Item | Value |
---|---|
geneid | 283987 |
ensemblid | ENSG00000167861.16 |
hgncid | 15736 |
symbol | HID1 |
name | HID1 domain containing |
refseq_nuc | NM_030630.3 |
refseq_prot | NP_085133.1 |
ensembl_nuc | ENST00000425042.7 |
ensembl_prot | ENSP00000413520.2 |
mane_status | MANE Select |
chr | chr17 |
start | 74950742 |
end | 74972759 |
strand | - |
ver | v1.2 |
region | chr17:74950742-74972759 |
region5000 | chr17:74945742-74977759 |
regionname0 | HID1_chr17_74950742_74972759 |
regionname5000 | HID1_chr17_74945742_74977759 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 788 | 350 | 89 | 74 | 129 | 16 | 40 | 83 | HID1_chr17_74945742_74977759 | HID1 | MGSTD others(783): Show |
chr17 | 74945742 | 74977759 |
a0002 | 0/0 | 788 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | MGSTD others(783): Show |
chr17 | 74945742 | 74977759 |
a0003 | 0/0 | 788 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | MGSTD others(783): Show |
chr17 | 74945742 | 74977759 |
a0004 | 0/0 | 788 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | HID1_chr17_74945742_74977759 | HID1 | MGSTD others(783): Show |
chr17 | 74945742 | 74977759 |
a0005 | 0/0 | 788 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | MGSTD others(783): Show |
chr17 | 74945742 | 74977759 |
a0006 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | MGSTD others(783): Show |
chr17 | 74945742 | 74977759 |
a0007 | 0/0 | 788 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | MGSTD others(783): Show |
chr17 | 74945742 | 74977759 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2364 | 89 | 22 | 30 | 20 | 2 | 15 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0002 | 0/0 | 2364 | 70 | 2 | 5 | 59 | 0 | 4 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0003 | 0/1 | 2364 | 67 | 10 | 11 | 34 | 7 | 4 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0004 | 0/0 | 2364 | 66 | 13 | 21 | 16 | 4 | 12 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0005 | 0/0 | 2364 | 16 | 14 | 2 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0006 | 0/0 | 2364 | 14 | 13 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0007 | 1/0 | 2364 | 6 | 1 | 1 | 0 | 0 | 3 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0008 | 0/0 | 2364 | 6 | 5 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0010 | 0/0 | 2364 | 4 | 3 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0011 | 0/0 | 2364 | 3 | 0 | 1 | 0 | 2 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0012 | 0/0 | 2364 | 2 | 0 | 0 | 0 | 0 | 2 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0018 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0019 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0020 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0021 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0022 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0023 | 0/0 | 2364 | 1 | 0 | 0 | 0 | 1 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0001c0024 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0002c0009 | 0/0 | 2364 | 6 | 5 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0003c0013 | 0/0 | 2364 | 2 | 2 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0003c0025 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0004c0014 | 0/0 | 2364 | 2 | 0 | 0 | 0 | 0 | 2 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0005c0016 | 0/0 | 2364 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0006c0017 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 | ||
a0007c0015 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | ATGGG others(2359): Show |
chr17 | 74945742 | 74977759 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3298 | 72 | 7 | 29 | 20 | 2 | 14 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0001t0002 | 0/0 | 3298 | 5 | 5 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0001t0004 | 0/0 | 3298 | 11 | 10 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0001t0010 | 0/0 | 3298 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0002t0001 | 0/0 | 3298 | 2 | 0 | 1 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0002t0002 | 0/0 | 3298 | 65 | 2 | 4 | 55 | 0 | 4 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0002t0003 | 0/0 | 3300 | 3 | 0 | 0 | 3 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3295): Show |
chr17 | 74945742 | 74977759 |
a0001c0003t0001 | 0/0 | 3298 | 2 | 0 | 0 | 2 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0003t0003 | 0/1 | 3300 | 56 | 7 | 6 | 31 | 7 | 4 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3295): Show |
chr17 | 74945742 | 74977759 |
a0001c0003t0005 | 0/0 | 3300 | 3 | 0 | 3 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3295): Show |
chr17 | 74945742 | 74977759 |
a0001c0003t0007 | 0/0 | 3300 | 2 | 2 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3295): Show |
chr17 | 74945742 | 74977759 |
a0001c0003t0008 | 0/0 | 3300 | 2 | 0 | 2 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3295): Show |
chr17 | 74945742 | 74977759 |
a0001c0003t0012 | 0/0 | 3300 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3295): Show |
chr17 | 74945742 | 74977759 |
a0001c0003t0013 | 0/0 | 3300 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3295): Show |
chr17 | 74945742 | 74977759 |
a0001c0004t0001 | 0/0 | 3298 | 66 | 13 | 21 | 16 | 4 | 12 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0005t0002 | 0/0 | 3298 | 16 | 14 | 2 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0006t0001 | 0/0 | 3298 | 14 | 13 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0007t0001 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0007t0002 | 1/0 | 3298 | 5 | 0 | 1 | 0 | 0 | 3 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0008t0001 | 0/0 | 3298 | 5 | 4 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0008t0009 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0010t0001 | 0/0 | 3298 | 4 | 3 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0011t0001 | 0/0 | 3298 | 3 | 0 | 1 | 0 | 2 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0012t0001 | 0/0 | 3298 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0012t0002 | 0/0 | 3298 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0018t0002 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0019t0002 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0020t0011 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0021t0006 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0022t0002 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0001c0023t0003 | 0/0 | 3300 | 1 | 0 | 0 | 0 | 1 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3295): Show |
chr17 | 74945742 | 74977759 |
a0001c0024t0001 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0002c0009t0002 | 0/0 | 3298 | 6 | 5 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0003c0013t0001 | 0/0 | 3298 | 2 | 2 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0003c0025t0002 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0004c0014t0001 | 0/0 | 3298 | 2 | 0 | 0 | 0 | 0 | 2 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
a0005c0016t0003 | 0/0 | 3300 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3295): Show |
chr17 | 74945742 | 74977759 |
a0006c0017t0003 | 0/0 | 3300 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3295): Show |
chr17 | 74945742 | 74977759 |
a0007c0015t0006 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | GTCTC others(3293): Show |
chr17 | 74945742 | 74977759 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 23 | 2 | 14 | 3 | 1 | 3 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0004g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0001t0010g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0004 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0011 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0003 | 0/0 | 17 | 0 | 2 | 11 | 3 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0007 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0005g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0007g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0008g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0003t0013g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0001 | 0/0 | 27 | 2 | 14 | 6 | 1 | 4 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0005t0002g0006 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0005t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0005t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0005t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0005t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0005t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0005t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0006t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0006t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0006t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0006t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0006t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0006t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0006t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0007t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0007t0002g0035 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0007t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0007t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0007t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0008t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0008t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0008t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0008t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0010t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0010t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0010t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0010t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0011t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0011t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0012t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0012t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0018t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0019t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0020t0011g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0021t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0022t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0023t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0001c0024t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0002c0009t0002g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0002c0009t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0002c0009t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0002c0009t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0002c0009t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0003c0013t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0003c0013t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0003c0025t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0004c0014t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0004c0014t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0005c0016t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0006c0017t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
