Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56941 |
| ensemblid | ENSG00000183624.14 |
| hgncid | 24446 |
| symbol | HMCES |
| name | 5-hydroxymethylcytosine binding, ES cell specific |
| refseq_nuc | NM_020187.3 |
| refseq_prot | NP_064572.2 |
| ensembl_nuc | ENST00000383463.9 |
| ensembl_prot | ENSP00000372955.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 129278870 |
| end | 129306186 |
| strand | + |
| ver | v1.2 |
| region | chr3:129278870-129306186 |
| region5000 | chr3:129273870-129311186 |
| regionname0 | HMCES_chr3_129278870_129306186 |
| regionname5000 | HMCES_chr3_129273870_129311186 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 354 | 308 | 83 | 74 | 108 | 8 | 33 | 80 | HMCES_chr3_129273870_129311186 | HMCES | MCGRT others(349): Show |
chr3 | 129273870 | 129311186 |
| a0002 | 0/0 | 354 | 28 | 1 | 0 | 22 | 0 | 5 | 12 | HMCES_chr3_129273870_129311186 | HMCES | MCGRT others(349): Show |
chr3 | 129273870 | 129311186 |
| a0003 | 0/0 | 354 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | MCGRT others(349): Show |
chr3 | 129273870 | 129311186 |
| a0004 | 0/0 | 129 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | MCGRT others(124): Show |
chr3 | 129273870 | 129311186 |
| a0005 | 0/0 | 354 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | MCGRT others(349): Show |
chr3 | 129273870 | 129311186 |
| a0006 | 0/0 | 354 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | MCGRT others(349): Show |
chr3 | 129273870 | 129311186 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1062 | 303 | 79 | 74 | 108 | 8 | 32 | HMCES_chr3_129273870_129311186 | HMCES | ATGTG others(1057): Show |
chr3 | 129273870 | 129311186 | ||
| a0001c0003 | 0/0 | 1062 | 2 | 2 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | ATGTG others(1057): Show |
chr3 | 129273870 | 129311186 | ||
| a0001c0005 | 0/0 | 1062 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | ATGTG others(1057): Show |
chr3 | 129273870 | 129311186 | ||
| a0001c0006 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | ATGTG others(1057): Show |
chr3 | 129273870 | 129311186 | ||
| a0001c0007 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | ATGTG others(1057): Show |
chr3 | 129273870 | 129311186 | ||
| a0002c0002 | 0/0 | 1062 | 27 | 1 | 0 | 21 | 0 | 5 | HMCES_chr3_129273870_129311186 | HMCES | ATGTG others(1057): Show |
chr3 | 129273870 | 129311186 | ||
| a0002c0008 | 0/0 | 1062 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | ATGTG others(1057): Show |
chr3 | 129273870 | 129311186 | ||
| a0003c0004 | 0/0 | 1062 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | ATGTG others(1057): Show |
chr3 | 129273870 | 129311186 | ||
| a0004c0010 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | ATGTG others(1057): Show |
chr3 | 129273870 | 129311186 | ||
| a0005c0009 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | ATGTG others(1057): Show |
chr3 | 129273870 | 129311186 | ||
| a0006c0011 | 0/0 | 1062 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | ATGTG others(1057): Show |
chr3 | 129273870 | 129311186 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2485 | 221 | 27 | 54 | 103 | 6 | 29 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0002 | 0/0 | 2485 | 46 | 32 | 9 | 0 | 2 | 3 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0003 | 0/0 | 2480 | 16 | 10 | 6 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2475): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0004 | 0/0 | 2485 | 5 | 4 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0005 | 0/0 | 2485 | 4 | 0 | 0 | 4 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0006 | 0/0 | 2485 | 2 | 1 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0007 | 0/0 | 2485 | 2 | 2 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0008 | 0/0 | 2485 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0009 | 0/0 | 2485 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0010 | 0/0 | 2471 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2466): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0011 | 0/0 | 2485 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0013 | 0/0 | 2485 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0014 | 0/0 | 2480 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2475): Show |
chr3 | 129273870 | 129311186 |
| a0001c0001t0015 | 0/0 | 2485 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0003t0006 | 0/0 | 2485 | 2 | 2 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0005t0001 | 0/0 | 2485 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0006t0001 | 0/0 | 2485 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0001c0007t0001 | 0/0 | 2485 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0002c0002t0002 | 0/0 | 2485 | 27 | 1 | 0 | 21 | 0 | 5 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0002c0008t0002 | 0/0 | 2485 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0003c0004t0001 | 0/0 | 2485 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0004c0010t0003 | 0/0 | 2480 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2475): Show |
chr3 | 129273870 | 129311186 |
| a0005c0009t0012 | 0/0 | 2485 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| a0006c0011t0002 | 0/0 | 2485 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | AGAGT others(2480): Show |
chr3 | 129273870 | 129311186 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 31 | 0 | 4 | 20 | 2 | 4 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0002 | 0/0 | 15 | 0 | 1 | 13 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0004 | 0/0 | 8 | 6 | 1 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0006 | 0/0 | 7 | 1 | 2 | 0 | 1 | 3 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0003g0003 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0004g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0005g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0009g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0010g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0013g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0014g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0001t0015g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0003t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0003t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0006t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0001c0007t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0008 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0002c0008t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0003c0004t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0004c0010t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0005c0009t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| a0006c0011t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | FIN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0100 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01496 | hp1 | a0001 | c0001 | t0013 | g0139 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01981 | hp1 | a0001 | c0001 | t0015 | g0177 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0146 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02015 | hp1 | a0001 | c0001 | t0010 | g0011 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | CDX | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02523 | hp2 | a0003 | c0004 | t0001 | g0011 | EAS | KHV | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02615 | hp1 | a0001 | c0007 | t0001 | g0209 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02647 | hp2 | a0001 | c0003 | t0006 | g0102 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0096 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02818 | hp2 | a0001 | c0001 | t0014 | g0003 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02886 | hp1 | a0001 | c0003 | t0006 | g0101 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02895 | hp2 | a0004 | c0010 | t0003 | g0060 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ESN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03491 | hp1 | a0001 | c0005 | t0001 | g0001 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0085 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0092 | SAS | BEB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0081 | SAS | STU | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | STU | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | YRI | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | YRI | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18612 | hp1 | a0006 | c0011 | t0002 | g0007 | EAS | CHB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | CHB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | YRI | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | YRI | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | LWK | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0074 | AFR | LWK | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19086 | hp2 | a0002 | c0008 | t0002 | g0094 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | YRI | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA19240 | hp2 | a0001 | c0006 | t0001 | g0205 | AFR | YRI | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ASW | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ASW | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | TSI | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | GIH | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03471 | hp1 | a0005 | c0009 | t0012 | g0058 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | USA | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | USA | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | USA | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0152 | AFR | LWK | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0142 | REF | REF | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | HMCES_chr3_129273870_129311186 | HMCES | chr3 | 129273870 | 129311186 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129288987 | G | A | 1 | a0003 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.317G>A | p.Arg106Gln | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/7 | 376/2485 | 317/1065 | 106/354 | chr3 | 129288987 | |||
| chr3:129290685 | C | G | 1 | a0006 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.334C>G | p.Leu112Val | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/7 | 393/2485 | 334/1065 | 112/354 | chr3 | 129290685 | |||
| chr3:129290739 | C | T | 1 | a0004 | 1 | HG02895.hp2 | stop_gained | HIGH | c.388C>T | p.Arg130* | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/7 | 447/2485 | 388/1065 | 130/354 | chr3 | 129290739 | |||
