Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3081 |
| ensemblid | ENSG00000113924.12 |
| hgncid | 4892 |
| symbol | HGD |
| name | homogentisate 1,2-dioxygenase |
| refseq_nuc | NM_000187.4 |
| refseq_prot | NP_000178.2 |
| ensembl_nuc | ENST00000283871.10 |
| ensembl_prot | ENSP00000283871.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 120628172 |
| end | 120682239 |
| strand | - |
| ver | v1.2 |
| region | chr3:120628172-120682239 |
| region5000 | chr3:120623172-120687239 |
| regionname0 | HGD_chr3_120628172_120682239 |
| regionname5000 | HGD_chr3_120623172_120687239 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 445 | 249 | 67 | 61 | 83 | 12 | 25 | 65 | HGD_chr3_120623172_120687239 | HGD | MAELK others(440): Show |
chr3 | 120623172 | 120687239 |
| a0002 | 1/0 | 445 | 115 | 15 | 12 | 64 | 4 | 19 | 48 | HGD_chr3_120623172_120687239 | HGD | MAELK others(440): Show |
chr3 | 120623172 | 120687239 |
| a0003 | 0/0 | 445 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | MAELK others(440): Show |
chr3 | 120623172 | 120687239 |
| a0004 | 0/0 | 445 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | MAELK others(440): Show |
chr3 | 120623172 | 120687239 |
| a0005 | 0/0 | 445 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | MAELK others(440): Show |
chr3 | 120623172 | 120687239 |
| a0006 | 0/0 | 445 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | MAELK others(440): Show |
chr3 | 120623172 | 120687239 |
| a0007 | 0/0 | 445 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | MAELK others(440): Show |
chr3 | 120623172 | 120687239 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1335 | 236 | 63 | 58 | 82 | 9 | 23 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 | ||
| a0001c0003 | 0/0 | 1335 | 5 | 4 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 | ||
| a0001c0004 | 0/0 | 1335 | 5 | 0 | 1 | 1 | 2 | 1 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 | ||
| a0001c0006 | 0/0 | 1335 | 3 | 0 | 2 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 | ||
| a0002c0002 | 1/0 | 1335 | 112 | 13 | 12 | 63 | 4 | 19 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 | ||
| a0002c0007 | 0/0 | 1335 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 | ||
| a0002c0010 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 | ||
| a0003c0005 | 0/0 | 1335 | 5 | 4 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 | ||
| a0004c0008 | 0/0 | 1335 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 | ||
| a0005c0011 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 | ||
| a0006c0012 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 | ||
| a0007c0009 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | ATGGC others(1330): Show |
chr3 | 120623172 | 120687239 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1674 | 235 | 63 | 57 | 82 | 9 | 23 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0001c0001t0002 | 0/0 | 1674 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0001c0003t0001 | 0/0 | 1674 | 5 | 4 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0001c0004t0001 | 0/0 | 1674 | 5 | 0 | 1 | 1 | 2 | 1 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0001c0006t0001 | 0/0 | 1674 | 3 | 0 | 2 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0002c0002t0001 | 1/0 | 1674 | 112 | 13 | 12 | 63 | 4 | 19 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0002c0007t0001 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0002c0010t0001 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0003c0005t0001 | 0/0 | 1674 | 5 | 4 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0004c0008t0001 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0005c0011t0001 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0006c0012t0001 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| a0007c0009t0001 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | AGTGA others(1669): Show |
chr3 | 120623172 | 120687239 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0001g0348 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0006t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0001c0006t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0007t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0007t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0002c0010t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0003c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0003c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0003c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0003c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0003c0005t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0004c0008t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0004c0008t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0005c0011t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0006c0012t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| a0007c0009t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0305 | EUR | GBR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0291 | EUR | FIN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0338 | EUR | FIN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | FIN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0312 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0298 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01099 | hp1 | a0003 | c0005 | t0001 | g0032 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0068 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0329 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01192 | hp2 | a0001 | c0006 | t0001 | g0015 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0304 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01496 | hp1 | a0001 | c0006 | t0001 | g0015 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0019 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01516 | hp2 | a0001 | c0004 | t0001 | g0067 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0019 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01884 | hp1 | a0005 | c0011 | t0001 | g0041 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0296 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0299 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0293 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0297 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02132 | hp2 | a0001 | c0004 | t0001 | g0076 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | CDX | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0308 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0258 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0267 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02622 | hp2 | a0004 | c0008 | t0001 | g0049 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0290 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0283 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0179 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0306 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02809 | hp1 | a0003 | c0005 | t0001 | g0028 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0260 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0177 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0320 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0294 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0070 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03209 | hp2 | a0006 | c0012 | t0001 | g0050 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0292 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0295 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03453 | hp1 | a0004 | c0008 | t0001 | g0054 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0058 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0269 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0257 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0327 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03579 | hp1 | a0002 | c0007 | t0001 | g0256 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0303 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0343 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0243 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03704 | hp1 | a0001 | c0006 | t0001 | g0221 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0018 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0339 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0302 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0272 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0326 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0317 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0307 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0340 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0088 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0347 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18983 | hp2 | a0007 | c0009 | t0001 | g0314 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18990 | hp1 | a0002 | c0010 | t0001 | g0315 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ASW | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0111 | EUR | TSI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0123 | EUR | TSI | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0259 | SAS | GIH | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | GIH | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02109 | hp1 | a0003 | c0005 | t0001 | g0029 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02109 | hp2 | a0003 | c0005 | t0001 | g0031 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02559 | hp1 | a0002 | c0007 | t0001 | g0321 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | USA | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | USA | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA20300 | hp2 | a0003 | c0005 | t0001 | g0030 | AFR | USA | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0348 | REF | REF | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0288 | REF | REF | HGD_chr3_120623172_120687239 | HGD | chr3 | 120623172 | 120687239 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:120633207 | G | C | 1 | a0005 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1128C>G | p.Asp376Glu | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/14 | 1256/1674 | 1128/1338 | 376/445 | chr3 | 120633207 | |||
| chr3:120638538 | G | C | 1 | a0007 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.923C>G | p.Pro308Arg | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/14 | 1051/1674 | 923/1338 | 308/445 | chr3 | 120638538 | |||
| chr3:120638542 | G | A | 1 | a0006 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.919C>T | p.Arg307Cys | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/14 | 1047/1674 | 919/1338 | 307/445 | chr3 | 120638542 | |||
| chr3:120638566 | T | C | 1 | a0004 | 2 | HG02622.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.895A>G | p.Thr299Ala | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/14 | 1023/1674 | 895/1338 | 299/445 | chr3 | 120638566 | |||
| chr3:120670469 | T | A | 5 | a0001 a0003 a0004 others(2): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
missense_variant | MODERATE | c.240A>T | p.Gln80His | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/14 | 368/1674 | 240/1338 | 80/445 | chr3 | 120670469 | |||
| chr3:120674935 | C | A | 1 | a0003 | 5 | HG01099.hp1 HG02109.hp1 HG02109.hp2 others(2): Show |
missense_variant | MODERATE | c.142G>T | p.Ala48Ser | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/14 | 270/1674 | 142/1338 | 48/445 | chr3 | 120674935 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:120628497 | C | T | 2 | a0001c0003 a0002c0007 |
7 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(4): Show |
synonymous_variant | LOW | c.1221G>A | p.Ala407Ala | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 14/14 | 1349/1674 | 1221/1338 | 407/445 | chr3 | 120628497 | |||
| chr3:120628527 | T | G | 1 | a0001c0004 | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.1191A>C | p.Ala397Ala | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 14/14 | 1319/1674 | 1191/1338 | 397/445 | chr3 | 120628527 | |||
| chr3:120633156 | A | G | 1 | a0001c0006 | 3 | HG01192.hp2 HG01496.hp1 HG03704.hp1 |
synonymous_variant | LOW | c.1179T>C | p.Asp393Asp | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/14 | 1307/1674 | 1179/1338 | 393/445 | chr3 | 120633156 | |||
| chr3:120647048 | C | A | 1 | a0002c0010 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.474G>T | p.Pro158Pro | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 8/14 | 602/1674 | 474/1338 | 158/445 | chr3 | 120647048 | |||
| chr3:120650836 | G | A | 1 | a0001c0004 | 5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
synonymous_variant | LOW | c.372C>T | p.Asp124Asp | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/14 | 500/1674 | 372/1338 | 124/445 | chr3 | 120650836 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:120682219 | A | G | 1 | a0001c0001t0002 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-108T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/14 | 108 | chr3 | 120682219 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:120629343 | C | T | 6 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 others(3): Show |
6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189-814G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120629343 | |||||||
| chr3:120629444 | A | G | 1 | a0006c0012t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1189-915T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120629444 | |||||||
| chr3:120629618 | G | A | 1 | a0006c0012t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1189-1089C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120629618 | |||||||
| chr3:120629868 | G | A | 1 | a0005c0011t0001g0041 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1189-1339C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120629868 | |||||||
| chr3:120629920 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1189-1391T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120629920 | |||||||
| chr3:120630033 | A | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1189-1504T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630033 | |||||||
| chr3:120630470 | G | A | 6 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 others(3): Show |
6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189-1941C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630470 | |||||||
| chr3:120630556 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1189-2027T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630556 | |||||||
| chr3:120630594 | C | T | 66 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(63): Show |
68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1189-2065G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630594 | |||||||
| chr3:120630684 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1189-2155G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630684 | |||||||
| chr3:120630708 | A | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1189-2179T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630708 | |||||||
| chr3:120630798 | T | TATATATA others(4): Show |
1 | a0002c0002t0001g0325 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1189-2270_1189-226 others(15): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TATATATA others(14): Show |
1 | a0001c0001t0001g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1189-2270_1189-226 others(25): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTA | 12 | a0001c0001t0001g0057 a0001c0001t0001g0105 a0001c0001t0001g0113 others(9): Show |
13 | HG01099.hp1 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1189-2271_1189-227 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATA | 13 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0056 others(10): Show |
13 | HG00280.hp1 HG00735.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1189-2273_1189-227 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATA | 16 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0062 others(13): Show |
16 | HG00738.hp2 HG01109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1189-2275_1189-227 others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0053 a0001c0001t0001g0099 a0001c0003t0001g0070 |
3 | HG00741.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1189-2277_1189-227 others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0034 a0002c0002t0001g0274 |
2 | HG01891.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1189-2279_1189-227 others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATAT others(5): Show |
8 | a0001c0001t0001g0043 a0001c0001t0001g0083 a0001c0003t0001g0088 others(5): Show |
8 | HG02717.hp1 HG02717.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-2281_1189-227 others(16): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATAT others(7): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0135 a0001c0001t0001g0231 |
4 | HG02572.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1189-2283_1189-227 others(18): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0234 |
2 | NA18993.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1189-2285_1189-227 others(20): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATAT others(11): Show |
9 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0052 others(6): Show |
12 | HG02451.hp2 HG02486.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1189-2287_1189-227 others(22): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATAT others(13): Show |
6 | a0001c0001t0001g0047 a0001c0001t0001g0082 a0002c0002t0001g0182 others(3): Show |
6 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-2289_1189-227 others(24): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATAT others(15): Show |
4 | a0001c0001t0001g0059 a0001c0001t0001g0162 a0002c0002t0001g0260 others(1): Show |
4 | HG00639.hp1 HG01175.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1189-2291_1189-227 others(26): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATAT others(17): Show |
1 | a0004c0008t0001g0054 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1189-2293_1189-227 others(28): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATAT others(19): Show |
1 | a0001c0001t0001g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1189-2295_1189-227 others(30): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | T | TTATATAT others(21): Show |
