Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80177 |
| ensemblid | ENSG00000120279.7 |
| hgncid | 23172 |
| symbol | MYCT1 |
| name | MYC target 1 |
| refseq_nuc | NM_025107.3 |
| refseq_prot | NP_079383.2 |
| ensembl_nuc | ENST00000367245.6 |
| ensembl_prot | ENSP00000356214.5 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 152697897 |
| end | 152724569 |
| strand | + |
| ver | v1.2 |
| region | chr6:152697897-152724569 |
| region5000 | chr6:152692897-152729569 |
| regionname0 | MYCT1_chr6_152697897_152724569 |
| regionname5000 | MYCT1_chr6_152692897_152729569 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 235 | 338 | 74 | 56 | 165 | 7 | 34 | 132 | MYCT1_chr6_152692897_152729569 | MYCT1 | MRTQV others(230): Show |
chr6 | 152692897 | 152729569 |
| a0002 | 0/0 | 54 | 51 | 7 | 6 | 37 | 0 | 1 | 30 | MYCT1_chr6_152692897_152729569 | MYCT1 | MRTQV others(49): Show |
chr6 | 152692897 | 152729569 |
| a0003 | 0/0 | 235 | 46 | 3 | 17 | 20 | 3 | 3 | 16 | MYCT1_chr6_152692897_152729569 | MYCT1 | MRTQV others(230): Show |
chr6 | 152692897 | 152729569 |
| a0004 | 0/0 | 235 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | MYCT1_chr6_152692897_152729569 | MYCT1 | MRTQV others(230): Show |
chr6 | 152692897 | 152729569 |
| a0005 | 0/0 | 235 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | MRTQV others(230): Show |
chr6 | 152692897 | 152729569 |
| a0006 | 0/0 | 235 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MYCT1_chr6_152692897_152729569 | MYCT1 | MRTQV others(230): Show |
chr6 | 152692897 | 152729569 |
| a0007 | 0/0 | 235 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | MRTQV others(230): Show |
chr6 | 152692897 | 152729569 |
| a0008 | 0/0 | 235 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | MRTQV others(230): Show |
chr6 | 152692897 | 152729569 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 705 | 336 | 74 | 54 | 165 | 7 | 34 | MYCT1_chr6_152692897_152729569 | MYCT1 | ATGCG others(700): Show |
chr6 | 152692897 | 152729569 | ||
| a0001c0006 | 0/0 | 705 | 2 | 0 | 2 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | ATGCG others(700): Show |
chr6 | 152692897 | 152729569 | ||
| a0002c0002 | 0/0 | 701 | 50 | 7 | 6 | 36 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | ATGCG others(696): Show |
chr6 | 152692897 | 152729569 | ||
| a0002c0008 | 0/0 | 701 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | ATGCG others(696): Show |
chr6 | 152692897 | 152729569 | ||
| a0003c0003 | 0/0 | 705 | 46 | 3 | 17 | 20 | 3 | 3 | MYCT1_chr6_152692897_152729569 | MYCT1 | ATGCG others(700): Show |
chr6 | 152692897 | 152729569 | ||
| a0004c0004 | 0/0 | 705 | 3 | 0 | 0 | 3 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | ATGCG others(700): Show |
chr6 | 152692897 | 152729569 | ||
| a0005c0007 | 0/0 | 705 | 2 | 2 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | ATGCG others(700): Show |
chr6 | 152692897 | 152729569 | ||
| a0006c0005 | 0/0 | 705 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | ATGCG others(700): Show |
chr6 | 152692897 | 152729569 | ||
| a0007c0010 | 0/0 | 705 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | ATGCG others(700): Show |
chr6 | 152692897 | 152729569 | ||
| a0008c0009 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | ATGCG others(700): Show |
chr6 | 152692897 | 152729569 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3030 | 71 | 3 | 6 | 60 | 2 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0002 | 1/0 | 3030 | 99 | 22 | 20 | 38 | 4 | 14 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0003 | 0/0 | 3031 | 94 | 18 | 16 | 43 | 1 | 16 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3026): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0004 | 0/0 | 3030 | 4 | 2 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0005 | 0/0 | 3030 | 18 | 0 | 3 | 14 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0006 | 0/0 | 3031 | 7 | 0 | 6 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3026): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0007 | 0/0 | 3029 | 7 | 7 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3024): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0008 | 0/0 | 3031 | 6 | 6 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3026): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0009 | 0/0 | 3030 | 5 | 1 | 0 | 4 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0012 | 0/0 | 3029 | 3 | 2 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3024): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0013 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0014 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3024): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0015 | 0/0 | 3029 | 2 | 2 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3024): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0016 | 0/0 | 3031 | 2 | 2 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3026): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0017 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3026): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0018 | 0/1 | 3030 | 1 | 0 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0020 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0021 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0022 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0023 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0024 | 0/0 | 3029 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3024): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0025 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0026 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0027 | 0/0 | 3031 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3026): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0028 | 0/0 | 3030 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0029 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0030 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0031 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0032 | 0/0 | 3030 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0001t0035 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0001c0006t0003 | 0/0 | 3031 | 2 | 0 | 2 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3026): Show |
chr6 | 152692897 | 152729569 |
| a0002c0002t0003 | 0/0 | 3027 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3022): Show |
chr6 | 152692897 | 152729569 |
| a0002c0002t0004 | 0/0 | 3026 | 37 | 4 | 5 | 27 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3021): Show |
chr6 | 152692897 | 152729569 |
| a0002c0002t0009 | 0/0 | 3026 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3021): Show |
chr6 | 152692897 | 152729569 |
| a0002c0002t0010 | 0/0 | 3026 | 4 | 0 | 0 | 4 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3021): Show |
chr6 | 152692897 | 152729569 |
| a0002c0002t0011 | 0/0 | 3026 | 3 | 2 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3021): Show |
chr6 | 152692897 | 152729569 |
| a0002c0002t0033 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3022): Show |
chr6 | 152692897 | 152729569 |
| a0002c0002t0034 | 0/0 | 3026 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3021): Show |
chr6 | 152692897 | 152729569 |
| a0002c0002t0036 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3020): Show |
chr6 | 152692897 | 152729569 |
| a0002c0008t0004 | 0/0 | 3026 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3021): Show |
chr6 | 152692897 | 152729569 |
| a0003c0003t0001 | 0/0 | 3030 | 44 | 3 | 15 | 20 | 3 | 3 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0003c0003t0014 | 0/0 | 3029 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3024): Show |
chr6 | 152692897 | 152729569 |
| a0003c0003t0019 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0004c0004t0001 | 0/0 | 3030 | 3 | 0 | 0 | 3 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0005c0007t0001 | 0/0 | 3030 | 2 | 2 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0006c0005t0001 | 0/0 | 3030 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0007c0010t0013 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| a0008c0009t0002 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | CCTTT others(3025): Show |
