Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 419 |
| ensemblid | ENSG00000156219.18 |
| hgncid | 725 |
| symbol | ART3 |
| name | ADP-ribosyltransferase 3 (inactive) |
| refseq_nuc | NM_001130016.3 |
| refseq_prot | NP_001123488.1 |
| ensembl_nuc | ENST00000355810.9 |
| ensembl_prot | ENSP00000348064.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 76074709 |
| end | 76112786 |
| strand | + |
| ver | v1.2 |
| region | chr4:76074709-76112786 |
| region5000 | chr4:76069709-76117786 |
| regionname0 | ART3_chr4_76074709_76112786 |
| regionname5000 | ART3_chr4_76069709_76117786 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 389 | 209 | 49 | 28 | 110 | 5 | 17 | 87 | ART3_chr4_76069709_76117786 | ART3 | MKTGH others(384): Show |
chr4 | 76069709 | 76117786 |
| a0002 | 1/1 | 389 | 163 | 29 | 35 | 63 | 11 | 23 | 50 | ART3_chr4_76069709_76117786 | ART3 | MKTGH others(384): Show |
chr4 | 76069709 | 76117786 |
| a0003 | 0/0 | 389 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | MKTGH others(384): Show |
chr4 | 76069709 | 76117786 |
| a0004 | 0/0 | 389 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | MKTGH others(384): Show |
chr4 | 76069709 | 76117786 |
| a0005 | 0/0 | 389 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | MKTGH others(384): Show |
chr4 | 76069709 | 76117786 |
| a0006 | 0/0 | 389 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | MKTGH others(384): Show |
chr4 | 76069709 | 76117786 |
| a0007 | 0/0 | 389 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | MKTGH others(384): Show |
chr4 | 76069709 | 76117786 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1167 | 207 | 47 | 28 | 110 | 5 | 17 | ART3_chr4_76069709_76117786 | ART3 | ATGAA others(1162): Show |
chr4 | 76069709 | 76117786 | ||
| a0001c0005 | 0/0 | 1167 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | ATGAA others(1162): Show |
chr4 | 76069709 | 76117786 | ||
| a0002c0002 | 1/1 | 1167 | 163 | 29 | 35 | 63 | 11 | 23 | ART3_chr4_76069709_76117786 | ART3 | ATGAA others(1162): Show |
chr4 | 76069709 | 76117786 | ||
| a0003c0003 | 0/0 | 1167 | 13 | 12 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | ATGAA others(1162): Show |
chr4 | 76069709 | 76117786 | ||
| a0004c0004 | 0/0 | 1167 | 3 | 0 | 0 | 3 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | ATGAA others(1162): Show |
chr4 | 76069709 | 76117786 | ||
| a0005c0006 | 0/0 | 1167 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | ATGAA others(1162): Show |
chr4 | 76069709 | 76117786 | ||
| a0006c0008 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | ATGAA others(1162): Show |
chr4 | 76069709 | 76117786 | ||
| a0007c0007 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | ATGAA others(1162): Show |
chr4 | 76069709 | 76117786 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1557 | 179 | 38 | 26 | 93 | 5 | 17 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1552): Show |
chr4 | 76069709 | 76117786 |
| a0001c0001t0002 | 0/0 | 1557 | 23 | 5 | 1 | 17 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1552): Show |
chr4 | 76069709 | 76117786 |
| a0001c0001t0004 | 0/0 | 1557 | 5 | 4 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1552): Show |
chr4 | 76069709 | 76117786 |
| a0001c0005t0001 | 0/0 | 1557 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1552): Show |
chr4 | 76069709 | 76117786 |
| a0002c0002t0002 | 1/1 | 1557 | 82 | 22 | 23 | 9 | 10 | 16 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1552): Show |
chr4 | 76069709 | 76117786 |
| a0002c0002t0003 | 0/0 | 1554 | 75 | 3 | 12 | 52 | 1 | 7 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1549): Show |
chr4 | 76069709 | 76117786 |
| a0002c0002t0005 | 0/0 | 1557 | 4 | 4 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1552): Show |
chr4 | 76069709 | 76117786 |
| a0002c0002t0006 | 0/0 | 1554 | 2 | 0 | 0 | 2 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1549): Show |
chr4 | 76069709 | 76117786 |
| a0003c0003t0001 | 0/0 | 1557 | 12 | 11 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1552): Show |
chr4 | 76069709 | 76117786 |
| a0003c0003t0002 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1552): Show |
chr4 | 76069709 | 76117786 |
| a0004c0004t0003 | 0/0 | 1554 | 3 | 0 | 0 | 3 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1549): Show |
chr4 | 76069709 | 76117786 |
| a0005c0006t0003 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1549): Show |
chr4 | 76069709 | 76117786 |
| a0005c0006t0007 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1549): Show |
chr4 | 76069709 | 76117786 |
| a0006c0008t0001 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1552): Show |
chr4 | 76069709 | 76117786 |
| a0007c0007t0002 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | TCTCA others(1552): Show |
chr4 | 76069709 | 76117786 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 13 | 0 | 5 | 8 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 7 | 0 | 1 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0003 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0001c0005t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0005 | 0/1 | 8 | 0 | 2 | 2 | 2 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0012 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0001 | 0/0 | 28 | 0 | 1 | 26 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0005g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0002c0002t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0003c0003t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0003c0003t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0003c0003t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0003c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0003c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0003c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0003c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0003c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0003c0003t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0004c0004t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0004c0004t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0005c0006t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0005c0006t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0006c0008t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| a0007c0007t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0013 | EUR | GBR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | GBR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0012 | EUR | GBR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0132 | EUR | GBR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0197 | EUR | FIN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0024 | EUR | FIN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0072 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00558 | hp2 | a0002 | c0002 | t0003 | g0060 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00597 | hp1 | a0002 | c0002 | t0003 | g0107 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00609 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00673 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | CHS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0069 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0191 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01069 | hp2 | a0002 | c0002 | t0003 | g0076 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01099 | hp1 | a0002 | c0002 | t0003 | g0067 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01106 | hp1 | a0002 | c0002 | t0003 | g0125 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0018 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0180 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01192 | hp1 | a0002 | c0002 | t0003 | g0055 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0221 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0238 | AMR | PUR | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0030 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01261 | hp1 | a0002 | c0002 | t0003 | g0104 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01346 | hp1 | a0002 | c0002 | t0003 | g0048 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0149 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0108 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0116 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0172 | AMR | CLM | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0199 | EUR | IBS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0012 | EUR | IBS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0005 | EUR | IBS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0005 | EUR | IBS | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01928 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0071 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0257 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0066 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02004 | hp2 | a0002 | c0002 | t0003 | g0250 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02027 | hp1 | a0004 | c0004 | t0003 | g0015 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02040 | hp2 | a0002 | c0002 | t0003 | g0190 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02055 | hp1 | a0002 | c0002 | t0003 | g0213 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0260 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02071 | hp2 | a0002 | c0002 | t0003 | g0061 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02080 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0263 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02155 | hp1 | a0002 | c0002 | t0003 | g0062 | EAS | CDX | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02258 | hp2 | a0002 | c0002 | t0005 | g0009 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0261 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0018 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0150 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0211 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0248 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0177 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0252 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0168 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0244 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0194 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0188 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0198 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02735 | hp2 | a0002 | c0002 | t0003 | g0014 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0214 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0037 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0176 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0040 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0175 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02896 | hp2 | a0002 | c0002 | t0005 | g0009 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02897 | hp2 | a0002 | c0002 | t0005 | g0009 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02922 | hp2 | a0005 | c0006 | t0007 | g0109 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0207 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02970 | hp2 | a0003 | c0003 | t0001 | g0038 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0222 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0038 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0179 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0037 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03209 | hp1 | a0006 | c0008 | t0001 | g0242 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03225 | hp1 | a0007 | c0007 | t0002 | g0225 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03453 | hp1 | a0005 | c0006 | t0003 | g0253 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03516 | hp1 | a0003 | c0003 | t0002 | g0254 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ESN | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | GWD | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03579 | hp2 | a0002 | c0002 | t0005 | g0210 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0193 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0206 | SAS | STU | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0079 | SAS | STU | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03710 | hp1 | a0002 | c0002 | t0003 | g0054 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0215 | SAS | BEB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03831 | hp2 | a0002 | c0002 | t0003 | g0014 | SAS | BEB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0148 | SAS | BEB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0001 | SAS | BEB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03927 | hp1 | a0002 | c0002 | t0003 | g0014 | SAS | BEB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0217 | SAS | STU | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0102 | SAS | BEB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0216 | SAS | STU | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0057 | SAS | STU | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0192 | SAS | STU | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18612 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | CHB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18747 | hp2 | a0004 | c0004 | t0003 | g0001 | EAS | CHB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0040 | AFR | YRI | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | YRI | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18939 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18940 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18941 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18942 | hp2 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18943 | hp1 | a0002 | c0002 | t0003 | g0103 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18945 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18946 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18947 | hp2 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18953 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18957 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18963 | hp2 | a0002 | c0002 | t0003 | g0105 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18964 | hp2 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18965 | hp2 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18966 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18968 | hp1 | a0002 | c0002 | t0006 | g0074 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18969 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18972 | hp1 | a0002 | c0002 | t0003 | g0065 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18973 | hp2 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18974 | hp1 | a0002 | c0002 | t0003 | g0020 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0093 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0063 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18984 | hp2 | a0004 | c0004 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18986 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18989 | hp2 | a0002 | c0002 | t0006 | g0106 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18990 | hp2 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18991 | hp1 | a0002 | c0002 | t0003 | g0045 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18994 | hp2 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19002 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19003 | hp2 | a0002 | c0002 | t0003 | g0064 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19009 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | LWK | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19058 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19065 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19068 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19074 | hp1 | a0002 | c0002 | t0003 | g0020 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19076 | hp2 | a0002 | c0002 | t0003 | g0046 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19077 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19080 | hp2 | a0002 | c0002 | t0003 | g0073 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19081 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19084 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19089 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0245 | AFR | YRI | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0231 | AFR | ASW | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | ASW | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0174 | EUR | TSI | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0088 | EUR | TSI | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0030 | SAS | GIH | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0129 | SAS | GIH | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02109 | hp1 | a0002 | c0002 | t0003 | g0051 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0209 | AFR | ACB | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0162 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG06807 | hp1 | a0003 | c0003 | t0001 | g0255 | AFR | USA | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | USA | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | USA | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0189 | AFR | USA | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | LWK | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0005 | REF | REF | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0181 | REF | REF | ART3_chr4_76069709_76117786 | ART3 | chr4 | 76069709 | 76117786 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76082058 | A | G | 1 | a0005 | 2 | HG02922.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.304A>G | p.Ile102Val | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/12 | 424/1557 | 304/1170 | 102/389 | chr4 | 76082058 | |||