1 | a0001c0001t0001g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1189-2297_1189-227 others(32): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | TTA | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(93): Show |
106 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1189-2271_1189-227 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | TTATATA | T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0104 others(28): Show |
35 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1189-2275_1189-227 others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | TTATATAT others(1): Show |
T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0152 |
3 | HG02055.hp2 NA18944.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1189-2277_1189-227 others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630798 | TTATATAT others(3): Show |
T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0073 |
2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1189-2279_1189-227 others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630798 | |||||||
| chr3:120630823 | T | TACAC | 3 | a0001c0001t0001g0197 a0002c0002t0001g0263 a0002c0002t0001g0285 |
3 | HG00621.hp2 HG02071.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1189-2295_1189-229 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630823 | |||||||
| chr3:120630825 | T | TATACAC | 14 | a0001c0001t0001g0063 a0001c0001t0001g0108 a0001c0001t0001g0144 others(11): Show |
15 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | |||||||
| chr3:120630825 | T | TATATACA others(1): Show |
4 | a0001c0001t0001g0064 a0001c0001t0001g0190 a0002c0002t0001g0294 others(1): Show |
4 | HG02145.hp1 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | |||||||
| chr3:120630825 | T | TATATATA others(1): Show |
13 | a0001c0001t0001g0007 a0001c0001t0001g0102 a0001c0001t0001g0103 others(10): Show |
14 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | |||||||
| chr3:120630825 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0060 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1189-2297_1189-229 others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | |||||||
| chr3:120630825 | T | TATATATA others(3): Show |
4 | a0001c0001t0001g0100 a0001c0001t0001g0156 a0002c0002t0001g0249 others(1): Show |
4 | HG00639.hp2 HG02083.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | |||||||
| chr3:120630825 | T | TATATATA others(5): Show |
2 | a0001c0001t0001g0208 a0002c0002t0001g0320 |
2 | HG02970.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(16): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | |||||||
| chr3:120630825 | T | TATATATA others(9): Show |
2 | a0002c0002t0001g0259 a0002c0002t0001g0299 |
2 | HG01975.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1189-2297_1189-229 others(20): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | |||||||
| chr3:120630825 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0336 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1189-2297_1189-229 others(30): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | |||||||
| chr3:120630825 | T | TATATATA others(23): Show |
1 | a0001c0001t0001g0101 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1189-2297_1189-229 others(34): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630825 | |||||||
| chr3:120630827 | C | T | 82 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(79): Show |
86 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1189-2298G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630827 | |||||||
| chr3:120630829 | C | T | 64 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(61): Show |
67 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1189-2300G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630829 | |||||||
| chr3:120630831 | T | C | 31 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0071 others(28): Show |
32 | HG00280.hp1 HG00621.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1189-2302A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | |||||||
| chr3:120630831 | T | TATAC | 6 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0184 others(3): Show |
7 | HG01516.hp1 HG01517.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | |||||||
| chr3:120630831 | T | TATATAC | 3 | a0001c0001t0001g0344 a0002c0002t0001g0267 a0003c0005t0001g0030 |
3 | HG02602.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | |||||||
| chr3:120630831 | T | TATATATA others(1): Show |
3 | a0002c0002t0001g0289 a0002c0002t0001g0290 a0002c0002t0001g0304 |
3 | HG01433.hp1 HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | |||||||
| chr3:120630831 | T | TATATATA others(5): Show |
5 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0081 others(2): Show |
6 | HG02258.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(16): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | |||||||
| chr3:120630831 | T | TATATATA others(7): Show |
2 | a0001c0001t0001g0089 a0002c0002t0001g0253 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(18): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | |||||||
| chr3:120630831 | T | TATATATA others(9): Show |
3 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0133 |
4 | HG00099.hp2 HG01515.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-2303_1189-230 others(20): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630831 | |||||||
| chr3:120630833 | C | T | 5 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0116 others(2): Show |
5 | HG02896.hp1 HG03098.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-2304G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630833 | |||||||
| chr3:120630835 | C | CACAT | 23 | a0001c0001t0001g0174 a0001c0001t0001g0194 a0001c0001t0001g0222 others(20): Show |
23 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1189-2307_1189-230 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630835 | |||||||
| chr3:120630835 | C | CAT | 7 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0095 others(4): Show |
7 | HG01346.hp1 HG01928.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189-2307_1189-230 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630835 | |||||||
| chr3:120630835 | C | T | 43 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(40): Show |
47 | HG00099.hp2 HG00280.hp1 HG01433.hp1 others(44): Show |
intron_variant | MODIFIER | c.1189-2306G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630835 | |||||||
| chr3:120630837 | C | T | 16 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0057 others(13): Show |
16 | HG00621.hp2 HG01099.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1189-2308G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630837 | |||||||
| chr3:120630839 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1188+2308G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630839 | |||||||
| chr3:120630843 | T | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(88): Show |
95 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1188+2304A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | |||||||
| chr3:120630843 | T | TAC | 18 | a0001c0001t0001g0051 a0001c0001t0001g0061 a0001c0001t0001g0080 others(15): Show |
18 | HG00735.hp1 HG01071.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1188+2302_1188+230 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | |||||||
| chr3:120630843 | T | TACAC | 9 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0117 others(6): Show |
10 | HG01099.hp2 HG02027.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.1188+2300_1188+230 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | |||||||
| chr3:120630843 | T | TACACACA others(3): Show |
4 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(1): Show |
4 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1188+2294_1188+230 others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | |||||||
| chr3:120630843 | TAC | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.1188+2302_1188+230 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | |||||||
| chr3:120630843 | TACAC | T | 20 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0066 others(17): Show |
22 | HG00558.hp2 HG00639.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1188+2300_1188+230 others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | |||||||
| chr3:120630843 | TACACAC | T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0136 a0001c0001t0001g0210 others(3): Show |
6 | HG02280.hp2 HG02523.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+2298_1188+230 others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630843 | |||||||
| chr3:120630845 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1188+2302G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630845 | |||||||
| chr3:120630847 | C | T | 72 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(69): Show |
76 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1188+2300G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630847 | |||||||
| chr3:120630849 | C | T | 13 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0057 others(10): Show |
13 | HG01099.hp1 HG01109.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1188+2298G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630849 | |||||||
| chr3:120630851 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1188+2296G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630851 | |||||||
| chr3:120630859 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1188+2288G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630859 | |||||||
| chr3:120630874 | A | G | 5 | a0001c0001t0001g0057 a0001c0001t0001g0071 a0003c0005t0001g0028 others(2): Show |
5 | HG01099.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1188+2273T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630874 | |||||||
| chr3:120630937 | C | T | 12 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0040 others(9): Show |
12 | HG00735.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1188+2210G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630937 | |||||||
| chr3:120630940 | C | T | 9 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0344 others(6): Show |
9 | HG02559.hp1 HG02922.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1188+2207G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630940 | |||||||
| chr3:120630961 | T | C | 8 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0051 others(5): Show |
8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1188+2186A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120630961 | |||||||
| chr3:120631399 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0225 |
2 | HG02148.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1188+1748C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631399 | |||||||
| chr3:120631451 | C | A | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1188+1696G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631451 | |||||||
| chr3:120631481 | CTTA | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(37): Show |
45 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1188+1663_1188+166 others(7): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631481 | |||||||
| chr3:120631570 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1188+1577G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631570 | |||||||
| chr3:120631658 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0073 |
2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1188+1489T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631658 | |||||||
| chr3:120631790 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1188+1357T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631790 | |||||||
| chr3:120631897 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1188+1250G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631897 | |||||||
| chr3:120631978 | C | T | 6 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 others(3): Show |
6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1188+1169G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120631978 | |||||||
| chr3:120632031 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1188+1116C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632031 | |||||||
| chr3:120632078 | T | C | 2 | a0001c0001t0001g0147 a0002c0002t0001g0317 |
2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1188+1069A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632078 | |||||||
| chr3:120632086 | C | T | 6 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 others(3): Show |
6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1188+1061G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632086 | |||||||
| chr3:120632089 | C | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0051 others(5): Show |
8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1188+1058G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632089 | |||||||
| chr3:120632151 | C | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1188+996G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632151 | |||||||
| chr3:120632448 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1188+699T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632448 | |||||||
| chr3:120632503 | G | A | 1 | a0002c0002t0001g0260 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1188+644C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632503 | |||||||
| chr3:120632504 | C | T | 1 | a0002c0002t0001g0260 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1188+643G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632504 | |||||||
| chr3:120632616 | C | T | 1 | a0002c0002t0001g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1188+531G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632616 | |||||||
| chr3:120632764 | A | C | 11 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 others(8): Show |
11 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1188+383T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632764 | |||||||
| chr3:120632768 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1188+379C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632768 | |||||||
| chr3:120632778 | G | A | 14 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0150 others(11): Show |
14 | HG00609.hp2 HG00621.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188+369C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632778 | |||||||
| chr3:120632787 | G | T | 1 | a0001c0001t0001g0242 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1188+360C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632787 | |||||||
| chr3:120632804 | C | T | 4 | a0002c0002t0001g0289 a0002c0002t0001g0290 a0002c0002t0001g0304 others(1): Show |
4 | HG01433.hp1 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1188+343G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632804 | |||||||
| chr3:120632944 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
81 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.1188+203G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120632944 | |||||||
| chr3:120633005 | C | A | 66 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(63): Show |
68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1188+142G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120633005 | |||||||
| chr3:120633081 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1188+66C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120633081 | |||||||
| chr3:120633096 | T | C | 23 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0040 others(20): Show |
23 | HG00735.hp1 HG01106.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.1188+51A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120633096 | |||||||
| chr3:120633118 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1188+29G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 13/13 | chr3 | 120633118 | |||||||
| chr3:120633679 | G | A | 1 | a0002c0002t0001g0323 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1007-351C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120633679 | |||||||
| chr3:120633719 | C | T | 11 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 others(8): Show |
11 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-391G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120633719 | |||||||
| chr3:120633796 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-468C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120633796 | |||||||
| chr3:120633863 | C | T | 1 | a0002c0002t0001g0274 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1007-535G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120633863 | |||||||
| chr3:120633942 | CTTCTA | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0132 a0001c0001t0001g0151 others(1): Show |
5 | NA18957.hp1 NA18995.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007-619_1007-615d others(7): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120633942 | |||||||
| chr3:120634053 | C | G | 31 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0063 others(28): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1007-725G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634053 | |||||||
| chr3:120634123 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1007-795G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634123 | |||||||
| chr3:120634129 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-801C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634129 | |||||||
| chr3:120634167 | C | T | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007-839G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634167 | |||||||
| chr3:120634250 | T | C | 3 | a0001c0001t0001g0006 a0002c0002t0001g0261 a0002c0002t0001g0262 |
4 | HG00639.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007-922A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634250 | |||||||
| chr3:120634368 | C | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1007-1040G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634368 | |||||||
| chr3:120634551 | A | G | 1 | a0002c0002t0001g0182 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1007-1223T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634551 | |||||||
| chr3:120634694 | G | C | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1007-1366C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634694 | |||||||
| chr3:120634896 | A | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1007-1568T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120634896 | |||||||
| chr3:120635065 | C | T | 6 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 others(3): Show |
6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007-1737G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635065 | |||||||
