Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 920 |
| ensemblid | ENSG00000010610.10 |
| hgncid | 1678 |
| symbol | CD4 |
| name | CD4 molecule |
| refseq_nuc | NM_000616.5 |
| refseq_prot | NP_000607.1 |
| ensembl_nuc | ENST00000011653.9 |
| ensembl_prot | ENSP00000011653.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 6789528 |
| end | 6820799 |
| strand | + |
| ver | v1.2 |
| region | chr12:6789528-6820799 |
| region5000 | chr12:6784528-6825799 |
| regionname0 | CD4_chr12_6789528_6820799 |
| regionname5000 | CD4_chr12_6784528_6825799 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 458 | 383 | 66 | 67 | 190 | 16 | 42 | 145 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| a0002 | 0/0 | 458 | 40 | 24 | 2 | 13 | 0 | 1 | 13 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| a0003 | 0/0 | 458 | 7 | 4 | 3 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| a0004 | 0/0 | 458 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| a0005 | 0/0 | 458 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| a0006 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| a0007 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| a0008 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| a0009 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| a0010 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| a0011 | 0/0 | 458 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| a0012 | 0/0 | 458 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | MNRGV others(453): Show |
chr12 | 6784528 | 6825799 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1374 | 290 | 45 | 43 | 170 | 7 | 24 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0001c0002 | 1/0 | 1374 | 78 | 15 | 23 | 15 | 9 | 15 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0001c0004 | 0/0 | 1374 | 7 | 0 | 0 | 4 | 0 | 3 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0001c0006 | 0/0 | 1374 | 4 | 3 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0001c0010 | 0/0 | 1374 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0001c0012 | 0/0 | 1374 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0001c0018 | 0/0 | 1374 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0002c0003 | 0/0 | 1374 | 38 | 22 | 2 | 13 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0002c0011 | 0/0 | 1374 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0003c0005 | 0/0 | 1374 | 5 | 3 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0003c0009 | 0/0 | 1374 | 2 | 1 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0004c0007 | 0/0 | 1374 | 3 | 0 | 0 | 3 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0005c0008 | 0/0 | 1374 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0006c0015 | 0/0 | 1374 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0007c0014 | 0/0 | 1374 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0008c0016 | 0/0 | 1374 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0009c0017 | 0/0 | 1374 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0010c0020 | 0/0 | 1374 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0011c0019 | 0/0 | 1374 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 | ||
| a0012c0013 | 0/0 | 1374 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | ATGAA others(1369): Show |
chr12 | 6784528 | 6825799 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3049 | 128 | 17 | 16 | 84 | 1 | 10 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0002 | 0/0 | 3049 | 97 | 2 | 26 | 56 | 6 | 7 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0003 | 0/0 | 3049 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0004 | 0/0 | 3049 | 54 | 21 | 1 | 25 | 0 | 7 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0009 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0010 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0011 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0012 | 0/0 | 3057 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3052): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0013 | 0/1 | 3049 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0014 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0015 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0016 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0001t0018 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0002t0002 | 1/0 | 3049 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0002t0003 | 0/0 | 3049 | 75 | 15 | 21 | 15 | 9 | 15 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0002t0008 | 0/0 | 3049 | 2 | 0 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0004t0006 | 0/0 | 3049 | 7 | 0 | 0 | 4 | 0 | 3 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0006t0001 | 0/0 | 3049 | 4 | 3 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0010t0003 | 0/0 | 3049 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0012t0002 | 0/0 | 3049 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0001c0018t0002 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0002c0003t0001 | 0/0 | 3049 | 5 | 5 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0002c0003t0002 | 0/0 | 3049 | 22 | 8 | 0 | 13 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0002c0003t0005 | 0/0 | 3051 | 6 | 6 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3046): Show |
chr12 | 6784528 | 6825799 |
| a0002c0003t0007 | 0/0 | 3049 | 4 | 2 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0002c0003t0019 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0002c0011t0001 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0002c0011t0005 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3046): Show |
chr12 | 6784528 | 6825799 |
| a0003c0005t0004 | 0/0 | 3049 | 5 | 3 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0003c0009t0004 | 0/0 | 3049 | 2 | 1 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0004c0007t0004 | 0/0 | 3049 | 3 | 0 | 0 | 3 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0005c0008t0004 | 0/0 | 3049 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0006c0015t0020 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0007c0014t0017 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0008c0016t0001 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0009c0017t0001 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0010c0020t0004 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0011c0019t0004 | 0/0 | 3049 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| a0012c0013t0009 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | CTCTC others(3044): Show |
chr12 | 6784528 | 6825799 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0001g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0002g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0004g0413 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0012g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0013g0295 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0014g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0015g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0016g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0001t0018g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0002g0401 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0402 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0003g0416 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0002t0008g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0004t0006g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0006t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0006t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0006t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0006t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0010t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0010t0003g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0012t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0001c0018t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0001g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0001g0409 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0001g0417 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0002g0412 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0007g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0007g0414 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0003t0019g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0011t0001g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0002c0011t0005g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0005t0004g0418 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0005t0004g0419 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0005t0004g0420 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0005t0004g0421 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0005t0004g0422 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0009t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0003c0009t0004g0415 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0004c0007t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0004c0007t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0004c0007t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0005c0008t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0006c0015t0020g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0007c0014t0017g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0008c0016t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0009c0017t0001g0407 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0010c0020t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0011c0019t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| a0012c0013t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0342 | EUR | GBR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0134 | EUR | GBR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | GBR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | GBR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0288 | EUR | FIN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0074 | EUR | FIN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0244 | EUR | FIN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00408 | hp1 | a0001 | c0004 | t0006 | g0369 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0395 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00597 | hp1 | a0001 | c0004 | t0006 | g0064 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00609 | hp1 | a0001 | c0004 | t0006 | g0209 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00639 | hp2 | a0001 | c0006 | t0001 | g0335 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0345 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0370 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00673 | hp1 | a0001 | c0001 | t0010 | g0233 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | CHS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0339 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0330 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00738 | hp1 | a0003 | c0009 | t0004 | g0415 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0005 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01069 | hp1 | a0001 | c0002 | t0008 | g0013 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0337 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01071 | hp2 | a0001 | c0002 | t0008 | g0013 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0228 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0196 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0216 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0336 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0402 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0289 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01167 | hp2 | a0003 | c0005 | t0004 | g0422 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01169 | hp2 | a0003 | c0005 | t0004 | g0421 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0163 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01256 | hp1 | a0001 | c0002 | t0003 | g0183 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0375 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0247 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0075 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01358 | hp1 | a0002 | c0003 | t0007 | g0414 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0291 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0009 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0198 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0246 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0124 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0009 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0125 | EUR | IBS | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0063 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01884 | hp2 | a0002 | c0003 | t0002 | g0412 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01891 | hp1 | a0006 | c0015 | t0020 | g0164 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0031 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0176 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01934 | hp2 | a0001 | c0002 | t0003 | g0333 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0388 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0387 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01993 | hp2 | a0002 | c0003 | t0007 | g0039 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0386 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0346 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0377 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02055 | hp1 | a0002 | c0003 | t0002 | g0403 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02071 | hp1 | a0004 | c0007 | t0004 | g0225 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02074 | hp1 | a0004 | c0007 | t0004 | g0224 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0106 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0394 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02135 | hp2 | a0004 | c0007 | t0004 | g0190 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02145 | hp1 | a0007 | c0014 | t0017 | g0268 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02145 | hp2 | a0002 | c0003 | t0007 | g0404 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0382 | EAS | CDX | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CDX | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CDX | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CDX | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02258 | hp1 | a0001 | c0001 | t0016 | g0250 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | KHV | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0259 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02615 | hp1 | a0002 | c0003 | t0005 | g0301 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02615 | hp2 | a0003 | c0005 | t0004 | g0418 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02622 | hp1 | a0002 | c0003 | t0019 | g0027 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02622 | hp2 | a0002 | c0003 | t0002 | g0041 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02630 | hp1 | a0001 | c0010 | t0003 | g0410 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0406 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02647 | hp2 | a0008 | c0016 | t0001 | g0044 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0145 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0155 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02717 | hp1 | a0009 | c0017 | t0001 | g0407 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0138 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0081 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0188 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0374 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02738 | hp2 | a0001 | c0002 | t0003 | g0069 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0273 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02809 | hp2 | a0003 | c0005 | t0004 | g0420 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02818 | hp2 | a0002 | c0003 | t0002 | g0271 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02886 | hp2 | a0002 | c0003 | t0005 | g0300 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02895 | hp2 | a0002 | c0003 | t0007 | g0269 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02896 | hp2 | a0002 | c0003 | t0005 | g0045 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02897 | hp2 | a0002 | c0003 | t0005 | g0046 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02965 | hp2 | a0001 | c0006 | t0001 | g0343 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02970 | hp1 | a0001 | c0006 | t0001 | g0329 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0092 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02976 | hp1 | a0002 | c0003 | t0005 | g0037 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0284 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0231 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0154 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0208 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03139 | hp2 | a0010 | c0020 | t0004 | g0315 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03195 | hp1 | a0001 | c0010 | t0003 | g0258 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0274 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0275 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0285 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0048 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03453 | hp1 | a0001 | c0006 | t0001 | g0019 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03486 | hp1 | a0002 | c0011 | t0001 | g0411 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0409 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0302 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0217 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03516 | hp2 | a0002 | c0003 | t0002 | g0267 | AFR | ESN | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03540 | hp1 | a0001 | c0018 | t0002 | g0158 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03579 | hp1 | a0003 | c0009 | t0004 | g0043 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03654 | hp1 | a0001 | c0004 | t0006 | g0153 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0341 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0257 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0143 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0230 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03704 | hp1 | a0002 | c0003 | t0002 | g0180 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03710 | hp1 | a0011 | c0019 | t0004 | g0082 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0347 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0204 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03927 | hp1 | a0001 | c0004 | t0006 | g0181 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0047 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0328 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0203 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0085 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0376 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0338 | SAS | BEB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0355 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04199 | hp2 | a0001 | c0004 | t0006 | g0252 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0080 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0234 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18522 | hp1 | a0012 | c0013 | t0009 | g0159 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18612 | hp1 | a0001 | c0001 | t0015 | g0127 | EAS | CHB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0354 | EAS | CHB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CHB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18906 | hp1 | a0002 | c0003 | t0002 | g0266 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0413 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0385 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18944 | hp2 | a0002 | c0003 | t0002 | g0006 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0380 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18951 | hp1 | a0001 | c0002 | t0003 | g0384 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18952 | hp1 | a0002 | c0003 | t0002 | g0202 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18956 | hp2 | a0002 | c0003 | t0002 | g0118 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0368 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0396 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0372 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18970 | hp2 | a0001 | c0002 | t0003 | g0226 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18972 | hp2 | a0001 | c0004 | t0006 | g0120 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18974 | hp2 | a0005 | c0008 | t0004 | g0017 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0400 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0383 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0392 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18981 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18984 | hp1 | a0001 | c0001 | t0018 | g0393 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18984 | hp2 | a0002 | c0003 | t0002 | g0110 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0398 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18992 | hp2 | a0002 | c0003 | t0002 | g0097 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18993 | hp2 | a0002 | c0003 | t0002 | g0260 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0357 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0373 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18999 | hp2 | a0002 | c0003 | t0002 | g0096 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19002 | hp1 | a0002 | c0003 | t0002 | g0006 