chr6 | 152692897 | 152729569 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 28 | 1 | 0 | 27 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0004 | 0/0 | 20 | 0 | 1 | 18 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0007 | 1/0 | 9 | 4 | 2 | 0 | 2 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0018 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0019 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0024 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0001 | 0/0 | 45 | 1 | 13 | 23 | 1 | 7 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0005g0006 | 0/0 | 16 | 0 | 3 | 12 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0006g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0006g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0007g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0008g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0009g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0009g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0012g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0012g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0013g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0014g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0016g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0017g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0018g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0020g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0021g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0022g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0023g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0024g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0025g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0026g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0027g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0028g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0029g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0030g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0031g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0032g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0001t0035g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0001c0006t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0003g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0004g0003 | 0/0 | 24 | 3 | 2 | 19 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0004g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0004g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0010g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0010g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0011g0029 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0033g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0034g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0002t0036g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0002c0008t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0005 | 0/0 | 15 | 0 | 2 | 10 | 1 | 2 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0011 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0013 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0014g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0003c0003t0019g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0004c0004t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0005c0007t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0005c0007t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0006c0005t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0007c0010t0013g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| a0008c0009t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | GBR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0156 | EUR | GBR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | GBR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | FIN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0011 | EUR | FIN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00558 | hp2 | a0002 | c0002 | t0036 | g0003 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00609 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0013 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00673 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0144 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0011 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00738 | hp1 | a0001 | c0006 | t0003 | g0001 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00741 | hp1 | a0002 | c0002 | t0004 | g0003 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0154 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01070 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01081 | hp2 | a0001 | c0001 | t0024 | g0129 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01099 | hp2 | a0001 | c0001 | t0012 | g0041 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0050 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01109 | hp2 | a0002 | c0002 | t0011 | g0029 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01167 | hp2 | a0003 | c0003 | t0001 | g0013 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01168 | hp2 | a0003 | c0003 | t0014 | g0011 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0013 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0047 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0050 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0119 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0013 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01361 | hp2 | a0003 | c0003 | t0001 | g0013 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01433 | hp1 | a0002 | c0002 | t0004 | g0003 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0138 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0005 | EUR | IBS | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0061 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01891 | hp2 | a0002 | c0002 | t0004 | g0003 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01934 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01934 | hp2 | a0002 | c0002 | t0004 | g0028 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01943 | hp1 | a0002 | c0002 | t0004 | g0028 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01975 | hp1 | a0001 | c0006 | t0003 | g0001 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01981 | hp1 | a0001 | c0001 | t0027 | g0082 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01993 | hp1 | a0003 | c0003 | t0019 | g0005 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02027 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02040 | hp2 | a0002 | c0002 | t0010 | g0163 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0145 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02129 | hp1 | a0002 | c0002 | t0033 | g0171 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02132 | hp1 | a0002 | c0002 | t0034 | g0173 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02145 | hp1 | a0002 | c0002 | t0004 | g0003 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02148 | hp2 | a0002 | c0002 | t0004 | g0028 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | CDX | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CDX | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0143 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02273 | hp1 | a0007 | c0010 | t0013 | g0077 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02280 | hp1 | a0002 | c0002 | t0004 | g0003 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0002 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02300 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | PEL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02451 | hp2 | a0001 | c0001 | t0023 | g0159 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02602 | hp2 | a0001 | c0001 | t0032 | g0004 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0125 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0041 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02723 | hp2 | a0001 | c0001 | t0030 | g0056 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0124 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02818 | hp1 | a0001 | c0001 | t0022 | g0160 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02896 | hp1 | a0001 | c0001 | t0021 | g0010 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02922 | hp2 | a0002 | c0002 | t0011 | g0029 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0033 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02976 | hp1 | a0001 | c0001 | t0026 | g0058 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03017 | hp1 | a0002 | c0002 | t0004 | g0170 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03195 | hp1 | a0001 | c0001 | t0016 | g0031 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03209 | hp1 | a0002 | c0002 | t0009 | g0167 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03225 | hp1 | a0002 | c0002 | t0011 | g0029 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0071 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0096 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03486 | hp2 | a0005 | c0007 | t0001 | g0135 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0105 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0036 | AFR | ESN | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0106 | AFR | MSL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0053 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | STU | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | STU | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03704 | hp2 | a0001 | c0001 | t0028 | g0009 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0151 | SAS | PJL | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | BEB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | BEB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | BEB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | STU | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | STU | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | STU | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | STU | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | STU | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0080 | SAS | STU | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | STU | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | YRI | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | YRI | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | CHB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | CHB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | CHB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | YRI | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | YRI | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18939 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18940 | hp2 | a0006 | c0005 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18941 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18942 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18942 | hp2 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18943 | hp1 | a0003 | c0003 | t0001 | g0147 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18943 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18944 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18949 | hp1 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18950 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18951 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18956 | hp1 | a0001 | c0001 | t0020 | g0025 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0017 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18962 | hp1 | a0001 | c0001 | t0014 | g0113 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18963 | hp1 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18965 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18966 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18967 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18969 | hp1 | a0006 | c0005 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18971 | hp2 | a0001 | c0001 | t0009 | g0034 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18974 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18977 | hp1 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18977 | hp2 | a0002 | c0002 | t0010 | g0165 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18978 | hp1 | a0002 | c0002 | t0010 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18981 | hp1 | a0002 | c0002 | t0004 | g0166 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18982 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18983 | hp2 | a0002 | c0002 | t0004 | g0162 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18984 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18988 | hp1 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18991 | hp1 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18991 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18994 | hp1 | a0002 | c0002 | t0004 | g0169 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18995 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19001 | hp1 | a0001 | c0001 | t0029 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19002 | hp1 | a0002 | c0002 | t0004 | g0161 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19002 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19003 | hp1 | a0008 | c0009 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19009 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | LWK | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0031 | AFR | LWK | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19043 | hp1 | a0001 | c0001 | t0017 | g0158 | AFR | LWK | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19043 | hp2 | a0002 | c0002 | t0004 | g0168 | AFR | LWK | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19055 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19055 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19056 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19059 | hp1 | a0001 | c0001 | t0031 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19059 | hp2 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19065 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19065 | hp2 | a0002 | c0002 | t0004 | g0174 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19066 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19067 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19068 | hp2 | a0002 | c0002 | t0004 | g0051 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19075 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19076 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19079 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19081 | hp1 | a0002 | c0008 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19081 | hp2 | a0002 | c0002 | t0004 | g0172 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19082 | hp1 | a0002 | c0002 | t0010 | g0164 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19083 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19085 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19088 | hp2 | a0002 | c0002 | t0004 | g0051 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19089 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | YRI | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA19240 | hp2 | a0001 | c0001 | t0015 | g0059 | AFR | YRI | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ASW | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA20129 | hp2 | a0005 | c0007 | t0001 | g0136 | AFR | ASW | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0068 | SAS | GIH | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | GIH | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0130 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02109 | hp2 | a0001 | c0001 | t0035 | g0126 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0108 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | USA | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| HG06807 | hp2 | a0001 | c0001 | t0025 | g0133 | AFR | USA | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18955 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0054 | AFR | USA | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | USA | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0047 | AFR | LWK | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0018 | g0089 | REF | REF | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0007 | REF | REF | MYCT1_chr6_152692897_152729569 | MYCT1 | chr6 | 152692897 | 152729569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:152697964 | GAGAT | G | 1 | a0002 | 51 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(48): Show |
frameshift_variant | HIGH | c.66_69delTAGA | p.Asp22fs | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/2 | 72/3030 | 66/708 | 22/235 | INFO_REALIGN_3_PRIME | chr6 | 152697964 | ||
| chr6:152698062 | A | G | 1 | a0005 | 2 | HG03486.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.160A>G | p.Thr54Ala | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/2 | 166/3030 | 160/708 | 54/235 | chr6 | 152698062 | |||
| chr6:152721793 | G | A | 1 | a0004 | 3 | NA18963.hp1 NA18977.hp1 NA19083.hp2 |
missense_variant | MODERATE | c.248G>A | p.Gly83Glu | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 254/3030 | 248/708 | 83/235 | chr6 | 152721793 | |||
| chr6:152721900 | G | A | 1 | a0003 | 46 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(43): Show |
missense_variant | MODERATE | c.355G>A | p.Gly119Ser | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 361/3030 | 355/708 | 119/235 | chr6 | 152721900 | |||
| chr6:152721943 | G | A | 1 | a0006 | 2 | NA18940.hp2 NA18969.hp1 |
missense_variant | MODERATE | c.398G>A | p.Arg133His | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 404/3030 | 398/708 | 133/235 | chr6 | 152721943 | |||
| chr6:152722075 | C | T | 1 | a0007 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.530C>T | p.Pro177Leu | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 536/3030 | 530/708 | 177/235 | chr6 | 152722075 | |||
| chr6:152722095 | C | A | 1 | a0008 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.550C>A | p.Leu184Met | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 556/3030 | 550/708 | 184/235 | chr6 | 152722095 | |||
| chr6:152722129 | C | T | 1 | a0002 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.584C>T | p.Thr195Ile | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 590/3030 | 584/708 | 195/235 | chr6 | 152722129 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:152721788 | A | T | 1 | a0001c0006 | 2 | HG00738.hp1 HG01975.hp1 |
synonymous_variant | LOW | c.243A>T | p.Val81Val | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 249/3030 | 243/708 | 81/235 | chr6 | 152721788 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:152722383 | T | G | 1 | a0001c0001t0017 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*130T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 130 | chr6 | 152722383 | ||||||
| chr6:152722439 | G | A | 1 | a0002c0002t0011 | 3 | HG01109.hp2 HG02922.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*186G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 186 | chr6 | 152722439 | ||||||
