Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9439 |
| ensemblid | ENSG00000112282.18 |
| hgncid | 2372 |
| symbol | MED23 |
| name | mediator complex subunit 23 |
| refseq_nuc | NM_004830.4 |
| refseq_prot | NP_004821.2 |
| ensembl_nuc | ENST00000368068.8 |
| ensembl_prot | ENSP00000357047.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 131586732 |
| end | 131628242 |
| strand | - |
| ver | v1.2 |
| region | chr6:131586732-131628242 |
| region5000 | chr6:131581732-131633242 |
| regionname0 | MED23_chr6_131586732_131628242 |
| regionname5000 | MED23_chr6_131581732_131633242 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1368 | 317 | 88 | 50 | 135 | 12 | 30 | 111 | MED23_chr6_131581732_131633242 | MED23 | METQL others(1363): Show |
chr6 | 131581732 | 131633242 |
| a0002 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | METQL others(1363): Show |
chr6 | 131581732 | 131633242 |
| a0003 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | METQL others(1363): Show |
chr6 | 131581732 | 131633242 |
| a0004 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | METQL others(1363): Show |
chr6 | 131581732 | 131633242 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4104 | 311 | 86 | 49 | 132 | 12 | 30 | MED23_chr6_131581732_131633242 | MED23 | ATGGA others(4099): Show |
chr6 | 131581732 | 131633242 | ||
| a0001c0002 | 0/0 | 4104 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | ATGGA others(4099): Show |
chr6 | 131581732 | 131633242 | ||
| a0001c0003 | 0/0 | 4104 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | ATGGA others(4099): Show |
chr6 | 131581732 | 131633242 | ||
| a0001c0004 | 0/0 | 4104 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | ATGGA others(4099): Show |
chr6 | 131581732 | 131633242 | ||
| a0001c0008 | 0/0 | 4104 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | ATGGA others(4099): Show |
chr6 | 131581732 | 131633242 | ||
| a0002c0006 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | ATGGA others(4099): Show |
chr6 | 131581732 | 131633242 | ||
| a0003c0005 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | ATGGA others(4099): Show |
chr6 | 131581732 | 131633242 | ||
| a0004c0007 | 0/0 | 4104 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | ATGGA others(4099): Show |
chr6 | 131581732 | 131633242 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5247 | 283 | 76 | 48 | 119 | 12 | 26 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0001t0002 | 0/0 | 5247 | 8 | 4 | 1 | 0 | 0 | 3 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0001t0003 | 0/0 | 5247 | 6 | 6 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0001t0004 | 0/0 | 5247 | 5 | 0 | 0 | 5 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0001t0005 | 0/0 | 5247 | 4 | 0 | 0 | 4 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0001t0006 | 0/0 | 5247 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0001t0007 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0001t0008 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0001t0009 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0002t0001 | 0/0 | 5247 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0003t0001 | 0/0 | 5247 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0004t0001 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0001c0008t0001 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0002c0006t0001 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0003c0005t0001 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| a0004c0007t0001 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | GTCTT others(5242): Show |
chr6 | 131581732 | 131633242 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 1 | 4 | 10 | 0 | 4 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0002 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 3 | 1 | 0 | 4 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0007 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0001t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0001c0008t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0002c0006t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0003c0005t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| a0004c0007t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0159 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0163 | EAS | KHV | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0098 | EAS | CDX | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02622 | hp1 | a0002 | c0006 | t0001 | g0151 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02809 | hp1 | a0003 | c0005 | t0001 | g0078 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03834 | hp1 | a0001 | c0001 | t0008 | g0110 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18953 | hp1 | a0001 | c0001 | t0007 | g0169 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18965 | hp2 | a0001 | c0004 | t0001 | g0195 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18991 | hp1 | a0004 | c0007 | t0001 | g0140 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19004 | hp2 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19006 | hp1 | a0001 | c0001 | t0009 | g0217 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19009 | hp2 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19072 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19085 | hp1 | a0001 | c0008 | t0001 | g0188 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ASW | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ASW | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | USA | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | USA | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | USA | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0111 | REF | REF | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0088 | REF | REF | MED23_chr6_131581732_131633242 | MED23 | chr6 | 131581732 | 131633242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:131589503 | T | G | 1 | a0004 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.3901A>C | p.Met1301Leu | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/29 | 4094/5247 | 3901/4107 | 1301/1368 | chr6 | 131589503 | |||
| chr6:131590387 | C | T | 1 | a0002 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.3742G>A | p.Val1248Ile | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/29 | 3935/5247 | 3742/4107 | 1248/1368 | chr6 | 131590387 | |||
| chr6:131590405 | C | T | 1 | a0003 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.3724G>A | p.Glu1242Lys | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/29 | 3917/5247 | 3724/4107 | 1242/1368 | chr6 | 131590405 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:131587706 | C | A | 1 | a0001c0002 | 2 | HG02258.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.4080G>T | p.Val1360Val | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 4273/5247 | 4080/4107 | 1360/1368 | chr6 | 131587706 | |||
| chr6:131602378 | G | A | 1 | a0001c0003 | 2 | HG01975.hp2 HG02165.hp2 |
synonymous_variant | LOW | c.1935C>T | p.Val645Val | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/29 | 2128/5247 | 1935/4107 | 645/1368 | chr6 | 131602378 | |||
| chr6:131618485 | C | T | 1 | a0001c0004 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.702G>A | p.Ser234Ser | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/29 | 895/5247 | 702/4107 | 234/1368 | chr6 | 131618485 | |||
| chr6:131621917 | G | A | 1 | a0001c0008 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.459C>T | p.Ser153Ser | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/29 | 652/5247 | 459/4107 | 153/1368 | chr6 | 131621917 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:131586748 | C | T | 1 | a0001c0001t0002 | 8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*931G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 931 | chr6 | 131586748 | ||||||
| chr6:131586987 | C | G | 3 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 |
10 | HG02083.hp2 NA18945.hp2 NA18952.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*692G>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 692 | chr6 | 131586987 | ||||||
| chr6:131587149 | T | G | 1 | a0001c0001t0004 | 5 | NA18945.hp2 NA18952.hp1 NA18959.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*530A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 530 | chr6 | 131587149 | ||||||
| chr6:131587411 | T | C | 1 | a0001c0001t0006 | 2 | NA19004.hp2 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*268A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 268 | chr6 | 131587411 | ||||||
| chr6:131587517 | T | G | 1 | a0001c0001t0005 | 4 | HG02083.hp2 NA18968.hp1 NA18972.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*162A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 162 | chr6 | 131587517 | ||||||
| chr6:131587660 | T | C | 1 | a0001c0001t0008 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 29/29 | 19 | chr6 | 131587660 | ||||||
| chr6:131628142 | T | C | 1 | a0001c0001t0003 | 6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-93A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/29 | 93 | chr6 | 131628142 | ||||||
| chr6:131628185 | C | A | 1 | a0001c0001t0009 | 1 | NA19006.hp1 | 5_prime_UTR_variant | MODIFIER | c.-136G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/29 | 136 | chr6 | 131628185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:131587886 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0134 |