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0399 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19003 | hp1 | a0002 | c0003 | t0002 | g0261 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0381 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0221 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19009 | hp1 | a0001 | c0001 | t0014 | g0360 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0240 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19011 | hp2 | a0001 | c0001 | t0011 | g0100 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0272 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19043 | hp1 | a0002 | c0003 | t0005 | g0040 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0282 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19054 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0371 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19058 | hp1 | a0001 | c0012 | t0002 | g0115 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19059 | hp2 | a0005 | c0008 | t0004 | g0017 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19067 | hp1 | a0002 | c0003 | t0002 | g0255 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19068 | hp2 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0390 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0105 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0378 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19086 | hp1 | a0001 | c0002 | t0003 | g0391 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0397 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0248 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0417 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | YRI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20129 | hp1 | a0002 | c0011 | t0005 | g0408 | AFR | ASW | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20129 | hp2 | a0002 | c0003 | t0002 | g0022 | AFR | ASW | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0107 | EUR | TSI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0210 | EUR | TSI | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0326 | AMR | CLM | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02109 | hp1 | a0002 | c0003 | t0002 | g0023 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0032 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0297 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0327 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0405 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG03471 | hp2 | a0003 | c0005 | t0004 | g0419 | AFR | MSL | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | USA | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0189 | AFR | USA | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18955 | hp1 | a0002 | c0003 | t0002 | g0218 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | USA | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | USA | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0416 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0162 | AFR | LWK | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0013 | g0295 | REF | REF | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0401 | REF | REF | CD4_chr12_6784528_6825799 | CD4 | chr12 | 6784528 | 6825799 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6800331 | G | A | 1 | a0005 | 2 | NA18974.hp2 NA19059.hp2 |
missense_variant | MODERATE | c.74G>A | p.Gly25Glu | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/10 | 276/3049 | 74/1377 | 25/458 | chr12 | 6800331 | |||
| chr12:6814791 | G | T | 1 | a0011 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.406G>T | p.Gly136Trp | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/10 | 608/3049 | 406/1377 | 136/458 | chr12 | 6814791 | |||
| chr12:6814828 | G | A | 1 | a0012 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.443G>A | p.Gly148Asp | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/10 | 645/3049 | 443/1377 | 148/458 | chr12 | 6814828 | |||
| chr12:6814956 | A | G | 1 | a0010 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.571A>G | p.Lys191Glu | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/10 | 773/3049 | 571/1377 | 191/458 | chr12 | 6814956 | |||
| chr12:6816128 | T | C | 2 | a0003 a0010 |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
missense_variant | MODERATE | c.680T>C | p.Phe227Ser | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/10 | 882/3049 | 680/1377 | 227/458 | chr12 | 6816128 | |||
| chr12:6816241 | C | T | 2 | a0002 a0009 |
41 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(38): Show |
missense_variant | MODERATE | c.793C>T | p.Arg265Trp | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/10 | 995/3049 | 793/1377 | 265/458 | chr12 | 6816241 | |||
| chr12:6817235 | G | A | 1 | a0007 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1061G>A | p.Arg354Gln | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/10 | 1263/3049 | 1061/1377 | 354/458 | chr12 | 6817235 | |||
| chr12:6818499 | T | C | 2 | a0006 a0009 |
2 | HG01891.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.1235T>C | p.Ile412Thr | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 8/10 | 1437/3049 | 1235/1377 | 412/458 | chr12 | 6818499 | |||
| chr12:6818538 | G | A | 1 | a0008 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1274G>A | p.Arg425Gln | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 8/10 | 1476/3049 | 1274/1377 | 425/458 | chr12 | 6818538 | |||
| chr12:6818860 | G | A | 1 | a0004 | 3 | HG02071.hp1 HG02074.hp1 HG02135.hp2 |
missense_variant | MODERATE | c.1292G>A | p.Arg431Gln | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/10 | 1494/3049 | 1292/1377 | 431/458 | chr12 | 6818860 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6800441 | C | T | 1 | a0002c0011 | 2 | HG03486.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.184C>T | p.Leu62Leu | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/10 | 386/3049 | 184/1377 | 62/458 | chr12 | 6800441 | |||
| chr12:6814278 | G | A | 1 | a0001c0012 | 1 | NA19058.hp1 | synonymous_variant | LOW | c.351G>A | p.Glu117Glu | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/10 | 553/3049 | 351/1377 | 117/458 | chr12 | 6814278 | |||
| chr12:6814296 | C | T | 2 | a0003c0005 a0010c0020 |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
synonymous_variant | LOW | c.369C>T | p.Phe123Phe | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/10 | 571/3049 | 369/1377 | 123/458 | chr12 | 6814296 | |||
| chr12:6814943 | C | T | 1 | a0001c0006 | 4 | HG00639.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.558C>T | p.Val186Val | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/10 | 760/3049 | 558/1377 | 186/458 | chr12 | 6814943 | |||
| chr12:6816147 | G | T | 3 | a0003c0005 a0003c0009 a0010c0020 |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
synonymous_variant | LOW | c.699G>T | p.Thr233Thr | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/10 | 901/3049 | 699/1377 | 233/458 | chr12 | 6816147 | |||
| chr12:6816156 | C | T | 1 | a0001c0018 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.708C>T | p.Gly236Gly | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/10 | 910/3049 | 708/1377 | 236/458 | chr12 | 6816156 | |||
| chr12:6817197 | T | C | 18 | a0001c0001 a0001c0004 a0001c0006 others(15): Show |
361 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(358): Show |
synonymous_variant | LOW | c.1023T>C | p.Ser341Ser | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/10 | 1225/3049 | 1023/1377 | 341/458 | chr12 | 6817197 | |||
| chr12:6817254 | G | A | 1 | a0007c0014 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1080G>A | p.Val360Val | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/10 | 1282/3049 | 1080/1377 | 360/458 | chr12 | 6817254 | |||
| chr12:6818909 | T | C | 19 | a0001c0001 a0001c0004 a0001c0006 others(16): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
synonymous_variant | LOW | c.1341T>C | p.Cys447Cys | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/10 | 1543/3049 | 1341/1377 | 447/458 | chr12 | 6818909 | |||
| chr12:6819320 | C | T | 1 | a0001c0004 | 7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
synonymous_variant | LOW | c.1368C>T | p.Ser456Ser | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1570/3049 | 1368/1377 | 456/458 | chr12 | 6819320 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6819384 | T | TTCCTGCC others(11): Show |
1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*57_*74dupCCTGCCTG others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 75 | INFO_REALIGN_3_PRIME | chr12 | 6819384 | |||||
| chr12:6819403 | T | A | 9 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0011 others(6): Show |
70 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*74T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 74 | chr12 | 6819403 | ||||||
| chr12:6819454 | T | C | 1 | a0001c0001t0014 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 125 | chr12 | 6819454 | ||||||
| chr12:6819581 | T | C | 4 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0008 others(1): Show |
81 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*252T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 252 | chr12 | 6819581 | ||||||
| chr12:6819614 | T | A | 2 | a0002c0003t0005 a0002c0011t0005 |
7 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*285T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 285 | chr12 | 6819614 | ||||||
| chr12:6819626 | G | C | 1 | a0001c0001t0015 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*297G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 297 | chr12 | 6819626 | ||||||
| chr12:6819670 | G | T | 1 | a0006c0015t0020 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 341 | chr12 | 6819670 | ||||||
| chr12:6819739 | A | G | 12 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(9): Show |
146 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*410A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 410 | chr12 | 6819739 | ||||||
| chr12:6819747 | A | G | 12 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0011 others(9): Show |
146 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*418A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 418 | chr12 | 6819747 | ||||||
| chr12:6819827 | C | CCA | 2 | a0002c0003t0005 a0002c0011t0005 |
7 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*499_*500insAC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 500 | INFO_REALIGN_3_PRIME | chr12 | 6819827 | |||||
| chr12:6819852 | A | G | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(18): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*523A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 523 | chr12 | 6819852 | ||||||
| chr12:6820060 | G | A | 1 | a0002c0003t0007 | 4 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*731G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 731 | chr12 | 6820060 | ||||||
| chr12:6820092 | A | G | 1 | a0001c0002t0008 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*763A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 763 | chr12 | 6820092 | ||||||
| chr12:6820313 | C | G | 2 | a0001c0001t0009 a0012c0013t0009 |
2 | HG02970.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*984C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 984 | chr12 | 6820313 | ||||||
| chr12:6820347 | C | T | 9 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(6): Show |
143 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*1018C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1018 | chr12 | 6820347 | ||||||
| chr12:6820471 | T | C | 10 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(7): Show |
144 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1142T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1142 | chr12 | 6820471 | ||||||
| chr12:6820494 | G | A | 2 | a0001c0001t0009 a0012c0013t0009 |
2 | HG02970.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1165G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1165 | chr12 | 6820494 | ||||||
| chr12:6820645 | CTTTTCCC others(3): Show |
C | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1319_*1328delTTCC others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1319 | INFO_REALIGN_3_PRIME | chr12 | 6820645 | |||||
| chr12:6820670 | G | C | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1341G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1341 | chr12 | 6820670 | ||||||
| chr12:6820674 | T | C | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1345T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1345 | chr12 | 6820674 | ||||||
| chr12:6820718 | G | C | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1389 | chr12 | 6820718 | ||||||
| chr12:6820723 | C | T | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1394C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1394 | chr12 | 6820723 | ||||||
| chr12:6820746 | G | A | 3 | a0001c0004t0006 a0002c0003t0005 a0002c0011t0005 |
14 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1417G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1417 | chr12 | 6820746 | ||||||
| chr12:6820790 | A | G | 1 | a0002c0003t0019 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1461A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 10/10 | 1461 | chr12 | 6820790 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6789680 | G | A | 1 | a0001c0006t0001g0019 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-68+18G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6789680 | |||||||
| chr12:6789703 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-68+41G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6789703 | |||||||
| chr12:6789791 | G | C | 4 | a0001c0001t0004g0021 a0001c0001t0004g0024 a0002c0003t0002g0022 others(1): Show |
4 | HG02109.hp1 HG03540.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+129G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6789791 | |||||||
| chr12:6789862 | C | T | 9 | a0001c0001t0004g0018 a0001c0002t0003g0416 a0002c0003t0001g0417 others(6): Show |
10 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-68+200C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6789862 | |||||||
| chr12:6789890 | A | G | 14 | a0001c0001t0004g0406 a0001c0001t0004g0413 a0001c0010t0003g0410 others(11): Show |
14 | HG01167.hp2 HG01169.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.-68+228A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6789890 | |||||||
| chr12:6790015 | T | G | 325 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(322): Show |
339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.-68+353T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790015 | |||||||
| chr12:6790020 | G | C | 22 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(19): Show |
22 | HG01109.hp2 HG01261.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-68+358G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790020 | |||||||
| chr12:6790056 | A | G | 12 | a0001c0001t0001g0305 a0001c0001t0001g0310 a0001c0001t0002g0014 others(9): Show |
14 | HG01106.hp1 HG01109.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.-68+394A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790056 | |||||||
| chr12:6790080 | T | C | 2 | a0001c0002t0003g0047 a0001c0002t0003g0048 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-68+418T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790080 | |||||||
| chr12:6790142 | C | CG | 205 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(202): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-68+480_-68+481ins others(1): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790142 | |||||||
| chr12:6790212 | CT | C | 419 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(416): Show |
439 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(436): Show |
intron_variant | MODIFIER | c.-68+552delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6790212 | ||||||
| chr12:6790342 | G | A | 183 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0160 others(180): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-68+680G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790342 | |||||||
| chr12:6790360 | G | A | 2 | a0001c0001t0002g0313 a0001c0001t0002g0314 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-68+698G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790360 | |||||||
| chr12:6790362 | T | C | 183 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0160 others(180): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-68+700T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790362 | |||||||
| chr12:6790416 | T | C | 128 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(125): Show |
135 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-68+754T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790416 | |||||||
| chr12:6790524 | A | C | 35 | a0001c0001t0001g0370 a0001c0001t0001g0374 a0001c0001t0001g0379 others(32): Show |
38 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.-68+862A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790524 | |||||||
| chr12:6790526 | C | T | 1 | a0001c0002t0003g0302 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-68+864C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790526 | |||||||
| chr12:6790631 | T | C | 1 | a0001c0001t0004g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-68+969T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790631 | |||||||
| chr12:6790721 | C | T | 6 | a0001c0001t0001g0296 a0001c0001t0001g0298 a0001c0001t0001g0299 others(3): Show |
6 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-68+1059C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790721 | |||||||
| chr12:6790722 | G | A | 1 | a0001c0004t0006g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-68+1060G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790722 | |||||||
| chr12:6790941 | T | C | 1 | a0001c0002t0003g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-68+1279T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6790941 | |||||||
| chr12:6791193 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-68+1531C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791193 | |||||||
| chr12:6791194 | G | C | 1 | a0001c0001t0002g0049 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-68+1532G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791194 | |||||||
| chr12:6791378 | G | T | 1 | a0001c0001t0001g0367 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-68+1716G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791378 | |||||||
| chr12:6791399 | C | G | 151 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(148): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.-68+1737C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791399 | |||||||
| chr12:6791447 | T | C | 117 | a0001c0001t0001g0056 a0001c0001t0001g0156 a0001c0001t0001g0157 others(114): Show |
120 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.-68+1785T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791447 | |||||||
| chr12:6791450 | A | G | 140 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0160 others(137): Show |
144 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.-68+1788A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791450 | |||||||
| chr12:6791502 | C | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-68+1840C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791502 | |||||||
| chr12:6791508 | G | A | 1 | a0010c0020t0004g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-68+1846G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791508 | |||||||
| chr12:6791602 | C | T | 1 | a0002c0003t0007g0414 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-68+1940C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791602 | |||||||
| chr12:6791629 | C | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(3): Show |
6 | HG01109.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-68+1967C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791629 | |||||||
| chr12:6791636 | T | C | 3 | a0001c0001t0004g0024 a0002c0003t0002g0022 a0002c0003t0002g0023 |
3 | HG02109.hp1 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-68+1974T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791636 | |||||||
| chr12:6791722 | C | T | 10 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0002t0003g0416 others(7): Show |
11 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-68+2060C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791722 | |||||||
| chr12:6791860 | C | T | 1 | a0001c0001t0001g0400 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-68+2198C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791860 | |||||||
| chr12:6791898 | G | T | 1 | a0001c0001t0002g0262 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-68+2236G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791898 | |||||||
| chr12:6791911 | A | G | 297 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(294): Show |
308 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-68+2249A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791911 | |||||||
| chr12:6791916 | G | A | 328 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(325): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.-68+2254G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791916 | |||||||
| chr12:6791964 | G | A | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | HG01168.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-68+2302G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791964 | |||||||
| chr12:6791968 | C | T | 119 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0160 others(116): Show |
122 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-68+2306C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6791968 | |||||||
| chr12:6792154 | G | A | 1 | a0001c0002t0003g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-68+2492G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792154 | |||||||