| chr6:152722467 | A | G | 2 | a0002c0002t0010 a0002c0002t0036 |
5 | HG00558.hp2 HG02040.hp2 NA18977.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*214A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 214 | chr6 | 152722467 | ||||||
| chr6:152722505 | C | T | 1 | a0001c0001t0012 | 3 | HG01099.hp2 HG02109.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*252C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 252 | chr6 | 152722505 | ||||||
| chr6:152722915 | T | G | 19 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(16): Show |
172 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*662T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 662 | chr6 | 152722915 | ||||||
| chr6:152722967 | C | T | 2 | a0001c0001t0035 a0002c0002t0034 |
2 | HG02109.hp2 HG02132.hp1 |
3_prime_UTR_variant | MODIFIER | c.*714C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 714 | chr6 | 152722967 | ||||||
| chr6:152722977 | G | A | 11 | a0001c0001t0004 a0001c0001t0023 a0001c0001t0024 others(8): Show |
55 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*724G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 724 | chr6 | 152722977 | ||||||
| chr6:152723019 | C | G | 1 | a0002c0002t0033 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*766C>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 766 | chr6 | 152723019 | ||||||
| chr6:152723165 | T | C | 1 | a0001c0001t0027 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*912T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 912 | chr6 | 152723165 | ||||||
| chr6:152723290 | G | A | 2 | a0001c0001t0013 a0007c0010t0013 |
2 | HG02273.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1037G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1037 | chr6 | 152723290 | ||||||
| chr6:152723474 | T | G | 1 | a0003c0003t0019 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1221 | chr6 | 152723474 | ||||||
| chr6:152723496 | G | T | 4 | a0001c0001t0012 a0001c0001t0024 a0001c0001t0025 others(1): Show |
6 | HG01081.hp2 HG01099.hp2 HG02109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1243G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1243 | chr6 | 152723496 | ||||||
| chr6:152723507 | A | G | 1 | a0001c0001t0032 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1254A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1254 | chr6 | 152723507 | ||||||
| chr6:152723515 | C | T | 1 | a0001c0001t0022 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1262C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1262 | chr6 | 152723515 | ||||||
| chr6:152723570 | G | T | 1 | a0001c0001t0031 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1317G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1317 | chr6 | 152723570 | ||||||
| chr6:152723578 | C | T | 1 | a0001c0001t0030 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1325C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1325 | chr6 | 152723578 | ||||||
| chr6:152723800 | A | T | 3 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0021 |
10 | HG01099.hp2 HG01891.hp1 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1547A>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1547 | chr6 | 152723800 | ||||||
| chr6:152723814 | T | C | 14 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0013 others(11): Show |
137 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1561T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1561 | chr6 | 152723814 | ||||||
| chr6:152724092 | A | G | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(37): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*1839A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1839 | chr6 | 152724092 | ||||||
| chr6:152724148 | C | A | 2 | a0001c0001t0008 a0001c0001t0021 |
7 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1895C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1895 | chr6 | 152724148 | ||||||
| chr6:152724179 | A | C | 1 | a0001c0001t0016 | 2 | HG03195.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1926A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1926 | chr6 | 152724179 | ||||||
| chr6:152724215 | A | T | 1 | a0001c0001t0020 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1962A>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1962 | chr6 | 152724215 | ||||||
| chr6:152724233 | C | CT | 9 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(6): Show |
116 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1998dupT | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1999 | INFO_REALIGN_3_PRIME | chr6 | 152724233 | |||||
| chr6:152724233 | CT | C | 7 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0014 others(4): Show |
16 | HG00558.hp2 HG01081.hp2 HG01099.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1998delT | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1998 | INFO_REALIGN_3_PRIME | chr6 | 152724233 | |||||
| chr6:152724251 | T | C | 1 | a0001c0001t0025 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1998T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 1998 | chr6 | 152724251 | ||||||
| chr6:152724428 | T | A | 1 | a0001c0001t0028 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2175T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 2175 | chr6 | 152724428 | ||||||
| chr6:152724451 | T | C | 1 | a0001c0001t0023 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 2198 | chr6 | 152724451 | ||||||
| chr6:152724478 | T | C | 1 | a0001c0001t0029 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2225T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 2225 | chr6 | 152724478 | ||||||
| chr6:152724497 | C | T | 1 | a0001c0001t0012 | 3 | HG01099.hp2 HG02109.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2244C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 2/2 | 2244 | chr6 | 152724497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:152698138 | G | A | 2 | a0003c0003t0001g0013 a0003c0003t0001g0053 |
6 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+40G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152698138 | |||||||
| chr6:152698297 | T | C | 5 | a0001c0001t0005g0006 a0001c0001t0005g0055 a0001c0001t0005g0057 others(2): Show |
20 | HG01358.hp2 HG01975.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.196+199T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152698297 | |||||||
| chr6:152698368 | G | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(117): Show |
280 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.196+270G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152698368 | |||||||
| chr6:152698426 | G | A | 1 | a0001c0001t0026g0058 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196+328G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152698426 | |||||||
| chr6:152698431 | T | C | 2 | a0001c0001t0002g0016 a0001c0001t0015g0059 |
5 | HG02630.hp1 HG02818.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+333T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152698431 | |||||||
| chr6:152698591 | G | C | 2 | a0001c0001t0001g0040 a0001c0001t0004g0107 |
3 | NA18974.hp2 NA18984.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.196+493G>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152698591 | |||||||
| chr6:152698766 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(117): Show |
280 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.196+668C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152698766 | |||||||
| chr6:152699228 | T | C | 4 | a0001c0001t0008g0010 a0001c0001t0008g0108 a0001c0001t0012g0041 others(1): Show |
9 | HG01099.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.196+1130T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699228 | |||||||
| chr6:152699258 | A | T | 1 | a0001c0001t0026g0058 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196+1160A>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699258 | |||||||
| chr6:152699266 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0020 others(25): Show |
71 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.196+1168G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699266 | |||||||
| chr6:152699307 | A | G | 22 | a0002c0002t0003g0052 a0002c0002t0004g0003 a0002c0002t0004g0028 others(19): Show |
51 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+1209A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699307 | |||||||
| chr6:152699311 | GA | G | 4 | a0001c0001t0008g0010 a0001c0001t0008g0108 a0001c0001t0012g0041 others(1): Show |
9 | HG01099.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.196+1221delA | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152699311 | ||||||
| chr6:152699337 | T | C | 1 | a0001c0001t0003g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.196+1239T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699337 | |||||||
| chr6:152699471 | A | G | 1 | a0001c0001t0026g0058 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196+1373A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699471 | |||||||
| chr6:152699588 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(117): Show |
280 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.196+1490G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699588 | |||||||