a0007c0015t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0004 | t0001 | g0001 | EUR | GBR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00280 | hp1 | a0001 | c0004 | t0001 | g0059 | EUR | FIN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00280 | hp2 | a0001 | c0003 | t0003 | g0003 | EUR | FIN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00323 | hp1 | a0001 | c0003 | t0003 | g0003 | EUR | FIN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00323 | hp2 | a0001 | c0023 | t0003 | g0060 | EUR | FIN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00544 | hp1 | a0001 | c0003 | t0003 | g0105 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00609 | hp1 | a0001 | c0003 | t0003 | g0064 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00609 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00621 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00639 | hp1 | a0002 | c0009 | t0002 | g0036 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00673 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | CHS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00733 | hp1 | a0001 | c0008 | t0001 | g0169 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00733 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00735 | hp1 | a0001 | c0003 | t0003 | g0007 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0048 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00738 | hp1 | a0001 | c0005 | t0002 | g0006 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00738 | hp2 | a0001 | c0003 | t0008 | g0114 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00741 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG00741 | hp2 | a0001 | c0007 | t0002 | g0159 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01069 | hp1 | a0001 | c0004 | t0001 | g0077 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01069 | hp2 | a0001 | c0010 | t0001 | g0178 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01070 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01071 | hp1 | a0001 | c0004 | t0001 | g0079 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01074 | hp2 | a0001 | c0004 | t0001 | g0080 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01099 | hp1 | a0005 | c0016 | t0003 | g0110 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01099 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01106 | hp1 | a0001 | c0005 | t0002 | g0006 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01106 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01109 | hp2 | a0001 | c0006 | t0001 | g0167 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01168 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01169 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01243 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0206 | AMR | PUR | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01255 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01255 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01257 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01258 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01258 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01261 | hp1 | a0001 | c0003 | t0003 | g0050 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01346 | hp2 | a0001 | c0004 | t0001 | g0061 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01358 | hp1 | a0001 | c0003 | t0003 | g0007 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01361 | hp1 | a0001 | c0004 | t0001 | g0068 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01361 | hp2 | a0001 | c0003 | t0008 | g0102 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01433 | hp2 | a0001 | c0004 | t0001 | g0051 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01496 | hp2 | a0001 | c0003 | t0003 | g0016 | AMR | CLM | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01515 | hp1 | a0001 | c0003 | t0003 | g0016 | EUR | IBS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01515 | hp2 | a0001 | c0004 | t0001 | g0024 | EUR | IBS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01516 | hp1 | a0001 | c0003 | t0003 | g0003 | EUR | IBS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01516 | hp2 | a0001 | c0003 | t0003 | g0049 | EUR | IBS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01517 | hp1 | a0001 | c0004 | t0001 | g0024 | EUR | IBS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01517 | hp2 | a0001 | c0003 | t0003 | g0016 | EUR | IBS | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01884 | hp1 | a0001 | c0005 | t0002 | g0006 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01884 | hp2 | a0001 | c0003 | t0012 | g0098 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01891 | hp1 | a0001 | c0005 | t0002 | g0006 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01934 | hp1 | a0001 | c0011 | t0001 | g0073 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01934 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01975 | hp1 | a0001 | c0003 | t0005 | g0018 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0117 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01993 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0135 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02015 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02027 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02040 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0136 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02055 | hp2 | a0001 | c0019 | t0002 | g0189 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02056 | hp2 | a0001 | c0003 | t0003 | g0142 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02071 | hp2 | a0001 | c0003 | t0003 | g0120 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02074 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02083 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02129 | hp1 | a0001 | c0003 | t0003 | g0084 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02129 | hp2 | a0001 | c0003 | t0013 | g0085 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02132 | hp2 | a0001 | c0003 | t0003 | g0007 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02145 | hp1 | a0003 | c0013 | t0001 | g0076 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02148 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02155 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | CDX | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02155 | hp2 | a0001 | c0003 | t0003 | g0123 | EAS | CDX | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CDX | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0132 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02258 | hp1 | a0001 | c0004 | t0001 | g0034 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02273 | hp1 | a0001 | c0003 | t0005 | g0018 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02280 | hp1 | a0001 | c0004 | t0001 | g0151 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02280 | hp2 | a0001 | c0005 | t0002 | g0173 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02293 | hp1 | a0001 | c0003 | t0005 | g0018 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02451 | hp1 | a0001 | c0004 | t0001 | g0001 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02523 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02523 | hp2 | a0001 | c0003 | t0003 | g0113 | EAS | KHV | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02572 | hp1 | a0001 | c0010 | t0001 | g0184 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02572 | hp2 | a0003 | c0013 | t0001 | g0074 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02615 | hp2 | a0001 | c0004 | t0001 | g0001 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02622 | hp2 | a0001 | c0006 | t0001 | g0020 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02630 | hp1 | a0001 | c0006 | t0001 | g0038 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02647 | hp1 | a0001 | c0006 | t0001 | g0038 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02647 | hp2 | a0001 | c0004 | t0001 | g0034 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02683 | hp1 | a0001 | c0003 | t0003 | g0003 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0097 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02698 | hp1 | a0001 | c0003 | t0003 | g0119 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02717 | hp1 | a0001 | c0005 | t0002 | g0125 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02717 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02735 | hp1 | a0001 | c0004 | t0001 | g0023 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02738 | hp2 | a0001 | c0004 | t0001 | g0001 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02809 | hp1 | a0001 | c0021 | t0006 | g0176 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02809 | hp2 | a0001 | c0006 | t0001 | g0020 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02818 | hp1 | a0001 | c0008 | t0009 | g0041 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02818 | hp2 | a0001 | c0008 | t0001 | g0017 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02886 | hp2 | a0001 | c0006 | t0001 | g0037 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0082 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02895 | hp2 | a0001 | c0004 | t0001 | g0072 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02896 | hp2 | a0001 | c0003 | t0003 | g0022 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02897 | hp2 | a0001 | c0003 | t0003 | g0022 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02922 | hp1 | a0001 | c0003 | t0003 | g0029 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02922 | hp2 | a0001 | c0006 | t0001 | g0170 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02965 | hp1 | a0001 | c0006 | t0001 | g0021 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02970 | hp1 | a0001 | c0003 | t0003 | g0029 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02970 | hp2 | a0001 | c0006 | t0001 | g0166 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02976 | hp1 | a0001 | c0006 | t0001 | g0020 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02976 | hp2 | a0002 | c0009 | t0002 | g0157 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03017 | hp1 | a0001 | c0004 | t0001 | g0069 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03041 | hp1 | a0001 | c0005 | t0002 | g0006 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03098 | hp1 | a0001 | c0010 | t0001 | g0182 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03098 | hp2 | a0001 | c0006 | t0001 | g0037 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03130 | hp1 | a0001 | c0003 | t0007 | g0026 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03139 | hp1 | a0001 | c0007 | t0001 | g0171 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03139 | hp2 | a0001 | c0006 | t0001 | g0021 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03195 | hp1 | a0001 | c0003 | t0003 | g0163 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03195 | hp2 | a0001 | c0006 | t0001 | g0193 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03209 | hp1 | a0001 | c0005 | t0002 | g0006 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03209 | hp2 | a0001 | c0008 | t0001 | g0081 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03225 | hp1 | a0001 | c0003 | t0003 | g0099 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03225 | hp2 | a0001 | c0018 | t0002 | g0078 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03239 | hp1 | a0001 | c0007 | t0002 | g0155 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03239 | hp2 | a0001 | c0003 | t0003 | g0109 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03453 | hp2 | a0001 | c0024 | t0001 | g0083 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03486 | hp1 | a0001 | c0008 | t0001 | g0017 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03491 | hp2 | a0004 | c0014 | t0001 | g0046 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03492 | hp2 | a0004 | c0014 | t0001 | g0045 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03516 | hp1 | a0001 | c0006 | t0001 | g0021 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03516 | hp2 | a0002 | c0009 | t0002 | g0036 | AFR | ESN | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03540 | hp1 | a0002 | c0009 | t0002 | g0192 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03540 | hp2 | a0001 | c0005 | t0002 | g0006 | AFR | GWD | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0057 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03579 | hp2 | a0001 | c0005 | t0002 | g0006 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03654 | hp1 | a0001 | c0004 | t0001 | g0070 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03654 | hp2 | a0001 | c0007 | t0002 | g0035 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03669 | hp1 | a0001 | c0004 | t0001 | g0023 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03704 | hp1 | a0001 | c0004 | t0001 | g0065 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0144 | SAS | PJL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03831 | hp1 | a0001 | c0012 | t0002 | g0130 | SAS | BEB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03831 | hp2 | a0001 | c0004 | t0001 | g0001 | SAS | BEB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03942 | hp2 | a0001 | c0004 | t0001 | g0054 | SAS | BEB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG04115 | hp1 | a0001 | c0007 | t0002 | g0115 | SAS | STU | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG04115 | hp2 | a0001 | c0001 | t0010 | g0042 | SAS | STU | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG04184 | hp1 | a0001 | c0012 | t0001 | g0160 | SAS | BEB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0011 | SAS | BEB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG04199 | hp1 | a0001 | c0004 | t0001 | g0055 | SAS | STU | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG04204 | hp1 | a0001 | c0004 | t0001 | g0062 | SAS | STU | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG04204 | hp2 | a0001 | c0004 | t0001 | g0001 | SAS | STU | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0011 | SAS | STU | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG04228 | hp2 | a0001 | c0004 | t0001 | g0001 | SAS | STU | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18522 | hp1 | a0001 | c0020 | t0011 | g0177 | AFR | YRI | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18522 | hp2 | a0001 | c0005 | t0002 | g0019 | AFR | YRI | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18612 | hp1 | a0001 | c0003 | t0003 | g0137 | EAS | CHB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18747 | hp1 | a0001 | c0003 | t0003 | g0121 | EAS | CHB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | YRI | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18942 | hp1 | a0001 | c0004 | t0001 | g0131 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18946 | hp1 | a0006 | c0017 | t0003 | g0122 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18952 | hp1 | a0001 | c0004 | t0001 | g0015 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18960 | hp1 | a0001 | c0004 | t0001 | g0071 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18961 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18962 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18964 | hp1 | a0001 | c0004 | t0001 | g0058 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18966 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18973 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18974 | hp1 | a0001 | c0003 | t0003 | g0111 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18977 | hp1 | a0001 | c0003 | t0003 | g0007 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18977 | hp2 | a0001 | c0002 | t0003 | g0086 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18979 | hp2 | a0001 | c0003 | t0003 | g0187 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18980 | hp1 | a0001 | c0004 | t0001 | g0056 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18980 | hp2 | a0001 | c0003 | t0003 | g0007 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18987 | hp2 | a0001 | c0003 | t0003 | g0007 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18994 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18994 | hp2 | a0001 | c0004 | t0001 | g0204 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18995 | hp1 | a0001 | c0004 | t0001 | g0066 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18997 | hp1 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA18997 | hp2 | a0001 | c0003 | t0003 | g0067 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19003 | hp1 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19003 | hp2 | a0001 | c0003 | t0003 | g0095 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19006 | hp1 | a0001 | c0003 | t0003 | g0134 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19009 | hp1 | a0001 | c0003 | t0003 | g0180 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19011 | hp1 | a0001 | c0004 | t0001 | g0015 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19030 | hp1 | a0002 | c0009 | t0002 | g0156 | AFR | LWK | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19030 | hp2 | a0007 | c0015 | t0006 | g0183 | AFR | LWK | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19043 | hp1 | a0003 | c0025 | t0002 | g0075 | AFR | LWK | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | LWK | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19057 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19060 | hp2 | a0001 | c0004 | t0001 | g0015 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19074 | hp1 | a0001 | c0003 | t0003 | g0007 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19075 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19075 | hp2 | a0001 | c0004 | t0001 | g0053 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19081 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19087 | hp2 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19090 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | YRI | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA19240 | hp2 | a0001 | c0005 | t0002 | g0019 | AFR | YRI | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA20752 | hp1 | a0001 | c0011 | t0001 | g0025 | EUR | TSI | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA20805 | hp1 | a0001 | c0003 | t0003 | g0063 | EUR | TSI | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA20805 | hp2 | a0001 | c0011 | t0001 | g0025 | EUR | TSI | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA20905 | hp1 | a0001 | c0003 | t0003 | g0174 | SAS | GIH | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | GIH | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02109 | hp1 | a0001 | c0008 | t0001 | g0017 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02109 | hp2 | a0001 | c0005 | t0002 | g0162 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02486 | hp2 | a0001 | c0003 | t0007 | g0026 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0207 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG02559 | hp2 | a0001 | c0005 | t0002 | g0172 | AFR | ACB | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG03471 | hp2 | a0001 | c0010 | t0001 | g0181 | AFR | MSL | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG06807 | hp1 | a0001 | c0003 | t0003 | g0118 | AFR | USA | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
HG06807 | hp2 | a0001 | c0005 | t0002 | g0019 | AFR | USA | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA20300 | hp1 | a0001 | c0005 | t0002 | g0126 | AFR | USA | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0104 | AFR | USA | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA21309 | hp1 | a0002 | c0009 | t0002 | g0161 | AFR | LWK | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
NA21309 | hp2 | a0001 | c0022 | t0002 | g0190 | AFR | LWK | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
homoSapiens | chm13v2 | a0001 | c0003 | t0003 | g0112 | REF | REF | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
homoSapiens | grch38p0 | a0001 | c0007 | t0002 | g0035 | REF | REF | HID1_chr17_74945742_74977759 | HID1 | chr17 | 74945742 | 74977759 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74954257 | C | T | 1 | a0006 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1745G>A | p.Arg582Gln | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 14/19 | 1848/3298 | 1745/2367 | 582/788 | chr17 | 74954257 | |||
chr17:74958457 | A | G | 1 | a0005 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1262T>C | p.Ile421Thr | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 11/19 | 1365/3298 | 1262/2367 | 421/788 | chr17 | 74958457 | |||
chr17:74962271 | G | A | 1 | a0002 | 6 | HG00639.hp1 HG02976.hp2 HG03516.hp2 others(3): Show |
missense_variant | MODERATE | c.574C>T | p.His192Tyr | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 5/19 | 677/3298 | 574/2367 | 192/788 | chr17 | 74962271 | |||
chr17:74963081 | G | C | 1 | a0003 | 3 | HG02145.hp1 HG02572.hp2 NA19043.hp1 |
missense_variant&splice_region_variant | MODERATE | c.388C>G | p.Gln130Glu | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/19 | 491/3298 | 388/2367 | 130/788 | chr17 | 74963081 | |||
chr17:74963868 | A | T | 1 | a0007 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.259T>A | p.Ser87Thr | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 3/19 | 362/3298 | 259/2367 | 87/788 | chr17 | 74963868 | |||
chr17:74964598 | T | C | 1 | a0004 | 2 | HG03491.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.101A>G | p.Gln34Arg | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 2/19 | 204/3298 | 101/2367 | 34/788 | chr17 | 74964598 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74951600 | G | A | 1 | a0001c0018 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.2337C>T | p.Asp779Asp | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 19/19 | 2440/3298 | 2337/2367 | 779/788 | chr17 | 74951600 | |||
chr17:74951997 | G | T | 1 | a0001c0020 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.2211C>A | p.Pro737Pro | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 18/19 | 2314/3298 | 2211/2367 | 737/788 | chr17 | 74951997 | |||
chr17:74952274 | A | G | 20 | a0001c0001 a0001c0002 a0001c0003 others(17): Show |
348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
synonymous_variant | LOW | c.2139T>C | p.Ile713Ile | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 17/19 | 2242/3298 | 2139/2367 | 713/788 | chr17 | 74952274 | |||