| chr12:6792236 | G | A | 8 | a0001c0001t0001g0265 a0001c0001t0001g0270 a0001c0001t0004g0272 others(5): Show |
8 | HG02145.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-68+2574G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792236 | |||||||
| chr12:6792285 | G | A | 1 | a0001c0002t0003g0155 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-68+2623G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792285 | |||||||
| chr12:6792300 | C | T | 2 | a0002c0003t0002g0260 a0002c0003t0002g0261 |
2 | NA18993.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-68+2638C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792300 | |||||||
| chr12:6792440 | C | CT | 25 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(22): Show |
28 | HG00408.hp2 HG00621.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.-68+2785dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6792440 | ||||||
| chr12:6792508 | A | G | 12 | a0001c0001t0004g0406 a0001c0001t0004g0413 a0001c0010t0003g0410 others(9): Show |
12 | HG01358.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-68+2846A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792508 | |||||||
| chr12:6792594 | C | T | 1 | a0001c0002t0003g0259 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-68+2932C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792594 | |||||||
| chr12:6792613 | C | T | 5 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+2951C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792613 | |||||||
| chr12:6792657 | G | A | 148 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(145): Show |
152 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-68+2995G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792657 | |||||||
| chr12:6792663 | G | T | 1 | a0001c0010t0003g0258 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-68+3001G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792663 | |||||||
| chr12:6792716 | C | G | 1 | a0001c0001t0001g0316 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-68+3054C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792716 | |||||||
| chr12:6792836 | G | T | 275 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(272): Show |
284 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.-68+3174G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6792836 | |||||||
| chr12:6793087 | C | T | 1 | a0001c0001t0004g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-68+3425C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793087 | |||||||
| chr12:6793411 | C | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(4): Show |
7 | HG00423.hp2 NA18963.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68+3749C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793411 | |||||||
| chr12:6793506 | C | G | 1 | a0001c0001t0004g0413 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-68+3844C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793506 | |||||||
| chr12:6793637 | GTATCTAT others(8): Show |
G | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-68+3988_-68+4002d others(17): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793637 | ||||||
| chr12:6793649 | CATCT | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0160 others(31): Show |
34 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.-68+4040_-68+4043d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793649 | ||||||
| chr12:6793649 | CATCTATC others(1): Show |
C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0034 others(79): Show |
87 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-68+4036_-68+4043d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793649 | ||||||
| chr12:6793649 | CATCTATC others(5): Show |
C | 22 | a0001c0001t0001g0318 a0001c0001t0001g0332 a0001c0001t0001g0340 others(19): Show |
22 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.-68+4032_-68+4043d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793649 | ||||||
| chr12:6793649 | CATCTATC others(9): Show |
C | 3 | a0001c0001t0001g0334 a0001c0001t0001g0355 a0001c0002t0003g0328 |
3 | HG02129.hp1 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-68+4028_-68+4043d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793649 | ||||||
| chr12:6793685 | TATCTATC others(10): Show |
T | 4 | a0001c0001t0001g0042 a0001c0001t0004g0038 a0002c0003t0002g0041 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+4024_-68+4040d others(19): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793685 | |||||||
| chr12:6793688 | CTATCTAT others(7): Show |
C | 98 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0091 others(95): Show |
104 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-68+4028_-68+4041d others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793688 | ||||||
| chr12:6793689 | TATCTATC others(6): Show |
T | 11 | a0001c0001t0004g0080 a0001c0001t0004g0081 a0001c0001t0004g0085 others(8): Show |
11 | HG01192.hp1 HG01891.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+4028_-68+4040d others(15): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793689 | |||||||
| chr12:6793689 | TATCTATC others(8): Show |
T | 1 | a0001c0004t0006g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-68+4028_-68+4042d others(17): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793689 | |||||||
| chr12:6793692 | CTATCTAT others(3): Show |
C | 90 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0073 others(87): Show |
92 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-68+4032_-68+4041d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793692 | ||||||
| chr12:6793693 | TATCTATC others(2): Show |
T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0232 a0001c0001t0001g0235 others(8): Show |
11 | HG01358.hp1 HG01993.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+4032_-68+4040d others(11): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793693 | |||||||
| chr12:6793693 | TATCTATC others(4): Show |
T | 2 | a0001c0001t0001g0056 a0003c0005t0004g0421 |
2 | HG01169.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-68+4032_-68+4042d others(13): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793693 | |||||||
| chr12:6793696 | CTATCTA | C | 30 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0186 others(27): Show |
30 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.-68+4036_-68+4041d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793696 | ||||||
| chr12:6793697 | TATCTA | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0029 others(7): Show |
10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-68+4036_-68+4040d others(7): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793697 | |||||||
| chr12:6793697 | TATCTATC | T | 4 | a0001c0001t0001g0156 a0001c0001t0004g0161 a0001c0018t0002g0158 others(1): Show |
4 | HG01928.hp1 HG03540.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+4036_-68+4042d others(9): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793697 | |||||||
| chr12:6793702 | A | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0270 a0002c0003t0002g0412 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+4040A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793702 | |||||||
| chr12:6793704 | C | T | 259 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(256): Show |
268 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.-68+4042C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793704 | |||||||
| chr12:6793716 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-68+4054T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793716 | |||||||
| chr12:6793738 | G | A | 1 | a0001c0001t0004g0018 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-68+4076G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793738 | |||||||
| chr12:6793758 | G | A | 7 | a0001c0001t0004g0010 a0001c0001t0004g0163 a0001c0001t0004g0249 others(4): Show |
8 | HG01192.hp1 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-68+4096G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793758 | |||||||
| chr12:6793798 | C | T | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0042 others(10): Show |
13 | HG01109.hp2 HG01993.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-68+4136C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793798 | |||||||
| chr12:6793831 | T | C | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-68+4169T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793831 | |||||||
| chr12:6793888 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-68+4226A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6793888 | |||||||
| chr12:6793958 | TTCTATCT others(7): Show |
T | 3 | a0001c0001t0004g0024 a0002c0003t0002g0022 a0002c0003t0002g0023 |
3 | HG02109.hp1 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-68+4310_-68+4323d others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793958 | ||||||
| chr12:6793960 | CTATCTAT others(3): Show |
C | 4 | a0001c0001t0002g0313 a0001c0001t0002g0314 a0001c0001t0002g0341 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+4310_-68+4319d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793960 | ||||||
| chr12:6793964 | CTATCTA | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0361 a0001c0001t0001g0374 others(6): Show |
9 | HG02040.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-68+4310_-68+4315d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793964 | ||||||
| chr12:6793968 | CTA | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0026 others(119): Show |
130 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-68+4310_-68+4311d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793968 | ||||||
| chr12:6793970 | A | ATATC | 4 | a0001c0001t0001g0212 a0001c0001t0002g0192 a0001c0001t0004g0053 others(1): Show |
4 | HG00741.hp1 HG02258.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+4341_-68+4344d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | ||||||
| chr12:6793970 | A | ATATCTAT others(1): Show |
115 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(112): Show |
119 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-68+4337_-68+4344d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | ||||||
| chr12:6793970 | A | ATATCTAT others(5): Show |
62 | a0001c0001t0001g0093 a0001c0001t0001g0133 a0001c0001t0001g0142 others(59): Show |
64 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-68+4333_-68+4344d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | ||||||
| chr12:6793970 | A | ATATCTAT others(9): Show |
63 | a0001c0001t0001g0056 a0001c0001t0001g0073 a0001c0001t0001g0103 others(60): Show |
63 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-68+4329_-68+4344d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | ||||||
| chr12:6793970 | A | ATATCTAT others(13): Show |
7 | a0001c0001t0002g0004 a0001c0001t0002g0124 a0001c0001t0002g0125 others(4): Show |
7 | HG01167.hp1 HG01192.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68+4325_-68+4344d others(22): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | ||||||
| chr12:6793970 | A | ATATCTAT others(17): Show |
5 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0184 others(2): Show |
5 | HG02135.hp1 HG03704.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+4321_-68+4344d others(26): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | ||||||
| chr12:6793970 | A | ATATCTAT others(21): Show |
1 | a0001c0001t0002g0012 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-68+4317_-68+4344d others(30): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | ||||||
| chr12:6793970 | A | ATC | 22 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0270 others(19): Show |
22 | HG00408.hp2 HG01993.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.-68+4309_-68+4310i others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | ||||||
| chr12:6793970 | A | ATCTATC | 7 | a0001c0001t0001g0020 a0001c0001t0001g0265 a0001c0001t0001g0334 others(4): Show |
7 | HG02129.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-68+4309_-68+4310i others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6793970 | ||||||
| chr12:6794030 | ATCTG | A | 32 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(29): Show |
32 | HG01109.hp2 HG01358.hp1 HG01993.hp2 others(29): Show |
intron_variant | MODIFIER | c.-68+4372_-68+4375d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794030 | ||||||
| chr12:6794075 | C | CTATCTTT others(5): Show |
1 | a0001c0001t0001g0156 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-68+4415_-68+4426d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794075 | ||||||
| chr12:6794079 | CT | C | 22 | a0001c0001t0001g0091 a0001c0001t0001g0165 a0001c0001t0001g0166 others(19): Show |
22 | HG00673.hp2 HG01167.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.-68+4430delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794079 | ||||||
| chr12:6794088 | T | TG | 3 | a0001c0001t0001g0051 a0001c0001t0003g0050 a0002c0003t0002g0412 |
3 | HG01884.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-68+4426_-68+4427i others(3): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794088 | |||||||
| chr12:6794142 | G | T | 113 | a0001c0001t0001g0056 a0001c0001t0001g0070 a0001c0001t0001g0073 others(110): Show |
119 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.-68+4480G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794142 | |||||||
| chr12:6794165 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0003g0050 a0001c0002t0003g0248 others(1): Show |
4 | HG01884.hp2 HG03139.hp1 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+4503C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794165 | |||||||
| chr12:6794465 | G | A | 32 | a0001c0001t0002g0012 a0001c0001t0002g0276 a0001c0001t0002g0277 others(29): Show |
36 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-68+4803G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794465 | |||||||
| chr12:6794468 | T | G | 4 | a0001c0001t0004g0024 a0001c0002t0003g0416 a0002c0003t0002g0022 others(1): Show |
4 | HG02109.hp1 HG06807.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+4806T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794468 | |||||||
| chr12:6794521 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-68+4859G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794521 | |||||||
| chr12:6794599 | C | T | 7 | a0001c0001t0001g0088 a0001c0001t0002g0086 a0001c0001t0002g0087 others(4): Show |
7 | NA18943.hp2 NA18977.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68+4937C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794599 | |||||||
| chr12:6794604 | TC | T | 3 | a0001c0001t0001g0347 a0001c0001t0001g0348 a0001c0001t0004g0346 |
3 | HG02015.hp1 HG02027.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-68+4943delC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794604 | |||||||
| chr12:6794724 | C | T | 2 | a0001c0002t0003g0246 a0001c0002t0003g0247 |
2 | HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-68+5062C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794724 | |||||||
| chr12:6794765 | C | A | 2 | a0001c0002t0003g0047 a0001c0002t0003g0048 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-68+5103C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794765 | |||||||
| chr12:6794769 | A | C | 2 | a0001c0002t0003g0047 a0001c0002t0003g0048 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-68+5107A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794769 | |||||||
| chr12:6794773 | C | T | 2 | a0001c0002t0003g0047 a0001c0002t0003g0048 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-68+5111C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794773 | |||||||
| chr12:6794775 | G | GTTTTTTT others(2): Show |
7 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0264 others(4): Show |
7 | HG01256.hp1 HG02897.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68+5115_-68+5123d others(11): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | ||||||
| chr12:6794775 | G | GTTTTTTT others(3): Show |
29 | a0001c0001t0001g0142 a0001c0001t0001g0186 a0001c0001t0001g0194 others(26): Show |
32 | HG00140.hp2 HG01081.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.-68+5114_-68+5123d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | ||||||
| chr12:6794775 | G | GTTTTTTT others(4): Show |
46 | a0001c0001t0001g0160 a0001c0001t0001g0166 a0001c0001t0001g0167 others(43): Show |
46 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.-68+5123_-68+5124i others(13): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | ||||||
| chr12:6794775 | G | GTTTTTTT others(5): Show |
31 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(28): Show |
31 | HG00673.hp1 HG01074.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.-68+5123_-68+5124i others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | ||||||
| chr12:6794775 | G | GTTTTTTT others(6): Show |
7 | a0001c0001t0001g0170 a0001c0001t0001g0242 a0001c0001t0002g0241 others(4): Show |
7 | HG00673.hp2 HG01261.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.-68+5123_-68+5124i others(15): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | ||||||
| chr12:6794775 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0004g0090 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-68+5123_-68+5124i others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | ||||||
| chr12:6794775 | G | GTTTTTTT others(8): Show |
2 | a0001c0001t0001g0245 a0001c0001t0002g0244 |
2 | HG00323.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-68+5123_-68+5124i others(17): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794775 | ||||||
| chr12:6794775 | G | T | 2 | a0001c0002t0003g0047 a0001c0002t0003g0048 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-68+5113G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794775 | |||||||
| chr12:6794776 | T | G | 94 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0056 others(91): Show |
99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-68+5114T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794776 | |||||||
| chr12:6794780 | TTTTTTG | T | 9 | a0001c0001t0001g0296 a0001c0001t0001g0298 a0001c0001t0001g0299 others(6): Show |
9 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-68+5124_-68+5129d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794780 | ||||||
| chr12:6794785 | TG | T | 3 | a0001c0001t0001g0179 a0001c0001t0002g0175 a0001c0001t0002g0177 |
3 | HG01069.hp2 HG02293.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-68+5124delG | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794785 | |||||||
| chr12:6794786 | G | GT | 29 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0070 others(26): Show |
29 | HG00438.hp1 HG00597.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.-68+5140dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794786 | ||||||
| chr12:6794786 | G | GTT | 6 | a0001c0001t0001g0132 a0001c0001t0002g0071 a0001c0001t0002g0128 others(3): Show |
6 | HG00597.hp1 HG03831.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.-68+5139_-68+5140d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794786 | ||||||
| chr12:6794786 | G | T | 128 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(125): Show |
131 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.-68+5124G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794786 | |||||||
| chr12:6794786 | GTT | G | 10 | a0001c0001t0001g0051 a0001c0001t0003g0030 a0001c0001t0003g0050 others(7): Show |
10 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-68+5139_-68+5140d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794786 | ||||||
| chr12:6794786 | GTTT | G | 11 | a0001c0001t0004g0406 a0001c0001t0004g0413 a0001c0010t0003g0410 others(8): Show |
11 | HG01358.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-68+5138_-68+5140d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6794786 | ||||||
| chr12:6794803 | G | T | 1 | a0001c0001t0002g0079 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-68+5141G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794803 | |||||||
| chr12:6794823 | C | T | 141 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(138): Show |
144 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.-68+5161C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794823 | |||||||
| chr12:6794980 | T | G | 29 | a0001c0001t0002g0012 a0001c0001t0002g0276 a0001c0001t0002g0277 others(26): Show |
32 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.-67-5092T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6794980 | |||||||
| chr12:6795070 | G | A | 2 | a0001c0001t0004g0089 a0001c0001t0004g0090 |
2 | NA18978.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-67-5002G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795070 | |||||||
| chr12:6795098 | C | CTCTA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(178): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-67-4937_-67-4934d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | ||||||
| chr12:6795098 | C | CTCTATCT others(1): Show |
161 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0029 others(158): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.-67-4941_-67-4934d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | ||||||
| chr12:6795098 | C | CTCTATCT others(5): Show |
28 | a0001c0001t0001g0026 a0001c0001t0001g0062 a0001c0001t0001g0165 others(25): Show |
28 | HG00558.hp1 HG00642.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-67-4945_-67-4934d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | ||||||
| chr12:6795098 | C | CTCTATCT others(9): Show |
7 | a0001c0001t0001g0184 a0001c0001t0001g0222 a0001c0001t0001g0347 others(4): Show |
7 | HG02015.hp1 HG02148.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67-4949_-67-4934d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | ||||||
| chr12:6795098 | C | CTCTATCT others(13): Show |
1 | a0001c0001t0004g0238 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-67-4953_-67-4934d others(22): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | ||||||
| chr12:6795098 | C | CTCTATCT others(5): Show |
2 | a0001c0001t0002g0223 a0001c0001t0002g0239 |