| chr3:129298363 | A | C | 1 | a0005 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.463A>C | p.Ile155Leu | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/7 | 522/2485 | 463/1065 | 155/354 | chr3 | 129298363 | |||
| chr3:129304787 | G | A | 1 | a0002 | 28 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(25): Show |
missense_variant | MODERATE | c.1027G>A | p.Glu343Lys | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1086/2485 | 1027/1065 | 343/354 | chr3 | 129304787 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129298425 | A | C | 1 | a0002c0008 | 1 | NA19086.hp2 | synonymous_variant | LOW | c.525A>C | p.Thr175Thr | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/7 | 584/2485 | 525/1065 | 175/354 | chr3 | 129298425 | |||
| chr3:129302010 | C | T | 1 | a0001c0003 | 2 | HG02647.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.696C>T | p.Val232Val | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/7 | 755/2485 | 696/1065 | 232/354 | chr3 | 129302010 | |||
| chr3:129304648 | C | A | 1 | a0001c0005 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.888C>A | p.Pro296Pro | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 947/2485 | 888/1065 | 296/354 | chr3 | 129304648 | |||
| chr3:129304699 | G | A | 1 | a0001c0006 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.939G>A | p.Gln313Gln | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 998/2485 | 939/1065 | 313/354 | chr3 | 129304699 | |||
| chr3:129304813 | T | C | 1 | a0001c0007 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.1053T>C | p.Pro351Pro | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1112/2485 | 1053/1065 | 351/354 | chr3 | 129304813 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129304917 | G | A | 1 | a0001c0001t0008 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*92G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 92 | chr3 | 129304917 | ||||||
| chr3:129305135 | C | T | 1 | a0001c0001t0015 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*310C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 310 | chr3 | 129305135 | ||||||
| chr3:129305196 | C | G | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(12): Show |
108 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*371C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 371 | chr3 | 129305196 | ||||||
| chr3:129305241 | AAAAAT | A | 3 | a0001c0001t0003 a0001c0001t0014 a0004c0010t0003 |
18 | HG00735.hp1 HG00738.hp1 HG01167.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*419_*423delAATAA | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 419 | INFO_REALIGN_3_PRIME | chr3 | 129305241 | |||||
| chr3:129305326 | G | T | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 501 | chr3 | 129305326 | ||||||
| chr3:129305327 | G | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*502G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 502 | chr3 | 129305327 | ||||||
| chr3:129305329 | G | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*504G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 504 | chr3 | 129305329 | ||||||
| chr3:129305331 | A | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*506A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 506 | chr3 | 129305331 | ||||||
| chr3:129305332 | A | C | 1 | a0001c0001t0014 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*507A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 507 | chr3 | 129305332 | ||||||
| chr3:129305335 | T | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*510T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 510 | chr3 | 129305335 | ||||||
| chr3:129305341 | T | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 516 | chr3 | 129305341 | ||||||
| chr3:129305342 | C | G | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*517C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 517 | chr3 | 129305342 | ||||||
| chr3:129305343 | T | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*518T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 518 | chr3 | 129305343 | ||||||
| chr3:129305345 | A | T | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*520A>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 520 | chr3 | 129305345 | ||||||
| chr3:129305346 | C | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 521 | chr3 | 129305346 | ||||||
| chr3:129305352 | T | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*527T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 527 | chr3 | 129305352 | ||||||
| chr3:129305353 | T | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*528T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 528 | chr3 | 129305353 | ||||||
| chr3:129305368 | C | G | 1 | a0001c0001t0013 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*543C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 543 | chr3 | 129305368 | ||||||
| chr3:129305373 | GGAATGGA others(7): Show |
G | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*549_*562delGAATGG others(8): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 549 | chr3 | 129305373 | ||||||
| chr3:129305378 | G | A | 1 | a0001c0003t0006 | 2 | HG02647.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*553G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 553 | chr3 | 129305378 | ||||||
| chr3:129305389 | C | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 564 | chr3 | 129305389 | ||||||
| chr3:129305390 | A | G | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*565A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 565 | chr3 | 129305390 | ||||||
| chr3:129305394 | G | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*569G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 569 | chr3 | 129305394 | ||||||
| chr3:129305395 | G | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*570G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 570 | chr3 | 129305395 | ||||||
| chr3:129305402 | G | T | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*577G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 577 | chr3 | 129305402 | ||||||
| chr3:129305403 | G | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 578 | chr3 | 129305403 | ||||||
| chr3:129305404 | G | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*579G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 579 | chr3 | 129305404 | ||||||
| chr3:129305405 | G | T | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*580G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 580 | chr3 | 129305405 | ||||||
| chr3:129305406 | C | G | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*581C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 581 | chr3 | 129305406 | ||||||
| chr3:129305407 | T | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 582 | chr3 | 129305407 | ||||||
| chr3:129305499 | T | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*674T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 674 | chr3 | 129305499 | ||||||
| chr3:129305543 | A | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*718A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 718 | chr3 | 129305543 | ||||||
| chr3:129305567 | G | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*742G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 742 | chr3 | 129305567 | ||||||
| chr3:129305612 | A | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*787A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 787 | chr3 | 129305612 | ||||||
| chr3:129305635 | A | T | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*810A>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 810 | chr3 | 129305635 | ||||||
| chr3:129305637 | G | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*812G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 812 | chr3 | 129305637 | ||||||
| chr3:129305652 | T | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*827T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 827 | chr3 | 129305652 | ||||||
| chr3:129305657 | G | T | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*832G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 832 | chr3 | 129305657 | ||||||
| chr3:129305661 | A | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 836 | chr3 | 129305661 | ||||||
| chr3:129305670 | G | T | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*845G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 845 | chr3 | 129305670 | ||||||
| chr3:129305681 | G | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*856G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 856 | chr3 | 129305681 | ||||||
| chr3:129305690 | G | T | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 865 | chr3 | 129305690 | ||||||
| chr3:129305711 | T | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*886T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 886 | chr3 | 129305711 | ||||||
| chr3:129305715 | G | T | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*890G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 890 | chr3 | 129305715 | ||||||
| chr3:129305724 | C | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*899C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 899 | chr3 | 129305724 | ||||||
| chr3:129305727 | T | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*902T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 902 | chr3 | 129305727 | ||||||
| chr3:129305733 | T | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*908T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 908 | chr3 | 129305733 | ||||||
| chr3:129305735 | G | T | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*910G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 910 | chr3 | 129305735 | ||||||
| chr3:129305745 | T | G | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*920T>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 920 | chr3 | 129305745 | ||||||
| chr3:129305754 | G | A | 1 | a0001c0001t0009 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*929G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 929 | chr3 | 129305754 | ||||||
| chr3:129305793 | G | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*968G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 968 | chr3 | 129305793 | ||||||
| chr3:129305794 | A | T | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*969A>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 969 | chr3 | 129305794 | ||||||
| chr3:129305795 | T | C | 3 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0011 |
4 | HG02015.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*970T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 970 | chr3 | 129305795 | ||||||
| chr3:129305823 | C | T | 1 | a0001c0001t0004 | 5 | HG01255.hp1 HG02055.hp2 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*998C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 998 | chr3 | 129305823 | ||||||