chr17:74952334 | C | A | 1 | a0001c0021 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.2079G>T | p.Pro693Pro | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 17/19 | 2182/3298 | 2079/2367 | 693/788 | chr17 | 74952334 | |||
chr17:74953015 | C | T | 2 | a0001c0022 a0003c0025 |
2 | NA19043.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.2043G>A | p.Thr681Thr | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 16/19 | 2146/3298 | 2043/2367 | 681/788 | chr17 | 74953015 | |||
chr17:74953051 | C | T | 4 | a0001c0003 a0001c0023 a0005c0016 others(1): Show |
69 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(66): Show |
synonymous_variant | LOW | c.2007G>A | p.Pro669Pro | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 16/19 | 2110/3298 | 2007/2367 | 669/788 | chr17 | 74953051 | |||
chr17:74953072 | T | C | 7 | a0001c0002 a0001c0006 a0001c0008 others(4): Show |
97 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(94): Show |
synonymous_variant | LOW | c.1986A>G | p.Ala662Ala | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 16/19 | 2089/3298 | 1986/2367 | 662/788 | chr17 | 74953072 | |||
chr17:74953554 | C | T | 1 | a0001c0002 | 70 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
synonymous_variant | LOW | c.1962G>A | p.Pro654Pro | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 15/19 | 2065/3298 | 1962/2367 | 654/788 | chr17 | 74953554 | |||
chr17:74954346 | G | A | 2 | a0001c0005 a0001c0024 |
17 | HG00738.hp1 HG01106.hp1 HG01884.hp1 others(14): Show |
synonymous_variant | LOW | c.1656C>T | p.Tyr552Tyr | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 14/19 | 1759/3298 | 1656/2367 | 552/788 | chr17 | 74954346 | |||
chr17:74955862 | G | A | 1 | a0001c0005 | 16 | HG00738.hp1 HG01106.hp1 HG01884.hp1 others(13): Show |
synonymous_variant | LOW | c.1566C>T | p.Ala522Ala | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/19 | 1669/3298 | 1566/2367 | 522/788 | chr17 | 74955862 | |||
chr17:74955922 | A | G | 19 | a0001c0001 a0001c0002 a0001c0003 others(16): Show |
326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
synonymous_variant | LOW | c.1506T>C | p.Thr502Thr | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/19 | 1609/3298 | 1506/2367 | 502/788 | chr17 | 74955922 | |||
chr17:74958743 | C | T | 1 | a0001c0011 | 3 | HG01934.hp1 NA20752.hp1 NA20805.hp2 |
synonymous_variant | LOW | c.1170G>A | p.Leu390Leu | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 10/19 | 1273/3298 | 1170/2367 | 390/788 | chr17 | 74958743 | |||
chr17:74960029 | G | A | 5 | a0001c0004 a0001c0023 a0001c0024 others(2): Show |
72 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
synonymous_variant | LOW | c.948C>T | p.Ala316Ala | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 7/19 | 1051/3298 | 948/2367 | 316/788 | chr17 | 74960029 | |||
chr17:74963043 | G | A | 1 | a0001c0010 | 4 | HG01069.hp2 HG02572.hp1 HG03098.hp1 others(1): Show |
synonymous_variant | LOW | c.426C>T | p.Ala142Ala | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/19 | 529/3298 | 426/2367 | 142/788 | chr17 | 74963043 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74950864 | C | A | 1 | a0001c0003t0007 | 2 | HG02486.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*706G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 19/19 | 706 | chr17 | 74950864 | ||||||
chr17:74950893 | G | T | 1 | a0001c0003t0012 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*677C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 19/19 | 677 | chr17 | 74950893 | ||||||
chr17:74950966 | T | C | 19 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(16): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*604A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 19/19 | 604 | chr17 | 74950966 | ||||||
chr17:74951031 | T | A | 1 | a0001c0003t0008 | 2 | HG00738.hp2 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*539A>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 19/19 | 539 | chr17 | 74951031 | ||||||
chr17:74951154 | T | C | 1 | a0001c0003t0005 | 3 | HG01975.hp1 HG02273.hp1 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*416A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 19/19 | 416 | chr17 | 74951154 | ||||||
chr17:74951223 | A | ATT | 10 | a0001c0002t0003 a0001c0003t0003 a0001c0003t0005 others(7): Show |
70 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*345_*346dupAA | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 19/19 | 346 | chr17 | 74951223 | ||||||
chr17:74951301 | A | G | 2 | a0001c0021t0006 a0007c0015t0006 |
2 | HG02809.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*269T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 19/19 | 269 | chr17 | 74951301 | ||||||
chr17:74951309 | C | T | 1 | a0001c0020t0011 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*261G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 19/19 | 261 | chr17 | 74951309 | ||||||
chr17:74951557 | G | A | 1 | a0001c0003t0013 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 19/19 | 13 | chr17 | 74951557 | ||||||
chr17:74972673 | C | T | 1 | a0001c0001t0010 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-17G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/19 | 17 | chr17 | 74972673 | ||||||
chr17:74972715 | A | G | 1 | a0001c0008t0009 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/19 | 59 | chr17 | 74972715 | ||||||
chr17:74972751 | G | A | 1 | a0001c0001t0004 | 11 | HG01243.hp2 HG02145.hp2 HG02559.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-95C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/19 | 95 | chr17 | 74972751 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74951698 | C | T | 1 | a0001c0008t0001g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2304-65G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 18/18 | chr17 | 74951698 | |||||||
chr17:74951756 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2304-123G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 18/18 | chr17 | 74951756 | |||||||
chr17:74951798 | T | G | 1 | a0001c0018t0002g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2303+107A>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 18/18 | chr17 | 74951798 | |||||||
chr17:74952142 | T | C | 1 | a0001c0001t0004g0207 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2145-79A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 17/18 | chr17 | 74952142 | |||||||
chr17:74952178 | C | T | 1 | a0001c0020t0011g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2144+91G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 17/18 | chr17 | 74952178 | |||||||
chr17:74952245 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2144+24G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 17/18 | chr17 | 74952245 | |||||||
chr17:74952372 | C | T | 1 | a0001c0021t0006g0176 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2053-12G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 16/18 | chr17 | 74952372 | |||||||
chr17:74952544 | C | A | 2 | a0001c0021t0006g0176 a0007c0015t0006g0183 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2053-184G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 16/18 | chr17 | 74952544 | |||||||
chr17:74952570 | G | A | 3 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0089 |
3 | HG02615.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2053-210C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 16/18 | chr17 | 74952570 | |||||||
chr17:74952725 | A | C | 2 | a0001c0021t0006g0176 a0007c0015t0006g0183 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2052+281T>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 16/18 | chr17 | 74952725 | |||||||
chr17:74952847 | C | T | 4 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0089 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2052+159G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 16/18 | chr17 | 74952847 | |||||||
chr17:74952863 | T | A | 55 | a0001c0002t0001g0124 a0001c0002t0001g0141 a0001c0002t0002g0004 others(52): Show |
103 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2052+143A>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 16/18 | chr17 | 74952863 | |||||||
chr17:74953125 | G | A | 4 | a0001c0004t0001g0015 a0001c0004t0001g0053 a0001c0004t0001g0058 others(1): Show |
6 | HG03209.hp2 NA18952.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1972-39C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 15/18 | chr17 | 74953125 | |||||||
chr17:74953144 | G | A | 5 | a0001c0006t0001g0037 a0001c0006t0001g0167 a0001c0006t0001g0170 others(2): Show |
8 | HG01109.hp2 HG02109.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1972-58C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 15/18 | chr17 | 74953144 | |||||||
chr17:74953291 | C | T | 1 | a0001c0004t0001g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1972-205G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 15/18 | chr17 | 74953291 | |||||||
chr17:74953341 | C | T | 15 | a0001c0005t0002g0006 a0001c0005t0002g0019 a0001c0005t0002g0125 others(12): Show |
29 | HG00733.hp1 HG00738.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1971+204G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 15/18 | chr17 | 74953341 | |||||||
chr17:74953473 | G | A | 1 | a0001c0003t0003g0029 | 2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1971+72C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 15/18 | chr17 | 74953473 | |||||||
chr17:74953775 | T | C | 19 | a0001c0005t0002g0006 a0001c0005t0002g0019 a0001c0005t0002g0125 others(16): Show |
33 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1865-124A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 14/18 | chr17 | 74953775 | |||||||
chr17:74953881 | C | T | 4 | a0001c0006t0001g0037 a0001c0006t0001g0167 a0001c0006t0001g0170 others(1): Show |
7 | HG01109.hp2 HG02109.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1865-230G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 14/18 | chr17 | 74953881 | |||||||
chr17:74953906 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0191 a0001c0004t0001g0072 |
4 | HG00639.hp2 HG02723.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1864+232C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 14/18 | chr17 | 74953906 | |||||||
chr17:74953932 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1864+206G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 14/18 | chr17 | 74953932 | |||||||
chr17:74954113 | C | G | 2 | a0001c0001t0002g0154 a0001c0001t0002g0158 |
2 | HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1864+25G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 14/18 | chr17 | 74954113 | |||||||
chr17:74954377 | G | A | 36 | a0001c0002t0001g0124 a0001c0002t0001g0141 a0001c0002t0002g0004 others(33): Show |
70 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1637-12C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954377 | |||||||
chr17:74954702 | A | C | 8 | a0001c0001t0001g0165 a0001c0001t0001g0188 a0001c0001t0004g0009 others(5): Show |
13 | HG01243.hp2 HG02145.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1637-337T>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954702 | |||||||
chr17:74954722 | A | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(193): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1637-357T>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954722 | |||||||