2 | NA18997.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3940-40C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131587886 | |||||||
| chr6:131588015 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3940-169A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588015 | |||||||
| chr6:131588075 | G | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.3940-229C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588075 | |||||||
| chr6:131588076 | C | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.3940-230G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588076 | |||||||
| chr6:131588294 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3940-448G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588294 | |||||||
| chr6:131588358 | T | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3940-512A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588358 | |||||||
| chr6:131588504 | A | T | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3940-658T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588504 | |||||||
| chr6:131588691 | A | T | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3939+774T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588691 | |||||||
| chr6:131588847 | G | A | 19 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(16): Show |
24 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.3939+618C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588847 | |||||||
| chr6:131588918 | C | T | 1 | a0001c0001t0005g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3939+547G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131588918 | |||||||
| chr6:131589075 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3939+390C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131589075 | |||||||
| chr6:131589160 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.3939+305T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131589160 | |||||||
| chr6:131589265 | T | G | 1 | a0001c0001t0001g0142 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3939+200A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 28/28 | chr6 | 131589265 | |||||||
| chr6:131589632 | C | CAA | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3808-38_3808-37dup others(2): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589632 | |||||||
| chr6:131589687 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3808-91G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589687 | |||||||
| chr6:131589774 | G | GA | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3808-179dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589774 | |||||||
| chr6:131589834 | A | T | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3808-238T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589834 | |||||||
| chr6:131589853 | C | T | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3808-257G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589853 | |||||||
| chr6:131589876 | T | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0106 a0001c0001t0001g0128 |
3 | HG01952.hp1 HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.3808-280A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589876 | |||||||
| chr6:131589977 | C | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3807+345G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131589977 | |||||||
| chr6:131590172 | A | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(15): Show |
23 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.3807+150T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 27/28 | chr6 | 131590172 | |||||||
| chr6:131590515 | A | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(113): Show |
164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.3687-73T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590515 | |||||||
| chr6:131590629 | T | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0189 |
2 | HG01123.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3687-187A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590629 | |||||||
| chr6:131590652 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0089 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3687-210C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590652 | |||||||
| chr6:131590714 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0109 a0001c0001t0001g0142 |
4 | HG00099.hp1 HG01243.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.3687-272G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590714 | |||||||
| chr6:131590793 | A | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3687-351T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590793 | |||||||
| chr6:131590807 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3687-365G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590807 | |||||||
| chr6:131590808 | G | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.3687-366C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590808 | |||||||
| chr6:131590908 | C | T | 32 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(29): Show |
38 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.3686+405G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590908 | |||||||
| chr6:131590935 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3686+378A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590935 | |||||||
| chr6:131590984 | AT | A | 69 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(66): Show |
107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.3686+328delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590984 | |||||||
| chr6:131590984 | ATTT | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0208 others(1): Show |
6 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3686+326_3686+328d others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131590984 | |||||||
| chr6:131591204 | G | A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(7): Show |
13 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3686+109C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 26/28 | chr6 | 131591204 | |||||||
| chr6:131591538 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0132 |
2 | NA18612.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.3472-11C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 25/28 | chr6 | 131591538 | |||||||
| chr6:131591549 | A | C | 1 | a0001c0001t0001g0091 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3472-22T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 25/28 | chr6 | 131591549 | |||||||
| chr6:131591897 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3472-370C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 25/28 | chr6 | 131591897 | |||||||
| chr6:131592103 | A | G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(15): Show |
23 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.3471+285T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 25/28 | chr6 | 131592103 | |||||||
| chr6:131592469 | G | A | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3399-9C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 24/28 | chr6 | 131592469 | |||||||
| chr6:131592953 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3398+53G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 24/28 | chr6 | 131592953 | |||||||
| chr6:131592970 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3398+36T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 24/28 | chr6 | 131592970 | |||||||
| chr6:131593002 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG03831.hp2 | splice_region_variant&intron_variant | LOW | c.3398+4T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 24/28 | chr6 | 131593002 | |||||||
| chr6:131593187 | G | A | 1 | a0001c0001t0003g0216 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3233-16C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593187 | |||||||
| chr6:131593260 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0166 a0001c0001t0001g0182 others(1): Show |
5 | HG02630.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3233-89G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593260 | |||||||
| chr6:131593424 | T | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(113): Show |
164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.3233-253A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593424 | |||||||
| chr6:131593426 | A | C | 3 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 |
3 | HG01255.hp1 HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.3233-255T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593426 | |||||||
| chr6:131593462 | TAA | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0210 |
3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3233-293_3233-292d others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593462 | |||||||
| chr6:131593628 | T | C | 4 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0052 others(1): Show |
4 | HG02723.hp2 HG02818.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.3233-457A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593628 | |||||||
| chr6:131593710 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3232+389G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593710 | |||||||