| chr6:152699589 | C | T | 3 | a0002c0002t0004g0172 a0002c0002t0004g0174 a0002c0002t0034g0173 |
3 | HG02132.hp1 NA19065.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.196+1491C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699589 | |||||||
| chr6:152699594 | T | G | 1 | a0001c0001t0007g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.196+1496T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699594 | |||||||
| chr6:152699711 | T | C | 3 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0035g0126 |
3 | HG02109.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.196+1613T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699711 | |||||||
| chr6:152699721 | T | A | 1 | a0002c0002t0004g0028 | 3 | HG01934.hp2 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.196+1623T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699721 | |||||||
| chr6:152699822 | T | A | 2 | a0001c0001t0003g0127 a0001c0001t0003g0128 |
2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.196+1724T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699822 | |||||||
| chr6:152699931 | G | T | 1 | a0002c0002t0033g0171 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.196+1833G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699931 | |||||||
| chr6:152699991 | A | G | 1 | a0001c0001t0022g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.196+1893A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699991 | |||||||
| chr6:152699993 | T | G | 1 | a0001c0001t0026g0058 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196+1895T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152699993 | |||||||
| chr6:152700091 | T | G | 1 | a0001c0001t0004g0107 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.196+1993T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700091 | |||||||
| chr6:152700092 | A | T | 1 | a0001c0001t0004g0107 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.196+1994A>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700092 | |||||||
| chr6:152700105 | A | G | 1 | a0001c0001t0007g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.196+2007A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700105 | |||||||
| chr6:152700171 | T | C | 1 | a0003c0003t0001g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.196+2073T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700171 | |||||||
| chr6:152700181 | C | T | 24 | a0001c0001t0017g0158 a0001c0001t0023g0159 a0002c0002t0003g0052 others(21): Show |
53 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.196+2083C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700181 | |||||||
| chr6:152700193 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.196+2095G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700193 | |||||||
| chr6:152700339 | C | T | 24 | a0001c0001t0017g0158 a0001c0001t0023g0159 a0002c0002t0003g0052 others(21): Show |
53 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.196+2241C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700339 | |||||||
| chr6:152700578 | T | G | 1 | a0001c0001t0002g0062 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.196+2480T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700578 | |||||||
| chr6:152700591 | G | T | 1 | a0001c0001t0003g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.196+2493G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700591 | |||||||
| chr6:152700674 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(117): Show |
280 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.196+2576G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700674 | |||||||
| chr6:152700681 | G | C | 2 | a0001c0001t0012g0130 a0001c0001t0024g0129 |
2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.196+2583G>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700681 | |||||||
| chr6:152700786 | C | T | 1 | a0001c0001t0035g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+2688C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700786 | |||||||
| chr6:152700864 | G | A | 48 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0127 others(45): Show |
101 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.196+2766G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700864 | |||||||
| chr6:152700978 | T | C | 5 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(2): Show |
9 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+2880T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152700978 | |||||||
| chr6:152701133 | T | C | 1 | a0001c0001t0003g0063 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196+3035T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152701133 | |||||||
| chr6:152701291 | C | T | 1 | a0002c0002t0004g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.196+3193C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152701291 | |||||||
| chr6:152701392 | C | G | 3 | a0002c0002t0003g0052 a0002c0002t0004g0051 a0002c0002t0004g0169 |
5 | NA18942.hp2 NA18988.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+3294C>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152701392 | |||||||
| chr6:152701486 | A | T | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.196+3388A>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152701486 | |||||||
| chr6:152701539 | T | C | 42 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(39): Show |
101 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.196+3441T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152701539 | |||||||
| chr6:152701618 | G | C | 1 | a0001c0001t0003g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.196+3520G>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152701618 | |||||||
| chr6:152701623 | G | GA | 4 | a0001c0001t0008g0010 a0001c0001t0008g0108 a0001c0001t0012g0041 others(1): Show |
9 | HG01099.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.196+3526dupA | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152701623 | ||||||
| chr6:152701752 | A | G | 1 | a0001c0001t0023g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.196+3654A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152701752 | |||||||
| chr6:152701777 | G | A | 42 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(39): Show |
101 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.196+3679G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152701777 | |||||||
| chr6:152701831 | C | G | 20 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0127 others(17): Show |
39 | HG01081.hp2 HG01358.hp2 HG01975.hp2 others(36): Show |
intron_variant | MODIFIER | c.196+3733C>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152701831 | |||||||
| chr6:152701918 | C | G | 16 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(13): Show |
31 | HG01081.hp2 HG01358.hp2 HG01975.hp2 others(28): Show |
intron_variant | MODIFIER | c.196+3820C>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152701918 | |||||||
| chr6:152702016 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(90): Show |
219 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.196+3918G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152702016 | |||||||
| chr6:152702049 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(90): Show |
219 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.196+3951A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152702049 | |||||||
| chr6:152702616 | C | G | 1 | a0001c0001t0005g0057 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.196+4518C>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152702616 | |||||||
| chr6:152702617 | A | C | 1 | a0001c0001t0005g0057 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.196+4519A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152702617 | |||||||
| chr6:152702630 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(84): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.196+4532A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152702630 | |||||||
| chr6:152702691 | A | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(84): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.196+4593A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152702691 | |||||||
| chr6:152702705 | T | G | 3 | a0001c0001t0002g0065 a0001c0001t0003g0017 a0001c0001t0009g0017 |
5 | NA18957.hp2 NA18960.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+4607T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152702705 | |||||||
| chr6:152702743 | G | A | 1 | a0001c0001t0023g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.196+4645G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152702743 | |||||||
| chr6:152702777 | G | A | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.196+4679G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152702777 | |||||||
| chr6:152702948 | G | A | 24 | a0001c0001t0017g0158 a0001c0001t0023g0159 a0002c0002t0003g0052 others(21): Show |
53 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.196+4850G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152702948 | |||||||
| chr6:152702982 | C | A | 4 | a0001c0001t0008g0010 a0001c0001t0008g0108 a0001c0001t0012g0041 others(1): Show |
9 | HG01099.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.196+4884C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152702982 | |||||||