chr17:74954731 | C | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(124): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1637-366G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954731 | |||||||
chr17:74954778 | A | G | 41 | a0001c0001t0001g0107 a0001c0001t0001g0133 a0001c0001t0001g0175 others(38): Show |
71 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1637-413T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954778 | |||||||
chr17:74954779 | C | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(124): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1637-414G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954779 | |||||||
chr17:74954821 | G | A | 10 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0089 others(7): Show |
10 | HG01069.hp2 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1637-456C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954821 | |||||||
chr17:74954832 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(126): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1637-467A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954832 | |||||||
chr17:74954856 | CA | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(126): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1637-492delT | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954856 | |||||||
chr17:74954909 | CT | C | 17 | a0001c0005t0002g0006 a0001c0005t0002g0019 a0001c0005t0002g0125 others(14): Show |
28 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1637-545delA | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954909 | |||||||
chr17:74954944 | G | A | 10 | a0001c0005t0002g0006 a0001c0005t0002g0019 a0001c0005t0002g0125 others(7): Show |
19 | HG00733.hp1 HG00738.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1637-579C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954944 | |||||||
chr17:74954955 | T | G | 36 | a0001c0002t0001g0124 a0001c0002t0001g0141 a0001c0002t0002g0004 others(33): Show |
70 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1637-590A>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74954955 | |||||||
chr17:74955053 | C | G | 1 | a0001c0006t0001g0037 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1637-688G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955053 | |||||||
chr17:74955123 | C | T | 5 | a0001c0010t0001g0178 a0001c0010t0001g0181 a0001c0010t0001g0182 others(2): Show |
5 | HG01069.hp2 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1636+669G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955123 | |||||||
chr17:74955212 | A | G | 1 | a0001c0001t0010g0042 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1636+580T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955212 | |||||||
chr17:74955299 | G | C | 20 | a0001c0001t0002g0089 a0001c0001t0002g0154 a0001c0001t0002g0158 others(17): Show |
29 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1636+493C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955299 | |||||||
chr17:74955501 | GA | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1636+290delT | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955501 | |||||||
chr17:74955528 | T | C | 1 | a0001c0006t0001g0037 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1636+264A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955528 | |||||||
chr17:74955530 | A | G | 21 | a0001c0001t0002g0089 a0001c0001t0002g0154 a0001c0001t0002g0158 others(18): Show |
30 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1636+262T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955530 | |||||||
chr17:74955682 | G | A | 1 | a0001c0004t0001g0070 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1636+110C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955682 | |||||||
chr17:74955711 | C | T | 1 | a0001c0002t0002g0010 | 5 | NA18963.hp2 NA18969.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1636+81G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955711 | |||||||
chr17:74955728 | C | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(193): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1636+64G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955728 | |||||||
chr17:74955750 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(117): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1636+42C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955750 | |||||||
chr17:74955769 | A | G | 1 | a0001c0002t0001g0124 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1636+23T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 13/18 | chr17 | 74955769 | |||||||
chr17:74955981 | C | A | 2 | a0001c0006t0001g0037 a0003c0025t0002g0075 |
3 | HG02886.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1472-25G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74955981 | |||||||
chr17:74956027 | G | A | 7 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0002c0009t0002g0036 others(4): Show |
8 | HG00639.hp1 HG02886.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1472-71C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956027 | |||||||
chr17:74956070 | G | C | 1 | a0001c0021t0006g0176 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1472-114C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956070 | |||||||
chr17:74956080 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1472-124C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956080 | |||||||
chr17:74956139 | G | A | 4 | a0001c0010t0001g0178 a0001c0010t0001g0181 a0001c0010t0001g0182 others(1): Show |
4 | HG01069.hp2 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1472-183C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956139 | |||||||
chr17:74956202 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1472-246T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956202 | |||||||
chr17:74956340 | C | T | 1 | a0001c0004t0001g0059 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1472-384G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956340 | |||||||
chr17:74956469 | T | C | 1 | a0001c0003t0003g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1472-513A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956469 | |||||||
chr17:74956492 | T | G | 10 | a0001c0001t0001g0165 a0001c0001t0001g0188 a0001c0001t0004g0009 others(7): Show |
16 | HG01243.hp2 HG01934.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1472-536A>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956492 | |||||||
chr17:74956693 | A | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(144): Show |
260 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.1472-737T>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956693 | |||||||
chr17:74956728 | C | T | 118 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0100 others(115): Show |
217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1472-772G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956728 | |||||||
chr17:74956795 | C | T | 1 | a0001c0003t0003g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1472-839G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956795 | |||||||
chr17:74956847 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
88 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1472-891C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74956847 | |||||||
chr17:74957051 | C | T | 3 | a0001c0002t0002g0136 a0001c0003t0003g0113 a0001c0003t0003g0137 |
3 | HG02055.hp1 HG02523.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1471+1090G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957051 | |||||||
chr17:74957212 | A | G | 1 | a0001c0006t0001g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1471+929T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957212 | |||||||
chr17:74957319 | CA | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(170): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1471+821delT | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957319 | |||||||
chr17:74957393 | A | C | 1 | a0001c0002t0002g0146 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1471+748T>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957393 | |||||||
chr17:74957582 | CA | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(201): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.1471+558delT | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957582 | |||||||
chr17:74957598 | A | T | 1 | a0001c0020t0011g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1471+543T>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957598 | |||||||
chr17:74957610 | TA | T | 5 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0002t0003g0198 others(2): Show |
5 | HG01099.hp1 HG02698.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1471+530delT | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957610 | |||||||
chr17:74957611 | A | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(140): Show |
256 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.1471+530T>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957611 | |||||||
chr17:74957612 | A | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(143): Show |
259 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1471+529T>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957612 | |||||||
chr17:74957613 | A | T | 87 | a0001c0001t0001g0031 a0001c0001t0001g0100 a0001c0001t0001g0128 others(84): Show |
155 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1471+528T>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957613 | |||||||
chr17:74957642 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1471+499C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957642 | |||||||
chr17:74957773 | G | A | 1 | a0001c0003t0003g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1471+368C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957773 | |||||||
chr17:74957968 | A | G | 1 | a0001c0006t0001g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1471+173T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957968 | |||||||
chr17:74957993 | T | C | 1 | a0001c0004t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1471+148A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74957993 | |||||||
chr17:74958004 | G | T | 1 | a0001c0006t0001g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1471+137C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74958004 | |||||||
chr17:74958070 | A | G | 1 | a0001c0002t0002g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1471+71T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 12/18 | chr17 | 74958070 | |||||||
chr17:74958316 | A | T | 2 | a0001c0003t0003g0111 a0001c0003t0003g0134 |
2 | NA18974.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1392+11T>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 11/18 | chr17 | 74958316 | |||||||
chr17:74958483 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG02615.hp1 | splice_region_variant&intron_variant | LOW | c.1241-5C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 10/18 | chr17 | 74958483 | |||||||
chr17:74958641 | C | A | 1 | a0001c0005t0002g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1240+32G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 10/18 | chr17 | 74958641 | |||||||
chr17:74958904 | G | A | 7 | a0001c0001t0001g0188 a0001c0001t0004g0009 a0001c0001t0004g0205 others(4): Show |