| chr4:76082059 | T | C | 1 | a0003 | 13 | HG01109.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
missense_variant | MODERATE | c.305T>C | p.Ile102Thr | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/12 | 425/1557 | 305/1170 | 102/389 | chr4 | 76082059 | |||
| chr4:76104626 | C | T | 1 | a0004 | 3 | HG02027.hp1 NA18747.hp2 NA18984.hp2 |
missense_variant | MODERATE | c.1000C>T | p.Pro334Ser | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/12 | 1120/1557 | 1000/1170 | 334/389 | chr4 | 76104626 | |||
| chr4:76112398 | T | C | 1 | a0007 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1049T>C | p.Val350Ala | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 12/12 | 1169/1557 | 1049/1170 | 350/389 | chr4 | 76112398 | |||
| chr4:76112437 | C | T | 4 | a0001 a0003 a0006 others(1): Show |
224 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(221): Show |
missense_variant | MODERATE | c.1088C>T | p.Ser363Leu | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 12/12 | 1208/1557 | 1088/1170 | 363/389 | chr4 | 76112437 | |||
| chr4:76112506 | T | C | 1 | a0006 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1157T>C | p.Phe386Ser | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 12/12 | 1277/1557 | 1157/1170 | 386/389 | chr4 | 76112506 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76104622 | A | G | 1 | a0001c0005 | 2 | HG02809.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.996A>G | p.Pro332Pro | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/12 | 1116/1557 | 996/1170 | 332/389 | chr4 | 76104622 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76074742 | T | G | 1 | a0002c0002t0005 | 4 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-87T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/12 | chr4 | 76074742 | |||||||
| chr4:76112568 | G | A | 5 | a0002c0002t0003 a0002c0002t0006 a0004c0004t0003 others(2): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*49G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 12/12 | 49 | chr4 | 76112568 | ||||||
| chr4:76112572 | C | A | 5 | a0001c0001t0001 a0001c0001t0004 a0001c0005t0001 others(2): Show |
199 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*53C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 12/12 | 53 | chr4 | 76112572 | ||||||
| chr4:76112606 | C | T | 1 | a0005c0006t0007 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 12/12 | 87 | chr4 | 76112606 | ||||||
| chr4:76112643 | A | G | 1 | a0001c0001t0004 | 5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*124A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 12/12 | 124 | chr4 | 76112643 | ||||||
| chr4:76112749 | ATAC | A | 5 | a0002c0002t0003 a0002c0002t0006 a0004c0004t0003 others(2): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*232_*234delACT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 12/12 | 232 | INFO_REALIGN_3_PRIME | chr4 | 76112749 | |||||
| chr4:76112763 | A | G | 1 | a0002c0002t0006 | 2 | NA18968.hp1 NA18989.hp2 |
3_prime_UTR_variant | MODIFIER | c.*244A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 12/12 | 244 | chr4 | 76112763 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76074840 | A | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.-10+21A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76074840 | |||||||
| chr4:76075045 | C | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.-10+226C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075045 | |||||||
| chr4:76075050 | G | A | 7 | a0001c0001t0001g0219 a0001c0001t0001g0223 a0001c0001t0002g0220 others(4): Show |
8 | HG01175.hp1 HG01243.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+231G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075050 | |||||||
| chr4:76075086 | C | A | 1 | a0007c0007t0002g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10+267C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075086 | |||||||
| chr4:76075100 | A | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.-10+281A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075100 | |||||||
| chr4:76075228 | G | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.-10+409G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075228 | |||||||
| chr4:76075454 | C | A | 1 | a0002c0002t0002g0033 | 2 | HG01081.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-9-427C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075454 | |||||||
| chr4:76075505 | T | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.-9-376T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075505 | |||||||
| chr4:76075529 | C | G | 1 | a0001c0001t0001g0218 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-9-352C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075529 | |||||||
| chr4:76075684 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02015.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-9-197G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075684 | |||||||
| chr4:76075771 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-110A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075771 | |||||||
| chr4:76075804 | C | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.-9-77C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075804 | |||||||
| chr4:76075805 | G | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
304 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.-9-76G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075805 | |||||||
| chr4:76075828 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0243 others(26): Show |
43 | HG01081.hp2 HG01109.hp1 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.-9-53C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 1/11 | chr4 | 76075828 | |||||||
| chr4:76075991 | G | A | 1 | a0007c0007t0002g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.69+33G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76075991 | |||||||
| chr4:76076004 | G | GT | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(92): Show |
134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.69+61dupT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76076004 | ||||||
| chr4:76076004 | G | GTT | 48 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0034 others(45): Show |
66 | HG00597.hp2 HG01081.hp2 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.69+60_69+61dupTT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76076004 | ||||||
| chr4:76076004 | G | GTTT | 11 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0262 others(8): Show |
12 | HG01884.hp1 HG01978.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.69+59_69+61dupTTT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76076004 | ||||||
| chr4:76076047 | A | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+89A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076047 | |||||||
| chr4:76076066 | T | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+108T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076066 | |||||||
| chr4:76076071 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+113T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076071 | |||||||
| chr4:76076073 | C | A | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+115C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076073 | |||||||
| chr4:76076105 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
304 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.69+147T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076105 | |||||||
| chr4:76076108 | C | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+150C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076108 | |||||||
| chr4:76076153 | T | C | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02523.hp1 HG02523.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+195T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076153 | |||||||
| chr4:76076270 | C | T | 2 | a0001c0005t0001g0037 a0006c0008t0001g0242 |
3 | HG02809.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.69+312C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076270 | |||||||
| chr4:76076342 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.69+384C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076342 | |||||||
| chr4:76076343 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.69+385T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076343 | |||||||
| chr4:76076344 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.69+386G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076344 | |||||||
| chr4:76076354 | A | G | 3 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0002c0002t0003g0238 |
3 | HG01243.hp2 HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.69+396A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076354 | |||||||
| chr4:76076357 | G | A | 1 | a0001c0001t0001g0006 | 7 | HG02040.hp1 HG02132.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+399G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076357 | |||||||
| chr4:76076397 | G | A | 6 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0003c0003t0001g0018 others(3): Show |
9 | HG01109.hp1 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+439G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076397 | |||||||
| chr4:76076401 | C | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+443C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076401 | |||||||
| chr4:76076416 | A | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
78 | HG01081.hp2 HG01109.hp1 HG01175.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+458A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076416 | |||||||
| chr4:76076556 | A | G | 1 | a0001c0001t0002g0160 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.69+598A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076556 | |||||||
| chr4:76076591 | C | A | 1 | a0001c0001t0002g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+633C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076591 | |||||||
| chr4:76076645 | T | C | 46 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(43): Show |
78 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.69+687T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076645 | |||||||
| chr4:76076647 | A | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69+689A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076647 | |||||||
| chr4:76076648 | C | T | 46 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(43): Show |
78 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.69+690C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076648 | |||||||
| chr4:76076881 | G | A | 7 | a0001c0001t0001g0219 a0001c0001t0001g0223 a0001c0001t0002g0220 others(4): Show |
8 | HG01175.hp1 HG01243.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+923G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76076881 | |||||||
| chr4:76076942 | CT | C | 46 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(43): Show |
78 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.69+990delT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76076942 | ||||||
| chr4:76077034 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.69+1076T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077034 | |||||||
| chr4:76077103 | G | A | 46 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(43): Show |
78 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.69+1145G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077103 | |||||||
| chr4:76077268 | G | A | 25 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0166 others(22): Show |
37 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.69+1310G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077268 | |||||||
| chr4:76077270 | A | T | 2 | a0001c0001t0001g0092 a0002c0002t0003g0093 |
2 | NA18942.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.69+1312A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077270 | |||||||
| chr4:76077374 | A | G | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.69+1416A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077374 | |||||||
| chr4:76077385 | G | A | 3 | a0002c0002t0003g0044 a0002c0002t0003g0102 a0002c0002t0003g0103 |
3 | HG04184.hp1 NA18943.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.69+1427G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077385 | |||||||
| chr4:76077390 | G | A | 46 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(43): Show |
78 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.69+1432G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077390 | |||||||
| chr4:76077430 | C | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0028 others(112): Show |
175 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.69+1472C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077430 | |||||||
| chr4:76077534 | T | C | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.69+1576T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077534 | |||||||
| chr4:76077719 | A | G | 1 | a0002c0002t0002g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.69+1761A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077719 | |||||||
| chr4:76077753 | T | C | 1 | a0002c0002t0002g0108 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.69+1795T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077753 | |||||||
| chr4:76077891 | C | T | 1 | a0001c0001t0004g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.69+1933C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077891 | |||||||
| chr4:76077900 | T | C | 1 | a0001c0001t0004g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.69+1942T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077900 | |||||||
| chr4:76077928 | A | G | 7 | a0001c0001t0001g0219 a0001c0001t0001g0223 a0001c0001t0002g0220 others(4): Show |
8 | HG01175.hp1 HG01243.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+1970A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76077928 | |||||||
| chr4:76078004 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0028 others(112): Show |
175 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.69+2046G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078004 | |||||||
| chr4:76078019 | C | G | 7 | a0001c0001t0001g0036 a0001c0001t0001g0233 a0001c0001t0001g0234 others(4): Show |
8 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+2061C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078019 | |||||||
| chr4:76078044 | A | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(70): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.69+2086A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078044 | |||||||
| chr4:76078091 | G | A | 46 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(43): Show |
78 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.69+2133G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078091 | |||||||