| chr6:131593768 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3232+331T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593768 | |||||||
| chr6:131593770 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3232+329A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593770 | |||||||
| chr6:131593804 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3232+295A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593804 | |||||||
| chr6:131593808 | A | G | 2 | a0001c0001t0006g0177 a0001c0001t0006g0184 |
2 | NA19004.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3232+291T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593808 | |||||||
| chr6:131593873 | G | A | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.3232+226C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 23/28 | chr6 | 131593873 | |||||||
| chr6:131594416 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2996-81T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594416 | |||||||
| chr6:131594677 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2996-342T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594677 | |||||||
| chr6:131594805 | AAAAC | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(38): Show |
74 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.2996-474_2996-471d others(6): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594805 | |||||||
| chr6:131594805 | AAAACAAA others(1): Show |
A | 6 | a0001c0001t0001g0167 a0001c0001t0003g0211 a0001c0001t0003g0212 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2996-478_2996-471d others(10): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594805 | |||||||
| chr6:131594807 | A | T | 1 | a0001c0001t0005g0175 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2996-472T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594807 | |||||||
| chr6:131594837 | C | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.2996-502G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131594837 | |||||||
| chr6:131595029 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2996-694G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131595029 | |||||||
| chr6:131595075 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2996-740T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131595075 | |||||||
| chr6:131595153 | A | G | 2 | a0001c0001t0001g0164 a0001c0008t0001g0188 |
2 | NA18944.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2995+794T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131595153 | |||||||
| chr6:131595682 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2995+265C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131595682 | |||||||
| chr6:131595922 | G | A | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2995+25C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 22/28 | chr6 | 131595922 | |||||||
| chr6:131596239 | A | G | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(59): Show |
99 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.2779-76T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 21/28 | chr6 | 131596239 | |||||||
| chr6:131596248 | A | AT | 14 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(11): Show |
16 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2779-86dupA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 21/28 | chr6 | 131596248 | |||||||
| chr6:131596333 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0066 a0001c0001t0001g0068 |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2779-170G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 21/28 | chr6 | 131596333 | |||||||
| chr6:131596502 | C | T | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2778+16G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 21/28 | chr6 | 131596502 | |||||||
| chr6:131596745 | G | A | 14 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0057 others(11): Show |
16 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2608-57C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131596745 | |||||||
| chr6:131596756 | A | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0210 |
3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2608-68T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131596756 | |||||||
| chr6:131596783 | T | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0210 |
3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2608-95A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131596783 | |||||||
| chr6:131596818 | C | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2608-130G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131596818 | |||||||
| chr6:131597131 | G | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0210 |
3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2608-443C>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597131 | |||||||
| chr6:131597165 | T | G | 1 | a0001c0001t0001g0126 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2608-477A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597165 | |||||||
| chr6:131597259 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0130 a0001c0001t0001g0133 |
4 | HG02109.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2608-571C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597259 | |||||||
| chr6:131597339 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0201 a0001c0001t0001g0203 |
4 | NA18961.hp1 NA18997.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608-651C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597339 | |||||||
| chr6:131597400 | C | T | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2608-712G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597400 | |||||||
| chr6:131597475 | C | CA | 32 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(29): Show |
42 | HG01496.hp1 HG01884.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.2608-788dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597475 | |||||||
| chr6:131597475 | C | CAA | 7 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0065 others(4): Show |
9 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2608-789_2608-788d others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597475 | |||||||
| chr6:131597475 | C | CAAA | 7 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0210 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2608-790_2608-788d others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597475 | |||||||
| chr6:131597475 | CAAAAAA | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(56): Show |
96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.2608-793_2608-788d others(8): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597475 | |||||||
| chr6:131597494 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0123 |
2 | HG04184.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2607+793T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597494 | |||||||
| chr6:131597498 | G | A | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2607+789C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597498 | |||||||
| chr6:131597499 | A | G | 1 | a0001c0002t0001g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2607+788T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597499 | |||||||
| chr6:131597542 | G | GA | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2607+744dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597542 | |||||||
| chr6:131597597 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0026 others(17): Show |
35 | HG00609.hp1 HG01109.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.2607+690C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597597 | |||||||
| chr6:131597632 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0210 |
2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2607+655A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597632 | |||||||
| chr6:131597636 | T | TC | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2607+650dupG | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597636 | |||||||
| chr6:131597699 | A | T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(59): Show |
99 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.2607+588T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597699 | |||||||
| chr6:131597703 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0165 a0001c0001t0001g0172 others(4): Show |
8 | HG01433.hp2 HG01928.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.2607+584C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597703 | |||||||
| chr6:131597864 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2607+423A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131597864 | |||||||
| chr6:131598053 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2607+234G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131598053 | |||||||
| chr6:131598090 | A | AAAAAACA others(11): Show |
6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2607+179_2607+196d others(20): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131598090 | |||||||
| chr6:131598143 | G | A | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2607+144C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131598143 | |||||||
| chr6:131598252 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2607+35A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 20/28 | chr6 | 131598252 | |||||||