| chr6:152703180 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(82): Show |
207 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.196+5082A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703180 | |||||||
| chr6:152703194 | T | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(81): Show |
206 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.196+5096T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703194 | |||||||
| chr6:152703205 | A | G | 1 | a0001c0001t0023g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.196+5107A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703205 | |||||||
| chr6:152703303 | G | A | 1 | a0001c0001t0003g0014 | 5 | HG00558.hp1 HG00621.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+5205G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703303 | |||||||
| chr6:152703318 | G | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(81): Show |
206 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.196+5220G>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703318 | |||||||
| chr6:152703444 | T | C | 1 | a0001c0001t0025g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.196+5346T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703444 | |||||||
| chr6:152703542 | A | G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0048 others(40): Show |
105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.196+5444A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703542 | |||||||
| chr6:152703558 | T | C | 5 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(2): Show |
9 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+5460T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703558 | |||||||
| chr6:152703593 | T | TTG | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(81): Show |
206 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.196+5497_196+5498d others(4): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703593 | ||||||
| chr6:152703630 | C | T | 1 | a0005c0007t0001g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.196+5532C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703630 | |||||||
| chr6:152703692 | A | AGAATTTT others(13): Show |
1 | a0001c0001t0001g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.196+5597_196+5616d others(22): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703692 | ||||||
| chr6:152703716 | T | C | 27 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(24): Show |
56 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.196+5618T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703716 | |||||||
| chr6:152703888 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.196+5790C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703888 | |||||||
| chr6:152703902 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.196+5804G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152703902 | |||||||
| chr6:152703940 | T | TTTTTA | 6 | a0001c0001t0002g0018 a0001c0001t0002g0037 a0001c0001t0002g0087 others(3): Show |
10 | HG01099.hp1 HG01256.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.196+5912_196+5916d others(7): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703940 | ||||||
| chr6:152703940 | T | TTTTTATT others(17): Show |
1 | a0002c0002t0004g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.196+5850_196+5851i others(26): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703940 | ||||||
| chr6:152703940 | T | TTTTTATT others(3): Show |
3 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0025g0133 |
3 | HG02083.hp2 HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.196+5907_196+5916d others(12): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703940 | ||||||
| chr6:152703940 | T | TTTTTATT others(8): Show |
2 | a0001c0001t0002g0084 a0001c0001t0002g0104 |
2 | HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.196+5902_196+5916d others(17): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703940 | ||||||
| chr6:152703940 | TTTTTA | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0112 others(11): Show |
27 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.196+5912_196+5916d others(7): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703940 | ||||||
| chr6:152703940 | TTTTTATT others(3): Show |
T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0025 others(20): Show |
63 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.196+5907_196+5916d others(12): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703940 | ||||||
| chr6:152703940 | TTTTTATT others(8): Show |
T | 24 | a0001c0001t0001g0026 a0001c0001t0001g0121 a0001c0001t0001g0122 others(21): Show |
52 | HG00323.hp2 HG00735.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.196+5902_196+5916d others(17): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703940 | ||||||
| chr6:152703940 | TTTTTATT others(13): Show |
T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0048 others(67): Show |
174 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.196+5897_196+5916d others(22): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703940 | ||||||
| chr6:152703940 | TTTTTATT others(18): Show |
T | 3 | a0001c0001t0001g0155 a0001c0001t0003g0036 a0001c0001t0009g0036 |
3 | HG02717.hp1 HG03516.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.196+5892_196+5916d others(27): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703940 | ||||||
| chr6:152703940 | TTTTTATT others(23): Show |
T | 6 | a0001c0001t0001g0110 a0001c0001t0002g0008 a0001c0001t0006g0050 others(3): Show |
15 | HG00140.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.196+5887_196+5916d others(32): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703940 | ||||||
| chr6:152703940 | TTTTTATT others(28): Show |
T | 2 | a0001c0001t0002g0065 a0001c0001t0003g0083 |
2 | HG01255.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.196+5882_196+5916d others(37): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703940 | ||||||
| chr6:152703941 | TTTTATTT others(22): Show |
T | 1 | a0001c0001t0002g0137 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.196+5847_196+5875d others(31): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703941 | ||||||
| chr6:152703945 | ATTTTAT | A | 8 | a0002c0002t0004g0003 a0002c0002t0004g0161 a0002c0002t0004g0172 others(5): Show |
12 | HG00741.hp1 HG01109.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+5851_196+5856d others(8): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703945 | ||||||
| chr6:152703945 | ATTTTATT others(4): Show |
A | 13 | a0001c0001t0004g0134 a0002c0002t0003g0052 a0002c0002t0004g0003 others(10): Show |
31 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.196+5851_196+5861d others(13): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703945 | ||||||
| chr6:152703945 | ATTTTATT others(9): Show |
A | 1 | a0002c0002t0010g0165 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.196+5851_196+5866d others(18): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703945 | ||||||
| chr6:152703945 | ATTTTATT others(14): Show |
A | 4 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0002c0002t0004g0003 others(1): Show |
8 | HG03516.hp1 HG06807.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+5851_196+5871d others(23): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152703945 | ||||||
| chr6:152704479 | A | C | 1 | a0001c0001t0001g0043 | 2 | NA18947.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.196+6381A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152704479 | |||||||
| chr6:152704681 | C | G | 1 | a0001c0001t0027g0082 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.196+6583C>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152704681 | |||||||
| chr6:152704686 | C | A | 1 | a0001c0001t0001g0045 | 2 | NA18941.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.196+6588C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152704686 | |||||||
| chr6:152704692 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(160): Show |
382 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.196+6594T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152704692 | |||||||
| chr6:152704965 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(78): Show |
203 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.196+6867G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152704965 | |||||||
| chr6:152704985 | C | T | 32 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(29): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.196+6887C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152704985 | |||||||
| chr6:152705004 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(121): Show |
305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.196+6906T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705004 | |||||||
| chr6:152705006 | C | T | 32 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(29): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.196+6908C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705006 | |||||||
| chr6:152705033 | C | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(153): Show |