2 | HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.-67-4965_-67-4964i others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | ||||||
| chr12:6795098 | CTCTA | C | 4 | a0001c0001t0001g0197 a0001c0001t0004g0010 a0001c0001t0004g0249 others(1): Show |
5 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-4937_-67-4934d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795098 | ||||||
| chr12:6795100 | C | G | 1 | a0008c0016t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-67-4972C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795100 | |||||||
| chr12:6795102 | A | C | 1 | a0008c0016t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-67-4970A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795102 | |||||||
| chr12:6795316 | A | T | 1 | a0001c0001t0004g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-67-4756A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795316 | |||||||
| chr12:6795317 | CCTGT | C | 133 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(130): Show |
136 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.-67-4752_-67-4749d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6795317 | ||||||
| chr12:6795457 | C | T | 1 | a0001c0004t0006g0120 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-67-4615C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795457 | |||||||
| chr12:6795624 | C | T | 18 | a0001c0001t0002g0012 a0001c0001t0002g0276 a0001c0001t0002g0277 others(15): Show |
20 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-67-4448C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795624 | |||||||
| chr12:6795679 | A | T | 7 | a0001c0002t0003g0416 a0003c0005t0004g0418 a0003c0005t0004g0419 others(4): Show |
7 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67-4393A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795679 | |||||||
| chr12:6795900 | C | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0174 |
2 | NA19080.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-67-4172C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795900 | |||||||
| chr12:6795955 | T | G | 1 | a0001c0001t0004g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-67-4117T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795955 | |||||||
| chr12:6795959 | C | A | 1 | a0001c0001t0004g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-67-4113C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795959 | |||||||
| chr12:6795962 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-67-4110C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6795962 | |||||||
| chr12:6796015 | T | C | 196 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(193): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.-67-4057T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796015 | |||||||
| chr12:6796098 | C | T | 185 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(182): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.-67-3974C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796098 | |||||||
| chr12:6796118 | A | G | 2 | a0001c0001t0004g0272 a0002c0003t0002g0271 |
2 | HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-67-3954A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796118 | |||||||
| chr12:6796251 | T | C | 294 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(291): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.-67-3821T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796251 | |||||||
| chr12:6796384 | C | G | 196 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(193): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.-67-3688C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796384 | |||||||
| chr12:6796442 | A | C | 199 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(196): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-67-3630A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796442 | |||||||
| chr12:6796524 | T | A | 11 | a0001c0001t0001g0051 a0001c0001t0003g0030 a0001c0001t0003g0050 others(8): Show |
11 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-67-3548T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796524 | |||||||
| chr12:6796549 | T | C | 199 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(196): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-67-3523T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796549 | |||||||
| chr12:6796772 | A | G | 1 | a0001c0001t0002g0311 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-67-3300A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796772 | |||||||
| chr12:6796823 | G | A | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-67-3249G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796823 | |||||||
| chr12:6796945 | C | T | 8 | a0001c0001t0001g0051 a0001c0002t0003g0416 a0003c0005t0004g0418 others(5): Show |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-67-3127C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6796945 | |||||||
| chr12:6797133 | A | G | 13 | a0001c0001t0001g0051 a0001c0001t0003g0030 a0001c0001t0003g0050 others(10): Show |
13 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-67-2939A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797133 | |||||||
| chr12:6797153 | G | A | 135 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(132): Show |
138 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.-67-2919G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797153 | |||||||
| chr12:6797312 | C | A | 1 | a0001c0001t0002g0345 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-67-2760C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797312 | |||||||
| chr12:6797502 | A | G | 6 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(3): Show |
6 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67-2570A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797502 | |||||||
| chr12:6797520 | C | T | 1 | a0001c0001t0004g0018 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-67-2552C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797520 | |||||||
| chr12:6797527 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0003g0030 a0001c0001t0003g0050 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-2545C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797527 | |||||||
| chr12:6797603 | G | A | 2 | a0001c0001t0002g0286 a0001c0002t0003g0416 |
2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-67-2469G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797603 | |||||||
| chr12:6797643 | G | C | 5 | a0001c0001t0001g0051 a0001c0001t0003g0030 a0001c0001t0003g0050 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-2429G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797643 | |||||||
| chr12:6797662 | T | C | 199 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(196): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-67-2410T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797662 | |||||||
| chr12:6797663 | A | G | 199 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(196): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-67-2409A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797663 | |||||||
| chr12:6797668 | C | T | 92 | a0001c0001t0001g0056 a0001c0001t0001g0070 a0001c0001t0001g0073 others(89): Show |
97 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-67-2404C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797668 | |||||||
| chr12:6797769 | A | G | 7 | a0001c0001t0001g0034 a0001c0001t0004g0021 a0001c0001t0004g0033 others(4): Show |
7 | HG01261.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67-2303A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797769 | |||||||
| chr12:6797799 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-67-2273G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797799 | |||||||
| chr12:6797838 | G | A | 4 | a0001c0001t0004g0024 a0001c0010t0003g0410 a0002c0003t0002g0022 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67-2234G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797838 | |||||||
| chr12:6797860 | C | T | 91 | a0001c0001t0001g0056 a0001c0001t0001g0070 a0001c0001t0001g0073 others(88): Show |
96 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-67-2212C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797860 | |||||||
| chr12:6797967 | C | T | 1 | a0001c0001t0004g0007 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-67-2105C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6797967 | |||||||
| chr12:6798067 | C | A | 2 | a0001c0001t0001g0349 a0001c0001t0001g0350 |
2 | NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-67-2005C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798067 | |||||||
| chr12:6798067 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-67-2005C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798067 | |||||||
| chr12:6798098 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(273): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-67-1974T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798098 | |||||||
| chr12:6798123 | C | T | 122 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(119): Show |
127 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.-67-1949C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798123 | |||||||
| chr12:6798139 | C | T | 2 | a0001c0001t0001g0316 a0010c0020t0004g0315 |
2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-67-1933C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798139 | |||||||
| chr12:6798172 | C | CT | 8 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0400 others(5): Show |
8 | HG02572.hp2 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-67-1885dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6798172 | ||||||
| chr12:6798172 | CT | C | 6 | a0001c0001t0002g0066 a0001c0001t0002g0121 a0001c0001t0004g0035 others(3): Show |
6 | HG01516.hp1 HG02280.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67-1885delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6798172 | ||||||
| chr12:6798208 | C | A | 4 | a0001c0001t0001g0397 a0001c0002t0003g0398 a0001c0002t0003g0399 others(1): Show |
4 | NA18989.hp2 NA19002.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67-1864C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798208 | |||||||
| chr12:6798208 | C | T | 90 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0088 others(87): Show |
95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-67-1864C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798208 | |||||||
| chr12:6798217 | TGGAGTGC others(249): Show |
T | 33 | a0001c0001t0002g0012 a0001c0001t0002g0276 a0001c0001t0002g0277 others(30): Show |
37 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.-67-1853_-67-1598d others(2): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 6798217 | ||||||
| chr12:6798221 | G | C | 1 | a0002c0003t0002g0412 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-67-1851G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798221 | |||||||
| chr12:6798230 | C | T | 5 | a0001c0001t0001g0270 a0001c0001t0001g0397 a0001c0002t0003g0398 others(2): Show |
5 | HG02895.hp2 NA18989.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-1842C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798230 | |||||||
| chr12:6798232 | C | T | 3 | a0001c0001t0001g0397 a0001c0002t0003g0398 a0001c0002t0003g0399 |
3 | NA18989.hp2 NA19002.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-67-1840C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798232 | |||||||
| chr12:6798318 | C | T | 2 | a0001c0002t0003g0047 a0001c0002t0003g0048 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-67-1754C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798318 | |||||||
| chr12:6798330 | C | A | 3 | a0001c0001t0004g0024 a0002c0003t0002g0022 a0002c0003t0002g0023 |
3 | HG02109.hp1 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-67-1742C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798330 | |||||||
| chr12:6798362 | T | C | 7 | a0001c0001t0004g0152 a0001c0001t0004g0297 a0001c0001t0004g0413 others(4): Show |
7 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67-1710T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798362 | |||||||
| chr12:6798364 | G | T | 1 | a0001c0006t0001g0343 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-67-1708G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798364 | |||||||
| chr12:6798379 | C | A | 1 | a0001c0002t0003g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-67-1693C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798379 | |||||||
| chr12:6798380 | A | G | 1 | a0001c0002t0003g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-67-1692A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798380 | |||||||
| chr12:6798449 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0003g0030 a0001c0001t0003g0050 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-1623C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798449 | |||||||
| chr12:6798480 | C | T | 1 | a0001c0001t0009g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-67-1592C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798480 | |||||||
| chr12:6798485 | G | A | 3 | a0001c0001t0001g0254 a0001c0001t0004g0018 a0002c0003t0002g0255 |
4 | HG02257.hp1 HG02280.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67-1587G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798485 | |||||||
| chr12:6798564 | T | A | 5 | a0001c0001t0001g0051 a0001c0001t0003g0030 a0001c0001t0003g0050 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-1508T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798564 | |||||||
| chr12:6798602 | G | C | 7 | a0001c0001t0004g0152 a0001c0001t0004g0297 a0001c0001t0004g0413 others(4): Show |
7 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67-1470G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798602 | |||||||
| chr12:6798766 | C | A | 2 | a0001c0004t0006g0181 a0001c0004t0006g0252 |
2 | HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-67-1306C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798766 | |||||||
| chr12:6798805 | C | G | 1 | a0001c0002t0003g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-67-1267C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798805 | |||||||
| chr12:6798951 | A | G | 3 | a0001c0001t0004g0024 a0002c0003t0002g0022 a0002c0003t0002g0023 |
3 | HG02109.hp1 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-67-1121A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798951 | |||||||
| chr12:6798980 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0003g0030 a0001c0001t0003g0050 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67-1092G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6798980 | |||||||
| chr12:6799023 | C | T | 1 | a0002c0003t0002g0118 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-67-1049C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799023 | |||||||
| chr12:6799027 | C | T | 1 | a0001c0002t0003g0388 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-67-1045C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799027 | |||||||
| chr12:6799049 | T | G | 5 | a0001c0001t0001g0051 a0001c0001t0003g0030 a0001c0001t0003g0050 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-1023T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799049 | |||||||
| chr12:6799059 | A | G | 4 | a0001c0001t0004g0024 a0001c0001t0004g0053 a0002c0003t0002g0022 others(1): Show |
4 | HG02109.hp1 HG02258.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67-1013A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799059 | |||||||
| chr12:6799221 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-67-851A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799221 | |||||||
| chr12:6799231 | A | T | 1 | a0001c0002t0003g0416 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-67-841A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799231 | |||||||
| chr12:6799298 | T | C | 2 | a0001c0004t0006g0181 a0001c0004t0006g0252 |
2 | HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-67-774T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799298 | |||||||
| chr12:6799357 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(274): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-67-715G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799357 | |||||||
| chr12:6799483 | G | A | 1 | a0001c0002t0003g0210 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-67-589G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799483 | |||||||
| chr12:6799626 | G | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(233): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-67-446G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799626 | |||||||
| chr12:6799637 | C | T | 2 | a0001c0001t0002g0294 a0001c0006t0001g0329 |
2 | HG01175.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-67-435C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799637 | |||||||
| chr12:6799641 | C | T | 1 | a0001c0001t0012g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-67-431C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799641 | |||||||
| chr12:6799713 | G | A | 3 | a0001c0001t0001g0256 a0001c0001t0002g0244 a0001c0002t0003g0198 |
3 | HG00323.hp2 HG01255.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-67-359G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799713 | |||||||
| chr12:6799770 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(258): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-67-302C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799770 | |||||||
| chr12:6799900 | C | T | 1 | a0001c0001t0002g0345 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-67-172C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 1/9 | chr12 | 6799900 | |||||||
| chr12:6800214 | TG | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(239): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.49+28delG | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 2/9 | chr12 | 6800214 | |||||||
| chr12:6800222 | A | G | 409 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(406): Show |
429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.49+35A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 2/9 | chr12 | 6800222 | |||||||
| chr12:6800269 | G | A | 3 | a0001c0002t0003g0031 a0001c0002t0003g0032 a0001c0002t0003g0282 |
3 | HG01891.hp2 HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.50-38G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 2/9 | chr12 | 6800269 | |||||||
| chr12:6800276 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(253): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.50-31T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 2/9 | chr12 | 6800276 | |||||||
| chr12:6800504 | A | G | 1 | a0001c0001t0004g0394 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.214+33A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800504 | |||||||
| chr12:6800605 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.214+134T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800605 | |||||||
| chr12:6800735 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.214+264C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800735 | |||||||
| chr12:6800759 | A | G | 1 | a0007c0014t0017g0268 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.214+288A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800759 | |||||||
| chr12:6800763 | AC | A | 5 | a0001c0001t0004g0297 a0002c0003t0007g0039 a0002c0003t0007g0404 others(2): Show |
5 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+294delC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6800763 | ||||||
| chr12:6800778 | A | G | 4 | a0001c0001t0004g0024 a0001c0010t0003g0410 a0002c0003t0002g0022 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+307A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800778 | |||||||
| chr12:6800807 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.214+336C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800807 | |||||||
| chr12:6800812 | A | G | 1 | a0003c0009t0004g0415 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.214+341A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800812 | |||||||
| chr12:6800904 | AT | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0186 a0001c0001t0001g0254 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+434delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800904 | |||||||
| chr12:6800905 | T | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(247): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.214+434T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800905 | |||||||
| chr12:6800907 | T | A | 15 | a0001c0001t0001g0186 a0001c0001t0001g0254 a0001c0001t0002g0071 others(12): Show |
15 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+436T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800907 | |||||||
| chr12:6800914 | AT | A | 11 | a0001c0001t0004g0283 a0001c0002t0003g0011 a0001c0002t0003g0031 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+451delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6800914 | ||||||
| chr12:6800916 | T | A | 28 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0051 others(25): Show |
29 | HG00735.hp1 HG01261.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.214+445T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800916 | |||||||
| chr12:6800974 | C | T | 8 | a0001c0001t0001g0051 a0001c0001t0001g0186 a0001c0001t0001g0254 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+503C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6800974 | |||||||
| chr12:6801121 | G | C | 8 | a0001c0001t0004g0053 a0002c0003t0001g0417 a0003c0005t0004g0418 others(5): Show |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+650G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801121 | |||||||
| chr12:6801152 | C | T | 1 | a0001c0002t0003g0285 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.214+681C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801152 | |||||||
| chr12:6801213 | A | T | 9 | a0001c0001t0001g0186 a0001c0001t0001g0254 a0002c0003t0002g0255 others(6): Show |