| chr3:120635367 | C | T | 3 | a0001c0001t0001g0163 a0002c0002t0001g0279 a0002c0002t0001g0328 |
3 | NA18940.hp2 NA18961.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1007-2039G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635367 | |||||||
| chr3:120635474 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1007-2146G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635474 | |||||||
| chr3:120635476 | C | CA | 6 | a0001c0001t0001g0151 a0001c0001t0001g0163 a0001c0001t0001g0190 others(3): Show |
6 | HG03927.hp2 HG04184.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007-2149dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635476 | |||||||
| chr3:120635476 | CA | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1007-2149delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635476 | |||||||
| chr3:120635476 | CAA | C | 7 | a0001c0001t0001g0116 a0001c0001t0001g0140 a0001c0001t0001g0184 others(4): Show |
7 | HG02896.hp1 HG02965.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1007-2150_1007-214 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635476 | |||||||
| chr3:120635644 | G | A | 11 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 others(8): Show |
11 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-2316C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635644 | |||||||
| chr3:120635674 | G | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0072 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1007-2346C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635674 | |||||||
| chr3:120635686 | C | A | 1 | a0001c0001t0001g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1007-2358G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635686 | |||||||
| chr3:120635928 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1006+2527T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120635928 | |||||||
| chr3:120636099 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1006+2356G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636099 | |||||||
| chr3:120636116 | C | CA | 32 | a0001c0001t0001g0023 a0001c0001t0001g0057 a0001c0001t0001g0060 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1006+2338dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636116 | |||||||
| chr3:120636116 | CA | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
213 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1006+2338delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636116 | |||||||
| chr3:120636116 | CAA | C | 20 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0040 others(17): Show |
20 | HG00735.hp1 HG01891.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1006+2337_1006+233 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636116 | |||||||
| chr3:120636125 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1006+2330T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636125 | |||||||
| chr3:120636139 | G | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(42): Show |
50 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1006+2316C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636139 | |||||||
| chr3:120636162 | C | G | 12 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0001g0144 others(9): Show |
13 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.1006+2293G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636162 | |||||||
| chr3:120636177 | G | C | 8 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0051 others(5): Show |
8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+2278C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636177 | |||||||
| chr3:120636184 | C | T | 1 | a0002c0002t0001g0171 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1006+2271G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636184 | |||||||
| chr3:120636280 | C | CA | 15 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0120 others(12): Show |
15 | HG00140.hp2 HG00673.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1006+2174dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636280 | |||||||
| chr3:120636280 | CA | C | 6 | a0001c0001t0001g0175 a0001c0004t0001g0067 a0001c0004t0001g0068 others(3): Show |
6 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006+2174delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636280 | |||||||
| chr3:120636518 | C | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0051 others(5): Show |
8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006+1937G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636518 | |||||||
| chr3:120636522 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(42): Show |
50 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1006+1933G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636522 | |||||||
| chr3:120636674 | T | C | 3 | a0002c0002t0001g0276 a0002c0002t0001g0277 a0002c0002t0001g0278 |
3 | NA18986.hp1 NA19056.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1006+1781A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636674 | |||||||
| chr3:120636757 | T | C | 1 | a0002c0002t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1006+1698A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636757 | |||||||
| chr3:120636872 | G | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(38): Show |
46 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1006+1583C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636872 | |||||||
| chr3:120636948 | G | C | 6 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 others(3): Show |
6 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006+1507C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120636948 | |||||||
| chr3:120637214 | A | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1006+1241T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637214 | |||||||
| chr3:120637224 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1006+1231G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637224 | |||||||
| chr3:120637257 | T | G | 1 | a0002c0002t0001g0306 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1006+1198A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637257 | |||||||
| chr3:120637307 | G | GA | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1006+1147dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637307 | |||||||
| chr3:120637307 | G | GAA | 8 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0107 others(5): Show |
8 | HG00639.hp2 HG00673.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006+1146_1006+114 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637307 | |||||||
| chr3:120637307 | GAA | G | 19 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0051 others(16): Show |
19 | HG00735.hp1 HG01106.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.1006+1146_1006+114 others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637307 | |||||||
| chr3:120637385 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1006+1070A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637385 | |||||||
| chr3:120637600 | GTCTCTCT others(5): Show |
G | 11 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 others(8): Show |
11 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1006+843_1006+854d others(14): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637600 | |||||||
| chr3:120637610 | CTCTCTCT others(3): Show |
C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0061 a0001c0001t0001g0085 |
3 | HG00735.hp1 HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1006+835_1006+844d others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637610 | |||||||
| chr3:120637701 | A | G | 1 | a0002c0002t0001g0179 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1006+754T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637701 | |||||||
| chr3:120637767 | C | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(32): Show |
38 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1006+688G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637767 | |||||||
| chr3:120637890 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1006+565T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120637890 | |||||||
| chr3:120638099 | C | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0078 a0001c0001t0001g0095 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1006+356G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120638099 | |||||||
| chr3:120638142 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1006+313A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120638142 | |||||||
| chr3:120638194 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1006+261G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120638194 | |||||||
| chr3:120638255 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1006+200G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120638255 | |||||||
| chr3:120638306 | G | A | 1 | a0002c0002t0001g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1006+149C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 12/13 | chr3 | 120638306 | |||||||
| chr3:120638608 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.880-27G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120638608 | |||||||
| chr3:120638611 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.880-30T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120638611 | |||||||
| chr3:120638694 | T | C | 7 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(4): Show |
7 | HG00639.hp2 HG01081.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-113A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120638694 | |||||||
| chr3:120638749 | C | G | 1 | a0002c0002t0001g0166 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.880-168G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120638749 | |||||||
| chr3:120639050 | C | G | 2 | a0001c0001t0001g0195 a0002c0002t0001g0284 |
2 | HG02015.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.880-469G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639050 | |||||||
| chr3:120639114 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.880-533G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639114 | |||||||
| chr3:120639466 | G | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | NA18948.hp1 NA18999.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.880-885C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639466 | |||||||
| chr3:120639537 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.880-956A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639537 | |||||||
| chr3:120639574 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0056 |
3 | HG01891.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.880-993C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639574 | |||||||
| chr3:120639856 | AAAT | A | 3 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 |
3 | HG03195.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.880-1278_880-1276d others(5): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639856 | |||||||
| chr3:120639910 | AT | A | 3 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0003t0001g0088 |
3 | HG03195.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.880-1330delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639910 | |||||||
| chr3:120639992 | C | G | 1 | a0001c0001t0001g0011 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.880-1411G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639992 | |||||||
| chr3:120639993 | T | G | 1 | a0001c0001t0001g0011 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.880-1412A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120639993 | |||||||
| chr3:120640016 | G | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-1435C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640016 | |||||||
| chr3:120640121 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+1468C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640121 | |||||||
| chr3:120640149 | A | AGAAG | 16 | a0001c0001t0001g0003 a0001c0001t0001g0065 a0001c0001t0001g0079 others(13): Show |
18 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.879+1436_879+1439d others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640149 | |||||||
| chr3:120640179 | C | T | 66 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(63): Show |
68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.879+1410G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640179 | |||||||
| chr3:120640256 | G | A | 1 | a0001c0001t0001g0021 | 2 | NA18983.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.879+1333C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640256 | |||||||
| chr3:120640319 | T | C | 3 | a0001c0001t0001g0006 a0002c0002t0001g0261 a0002c0002t0001g0262 |
4 | HG00639.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+1270A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640319 | |||||||
| chr3:120640381 | G | A | 5 | a0001c0001t0001g0148 a0002c0002t0001g0018 a0002c0002t0001g0298 others(2): Show |
6 | HG00099.hp1 HG00140.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+1208C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640381 | |||||||
| chr3:120640405 | G | T | 66 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(63): Show |
68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.879+1184C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640405 | |||||||
| chr3:120640412 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.879+1177C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640412 | |||||||
| chr3:120640534 | A | G | 1 | a0001c0001t0001g0337 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.879+1055T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640534 | |||||||
| chr3:120640557 | A | G | 1 | a0003c0005t0001g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.879+1032T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640557 | |||||||
| chr3:120640574 | C | T | 62 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(59): Show |
64 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.879+1015G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640574 | |||||||
| chr3:120640622 | G | A | 7 | a0001c0003t0001g0058 a0001c0003t0001g0070 a0001c0004t0001g0067 others(4): Show |
7 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+967C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640622 | |||||||
| chr3:120640877 | G | C | 15 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0001g0144 others(12): Show |
16 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.879+712C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640877 | |||||||
| chr3:120640966 | C | T | 2 | a0001c0003t0001g0058 a0001c0003t0001g0070 |
2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.879+623G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640966 | |||||||
| chr3:120640998 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.879+591A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120640998 | |||||||
| chr3:120641029 | G | C | 74 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0033 others(71): Show |
76 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.879+560C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641029 | |||||||
| chr3:120641085 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0002c0002t0001g0253 |
3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.879+504G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641085 | |||||||
| chr3:120641164 | C | T | 65 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(62): Show |
67 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.879+425G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641164 | |||||||
| chr3:120641265 | C | T | 1 | a0002c0002t0001g0330 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.879+324G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641265 | |||||||
| chr3:120641484 | T | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(253): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.879+105A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641484 | |||||||
| chr3:120641525 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.879+64A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641525 | |||||||
| chr3:120641571 | T | C | 1 | a0002c0002t0001g0283 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.879+18A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 11/13 | chr3 | 120641571 | |||||||
| chr3:120641889 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.775-196G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120641889 | |||||||
| chr3:120641984 | T | G | 1 | a0001c0001t0001g0008 | 2 | HG00099.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.775-291A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120641984 | |||||||
| chr3:120642009 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.775-316T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642009 | |||||||
| chr3:120642106 | C | T | 1 | a0002c0002t0001g0289 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.775-413G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642106 | |||||||
| chr3:120642178 | A | G | 1 | a0002c0002t0001g0343 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.775-485T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642178 | |||||||
| chr3:120642218 | T | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0062 a0001c0001t0001g0086 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-525A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642218 | |||||||
| chr3:120642229 | T | C | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-536A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642229 | |||||||
| chr3:120642462 | A | G | 1 | a0001c0003t0001g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.775-769T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642462 | |||||||
| chr3:120642478 | G | T | 1 | a0002c0002t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.775-785C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642478 | |||||||
| chr3:120642544 | T | TGACATAT others(4): Show |
1 | a0001c0001t0001g0130 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.775-862_775-852dup others(11): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642544 | |||||||
| chr3:120642642 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.775-949T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642642 | |||||||
| chr3:120642682 | C | G | 1 | a0002c0002t0001g0247 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.775-989G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642682 | |||||||