12 | HG01243.hp2 HG02145.hp2 HG02559.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1149+7C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 9/18 | chr17 | 74958904 | |||||||
chr17:74959132 | C | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.1009-81G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 8/18 | chr17 | 74959132 | |||||||
chr17:74959215 | T | A | 95 | a0001c0001t0001g0031 a0001c0001t0001g0100 a0001c0001t0001g0128 others(92): Show |
166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1009-164A>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 8/18 | chr17 | 74959215 | |||||||
chr17:74959228 | G | A | 1 | a0001c0004t0001g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1009-177C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 8/18 | chr17 | 74959228 | |||||||
chr17:74959428 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(49): Show |
94 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1009-377G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 8/18 | chr17 | 74959428 | |||||||
chr17:74959460 | T | C | 3 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0022t0002g0190 |
3 | HG02886.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1009-409A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 8/18 | chr17 | 74959460 | |||||||
chr17:74959493 | G | A | 1 | a0001c0020t0011g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1008+388C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 8/18 | chr17 | 74959493 | |||||||
chr17:74959874 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG00408.hp1 | splice_region_variant&intron_variant | LOW | c.1008+7C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 8/18 | chr17 | 74959874 | |||||||
chr17:74960304 | C | A | 86 | a0001c0001t0001g0031 a0001c0001t0001g0100 a0001c0001t0001g0128 others(83): Show |
154 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.729-56G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960304 | |||||||
chr17:74960441 | T | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(30): Show |
65 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.729-193A>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960441 | |||||||
chr17:74960486 | G | A | 1 | a0001c0008t0001g0169 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.729-238C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960486 | |||||||
chr17:74960530 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(52): Show |
98 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.729-282C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960530 | |||||||
chr17:74960590 | G | A | 1 | a0001c0021t0006g0176 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.729-342C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960590 | |||||||
chr17:74960643 | G | A | 8 | a0001c0001t0001g0165 a0001c0001t0001g0188 a0001c0001t0004g0009 others(5): Show |
13 | HG01243.hp2 HG02145.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.729-395C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960643 | |||||||
chr17:74960693 | T | C | 1 | a0001c0002t0002g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.729-445A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960693 | |||||||
chr17:74960706 | G | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(52): Show |
98 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.729-458C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960706 | |||||||
chr17:74960745 | C | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
87 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.729-497G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960745 | |||||||
chr17:74960764 | G | A | 1 | a0001c0005t0002g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.729-516C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960764 | |||||||
chr17:74960801 | G | A | 1 | a0001c0008t0001g0169 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.729-553C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960801 | |||||||
chr17:74960871 | C | A | 1 | a0001c0004t0001g0023 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.729-623G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960871 | |||||||
chr17:74960912 | A | T | 88 | a0001c0001t0001g0031 a0001c0001t0001g0100 a0001c0001t0001g0128 others(85): Show |
156 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.729-664T>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960912 | |||||||
chr17:74960929 | G | A | 1 | a0001c0002t0002g0117 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.729-681C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74960929 | |||||||
chr17:74961009 | C | T | 7 | a0001c0005t0002g0006 a0001c0005t0002g0019 a0001c0005t0002g0125 others(4): Show |
16 | HG00738.hp1 HG01106.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.729-761G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961009 | |||||||
chr17:74961013 | G | A | 1 | a0001c0002t0002g0201 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.729-765C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961013 | |||||||
chr17:74961043 | T | A | 1 | a0001c0003t0003g0022 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.729-795A>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961043 | |||||||
chr17:74961102 | G | A | 5 | a0001c0006t0001g0037 a0001c0006t0001g0167 a0001c0006t0001g0170 others(2): Show |
8 | HG01109.hp2 HG02109.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.728+771C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961102 | |||||||
chr17:74961107 | G | A | 5 | a0001c0006t0001g0020 a0001c0006t0001g0021 a0001c0006t0001g0038 others(2): Show |
10 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.728+766C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961107 | |||||||
chr17:74961117 | G | A | 1 | a0007c0015t0006g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.728+756C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961117 | |||||||
chr17:74961273 | A | AT | 9 | a0001c0001t0001g0052 a0001c0001t0001g0103 a0001c0001t0001g0127 others(6): Show |
9 | HG01168.hp2 HG01361.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.728+599dupA | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961273 | |||||||
chr17:74961273 | AT | A | 7 | a0001c0001t0002g0158 a0001c0006t0001g0020 a0001c0006t0001g0021 others(4): Show |
12 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+599delA | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961273 | |||||||
chr17:74961302 | C | T | 1 | a0001c0008t0001g0017 | 3 | HG02109.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.728+571G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961302 | |||||||
chr17:74961306 | C | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
86 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.728+567G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961306 | |||||||
chr17:74961321 | G | A | 1 | a0001c0011t0001g0073 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.728+552C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961321 | |||||||
chr17:74961354 | G | A | 7 | a0001c0010t0001g0178 a0001c0010t0001g0181 a0001c0010t0001g0182 others(4): Show |
8 | HG01069.hp2 HG01934.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.728+519C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961354 | |||||||
chr17:74961361 | G | A | 1 | a0001c0004t0001g0132 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.728+512C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961361 | |||||||
chr17:74961403 | G | C | 2 | a0001c0002t0002g0116 a0001c0002t0002g0145 |
2 | HG02027.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.728+470C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961403 | |||||||
chr17:74961465 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.728+408T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961465 | |||||||
chr17:74961469 | T | A | 1 | a0001c0001t0001g0039 | 2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.728+404A>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961469 | |||||||
chr17:74961584 | C | CT | 46 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
88 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.728+288dupA | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961584 | |||||||
chr17:74961616 | G | T | 1 | a0002c0009t0002g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.728+257C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961616 | |||||||
chr17:74961620 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(147): Show |
264 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.728+253A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961620 | |||||||
chr17:74961647 | G | C | 1 | a0001c0004t0001g0080 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.728+226C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961647 | |||||||
chr17:74961699 | G | A | 1 | a0001c0002t0002g0150 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.728+174C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961699 | |||||||
chr17:74961742 | T | G | 8 | a0001c0001t0001g0165 a0001c0001t0001g0188 a0001c0001t0004g0009 others(5): Show |
13 | HG01243.hp2 HG02145.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.728+131A>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961742 | |||||||
chr17:74961781 | C | G | 1 | a0001c0003t0003g0120 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.728+92G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961781 | |||||||
chr17:74961867 | CT | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(146): Show |
263 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(260): Show |
splice_region_variant&intron_variant | LOW | c.728+5delA | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 6/18 | chr17 | 74961867 | |||||||
chr17:74962004 | G | C | 2 | a0001c0006t0001g0167 a0001c0006t0001g0170 |
2 | HG01109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.612-15C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 5/18 | chr17 | 74962004 | |||||||
chr17:74962087 | A | G | 1 | a0001c0003t0003g0022 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.612-98T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 5/18 | chr17 | 74962087 | |||||||
chr17:74962167 | T | C | 1 | a0001c0004t0001g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.611+67A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 5/18 | chr17 | 74962167 | |||||||
chr17:74962177 | G | A | 1 | a0001c0022t0002g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.611+57C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 5/18 | chr17 | 74962177 | |||||||
chr17:74962383 | G | A | 6 | a0001c0006t0001g0037 a0001c0006t0001g0166 a0001c0006t0001g0167 others(3): Show |
9 | HG01109.hp2 HG02109.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.505-43C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/18 | chr17 | 74962383 | |||||||
chr17:74962478 | T | C | 1 | a0001c0004t0001g0024 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.505-138A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/18 | chr17 | 74962478 | |||||||
chr17:74962558 | G | C | 1 | a0001c0004t0001g0080 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.505-218C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/18 | chr17 | 74962558 | |||||||