| chr6:131598519 | T | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0166 a0001c0001t0001g0182 others(1): Show |
5 | HG02630.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2426+37A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 19/28 | chr6 | 131598519 | |||||||
| chr6:131598855 | C | T | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2221-94G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131598855 | |||||||
| chr6:131598923 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2221-162T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131598923 | |||||||
| chr6:131599077 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0208 |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2221-316G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599077 | |||||||
| chr6:131599106 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2221-345G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599106 | |||||||
| chr6:131599263 | A | T | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2221-502T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599263 | |||||||
| chr6:131599463 | G | A | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0210 |
3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2220+575C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599463 | |||||||
| chr6:131599517 | G | C | 1 | a0001c0001t0003g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2220+521C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599517 | |||||||
| chr6:131599841 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2220+197G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599841 | |||||||
| chr6:131599908 | C | T | 3 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 |
3 | HG01255.hp1 HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2220+130G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599908 | |||||||
| chr6:131599984 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0208 |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2220+54C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 18/28 | chr6 | 131599984 | |||||||
| chr6:131600180 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2096-18C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600180 | |||||||
| chr6:131600333 | T | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0199 |
5 | HG00609.hp2 HG02027.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.2096-171A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600333 | |||||||
| chr6:131600426 | C | A | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2096-264G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600426 | |||||||
| chr6:131600517 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2096-355T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600517 | |||||||
| chr6:131600600 | A | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(15): Show |
23 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2096-438T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600600 | |||||||
| chr6:131600639 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0209 |
3 | HG03041.hp1 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2096-477A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600639 | |||||||
| chr6:131600749 | A | ATT | 19 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(16): Show |
24 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.2096-588_2096-587i others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600749 | |||||||
| chr6:131600755 | T | C | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0210 |
3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2096-593A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600755 | |||||||
| chr6:131600908 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2096-746C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131600908 | |||||||
| chr6:131601038 | CT | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(87): Show |
132 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.2096-877delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601038 | |||||||
| chr6:131601038 | CTT | C | 23 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(20): Show |
29 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.2096-878_2096-877d others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601038 | |||||||
| chr6:131601109 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2096-947C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601109 | |||||||
| chr6:131601442 | T | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(15): Show |
23 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2095+776A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601442 | |||||||
| chr6:131601471 | A | G | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0103 others(2): Show |
5 | HG00423.hp2 HG03942.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2095+747T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601471 | |||||||
| chr6:131601728 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2095+490T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601728 | |||||||
| chr6:131601762 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2095+456A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601762 | |||||||
| chr6:131601855 | ACTT | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2095+360_2095+362d others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601855 | |||||||
| chr6:131601920 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2095+298A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131601920 | |||||||
| chr6:131602143 | C | T | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2095+75G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 17/28 | chr6 | 131602143 | |||||||
| chr6:131602414 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1932-33T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 16/28 | chr6 | 131602414 | |||||||
| chr6:131602631 | T | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0130 a0001c0001t0001g0133 |
4 | HG02109.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1932-250A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 16/28 | chr6 | 131602631 | |||||||
| chr6:131602641 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1932-260C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 16/28 | chr6 | 131602641 | |||||||
| chr6:131602991 | T | C | 3 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 |
3 | HG02257.hp1 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1931+39A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 16/28 | chr6 | 131602991 | |||||||
| chr6:131603270 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1757-66T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603270 | |||||||
| chr6:131603421 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1757-217A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603421 | |||||||
| chr6:131603469 | T | C | 1 | a0001c0001t0003g0215 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1757-265A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603469 | |||||||
| chr6:131603495 | TC | T | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1757-292delG | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603495 | |||||||
| chr6:131603516 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1757-312T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603516 | |||||||
| chr6:131603549 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(59): Show |
99 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1757-345C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603549 | |||||||
| chr6:131603565 | A | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0150 a0001c0001t0001g0152 others(2): Show |
6 | HG02622.hp1 HG03098.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1757-361T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603565 | |||||||
| chr6:131603678 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1757-474C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603678 | |||||||
| chr6:131603780 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0210 |
2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1756+398A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603780 | |||||||
| chr6:131603852 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0208 |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1756+326T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603852 | |||||||
| chr6:131603963 | C | A | 1 | a0003c0005t0001g0078 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1756+215G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603963 | |||||||
| chr6:131603987 | C | T | 1 | a0001c0001t0003g0215 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1756+191G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 15/28 | chr6 | 131603987 | |||||||
| chr6:131604518 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1614-198G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131604518 | |||||||
| chr6:131604569 | A | G | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614-249T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131604569 | |||||||
| chr6:131604667 | T | C | 3 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 |
3 | HG02257.hp1 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1614-347A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131604667 | |||||||