| chr3:129305881 | T | C | 1 | a0005c0009t0012 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1056T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1056 | chr3 | 129305881 | ||||||
| chr3:129305922 | C | T | 2 | a0001c0001t0006 a0001c0003t0006 |
4 | HG00642.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1097C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1097 | chr3 | 129305922 | ||||||
| chr3:129305924 | G | A | 1 | a0001c0001t0011 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1099G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1099 | chr3 | 129305924 | ||||||
| chr3:129305946 | C | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1121C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1121 | chr3 | 129305946 | ||||||
| chr3:129305962 | T | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1137T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1137 | chr3 | 129305962 | ||||||
| chr3:129305981 | A | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1156A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1156 | chr3 | 129305981 | ||||||
| chr3:129306005 | G | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1180G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1180 | chr3 | 129306005 | ||||||
| chr3:129306006 | C | G | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1181 | chr3 | 129306006 | ||||||
| chr3:129306007 | G | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1182G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1182 | chr3 | 129306007 | ||||||
| chr3:129306012 | T | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1187T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1187 | chr3 | 129306012 | ||||||
| chr3:129306015 | G | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1190G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1190 | chr3 | 129306015 | ||||||
| chr3:129306019 | G | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1194G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1194 | chr3 | 129306019 | ||||||
| chr3:129306020 | T | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1195T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1195 | chr3 | 129306020 | ||||||
| chr3:129306034 | G | A | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1209G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1209 | chr3 | 129306034 | ||||||
| chr3:129306035 | T | C | 1 | a0001c0001t0010 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1210T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1210 | chr3 | 129306035 | ||||||
| chr3:129306054 | C | G | 1 | a0001c0001t0005 | 4 | NA18952.hp2 NA18954.hp2 NA18985.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1229C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 7/7 | 1229 | chr3 | 129306054 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129278958 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-24+53G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 1/6 | chr3 | 129278958 | |||||||
| chr3:129278990 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-24+85G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 1/6 | chr3 | 129278990 | |||||||
| chr3:129279058 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-24+153G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 1/6 | chr3 | 129279058 | |||||||
| chr3:129279214 | C | T | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-24+309C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 1/6 | chr3 | 129279214 | |||||||
| chr3:129279274 | G | C | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-24+369G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 1/6 | chr3 | 129279274 | |||||||
| chr3:129279379 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0213 |
3 | HG00741.hp1 HG01168.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-23-331C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 1/6 | chr3 | 129279379 | |||||||
| chr3:129280271 | T | C | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.183+356T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129280271 | |||||||
| chr3:129280426 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0021 others(22): Show |
42 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.183+511G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129280426 | |||||||
| chr3:129280507 | T | A | 7 | a0001c0001t0002g0013 a0001c0001t0002g0054 a0001c0001t0002g0055 others(4): Show |
10 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.183+592T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129280507 | |||||||
| chr3:129280638 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | NA18975.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.183+723G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129280638 | |||||||
| chr3:129280758 | T | A | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.183+843T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129280758 | |||||||
| chr3:129280865 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0038 |
3 | HG00280.hp2 HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.183+950G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129280865 | |||||||
| chr3:129280961 | C | T | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+1046C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129280961 | |||||||
| chr3:129280962 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.183+1047G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129280962 | |||||||
| chr3:129280994 | C | T | 2 | a0001c0003t0006g0101 a0001c0003t0006g0102 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.183+1079C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129280994 | |||||||
| chr3:129280999 | G | A | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+1084G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129280999 | |||||||
| chr3:129281011 | C | G | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.183+1096C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129281011 | |||||||
| chr3:129281019 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.183+1104C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129281019 | |||||||
| chr3:129281208 | G | A | 8 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0039 others(5): Show |
10 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.183+1293G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129281208 | |||||||
| chr3:129281317 | C | G | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.183+1402C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129281317 | |||||||
| chr3:129281453 | G | A | 51 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(48): Show |
65 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.183+1538G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129281453 | |||||||
| chr3:129281464 | C | G | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.183+1549C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129281464 | |||||||
| chr3:129281494 | C | T | 1 | a0001c0003t0006g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.183+1579C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129281494 | |||||||
| chr3:129281520 | G | A | 1 | a0001c0003t0006g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.183+1605G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129281520 | |||||||
| chr3:129281796 | G | A | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.183+1881G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129281796 | |||||||
| chr3:129281860 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.183+1945G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129281860 | |||||||
| chr3:129281926 | C | CA | 12 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(9): Show |
13 | HG01361.hp1 HG01433.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.183+2033dupA | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129281926 | ||||||
| chr3:129281926 | CA | C | 60 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0197 others(57): Show |
72 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.183+2033delA | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129281926 | ||||||
| chr3:129281926 | CAA | C | 16 | a0001c0001t0002g0013 a0001c0001t0002g0037 a0001c0001t0002g0052 others(13): Show |
19 | HG00642.hp1 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.183+2032_183+2033d others(4): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129281926 | ||||||
| chr3:129282264 | C | G | 8 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0206 others(5): Show |
8 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+2349C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129282264 | |||||||
| chr3:129282267 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.183+2352G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129282267 | |||||||
| chr3:129282295 | C | CA | 11 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(8): Show |
14 | HG00280.hp1 HG00642.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.183+2397dupA | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129282295 | ||||||
| chr3:129282295 | C | CAAAAA | 21 | a0001c0001t0006g0098 a0002c0002t0002g0008 a0002c0002t0002g0074 others(18): Show |
26 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.183+2393_183+2397d others(7): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129282295 | ||||||
| chr3:129282295 | C | CAAAAAA | 25 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(22): Show |
34 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.183+2392_183+2397d others(8): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129282295 | ||||||
| chr3:129282298 | A | C | 25 | a0001c0001t0001g0194 a0001c0001t0002g0007 a0001c0001t0002g0012 others(22): Show |
32 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.183+2383A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129282298 | |||||||
| chr3:129282301 | A | C | 25 | a0001c0001t0001g0194 a0001c0001t0002g0007 a0001c0001t0002g0012 others(22): Show |
32 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.183+2386A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129282301 | |||||||
| chr3:129282304 | A | C | 23 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(20): Show |
30 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.183+2389A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129282304 | |||||||
| chr3:129282440 | G | A | 31 | a0001c0001t0006g0098 a0001c0001t0006g0100 a0001c0001t0007g0020 others(28): Show |
36 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.183+2525G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129282440 | |||||||