9 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+742A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801213 | |||||||
| chr12:6801225 | A | T | 1 | a0003c0009t0004g0415 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.214+754A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801225 | |||||||
| chr12:6801257 | C | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0157 others(8): Show |
14 | HG00408.hp2 HG00621.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.214+786C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801257 | |||||||
| chr12:6801264 | T | C | 3 | a0001c0001t0012g0063 a0002c0003t0001g0417 a0007c0014t0017g0268 |
3 | HG01884.hp1 HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.214+793T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801264 | |||||||
| chr12:6801295 | T | C | 1 | a0001c0001t0004g0099 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.214+824T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801295 | |||||||
| chr12:6801299 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.214+828C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801299 | |||||||
| chr12:6801300 | G | A | 28 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(25): Show |
28 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+829G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801300 | |||||||
| chr12:6801343 | C | A | 8 | a0001c0001t0004g0152 a0001c0001t0004g0297 a0001c0001t0004g0413 others(5): Show |
8 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+872C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801343 | |||||||
| chr12:6801343 | C | T | 1 | a0001c0001t0009g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.214+872C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801343 | |||||||
| chr12:6801377 | T | C | 1 | a0001c0001t0001g0370 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.214+906T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801377 | |||||||
| chr12:6801382 | G | T | 303 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(300): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.214+911G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801382 | |||||||
| chr12:6801384 | G | T | 1 | a0001c0002t0003g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.214+913G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801384 | |||||||
| chr12:6801399 | T | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(289): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.214+928T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801399 | |||||||
| chr12:6801494 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(203): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.214+1023G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801494 | |||||||
| chr12:6801516 | C | CA | 88 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0042 others(85): Show |
92 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.214+1060dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6801516 | ||||||
| chr12:6801516 | C | CAA | 6 | a0001c0001t0001g0160 a0001c0001t0002g0193 a0001c0001t0004g0089 others(3): Show |
6 | HG02132.hp2 HG04228.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+1059_214+1060d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6801516 | ||||||
| chr12:6801516 | CA | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(119): Show |
129 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.214+1060delA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6801516 | ||||||
| chr12:6801540 | TTTA | T | 19 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0042 others(16): Show |
19 | HG01109.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.214+1085_214+1087d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6801540 | ||||||
| chr12:6801558 | AGTTT | A | 11 | a0001c0002t0003g0011 a0001c0002t0003g0031 a0001c0002t0003g0032 others(8): Show |
12 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+1088_214+1091d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801558 | |||||||
| chr12:6801593 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.214+1122T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801593 | |||||||
| chr12:6801598 | T | C | 1 | a0002c0003t0001g0208 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.214+1127T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801598 | |||||||
| chr12:6801599 | C | T | 7 | a0001c0001t0001g0270 a0002c0003t0001g0405 a0002c0003t0001g0409 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+1128C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801599 | |||||||
| chr12:6801600 | G | A | 1 | a0006c0015t0020g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+1129G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801600 | |||||||
| chr12:6801615 | C | T | 8 | a0001c0001t0001g0270 a0001c0010t0003g0410 a0002c0003t0001g0405 others(5): Show |
8 | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+1144C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801615 | |||||||
| chr12:6801616 | G | A | 346 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(343): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.214+1145G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801616 | |||||||
| chr12:6801708 | A | G | 4 | a0001c0001t0003g0030 a0001c0001t0003g0050 a0001c0001t0004g0297 others(1): Show |
4 | HG02145.hp1 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1237A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801708 | |||||||
| chr12:6801717 | T | C | 2 | a0001c0001t0001g0374 a0001c0001t0004g0283 |
2 | HG02738.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.214+1246T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801717 | |||||||
| chr12:6801718 | G | A | 1 | a0001c0001t0001g0374 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.214+1247G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801718 | |||||||
| chr12:6801753 | A | G | 6 | a0001c0001t0001g0034 a0001c0001t0004g0021 a0001c0001t0004g0033 others(3): Show |
6 | HG01261.hp1 HG02280.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+1282A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801753 | |||||||
| chr12:6801767 | A | G | 90 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0001t0001g0052 others(87): Show |
93 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.214+1296A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801767 | |||||||
| chr12:6801769 | C | T | 2 | a0001c0001t0002g0223 a0001c0001t0002g0239 |
2 | HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.214+1298C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801769 | |||||||
| chr12:6801774 | C | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | HG02572.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.214+1303C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801774 | |||||||
| chr12:6801778 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | HG02572.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.214+1307T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801778 | |||||||
| chr12:6801817 | C | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 |
3 | HG02630.hp2 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.214+1346C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801817 | |||||||
| chr12:6801845 | T | C | 1 | a0001c0001t0002g0262 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.214+1374T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801845 | |||||||
| chr12:6801903 | C | T | 5 | a0002c0003t0001g0208 a0002c0003t0007g0039 a0002c0003t0007g0269 others(2): Show |
5 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+1432C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801903 | |||||||
| chr12:6801911 | T | C | 2 | a0001c0001t0002g0286 a0001c0001t0002g0293 |
2 | HG00733.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.214+1440T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801911 | |||||||
| chr12:6801942 | T | C | 1 | a0001c0001t0002g0377 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.214+1471T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6801942 | |||||||
| chr12:6802036 | G | T | 1 | a0006c0015t0020g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+1565G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802036 | |||||||
| chr12:6802122 | C | T | 1 | a0001c0002t0003g0134 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.214+1651C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802122 | |||||||
| chr12:6802218 | T | C | 1 | a0001c0001t0004g0201 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.214+1747T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802218 | |||||||
| chr12:6802271 | T | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(341): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.214+1800T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802271 | |||||||
| chr12:6802319 | C | CT | 20 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0117 others(17): Show |
22 | HG01515.hp2 HG01884.hp2 HG03225.hp1 others(19): Show |
intron_variant | MODIFIER | c.214+1863dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6802319 | ||||||
| chr12:6802541 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(201): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.214+2070C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802541 | |||||||
| chr12:6802617 | C | T | 2 | a0001c0001t0003g0030 a0001c0001t0003g0050 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.214+2146C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802617 | |||||||
| chr12:6802759 | C | G | 1 | a0002c0003t0007g0414 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.214+2288C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802759 | |||||||
| chr12:6802759 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.214+2288C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802759 | |||||||
| chr12:6802800 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.214+2329G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6802800 | |||||||
| chr12:6803016 | A | G | 27 | a0001c0001t0001g0156 a0001c0001t0001g0316 a0001c0001t0002g0175 others(24): Show |
29 | HG01928.hp1 HG01978.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.214+2545A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803016 | |||||||
| chr12:6803102 | A | C | 2 | a0001c0001t0001g0364 a0001c0001t0001g0396 |
2 | NA18943.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.214+2631A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803102 | |||||||
| chr12:6803151 | C | T | 1 | a0001c0001t0004g0187 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.214+2680C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803151 | |||||||
| chr12:6803294 | G | A | 1 | a0008c0016t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.214+2823G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803294 | |||||||
| chr12:6803391 | T | C | 110 | a0001c0001t0001g0034 a0001c0001t0001g0094 a0001c0001t0001g0156 others(107): Show |
116 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.214+2920T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803391 | |||||||
| chr12:6803396 | A | C | 1 | a0003c0009t0004g0415 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.214+2925A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803396 | |||||||
| chr12:6803429 | G | T | 2 | a0001c0001t0003g0030 a0001c0001t0003g0050 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.214+2958G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803429 | |||||||
| chr12:6803507 | G | A | 4 | a0002c0003t0007g0039 a0002c0003t0007g0269 a0002c0003t0007g0404 others(1): Show |
4 | HG01358.hp1 HG01993.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3036G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803507 | |||||||
| chr12:6803601 | G | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(293): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.214+3130G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803601 | |||||||
| chr12:6803611 | C | G | 1 | a0006c0015t0020g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+3140C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803611 | |||||||
| chr12:6803647 | T | G | 6 | a0002c0003t0005g0037 a0002c0003t0005g0045 a0002c0003t0005g0046 others(3): Show |
6 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+3176T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803647 | |||||||
| chr12:6803740 | G | A | 6 | a0001c0001t0001g0091 a0001c0001t0004g0089 a0001c0001t0004g0090 others(3): Show |
6 | HG02132.hp2 NA18961.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.214+3269G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803740 | |||||||
| chr12:6803783 | A | T | 1 | a0006c0015t0020g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+3312A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803783 | |||||||
| chr12:6803791 | T | A | 3 | a0002c0003t0002g0022 a0002c0003t0002g0023 a0002c0003t0002g0041 |
3 | HG02109.hp1 HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.214+3320T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803791 | |||||||
| chr12:6803849 | C | T | 1 | a0001c0002t0008g0013 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.214+3378C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803849 | |||||||
| chr12:6803858 | T | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(217): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.214+3387T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803858 | |||||||
| chr12:6803885 | A | G | 341 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(338): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.214+3414A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803885 | |||||||
| chr12:6803965 | T | G | 368 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(365): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.214+3494T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6803965 | |||||||
| chr12:6804054 | T | C | 1 | a0001c0010t0003g0410 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.214+3583T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804054 | |||||||
| chr12:6804067 | C | T | 1 | a0001c0001t0001g0395 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.214+3596C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804067 | |||||||
| chr12:6804090 | G | A | 7 | a0001c0004t0006g0064 a0001c0004t0006g0120 a0001c0004t0006g0153 others(4): Show |
7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+3619G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804090 | |||||||
| chr12:6804111 | A | AAAAT | 17 | a0001c0001t0004g0065 a0001c0001t0004g0109 a0001c0001t0004g0141 others(14): Show |
19 | HG00738.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.214+3680_214+3683d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804111 | ||||||
| chr12:6804111 | A | AAAATAAA others(1): Show |
8 | a0002c0003t0002g0022 a0002c0003t0002g0023 a0002c0003t0002g0041 others(5): Show |
8 | HG01358.hp1 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+3676_214+3683d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804111 | ||||||
| chr12:6804111 | AAAAT | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0157 others(21): Show |
27 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.214+3680_214+3683d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804111 | ||||||
| chr12:6804111 | AAAATAAA others(1): Show |
A | 196 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(193): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.214+3676_214+3683d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804111 | ||||||
| chr12:6804111 | AAAATAAA others(5): Show |
A | 107 | a0001c0001t0001g0034 a0001c0001t0001g0094 a0001c0001t0001g0156 others(104): Show |
112 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.214+3672_214+3683d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804111 | ||||||
| chr12:6804127 | T | C | 4 | a0002c0003t0002g0266 a0002c0003t0002g0267 a0002c0003t0002g0271 others(1): Show |
4 | HG02055.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3656T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804127 | |||||||
| chr12:6804162 | G | GCA | 9 | a0001c0001t0004g0383 a0002c0003t0001g0405 a0002c0003t0001g0409 others(6): Show |
9 | HG02559.hp1 HG03486.hp1 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+3720_214+3721d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804162 | ||||||
| chr12:6804162 | G | GCACA | 3 | a0002c0003t0002g0006 a0002c0003t0002g0110 a0002c0003t0002g0255 |
4 | NA18944.hp2 NA18984.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+3718_214+3721d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804162 | ||||||
| chr12:6804162 | GCA | G | 10 | a0001c0001t0001g0182 a0001c0001t0001g0316 a0001c0001t0004g0163 others(7): Show |
11 | HG00673.hp1 HG01192.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.214+3720_214+3721d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804162 | ||||||
| chr12:6804162 | GCACACAC others(1): Show |
G | 4 | a0002c0003t0002g0266 a0002c0003t0002g0267 a0002c0003t0002g0271 others(1): Show |
4 | HG02055.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3714_214+3721d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804162 | ||||||
| chr12:6804162 | GCACACAC others(9): Show |
G | 338 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(335): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.214+3706_214+3721d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6804162 | ||||||
| chr12:6804170 | A | G | 1 | a0006c0015t0020g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+3699A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804170 | |||||||
| chr12:6804180 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.214+3709A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804180 | |||||||
| chr12:6804190 | A | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(209): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.214+3719A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804190 | |||||||
| chr12:6804207 | C | T | 8 | a0001c0001t0001g0321 a0001c0004t0006g0064 a0001c0004t0006g0120 others(5): Show |
8 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+3736C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804207 | |||||||
| chr12:6804307 | A | G | 1 | a0009c0017t0001g0407 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.214+3836A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804307 | |||||||
| chr12:6804380 | A | G | 336 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(333): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.214+3909A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804380 | |||||||
| chr12:6804437 | A | G | 2 | a0001c0001t0001g0316 a0002c0003t0019g0027 |
2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.214+3966A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804437 | |||||||
| chr12:6804524 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(163): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.214+4053A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804524 | |||||||
| chr12:6804600 | T | C | 1 | a0001c0002t0003g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.214+4129T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804600 | |||||||
| chr12:6804665 | G | A | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | HG01168.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.214+4194G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804665 | |||||||
| chr12:6804694 | G | A | 1 | a0001c0002t0003g0402 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.214+4223G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804694 | |||||||
| chr12:6804734 | T | C | 2 | a0001c0001t0002g0223 a0001c0001t0002g0239 |
2 | HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.214+4263T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804734 | |||||||
| chr12:6804788 | G | A | 2 | a0001c0001t0001g0054 a0006c0015t0020g0164 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.214+4317G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804788 | |||||||
| chr12:6804792 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0009g0092 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+4321G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804792 | |||||||
| chr12:6804941 | G | A | 1 | a0001c0002t0003g0398 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.214+4470G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804941 | |||||||
| chr12:6804948 | G | A | 1 | a0006c0015t0020g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+4477G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6804948 | |||||||
| chr12:6805015 | C | CA | 22 | a0001c0001t0001g0020 a0001c0001t0001g0088 a0001c0001t0001g0305 others(19): Show |
22 | HG00621.hp2 HG01192.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.214+4563dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805015 | ||||||
| chr12:6805015 | C | CAA | 62 | a0001c0001t0001g0245 a0001c0001t0001g0316 a0001c0001t0002g0057 others(59): Show |
69 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.214+4562_214+4563d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805015 | ||||||
| chr12:6805015 | C | CAAA | 12 | a0001c0001t0001g0182 a0001c0001t0004g0089 a0001c0001t0004g0219 others(9): Show |
12 | HG02055.hp1 HG02074.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+4561_214+4563d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805015 | ||||||
| chr12:6805015 | CA | C | 112 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0029 others(109): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.214+4563delA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805015 | ||||||
| chr12:6805015 | CAA | C | 15 | a0001c0001t0001g0142 a0001c0001t0004g0099 a0001c0002t0003g0105 others(12): Show |
15 | HG01928.hp2 HG01978.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.214+4562_214+4563d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805015 | ||||||