| chr4:76078109 | A | G | 1 | a0002c0002t0002g0158 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.69+2151A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078109 | |||||||
| chr4:76078179 | G | A | 2 | a0001c0005t0001g0037 a0006c0008t0001g0242 |
3 | HG02809.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.69+2221G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078179 | |||||||
| chr4:76078229 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.69+2271A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078229 | |||||||
| chr4:76078280 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG03195.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69+2322C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078280 | |||||||
| chr4:76078341 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02015.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.69+2383T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078341 | |||||||
| chr4:76078370 | G | A | 62 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0047 others(59): Show |
102 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.69+2412G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078370 | |||||||
| chr4:76078387 | C | T | 1 | a0001c0001t0004g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.69+2429C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078387 | |||||||
| chr4:76078456 | G | A | 55 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0049 others(52): Show |
88 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.69+2498G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078456 | |||||||
| chr4:76078576 | G | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0208 |
3 | NA18965.hp1 NA19009.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.69+2618G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078576 | |||||||
| chr4:76078648 | T | A | 10 | a0001c0001t0001g0219 a0001c0001t0001g0239 a0001c0001t0002g0220 others(7): Show |
10 | HG01175.hp1 HG01243.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+2690T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078648 | |||||||
| chr4:76078652 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(178): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.69+2694C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078652 | |||||||
| chr4:76078661 | G | GT | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(217): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.69+2705dupT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76078661 | ||||||
| chr4:76078688 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.69+2730A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078688 | |||||||
| chr4:76078807 | A | G | 1 | a0002c0002t0002g0259 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.69+2849A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078807 | |||||||
| chr4:76078847 | G | A | 10 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(7): Show |
19 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(16): Show |
intron_variant | MODIFIER | c.69+2889G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078847 | |||||||
| chr4:76078866 | G | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(197): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.69+2908G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078866 | |||||||
| chr4:76078869 | G | A | 29 | a0001c0001t0001g0070 a0001c0001t0001g0239 a0001c0001t0002g0173 others(26): Show |
39 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+2911G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078869 | |||||||
| chr4:76078949 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.70-2875C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76078949 | |||||||
| chr4:76079012 | C | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0034 others(14): Show |
23 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-2812C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079012 | |||||||
| chr4:76079030 | G | A | 1 | a0006c0008t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.70-2794G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079030 | |||||||
| chr4:76079086 | A | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(217): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.70-2738A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079086 | |||||||
| chr4:76079157 | T | G | 8 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0118 others(5): Show |
17 | HG00673.hp1 HG02083.hp1 NA18948.hp1 others(14): Show |
intron_variant | MODIFIER | c.70-2667T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079157 | |||||||
| chr4:76079176 | T | TA | 29 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0047 others(26): Show |
42 | HG00423.hp1 HG01109.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.70-2630dupA | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76079176 | ||||||
| chr4:76079176 | T | TAA | 102 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(99): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.70-2631_70-2630dup others(2): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76079176 | ||||||
| chr4:76079176 | T | TAAA | 41 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(38): Show |
59 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.70-2632_70-2630dup others(3): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76079176 | ||||||
| chr4:76079176 | T | TAAAA | 20 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(17): Show |
29 | HG00673.hp1 HG01243.hp2 HG02083.hp1 others(26): Show |
intron_variant | MODIFIER | c.70-2633_70-2630dup others(4): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76079176 | ||||||
| chr4:76079176 | T | TAAAAA | 8 | a0001c0001t0001g0078 a0001c0001t0002g0118 a0001c0001t0002g0119 others(5): Show |
9 | HG01168.hp2 HG02809.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-2634_70-2630dup others(5): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76079176 | ||||||
| chr4:76079176 | T | TAAAAAA | 21 | a0001c0001t0001g0219 a0001c0001t0002g0173 a0001c0001t0002g0220 others(18): Show |
31 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.70-2635_70-2630dup others(6): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76079176 | ||||||
| chr4:76079288 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(165): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.70-2536A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079288 | |||||||
| chr4:76079318 | G | A | 1 | a0002c0002t0003g0238 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.70-2506G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079318 | |||||||
| chr4:76079409 | G | C | 2 | a0002c0002t0002g0030 a0002c0002t0002g0214 |
3 | HG01257.hp2 HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.70-2415G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079409 | |||||||
| chr4:76079428 | T | G | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-2396T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079428 | |||||||
| chr4:76079814 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.70-2010G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079814 | |||||||
| chr4:76079852 | C | T | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-1972C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079852 | |||||||
| chr4:76079867 | ATCTCTGT others(7): Show |
A | 1 | a0001c0001t0001g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.70-1939_70-1926del others(14): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76079867 | ||||||
| chr4:76079914 | T | A | 1 | a0002c0002t0002g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.70-1910T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079914 | |||||||
| chr4:76079916 | T | A | 1 | a0002c0002t0002g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.70-1908T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079916 | |||||||
| chr4:76079916 | T | TCACA | 42 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(39): Show |
60 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.70-1907_70-1906ins others(4): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76079916 | ||||||
| chr4:76079918 | T | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
127 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.70-1906T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079918 | |||||||
| chr4:76079918 | T | TCA | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-1893_70-1892dup others(2): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76079918 | ||||||
| chr4:76079931 | C | G | 5 | a0001c0001t0001g0264 a0002c0002t0002g0019 a0002c0002t0002g0108 others(2): Show |
7 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-1893C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079931 | |||||||
| chr4:76079931 | CAGAG | C | 19 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0034 others(16): Show |
25 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.70-1876_70-1873del others(4): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76079931 | ||||||
| chr4:76079933 | G | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(87): Show |
127 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.70-1891G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079933 | |||||||
| chr4:76079935 | G | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0219 a0001c0001t0001g0239 others(4): Show |
7 | HG01175.hp1 HG02818.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-1889G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76079935 | |||||||
| chr4:76080017 | A | G | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-1807A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080017 | |||||||
| chr4:76080031 | A | G | 8 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0118 others(5): Show |
17 | HG00673.hp1 HG02083.hp1 NA18948.hp1 others(14): Show |
intron_variant | MODIFIER | c.70-1793A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080031 | |||||||
| chr4:76080178 | A | G | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-1646A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080178 | |||||||
| chr4:76080273 | C | T | 136 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
206 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.70-1551C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080273 | |||||||
| chr4:76080382 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0126 a0001c0001t0001g0155 others(1): Show |
6 | NA18964.hp1 NA18971.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-1442C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080382 | |||||||
| chr4:76080445 | A | G | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-1379A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080445 | |||||||
| chr4:76080566 | T | C | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-1258T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080566 | |||||||
| chr4:76080569 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.70-1255G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080569 | |||||||
| chr4:76080577 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-1247C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080577 | |||||||
| chr4:76080579 | C | T | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-1245C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080579 | |||||||
| chr4:76080667 | C | T | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-1157C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080667 | |||||||
| chr4:76080685 | A | G | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-1139A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080685 | |||||||
| chr4:76080702 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.70-1122G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080702 | |||||||
| chr4:76080709 | T | TC | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
64 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.70-1114dupC | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 76080709 | ||||||
| chr4:76080711 | A | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
64 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.70-1113A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080711 | |||||||
| chr4:76080730 | T | C | 2 | a0002c0002t0002g0024 a0002c0002t0002g0158 |
3 | HG00323.hp2 HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.70-1094T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080730 | |||||||
| chr4:76080770 | G | C | 1 | a0003c0003t0001g0038 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.70-1054G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080770 | |||||||
| chr4:76080960 | T | G | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-864T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76080960 | |||||||
| chr4:76081097 | G | A | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-727G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081097 | |||||||
| chr4:76081129 | T | G | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-695T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081129 | |||||||
| chr4:76081139 | T | C | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-685T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081139 | |||||||
| chr4:76081283 | T | G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0075 a0002c0002t0003g0048 others(1): Show |
4 | HG01346.hp1 HG01934.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-541T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081283 | |||||||
| chr4:76081364 | A | G | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-460A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081364 | |||||||
| chr4:76081419 | A | G | 29 | a0001c0001t0001g0070 a0001c0001t0002g0173 a0001c0001t0002g0178 others(26): Show |
40 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.70-405A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081419 | |||||||
| chr4:76081436 | G | A | 29 | a0001c0001t0001g0070 a0001c0001t0002g0173 a0001c0001t0002g0178 others(26): Show |
40 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.70-388G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081436 | |||||||
| chr4:76081555 | C | G | 1 | a0002c0002t0005g0210 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.70-269C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081555 | |||||||
| chr4:76081570 | A | C | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-254A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081570 | |||||||
| chr4:76081590 | C | G | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-234C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081590 | |||||||
| chr4:76081639 | G | T | 47 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(44): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.70-185G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081639 | |||||||
| chr4:76081781 | G | A | 51 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(48): Show |
83 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.70-43G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081781 | |||||||
| chr4:76081799 | G | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(41): Show |
62 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.70-25G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 2/11 | chr4 | 76081799 | |||||||
| chr4:76082644 | C | T | 4 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | HG00642.hp2 HG03239.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+109C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76082644 | |||||||
| chr4:76082846 | C | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(102): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.781+311C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76082846 | |||||||
| chr4:76082937 | T | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(32): Show |
53 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.781+402T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76082937 | |||||||
| chr4:76082958 | AC | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(102): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.781+426delC | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 76082958 | ||||||
| chr4:76083009 | G | A | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.781+474G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76083009 | |||||||
| chr4:76083025 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(210): Show |