371 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.196+6935C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705033 | |||||||
| chr6:152705070 | C | T | 32 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(29): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.196+6972C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705070 | |||||||
| chr6:152705084 | G | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(153): Show |
371 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.196+6986G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705084 | |||||||
| chr6:152705104 | G | A | 1 | a0001c0001t0003g0032 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.196+7006G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705104 | |||||||
| chr6:152705310 | T | A | 1 | a0001c0001t0003g0014 | 5 | HG00558.hp1 HG00621.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+7212T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705310 | |||||||
| chr6:152705339 | G | A | 32 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(29): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.196+7241G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705339 | |||||||
| chr6:152705420 | AT | A | 3 | a0001c0001t0002g0065 a0001c0001t0003g0017 a0001c0001t0009g0017 |
5 | NA18957.hp2 NA18960.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+7323delT | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705420 | |||||||
| chr6:152705643 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(121): Show |
305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.196+7545A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705643 | |||||||
| chr6:152705669 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(153): Show |
371 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.196+7571A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705669 | |||||||
| chr6:152705707 | TTTA | T | 42 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(39): Show |
101 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.196+7623_196+7625d others(5): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152705707 | ||||||
| chr6:152705800 | G | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(150): Show |
368 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.196+7702G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705800 | |||||||
| chr6:152705895 | G | A | 1 | a0001c0001t0012g0041 | 2 | HG01099.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.196+7797G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705895 | |||||||
| chr6:152705995 | G | A | 1 | a0003c0003t0001g0012 | 6 | NA18951.hp2 NA18974.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+7897G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152705995 | |||||||
| chr6:152706019 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(128): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.196+7921A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706019 | |||||||
| chr6:152706019 | A | T | 32 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(29): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.196+7921A>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706019 | |||||||
| chr6:152706055 | TA | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(150): Show |
368 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.196+7964delA | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152706055 | ||||||
| chr6:152706149 | C | A | 1 | a0001c0001t0003g0027 | 3 | HG02258.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.196+8051C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706149 | |||||||
| chr6:152706168 | C | T | 3 | a0001c0001t0002g0039 a0001c0001t0002g0086 a0001c0001t0002g0103 |
4 | HG02258.hp2 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+8070C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706168 | |||||||
| chr6:152706185 | A | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(150): Show |
368 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.196+8087A>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706185 | |||||||
| chr6:152706285 | T | C | 1 | a0003c0003t0001g0154 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.196+8187T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706285 | |||||||
| chr6:152706295 | G | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(150): Show |
368 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.196+8197G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706295 | |||||||
| chr6:152706339 | T | C | 1 | a0001c0001t0002g0046 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.196+8241T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706339 | |||||||
| chr6:152706357 | A | G | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.196+8259A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706357 | |||||||
| chr6:152706386 | A | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(158): Show |
380 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(377): Show |
intron_variant | MODIFIER | c.196+8288A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706386 | |||||||
| chr6:152706410 | C | A | 1 | a0001c0001t0007g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.196+8312C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706410 | |||||||
| chr6:152706502 | A | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(118): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.196+8404A>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706502 | |||||||
| chr6:152706555 | T | C | 4 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(1): Show |
8 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+8457T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706555 | |||||||
| chr6:152706596 | A | T | 4 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(1): Show |
8 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+8498A>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706596 | |||||||
| chr6:152706768 | C | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(150): Show |
368 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.196+8670C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706768 | |||||||
| chr6:152706847 | A | ATG | 33 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0048 others(30): Show |
73 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.196+8775_196+8776d others(4): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152706847 | ||||||
| chr6:152706847 | A | ATGTG | 3 | a0001c0001t0001g0120 a0001c0001t0025g0133 a0001c0001t0026g0058 |
3 | HG00544.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.196+8773_196+8776d others(6): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152706847 | ||||||
| chr6:152706847 | A | ATGTGTGT others(3): Show |
3 | a0001c0001t0008g0010 a0001c0001t0021g0010 a0002c0002t0004g0172 |
7 | HG01891.hp1 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+8767_196+8776d others(12): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152706847 | ||||||
| chr6:152706847 | A | ATGTGTGT others(5): Show |
20 | a0001c0001t0003g0127 a0001c0001t0008g0108 a0001c0001t0012g0041 others(17): Show |
50 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.196+8765_196+8776d others(14): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152706847 | ||||||
| chr6:152706847 | A | ATGTGTGT others(7): Show |
5 | a0001c0001t0003g0128 a0001c0001t0004g0134 a0002c0002t0004g0168 others(2): Show |
5 | HG02809.hp1 HG03209.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+8763_196+8776d others(16): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152706847 | ||||||
| chr6:152706847 | A | ATGTGTGT others(11): Show |
2 | a0001c0001t0017g0158 a0001c0001t0023g0159 |
2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.196+8759_196+8776d others(20): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152706847 | ||||||
| chr6:152706847 | ATG | A | 46 | a0001c0001t0001g0075 a0001c0001t0001g0141 a0001c0001t0002g0062 others(43): Show |
105 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.196+8775_196+8776d others(4): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152706847 | ||||||
| chr6:152706855 | G | A | 3 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0035g0126 |
3 | HG02109.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.196+8757G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706855 | |||||||
| chr6:152706869 | G | GTGTGTGT others(11): Show |
1 | a0002c0002t0004g0166 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.196+8776_196+8777i others(20): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152706869 | ||||||
| chr6:152706876 | T | C | 1 | a0001c0001t0025g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.196+8778T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706876 | |||||||
| chr6:152706964 | A | G | 1 | a0001c0001t0002g0019 | 4 | HG02683.hp2 HG03491.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+8866A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706964 | |||||||
| chr6:152706988 | C | T | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.196+8890C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706988 | |||||||