| chr6:131605027 | T | G | 1 | a0001c0001t0001g0011 | 3 | HG03831.hp1 HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1613+213A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605027 | |||||||
| chr6:131605040 | A | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0026 others(17): Show |
35 | HG00609.hp1 HG01109.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.1613+200T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605040 | |||||||
| chr6:131605067 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1613+173G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605067 | |||||||
| chr6:131605119 | CT | C | 17 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0072 others(14): Show |
19 | HG00642.hp2 HG01109.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1613+120delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605119 | |||||||
| chr6:131605194 | C | T | 52 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(49): Show |
88 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1613+46G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605194 | |||||||
| chr6:131605199 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1613+41G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605199 | |||||||
| chr6:131605204 | C | T | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1613+36G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 14/28 | chr6 | 131605204 | |||||||
| chr6:131605572 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0174 a0001c0001t0006g0177 others(1): Show |
5 | HG00621.hp1 HG01978.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1368-87G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131605572 | |||||||
| chr6:131605726 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1368-241A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131605726 | |||||||
| chr6:131605867 | C | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(113): Show |
164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1368-382G>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131605867 | |||||||
| chr6:131606253 | T | TA | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367+225dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606253 | |||||||
| chr6:131606254 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1367+225T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606254 | |||||||
| chr6:131606329 | C | T | 1 | a0001c0001t0003g0215 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1367+150G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606329 | |||||||
| chr6:131606331 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1367+148C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606331 | |||||||
| chr6:131606369 | G | C | 8 | a0001c0001t0001g0033 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
9 | HG02451.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1367+110C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606369 | |||||||
| chr6:131606431 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1367+48C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 13/28 | chr6 | 131606431 | |||||||
| chr6:131606724 | G | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1222-100C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131606724 | |||||||
| chr6:131606856 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1222-232A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131606856 | |||||||
| chr6:131606868 | G | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(113): Show |
164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1222-244C>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131606868 | |||||||
| chr6:131607468 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG00621.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.1221+460G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131607468 | |||||||
| chr6:131607502 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02080.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1221+426C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131607502 | |||||||
| chr6:131607542 | T | TAAC | 4 | a0001c0001t0001g0174 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00621.hp1 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221+383_1221+385d others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131607542 | |||||||
| chr6:131607731 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1221+197A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 12/28 | chr6 | 131607731 | |||||||
| chr6:131608132 | G | GT | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078-62dupA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608132 | |||||||
| chr6:131608169 | A | AC | 138 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
201 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1078-99dupG | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608169 | |||||||
| chr6:131608248 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1078-177C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608248 | |||||||
| chr6:131608314 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0208 |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-243C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608314 | |||||||
| chr6:131608319 | T | TA | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078-249dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608319 | |||||||
| chr6:131608384 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1078-313G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608384 | |||||||
| chr6:131608475 | A | AT | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078-405dupA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608475 | |||||||
| chr6:131608611 | T | G | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(114): Show |
165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.1078-540A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608611 | |||||||
| chr6:131608651 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1078-580G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608651 | |||||||
| chr6:131608846 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1078-775A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608846 | |||||||
| chr6:131608984 | C | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1078-913G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608984 | |||||||
| chr6:131608988 | A | G | 8 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(5): Show |
8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-917T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131608988 | |||||||
| chr6:131609326 | G | A | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1077+720C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609326 | |||||||
| chr6:131609494 | T | C | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1077+552A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609494 | |||||||
| chr6:131609506 | C | CT | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0143 others(2): Show |
7 | HG01934.hp2 HG02165.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+539dupA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609506 | |||||||
| chr6:131609506 | CT | C | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(89): Show |
136 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1077+539delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609506 | |||||||
| chr6:131609506 | CTT | C | 13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
16 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1077+538_1077+539d others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609506 | |||||||
| chr6:131609506 | CTTTTTTT others(2): Show |
C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+531_1077+539d others(11): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609506 | |||||||
| chr6:131609555 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1077+491C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609555 | |||||||
| chr6:131609572 | G | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1077+474C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609572 | |||||||
| chr6:131609616 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1077+430A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609616 | |||||||
| chr6:131609716 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1077+330T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609716 | |||||||
| chr6:131609733 | CATATATA others(7): Show |
C | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0210 |
3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1077+299_1077+312d others(16): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609733 | |||||||
| chr6:131609746 | G | GTATA | 2 | a0001c0001t0001g0016 a0001c0001t0001g0208 |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+296_1077+299d others(6): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609746 | |||||||
| chr6:131609746 | GTA | G | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+298_1077+299d others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609746 | |||||||
| chr6:131609809 | C | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1077+237G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609809 | |||||||