chr17:74962631 | T | A | 2 | a0001c0001t0002g0154 a0001c0001t0002g0158 |
2 | HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.505-291A>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/18 | chr17 | 74962631 | |||||||
chr17:74962742 | G | T | 1 | a0001c0002t0002g0117 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.504+223C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/18 | chr17 | 74962742 | |||||||
chr17:74962831 | G | A | 12 | a0001c0001t0001g0028 a0001c0001t0001g0129 a0001c0001t0001g0148 others(9): Show |
25 | HG00423.hp1 HG01175.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.504+134C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/18 | chr17 | 74962831 | |||||||
chr17:74962852 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG01070.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.504+113G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/18 | chr17 | 74962852 | |||||||
chr17:74962860 | C | T | 11 | a0001c0001t0002g0043 a0001c0003t0003g0099 a0001c0003t0003g0163 others(8): Show |
15 | HG01884.hp2 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.504+105G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/18 | chr17 | 74962860 | |||||||
chr17:74962881 | G | A | 1 | a0002c0009t0002g0036 | 2 | HG00639.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.504+84C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/18 | chr17 | 74962881 | |||||||
chr17:74962905 | G | C | 39 | a0001c0003t0003g0016 a0001c0003t0003g0049 a0001c0003t0003g0050 others(36): Show |
72 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.504+60C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/18 | chr17 | 74962905 | |||||||
chr17:74962944 | G | T | 1 | a0001c0004t0001g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.504+21C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 4/18 | chr17 | 74962944 | |||||||
chr17:74963082 | C | A | 6 | a0001c0001t0001g0188 a0001c0006t0001g0020 a0001c0006t0001g0021 others(3): Show |
11 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(8): Show |
splice_acceptor_variant&intron_variant | HIGH | c.388-1G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 3/18 | chr17 | 74963082 | |||||||
chr17:74963238 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0179 others(16): Show |
23 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.388-157G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 3/18 | chr17 | 74963238 | |||||||
chr17:74963374 | C | T | 1 | a0001c0007t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.388-293G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 3/18 | chr17 | 74963374 | |||||||
chr17:74963394 | C | A | 24 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0179 others(21): Show |
33 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.388-313G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 3/18 | chr17 | 74963394 | |||||||
chr17:74963394 | C | T | 5 | a0001c0011t0001g0025 a0001c0011t0001g0073 a0003c0013t0001g0074 others(2): Show |
6 | HG01934.hp1 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-313G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 3/18 | chr17 | 74963394 | |||||||
chr17:74963625 | C | T | 4 | a0001c0006t0001g0166 a0001c0006t0001g0167 a0001c0006t0001g0170 others(1): Show |
4 | HG01109.hp2 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+115G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 3/18 | chr17 | 74963625 | |||||||
chr17:74963683 | C | T | 1 | a0001c0004t0001g0048 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.387+57G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 3/18 | chr17 | 74963683 | |||||||
chr17:74963915 | G | C | 1 | a0001c0002t0002g0032 | 2 | NA18970.hp1 NA19066.hp2 |
splice_region_variant&intron_variant | LOW | c.217-5C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 2/18 | chr17 | 74963915 | |||||||
chr17:74963955 | A | G | 61 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0165 others(58): Show |
88 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.217-45T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 2/18 | chr17 | 74963955 | |||||||
chr17:74963980 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.217-70C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 2/18 | chr17 | 74963980 | |||||||
chr17:74964255 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.216+228G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 2/18 | chr17 | 74964255 | |||||||
chr17:74964263 | T | G | 1 | a0001c0001t0004g0208 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.216+220A>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 2/18 | chr17 | 74964263 | |||||||
chr17:74964318 | C | T | 1 | a0001c0008t0001g0169 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.216+165G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 2/18 | chr17 | 74964318 | |||||||
chr17:74964423 | C | G | 1 | a0001c0022t0002g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.216+60G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 2/18 | chr17 | 74964423 | |||||||
chr17:74964762 | A | G | 38 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0165 others(35): Show |
56 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.67-130T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74964762 | |||||||
chr17:74964771 | G | A | 1 | a0001c0022t0002g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67-139C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74964771 | |||||||
chr17:74964873 | A | G | 1 | a0001c0007t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.67-241T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74964873 | |||||||
chr17:74964918 | C | T | 26 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0165 others(23): Show |
39 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.67-286G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74964918 | |||||||
chr17:74964969 | C | G | 1 | a0001c0008t0001g0169 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.67-337G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74964969 | |||||||
chr17:74965029 | T | C | 12 | a0001c0001t0001g0188 a0001c0004t0001g0077 a0001c0004t0001g0079 others(9): Show |
19 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.67-397A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965029 | |||||||
chr17:74965147 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.67-515T>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965147 | |||||||
chr17:74965179 | T | A | 1 | a0001c0003t0003g0029 | 2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.67-547A>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965179 | |||||||
chr17:74965186 | G | A | 1 | a0001c0003t0003g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.67-554C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965186 | |||||||
chr17:74965301 | G | C | 5 | a0001c0003t0003g0120 a0001c0003t0003g0121 a0001c0003t0003g0123 others(2): Show |
7 | HG01975.hp1 HG02071.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-669C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965301 | |||||||
chr17:74965426 | A | G | 2 | a0001c0004t0001g0051 a0001c0004t0001g0055 |
2 | HG01433.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.67-794T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965426 | |||||||
chr17:74965505 | A | G | 1 | a0002c0009t0002g0036 | 2 | HG00639.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.67-873T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965505 | |||||||
chr17:74965715 | G | A | 2 | a0001c0002t0001g0124 a0001c0008t0001g0169 |
2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.67-1083C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965715 | |||||||
chr17:74965763 | A | C | 8 | a0001c0001t0001g0165 a0001c0005t0002g0006 a0001c0005t0002g0019 others(5): Show |
17 | HG00738.hp1 HG01106.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.67-1131T>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965763 | |||||||
chr17:74965800 | C | T | 1 | a0001c0007t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.67-1168G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965800 | |||||||
chr17:74965886 | C | T | 6 | a0001c0003t0001g0030 a0001c0011t0001g0025 a0001c0011t0001g0073 others(3): Show |
8 | HG01934.hp1 HG02145.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-1254G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965886 | |||||||
chr17:74965917 | C | CA | 38 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0165 others(35): Show |
56 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.67-1286dupT | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74965917 | |||||||
chr17:74966057 | C | T | 1 | a0001c0004t0001g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.67-1425G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966057 | |||||||
chr17:74966063 | G | C | 2 | a0001c0010t0001g0181 a0001c0010t0001g0182 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.67-1431C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966063 | |||||||
chr17:74966153 | C | T | 3 | a0001c0003t0001g0030 a0001c0011t0001g0025 a0001c0011t0001g0073 |
5 | HG01934.hp1 NA19075.hp1 NA19090.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-1521G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966153 | |||||||
chr17:74966232 | C | T | 1 | a0001c0004t0001g0048 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.67-1600G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966232 | |||||||
chr17:74966283 | C | CA | 9 | a0001c0001t0004g0209 a0001c0002t0002g0033 a0001c0002t0002g0152 others(6): Show |
12 | HG00639.hp1 HG00741.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.67-1652dupT | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966283 | |||||||
chr17:74966283 | CA | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0027 others(104): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.67-1652delT | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966283 | |||||||
chr17:74966283 | CAA | C | 7 | a0001c0001t0001g0052 a0001c0001t0001g0094 a0001c0001t0001g0203 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-1653_67-1652del others(2): Show |
HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966283 | |||||||
chr17:74966283 | CAAAAAAA | C | 6 | a0001c0001t0001g0188 a0001c0006t0001g0020 a0001c0006t0001g0021 others(3): Show |
11 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.67-1658_67-1652del others(7): Show |
HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966283 | |||||||
chr17:74966393 | CAT | C | 12 | a0001c0001t0001g0188 a0001c0004t0001g0077 a0001c0004t0001g0079 others(9): Show |
19 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.67-1763_67-1762del others(2): Show |
HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966393 | |||||||
chr17:74966443 | T | C | 2 | a0001c0002t0003g0198 a0001c0002t0003g0199 |
2 | NA19003.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.67-1811A>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966443 | |||||||
chr17:74966467 | G | A | 1 | a0001c0007t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.67-1835C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966467 | |||||||