| chr3:120642764 | C | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-1071G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642764 | |||||||
| chr3:120642805 | C | T | 1 | a0002c0002t0001g0168 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.775-1112G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642805 | |||||||
| chr3:120642887 | C | G | 1 | a0001c0001t0001g0005 | 2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.775-1194G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642887 | |||||||
| chr3:120642977 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.775-1284G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120642977 | |||||||
| chr3:120643050 | G | A | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+1269C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643050 | |||||||
| chr3:120643057 | A | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+1262T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643057 | |||||||
| chr3:120643163 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0112 others(1): Show |
4 | HG00738.hp2 HG00741.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+1156C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643163 | |||||||
| chr3:120643167 | G | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(45): Show |
53 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.774+1152C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643167 | |||||||
| chr3:120643417 | C | A | 1 | a0001c0001t0001g0211 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.774+902G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643417 | |||||||
| chr3:120643474 | C | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(45): Show |
53 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.774+845G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643474 | |||||||
| chr3:120643575 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0073 |
2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.774+744A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120643575 | |||||||
| chr3:120644014 | A | G | 65 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(62): Show |
67 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.774+305T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120644014 | |||||||
| chr3:120644116 | G | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(89): Show |
99 | HG00323.hp2 HG00639.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.774+203C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120644116 | |||||||
| chr3:120644153 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.774+166T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120644153 | |||||||
| chr3:120644201 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.774+118C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120644201 | |||||||
| chr3:120644233 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.774+86A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 10/13 | chr3 | 120644233 | |||||||
| chr3:120644481 | C | CA | 5 | a0002c0002t0001g0246 a0002c0002t0001g0250 a0002c0002t0001g0271 others(2): Show |
5 | NA18941.hp1 NA19011.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.650-39dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644481 | |||||||
| chr3:120644496 | A | G | 1 | a0002c0002t0001g0326 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.650-53T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644496 | |||||||
| chr3:120644528 | T | C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0021 others(19): Show |
25 | HG02015.hp2 HG02129.hp1 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.650-85A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644528 | |||||||
| chr3:120644622 | G | A | 1 | a0002c0002t0001g0343 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.650-179C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644622 | |||||||
| chr3:120644676 | T | A | 1 | a0002c0002t0001g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.650-233A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644676 | |||||||
| chr3:120644863 | A | G | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.650-420T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644863 | |||||||
| chr3:120644893 | CT | C | 65 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(62): Show |
67 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.650-451delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644893 | |||||||
| chr3:120644926 | T | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0026 others(17): Show |
22 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.650-483A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120644926 | |||||||
| chr3:120645160 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.650-717T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120645160 | |||||||
| chr3:120645294 | G | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(45): Show |
53 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.650-851C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120645294 | |||||||
| chr3:120645460 | A | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0057 others(31): Show |
37 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.649+807T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120645460 | |||||||
| chr3:120645464 | C | A | 1 | a0001c0001t0001g0011 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.649+803G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120645464 | |||||||
| chr3:120645599 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.649+668A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120645599 | |||||||
| chr3:120646073 | T | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0073 |
2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.649+194A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120646073 | |||||||
| chr3:120646163 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(58): Show |
66 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.649+104C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120646163 | |||||||
| chr3:120646182 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.649+85C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120646182 | |||||||
| chr3:120646208 | T | C | 1 | a0001c0001t0001g0007 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.649+59A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 9/13 | chr3 | 120646208 | |||||||
| chr3:120646656 | T | TA | 49 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(46): Show |
54 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.550-291dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 8/13 | chr3 | 120646656 | |||||||
| chr3:120646692 | G | A | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.549+281C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 8/13 | chr3 | 120646692 | |||||||
| chr3:120646784 | T | C | 66 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(63): Show |
68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.549+189A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 8/13 | chr3 | 120646784 | |||||||
| chr3:120647215 | A | G | 8 | a0001c0001t0001g0124 a0001c0001t0001g0158 a0002c0002t0001g0166 others(5): Show |
8 | HG00609.hp2 HG02074.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-163T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647215 | |||||||
| chr3:120647263 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0203 |
2 | HG02074.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.470-211C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647263 | |||||||
| chr3:120647314 | A | AG | 4 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0001g0153 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-263dupC | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647314 | |||||||
| chr3:120647341 | C | T | 1 | a0002c0002t0001g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.470-289G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647341 | |||||||
| chr3:120647391 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.470-339A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647391 | |||||||
| chr3:120647395 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.470-343G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647395 | |||||||
| chr3:120647675 | CA | C | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+201delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 7/13 | chr3 | 120647675 | |||||||
| chr3:120648056 | C | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0003t0001g0177 |
3 | HG02922.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.435-145G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648056 | |||||||
| chr3:120648232 | G | T | 283 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.435-321C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648232 | |||||||
| chr3:120648364 | G | A | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-453C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648364 | |||||||
| chr3:120648382 | G | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0002c0002t0001g0253 |
3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.435-471C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648382 | |||||||
| chr3:120648476 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0056 |
3 | HG01891.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.435-565G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648476 | |||||||
| chr3:120648555 | G | T | 66 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(63): Show |
68 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.435-644C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648555 | |||||||
| chr3:120648666 | T | C | 9 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(6): Show |
9 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.435-755A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648666 | |||||||
| chr3:120648799 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0073 |
2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.435-888G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648799 | |||||||
| chr3:120648838 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.435-927A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648838 | |||||||
| chr3:120648933 | G | A | 1 | a0001c0003t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.435-1022C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648933 | |||||||
| chr3:120648958 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0002c0002t0001g0253 |
3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.435-1047C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648958 | |||||||
| chr3:120648972 | C | T | 35 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0057 others(32): Show |
38 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(35): Show |
intron_variant | MODIFIER | c.435-1061G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120648972 | |||||||
| chr3:120649139 | C | CT | 7 | a0001c0001t0001g0112 a0001c0001t0001g0153 a0001c0001t0001g0161 others(4): Show |
7 | HG01243.hp1 HG02258.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.435-1229dupA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649139 | |||||||
| chr3:120649139 | CT | C | 8 | a0001c0001t0001g0095 a0001c0001t0001g0126 a0001c0001t0001g0186 others(5): Show |
8 | HG02735.hp1 HG03491.hp2 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.435-1229delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649139 | |||||||
| chr3:120649139 | CTT | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(185): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.435-1230_435-1229d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649139 | |||||||
| chr3:120649143 | T | C | 1 | a0002c0002t0001g0323 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.435-1232A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649143 | |||||||
| chr3:120649144 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.435-1233A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649144 | |||||||
| chr3:120649175 | C | A | 2 | a0001c0003t0001g0058 a0001c0003t0001g0070 |
2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.435-1264G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649175 | |||||||
| chr3:120649186 | G | A | 1 | a0006c0012t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.435-1275C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649186 | |||||||
| chr3:120649229 | G | A | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-1318C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649229 | |||||||
| chr3:120649231 | C | T | 62 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(59): Show |
64 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.435-1320G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649231 | |||||||
| chr3:120649286 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.435-1375C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649286 | |||||||
| chr3:120649353 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.434+1421A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649353 | |||||||
| chr3:120649423 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.434+1351C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649423 | |||||||
| chr3:120649438 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(31): Show |
38 | HG00639.hp1 HG01175.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.434+1336G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649438 | |||||||
| chr3:120649625 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0002c0002t0001g0253 |
3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.434+1149G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649625 | |||||||
| chr3:120649638 | G | A | 2 | a0002c0002t0001g0324 a0002c0002t0001g0325 |
2 | NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.434+1136C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649638 | |||||||
| chr3:120649674 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.434+1100G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649674 | |||||||
| chr3:120649675 | C | A | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+1099G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649675 | |||||||
| chr3:120649738 | G | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(199): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.434+1036C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649738 | |||||||
| chr3:120649824 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.434+950C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649824 | |||||||
| chr3:120649952 | C | G | 1 | a0001c0003t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.434+822G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120649952 | |||||||
| chr3:120650003 | A | T | 1 | a0001c0003t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.434+771T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650003 | |||||||
| chr3:120650014 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+760C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650014 | |||||||
| chr3:120650047 | T | C | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+727A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650047 | |||||||
| chr3:120650048 | A | T | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+726T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650048 | |||||||
| chr3:120650418 | C | T | 1 | a0002c0002t0001g0308 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.434+356G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650418 | |||||||
| chr3:120650490 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0191 |
2 | HG00323.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.434+284G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650490 | |||||||
| chr3:120650491 | G | A | 1 | a0001c0001t0001g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.434+283C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650491 | |||||||
| chr3:120650503 | C | T | 1 | a0002c0002t0001g0257 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.434+271G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650503 | |||||||
| chr3:120650728 | T | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(199): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.434+46A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 6/13 | chr3 | 120650728 | |||||||
| chr3:120650876 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.343-11G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120650876 | |||||||
| chr3:120651390 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.343-525A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651390 | |||||||
| chr3:120651427 | C | T | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-562G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651427 | |||||||
| chr3:120651545 | T | C | 36 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0057 others(33): Show |
39 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.343-680A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651545 | |||||||
| chr3:120651793 | T | C | 1 | a0001c0006t0001g0015 | 2 | HG01192.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.342+799A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651793 | |||||||
| chr3:120651801 | C | T | 69 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(66): Show |
71 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.342+791G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651801 | |||||||
| chr3:120651807 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.342+785T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651807 | |||||||
| chr3:120651857 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0002c0002t0001g0253 |
3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.342+735C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651857 | |||||||
| chr3:120651979 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.342+613C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120651979 | |||||||
| chr3:120652071 | G | A | 1 | a0001c0004t0001g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.342+521C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652071 | |||||||
| chr3:120652143 | G | A | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+449C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652143 | |||||||
| chr3:120652335 | TTAAG | T | 47 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(44): Show |
52 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.342+253_342+256del others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652335 | |||||||