| chr6:131609952 | T | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(60): Show |
100 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1077+94A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 11/28 | chr6 | 131609952 | |||||||
| chr6:131610423 | G | A | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.877-177C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131610423 | |||||||
| chr6:131610862 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.877-616G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131610862 | |||||||
| chr6:131611143 | T | C | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.877-897A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131611143 | |||||||
| chr6:131611207 | A | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0136 |
3 | NA18966.hp2 NA19070.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.877-961T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131611207 | |||||||
| chr6:131611472 | T | C | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.877-1226A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131611472 | |||||||
| chr6:131611810 | A | C | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.877-1564T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131611810 | |||||||
| chr6:131612221 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.877-1975A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131612221 | |||||||
| chr6:131612443 | A | C | 5 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(2): Show |
5 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.877-2197T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131612443 | |||||||
| chr6:131612598 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.877-2352T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131612598 | |||||||
| chr6:131613076 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.877-2830A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613076 | |||||||
| chr6:131613080 | CAAGA | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(61): Show |
101 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.876+2823_876+2826d others(6): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613080 | |||||||
| chr6:131613082 | A | G | 8 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(5): Show |
8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.876+2825T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613082 | |||||||
| chr6:131613145 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.876+2762C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613145 | |||||||
| chr6:131613311 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.876+2596C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613311 | |||||||
| chr6:131613592 | G | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
8 | HG01891.hp1 HG02300.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.876+2315C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613592 | |||||||
| chr6:131613672 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.876+2235G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613672 | |||||||
| chr6:131613823 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.876+2084A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613823 | |||||||
| chr6:131613841 | CAAT | C | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(50): Show |
89 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.876+2063_876+2065d others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613841 | |||||||
| chr6:131613846 | G | A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(50): Show |
89 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.876+2061C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613846 | |||||||
| chr6:131613849 | T | C | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(50): Show |
89 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.876+2058A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131613849 | |||||||
| chr6:131614266 | T | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(114): Show |
165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.876+1641A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131614266 | |||||||
| chr6:131614841 | T | C | 5 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(2): Show |
5 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+1066A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131614841 | |||||||
| chr6:131614862 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.876+1045A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131614862 | |||||||
| chr6:131615065 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.876+842G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615065 | |||||||
| chr6:131615066 | CA | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.876+840delT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615066 | |||||||
| chr6:131615066 | CAA | C | 18 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(15): Show |
22 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.876+839_876+840del others(2): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615066 | |||||||
| chr6:131615082 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.876+825T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615082 | |||||||
| chr6:131615184 | GTTT | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(52): Show |
91 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.876+720_876+722del others(3): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615184 | |||||||
| chr6:131615503 | C | CA | 40 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(37): Show |
51 | HG00741.hp1 HG00741.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.876+403dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | |||||||
| chr6:131615503 | C | CAA | 13 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0027 others(10): Show |
17 | HG01123.hp2 HG01884.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.876+402_876+403dup others(2): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | |||||||
| chr6:131615503 | C | CAAA | 11 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(8): Show |
21 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.876+401_876+403dup others(3): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | |||||||
| chr6:131615503 | C | CAAAA | 29 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(26): Show |
45 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.876+400_876+403dup others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | |||||||
| chr6:131615503 | C | CAAAAA | 13 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0036 others(10): Show |
17 | HG02148.hp2 HG02895.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.876+399_876+403dup others(5): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | |||||||
| chr6:131615503 | C | CAAAAAA | 7 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0162 others(4): Show |
13 | HG00423.hp1 HG01192.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.876+398_876+403dup others(6): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | |||||||
| chr6:131615503 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0208 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.876+387_876+403dup others(17): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | |||||||
| chr6:131615503 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0016 | 3 | HG02572.hp2 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.876+386_876+403dup others(18): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | |||||||
| chr6:131615503 | CA | C | 9 | a0001c0001t0001g0059 a0001c0001t0001g0091 a0001c0001t0001g0092 others(6): Show |
9 | HG02257.hp1 HG02258.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.876+403delT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 10/28 | chr6 | 131615503 | |||||||
| chr6:131616266 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.781-264G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131616266 | |||||||
| chr6:131616445 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.781-443T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131616445 | |||||||
| chr6:131616915 | T | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.781-913A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131616915 | |||||||
| chr6:131616991 | C | T | 3 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 |
3 | HG01255.hp1 HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.781-989G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131616991 | |||||||
| chr6:131617016 | G | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0197 |
6 | HG01934.hp1 HG02083.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-1014C>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617016 | |||||||
| chr6:131617037 | A | G | 8 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(5): Show |
8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-1035T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617037 | |||||||
| chr6:131617041 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.781-1039A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617041 | |||||||
| chr6:131617165 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.781-1163A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617165 | |||||||