313 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.781+490G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76083025 | |||||||
| chr4:76083525 | C | T | 1 | a0006c0008t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781+990C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76083525 | |||||||
| chr4:76083538 | A | G | 1 | a0002c0002t0002g0199 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.781+1003A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76083538 | |||||||
| chr4:76083732 | T | A | 1 | a0001c0001t0001g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.781+1197T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76083732 | |||||||
| chr4:76083865 | G | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(103): Show |
146 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.781+1330G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76083865 | |||||||
| chr4:76083876 | T | G | 1 | a0002c0002t0002g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.781+1341T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76083876 | |||||||
| chr4:76083912 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.781+1377C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76083912 | |||||||
| chr4:76083975 | C | T | 3 | a0001c0001t0001g0219 a0001c0001t0002g0220 a0001c0001t0002g0224 |
3 | HG01175.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.781+1440C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76083975 | |||||||
| chr4:76084048 | T | G | 10 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(7): Show |
19 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(16): Show |
intron_variant | MODIFIER | c.781+1513T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76084048 | |||||||
| chr4:76084130 | T | C | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.781+1595T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76084130 | |||||||
| chr4:76084262 | C | T | 10 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(7): Show |
19 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(16): Show |
intron_variant | MODIFIER | c.781+1727C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76084262 | |||||||
| chr4:76084661 | T | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(35): Show |
57 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.781+2126T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76084661 | |||||||
| chr4:76084812 | C | A | 1 | a0002c0002t0002g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.781+2277C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76084812 | |||||||
| chr4:76084866 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+2331C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76084866 | |||||||
| chr4:76084949 | A | C | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.781+2414A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76084949 | |||||||
| chr4:76084999 | C | A | 4 | a0001c0001t0001g0219 a0001c0001t0002g0220 a0001c0001t0002g0224 others(1): Show |
4 | HG01175.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+2464C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76084999 | |||||||
| chr4:76085040 | A | G | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG03195.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+2505A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085040 | |||||||
| chr4:76085087 | C | T | 16 | a0001c0001t0001g0219 a0001c0001t0002g0003 a0001c0001t0002g0022 others(13): Show |
25 | HG00673.hp1 HG01175.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.781+2552C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085087 | |||||||
| chr4:76085461 | C | G | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.781+2926C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085461 | |||||||
| chr4:76085566 | A | C | 1 | a0001c0001t0004g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.781+3031A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085566 | |||||||
| chr4:76085618 | T | C | 1 | a0002c0002t0002g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.781+3083T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085618 | |||||||
| chr4:76085651 | C | T | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.781+3116C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085651 | |||||||
| chr4:76085652 | G | A | 83 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
122 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.781+3117G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085652 | |||||||
| chr4:76085809 | T | C | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG03195.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+3274T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085809 | |||||||
| chr4:76085824 | C | T | 29 | a0001c0001t0001g0070 a0001c0001t0002g0173 a0001c0001t0002g0178 others(26): Show |
40 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.781+3289C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085824 | |||||||
| chr4:76085905 | C | T | 4 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0114 others(1): Show |
4 | HG00323.hp1 HG03492.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+3370C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085905 | |||||||
| chr4:76085943 | G | A | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.781+3408G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085943 | |||||||
| chr4:76085969 | G | A | 29 | a0001c0001t0001g0070 a0001c0001t0002g0173 a0001c0001t0002g0178 others(26): Show |
40 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.781+3434G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085969 | |||||||
| chr4:76085977 | C | T | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.781+3442C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76085977 | |||||||
| chr4:76086059 | T | TC | 13 | a0001c0001t0001g0200 a0001c0001t0001g0236 a0001c0001t0002g0003 others(10): Show |
21 | HG00673.hp1 HG01261.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.781+3534dupC | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 76086059 | ||||||
| chr4:76086059 | TC | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(41): Show |
63 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.781+3534delC | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 76086059 | ||||||
| chr4:76086060 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.781+3525C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086060 | |||||||
| chr4:76086063 | C | CA | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+3528_781+3529i others(3): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086063 | |||||||
| chr4:76086065 | C | G | 49 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(46): Show |
81 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.781+3530C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086065 | |||||||
| chr4:76086066 | C | T | 1 | a0002c0002t0002g0198 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.781+3531C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086066 | |||||||
| chr4:76086067 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.781+3532C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086067 | |||||||
| chr4:76086080 | C | T | 3 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 |
4 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+3545C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086080 | |||||||
| chr4:76086099 | C | T | 1 | a0002c0002t0003g0071 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.781+3564C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086099 | |||||||
| chr4:76086193 | A | T | 1 | a0001c0001t0001g0028 | 2 | HG03491.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.781+3658A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086193 | |||||||
| chr4:76086246 | A | C | 1 | a0002c0002t0003g0107 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.781+3711A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086246 | |||||||
| chr4:76086353 | G | A | 1 | a0001c0001t0001g0010 | 4 | HG00609.hp2 NA19004.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+3818G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086353 | |||||||
| chr4:76086379 | A | G | 6 | a0001c0001t0001g0219 a0001c0001t0002g0220 a0001c0001t0002g0224 others(3): Show |
6 | HG01175.hp1 HG01243.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.781+3844A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086379 | |||||||
| chr4:76086597 | G | A | 4 | a0001c0001t0001g0219 a0001c0001t0002g0220 a0001c0001t0002g0224 others(1): Show |
4 | HG01175.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+4062G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086597 | |||||||
| chr4:76086610 | A | G | 1 | a0002c0002t0002g0180 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.781+4075A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086610 | |||||||
| chr4:76086631 | G | T | 1 | a0002c0002t0003g0065 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.781+4096G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086631 | |||||||
| chr4:76086712 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.781+4177T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086712 | |||||||
| chr4:76086759 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(102): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.781+4224C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76086759 | |||||||
| chr4:76087064 | G | A | 6 | a0001c0001t0001g0219 a0001c0001t0002g0220 a0001c0001t0002g0224 others(3): Show |
6 | HG01175.hp1 HG01243.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.781+4529G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76087064 | |||||||
| chr4:76087289 | A | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+4754A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76087289 | |||||||
| chr4:76087585 | G | A | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG03195.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+5050G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76087585 | |||||||
| chr4:76087606 | A | G | 4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+5071A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76087606 | |||||||
| chr4:76087651 | T | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(210): Show |
313 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.781+5116T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76087651 | |||||||
| chr4:76087697 | C | T | 50 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(47): Show |
82 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.781+5162C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76087697 | |||||||
| chr4:76087814 | T | C | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG03195.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+5279T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76087814 | |||||||
| chr4:76088022 | G | A | 137 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
208 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.781+5487G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088022 | |||||||
| chr4:76088028 | G | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.781+5493G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088028 | |||||||
| chr4:76088189 | T | C | 50 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0059 others(47): Show |
82 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.781+5654T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088189 | |||||||
| chr4:76088248 | CT | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(207): Show |
310 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.781+5726delT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 76088248 | ||||||
| chr4:76088251 | T | C | 1 | a0002c0002t0003g0050 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.781+5716T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088251 | |||||||
| chr4:76088282 | A | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+5747A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088282 | |||||||
| chr4:76088321 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.781+5786C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088321 | |||||||
| chr4:76088425 | C | T | 2 | a0002c0002t0006g0074 a0002c0002t0006g0106 |
2 | NA18968.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.781+5890C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088425 | |||||||
| chr4:76088456 | A | AC | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+5922dupC | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 76088456 | ||||||
| chr4:76088468 | T | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+5933T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088468 | |||||||
| chr4:76088495 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.781+5960A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088495 | |||||||
| chr4:76088622 | T | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+6087T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088622 | |||||||
| chr4:76088793 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.781+6258G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088793 | |||||||
| chr4:76088905 | A | C | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.781+6370A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088905 | |||||||
| chr4:76088965 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.781+6430A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76088965 | |||||||
| chr4:76089188 | C | G | 10 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(7): Show |
19 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(16): Show |
intron_variant | MODIFIER | c.781+6653C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089188 | |||||||
| chr4:76089327 | A | G | 1 | a0002c0002t0003g0238 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.781+6792A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089327 | |||||||
| chr4:76089352 | G | T | 1 | a0002c0002t0002g0177 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.781+6817G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089352 | |||||||
| chr4:76089362 | T | TGTTTCTA others(5): Show |
4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+6827_781+6828i others(14): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089362 | |||||||
| chr4:76089363 | C | A | 4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+6828C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089363 | |||||||
| chr4:76089365 | T | G | 4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+6830T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089365 | |||||||
| chr4:76089367 | G | A | 4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+6832G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089367 | |||||||
| chr4:76089393 | G | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0223 a0001c0001t0001g0227 others(15): Show |
26 | HG01255.hp2 HG01358.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.781+6858G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089393 | |||||||
| chr4:76089547 | G | T | 49 | a0001c0001t0001g0070 a0001c0001t0001g0094 a0001c0001t0001g0095 others(46): Show |
70 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.781+7012G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089547 | |||||||
| chr4:76089548 | G | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+7013G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089548 | |||||||
| chr4:76089562 | G | T | 1 | a0001c0001t0004g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.781+7027G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089562 | |||||||
| chr4:76089637 | C | A | 28 | a0001c0001t0001g0070 a0001c0001t0002g0173 a0001c0001t0002g0178 others(25): Show |
39 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.781+7102C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089637 | |||||||
| chr4:76089723 | AAGCTAGT | A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
123 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.781+7191_781+7197d others(9): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 76089723 | ||||||
| chr4:76089739 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+7204C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089739 | |||||||
| chr4:76089807 | C | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0165 |