| chr3:129282472 | C | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.183+2557C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129282472 | |||||||
| chr3:129282927 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.183+3012T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129282927 | |||||||
| chr3:129283110 | A | G | 27 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 others(24): Show |
32 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+3195A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129283110 | |||||||
| chr3:129283277 | G | A | 21 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0023 others(18): Show |
31 | HG00280.hp1 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.183+3362G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129283277 | |||||||
| chr3:129283334 | C | CT | 6 | a0001c0001t0001g0009 a0001c0001t0001g0122 a0001c0001t0001g0138 others(3): Show |
11 | HG01123.hp2 HG01928.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.183+3433dupT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129283334 | ||||||
| chr3:129283393 | G | A | 1 | a0001c0001t0002g0214 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.183+3478G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129283393 | |||||||
| chr3:129283491 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.183+3576T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129283491 | |||||||
| chr3:129283576 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.183+3661A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129283576 | |||||||
| chr3:129283712 | C | T | 51 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(48): Show |
65 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.183+3797C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129283712 | |||||||
| chr3:129283753 | G | C | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.183+3838G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129283753 | |||||||
| chr3:129283832 | A | C | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.183+3917A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129283832 | |||||||
| chr3:129284166 | C | G | 1 | a0001c0001t0001g0192 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.183+4251C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129284166 | |||||||
| chr3:129284210 | T | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(17): Show |
29 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.183+4295T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129284210 | |||||||
| chr3:129284322 | A | C | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.183+4407A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129284322 | |||||||
| chr3:129284532 | G | GCAGTTCA others(38): Show |
1 | a0001c0001t0001g0198 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.184-4321_184-4277d others(47): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129284532 | ||||||
| chr3:129284591 | C | A | 1 | a0001c0001t0002g0045 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.184-4263C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129284591 | |||||||
| chr3:129284831 | G | A | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.184-4023G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129284831 | |||||||
| chr3:129284854 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.184-4000T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129284854 | |||||||
| chr3:129284899 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.184-3955G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129284899 | |||||||
| chr3:129284977 | G | A | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-3877G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129284977 | |||||||
| chr3:129284978 | C | A | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-3876C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129284978 | |||||||
| chr3:129285111 | C | T | 51 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(48): Show |
65 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.184-3743C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285111 | |||||||
| chr3:129285127 | T | C | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.184-3727T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285127 | |||||||
| chr3:129285169 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG00621.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.184-3685C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285169 | |||||||
| chr3:129285234 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.184-3620T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285234 | |||||||
| chr3:129285254 | A | C | 1 | a0001c0001t0002g0045 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.184-3600A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285254 | |||||||
| chr3:129285378 | G | T | 1 | a0001c0001t0002g0052 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.184-3476G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285378 | |||||||
| chr3:129285455 | A | AT | 8 | a0001c0001t0001g0122 a0001c0001t0001g0148 a0001c0001t0001g0150 others(5): Show |
8 | HG01109.hp2 HG01175.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-3385dupT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129285455 | ||||||
| chr3:129285566 | C | T | 1 | a0002c0008t0002g0094 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.184-3288C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285566 | |||||||
| chr3:129285751 | A | AT | 11 | a0001c0001t0001g0147 a0001c0001t0001g0190 a0001c0001t0001g0196 others(8): Show |
11 | HG00735.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-3090dupT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129285751 | ||||||
| chr3:129285804 | A | G | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-3050A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285804 | |||||||
| chr3:129285838 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.184-3016T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285838 | |||||||
| chr3:129285865 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(17): Show |
29 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.184-2989G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285865 | |||||||
| chr3:129285879 | G | T | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.184-2975G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285879 | |||||||
| chr3:129285882 | A | T | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.184-2972A>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129285882 | |||||||
| chr3:129286052 | G | T | 1 | a0001c0001t0003g0071 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.184-2802G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129286052 | |||||||
| chr3:129286106 | C | T | 1 | a0002c0002t0002g0081 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.184-2748C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129286106 | |||||||
| chr3:129286217 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.184-2637A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129286217 | |||||||
| chr3:129286342 | C | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(17): Show |
29 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.184-2512C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129286342 | |||||||
| chr3:129286369 | A | G | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.184-2485A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129286369 | |||||||
| chr3:129286383 | C | G | 3 | a0001c0001t0002g0036 a0001c0001t0002g0045 a0001c0001t0002g0050 |
3 | HG01358.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.184-2471C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129286383 | |||||||
| chr3:129286825 | C | A | 1 | a0004c0010t0003g0060 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.184-2029C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129286825 | |||||||
| chr3:129287134 | G | C | 51 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(48): Show |
65 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.184-1720G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287134 | |||||||
| chr3:129287149 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.184-1705T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287149 | |||||||
| chr3:129287187 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.184-1667T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287187 | |||||||
| chr3:129287188 | G | GT | 2 | a0001c0001t0002g0054 a0001c0001t0004g0014 |
4 | HG01255.hp1 HG02055.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1661dupT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129287188 | ||||||
| chr3:129287192 | TTGTTTTT others(7): Show |
T | 2 | a0001c0001t0006g0098 a0001c0001t0006g0100 |
2 | HG00642.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.184-1661_184-1648d others(16): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287192 | |||||||
| chr3:129287194 | G | GT | 7 | a0001c0001t0001g0024 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
8 | HG00280.hp1 HG01891.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-1651dupT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129287194 | ||||||
| chr3:129287194 | G | T | 7 | a0001c0001t0002g0013 a0001c0001t0002g0054 a0001c0001t0002g0055 others(4): Show |
10 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.184-1660G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287194 | |||||||
| chr3:129287209 | G | T | 2 | a0001c0001t0006g0098 a0001c0001t0006g0100 |
2 | HG00642.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.184-1645G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287209 | |||||||
| chr3:129287212 | TTTTTG | T | 19 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(16): Show |
28 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.184-1622_184-1618d others(7): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129287212 | ||||||
| chr3:129287258 | C | T | 6 | a0002c0002t0002g0075 a0002c0002t0002g0076 a0002c0002t0002g0090 others(3): Show |
6 | HG02056.hp2 NA18747.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-1596C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287258 | |||||||
| chr3:129287279 | G | C | 17 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(14): Show |
26 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.184-1575G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287279 | |||||||
| chr3:129287390 | A | AT | 7 | a0001c0001t0001g0034 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
8 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-1450dupT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129287390 | ||||||
| chr3:129287526 | C | G | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.184-1328C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287526 | |||||||