| chr3:120652360 | A | G | 1 | a0002c0002t0001g0291 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.342+232T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652360 | |||||||
| chr3:120652522 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(88): Show |
100 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.342+70C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652522 | |||||||
| chr3:120652567 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.342+25C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652567 | |||||||
| chr3:120652570 | G | T | 1 | a0002c0002t0001g0275 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.342+22C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 5/13 | chr3 | 120652570 | |||||||
| chr3:120652655 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0042 |
3 | HG03041.hp1 HG03486.hp1 NA18522.hp2 |
splice_region_variant&intron_variant | LOW | c.283-4C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652655 | |||||||
| chr3:120652674 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.283-23C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652674 | |||||||
| chr3:120652683 | C | T | 1 | a0002c0002t0001g0283 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.283-32G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652683 | |||||||
| chr3:120652796 | A | G | 71 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0035 others(68): Show |
73 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.283-145T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652796 | |||||||
| chr3:120652796 | A | T | 1 | a0001c0001t0001g0193 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.283-145T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652796 | |||||||
| chr3:120652942 | T | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.283-291A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652942 | |||||||
| chr3:120652990 | G | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0002c0002t0001g0253 |
3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283-339C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120652990 | |||||||
| chr3:120653108 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.283-457G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653108 | |||||||
| chr3:120653192 | G | A | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-541C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653192 | |||||||
| chr3:120653279 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283-628A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653279 | |||||||
| chr3:120653401 | G | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-750C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653401 | |||||||
| chr3:120653474 | G | A | 9 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0051 others(6): Show |
9 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-823C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653474 | |||||||
| chr3:120653491 | G | T | 1 | a0002c0002t0001g0331 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.283-840C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653491 | |||||||
| chr3:120653504 | G | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(74): Show |
84 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.283-853C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653504 | |||||||
| chr3:120653693 | G | T | 63 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(60): Show |
65 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.283-1042C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120653693 | |||||||
| chr3:120654013 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.283-1362G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654013 | |||||||
| chr3:120654130 | G | A | 1 | a0001c0003t0001g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.283-1479C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654130 | |||||||
| chr3:120654191 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.283-1540T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654191 | |||||||
| chr3:120654336 | T | C | 2 | a0001c0001t0001g0122 a0001c0003t0001g0123 |
2 | HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.283-1685A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654336 | |||||||
| chr3:120654389 | G | A | 2 | a0001c0001t0002g0022 a0002c0002t0001g0270 |
2 | HG01109.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.283-1738C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654389 | |||||||
| chr3:120654438 | A | G | 1 | a0001c0001t0001g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.283-1787T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654438 | |||||||
| chr3:120654497 | T | C | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.283-1846A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654497 | |||||||
| chr3:120654541 | A | C | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0003t0001g0177 |
3 | HG02922.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.283-1890T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654541 | |||||||
| chr3:120654613 | C | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-1962G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654613 | |||||||
| chr3:120654840 | A | G | 2 | a0001c0001t0001g0081 a0002c0002t0001g0253 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283-2189T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654840 | |||||||
| chr3:120654948 | G | T | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.283-2297C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120654948 | |||||||
| chr3:120655039 | C | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283-2388G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655039 | |||||||
| chr3:120655049 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.283-2398A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655049 | |||||||
| chr3:120655095 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0026 others(15): Show |
20 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.283-2444G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655095 | |||||||
| chr3:120655138 | G | T | 2 | a0002c0007t0001g0256 a0002c0007t0001g0321 |
2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.283-2487C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655138 | |||||||
| chr3:120655167 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283-2516C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655167 | |||||||
| chr3:120655192 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.283-2541A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655192 | |||||||
| chr3:120655261 | G | A | 1 | a0001c0003t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.283-2610C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655261 | |||||||
| chr3:120655358 | C | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.283-2707G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655358 | |||||||
| chr3:120655370 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283-2719G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655370 | |||||||
| chr3:120655482 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.283-2831T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655482 | |||||||
| chr3:120655597 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283-2946A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655597 | |||||||
| chr3:120655623 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-2972C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655623 | |||||||
| chr3:120655761 | T | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(83): Show |
93 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.283-3110A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655761 | |||||||
| chr3:120655799 | T | A | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.283-3148A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655799 | |||||||
| chr3:120655863 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(78): Show |
88 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.283-3212G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655863 | |||||||
| chr3:120655864 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.283-3213T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120655864 | |||||||
| chr3:120656052 | C | G | 64 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0100 others(61): Show |
66 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.283-3401G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656052 | |||||||
| chr3:120656133 | T | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(83): Show |
93 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.283-3482A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656133 | |||||||
| chr3:120656214 | C | T | 1 | a0002c0002t0001g0275 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.283-3563G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656214 | |||||||
| chr3:120656247 | A | T | 2 | a0001c0001t0001g0174 a0002c0002t0001g0339 |
2 | HG02683.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.283-3596T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656247 | |||||||
| chr3:120656361 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.283-3710A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656361 | |||||||
| chr3:120656366 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.283-3715A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656366 | |||||||
| chr3:120656376 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.283-3725C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656376 | |||||||
| chr3:120656519 | A | G | 4 | a0002c0002t0001g0169 a0002c0002t0001g0255 a0002c0002t0001g0265 others(1): Show |
4 | HG00597.hp1 HG00621.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-3868T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656519 | |||||||
| chr3:120656563 | T | TG | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.283-3913dupC | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656563 | |||||||
| chr3:120656565 | G | C | 1 | a0001c0001t0001g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283-3914C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656565 | |||||||
| chr3:120656582 | C | T | 2 | a0001c0001t0001g0174 a0002c0002t0001g0339 |
2 | HG02683.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.283-3931G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656582 | |||||||
| chr3:120656603 | G | C | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.283-3952C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656603 | |||||||
| chr3:120656613 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.283-3962C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656613 | |||||||
| chr3:120656706 | C | T | 71 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(68): Show |
74 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.283-4055G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656706 | |||||||
| chr3:120656712 | C | A | 1 | a0002c0002t0001g0320 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.283-4061G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656712 | |||||||
| chr3:120656763 | G | A | 2 | a0002c0007t0001g0256 a0002c0007t0001g0321 |
2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.283-4112C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656763 | |||||||
| chr3:120656932 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0034 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.283-4281C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120656932 | |||||||
| chr3:120657004 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.283-4353C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657004 | |||||||
| chr3:120657168 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283-4517C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657168 | |||||||
| chr3:120657537 | T | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0034 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.283-4886A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657537 | |||||||
| chr3:120657548 | G | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.283-4897C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657548 | |||||||
| chr3:120657584 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0002c0002t0001g0253 |
3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283-4933G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657584 | |||||||
| chr3:120657812 | C | G | 1 | a0001c0001t0001g0232 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.283-5161G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657812 | |||||||
| chr3:120657818 | TGA | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(291): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.283-5169_283-5168d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657818 | |||||||
| chr3:120657825 | GAGAGAGA others(7): Show |
G | 1 | a0001c0001t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.283-5188_283-5175d others(16): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657825 | |||||||
| chr3:120657899 | C | T | 15 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0001g0144 others(12): Show |
16 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.283-5248G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657899 | |||||||
| chr3:120657943 | C | G | 9 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0051 others(6): Show |
9 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-5292G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657943 | |||||||
| chr3:120657981 | A | C | 46 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(43): Show |
51 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.283-5330T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120657981 | |||||||
| chr3:120658018 | A | G | 1 | a0002c0002t0001g0283 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.283-5367T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658018 | |||||||
| chr3:120658274 | G | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0057 others(34): Show |
40 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.283-5623C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658274 | |||||||
| chr3:120658292 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.283-5641A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658292 | |||||||
| chr3:120658349 | G | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.283-5698C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658349 | |||||||
| chr3:120658394 | C | A | 1 | a0002c0002t0001g0340 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.283-5743G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658394 | |||||||
| chr3:120658394 | C | G | 2 | a0001c0001t0001g0124 a0002c0002t0001g0172 |
2 | NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.283-5743G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658394 | |||||||
| chr3:120658440 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0036 others(23): Show |
29 | HG00639.hp1 HG01175.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.283-5789C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658440 | |||||||
| chr3:120658520 | A | G | 4 | a0002c0002t0001g0309 a0002c0002t0001g0310 a0002c0002t0001g0311 others(1): Show |
4 | NA18956.hp2 NA18957.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-5869T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658520 | |||||||
| chr3:120658582 | A | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | NA18941.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.283-5931T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658582 | |||||||
| chr3:120658603 | T | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(79): Show |
89 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.283-5952A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658603 | |||||||
| chr3:120658644 | C | T | 1 | a0002c0002t0001g0271 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.283-5993G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658644 | |||||||
| chr3:120658721 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0220 |
3 | HG02523.hp2 NA18988.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.283-6070C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658721 | |||||||
| chr3:120658920 | T | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(76): Show |
82 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.283-6269A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658920 | |||||||
| chr3:120658973 | C | T | 1 | a0002c0002t0001g0270 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.283-6322G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658973 | |||||||
| chr3:120658987 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.283-6336G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120658987 | |||||||
| chr3:120659096 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.283-6445G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659096 | |||||||
| chr3:120659114 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(93): Show |
105 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.283-6463A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659114 | |||||||
| chr3:120659125 | A | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.283-6474T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659125 | |||||||
| chr3:120659251 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.283-6600A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659251 | |||||||
| chr3:120659408 | G | A | 1 | a0001c0001t0001g0021 | 2 | NA18983.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.283-6757C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659408 | |||||||
| chr3:120659420 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.283-6769G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659420 | |||||||
| chr3:120659604 | A | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.283-6953T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659604 | |||||||
| chr3:120659723 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.283-7072G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659723 | |||||||
| chr3:120659743 | G | A | 3 | a0001c0001t0001g0057 a0003c0005t0001g0028 a0003c0005t0001g0032 |
3 | HG01099.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-7092C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659743 | |||||||