| chr12:6805166 | G | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(335): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.214+4695G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805166 | |||||||
| chr12:6805184 | C | CA | 11 | a0001c0001t0001g0182 a0001c0001t0002g0057 a0001c0001t0002g0304 others(8): Show |
13 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.214+4735dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805184 | ||||||
| chr12:6805198 | AAAAAAAA others(2): Show |
A | 47 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0051 others(44): Show |
47 | HG00741.hp1 HG01069.hp2 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+4732_214+4740d others(11): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805198 | ||||||
| chr12:6805199 | AAAAAAAA others(1): Show |
A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0028 others(146): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.214+4733_214+4740d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805199 | ||||||
| chr12:6805200 | AAAAAAAG | A | 15 | a0001c0001t0001g0020 a0001c0001t0001g0088 a0001c0001t0001g0270 others(12): Show |
15 | HG00099.hp1 HG01175.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+4734_214+4740d others(9): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805200 | ||||||
| chr12:6805202 | AAAAAG | A | 10 | a0001c0001t0002g0078 a0001c0001t0002g0126 a0001c0001t0002g0373 others(7): Show |
10 | HG02027.hp1 HG02040.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.214+4756_214+4760d others(7): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805202 | ||||||
| chr12:6805203 | AAAAG | A | 120 | a0001c0001t0001g0034 a0001c0001t0001g0094 a0001c0001t0001g0156 others(117): Show |
127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.214+4736_214+4739d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805203 | ||||||
| chr12:6805204 | AAAG | A | 20 | a0001c0001t0002g0014 a0001c0001t0002g0049 a0001c0001t0002g0067 others(17): Show |
20 | HG01358.hp1 HG02055.hp1 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.214+4736_214+4738d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805204 | ||||||
| chr12:6805206 | AG | A | 7 | a0001c0004t0006g0064 a0001c0004t0006g0120 a0001c0004t0006g0153 others(4): Show |
7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+4736delG | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805206 | |||||||
| chr12:6805256 | G | T | 1 | a0001c0001t0004g0283 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214+4785G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805256 | |||||||
| chr12:6805285 | A | G | 19 | a0001c0001t0004g0099 a0001c0002t0003g0105 a0001c0002t0003g0106 others(16): Show |
19 | HG00673.hp2 HG01928.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.214+4814A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805285 | |||||||
| chr12:6805293 | T | A | 1 | a0001c0001t0001g0355 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.214+4822T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805293 | |||||||
| chr12:6805368 | G | A | 1 | a0001c0001t0010g0233 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.214+4897G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805368 | |||||||
| chr12:6805559 | TC | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0168 a0001c0001t0001g0380 others(3): Show |
6 | HG01070.hp1 HG02897.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+5091delC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6805559 | ||||||
| chr12:6805560 | C | CA | 88 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0321 others(85): Show |
93 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.214+5089_214+5090i others(3): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805560 | |||||||
| chr12:6805560 | C | CAA | 7 | a0002c0003t0002g0003 a0002c0003t0002g0006 a0002c0003t0002g0097 others(4): Show |
9 | HG03704.hp1 NA18944.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+5089_214+5090i others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805560 | |||||||
| chr12:6805561 | C | A | 414 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(411): Show |
434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.214+5090C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805561 | |||||||
| chr12:6805577 | G | A | 1 | a0001c0001t0004g0220 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.214+5106G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805577 | |||||||
| chr12:6805578 | A | G | 1 | a0001c0001t0004g0220 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.214+5107A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805578 | |||||||
| chr12:6805816 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.214+5345C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805816 | |||||||
| chr12:6805828 | G | A | 1 | a0001c0002t0003g0243 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.214+5357G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805828 | |||||||
| chr12:6805945 | C | A | 5 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0024 others(2): Show |
7 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+5474C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805945 | |||||||
| chr12:6805994 | T | A | 86 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(83): Show |
93 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.214+5523T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805994 | |||||||
| chr12:6805996 | C | T | 2 | a0001c0001t0001g0316 a0002c0003t0019g0027 |
2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.214+5525C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6805996 | |||||||
| chr12:6806037 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.214+5566C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806037 | |||||||
| chr12:6806072 | G | C | 83 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(80): Show |
90 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.214+5601G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806072 | |||||||
| chr12:6806136 | C | CA | 113 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0156 others(110): Show |
120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.214+5678dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806136 | ||||||
| chr12:6806149 | AG | A | 8 | a0001c0001t0001g0321 a0001c0004t0006g0064 a0001c0004t0006g0120 others(5): Show |
8 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+5680delG | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806149 | ||||||
| chr12:6806150 | G | A | 411 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(408): Show |
431 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(428): Show |
intron_variant | MODIFIER | c.214+5679G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806150 | |||||||
| chr12:6806154 | C | A | 1 | a0001c0001t0004g0141 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.214+5683C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806154 | |||||||
| chr12:6806155 | A | G | 1 | a0001c0001t0004g0141 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.214+5684A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806155 | |||||||
| chr12:6806156 | T | TAC | 16 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0136 others(13): Show |
17 | HG01261.hp2 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.214+5711_214+5712d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806156 | ||||||
| chr12:6806156 | TAC | T | 5 | a0001c0001t0001g0073 a0001c0001t0001g0265 a0001c0001t0001g0299 others(2): Show |
5 | HG02056.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+5711_214+5712d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806156 | ||||||
| chr12:6806156 | TACAC | T | 81 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(78): Show |
88 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.214+5709_214+5712d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806156 | ||||||
| chr12:6806156 | TACACACA others(5): Show |
T | 1 | a0001c0018t0002g0158 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.214+5701_214+5712d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806156 | ||||||
| chr12:6806160 | C | T | 1 | a0001c0001t0004g0141 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.214+5689C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806160 | |||||||
| chr12:6806176 | CACACACA others(9): Show |
C | 1 | a0001c0001t0004g0413 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.214+5707_214+5722d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806176 | ||||||
| chr12:6806178 | CACACATA others(7): Show |
C | 92 | a0001c0001t0001g0034 a0001c0001t0001g0156 a0001c0001t0002g0002 others(89): Show |
98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.214+5709_214+5722d others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806178 | ||||||
| chr12:6806180 | CACATACA others(5): Show |
C | 18 | a0001c0001t0002g0211 a0001c0001t0002g0276 a0001c0001t0002g0277 others(15): Show |
18 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+5711_214+5722d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806180 | ||||||
| chr12:6806182 | C | CAT | 8 | a0001c0001t0001g0321 a0001c0004t0006g0064 a0001c0004t0006g0120 others(5): Show |
8 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+5713_214+5714d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806182 | ||||||
| chr12:6806182 | C | T | 83 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(80): Show |
90 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.214+5711C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806182 | |||||||
| chr12:6806182 | CATACACA others(3): Show |
C | 1 | a0006c0015t0020g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+5715_214+5724d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6806182 | ||||||
| chr12:6806184 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.214+5713T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806184 | |||||||
| chr12:6806191 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(305): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.214+5720G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806191 | |||||||
| chr12:6806202 | T | A | 112 | a0001c0001t0001g0034 a0001c0001t0001g0156 a0001c0001t0002g0002 others(109): Show |
118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.214+5731T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806202 | |||||||
| chr12:6806242 | T | C | 6 | a0002c0003t0005g0037 a0002c0003t0005g0045 a0002c0003t0005g0046 others(3): Show |
6 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+5771T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806242 | |||||||
| chr12:6806269 | C | T | 25 | a0001c0001t0001g0316 a0002c0003t0001g0162 a0002c0003t0001g0208 others(22): Show |
27 | HG02055.hp1 HG02109.hp1 HG02559.hp1 others(24): Show |
intron_variant | MODIFIER | c.214+5798C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806269 | |||||||
| chr12:6806286 | A | C | 85 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(82): Show |
92 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.214+5815A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806286 | |||||||
| chr12:6806345 | CCCAGGCT others(1): Show |
C | 55 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0015 others(52): Show |
58 | HG00558.hp1 HG00621.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.214+5875_214+5882d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806345 | |||||||
| chr12:6806353 | G | A | 1 | a0002c0003t0007g0039 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.214+5882G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806353 | |||||||
| chr12:6806420 | G | T | 4 | a0002c0003t0002g0266 a0002c0003t0002g0267 a0002c0003t0002g0271 others(1): Show |
4 | HG02055.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+5949G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806420 | |||||||
| chr12:6806740 | G | A | 103 | a0001c0001t0001g0156 a0001c0001t0002g0002 a0001c0001t0002g0004 others(100): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.214+6269G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806740 | |||||||
| chr12:6806797 | T | C | 28 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0112 others(25): Show |
28 | HG00741.hp1 HG01069.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+6326T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806797 | |||||||
| chr12:6806820 | G | A | 6 | a0002c0003t0005g0037 a0002c0003t0005g0045 a0002c0003t0005g0046 others(3): Show |
6 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+6349G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806820 | |||||||
| chr12:6806893 | C | T | 2 | a0001c0001t0001g0361 a0001c0001t0014g0360 |
2 | NA18997.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.214+6422C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806893 | |||||||
| chr12:6806949 | C | T | 1 | a0001c0001t0002g0375 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.214+6478C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806949 | |||||||
| chr12:6806994 | T | C | 84 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(81): Show |
91 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.214+6523T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6806994 | |||||||
| chr12:6807023 | C | T | 1 | a0001c0001t0002g0281 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+6552C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807023 | |||||||
| chr12:6807083 | T | C | 25 | a0001c0001t0001g0316 a0002c0003t0001g0162 a0002c0003t0001g0208 others(22): Show |
27 | HG02055.hp1 HG02109.hp1 HG02559.hp1 others(24): Show |
intron_variant | MODIFIER | c.214+6612T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807083 | |||||||
| chr12:6807099 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.214+6628G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807099 | |||||||
| chr12:6807113 | G | A | 53 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0002g0131 others(50): Show |
58 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.214+6642G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807113 | |||||||
| chr12:6807128 | T | C | 90 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(87): Show |
97 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.214+6657T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807128 | |||||||
| chr12:6807148 | C | G | 7 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0263 others(4): Show |
7 | HG01261.hp1 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+6677C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807148 | |||||||
| chr12:6807149 | G | C | 8 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(5): Show |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+6678G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807149 | |||||||
| chr12:6807174 | CAA | C | 82 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(79): Show |
89 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.214+6707_214+6708d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6807174 | ||||||
| chr12:6807344 | G | A | 1 | a0001c0010t0003g0258 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215-6798G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807344 | |||||||
| chr12:6807345 | T | G | 90 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(87): Show |
97 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.215-6797T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807345 | |||||||
| chr12:6807412 | C | A | 1 | a0002c0003t0002g0412 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.215-6730C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807412 | |||||||
| chr12:6807419 | G | C | 1 | a0001c0002t0008g0013 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.215-6723G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807419 | |||||||
| chr12:6807615 | C | T | 8 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(5): Show |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-6527C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807615 | |||||||
| chr12:6807725 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.215-6417T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807725 | |||||||
| chr12:6807851 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.215-6291C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807851 | |||||||
| chr12:6807887 | C | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0051 |
2 | HG01261.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.215-6255C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807887 | |||||||
| chr12:6807936 | T | C | 1 | a0001c0001t0001g0382 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.215-6206T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807936 | |||||||
| chr12:6807940 | C | T | 1 | a0001c0010t0003g0258 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215-6202C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807940 | |||||||
| chr12:6807973 | G | A | 2 | a0001c0001t0003g0030 a0001c0001t0003g0050 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.215-6169G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6807973 | |||||||
| chr12:6808052 | C | T | 2 | a0001c0001t0001g0379 a0001c0001t0001g0381 |
2 | NA19003.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.215-6090C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808052 | |||||||
| chr12:6808076 | T | A | 90 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(87): Show |
97 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.215-6066T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808076 | |||||||
| chr12:6808079 | C | CA | 27 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0001g0156 others(24): Show |
27 | HG00423.hp2 HG00642.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.215-6039dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808079 | ||||||
| chr12:6808079 | CA | C | 150 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0034 others(147): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.215-6039delA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808079 | ||||||
| chr12:6808079 | CAA | C | 12 | a0001c0001t0001g0136 a0001c0001t0001g0182 a0001c0001t0001g0227 others(9): Show |
13 | HG01884.hp2 HG01943.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.215-6040_215-6039d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808079 | ||||||
| chr12:6808079 | CAAA | C | 72 | a0001c0001t0001g0245 a0001c0001t0002g0131 a0001c0001t0002g0137 others(69): Show |
78 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.215-6041_215-6039d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808079 | ||||||
| chr12:6808079 | CAAAA | C | 20 | a0001c0001t0001g0316 a0002c0003t0001g0162 a0002c0003t0001g0405 others(17): Show |
20 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-6042_215-6039d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808079 | ||||||
| chr12:6808167 | A | C | 2 | a0001c0001t0009g0092 a0012c0013t0009g0159 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.215-5975A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808167 | |||||||
| chr12:6808192 | CGCCTGTA others(7): Show |
C | 7 | a0001c0001t0001g0156 a0001c0001t0001g0310 a0001c0001t0001g0319 others(4): Show |
7 | HG01257.hp1 HG01358.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-5949_215-5936d others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808192 | |||||||
| chr12:6808193 | G | T | 5 | a0001c0001t0004g0080 a0001c0001t0004g0081 a0001c0001t0004g0085 others(2): Show |
5 | HG01192.hp1 HG02735.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-5949G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808193 | |||||||
| chr12:6808270 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0254 |
2 | NA18945.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.215-5872A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808270 | |||||||
| chr12:6808318 | G | A | 152 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0034 others(149): Show |
158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.215-5824G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808318 | |||||||
| chr12:6808324 | C | T | 82 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(79): Show |
89 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.215-5818C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808324 | |||||||
| chr12:6808369 | T | C | 5 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0024 others(2): Show |
7 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-5773T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808369 | |||||||
| chr12:6808386 | A | AG | 92 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(89): Show |
99 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-5755dupG | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808386 | ||||||
| chr12:6808387 | G | GC | 328 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(325): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.215-5755_215-5754i others(3): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808387 | |||||||
| chr12:6808445 | T | C | 1 | a0001c0018t0002g0158 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.215-5697T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808445 | |||||||
| chr12:6808450 | C | CA | 59 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0060 others(56): Show |
59 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.215-5660dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAA | 22 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0042 others(19): Show |
23 | HG01099.hp1 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.215-5661_215-5660d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAA | 6 | a0001c0001t0001g0059 a0001c0001t0001g0093 a0001c0002t0003g0011 others(3): Show |
7 | HG01361.hp2 HG02451.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-5662_215-5660d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAAAA | 5 | a0001c0001t0002g0012 a0001c0001t0002g0116 a0001c0001t0002g0280 others(2): Show |