| chr3:129287738 | C | T | 2 | a0001c0001t0006g0098 a0001c0001t0006g0100 |
2 | HG00642.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.184-1116C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287738 | |||||||
| chr3:129287753 | A | G | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.184-1101A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287753 | |||||||
| chr3:129287918 | G | A | 2 | a0001c0001t0008g0152 a0001c0001t0013g0139 |
2 | HG01496.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.184-936G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287918 | |||||||
| chr3:129287942 | G | A | 51 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(48): Show |
65 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.184-912G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287942 | |||||||
| chr3:129287949 | C | T | 2 | a0001c0003t0006g0101 a0001c0003t0006g0102 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.184-905C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287949 | |||||||
| chr3:129287952 | G | A | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.184-902G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129287952 | |||||||
| chr3:129288144 | G | A | 2 | a0001c0003t0006g0101 a0001c0003t0006g0102 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.184-710G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129288144 | |||||||
| chr3:129288149 | C | T | 1 | a0001c0001t0006g0098 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.184-705C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129288149 | |||||||
| chr3:129288557 | TG | T | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.184-290delG | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129288557 | ||||||
| chr3:129288695 | C | CA | 27 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 others(24): Show |
32 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.184-151dupA | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 129288695 | ||||||
| chr3:129288749 | G | C | 1 | a0001c0001t0002g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.184-105G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 2/6 | chr3 | 129288749 | |||||||
| chr3:129289145 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.327+148G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289145 | |||||||
| chr3:129289153 | A | C | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+156A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289153 | |||||||
| chr3:129289278 | G | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(17): Show |
29 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.327+281G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289278 | |||||||
| chr3:129289379 | G | A | 51 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(48): Show |
65 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.327+382G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289379 | |||||||
| chr3:129289403 | G | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(17): Show |
29 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.327+406G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289403 | |||||||
| chr3:129289460 | T | C | 84 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(81): Show |
108 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.327+463T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289460 | |||||||
| chr3:129289666 | C | T | 1 | a0001c0001t0006g0098 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.327+669C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289666 | |||||||
| chr3:129289692 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.327+695A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289692 | |||||||
| chr3:129289695 | G | T | 23 | a0002c0002t0002g0008 a0002c0002t0002g0074 a0002c0002t0002g0075 others(20): Show |
28 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.327+698G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289695 | |||||||
| chr3:129289915 | C | T | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.328-764C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289915 | |||||||
| chr3:129289921 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.328-758C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289921 | |||||||
| chr3:129289962 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG01175.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.328-717C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129289962 | |||||||
| chr3:129290014 | C | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(17): Show |
29 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.328-665C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129290014 | |||||||
| chr3:129290015 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.328-664G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129290015 | |||||||
| chr3:129290057 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0153 |
4 | HG00558.hp1 HG02523.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-622G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129290057 | |||||||
| chr3:129290185 | C | T | 1 | a0001c0001t0009g0146 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.328-494C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129290185 | |||||||
| chr3:129290190 | C | CA | 50 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0136 others(47): Show |
61 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.328-472dupA | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 129290190 | ||||||
| chr3:129290282 | A | ATTTG | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.328-389_328-386dup others(4): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 129290282 | ||||||
| chr3:129290394 | G | A | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.328-285G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129290394 | |||||||
| chr3:129290539 | C | T | 2 | a0001c0001t0005g0018 a0001c0001t0005g0135 |
4 | NA18952.hp2 NA18954.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-140C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 3/6 | chr3 | 129290539 | |||||||
| chr3:129290818 | C | G | 1 | a0004c0010t0003g0060 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.453+14C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129290818 | |||||||
| chr3:129290872 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.453+68T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129290872 | |||||||
| chr3:129291048 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.453+244C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129291048 | |||||||
| chr3:129291109 | G | C | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.453+305G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129291109 | |||||||
| chr3:129291310 | G | C | 3 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 |
3 | HG02922.hp2 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.453+506G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129291310 | |||||||
| chr3:129291444 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.453+640C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129291444 | |||||||
| chr3:129291638 | C | T | 31 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0013 others(28): Show |
41 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.453+834C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129291638 | |||||||
| chr3:129291720 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(17): Show |
29 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.453+916C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129291720 | |||||||
| chr3:129291745 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(17): Show |
29 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.453+941A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129291745 | |||||||
| chr3:129291984 | G | A | 20 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(17): Show |
29 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.453+1180G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129291984 | |||||||
| chr3:129292036 | A | C | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.453+1232A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292036 | |||||||
| chr3:129292202 | G | A | 31 | a0001c0001t0006g0098 a0001c0001t0006g0100 a0001c0001t0007g0020 others(28): Show |
36 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.453+1398G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292202 | |||||||
| chr3:129292230 | T | A | 1 | a0001c0001t0005g0135 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.453+1426T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292230 | |||||||
| chr3:129292277 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.453+1473C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292277 | |||||||
| chr3:129292473 | C | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
144 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.453+1669C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292473 | |||||||
| chr3:129292482 | GT | G | 48 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(45): Show |
62 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.453+1689delT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129292482 | ||||||
| chr3:129292484 | T | A | 2 | a0001c0003t0006g0101 a0001c0003t0006g0102 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.453+1680T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292484 | |||||||
| chr3:129292497 | C | CT | 7 | a0001c0001t0002g0013 a0001c0001t0002g0054 a0001c0001t0002g0055 others(4): Show |
10 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+1706dupT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129292497 | ||||||
| chr3:129292507 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.453+1703T>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292507 | |||||||
| chr3:129292516 | A | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0191 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.453+1712A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292516 | |||||||
| chr3:129292523 | C | G | 7 | a0001c0001t0002g0013 a0001c0001t0002g0054 a0001c0001t0002g0055 others(4): Show |
10 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+1719C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292523 | |||||||
| chr3:129292529 | G | C | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+1725G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292529 | |||||||
| chr3:129292554 | G | A | 2 | a0001c0001t0008g0152 a0001c0001t0013g0139 |