| chr3:120659879 | TC | T | 8 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0051 others(5): Show |
8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-7229delG | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659879 | |||||||
| chr3:120659934 | AAG | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(37): Show |
44 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.283-7285_283-7284d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659934 | |||||||
| chr3:120659936 | GA | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0145 others(1): Show |
4 | HG01106.hp2 HG01169.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-7286delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659936 | |||||||
| chr3:120659938 | GA | G | 16 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0065 others(13): Show |
19 | HG00558.hp2 HG01070.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.283-7288delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659938 | |||||||
| chr3:120659939 | A | G | 9 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0145 others(6): Show |
9 | HG00673.hp1 HG01106.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-7288T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659939 | |||||||
| chr3:120659941 | A | C | 8 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0051 others(5): Show |
8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-7290T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659941 | |||||||
| chr3:120659941 | A | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(67): Show |
77 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.283-7290T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659941 | |||||||
| chr3:120659943 | T | G | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(79): Show |
89 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.283-7292A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659943 | |||||||
| chr3:120659944 | G | A | 9 | a0001c0001t0001g0124 a0001c0001t0001g0150 a0001c0001t0001g0158 others(6): Show |
9 | HG00609.hp2 HG02074.hp2 NA18982.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-7293C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659944 | |||||||
| chr3:120659947 | G | C | 10 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0051 others(7): Show |
10 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-7296C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659947 | |||||||
| chr3:120659968 | G | A | 2 | a0001c0003t0001g0058 a0001c0003t0001g0070 |
2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.283-7317C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659968 | |||||||
| chr3:120659980 | A | T | 1 | a0001c0001t0001g0200 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.283-7329T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120659980 | |||||||
| chr3:120660114 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0065 a0001c0001t0001g0079 others(13): Show |
18 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.283-7463G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660114 | |||||||
| chr3:120660129 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.283-7478T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660129 | |||||||
| chr3:120660505 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.283-7854A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660505 | |||||||
| chr3:120660550 | C | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0002c0002t0001g0253 |
3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283-7899G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660550 | |||||||
| chr3:120660556 | G | A | 1 | a0002c0002t0001g0020 | 2 | NA18942.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.283-7905C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660556 | |||||||
| chr3:120660558 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0002c0002t0001g0253 |
3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283-7907A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660558 | |||||||
| chr3:120660588 | G | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(79): Show |
89 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.283-7937C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660588 | |||||||
| chr3:120660623 | G | A | 1 | a0002c0002t0001g0264 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.283-7972C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660623 | |||||||
| chr3:120660744 | G | C | 5 | a0001c0004t0001g0067 a0001c0004t0001g0068 a0001c0004t0001g0076 others(2): Show |
5 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-8093C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660744 | |||||||
| chr3:120660873 | GAAAACTT others(14): Show |
G | 1 | a0005c0011t0001g0041 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.283-8243_283-8223d others(23): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660873 | |||||||
| chr3:120660895 | C | G | 1 | a0005c0011t0001g0041 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.283-8244G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660895 | |||||||
| chr3:120660950 | C | T | 1 | a0001c0001t0001g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.283-8299G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660950 | |||||||
| chr3:120660989 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.283-8338A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120660989 | |||||||
| chr3:120661156 | C | T | 78 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(75): Show |
81 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.283-8505G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661156 | |||||||
| chr3:120661327 | C | T | 8 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0051 others(5): Show |
8 | HG00735.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-8676G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661327 | |||||||
| chr3:120661549 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.282+8878G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661549 | |||||||
| chr3:120661656 | C | A | 2 | a0001c0003t0001g0058 a0001c0003t0001g0070 |
2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.282+8771G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661656 | |||||||
| chr3:120661667 | C | T | 79 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(76): Show |
82 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.282+8760G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661667 | |||||||
| chr3:120661672 | AGCGCCAA others(7): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.282+8741_282+8754d others(16): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661672 | |||||||
| chr3:120661675 | G | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(291): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.282+8752C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120661675 | |||||||
| chr3:120662014 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(79): Show |
89 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.282+8413G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662014 | |||||||
| chr3:120662015 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.282+8412C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662015 | |||||||
| chr3:120662082 | C | T | 1 | a0002c0002t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.282+8345G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662082 | |||||||
| chr3:120662248 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(79): Show |
89 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.282+8179C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662248 | |||||||
| chr3:120662277 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0026 others(25): Show |
30 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.282+8150G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662277 | |||||||
| chr3:120662328 | A | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.282+8099T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662328 | |||||||
| chr3:120662735 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.282+7692C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662735 | |||||||
| chr3:120662769 | C | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(291): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.282+7658G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120662769 | |||||||
| chr3:120663049 | G | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(76): Show |
82 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.282+7378C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663049 | |||||||
| chr3:120663153 | A | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0104 others(26): Show |
32 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.282+7274T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663153 | |||||||
| chr3:120663167 | G | T | 2 | a0001c0001t0001g0124 a0002c0002t0001g0172 |
2 | NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.282+7260C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663167 | |||||||
| chr3:120663253 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.282+7174G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663253 | |||||||
| chr3:120663393 | A | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0033 others(60): Show |
68 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.282+7034T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663393 | |||||||
| chr3:120663494 | C | T | 122 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(119): Show |
129 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.282+6933G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663494 | |||||||
| chr3:120663516 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0002c0002t0001g0253 |
3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.282+6911C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663516 | |||||||
| chr3:120663518 | G | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0026 others(14): Show |
19 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.282+6909C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663518 | |||||||
| chr3:120663625 | C | G | 1 | a0002c0002t0001g0296 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.282+6802G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663625 | |||||||
| chr3:120663639 | A | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0033 others(60): Show |
68 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.282+6788T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663639 | |||||||
| chr3:120663695 | G | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+6732C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663695 | |||||||
| chr3:120663779 | T | TTG | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.282+6647_282+6648i others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663779 | |||||||
| chr3:120663800 | TTATAA | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(46): Show |
54 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.282+6622_282+6626d others(7): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663800 | |||||||
| chr3:120663851 | G | GA | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0036 others(23): Show |
29 | HG00639.hp1 HG01175.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.282+6575dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663851 | |||||||
| chr3:120663941 | AT | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.282+6485delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120663941 | |||||||
| chr3:120664226 | G | A | 1 | a0002c0002t0001g0167 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.282+6201C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664226 | |||||||
| chr3:120664426 | C | CT | 52 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(49): Show |
59 | HG00323.hp1 HG01074.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.282+6000dupA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664426 | |||||||
| chr3:120664426 | C | CTT | 81 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(78): Show |
86 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.282+5999_282+6000d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664426 | |||||||
| chr3:120664426 | CT | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(84): Show |
92 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.282+6000delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664426 | |||||||
| chr3:120664426 | CTT | C | 8 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(5): Show |
8 | HG00639.hp2 HG01081.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+5999_282+6000d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664426 | |||||||
| chr3:120664581 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.282+5846G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664581 | |||||||
| chr3:120664630 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0056 |
3 | HG01891.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.282+5797A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664630 | |||||||
| chr3:120664676 | T | C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0074 others(44): Show |
52 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.282+5751A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120664676 | |||||||
| chr3:120665032 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0002c0002t0001g0253 |
3 | HG01884.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.282+5395A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665032 | |||||||
| chr3:120665086 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.282+5341C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665086 | |||||||
| chr3:120665325 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0061 a0001c0001t0001g0085 others(1): Show |
4 | HG00735.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+5102G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665325 | |||||||
| chr3:120665434 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.282+4993A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665434 | |||||||
| chr3:120665463 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(96): Show |
109 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.282+4964A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665463 | |||||||
| chr3:120665466 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0144 a0001c0001t0001g0338 |
3 | HG00323.hp1 HG01169.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.282+4961C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665466 | |||||||
| chr3:120665468 | T | C | 6 | a0001c0003t0001g0088 a0001c0004t0001g0067 a0001c0004t0001g0068 others(3): Show |
6 | HG01106.hp1 HG01516.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+4959A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665468 | |||||||
| chr3:120665495 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(102): Show |
115 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.282+4932G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665495 | |||||||
| chr3:120665589 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0026 others(19): Show |
24 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.282+4838G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665589 | |||||||
| chr3:120665599 | G | C | 3 | a0001c0001t0001g0337 a0001c0003t0001g0058 a0006c0012t0001g0050 |
3 | HG03209.hp2 HG03453.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.282+4828C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665599 | |||||||
| chr3:120665771 | G | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(43): Show |
51 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.282+4656C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665771 | |||||||
| chr3:120665777 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0034 others(2): Show |
6 | HG01891.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+4650T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665777 | |||||||
| chr3:120665816 | G | C | 1 | a0002c0002t0001g0301 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.282+4611C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120665816 | |||||||
| chr3:120666019 | T | C | 4 | a0001c0001t0001g0071 a0001c0001t0001g0084 a0001c0001t0001g0244 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+4408A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666019 | |||||||
| chr3:120666181 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.282+4246C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666181 | |||||||
| chr3:120666293 | G | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.282+4134C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666293 | |||||||
| chr3:120666395 | G | A | 2 | a0001c0004t0001g0067 a0001c0004t0001g0068 |
2 | HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.282+4032C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666395 | |||||||
| chr3:120666409 | G | A | 61 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0033 others(58): Show |
63 | HG00438.hp2 HG00609.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.282+4018C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666409 | |||||||
| chr3:120666624 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.282+3803T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666624 | |||||||
| chr3:120666625 | G | A | 15 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0066 others(12): Show |
17 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.282+3802C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666625 | |||||||
| chr3:120666958 | G | A | 2 | a0001c0004t0001g0067 a0001c0004t0001g0068 |
2 | HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.282+3469C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120666958 | |||||||
| chr3:120667089 | C | T | 15 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0184 others(12): Show |
15 | HG00323.hp1 HG00323.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.282+3338G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667089 | |||||||
| chr3:120667098 | G | A | 15 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0184 others(12): Show |
15 | HG00323.hp1 HG00323.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.282+3329C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667098 | |||||||
| chr3:120667297 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.282+3130C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667297 | |||||||
| chr3:120667326 | C | CA | 48 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.282+3100dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667326 | |||||||