4 | NA18964.hp1 NA18971.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+7272C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089807 | |||||||
| chr4:76089820 | G | C | 1 | a0002c0002t0003g0048 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.781+7285G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089820 | |||||||
| chr4:76089847 | C | T | 3 | a0001c0001t0001g0219 a0001c0001t0002g0220 a0001c0001t0002g0224 |
3 | HG01175.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.781+7312C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089847 | |||||||
| chr4:76089856 | C | A | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.781+7321C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089856 | |||||||
| chr4:76089877 | C | T | 4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+7342C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089877 | |||||||
| chr4:76089970 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0085 others(6): Show |
18 | HG00544.hp1 HG01070.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.781+7435C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76089970 | |||||||
| chr4:76090019 | G | A | 1 | a0002c0002t0002g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.781+7484G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090019 | |||||||
| chr4:76090037 | G | A | 44 | a0001c0001t0001g0059 a0002c0002t0002g0056 a0002c0002t0003g0001 others(41): Show |
76 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.781+7502G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090037 | |||||||
| chr4:76090062 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.781+7527A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090062 | |||||||
| chr4:76090204 | T | G | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG03195.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.782-7440T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090204 | |||||||
| chr4:76090260 | G | A | 46 | a0001c0001t0001g0059 a0002c0002t0002g0056 a0002c0002t0003g0001 others(43): Show |
78 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.782-7384G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090260 | |||||||
| chr4:76090540 | T | G | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.782-7104T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090540 | |||||||
| chr4:76090651 | C | A | 1 | a0001c0001t0001g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.782-6993C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090651 | |||||||
| chr4:76090652 | T | G | 1 | a0001c0001t0001g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.782-6992T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090652 | |||||||
| chr4:76090653 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.782-6991T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090653 | |||||||
| chr4:76090706 | C | T | 2 | a0001c0001t0001g0239 a0006c0008t0001g0242 |
2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.782-6938C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090706 | |||||||
| chr4:76090731 | T | C | 1 | a0001c0001t0001g0017 | 3 | HG01891.hp2 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.782-6913T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090731 | |||||||
| chr4:76090762 | G | T | 1 | a0002c0002t0003g0076 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.782-6882G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090762 | |||||||
| chr4:76090817 | A | G | 4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.782-6827A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090817 | |||||||
| chr4:76090948 | T | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.782-6696T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090948 | |||||||
| chr4:76090949 | T | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.782-6695T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76090949 | |||||||
| chr4:76091001 | C | T | 2 | a0002c0002t0002g0176 a0002c0002t0002g0209 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.782-6643C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76091001 | |||||||
| chr4:76091242 | T | C | 4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.782-6402T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76091242 | |||||||
| chr4:76091246 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.782-6398A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76091246 | |||||||
| chr4:76091316 | T | C | 1 | a0001c0005t0001g0037 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.782-6328T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76091316 | |||||||
| chr4:76091385 | A | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.782-6259A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76091385 | |||||||
| chr4:76091447 | G | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.782-6197G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76091447 | |||||||
| chr4:76091495 | T | C | 1 | a0002c0002t0003g0051 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.782-6149T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76091495 | |||||||
| chr4:76091679 | C | CT | 13 | a0001c0001t0001g0100 a0001c0001t0001g0145 a0001c0001t0001g0146 others(10): Show |
13 | HG00280.hp1 HG02080.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.782-5945dupT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 76091679 | ||||||
| chr4:76091679 | CT | C | 46 | a0001c0001t0001g0036 a0001c0001t0001g0070 a0001c0001t0001g0169 others(43): Show |
67 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.782-5945delT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 76091679 | ||||||
| chr4:76091679 | CTT | C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
116 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.782-5946_782-5945d others(4): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 76091679 | ||||||
| chr4:76092021 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.782-5623G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76092021 | |||||||
| chr4:76092038 | A | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(99): Show |
154 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.782-5606A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76092038 | |||||||
| chr4:76092140 | C | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.782-5504C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76092140 | |||||||
| chr4:76092315 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.782-5329A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76092315 | |||||||
| chr4:76092573 | A | T | 1 | a0002c0002t0002g0197 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.782-5071A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76092573 | |||||||
| chr4:76092590 | T | C | 1 | a0002c0002t0002g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.782-5054T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76092590 | |||||||
| chr4:76093002 | G | C | 2 | a0001c0001t0001g0239 a0006c0008t0001g0242 |
2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.782-4642G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76093002 | |||||||
| chr4:76093009 | T | C | 3 | a0001c0001t0001g0133 a0001c0001t0001g0145 a0001c0001t0001g0164 |
3 | NA18983.hp1 NA19012.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.782-4635T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76093009 | |||||||
| chr4:76093190 | G | T | 25 | a0001c0001t0001g0070 a0002c0002t0002g0009 a0002c0002t0002g0011 others(22): Show |
35 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.782-4454G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76093190 | |||||||
| chr4:76093228 | C | T | 16 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(13): Show |
26 | HG00673.hp1 HG01243.hp1 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.782-4416C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76093228 | |||||||
| chr4:76093402 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.782-4242C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76093402 | |||||||
| chr4:76093596 | A | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(230): Show |
343 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.782-4048A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76093596 | |||||||
| chr4:76093713 | G | A | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG03195.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.782-3931G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76093713 | |||||||
| chr4:76093931 | G | A | 2 | a0001c0001t0001g0239 a0006c0008t0001g0242 |
2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.782-3713G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76093931 | |||||||
| chr4:76094106 | C | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(181): Show |
273 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.782-3538C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76094106 | |||||||
| chr4:76094238 | T | C | 1 | a0001c0001t0004g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.782-3406T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76094238 | |||||||
| chr4:76094438 | A | T | 48 | a0001c0001t0001g0059 a0001c0001t0001g0228 a0002c0002t0002g0056 others(45): Show |
80 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.782-3206A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76094438 | |||||||
| chr4:76094512 | A | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(49): Show |
72 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.782-3132A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76094512 | |||||||
| chr4:76094742 | A | T | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.782-2902A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76094742 | |||||||
| chr4:76094898 | G | T | 3 | a0002c0002t0003g0060 a0002c0002t0003g0061 a0002c0002t0003g0062 |
3 | HG00558.hp2 HG02071.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.782-2746G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76094898 | |||||||
| chr4:76095154 | G | T | 1 | a0002c0002t0002g0196 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.782-2490G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76095154 | |||||||
| chr4:76095222 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.782-2422A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76095222 | |||||||
| chr4:76095303 | T | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0145 a0001c0001t0001g0164 |
3 | NA18983.hp1 NA19012.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.782-2341T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76095303 | |||||||
| chr4:76095444 | G | T | 1 | a0001c0001t0001g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.782-2200G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76095444 | |||||||
| chr4:76095541 | A | G | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.782-2103A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76095541 | |||||||
| chr4:76095596 | T | C | 1 | a0001c0001t0002g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.782-2048T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76095596 | |||||||
| chr4:76095839 | T | C | 2 | a0002c0002t0002g0011 a0002c0002t0002g0179 |
5 | HG01884.hp2 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-1805T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76095839 | |||||||
| chr4:76095923 | AT | A | 17 | a0001c0001t0001g0081 a0001c0001t0002g0003 a0001c0001t0002g0022 others(14): Show |
27 | HG00673.hp1 HG01243.hp1 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.782-1710delT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 76095923 | ||||||
| chr4:76095973 | G | A | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.782-1671G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76095973 | |||||||
| chr4:76096023 | A | T | 1 | a0002c0002t0002g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.782-1621A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096023 | |||||||
| chr4:76096069 | C | T | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG01243.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-1575C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096069 | |||||||
| chr4:76096177 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.782-1467G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096177 | |||||||
| chr4:76096318 | A | G | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.782-1326A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096318 | |||||||
| chr4:76096361 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.782-1283C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096361 | |||||||
| chr4:76096410 | C | G | 2 | a0002c0002t0002g0175 a0002c0002t0002g0207 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.782-1234C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096410 | |||||||
| chr4:76096470 | T | C | 2 | a0002c0002t0002g0011 a0002c0002t0002g0179 |
5 | HG01884.hp2 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-1174T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096470 | |||||||
| chr4:76096472 | G | C | 1 | a0002c0002t0003g0107 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.782-1172G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096472 | |||||||
| chr4:76096485 | C | T | 1 | a0001c0001t0001g0025 | 2 | NA18984.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.782-1159C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096485 | |||||||
| chr4:76096526 | G | A | 1 | a0007c0007t0002g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.782-1118G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096526 | |||||||
| chr4:76096527 | C | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(230): Show |
343 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.782-1117C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096527 | |||||||
| chr4:76096571 | G | A | 27 | a0001c0001t0001g0070 a0001c0001t0001g0145 a0001c0005t0001g0037 others(24): Show |
38 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.782-1073G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096571 | |||||||
| chr4:76096590 | G | A | 1 | a0002c0002t0003g0060 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.782-1054G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096590 | |||||||
| chr4:76096834 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.782-810A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76096834 | |||||||
| chr4:76097010 | C | T | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.782-634C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76097010 | |||||||
| chr4:76097156 | T | C | 4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.782-488T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76097156 | |||||||
| chr4:76097231 | G | T | 1 | a0001c0001t0002g0224 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.782-413G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76097231 | |||||||
| chr4:76097299 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0127 a0001c0001t0001g0130 others(2): Show |
5 | HG00558.hp1 HG00639.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-345G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76097299 | |||||||
| chr4:76097386 | T | C | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.782-258T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76097386 | |||||||
| chr4:76097456 | A | G | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.782-188A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 3/11 | chr4 | 76097456 | |||||||
| chr4:76097704 | A | G | 1 | a0002c0002t0002g0177 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.814+28A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76097704 | |||||||
| chr4:76097723 | T | A | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.814+47T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76097723 | |||||||
| chr4:76097738 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.814+62A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76097738 | |||||||
| chr4:76097759 | A | G | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.814+83A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76097759 | |||||||
| chr4:76097987 | C | T | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.814+311C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76097987 | |||||||
| chr4:76098033 | T | G | 1 | a0005c0006t0003g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.814+357T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76098033 | |||||||