6 | HG00140.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-5664_215-5660d others(7): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAAAAA | 33 | a0001c0001t0002g0066 a0001c0001t0002g0068 a0001c0001t0002g0071 others(30): Show |
33 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.215-5665_215-5660d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAAAAAA | 27 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0015 others(24): Show |
31 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.215-5666_215-5660d others(9): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0002g0014 a0001c0001t0002g0083 a0001c0001t0002g0086 others(5): Show |
9 | HG01169.hp1 HG02257.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.215-5667_215-5660d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAAAAAA others(3): Show |
4 | a0002c0003t0005g0037 a0002c0003t0005g0045 a0002c0003t0005g0046 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-5669_215-5660d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAAAAAA others(4): Show |
1 | a0012c0013t0009g0159 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.215-5670_215-5660d others(13): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAAAAAA others(5): Show |
5 | a0001c0001t0009g0092 a0001c0004t0006g0064 a0001c0004t0006g0181 others(2): Show |
5 | HG00597.hp1 HG02615.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-5671_215-5660d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAAAAAA others(6): Show |
1 | a0002c0003t0005g0300 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.215-5672_215-5660d others(15): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAAAAAA others(9): Show |
2 | a0001c0004t0006g0120 a0001c0004t0006g0153 |
2 | HG03654.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.215-5675_215-5660d others(18): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAAAAAA others(10): Show |
1 | a0001c0004t0006g0369 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.215-5676_215-5660d others(19): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | C | CAAAAAAA others(11): Show |
1 | a0001c0004t0006g0209 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.215-5677_215-5660d others(20): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | CA | C | 32 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(29): Show |
32 | HG01069.hp2 HG01255.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.215-5660delA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | CAAAAAA | C | 14 | a0001c0001t0002g0049 a0001c0001t0002g0077 a0001c0001t0002g0078 others(11): Show |
14 | HG00558.hp1 HG01109.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.215-5665_215-5660d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0317 a0001c0001t0002g0276 a0001c0001t0002g0277 |
3 | HG03490.hp2 HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.215-5670_215-5660d others(13): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0270 a0001c0001t0003g0030 a0001c0001t0003g0050 |
3 | HG02572.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.215-5671_215-5660d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0010t0003g0258 |
3 | HG01261.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.215-5672_215-5660d others(15): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | CAAAAAAA others(10): Show |
C | 2 | a0002c0003t0007g0414 a0010c0020t0004g0315 |
2 | HG01358.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.215-5676_215-5660d others(19): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | CAAAAAAA others(11): Show |
C | 86 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(83): Show |
93 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.215-5677_215-5660d others(20): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808450 | CAAAAAAA others(12): Show |
C | 4 | a0002c0003t0002g0266 a0002c0003t0002g0267 a0002c0003t0002g0271 others(1): Show |
4 | HG02055.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-5678_215-5660d others(21): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6808450 | ||||||
| chr12:6808489 | T | A | 92 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0001t0001g0316 others(89): Show |
99 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-5653T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808489 | |||||||
| chr12:6808502 | T | A | 2 | a0001c0004t0006g0064 a0001c0004t0006g0120 |
2 | HG00597.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.215-5640T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808502 | |||||||
| chr12:6808503 | T | A | 29 | a0001c0001t0001g0316 a0001c0004t0006g0064 a0001c0004t0006g0120 others(26): Show |
31 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.215-5639T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808503 | |||||||
| chr12:6808666 | G | A | 147 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0034 others(144): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.215-5476G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808666 | |||||||
| chr12:6808801 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.215-5341T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808801 | |||||||
| chr12:6808900 | G | T | 2 | a0003c0009t0004g0043 a0003c0009t0004g0415 |
2 | HG00738.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.215-5242G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808900 | |||||||
| chr12:6808955 | C | T | 6 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-5187C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6808955 | |||||||
| chr12:6809030 | A | G | 92 | a0001c0001t0001g0182 a0001c0001t0002g0057 a0001c0001t0002g0131 others(89): Show |
99 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-5112A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809030 | |||||||
| chr12:6809269 | C | A | 1 | a0002c0003t0007g0414 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.215-4873C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809269 | |||||||
| chr12:6809294 | G | A | 7 | a0001c0004t0006g0064 a0001c0004t0006g0120 a0001c0004t0006g0153 others(4): Show |
7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-4848G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809294 | |||||||
| chr12:6809358 | T | C | 8 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(5): Show |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-4784T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809358 | |||||||
| chr12:6809373 | G | A | 6 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-4769G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809373 | |||||||
| chr12:6809444 | C | A | 2 | a0001c0002t0003g0047 a0001c0002t0003g0048 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.215-4698C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809444 | |||||||
| chr12:6809449 | T | C | 1 | a0002c0003t0007g0414 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.215-4693T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809449 | |||||||
| chr12:6809495 | C | CA | 6 | a0001c0001t0001g0310 a0001c0001t0002g0067 a0001c0001t0004g0272 others(3): Show |
6 | HG02293.hp2 HG02735.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-4634dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809495 | ||||||
| chr12:6809495 | CA | C | 40 | a0001c0002t0003g0155 a0001c0004t0006g0209 a0001c0004t0006g0369 others(37): Show |
42 | HG00408.hp1 HG00609.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.215-4634delA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809495 | ||||||
| chr12:6809646 | T | C | 7 | a0002c0003t0005g0037 a0002c0003t0005g0040 a0002c0003t0005g0045 others(4): Show |
7 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-4496T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809646 | |||||||
| chr12:6809666 | C | T | 6 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-4476C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809666 | |||||||
| chr12:6809752 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0073 |
2 | HG02056.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.215-4390G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6809752 | |||||||
| chr12:6809890 | C | CT | 33 | a0001c0001t0002g0223 a0001c0004t0006g0064 a0001c0004t0006g0120 others(30): Show |
35 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.215-4235dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809890 | ||||||
| chr12:6809890 | C | CTT | 154 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0034 others(151): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.215-4236_215-4235d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809890 | ||||||
| chr12:6809890 | C | CTTT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(82): Show |
88 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.215-4237_215-4235d others(5): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809890 | ||||||
| chr12:6809916 | GTC | G | 92 | a0001c0001t0001g0182 a0001c0001t0002g0057 a0001c0001t0002g0131 others(89): Show |
99 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-4215_215-4214d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6809916 | ||||||
| chr12:6810034 | C | T | 4 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0230 others(1): Show |
4 | HG03017.hp1 HG03239.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-4108C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810034 | |||||||
| chr12:6810142 | G | A | 8 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(5): Show |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-4000G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810142 | |||||||
| chr12:6810153 | G | C | 83 | a0001c0001t0001g0182 a0001c0001t0001g0316 a0001c0001t0001g0400 others(80): Show |
90 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.215-3989G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810153 | |||||||
| chr12:6810239 | A | G | 1 | a0003c0009t0004g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.215-3903A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810239 | |||||||
| chr12:6810255 | C | T | 1 | a0001c0018t0002g0158 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.215-3887C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810255 | |||||||
| chr12:6810403 | A | G | 92 | a0001c0001t0001g0182 a0001c0001t0001g0400 a0001c0001t0002g0057 others(89): Show |
99 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-3739A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810403 | |||||||
| chr12:6810510 | G | T | 1 | a0001c0001t0012g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.215-3632G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810510 | |||||||
| chr12:6810589 | A | G | 2 | a0001c0001t0003g0030 a0001c0001t0003g0050 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.215-3553A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810589 | |||||||
| chr12:6810592 | C | A | 1 | a0001c0001t0001g0298 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.215-3550C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810592 | |||||||
| chr12:6810685 | C | T | 8 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(5): Show |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-3457C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6810685 | |||||||
| chr12:6811099 | A | G | 6 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-3043A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811099 | |||||||
| chr12:6811106 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.215-3036C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811106 | |||||||
| chr12:6811468 | CTTTTCTT | C | 5 | a0001c0001t0002g0072 a0001c0001t0002g0129 a0001c0001t0002g0139 others(2): Show |
5 | HG00621.hp1 NA18952.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-2664_215-2658d others(9): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811468 | ||||||
| chr12:6811472 | T | C | 1 | a0003c0005t0004g0420 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.215-2670T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811472 | |||||||
| chr12:6811477 | TTTCTTTT others(7): Show |
T | 5 | a0002c0003t0002g0003 a0002c0003t0002g0096 a0002c0003t0002g0097 others(2): Show |
6 | NA18952.hp1 NA18956.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-2662_215-2649d others(16): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811477 | ||||||
| chr12:6811478 | TTCTTTTC others(6): Show |
T | 7 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0421 others(4): Show |
7 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-2662_215-2650d others(15): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811478 | ||||||
| chr12:6811491 | C | CT | 20 | a0001c0001t0002g0067 a0001c0001t0002g0086 a0001c0001t0002g0087 others(17): Show |
20 | HG00408.hp1 HG00609.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-2632dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811491 | ||||||
| chr12:6811491 | CT | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(135): Show |
141 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.215-2632delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811491 | ||||||
| chr12:6811491 | CTT | C | 74 | a0001c0001t0001g0060 a0001c0001t0001g0400 a0001c0001t0002g0131 others(71): Show |
80 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.215-2633_215-2632d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811491 | ||||||
| chr12:6811492 | T | C | 7 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0421 others(4): Show |
7 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-2650T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811492 | |||||||
| chr12:6811493 | T | C | 6 | a0002c0003t0002g0003 a0002c0003t0002g0096 a0002c0003t0002g0097 others(3): Show |
7 | HG01891.hp1 NA18952.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-2649T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811493 | |||||||
| chr12:6811495 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.215-2647T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811495 | |||||||
| chr12:6811553 | C | T | 1 | a0001c0001t0004g0018 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.215-2589C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811553 | |||||||
| chr12:6811671 | C | CT | 102 | a0001c0001t0002g0049 a0001c0001t0002g0072 a0001c0001t0002g0077 others(99): Show |
109 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.215-2460dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6811671 | ||||||
| chr12:6811791 | G | A | 83 | a0001c0001t0002g0131 a0001c0001t0002g0137 a0001c0001t0002g0144 others(80): Show |
90 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.215-2351G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811791 | |||||||
| chr12:6811807 | G | A | 6 | a0002c0003t0005g0037 a0002c0003t0005g0045 a0002c0003t0005g0046 others(3): Show |
6 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-2335G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811807 | |||||||
| chr12:6811925 | T | A | 1 | a0001c0001t0004g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.215-2217T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811925 | |||||||
| chr12:6811985 | A | T | 7 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0015 others(4): Show |
10 | NA18942.hp1 NA18948.hp1 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-2157A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6811985 | |||||||
| chr12:6812074 | C | T | 1 | a0001c0001t0004g0283 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.215-2068C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812074 | |||||||
| chr12:6812078 | T | G | 84 | a0001c0001t0002g0131 a0001c0001t0002g0137 a0001c0001t0002g0144 others(81): Show |
91 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.215-2064T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812078 | |||||||
| chr12:6812129 | G | A | 1 | a0001c0001t0004g0084 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.215-2013G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812129 | |||||||
| chr12:6812140 | C | G | 1 | a0002c0003t0019g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.215-2002C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812140 | |||||||
| chr12:6812229 | T | C | 84 | a0001c0001t0002g0131 a0001c0001t0002g0137 a0001c0001t0002g0144 others(81): Show |
91 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.215-1913T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812229 | |||||||
| chr12:6812263 | G | A | 1 | a0001c0001t0004g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.215-1879G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812263 | |||||||
| chr12:6812548 | G | A | 4 | a0001c0002t0003g0185 a0001c0002t0003g0226 a0001c0002t0003g0240 others(1): Show |
4 | NA18970.hp2 NA19010.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1594G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812548 | |||||||
| chr12:6812619 | C | T | 2 | a0001c0004t0006g0064 a0001c0004t0006g0120 |
2 | HG00597.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.215-1523C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812619 | |||||||
| chr12:6812620 | G | A | 5 | a0002c0003t0002g0266 a0002c0003t0002g0267 a0002c0003t0002g0271 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-1522G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812620 | |||||||
| chr12:6812660 | C | T | 1 | a0001c0002t0003g0273 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.215-1482C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812660 | |||||||
| chr12:6812679 | C | CA | 7 | a0001c0001t0001g0132 a0001c0001t0004g0394 a0002c0003t0002g0266 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-1451dupA | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812679 | ||||||
| chr12:6812767 | ATT | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0002c0003t0001g0162 others(15): Show |
19 | HG01358.hp1 HG01993.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.215-1371_215-1370d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | ||||||
| chr12:6812767 | ATTTT | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0173 others(5): Show |
10 | HG00642.hp2 HG03130.hp1 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-1373_215-1370d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | ||||||
| chr12:6812767 | ATTTTTG | A | 121 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0028 others(118): Show |
122 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.215-1373_215-1368d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | ||||||
| chr12:6812767 | ATTTTTGT others(1): Show |
A | 6 | a0002c0003t0005g0037 a0002c0003t0005g0045 a0002c0003t0005g0046 others(3): Show |
6 | HG02615.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-1373_215-1366d others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | ||||||
| chr12:6812767 | ATTTTTGT others(3): Show |
A | 2 | a0001c0001t0001g0103 a0001c0001t0002g0294 |
2 | HG01175.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.215-1373_215-1364d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | ||||||
| chr12:6812767 | ATTTTTGT others(5): Show |
A | 98 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(95): Show |
104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.215-1373_215-1362d others(14): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812767 | ||||||
| chr12:6812769 | T | G | 1 | a0008c0016t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.215-1373T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812769 | |||||||
| chr12:6812769 | T | TTG | 9 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0024 others(6): Show |
13 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.215-1372_215-1371i others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | ||||||
| chr12:6812769 | T | TTGTG | 26 | a0001c0001t0004g0008 a0001c0001t0004g0065 a0001c0001t0004g0090 others(23): Show |
27 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.215-1372_215-1371i others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | ||||||
| chr12:6812769 | T | TTGTGTG | 3 | a0001c0001t0004g0038 a0001c0001t0004g0089 a0001c0001t0004g0143 |
3 | HG03453.hp2 HG03669.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.215-1372_215-1371i others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | ||||||
| chr12:6812769 | T | TTGTGTGT others(1): Show |
3 | a0001c0001t0004g0109 a0001c0001t0009g0092 a0012c0013t0009g0159 |
3 | HG02129.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.215-1372_215-1371i others(10): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | ||||||
| chr12:6812769 | T | TTGTGTGT others(3): Show |
2 | a0001c0001t0004g0084 a0001c0001t0004g0099 |
2 | NA18995.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.215-1372_215-1371i others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | ||||||
| chr12:6812769 | TTTTG | T | 7 | a0001c0004t0006g0064 a0001c0004t0006g0120 a0001c0004t0006g0153 others(4): Show |
7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.215-1371_215-1368d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | ||||||
| chr12:6812769 | TTTTGTG | T | 7 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(4): Show |
7 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.215-1371_215-1366d others(8): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812769 | ||||||
| chr12:6812771 | T | G | 73 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0002g0144 others(70): Show |
79 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.215-1371T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812771 | |||||||
| chr12:6812771 | T | TTG | 11 | a0001c0001t0001g0324 a0001c0001t0002g0079 a0001c0001t0002g0101 others(8): Show |
11 | HG00438.hp1 HG00597.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.215-1335_215-1334d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812771 | ||||||
| chr12:6812771 | T | TTGTG | 5 | a0001c0001t0003g0050 a0001c0002t0003g0105 a0001c0002t0003g0106 others(2): Show |
5 | HG02080.hp2 HG02735.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-1337_215-1334d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812771 | ||||||
