336840 | |||||||
chr12:66336862 | CTG | C | 5 | a0010c0027t0001g0220 a0010c0027t0001g0223 a0016c0021t0001g0221 others(2): Show |
5 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3163-1136_3163-113 others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66336862 | ||||||
chr12:66336889 | A | G | 14 | a0001c0022t0001g0174 a0001c0024t0001g0180 a0001c0024t0001g0181 others(11): Show |
14 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3163-1112A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336889 | |||||||
chr12:66337039 | G | A | 1 | a0003c0003t0001g0212 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3163-962G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337039 | |||||||
chr12:66337301 | A | T | 4 | a0007c0009t0001g0042 a0007c0009t0001g0243 a0007c0009t0001g0245 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3163-700A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337301 | |||||||
chr12:66337418 | C | A | 6 | a0005c0033t0001g0236 a0010c0027t0001g0220 a0010c0027t0001g0223 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3163-583C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337418 | |||||||
chr12:66337505 | T | C | 1 | a0005c0033t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3163-496T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337505 | |||||||
chr12:66337563 | G | A | 1 | a0001c0002t0001g0275 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3163-438G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337563 | |||||||
chr12:66337619 | T | TA | 6 | a0001c0002t0001g0269 a0003c0003t0001g0124 a0004c0004t0001g0097 others(3): Show |
6 | HG01192.hp1 NA18952.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.3163-366dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66337619 | ||||||
chr12:66337619 | TA | T | 25 | a0001c0024t0001g0180 a0001c0024t0001g0181 a0001c0024t0001g0182 others(22): Show |
25 | HG01074.hp2 HG01168.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.3163-366delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66337619 | ||||||
chr12:66337635 | A | C | 1 | a0012c0025t0001g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3163-366A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337635 | |||||||
chr12:66337643 | A | G | 1 | a0003c0003t0001g0011 | 3 | HG01123.hp2 HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.3163-358A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337643 |