| chr4:76098200 | C | CA | 7 | a0001c0001t0001g0031 a0001c0001t0001g0187 a0001c0001t0002g0120 others(4): Show |
8 | HG02622.hp2 HG02738.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.814+541dupA | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 76098200 | ||||||
| chr4:76098200 | CA | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
266 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.814+541delA | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 76098200 | ||||||
| chr4:76098200 | CAA | C | 9 | a0001c0001t0001g0059 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
9 | HG02818.hp1 HG03195.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.814+540_814+541del others(2): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 76098200 | ||||||
| chr4:76098360 | G | A | 1 | a0002c0002t0005g0210 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.815-595G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76098360 | |||||||
| chr4:76098428 | A | G | 132 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
201 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.815-527A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76098428 | |||||||
| chr4:76098436 | A | G | 4 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | HG00642.hp2 HG03239.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.815-519A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76098436 | |||||||
| chr4:76098497 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.815-458T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76098497 | |||||||
| chr4:76098684 | C | T | 14 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(11): Show |
23 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(20): Show |
intron_variant | MODIFIER | c.815-271C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76098684 | |||||||
| chr4:76098816 | G | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
305 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.815-139G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76098816 | |||||||
| chr4:76098932 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.815-23A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 4/11 | chr4 | 76098932 | |||||||
| chr4:76099160 | G | A | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.847+173G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | chr4 | 76099160 | |||||||
| chr4:76099165 | G | C | 2 | a0001c0001t0001g0239 a0006c0008t0001g0242 |
2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.847+178G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | chr4 | 76099165 | |||||||
| chr4:76099458 | T | G | 8 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0118 others(5): Show |
17 | HG00673.hp1 HG02083.hp1 NA18948.hp1 others(14): Show |
intron_variant | MODIFIER | c.847+471T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | chr4 | 76099458 | |||||||
| chr4:76099629 | C | CA | 12 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(9): Show |
21 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(18): Show |
intron_variant | MODIFIER | c.847+643dupA | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 76099629 | ||||||
| chr4:76099684 | A | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(50): Show |
73 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.848-607A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | chr4 | 76099684 | |||||||
| chr4:76099837 | A | G | 1 | a0002c0002t0003g0057 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.848-454A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | chr4 | 76099837 | |||||||
| chr4:76099924 | G | A | 140 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
210 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.848-367G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | chr4 | 76099924 | |||||||
| chr4:76100093 | G | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-198G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | chr4 | 76100093 | |||||||
| chr4:76100100 | A | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(50): Show |
73 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.848-191A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | chr4 | 76100100 | |||||||
| chr4:76100135 | G | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(212): Show |
315 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.848-156G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | chr4 | 76100135 | |||||||
| chr4:76100143 | CAACTT | C | 16 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(13): Show |
25 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(22): Show |
intron_variant | MODIFIER | c.848-145_848-141del others(5): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 76100143 | ||||||
| chr4:76100228 | A | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-63A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | chr4 | 76100228 | |||||||
| chr4:76100280 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(84): Show |
119 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.848-11C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 5/11 | chr4 | 76100280 | |||||||
| chr4:76100398 | C | T | 3 | a0001c0001t0001g0167 a0002c0002t0002g0030 a0002c0002t0002g0214 |
4 | HG01257.hp2 HG02738.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+78C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 6/11 | chr4 | 76100398 | |||||||
| chr4:76100403 | C | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+83C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 6/11 | chr4 | 76100403 | |||||||
| chr4:76100579 | T | C | 8 | a0003c0003t0001g0018 a0003c0003t0001g0038 a0003c0003t0001g0040 others(5): Show |
12 | HG01109.hp1 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.878-216T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 6/11 | chr4 | 76100579 | |||||||
| chr4:76100629 | C | CA | 17 | a0001c0001t0001g0110 a0001c0001t0001g0142 a0001c0001t0001g0143 others(14): Show |
18 | HG01099.hp2 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.878-147dupA | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 76100629 | ||||||
| chr4:76100629 | C | CAA | 48 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(45): Show |
68 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.878-148_878-147dup others(2): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 76100629 | ||||||
| chr4:76100629 | CA | C | 16 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0094 others(13): Show |
19 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.878-147delA | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 76100629 | ||||||
| chr4:76100762 | G | A | 24 | a0001c0001t0001g0070 a0001c0005t0001g0037 a0002c0002t0002g0009 others(21): Show |
35 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.878-33G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 6/11 | chr4 | 76100762 | |||||||
| chr4:76100863 | A | G | 1 | a0002c0002t0002g0194 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.907+39A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 7/11 | chr4 | 76100863 | |||||||
| chr4:76101133 | C | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(50): Show |
73 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.937+114C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101133 | |||||||
| chr4:76101162 | C | G | 1 | a0002c0002t0002g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.937+143C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101162 | |||||||
| chr4:76101217 | T | G | 1 | a0002c0002t0002g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.937+198T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101217 | |||||||
| chr4:76101379 | C | A | 1 | a0001c0001t0004g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.937+360C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101379 | |||||||
| chr4:76101434 | G | A | 24 | a0001c0001t0001g0070 a0001c0005t0001g0037 a0002c0002t0002g0009 others(21): Show |
35 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.937+415G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101434 | |||||||
| chr4:76101494 | G | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG01070.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.937+475G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101494 | |||||||
| chr4:76101505 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+486C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101505 | |||||||
| chr4:76101608 | C | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+589C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101608 | |||||||
| chr4:76101701 | G | A | 45 | a0001c0001t0001g0059 a0002c0002t0002g0056 a0002c0002t0003g0001 others(42): Show |
77 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.937+682G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101701 | |||||||
| chr4:76101706 | C | T | 12 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(9): Show |
21 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(18): Show |
intron_variant | MODIFIER | c.937+687C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101706 | |||||||
| chr4:76101733 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.937+714C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101733 | |||||||
| chr4:76101753 | GA | G | 24 | a0001c0001t0001g0070 a0001c0005t0001g0037 a0002c0002t0002g0009 others(21): Show |
35 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.937+744delA | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76101753 | ||||||
| chr4:76101758 | A | G | 16 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(13): Show |
25 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(22): Show |
intron_variant | MODIFIER | c.937+739A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101758 | |||||||
| chr4:76101789 | G | A | 1 | a0002c0002t0003g0014 | 3 | HG02735.hp2 HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.937+770G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101789 | |||||||
| chr4:76101907 | A | G | 12 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(9): Show |
21 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(18): Show |
intron_variant | MODIFIER | c.937+888A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101907 | |||||||
| chr4:76101909 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.937+890C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76101909 | |||||||
| chr4:76102039 | AT | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+1023delT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76102039 | ||||||
| chr4:76102045 | GATTCTAG others(3): Show |
G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+1027_937+1036d others(12): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76102045 | |||||||
| chr4:76102085 | A | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): Show |
301 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.937+1066A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76102085 | |||||||
| chr4:76102089 | A | G | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
6 | HG02280.hp1 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.937+1070A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76102089 | |||||||
| chr4:76102315 | CTGTTATT | C | 12 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(9): Show |
21 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(18): Show |
intron_variant | MODIFIER | c.937+1298_937+1304d others(9): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76102315 | ||||||
| chr4:76102346 | T | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(66): Show |
98 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.937+1327T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76102346 | |||||||
| chr4:76102400 | G | A | 6 | a0002c0002t0002g0009 a0002c0002t0002g0172 a0002c0002t0002g0176 others(3): Show |
9 | HG01255.hp1 HG01496.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.937+1381G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76102400 | |||||||
| chr4:76102427 | T | A | 16 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(13): Show |
25 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(22): Show |
intron_variant | MODIFIER | c.937+1408T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76102427 | |||||||
| chr4:76102538 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(206): Show |
308 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.938-1399C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76102538 | |||||||
| chr4:76102638 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(206): Show |
308 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.938-1299G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76102638 | |||||||
| chr4:76102655 | T | TAATATTA others(302): Show |
2 | a0001c0001t0001g0115 a0001c0001t0001g0161 |
2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.938-1269_938-1268i others(311): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76102655 | ||||||
| chr4:76102655 | T | TAATATTA others(309): Show |
1 | a0001c0001t0001g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.938-1269_938-1268i others(318): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76102655 | ||||||
| chr4:76102655 | T | TAATATTA others(310): Show |
28 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0025 others(25): Show |
40 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.938-1269_938-1268i others(319): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76102655 | ||||||
| chr4:76102655 | T | TAATATTA others(310): Show |
4 | a0001c0001t0001g0016 a0001c0001t0001g0126 a0001c0001t0001g0155 others(1): Show |
6 | NA18964.hp1 NA18971.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.938-1269_938-1268i others(319): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76102655 | ||||||
| chr4:76102655 | T | TAATATTA others(311): Show |
17 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0041 others(14): Show |
21 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.938-1269_938-1268i others(320): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76102655 | ||||||
| chr4:76102655 | T | TAATATTA others(311): Show |
1 | a0001c0001t0001g0143 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.938-1269_938-1268i others(320): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76102655 | ||||||
| chr4:76102655 | T | TAATATTA others(312): Show |
2 | a0001c0001t0001g0140 a0001c0001t0001g0142 |
2 | HG02027.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.938-1269_938-1268i others(321): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76102655 | ||||||
| chr4:76102806 | A | C | 12 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(9): Show |
21 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(18): Show |
intron_variant | MODIFIER | c.938-1131A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76102806 | |||||||
| chr4:76102889 | T | G | 12 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(9): Show |
21 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(18): Show |
intron_variant | MODIFIER | c.938-1048T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76102889 | |||||||
| chr4:76103027 | C | T | 55 | a0001c0001t0001g0059 a0001c0001t0001g0239 a0001c0001t0002g0220 others(52): Show |
87 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.938-910C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103027 | |||||||
| chr4:76103086 | G | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(212): Show |
315 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.938-851G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103086 | |||||||
| chr4:76103089 | AT | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.938-841delT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76103089 | ||||||
| chr4:76103117 | G | A | 16 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(13): Show |
25 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(22): Show |
intron_variant | MODIFIER | c.938-820G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103117 | |||||||
| chr4:76103201 | G | A | 16 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(13): Show |
25 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(22): Show |
intron_variant | MODIFIER | c.938-736G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103201 | |||||||
| chr4:76103244 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