2 | HG01496.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.453+1750G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292554 | |||||||
| chr3:129292561 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.453+1757C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292561 | |||||||
| chr3:129292683 | G | A | 2 | a0001c0003t0006g0101 a0001c0003t0006g0102 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.453+1879G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292683 | |||||||
| chr3:129292684 | C | T | 2 | a0001c0001t0006g0098 a0001c0001t0006g0100 |
2 | HG00642.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.453+1880C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292684 | |||||||
| chr3:129292731 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.453+1927G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292731 | |||||||
| chr3:129292776 | G | A | 51 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(48): Show |
65 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.453+1972G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129292776 | |||||||
| chr3:129293009 | G | T | 4 | a0001c0001t0006g0098 a0001c0001t0006g0100 a0001c0003t0006g0101 others(1): Show |
4 | HG00642.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+2205G>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293009 | |||||||
| chr3:129293072 | C | T | 2 | a0001c0001t0008g0152 a0001c0001t0013g0139 |
2 | HG01496.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.453+2268C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293072 | |||||||
| chr3:129293130 | G | A | 1 | a0001c0001t0003g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.453+2326G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293130 | |||||||
| chr3:129293132 | A | T | 1 | a0001c0001t0003g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.453+2328A>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293132 | |||||||
| chr3:129293198 | G | A | 1 | a0002c0002t0002g0084 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.453+2394G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293198 | |||||||
| chr3:129293236 | G | A | 23 | a0002c0002t0002g0008 a0002c0002t0002g0074 a0002c0002t0002g0075 others(20): Show |
28 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.453+2432G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293236 | |||||||
| chr3:129293561 | C | CT | 27 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0026 others(24): Show |
33 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.453+2783dupT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129293561 | ||||||
| chr3:129293561 | CT | C | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0129 others(4): Show |
7 | HG00738.hp2 HG01496.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.453+2783delT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129293561 | ||||||
| chr3:129293561 | CTT | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0036 a0001c0001t0002g0040 others(7): Show |
13 | HG00642.hp1 HG01123.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.453+2782_453+2783d others(4): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129293561 | ||||||
| chr3:129293561 | CTTT | C | 23 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(20): Show |
30 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.453+2781_453+2783d others(5): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129293561 | ||||||
| chr3:129293561 | CTTTT | C | 24 | a0001c0001t0002g0010 a0001c0001t0002g0052 a0001c0001t0002g0063 others(21): Show |
33 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.453+2780_453+2783d others(6): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129293561 | ||||||
| chr3:129293561 | CTTTTT | C | 25 | a0001c0001t0002g0062 a0002c0002t0002g0008 a0002c0002t0002g0074 others(22): Show |
30 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.453+2779_453+2783d others(7): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129293561 | ||||||
| chr3:129293653 | C | T | 1 | a0002c0002t0002g0083 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.453+2849C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293653 | |||||||
| chr3:129293689 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.453+2885G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293689 | |||||||
| chr3:129293715 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.453+2911G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293715 | |||||||
| chr3:129293827 | C | A | 1 | a0001c0001t0008g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.453+3023C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293827 | |||||||
| chr3:129293901 | A | G | 86 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0007 others(83): Show |
110 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.453+3097A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293901 | |||||||
| chr3:129293952 | A | G | 1 | a0002c0002t0002g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.453+3148A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129293952 | |||||||
| chr3:129294026 | C | T | 2 | a0001c0001t0002g0068 a0001c0001t0002g0069 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.453+3222C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294026 | |||||||
| chr3:129294031 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.453+3227C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294031 | |||||||
| chr3:129294082 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.453+3278T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294082 | |||||||
| chr3:129294145 | G | A | 31 | a0001c0001t0006g0098 a0001c0001t0006g0100 a0001c0001t0007g0020 others(28): Show |
36 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.453+3341G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294145 | |||||||
| chr3:129294285 | C | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
134 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.453+3481C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294285 | |||||||
| chr3:129294312 | A | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
145 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.453+3508A>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294312 | |||||||
| chr3:129294491 | A | AAT | 26 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 others(23): Show |
31 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.453+3689_453+3690d others(4): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129294491 | ||||||
| chr3:129294512 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.453+3708A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294512 | |||||||
| chr3:129294555 | T | G | 7 | a0001c0001t0002g0013 a0001c0001t0002g0054 a0001c0001t0002g0055 others(4): Show |
10 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+3751T>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294555 | |||||||
| chr3:129294557 | C | A | 23 | a0002c0002t0002g0008 a0002c0002t0002g0074 a0002c0002t0002g0075 others(20): Show |
28 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.453+3753C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294557 | |||||||
| chr3:129294615 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.454-3739A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294615 | |||||||
| chr3:129294688 | C | T | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.454-3666C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294688 | |||||||
| chr3:129294915 | C | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG01070.hp1 HG01074.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-3439C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294915 | |||||||
| chr3:129294923 | C | T | 2 | a0001c0003t0006g0101 a0001c0003t0006g0102 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.454-3431C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294923 | |||||||
| chr3:129294950 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.454-3404A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294950 | |||||||
| chr3:129294973 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.454-3381C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129294973 | |||||||
| chr3:129295014 | C | T | 1 | a0001c0001t0015g0177 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.454-3340C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129295014 | |||||||
| chr3:129295158 | C | CA | 37 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0112 others(34): Show |
42 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.454-3177dupA | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129295158 | ||||||
| chr3:129295158 | C | CAA | 16 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0065 others(13): Show |
25 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.454-3178_454-3177d others(4): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129295158 | ||||||
| chr3:129295158 | C | CAAA | 6 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0067 others(3): Show |
6 | HG01175.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.454-3179_454-3177d others(5): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129295158 | ||||||
| chr3:129295158 | CA | C | 16 | a0001c0001t0001g0130 a0001c0001t0001g0150 a0001c0001t0001g0165 others(13): Show |
19 | HG00099.hp1 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.454-3177delA | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129295158 | ||||||
| chr3:129295341 | G | A | 23 | a0002c0002t0002g0008 a0002c0002t0002g0074 a0002c0002t0002g0075 others(20): Show |
28 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.454-3013G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129295341 | |||||||
| chr3:129295434 | C | CA | 74 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(71): Show |
95 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.454-2909dupA | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 129295434 | ||||||
| chr3:129295455 | C | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
166 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.454-2899C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129295455 | |||||||
| chr3:129295619 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.454-2735T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129295619 | |||||||
| chr3:129295646 | A | G | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.454-2708A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129295646 | |||||||
| chr3:129295713 | T | C | 4 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG01070.hp1 HG01074.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-2641T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129295713 | |||||||
| chr3:129295722 | T | G | 45 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(42): Show |