| chr3:120667326 | C | CAA | 18 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0045 others(15): Show |
21 | HG00741.hp1 HG01243.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.282+3099_282+3100d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667326 | |||||||
| chr3:120667326 | C | CAAA | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0064 others(3): Show |
6 | HG02145.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+3098_282+3100d others(5): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667326 | |||||||
| chr3:120667326 | CA | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0027 others(33): Show |
37 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.282+3100delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667326 | |||||||
| chr3:120667326 | CAA | C | 56 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(53): Show |
59 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.282+3099_282+3100d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667326 | |||||||
| chr3:120667443 | A | G | 4 | a0003c0005t0001g0028 a0003c0005t0001g0030 a0003c0005t0001g0031 others(1): Show |
4 | HG01099.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+2984T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667443 | |||||||
| chr3:120667456 | T | C | 53 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(50): Show |
56 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.282+2971A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667456 | |||||||
| chr3:120667591 | G | A | 53 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(50): Show |
56 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.282+2836C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667591 | |||||||
| chr3:120667879 | A | G | 1 | a0002c0002t0001g0328 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.282+2548T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667879 | |||||||
| chr3:120667885 | A | G | 3 | a0001c0001t0001g0066 a0001c0004t0001g0067 a0001c0004t0001g0068 |
3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.282+2542T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120667885 | |||||||
| chr3:120668019 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+2408A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668019 | |||||||
| chr3:120668034 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.282+2393G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668034 | |||||||
| chr3:120668288 | T | G | 4 | a0003c0005t0001g0028 a0003c0005t0001g0030 a0003c0005t0001g0031 others(1): Show |
4 | HG01099.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+2139A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668288 | |||||||
| chr3:120668444 | G | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.282+1983C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668444 | |||||||
| chr3:120668486 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+1941C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668486 | |||||||
| chr3:120668531 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0074 others(15): Show |
20 | HG00735.hp1 HG01099.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.282+1896C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668531 | |||||||
| chr3:120668673 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.282+1754G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668673 | |||||||
| chr3:120668740 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0044 others(23): Show |
29 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.282+1687G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668740 | |||||||
| chr3:120668759 | AT | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0033 others(12): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.282+1667delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668759 | |||||||
| chr3:120668812 | G | C | 56 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(53): Show |
59 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.282+1615C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668812 | |||||||
| chr3:120668869 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.282+1558G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668869 | |||||||
| chr3:120668910 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.282+1517C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668910 | |||||||
| chr3:120668940 | C | T | 1 | a0002c0007t0001g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.282+1487G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668940 | |||||||
| chr3:120668941 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.282+1486C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668941 | |||||||
| chr3:120668968 | CTA | C | 57 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(54): Show |
60 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.282+1457_282+1458d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120668968 | |||||||
| chr3:120669033 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.282+1394C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669033 | |||||||
| chr3:120669048 | C | T | 3 | a0002c0002t0001g0263 a0002c0002t0001g0264 a0002c0002t0001g0345 |
3 | HG02071.hp2 HG02135.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.282+1379G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669048 | |||||||
| chr3:120669056 | A | G | 1 | a0003c0005t0001g0029 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.282+1371T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669056 | |||||||
| chr3:120669062 | A | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0033 others(10): Show |
14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.282+1365T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669062 | |||||||
| chr3:120669139 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+1288G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669139 | |||||||
| chr3:120669267 | C | CA | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0042 others(27): Show |
33 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.282+1159dupT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669267 | |||||||
| chr3:120669277 | A | C | 3 | a0001c0001t0001g0066 a0001c0004t0001g0067 a0001c0004t0001g0068 |
3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.282+1150T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669277 | |||||||
| chr3:120669440 | C | T | 50 | a0002c0002t0001g0019 a0002c0002t0001g0069 a0002c0002t0001g0181 others(47): Show |
51 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.282+987G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669440 | |||||||
| chr3:120669441 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.282+986C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669441 | |||||||
| chr3:120669447 | G | GCA | 62 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
69 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.282+978_282+979dup others(2): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | |||||||
| chr3:120669447 | G | GCACA | 41 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0021 others(38): Show |
45 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.282+976_282+979dup others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | |||||||
| chr3:120669447 | G | GCACACA | 10 | a0001c0001t0001g0023 a0001c0001t0001g0117 a0001c0001t0001g0234 others(7): Show |
10 | HG00323.hp1 HG00558.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.282+974_282+979dup others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | |||||||
| chr3:120669447 | G | GCACACAC others(1): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(4): Show |
12 | HG01074.hp1 HG01106.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.282+972_282+979dup others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | |||||||
| chr3:120669447 | G | GCGCGCAC others(1): Show |
4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0341 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+979_282+980ins others(8): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | |||||||
| chr3:120669447 | GCA | G | 62 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0033 others(59): Show |
64 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.282+978_282+979del others(2): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | |||||||
| chr3:120669447 | GCACA | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
56 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.282+976_282+979del others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | |||||||
| chr3:120669447 | GCACACA | G | 5 | a0001c0001t0001g0044 a0001c0001t0001g0094 a0001c0001t0002g0022 others(2): Show |
5 | HG01109.hp1 HG01358.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+974_282+979del others(6): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | |||||||
| chr3:120669447 | GCACACAC others(3): Show |
G | 1 | a0001c0001t0001g0074 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.282+970_282+979del others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | |||||||
| chr3:120669447 | GCACACAC others(5): Show |
G | 1 | a0002c0002t0001g0164 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.282+968_282+979del others(12): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669447 | |||||||
| chr3:120669449 | A | G | 1 | a0001c0003t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.282+978T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669449 | |||||||
| chr3:120669507 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.282+920C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669507 | |||||||
| chr3:120669520 | C | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.282+907G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669520 | |||||||
| chr3:120669576 | C | G | 1 | a0002c0002t0001g0254 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.282+851G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669576 | |||||||
| chr3:120669624 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(111): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.282+803T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669624 | |||||||
| chr3:120669923 | T | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(111): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.282+504A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669923 | |||||||
| chr3:120669925 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.282+502A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120669925 | |||||||
| chr3:120670034 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.282+393A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670034 | |||||||
| chr3:120670082 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0074 others(12): Show |
17 | HG01099.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.282+345G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670082 | |||||||
| chr3:120670083 | A | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.282+344T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670083 | |||||||
| chr3:120670140 | C | T | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.282+287G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670140 | |||||||
| chr3:120670188 | G | A | 1 | a0001c0004t0001g0243 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.282+239C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670188 | |||||||
| chr3:120670205 | G | A | 1 | a0002c0002t0001g0250 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.282+222C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670205 | |||||||
| chr3:120670250 | T | C | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG00735.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+177A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670250 | |||||||
| chr3:120670369 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.282+58C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670369 | |||||||
| chr3:120670375 | C | G | 1 | a0002c0002t0001g0253 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.282+52G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670375 | |||||||
| chr3:120670396 | T | C | 1 | a0001c0004t0001g0243 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.282+31A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670396 | |||||||
| chr3:120670413 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.282+14G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 4/13 | chr3 | 120670413 | |||||||
| chr3:120670582 | G | A | 3 | a0001c0001t0001g0066 a0001c0004t0001g0067 a0001c0004t0001g0068 |
3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.177-50C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670582 | |||||||
| chr3:120670584 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.177-52C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670584 | |||||||
| chr3:120670644 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.177-112T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670644 | |||||||
| chr3:120670739 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.177-207G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670739 | |||||||
| chr3:120670742 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.177-210G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670742 | |||||||
| chr3:120670804 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0081 |
2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.177-272A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670804 | |||||||
| chr3:120670833 | G | T | 1 | a0002c0002t0001g0246 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.177-301C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120670833 | |||||||
| chr3:120671071 | A | G | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0082 others(1): Show |
4 | HG02055.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.177-539T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671071 | |||||||
| chr3:120671177 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0074 others(7): Show |
12 | HG02132.hp2 HG02257.hp1 HG03195.hp1 others(9): Show |
intron_variant | MODIFIER | c.177-645G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671177 | |||||||
| chr3:120671264 | C | A | 1 | a0001c0001t0001g0163 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.177-732G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671264 | |||||||
| chr3:120671460 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0074 others(16): Show |
21 | HG00735.hp1 HG01099.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.177-928C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671460 | |||||||
| chr3:120671672 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(59): Show |
69 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.177-1140A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671672 | |||||||
| chr3:120671673 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.177-1141C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671673 | |||||||
| chr3:120671701 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.177-1169G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671701 | |||||||
| chr3:120671758 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.177-1226G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671758 | |||||||
| chr3:120671779 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.177-1247G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671779 | |||||||
| chr3:120671907 | T | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.177-1375A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120671907 | |||||||
| chr3:120672068 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.177-1536T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672068 | |||||||
| chr3:120672082 | C | G | 3 | a0001c0001t0001g0071 a0001c0001t0002g0022 a0001c0003t0001g0070 |
3 | HG01109.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.177-1550G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672082 | |||||||
| chr3:120672237 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.177-1705G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672237 | |||||||
| chr3:120672343 | A | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.177-1811T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672343 | |||||||
| chr3:120672358 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.177-1826G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672358 | |||||||
| chr3:120672367 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | NA18941.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.177-1835T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672367 | |||||||
| chr3:120672439 | G | A | 5 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0341 others(2): Show |
5 | HG02280.hp2 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.177-1907C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672439 | |||||||
| chr3:120672570 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.177-2038A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672570 | |||||||
| chr3:120672756 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | NA18941.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.176+2145G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120672756 | |||||||
| chr3:120673036 | A | T | 1 | a0002c0002t0001g0251 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.176+1865T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673036 | |||||||
| chr3:120673097 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(55): Show |
65 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.176+1804A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673097 | |||||||
| chr3:120673158 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.176+1743G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673158 | |||||||
| chr3:120673165 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.176+1736C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673165 | |||||||
| chr3:120673220 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.176+1681G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673220 | |||||||
| chr3:120673471 | A | G | 51 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
54 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.176+1430T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673471 | |||||||
| chr3:120673479 | C | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(61): Show |