305 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.938-693G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103244 | |||||||
| chr4:76103318 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.938-619T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103318 | |||||||
| chr4:76103329 | C | G | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.938-608C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103329 | |||||||
| chr4:76103340 | C | T | 17 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(14): Show |
26 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(23): Show |
intron_variant | MODIFIER | c.938-597C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103340 | |||||||
| chr4:76103347 | G | T | 17 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(14): Show |
26 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(23): Show |
intron_variant | MODIFIER | c.938-590G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103347 | |||||||
| chr4:76103370 | GA | G | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.938-558delA | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76103370 | ||||||
| chr4:76103381 | A | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
124 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.938-556A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103381 | |||||||
| chr4:76103448 | C | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.938-489C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103448 | |||||||
| chr4:76103642 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.938-295A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103642 | |||||||
| chr4:76103699 | C | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.938-238C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | chr4 | 76103699 | |||||||
| chr4:76103829 | C | CT | 51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(48): Show |
71 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.938-95dupT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76103829 | ||||||
| chr4:76103829 | C | CTT | 14 | a0001c0001t0001g0143 a0001c0001t0001g0262 a0001c0001t0002g0003 others(11): Show |
23 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(20): Show |
intron_variant | MODIFIER | c.938-96_938-95dupTT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 76103829 | ||||||
| chr4:76103983 | C | T | 25 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0001t0001g0223 others(22): Show |
32 | HG01109.hp1 HG01255.hp2 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.970+14C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 9/11 | chr4 | 76103983 | |||||||
| chr4:76104120 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(187): Show |
280 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.970+151C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 9/11 | chr4 | 76104120 | |||||||
| chr4:76104204 | G | A | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.970+235G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 9/11 | chr4 | 76104204 | |||||||
| chr4:76104206 | T | G | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.970+237T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 9/11 | chr4 | 76104206 | |||||||
| chr4:76104215 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(233): Show |
347 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.970+246G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 9/11 | chr4 | 76104215 | |||||||
| chr4:76104420 | A | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.971-177A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 9/11 | chr4 | 76104420 | |||||||
| chr4:76104433 | G | T | 1 | a0001c0001t0001g0010 | 4 | HG00609.hp2 NA19004.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.971-164G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 9/11 | chr4 | 76104433 | |||||||
| chr4:76104449 | C | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.971-148C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 9/11 | chr4 | 76104449 | |||||||
| chr4:76104657 | G | A | 7 | a0002c0002t0003g0051 a0002c0002t0003g0054 a0002c0002t0003g0055 others(4): Show |
7 | HG01069.hp2 HG01099.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1003+28G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76104657 | |||||||
| chr4:76104687 | C | T | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1003+58C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76104687 | |||||||
| chr4:76104718 | A | G | 2 | a0002c0002t0002g0193 a0002c0002t0002g0216 |
2 | HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1003+89A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76104718 | |||||||
| chr4:76105168 | C | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.1003+539C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76105168 | |||||||
| chr4:76105182 | C | A | 1 | a0002c0002t0002g0023 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1003+553C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76105182 | |||||||
| chr4:76105230 | C | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.1003+601C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76105230 | |||||||
| chr4:76105364 | C | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.1003+735C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76105364 | |||||||
| chr4:76105365 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1003+736G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76105365 | |||||||
| chr4:76105632 | T | C | 1 | a0001c0005t0001g0037 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1003+1003T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76105632 | |||||||
| chr4:76105668 | T | A | 2 | a0003c0003t0001g0255 a0003c0003t0001g0263 |
2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1003+1039T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76105668 | |||||||
| chr4:76105956 | AC | A | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.1003+1328delC | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76105956 | |||||||
| chr4:76105957 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(50): Show |
73 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1003+1328C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76105957 | |||||||
| chr4:76105958 | A | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.1003+1329A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76105958 | |||||||
| chr4:76105967 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(63): Show |
95 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1003+1338G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76105967 | |||||||
| chr4:76106022 | T | A | 1 | a0002c0002t0003g0238 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1003+1393T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106022 | |||||||
| chr4:76106047 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0082 |
2 | HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1003+1418G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106047 | |||||||
| chr4:76106083 | C | A | 235 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(232): Show |
346 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.1003+1454C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106083 | |||||||
| chr4:76106084 | G | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1003+1455G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106084 | |||||||
| chr4:76106097 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(50): Show |
73 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1003+1468G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106097 | |||||||
| chr4:76106336 | G | A | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.1004-1425G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106336 | |||||||
| chr4:76106454 | G | A | 235 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(232): Show |
346 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.1004-1307G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106454 | |||||||
| chr4:76106512 | C | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(179): Show |
261 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1004-1249C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106512 | |||||||
| chr4:76106529 | G | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.1004-1232G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106529 | |||||||
| chr4:76106544 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1004-1217G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106544 | |||||||
| chr4:76106555 | A | G | 1 | a0006c0008t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1004-1206A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106555 | |||||||
| chr4:76106603 | A | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.1004-1158A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106603 | |||||||
| chr4:76106697 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1004-1064T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106697 | |||||||
| chr4:76106710 | A | C | 24 | a0001c0001t0001g0070 a0001c0005t0001g0037 a0002c0002t0002g0009 others(21): Show |
35 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1004-1051A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106710 | |||||||
| chr4:76106735 | C | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(179): Show |
261 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1004-1026C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106735 | |||||||
| chr4:76106737 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1004-1024C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106737 | |||||||
| chr4:76106800 | C | T | 1 | a0002c0002t0002g0069 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1004-961C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106800 | |||||||
| chr4:76106850 | A | G | 1 | a0001c0001t0001g0006 | 7 | HG02040.hp1 HG02132.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.1004-911A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106850 | |||||||
| chr4:76106887 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1004-874C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106887 | |||||||
| chr4:76106935 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1004-826A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106935 | |||||||
| chr4:76106989 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(179): Show |
261 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1004-772G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76106989 | |||||||
| chr4:76107048 | AT | A | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.1004-711delT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 76107048 | ||||||
| chr4:76107069 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1004-692T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76107069 | |||||||
| chr4:76107226 | T | C | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.1004-535T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76107226 | |||||||
| chr4:76107297 | G | A | 129 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(126): Show |
188 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1004-464G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76107297 | |||||||
| chr4:76107302 | C | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
166 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1004-459C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76107302 | |||||||
| chr4:76107421 | A | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(50): Show |
73 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1004-340A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76107421 | |||||||
| chr4:76107630 | G | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
166 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1004-131G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 10/11 | chr4 | 76107630 | |||||||
| chr4:76107801 | G | A | 1 | a0006c0008t0001g0242 | 1 | HG03209.hp1 | splice_region_variant&intron_variant | LOW | c.1036+8G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76107801 | |||||||
| chr4:76107949 | G | A | 1 | a0002c0002t0003g0063 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1036+156G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76107949 | |||||||
| chr4:76108168 | C | T | 1 | a0006c0008t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1036+375C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108168 | |||||||
| chr4:76108260 | T | C | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1036+467T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108260 | |||||||
| chr4:76108315 | A | G | 13 | a0001c0001t0002g0003 a0001c0001t0002g0022 a0001c0001t0002g0043 others(10): Show |
22 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.1036+522A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108315 | |||||||
| chr4:76108362 | T | TATC | 118 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
168 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1036+571_1036+573d others(5): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76108362 | ||||||
| chr4:76108460 | T | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(213): Show |
316 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1036+667T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108460 | |||||||
| chr4:76108524 | T | G | 15 | a0001c0001t0001g0095 a0001c0001t0001g0243 a0001c0001t0002g0003 others(12): Show |
24 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(21): Show |
intron_variant | MODIFIER | c.1036+731T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108524 | |||||||
| chr4:76108557 | T | TA | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1036+775dupA | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76108557 | ||||||
| chr4:76108557 | TA | T | 16 | a0001c0001t0001g0095 a0001c0001t0001g0141 a0001c0001t0001g0243 others(13): Show |
25 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(22): Show |
intron_variant | MODIFIER | c.1036+775delA | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76108557 | ||||||
| chr4:76108568 | A | AC | 25 | a0001c0001t0001g0070 a0001c0001t0001g0223 a0001c0005t0001g0037 others(22): Show |
36 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1036+776dupC | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76108568 | ||||||
| chr4:76108615 | GC | G | 24 | a0001c0001t0001g0070 a0001c0005t0001g0037 a0002c0002t0002g0009 others(21): Show |
35 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1036+828delC | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76108615 | ||||||
| chr4:76108667 | CAA | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(181): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1036+875_1036+876d others(4): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108667 | |||||||
| chr4:76108676 | G | GA | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(181): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1036+883_1036+884i others(3): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108676 | |||||||
| chr4:76108699 | G | A | 1 | a0003c0003t0001g0245 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1036+906G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108699 | |||||||
| chr4:76108755 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1036+962T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108755 | |||||||
| chr4:76108804 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1036+1011T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108804 | |||||||
| chr4:76108828 | G | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(168): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1036+1035G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108828 | |||||||
| chr4:76108858 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(181): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1036+1065G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108858 | |||||||
| chr4:76108994 | G | A | 69 | a0001c0001t0001g0059 a0001c0001t0002g0003 a0001c0001t0002g0022 others(66): Show |
110 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.1036+1201G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76108994 | |||||||
| chr4:76109007 | G | A | 56 | a0001c0001t0001g0059 a0001c0001t0002g0220 a0001c0001t0002g0224 others(53): Show |