| chr6:131617195 | G | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-1193C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617195 | |||||||
| chr6:131617331 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.780+1076G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617331 | |||||||
| chr6:131617369 | A | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0196 |
3 | NA18946.hp1 NA18999.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.780+1038T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617369 | |||||||
| chr6:131617398 | C | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0066 others(3): Show |
9 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.780+1009G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617398 | |||||||
| chr6:131617398 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+1009G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617398 | |||||||
| chr6:131617445 | C | T | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+962G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617445 | |||||||
| chr6:131617452 | G | A | 1 | a0001c0001t0001g0011 | 3 | HG03831.hp1 HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.780+955C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617452 | |||||||
| chr6:131617464 | CT | C | 23 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0040 others(20): Show |
29 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.780+942delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617464 | |||||||
| chr6:131617647 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.780+760A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617647 | |||||||
| chr6:131617920 | T | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.780+487A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131617920 | |||||||
| chr6:131618021 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.780+386A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618021 | |||||||
| chr6:131618126 | TAATC | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+277_780+280del others(4): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618126 | |||||||
| chr6:131618215 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.780+192C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618215 | |||||||
| chr6:131618245 | G | A | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+162C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618245 | |||||||
| chr6:131618302 | T | C | 24 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(21): Show |
30 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.780+105A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618302 | |||||||
| chr6:131618389 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.780+18A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 9/28 | chr6 | 131618389 | |||||||
| chr6:131618641 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0208 |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-122A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131618641 | |||||||
| chr6:131618834 | C | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.668-315G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131618834 | |||||||
| chr6:131618911 | A | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0210 |
3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.668-392T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131618911 | |||||||
| chr6:131618925 | A | G | 8 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(5): Show |
8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.668-406T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131618925 | |||||||
| chr6:131619048 | G | A | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.668-529C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619048 | |||||||
| chr6:131619224 | G | C | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.667+603C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619224 | |||||||
| chr6:131619282 | A | G | 3 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 |
3 | HG02257.hp1 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.667+545T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619282 | |||||||
| chr6:131619283 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.667+544T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619283 | |||||||
| chr6:131619344 | T | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(114): Show |
165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.667+483A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619344 | |||||||
| chr6:131619476 | T | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.667+351A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619476 | |||||||
| chr6:131619722 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.667+105T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619722 | |||||||
| chr6:131619750 | A | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(114): Show |
165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.667+77T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619750 | |||||||
| chr6:131619756 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0082 a0001c0001t0001g0142 others(1): Show |
5 | HG00099.hp2 HG01243.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.667+71G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 8/28 | chr6 | 131619756 | |||||||
| chr6:131620539 | C | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02559.hp2 HG02976.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.597+89G>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 7/28 | chr6 | 131620539 | |||||||
| chr6:131620589 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.597+39C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 7/28 | chr6 | 131620589 | |||||||
| chr6:131620593 | AT | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
7 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.597+34delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 7/28 | chr6 | 131620593 | |||||||
| chr6:131620804 | A | T | 1 | a0001c0001t0001g0081 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.496-75T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620804 | |||||||
| chr6:131620807 | T | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.496-78A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620807 | |||||||
| chr6:131620943 | T | C | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.496-214A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620943 | |||||||
| chr6:131620949 | T | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
7 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.496-220A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620949 | |||||||
| chr6:131620953 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.496-224G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620953 | |||||||
| chr6:131620983 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496-254A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131620983 | |||||||
| chr6:131621002 | C | A | 1 | a0001c0004t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.496-273G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621002 | |||||||
| chr6:131621003 | A | G | 1 | a0001c0004t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.496-274T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621003 | |||||||
| chr6:131621049 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.496-320C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621049 | |||||||
| chr6:131621148 | C | T | 19 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(16): Show |
24 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.496-419G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621148 | |||||||
| chr6:131621224 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0208 |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-495C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621224 | |||||||
| chr6:131621297 | A | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0210 |
3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.496-568T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621297 | |||||||
| chr6:131621370 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | NA18939.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.495+511G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621370 | |||||||
| chr6:131621391 | A | C | 1 | a0001c0004t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.495+490T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621391 | |||||||
| chr6:131621572 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.495+309C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621572 | |||||||
| chr6:131621690 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0019 others(7): Show |
14 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.495+191T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 6/28 | chr6 | 131621690 | |||||||
| chr6:131622098 | C | CAG | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.397-121_397-120dup others(2): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622098 | |||||||
| chr6:131622328 | C | T | 8 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(5): Show |
8 | HG01255.hp1 HG02698.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.397-349G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622328 | |||||||