61 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.454-2632T>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129295722 | |||||||
| chr3:129295796 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0180 |
3 | HG00621.hp2 HG02080.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.454-2558C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129295796 | |||||||
| chr3:129295825 | G | A | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.454-2529G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129295825 | |||||||
| chr3:129295970 | G | C | 2 | a0001c0001t0006g0098 a0001c0001t0006g0100 |
2 | HG00642.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.454-2384G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129295970 | |||||||
| chr3:129296032 | C | T | 3 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 |
3 | HG02922.hp2 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.454-2322C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296032 | |||||||
| chr3:129296105 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.454-2249A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296105 | |||||||
| chr3:129296147 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.454-2207A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296147 | |||||||
| chr3:129296352 | C | T | 3 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 |
3 | HG02922.hp2 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.454-2002C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296352 | |||||||
| chr3:129296409 | C | A | 8 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0039 others(5): Show |
10 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-1945C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296409 | |||||||
| chr3:129296557 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.454-1797A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296557 | |||||||
| chr3:129296561 | C | G | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.454-1793C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296561 | |||||||
| chr3:129296582 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.454-1772C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296582 | |||||||
| chr3:129296635 | C | T | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.454-1719C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296635 | |||||||
| chr3:129296645 | G | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0156 a0001c0001t0001g0200 |
4 | HG01074.hp1 HG01106.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-1709G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296645 | |||||||
| chr3:129296788 | A | G | 84 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(81): Show |
108 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.454-1566A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296788 | |||||||
| chr3:129296833 | C | T | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.454-1521C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296833 | |||||||
| chr3:129296940 | G | A | 51 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(48): Show |
65 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.454-1414G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296940 | |||||||
| chr3:129296990 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01496.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.454-1364G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129296990 | |||||||
| chr3:129297030 | G | C | 1 | a0002c0002t0002g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.454-1324G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297030 | |||||||
| chr3:129297031 | A | C | 74 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(71): Show |
95 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.454-1323A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297031 | |||||||
| chr3:129297031 | A | G | 1 | a0002c0002t0002g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.454-1323A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297031 | |||||||
| chr3:129297114 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.454-1240G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297114 | |||||||
| chr3:129297206 | T | C | 1 | a0002c0002t0002g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.454-1148T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297206 | |||||||
| chr3:129297214 | G | A | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.454-1140G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297214 | |||||||
| chr3:129297215 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.454-1139T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297215 | |||||||
| chr3:129297247 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.454-1107C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297247 | |||||||
| chr3:129297283 | A | G | 51 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(48): Show |
65 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.454-1071A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297283 | |||||||
| chr3:129297555 | G | A | 27 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 others(24): Show |
32 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.454-799G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297555 | |||||||
| chr3:129297687 | T | C | 3 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG02109.hp2 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.454-667T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297687 | |||||||
| chr3:129297721 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.454-633C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129297721 | |||||||
| chr3:129298105 | C | T | 3 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 |
3 | HG02922.hp2 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.454-249C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129298105 | |||||||
| chr3:129298237 | G | A | 2 | a0001c0003t0006g0101 a0001c0003t0006g0102 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.454-117G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129298237 | |||||||
| chr3:129298290 | C | G | 1 | a0001c0003t0006g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.454-64C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 4/6 | chr3 | 129298290 | |||||||
| chr3:129298731 | G | A | 4 | a0002c0002t0002g0080 a0002c0002t0002g0083 a0002c0002t0002g0087 others(1): Show |
4 | HG00544.hp1 HG02027.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.635+196G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129298731 | |||||||
| chr3:129298786 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.635+251A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129298786 | |||||||
| chr3:129298872 | C | T | 2 | a0001c0001t0006g0098 a0001c0001t0006g0100 |
2 | HG00642.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.635+337C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129298872 | |||||||
| chr3:129298883 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.635+348G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129298883 | |||||||
| chr3:129299072 | C | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(17): Show |
29 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.635+537C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129299072 | |||||||
| chr3:129299600 | T | C | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.635+1065T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129299600 | |||||||
| chr3:129299647 | T | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0117 |
2 | NA18947.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.635+1112T>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129299647 | |||||||
| chr3:129299648 | C | CT | 86 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(83): Show |
127 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.635+1134dupT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129299648 | ||||||
| chr3:129299648 | CT | C | 10 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0141 others(7): Show |
10 | HG00642.hp1 HG00735.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.635+1134delT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129299648 | ||||||
| chr3:129299648 | CTT | C | 31 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0013 others(28): Show |
45 | HG00639.hp1 HG00738.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.635+1133_635+1134d others(4): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129299648 | ||||||
| chr3:129299648 | CTTT | C | 15 | a0001c0001t0002g0007 a0001c0001t0002g0019 a0001c0001t0002g0036 others(12): Show |
20 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.635+1132_635+1134d others(5): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129299648 | ||||||
| chr3:129299831 | A | G | 1 | a0001c0001t0002g0214 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.635+1296A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129299831 | |||||||
| chr3:129300005 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.635+1470T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129300005 | |||||||
| chr3:129300043 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.635+1508T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129300043 | |||||||
| chr3:129300066 | A | G | 1 | a0001c0001t0002g0019 | 2 | HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.635+1531A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129300066 | |||||||
| chr3:129300080 | AT | A | 26 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 others(23): Show |
31 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.635+1548delT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129300080 | ||||||
| chr3:129300166 | T | TTA | 17 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0034 others(14): Show |
27 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.635+1656_635+1657d others(4): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129300166 | ||||||
| chr3:129300166 | T | TTATA | 2 | a0001c0001t0001g0028 a0001c0001t0001g0187 |
3 | HG00423.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.635+1654_635+1657d others(6): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129300166 | ||||||
| chr3:129300166 | T | TTATATAT others(3): Show |
7 | a0001c0001t0001g0159 a0001c0001t0001g0196 a0001c0001t0001g0206 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.635+1648_635+1657d others(12): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129300166 | ||||||
| chr3:129300166 | T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0208 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.635+1644_635+1657d others(16): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129300166 | ||||||