88 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1036+1214G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109007 | |||||||
| chr4:76109102 | C | T | 56 | a0001c0001t0001g0059 a0001c0001t0002g0220 a0001c0001t0002g0224 others(53): Show |
88 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1036+1309C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109102 | |||||||
| chr4:76109134 | C | G | 69 | a0001c0001t0001g0059 a0001c0001t0002g0003 a0001c0001t0002g0022 others(66): Show |
110 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.1036+1341C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109134 | |||||||
| chr4:76109145 | TCTGA | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1036+1355_1036+135 others(8): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76109145 | ||||||
| chr4:76109189 | C | G | 69 | a0001c0001t0001g0059 a0001c0001t0002g0003 a0001c0001t0002g0022 others(66): Show |
110 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.1036+1396C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109189 | |||||||
| chr4:76109245 | CT | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(136): Show |
203 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.1036+1461delT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76109245 | ||||||
| chr4:76109322 | A | G | 5 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0140 others(2): Show |
5 | HG02027.hp2 NA18983.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+1529A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109322 | |||||||
| chr4:76109337 | A | G | 1 | a0002c0002t0002g0259 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1036+1544A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109337 | |||||||
| chr4:76109384 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1036+1591T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109384 | |||||||
| chr4:76109390 | C | T | 1 | a0002c0002t0003g0055 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1036+1597C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109390 | |||||||
| chr4:76109391 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(50): Show |
73 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1036+1598G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109391 | |||||||
| chr4:76109477 | T | C | 2 | a0002c0002t0003g0260 a0005c0006t0003g0253 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1036+1684T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109477 | |||||||
| chr4:76109544 | CAT | C | 56 | a0001c0001t0001g0059 a0001c0001t0002g0220 a0001c0001t0002g0224 others(53): Show |
88 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1036+1753_1036+175 others(6): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76109544 | ||||||
| chr4:76109561 | AAAT | A | 56 | a0001c0001t0001g0059 a0001c0001t0002g0220 a0001c0001t0002g0224 others(53): Show |
88 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1036+1769_1036+177 others(7): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109561 | |||||||
| chr4:76109699 | T | G | 1 | a0001c0001t0001g0186 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1036+1906T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109699 | |||||||
| chr4:76109714 | T | A | 23 | a0001c0005t0001g0037 a0002c0002t0002g0009 a0002c0002t0002g0011 others(20): Show |
34 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1036+1921T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109714 | |||||||
| chr4:76109719 | G | A | 131 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
190 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1036+1926G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109719 | |||||||
| chr4:76109733 | C | G | 1 | a0006c0008t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1036+1940C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109733 | |||||||
| chr4:76109776 | A | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(184): Show |
266 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1036+1983A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109776 | |||||||
| chr4:76109793 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1036+2000A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109793 | |||||||
| chr4:76109805 | A | G | 48 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(45): Show |
69 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.1036+2012A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109805 | |||||||
| chr4:76109818 | C | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(186): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.1036+2025C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109818 | |||||||
| chr4:76109838 | C | T | 132 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
191 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1036+2045C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109838 | |||||||
| chr4:76109869 | T | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
123 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1036+2076T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109869 | |||||||
| chr4:76109972 | C | G | 1 | a0002c0002t0002g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1036+2179C>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76109972 | |||||||
| chr4:76110037 | T | G | 1 | a0002c0002t0003g0238 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1036+2244T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110037 | |||||||
| chr4:76110110 | AT | A | 107 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1037-2266delT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76110110 | ||||||
| chr4:76110110 | ATT | A | 60 | a0001c0001t0001g0059 a0001c0001t0001g0113 a0001c0001t0001g0131 others(57): Show |
92 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1037-2267_1037-226 others(6): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76110110 | ||||||
| chr4:76110134 | G | T | 1 | a0001c0001t0002g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1037-2252G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110134 | |||||||
| chr4:76110199 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(28): Show |
56 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1037-2187G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110199 | |||||||
| chr4:76110206 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0025 others(63): Show |
94 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1037-2180G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110206 | |||||||
| chr4:76110217 | T | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(67): Show |
100 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1037-2169T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110217 | |||||||
| chr4:76110238 | T | A | 1 | a0006c0008t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1037-2148T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110238 | |||||||
| chr4:76110253 | TACA | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
10 | HG02132.hp1 NA18943.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-2127_1037-212 others(7): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76110253 | ||||||
| chr4:76110271 | T | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(180): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.1037-2115T>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110271 | |||||||
| chr4:76110319 | G | A | 4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-2067G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110319 | |||||||
| chr4:76110431 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0204 |
3 | HG00642.hp2 HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1037-1955C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110431 | |||||||
| chr4:76110514 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(59): Show |
83 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1037-1872T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110514 | |||||||
| chr4:76110580 | TA | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(128): Show |
193 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.1037-1797delA | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76110580 | ||||||
| chr4:76110646 | G | T | 76 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
113 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1037-1740G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110646 | |||||||
| chr4:76110777 | C | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(57): Show |
80 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1037-1609C>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110777 | |||||||
| chr4:76110802 | A | T | 1 | a0006c0008t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1037-1584A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110802 | |||||||
| chr4:76110850 | A | T | 1 | a0001c0001t0001g0228 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1037-1536A>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110850 | |||||||
| chr4:76110866 | T | C | 76 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
113 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1037-1520T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110866 | |||||||
| chr4:76110898 | A | G | 1 | a0002c0002t0002g0023 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1037-1488A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110898 | |||||||
| chr4:76110929 | C | T | 2 | a0002c0002t0002g0192 a0002c0002t0002g0194 |
2 | HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1037-1457C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110929 | |||||||
| chr4:76110945 | CGTTA | C | 4 | a0001c0001t0002g0220 a0001c0001t0002g0224 a0003c0003t0002g0254 others(1): Show |
4 | HG01175.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037-1438_1037-143 others(8): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76110945 | ||||||
| chr4:76110948 | TAGTA | T | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-1437_1037-143 others(8): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76110948 | |||||||
| chr4:76111009 | C | T | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-1377C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111009 | |||||||
| chr4:76111026 | G | A | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-1360G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111026 | |||||||
| chr4:76111057 | A | G | 1 | a0002c0002t0002g0259 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1037-1329A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111057 | |||||||
| chr4:76111122 | A | G | 1 | a0002c0002t0002g0197 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1037-1264A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111122 | |||||||
| chr4:76111123 | A | G | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-1263A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111123 | |||||||
| chr4:76111130 | G | C | 1 | a0001c0001t0001g0021 | 2 | NA18612.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1037-1256G>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111130 | |||||||
| chr4:76111131 | A | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(74): Show |
114 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1037-1255A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111131 | |||||||
| chr4:76111207 | A | G | 1 | a0002c0002t0002g0199 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1037-1179A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111207 | |||||||
| chr4:76111223 | GT | G | 15 | a0001c0001t0001g0039 a0001c0001t0001g0070 a0001c0001t0001g0223 others(12): Show |
20 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1037-1161delT | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76111223 | ||||||
| chr4:76111244 | T | G | 1 | a0006c0008t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1037-1142T>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111244 | |||||||
| chr4:76111342 | C | T | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-1044C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111342 | |||||||
| chr4:76111372 | T | C | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-1014T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111372 | |||||||
| chr4:76111541 | G | GTTTA | 141 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(138): Show |
199 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1037-829_1037-826d others(6): Show |
ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 76111541 | ||||||
| chr4:76111573 | T | C | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-813T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111573 | |||||||
| chr4:76111644 | A | G | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-742A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111644 | |||||||
| chr4:76111647 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1037-739A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111647 | |||||||
| chr4:76111675 | G | T | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-711G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111675 | |||||||
| chr4:76111703 | C | T | 1 | a0002c0002t0002g0207 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1037-683C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111703 | |||||||
| chr4:76111712 | C | T | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-674C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111712 | |||||||
| chr4:76111729 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1037-657A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111729 | |||||||
| chr4:76111730 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1037-656C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111730 | |||||||
| chr4:76111742 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0234 a0001c0001t0001g0235 others(4): Show |
8 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1037-644G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111742 | |||||||
| chr4:76111806 | C | T | 4 | a0001c0001t0002g0220 a0001c0001t0002g0224 a0003c0003t0002g0254 others(1): Show |
4 | HG01175.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037-580C>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111806 | |||||||
| chr4:76111820 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1037-566G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111820 | |||||||
| chr4:76111919 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1037-467G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76111919 | |||||||
| chr4:76112033 | A | C | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-353A>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76112033 | |||||||
| chr4:76112066 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1037-320A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76112066 | |||||||
| chr4:76112072 | A | G | 8 | a0001c0001t0001g0036 a0001c0001t0001g0233 a0001c0001t0001g0234 others(5): Show |
9 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1037-314A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76112072 | |||||||
| chr4:76112131 | G | A | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-255G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76112131 | |||||||
| chr4:76112154 | G | A | 4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-232G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76112154 | |||||||
| chr4:76112174 | A | G | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-212A>G | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76112174 | |||||||
| chr4:76112178 | G | A | 50 | a0002c0002t0003g0001 a0002c0002t0003g0014 a0002c0002t0003g0015 others(47): Show |
82 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1037-208G>A | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76112178 | |||||||
| chr4:76112207 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1037-179T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76112207 | |||||||
| chr4:76112237 | T | C | 4 | a0001c0001t0004g0032 a0001c0001t0004g0159 a0001c0001t0004g0221 others(1): Show |
5 | HG01243.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-149T>C | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76112237 | |||||||
| chr4:76112378 | G | T | 1 | a0002c0002t0002g0174 | 1 | NA20752.hp1 | splice_region_variant&intron_variant | LOW | c.1037-8G>T | ART3 | ENSG00000156219.18 | transcript | ENST00000355810.9 | protein_coding | 11/11 | chr4 | 76112378 |