| chr6:131622374 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.397-395T>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622374 | |||||||
| chr6:131622510 | T | C | 1 | a0004c0007t0001g0140 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.397-531A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622510 | |||||||
| chr6:131622557 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0066 others(3): Show |
9 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.397-578A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622557 | |||||||
| chr6:131622572 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397-593C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622572 | |||||||
| chr6:131622643 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.397-664A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622643 | |||||||
| chr6:131622647 | A | G | 1 | a0003c0005t0001g0078 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.397-668T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131622647 | |||||||
| chr6:131623119 | G | A | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(8): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.396+232C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131623119 | |||||||
| chr6:131623177 | C | A | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.396+174G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131623177 | |||||||
| chr6:131623311 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.396+40A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 5/28 | chr6 | 131623311 | |||||||
| chr6:131623529 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.285-67T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131623529 | |||||||
| chr6:131623648 | T | G | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
8 | HG01891.hp1 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.285-186A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131623648 | |||||||
| chr6:131623934 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.285-472C>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131623934 | |||||||
| chr6:131624155 | T | G | 1 | a0001c0001t0001g0142 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.285-693A>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624155 | |||||||
| chr6:131624159 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.285-697T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624159 | |||||||
| chr6:131624334 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.284+531A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624334 | |||||||
| chr6:131624469 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0045 |
3 | HG01884.hp2 HG02257.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284+396G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624469 | |||||||
| chr6:131624591 | G | A | 24 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(21): Show |
30 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.284+274C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624591 | |||||||
| chr6:131624597 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.284+268C>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624597 | |||||||
| chr6:131624821 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
7 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+44A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 4/28 | chr6 | 131624821 | |||||||
| chr6:131625352 | G | C | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-363C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131625352 | |||||||
| chr6:131625385 | G | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(13): Show |
21 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.160-396C>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131625385 | |||||||
| chr6:131625434 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0208 |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-445G>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131625434 | |||||||
| chr6:131625863 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160-874G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131625863 | |||||||
| chr6:131625888 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.160-899G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131625888 | |||||||
| chr6:131626100 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01109.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.160-1111G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626100 | |||||||
| chr6:131626122 | C | CA | 30 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(27): Show |
37 | HG01496.hp2 HG01884.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.160-1134dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626122 | |||||||
| chr6:131626122 | CA | C | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
11 | HG01257.hp1 HG01891.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.160-1134delT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626122 | |||||||
| chr6:131626137 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.160-1148T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626137 | |||||||
| chr6:131626280 | T | A | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+1116A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626280 | |||||||
| chr6:131626558 | A | C | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+838T>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626558 | |||||||
| chr6:131626821 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.159+575T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131626821 | |||||||
| chr6:131627010 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0019 others(7): Show |
14 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.159+386A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627010 | |||||||
| chr6:131627045 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0045 |
3 | HG01884.hp2 HG02257.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.159+351T>C | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627045 | |||||||
| chr6:131627134 | C | T | 6 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+262G>A | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627134 | |||||||
| chr6:131627156 | G | GT | 7 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0207 others(4): Show |
9 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+239dupA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627156 | |||||||
| chr6:131627156 | GT | G | 7 | a0001c0001t0001g0158 a0001c0001t0003g0211 a0001c0001t0003g0212 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+239delA | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627156 | |||||||
| chr6:131627167 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.159+229A>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627167 | |||||||
| chr6:131627182 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.159+214C>T | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627182 | |||||||
| chr6:131627317 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.159+79A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627317 | |||||||
| chr6:131627329 | GA | G | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(97): Show |
142 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.159+66delT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627329 | |||||||
| chr6:131627329 | GAA | G | 11 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(8): Show |
16 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.159+65_159+66delTT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627329 | |||||||
| chr6:131627329 | GAAA | G | 8 | a0001c0001t0001g0205 a0001c0001t0001g0210 a0001c0001t0003g0211 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+64_159+66delTT others(1): Show |
MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 3/28 | chr6 | 131627329 | |||||||
| chr6:131627579 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG00621.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.71+62A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 2/28 | chr6 | 131627579 | |||||||
| chr6:131627676 | T | TA | 13 | a0001c0001t0001g0028 a0001c0001t0001g0148 a0001c0001t0001g0149 others(10): Show |
14 | HG01192.hp2 HG02622.hp1 HG02683.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.40-5dupT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/28 | chr6 | 131627676 | |||||||
| chr6:131627676 | T | TAA | 51 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
78 | HG00140.hp2 HG00280.hp1 HG00609.hp2 others(75): Show |
splice_region_variant&intron_variant | LOW | c.40-6_40-5dupTT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/28 | chr6 | 131627676 | |||||||
| chr6:131627676 | T | TAAA | 22 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
37 | HG00408.hp1 HG00423.hp1 HG02027.hp2 others(34): Show |
splice_region_variant&intron_variant | LOW | c.40-7_40-5dupTTT | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/28 | chr6 | 131627676 | |||||||
| chr6:131627865 | T | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(13): Show |
21 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.39+146A>G | MED23 | ENSG00000112282.18 | transcript | ENST00000368068.8 | protein_coding | 1/28 | chr6 | 131627865 |