| chr3:129300166 | TTA | T | 4 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 others(1): Show |
4 | HG01496.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.635+1656_635+1657d others(4): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129300166 | ||||||
| chr3:129300166 | TTATA | T | 3 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0008g0152 |
3 | HG03098.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.635+1654_635+1657d others(6): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129300166 | ||||||
| chr3:129300166 | TTATATA | T | 73 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(70): Show |
97 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.635+1652_635+1657d others(8): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129300166 | ||||||
| chr3:129300402 | G | A | 7 | a0001c0001t0002g0013 a0001c0001t0002g0054 a0001c0001t0002g0055 others(4): Show |
10 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.636-1548G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129300402 | |||||||
| chr3:129300619 | A | G | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.636-1331A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129300619 | |||||||
| chr3:129300626 | G | C | 7 | a0001c0001t0002g0013 a0001c0001t0002g0054 a0001c0001t0002g0055 others(4): Show |
10 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.636-1324G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129300626 | |||||||
| chr3:129300758 | C | T | 3 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 |
3 | HG02922.hp2 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.636-1192C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129300758 | |||||||
| chr3:129300827 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.636-1123G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129300827 | |||||||
| chr3:129300910 | A | T | 1 | a0001c0001t0002g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.636-1040A>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129300910 | |||||||
| chr3:129300991 | A | G | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.636-959A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129300991 | |||||||
| chr3:129301030 | C | CAAAAA | 48 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(45): Show |
62 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.636-912_636-908dup others(5): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129301030 | ||||||
| chr3:129301030 | C | CAAAAAA | 21 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(18): Show |
28 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.636-913_636-908dup others(6): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129301030 | ||||||
| chr3:129301030 | C | CAAAAAAA others(1): Show |
5 | a0001c0001t0002g0013 a0001c0001t0002g0055 a0001c0001t0002g0057 others(2): Show |
8 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.636-915_636-908dup others(8): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129301030 | ||||||
| chr3:129301085 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.636-865A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129301085 | |||||||
| chr3:129301155 | G | A | 22 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(19): Show |
29 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.636-795G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129301155 | |||||||
| chr3:129301161 | C | G | 23 | a0002c0002t0002g0008 a0002c0002t0002g0074 a0002c0002t0002g0075 others(20): Show |
28 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.636-789C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129301161 | |||||||
| chr3:129301169 | G | GACGTC | 7 | a0001c0001t0002g0013 a0001c0001t0002g0054 a0001c0001t0002g0055 others(4): Show |
10 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.636-781_636-780ins others(5): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129301169 | |||||||
| chr3:129301170 | C | T | 7 | a0001c0001t0002g0013 a0001c0001t0002g0054 a0001c0001t0002g0055 others(4): Show |
10 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.636-780C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129301170 | |||||||
| chr3:129301171 | A | C | 7 | a0001c0001t0002g0013 a0001c0001t0002g0054 a0001c0001t0002g0055 others(4): Show |
10 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.636-779A>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129301171 | |||||||
| chr3:129301191 | C | CA | 130 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(127): Show |
182 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.636-744dupA | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129301191 | ||||||
| chr3:129301191 | C | CAAA | 6 | a0001c0001t0002g0013 a0001c0001t0002g0055 a0001c0001t0002g0056 others(3): Show |
9 | HG01123.hp1 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.636-746_636-744dup others(3): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129301191 | ||||||
| chr3:129301210 | GA | G | 14 | a0001c0001t0001g0030 a0001c0001t0001g0150 a0001c0001t0001g0160 others(11): Show |
15 | HG01496.hp1 HG02004.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.636-727delA | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129301210 | ||||||
| chr3:129301219 | A | AAAAC | 77 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(74): Show |
101 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.636-728_636-727ins others(4): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129301219 | ||||||
| chr3:129301246 | C | G | 82 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(79): Show |
106 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.636-704C>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129301246 | |||||||
| chr3:129301435 | C | CTT | 84 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(81): Show |
108 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.636-514_636-513ins others(2): Show |
HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 129301435 | ||||||
| chr3:129301677 | A | G | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.636-273A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129301677 | |||||||
| chr3:129301744 | T | C | 2 | a0001c0001t0003g0072 a0001c0001t0003g0073 |
2 | HG01175.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.636-206T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129301744 | |||||||
| chr3:129301935 | A | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
264 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.636-15A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 5/6 | chr3 | 129301935 | |||||||
| chr3:129302159 | G | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG01496.hp2 HG03834.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.828+17G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129302159 | |||||||
| chr3:129302311 | G | C | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.828+169G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129302311 | |||||||
| chr3:129302338 | G | C | 1 | a0002c0008t0002g0094 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.828+196G>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129302338 | |||||||
| chr3:129302542 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.828+400G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129302542 | |||||||
| chr3:129302702 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.828+560C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129302702 | |||||||
| chr3:129302952 | C | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
19 | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.828+810C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129302952 | |||||||
| chr3:129303015 | G | A | 26 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 others(23): Show |
31 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.828+873G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129303015 | |||||||
| chr3:129303170 | G | A | 31 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0013 others(28): Show |
41 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.828+1028G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129303170 | |||||||
| chr3:129303193 | C | T | 20 | a0001c0001t0002g0010 a0001c0001t0002g0062 a0001c0001t0002g0063 others(17): Show |
29 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.828+1051C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129303193 | |||||||
| chr3:129303243 | G | A | 3 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 |
3 | HG02922.hp2 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.828+1101G>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129303243 | |||||||
| chr3:129303385 | C | A | 3 | a0001c0001t0007g0020 a0001c0001t0007g0078 a0001c0001t0011g0020 |
3 | HG02922.hp2 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.829-1204C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129303385 | |||||||
| chr3:129303425 | C | T | 2 | a0001c0003t0006g0101 a0001c0003t0006g0102 |
2 | HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.829-1164C>T | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129303425 | |||||||
| chr3:129303577 | C | A | 1 | a0005c0009t0012g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.829-1012C>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129303577 | |||||||
| chr3:129303583 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.829-1006T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129303583 | |||||||
| chr3:129303650 | A | G | 1 | a0002c0002t0002g0088 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.829-939A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129303650 | |||||||
| chr3:129303872 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0174 |
2 | HG00099.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.829-717A>G | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129303872 | |||||||
| chr3:129303916 | T | A | 24 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0019 others(21): Show |
31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.829-673T>A | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129303916 | |||||||
| chr3:129304512 | CCT | C | 23 | a0002c0002t0002g0008 a0002c0002t0002g0074 a0002c0002t0002g0075 others(20): Show |
28 | HG00408.hp2 HG00544.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.829-76_829-75delCT | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129304512 | |||||||
| chr3:129304532 | T | C | 1 | a0002c0002t0002g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.829-57T>C | HMCES | ENSG00000183624.14 | transcript | ENST00000383463.9 | protein_coding | 6/6 | chr3 | 129304532 |