68 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.176+1422G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673479 | |||||||
| chr3:120673496 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.176+1405T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673496 | |||||||
| chr3:120673507 | CAG | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
92 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.176+1392_176+1393d others(4): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673507 | |||||||
| chr3:120673581 | C | A | 50 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(47): Show |
53 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.176+1320G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673581 | |||||||
| chr3:120673624 | T | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.176+1277A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673624 | |||||||
| chr3:120673657 | G | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.176+1244C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673657 | |||||||
| chr3:120673745 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.176+1156C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673745 | |||||||
| chr3:120673876 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.176+1025G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120673876 | |||||||
| chr3:120674148 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.176+753A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674148 | |||||||
| chr3:120674259 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0074 others(16): Show |
21 | HG00735.hp1 HG01099.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.176+642G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674259 | |||||||
| chr3:120674270 | C | T | 5 | a0002c0002t0001g0246 a0002c0002t0001g0247 a0002c0002t0001g0248 others(2): Show |
5 | NA18947.hp1 NA19005.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.176+631G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674270 | |||||||
| chr3:120674459 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0044 others(22): Show |
28 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.176+442C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674459 | |||||||
| chr3:120674511 | T | C | 3 | a0001c0001t0001g0066 a0001c0004t0001g0067 a0001c0004t0001g0068 |
3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.176+390A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674511 | |||||||
| chr3:120674550 | T | TAAAACAA others(3): Show |
31 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0025 others(28): Show |
34 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.176+341_176+350dup others(10): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674550 | |||||||
| chr3:120674550 | T | TAAAACAA others(8): Show |
33 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(30): Show |
37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.176+336_176+350dup others(15): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674550 | |||||||
| chr3:120674787 | A | C | 3 | a0001c0001t0001g0066 a0001c0004t0001g0067 a0001c0004t0001g0068 |
3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.176+114T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 3/13 | chr3 | 120674787 | |||||||
| chr3:120675112 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.88-123C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675112 | |||||||
| chr3:120675117 | G | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | NA18984.hp1 NA18991.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.88-128C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675117 | |||||||
| chr3:120675152 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0002g0022 a0001c0003t0001g0070 |
3 | HG01109.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.88-163G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675152 | |||||||
| chr3:120675205 | A | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.88-216T>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675205 | |||||||
| chr3:120675239 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
75 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.88-250C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675239 | |||||||
| chr3:120675330 | CT | C | 62 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
66 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.88-342delA | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675330 | |||||||
| chr3:120675447 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.87+345A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675447 | |||||||
| chr3:120675536 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.87+256A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675536 | |||||||
| chr3:120675542 | T | G | 1 | a0001c0001t0001g0021 | 2 | NA18983.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.87+250A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675542 | |||||||
| chr3:120675579 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.87+213G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675579 | |||||||
| chr3:120675608 | A | G | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | NA18961.hp2 NA19064.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.87+184T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675608 | |||||||
| chr3:120675674 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.87+118A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675674 | |||||||
| chr3:120675757 | T | A | 51 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
54 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.87+35A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 2/13 | chr3 | 120675757 | |||||||
| chr3:120676038 | G | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.16-175C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676038 | |||||||
| chr3:120676441 | AG | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.16-579delC | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676441 | |||||||
| chr3:120676453 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.16-590C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676453 | |||||||
| chr3:120676609 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(41): Show |
49 | HG00735.hp1 HG01099.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.16-746C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676609 | |||||||
| chr3:120676771 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.16-908T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676771 | |||||||
| chr3:120676775 | G | A | 3 | a0001c0001t0001g0066 a0001c0004t0001g0067 a0001c0004t0001g0068 |
3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.16-912C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676775 | |||||||
| chr3:120676905 | C | T | 51 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
54 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.16-1042G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120676905 | |||||||
| chr3:120677019 | A | G | 32 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(29): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.16-1156T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677019 | |||||||
| chr3:120677279 | A | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
43 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.16-1416T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677279 | |||||||
| chr3:120677292 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.16-1429G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677292 | |||||||
| chr3:120677379 | G | A | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG00323.hp1 HG02293.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-1516C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677379 | |||||||
| chr3:120677414 | C | G | 3 | a0001c0001t0001g0066 a0001c0004t0001g0067 a0001c0004t0001g0068 |
3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.16-1551G>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677414 | |||||||
| chr3:120677422 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.16-1559C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677422 | |||||||
| chr3:120677442 | A | G | 2 | a0002c0002t0001g0179 a0002c0002t0001g0180 |
2 | HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.16-1579T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677442 | |||||||
| chr3:120677478 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.16-1615C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677478 | |||||||
| chr3:120677481 | C | T | 3 | a0001c0001t0001g0066 a0001c0004t0001g0067 a0001c0004t0001g0068 |
3 | HG01106.hp1 HG01192.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.16-1618G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677481 | |||||||
| chr3:120677619 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.16-1756G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677619 | |||||||
| chr3:120677627 | T | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
96 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.16-1764A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677627 | |||||||
| chr3:120677756 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0033 others(10): Show |
14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.16-1893G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677756 | |||||||
| chr3:120677793 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.16-1930G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677793 | |||||||
| chr3:120677852 | C | A | 2 | a0002c0002t0001g0339 a0002c0002t0001g0340 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.16-1989G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677852 | |||||||
| chr3:120677889 | T | C | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.16-2026A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677889 | |||||||
| chr3:120677959 | G | A | 1 | a0002c0002t0001g0343 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.16-2096C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120677959 | |||||||
| chr3:120678021 | T | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0074 others(12): Show |
17 | HG01099.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-2158A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678021 | |||||||
| chr3:120678128 | A | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(105): Show |
117 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(114): Show |
intron_variant | MODIFIER | c.16-2265T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678128 | |||||||
| chr3:120678246 | A | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
96 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.16-2383T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678246 | |||||||
| chr3:120678248 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.16-2385C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678248 | |||||||
| chr3:120678249 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0074 others(12): Show |
17 | HG01099.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-2386G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678249 | |||||||
| chr3:120678526 | G | A | 1 | a0001c0001t0001g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.16-2663C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678526 | |||||||
| chr3:120678666 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.16-2803C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678666 | |||||||
| chr3:120678699 | A | G | 1 | a0001c0003t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.16-2836T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678699 | |||||||
| chr3:120678769 | CAG | C | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG00735.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-2908_16-2907del others(2): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678769 | |||||||
| chr3:120678806 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.16-2943G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678806 | |||||||
| chr3:120678837 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.16-2974T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678837 | |||||||
| chr3:120678868 | CA | C | 3 | a0001c0001t0001g0071 a0001c0001t0002g0022 a0001c0003t0001g0070 |
3 | HG01109.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.16-3006delT | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678868 | |||||||
| chr3:120678903 | C | T | 51 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
54 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.16-3040G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678903 | |||||||
| chr3:120678904 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.16-3041C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678904 | |||||||
| chr3:120678922 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
101 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.16-3059A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120678922 | |||||||
| chr3:120679003 | G | T | 3 | a0001c0001t0001g0071 a0001c0001t0002g0022 a0001c0003t0001g0070 |
3 | HG01109.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.15+3094C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679003 | |||||||
| chr3:120679012 | C | T | 1 | a0002c0002t0001g0176 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.15+3085G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679012 | |||||||
| chr3:120679118 | G | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02683.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.15+2979C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679118 | |||||||
| chr3:120679135 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.15+2962A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679135 | |||||||
| chr3:120679219 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.15+2878C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679219 | |||||||
| chr3:120679247 | G | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0074 others(7): Show |
12 | HG02132.hp2 HG02257.hp1 HG03195.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+2850C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679247 | |||||||
| chr3:120679275 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.15+2822G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679275 | |||||||
| chr3:120679447 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.15+2650C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679447 | |||||||
| chr3:120679523 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.15+2574A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679523 | |||||||
| chr3:120679651 | T | A | 1 | a0002c0002t0001g0345 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.15+2446A>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679651 | |||||||
| chr3:120679698 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.15+2399G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679698 | |||||||
| chr3:120679724 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG00735.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+2373G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679724 | |||||||
| chr3:120679757 | G | T | 1 | a0001c0001t0001g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.15+2340C>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679757 | |||||||
| chr3:120679837 | C | T | 10 | a0002c0002t0001g0164 a0002c0002t0001g0165 a0002c0002t0001g0166 others(7): Show |
10 | HG00597.hp1 HG00609.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+2260G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679837 | |||||||
| chr3:120679850 | G | C | 1 | a0001c0001t0001g0346 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.15+2247C>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679850 | |||||||
| chr3:120679970 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
101 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.15+2127T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679970 | |||||||
| chr3:120679975 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0074 others(11): Show |
16 | HG00735.hp1 HG02132.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+2122C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120679975 | |||||||
| chr3:120680106 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.15+1991C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120680106 | |||||||
| chr3:120680322 | A | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.15+1775T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120680322 | |||||||
| chr3:120680512 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.15+1585C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120680512 | |||||||
| chr3:120680728 | C | A | 1 | a0002c0002t0001g0347 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.15+1369G>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120680728 | |||||||
| chr3:120680858 | CCAGTTCC others(18): Show |
C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG00735.hp1 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.15+1214_15+1238del others(25): Show |
HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120680858 | |||||||
| chr3:120681015 | A | C | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02258.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+1082T>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681015 | |||||||
| chr3:120681070 | T | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG00735.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+1027A>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681070 | |||||||
| chr3:120681268 | T | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(29): Show |
36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.15+829A>G | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681268 | |||||||
| chr3:120681287 | G | A | 51 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
54 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.15+810C>T | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681287 | |||||||
| chr3:120681568 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.15+529G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681568 | |||||||
| chr3:120681628 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.15+469T>C | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681628 | |||||||
| chr3:120681811 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.15+286G>A | HGD | ENSG00000113924.12 | transcript | ENST00000283871.10 | protein_coding | 1/13 | chr3 | 120681811 |