chr17:74966593 | C | G | 1 | a0001c0002t0002g0093 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.67-1961G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966593 | |||||||
chr17:74966639 | A | T | 6 | a0001c0001t0001g0188 a0001c0006t0001g0020 a0001c0006t0001g0021 others(3): Show |
11 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.67-2007T>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74966639 | |||||||
chr17:74967067 | C | T | 1 | a0001c0004t0001g0051 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.67-2435G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74967067 | |||||||
chr17:74967192 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(191): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.67-2560C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74967192 | |||||||
chr17:74967323 | G | A | 3 | a0001c0006t0001g0037 a0001c0020t0011g0177 a0001c0021t0006g0176 |
4 | HG02809.hp1 HG02886.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-2691C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74967323 | |||||||
chr17:74967455 | C | T | 3 | a0001c0006t0001g0037 a0001c0020t0011g0177 a0001c0021t0006g0176 |
4 | HG02809.hp1 HG02886.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-2823G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74967455 | |||||||
chr17:74967487 | C | A | 1 | a0001c0010t0001g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67-2855G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74967487 | |||||||
chr17:74967551 | A | C | 5 | a0001c0004t0001g0077 a0001c0004t0001g0079 a0001c0004t0001g0080 others(2): Show |
7 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-2919T>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74967551 | |||||||
chr17:74967553 | T | A | 2 | a0001c0001t0001g0153 a0001c0004t0001g0034 |
3 | HG01261.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.67-2921A>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74967553 | |||||||
chr17:74967555 | T | A | 2 | a0001c0001t0001g0153 a0001c0004t0001g0034 |
3 | HG01261.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.67-2923A>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74967555 | |||||||
chr17:74967954 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.67-3322T>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74967954 | |||||||
chr17:74968266 | C | G | 6 | a0001c0001t0001g0188 a0001c0006t0001g0020 a0001c0006t0001g0021 others(3): Show |
11 | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.67-3634G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74968266 | |||||||
chr17:74968373 | G | A | 1 | a0002c0009t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67-3741C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74968373 | |||||||
chr17:74968605 | C | T | 2 | a0001c0002t0002g0090 a0001c0002t0002g0091 |
2 | NA19002.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.67-3973G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74968605 | |||||||
chr17:74968650 | G | T | 8 | a0001c0006t0001g0037 a0001c0011t0001g0025 a0001c0011t0001g0073 others(5): Show |
10 | HG01934.hp1 HG02145.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+3941C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74968650 | |||||||
chr17:74968754 | G | A | 1 | a0001c0006t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.66+3837C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74968754 | |||||||
chr17:74968869 | G | A | 1 | a0001c0004t0001g0068 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.66+3722C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74968869 | |||||||
chr17:74968969 | A | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0179 a0001c0001t0001g0185 others(7): Show |
13 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.66+3622T>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74968969 | |||||||
chr17:74968986 | C | G | 1 | a0001c0020t0011g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.66+3605G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74968986 | |||||||
chr17:74969061 | G | C | 2 | a0001c0004t0001g0069 a0001c0004t0001g0070 |
2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.66+3530C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969061 | |||||||
chr17:74969165 | AGCCC | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(194): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.66+3422_66+3425del others(4): Show |
HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969165 | |||||||
chr17:74969205 | T | G | 1 | a0001c0008t0001g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.66+3386A>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969205 | |||||||
chr17:74969295 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.66+3296G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969295 | |||||||
chr17:74969530 | G | T | 4 | a0001c0001t0001g0197 a0001c0002t0002g0011 a0001c0002t0003g0198 others(1): Show |
8 | HG01081.hp1 HG01928.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+3061C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969530 | |||||||
chr17:74969829 | G | C | 3 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0203 |
3 | HG02698.hp2 HG03017.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.66+2762C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969829 | |||||||
chr17:74969893 | G | A | 2 | a0001c0005t0002g0172 a0001c0005t0002g0173 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.66+2698C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969893 | |||||||
chr17:74969922 | C | CT | 128 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0027 others(125): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.66+2668dupA | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969922 | |||||||
chr17:74969922 | C | CTT | 9 | a0001c0001t0001g0047 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
9 | HG01261.hp1 HG01516.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+2667_66+2668dup others(2): Show |
HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969922 | |||||||
chr17:74969922 | C | CTTT | 21 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0185 others(18): Show |
35 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.66+2666_66+2668dup others(3): Show |
HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969922 | |||||||
chr17:74969922 | C | CTTTT | 9 | a0001c0001t0001g0179 a0001c0001t0004g0205 a0001c0003t0003g0180 others(6): Show |
9 | HG01069.hp2 HG02056.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+2665_66+2668dup others(4): Show |
HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969922 | |||||||
chr17:74969968 | A | G | 1 | a0001c0004t0001g0048 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.66+2623T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74969968 | |||||||
chr17:74970066 | T | G | 32 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0179 others(29): Show |
46 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.66+2525A>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74970066 | |||||||
chr17:74970106 | G | A | 1 | a0001c0003t0003g0174 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.66+2485C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74970106 | |||||||
chr17:74970122 | G | A | 1 | a0001c0008t0001g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.66+2469C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74970122 | |||||||
chr17:74970210 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.66+2381G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74970210 | |||||||
chr17:74970364 | G | A | 1 | a0001c0020t0011g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.66+2227C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74970364 | |||||||
chr17:74970554 | G | A | 1 | a0001c0004t0001g0072 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.66+2037C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74970554 | |||||||
chr17:74971080 | G | T | 3 | a0001c0004t0001g0012 a0001c0004t0001g0082 a0001c0024t0001g0083 |
6 | HG01891.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+1511C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74971080 | |||||||
chr17:74971089 | G | T | 11 | a0001c0004t0001g0077 a0001c0004t0001g0079 a0001c0004t0001g0080 others(8): Show |
14 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.66+1502C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74971089 | |||||||
chr17:74971183 | A | C | 32 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0179 others(29): Show |
46 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.66+1408T>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74971183 | |||||||
chr17:74971290 | C | T | 1 | a0001c0010t0001g0178 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.66+1301G>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74971290 | |||||||
chr17:74971417 | G | A | 3 | a0001c0006t0001g0037 a0001c0020t0011g0177 a0001c0021t0006g0176 |
4 | HG02809.hp1 HG02886.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+1174C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74971417 | |||||||
chr17:74971645 | C | A | 32 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0179 others(29): Show |
46 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.66+946G>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74971645 | |||||||
chr17:74971679 | G | A | 1 | a0001c0002t0002g0040 | 2 | HG00438.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.66+912C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74971679 | |||||||
chr17:74971697 | G | A | 7 | a0001c0001t0001g0197 a0001c0002t0002g0011 a0001c0002t0002g0040 others(4): Show |
12 | HG00438.hp1 HG01081.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+894C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74971697 | |||||||
chr17:74971705 | G | C | 1 | a0001c0002t0002g0202 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.66+886C>G | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74971705 | |||||||
chr17:74971722 | G | A | 6 | a0001c0001t0004g0009 a0001c0001t0004g0205 a0001c0001t0004g0206 others(3): Show |
11 | HG01243.hp2 HG02145.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.66+869C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74971722 | |||||||
chr17:74972059 | G | T | 34 | a0001c0001t0001g0052 a0001c0003t0003g0016 a0001c0003t0003g0022 others(31): Show |
67 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.66+532C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74972059 | |||||||
chr17:74972208 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.66+383C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74972208 | |||||||
chr17:74972217 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.66+374C>A | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74972217 | |||||||
chr17:74972225 | C | G | 2 | a0004c0014t0001g0045 a0004c0014t0001g0046 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.66+366G>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74972225 | |||||||
chr17:74972372 | G | A | 1 | a0001c0004t0001g0204 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.66+219C>T | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74972372 | |||||||
chr17:74972515 | A | G | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.66+76T>C | HID1 | ENSG00000167861.16 | transcript | ENST00000425042.7 | protein_coding | 1/18 | chr17 | 74972515 |