| chr12:6812773 | G | T | 2 | a0001c0002t0003g0009 a0001c0002t0003g0183 |
2 | HG01256.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.215-1369G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812773 | |||||||
| chr12:6812912 | GT | G | 4 | a0001c0001t0009g0092 a0001c0018t0002g0158 a0005c0008t0004g0017 others(1): Show |
5 | HG02970.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-1221delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6812912 | ||||||
| chr12:6812947 | G | A | 3 | a0001c0001t0009g0092 a0001c0018t0002g0158 a0012c0013t0009g0159 |
3 | HG02970.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.215-1195G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812947 | |||||||
| chr12:6812974 | C | G | 1 | a0008c0016t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.215-1168C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6812974 | |||||||
| chr12:6813008 | G | A | 1 | a0001c0001t0004g0084 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.215-1134G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813008 | |||||||
| chr12:6813082 | C | T | 1 | a0001c0001t0001g0390 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.215-1060C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813082 | |||||||
| chr12:6813083 | T | C | 1 | a0001c0001t0001g0390 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.215-1059T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813083 | |||||||
| chr12:6813219 | A | T | 2 | a0001c0002t0003g0391 a0001c0002t0003g0392 |
2 | NA18980.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.215-923A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813219 | |||||||
| chr12:6813220 | A | AT | 75 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(72): Show |
78 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.215-903dupT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6813220 | ||||||
| chr12:6813220 | A | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0002t0003g0284 others(1): Show |
4 | HG00639.hp2 HG01109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-922A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813220 | |||||||
| chr12:6813220 | AT | A | 84 | a0001c0001t0002g0144 a0001c0001t0002g0223 a0001c0001t0002g0311 others(81): Show |
90 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.215-903delT | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6813220 | ||||||
| chr12:6813220 | ATTT | A | 8 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(5): Show |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-905_215-903del others(3): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 6813220 | ||||||
| chr12:6813222 | T | A | 2 | a0002c0003t0002g0412 a0007c0014t0017g0268 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.215-920T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813222 | |||||||
| chr12:6813223 | T | A | 1 | a0001c0001t0001g0347 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.215-919T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813223 | |||||||
| chr12:6813224 | T | A | 8 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(5): Show |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-918T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813224 | |||||||
| chr12:6813328 | A | T | 99 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(96): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.215-814A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813328 | |||||||
| chr12:6813466 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.215-676A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813466 | |||||||
| chr12:6813536 | G | T | 342 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(339): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.215-606G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813536 | |||||||
| chr12:6813841 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.215-301A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813841 | |||||||
| chr12:6813852 | G | A | 148 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0034 others(145): Show |
154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.215-290G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813852 | |||||||
| chr12:6813935 | T | A | 81 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(78): Show |
88 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.215-207T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6813935 | |||||||
| chr12:6814054 | A | G | 1 | a0001c0001t0004g0383 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.215-88A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6814054 | |||||||
| chr12:6814068 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.215-74G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6814068 | |||||||
| chr12:6814120 | C | G | 81 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(78): Show |
88 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.215-22C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6814120 | |||||||
| chr12:6814122 | C | T | 2 | a0001c0001t0002g0307 a0001c0001t0002g0309 |
2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.215-20C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 3/9 | chr12 | 6814122 | |||||||
| chr12:6814305 | G | A | 1 | a0001c0001t0002g0177 | 1 | NA20300.hp1 | splice_region_variant&intron_variant | LOW | c.373+5G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/9 | chr12 | 6814305 | |||||||
| chr12:6814365 | C | T | 2 | a0001c0001t0004g0371 a0005c0008t0004g0017 |
3 | NA18974.hp2 NA19056.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.373+65C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/9 | chr12 | 6814365 | |||||||
| chr12:6814370 | C | A | 1 | a0001c0001t0001g0123 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.373+70C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/9 | chr12 | 6814370 | |||||||
| chr12:6814549 | A | G | 1 | a0001c0001t0004g0283 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.374-210A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/9 | chr12 | 6814549 | |||||||
| chr12:6814665 | C | T | 84 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(81): Show |
91 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.374-94C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 4/9 | chr12 | 6814665 | |||||||
| chr12:6815131 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(235): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.607+139C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815131 | |||||||
| chr12:6815154 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.607+162G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815154 | |||||||
| chr12:6815168 | G | A | 1 | a0001c0018t0002g0158 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.607+176G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815168 | |||||||
| chr12:6815179 | G | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0054 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.607+187G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815179 | |||||||
| chr12:6815241 | G | A | 1 | a0001c0002t0003g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.607+249G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815241 | |||||||
| chr12:6815320 | C | T | 1 | a0001c0002t0003g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.607+328C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815320 | |||||||
| chr12:6815349 | G | A | 1 | a0007c0014t0017g0268 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.607+357G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815349 | |||||||
| chr12:6815495 | G | A | 8 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(5): Show |
8 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.607+503G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815495 | |||||||
| chr12:6815516 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.607+524G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815516 | |||||||
| chr12:6815552 | C | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(235): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.608-504C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815552 | |||||||
| chr12:6815614 | G | C | 1 | a0007c0014t0017g0268 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.608-442G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815614 | |||||||
| chr12:6815661 | C | T | 1 | a0001c0018t0002g0158 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.608-395C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815661 | |||||||
| chr12:6815691 | G | A | 1 | a0002c0003t0002g0255 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.608-365G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815691 | |||||||
| chr12:6815827 | T | A | 1 | a0010c0020t0004g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.608-229T>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815827 | |||||||
| chr12:6815954 | C | T | 1 | a0001c0001t0001g0385 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.608-102C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815954 | |||||||
| chr12:6815983 | C | T | 98 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(95): Show |
104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.608-73C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6815983 | |||||||
| chr12:6816052 | C | G | 1 | a0002c0003t0007g0414 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.608-4C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 5/9 | chr12 | 6816052 | |||||||
| chr12:6816660 | C | T | 1 | a0001c0002t0003g0416 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955+257C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/9 | chr12 | 6816660 | |||||||
| chr12:6816763 | T | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.955+360T>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/9 | chr12 | 6816763 | |||||||
| chr12:6816769 | G | C | 1 | a0001c0001t0014g0360 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.956-361G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 6/9 | chr12 | 6816769 | |||||||
| chr12:6817505 | A | G | 56 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(53): Show |
61 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1156+175A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817505 | |||||||
| chr12:6817610 | G | GC | 17 | a0002c0003t0001g0162 a0002c0003t0001g0208 a0002c0003t0001g0405 others(14): Show |
17 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.1156+286dupC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817610 | ||||||
| chr12:6817649 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1156+319C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817649 | |||||||
| chr12:6817675 | T | C | 2 | a0001c0001t0002g0131 a0001c0001t0002g0137 |
2 | NA18946.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1156+345T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817675 | |||||||
| chr12:6817691 | T | C | 7 | a0001c0004t0006g0064 a0001c0004t0006g0120 a0001c0004t0006g0153 others(4): Show |
7 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156+361T>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817691 | |||||||
| chr12:6817694 | A | G | 1 | a0001c0001t0004g0376 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1156+364A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817694 | |||||||
| chr12:6817731 | ACT | A | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0034 others(46): Show |
49 | HG00741.hp1 HG01069.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.1156+403_1156+404d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817731 | ||||||
| chr12:6817743 | G | A | 1 | a0009c0017t0001g0407 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1156+413G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817743 | |||||||
| chr12:6817753 | ATACACAC others(2): Show |
A | 84 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(81): Show |
89 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1156+433_1156+441d others(11): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817753 | ||||||
| chr12:6817767 | C | T | 1 | a0001c0002t0003g0416 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1156+437C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817767 | |||||||
| chr12:6817778 | ACT | A | 18 | a0002c0003t0001g0162 a0002c0003t0001g0208 a0002c0003t0001g0405 others(15): Show |
18 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.1156+450_1156+451d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817778 | ||||||
| chr12:6817796 | AC | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(79): Show |
85 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1156+470delC | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817796 | ||||||
| chr12:6817819 | A | G | 105 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(102): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1156+489A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817819 | |||||||
| chr12:6817824 | C | T | 1 | a0001c0010t0003g0258 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1156+494C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817824 | |||||||
| chr12:6817828 | C | T | 1 | a0001c0002t0003g0204 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1156+498C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817828 | |||||||
| chr12:6817857 | T | TCA | 83 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(80): Show |
88 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1156+532_1156+533d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817857 | ||||||
| chr12:6817869 | GCA | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(16): Show |
22 | HG00621.hp2 HG01891.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.1157-542_1157-541d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817869 | ||||||
| chr12:6817872 | C | T | 8 | a0002c0003t0001g0162 a0002c0003t0001g0208 a0002c0003t0001g0405 others(5): Show |
8 | HG02559.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1156+542C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817872 | |||||||
| chr12:6817878 | CACTT | C | 3 | a0001c0004t0006g0153 a0001c0004t0006g0181 a0001c0004t0006g0252 |
3 | HG03654.hp1 HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1157-540_1157-537d others(6): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817878 | ||||||
| chr12:6817879 | A | ACT | 66 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(63): Show |
71 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.1157-541_1157-540d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6817879 | ||||||
| chr12:6817879 | A | T | 17 | a0002c0003t0001g0162 a0002c0003t0001g0208 a0002c0003t0001g0405 others(14): Show |
17 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.1157-542A>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817879 | |||||||
| chr12:6817887 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0166 |
2 | NA18939.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1157-534A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817887 | |||||||
| chr12:6817925 | G | A | 1 | a0001c0002t0003g0176 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1157-496G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817925 | |||||||
| chr12:6817938 | C | A | 18 | a0002c0003t0001g0162 a0002c0003t0001g0208 a0002c0003t0001g0405 others(15): Show |
18 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.1157-483C>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817938 | |||||||
| chr12:6817980 | A | G | 17 | a0002c0003t0001g0162 a0002c0003t0001g0208 a0002c0003t0001g0405 others(14): Show |
17 | HG01358.hp1 HG01884.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.1157-441A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817980 | |||||||
| chr12:6817989 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1157-432C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817989 | |||||||
| chr12:6817990 | G | A | 2 | a0001c0002t0003g0328 a0001c0002t0003g0336 |
2 | HG01099.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1157-431G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817990 | |||||||
| chr12:6817992 | G | A | 343 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(340): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1157-429G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6817992 | |||||||
| chr12:6818000 | A | C | 90 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(87): Show |
95 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.1157-421A>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818000 | |||||||
| chr12:6818027 | C | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0263 others(1): Show |
4 | HG01261.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1157-394C>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818027 | |||||||
| chr12:6818068 | A | G | 90 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(87): Show |
95 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.1157-353A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818068 | |||||||
| chr12:6818081 | G | C | 90 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(87): Show |
95 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.1157-340G>C | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818081 | |||||||
| chr12:6818088 | ACGCGCAC others(3): Show |
A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(242): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1157-323_1157-314d others(12): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6818088 | ||||||
| chr12:6818092 | G | A | 90 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(87): Show |
95 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.1157-329G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818092 | |||||||
| chr12:6818092 | G | GCA | 6 | a0001c0002t0003g0011 a0001c0002t0003g0138 a0001c0002t0003g0154 others(3): Show |
7 | HG02451.hp1 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1157-325_1157-324d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6818092 | ||||||
| chr12:6818101 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1157-320C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818101 | |||||||
| chr12:6818102 | G | A | 20 | a0001c0002t0003g0339 a0002c0003t0001g0162 a0002c0003t0001g0208 others(17): Show |
20 | HG00733.hp2 HG01358.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1157-319G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818102 | |||||||
| chr12:6818102 | GCA | G | 3 | a0002c0003t0002g0022 a0002c0003t0002g0023 a0002c0003t0002g0041 |
3 | HG02109.hp1 HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1157-308_1157-307d others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 6818102 | ||||||
| chr12:6818108 | A | G | 87 | a0001c0001t0002g0144 a0001c0001t0004g0007 a0001c0001t0004g0008 others(84): Show |
92 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.1157-313A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818108 | |||||||
| chr12:6818110 | A | G | 3 | a0002c0003t0002g0022 a0002c0003t0002g0023 a0002c0003t0002g0041 |
3 | HG02109.hp1 HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1157-311A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818110 | |||||||
| chr12:6818119 | C | T | 4 | a0001c0001t0003g0030 a0001c0001t0003g0050 a0001c0010t0003g0258 others(1): Show |
4 | HG02572.hp1 HG02630.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1157-302C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818119 | |||||||
| chr12:6818297 | C | T | 1 | a0001c0002t0003g0106 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1157-124C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818297 | |||||||
| chr12:6818304 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(236): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1157-117C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818304 | |||||||
| chr12:6818374 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG01109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1157-47G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 7/9 | chr12 | 6818374 | |||||||
| chr12:6818618 | A | G | 2 | a0001c0001t0003g0030 a0001c0001t0003g0050 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1278+76A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 8/9 | chr12 | 6818618 | |||||||
| chr12:6818651 | G | A | 1 | a0001c0002t0003g0247 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1278+109G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 8/9 | chr12 | 6818651 | |||||||
| chr12:6818762 | C | T | 1 | a0006c0015t0020g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1279-85C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 8/9 | chr12 | 6818762 | |||||||
| chr12:6818933 | G | A | 1 | a0001c0001t0004g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1346+19G>A | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/9 | chr12 | 6818933 | |||||||
| chr12:6818958 | GGGGA | G | 6 | a0003c0005t0004g0418 a0003c0005t0004g0419 a0003c0005t0004g0420 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346+50_1346+53del others(4): Show |
CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 6818958 | ||||||
| chr12:6818964 | G | T | 5 | a0001c0001t0009g0092 a0002c0003t0002g0022 a0002c0003t0002g0023 others(2): Show |
5 | HG02109.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346+50G>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/9 | chr12 | 6818964 | |||||||
| chr12:6818970 | A | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(267): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1346+56A>G | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/9 | chr12 | 6818970 | |||||||
| chr12:6819048 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(183): Show |
194 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.1346+134C>T | CD4 | ENSG00000010610.10 | transcript | ENST00000011653.9 | protein_coding | 9/9 | chr12 | 6819048 |