| chr6:152706992 | G | A | 1 | a0001c0001t0017g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.196+8894G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152706992 | |||||||
| chr6:152707019 | G | A | 2 | a0001c0001t0012g0130 a0001c0001t0024g0129 |
2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.196+8921G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152707019 | |||||||
| chr6:152707447 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(74): Show |
199 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.196+9349C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152707447 | |||||||
| chr6:152707510 | A | G | 1 | a0001c0001t0035g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+9412A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152707510 | |||||||
| chr6:152707613 | GT | G | 32 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(29): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.196+9521delT | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152707613 | ||||||
| chr6:152707615 | T | A | 32 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(29): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.196+9517T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152707615 | |||||||
| chr6:152707724 | T | C | 4 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(1): Show |
8 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+9626T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152707724 | |||||||
| chr6:152707852 | A | C | 1 | a0001c0001t0002g0049 | 2 | HG00423.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.196+9754A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152707852 | |||||||
| chr6:152707912 | T | A | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.196+9814T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152707912 | |||||||
| chr6:152707988 | G | A | 1 | a0001c0001t0003g0067 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.196+9890G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152707988 | |||||||
| chr6:152708165 | G | A | 42 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(39): Show |
101 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.196+10067G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152708165 | |||||||
| chr6:152708296 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.196+10198C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152708296 | |||||||
| chr6:152708417 | T | C | 1 | a0002c0002t0004g0161 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.196+10319T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152708417 | |||||||
| chr6:152708577 | T | C | 1 | a0001c0001t0023g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.196+10479T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152708577 | |||||||
| chr6:152708649 | G | T | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.196+10551G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152708649 | |||||||
| chr6:152708666 | A | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(150): Show |
368 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.196+10568A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152708666 | |||||||
| chr6:152708737 | C | T | 1 | a0002c0002t0004g0172 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.196+10639C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152708737 | |||||||
| chr6:152708759 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.196+10661A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152708759 | |||||||
| chr6:152708836 | ACCTGAAA others(3811): Show |
A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(150): Show |
368 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.196+10758_197-9069 others(3): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152708836 | ||||||
| chr6:152708860 | AT | A | 6 | a0001c0001t0002g0018 a0001c0001t0003g0021 a0001c0001t0003g0044 others(3): Show |
10 | HG01496.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+10773delT | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152708860 | ||||||
| chr6:152709024 | C | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(1): Show |
8 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+10926C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152709024 | |||||||
| chr6:152709203 | G | A | 1 | a0001c0001t0007g0125 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.196+11105G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152709203 | |||||||
| chr6:152709230 | G | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(1): Show |
8 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+11132G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152709230 | |||||||
| chr6:152709326 | G | T | 1 | a0001c0001t0002g0094 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.196+11228G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152709326 | |||||||
| chr6:152709762 | A | C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0016 others(40): Show |
74 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.196+11664A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152709762 | |||||||
| chr6:152709937 | C | T | 4 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(1): Show |
8 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-11805C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152709937 | |||||||
| chr6:152710001 | G | A | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.197-11741G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152710001 | |||||||
| chr6:152710116 | G | T | 4 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(1): Show |
8 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-11626G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152710116 | |||||||
| chr6:152710263 | A | G | 8 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(5): Show |
12 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.197-11479A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152710263 | |||||||
| chr6:152710283 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.197-11459G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152710283 | |||||||
| chr6:152710643 | C | T | 1 | a0001c0001t0002g0019 | 4 | HG02683.hp2 HG03491.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-11099C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152710643 | |||||||
| chr6:152710773 | G | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(1): Show |
8 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-10969G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152710773 | |||||||
| chr6:152711330 | G | T | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.197-10412G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152711330 | |||||||
| chr6:152711540 | G | T | 1 | a0001c0001t0002g0018 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.197-10202G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152711540 | |||||||
| chr6:152711586 | C | T | 1 | a0001c0001t0035g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-10156C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152711586 | |||||||
| chr6:152711616 | T | A | 3 | a0001c0001t0002g0098 a0001c0001t0003g0088 a0001c0001t0003g0092 |
3 | NA18747.hp2 NA18952.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.197-10126T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152711616 | |||||||
| chr6:152712451 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.197-9291G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152712451 | |||||||
| chr6:152712484 | C | T | 1 | a0001c0001t0002g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.197-9258C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152712484 | |||||||
| chr6:152712492 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.197-9250G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152712492 | |||||||
| chr6:152712706 | T | C | 2 | a0001c0001t0005g0055 a0001c0001t0005g0057 |
2 | NA18947.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.197-9036T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152712706 | |||||||
| chr6:152712724 | C | A | 8 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(5): Show |
12 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.197-9018C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152712724 | |||||||
| chr6:152712796 | T | C | 42 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(39): Show |
101 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.197-8946T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152712796 | |||||||
| chr6:152712797 | G | T | 1 | a0001c0001t0026g0058 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.197-8945G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152712797 | |||||||
| chr6:152712821 | A | G | 1 | a0001c0001t0003g0066 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.197-8921A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152712821 | |||||||
| chr6:152712823 | T | C | 4 | a0001c0001t0008g0010 a0001c0001t0008g0108 a0001c0001t0012g0041 others(1): Show |
9 | HG01099.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.197-8919T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152712823 | |||||||
| chr6:152712881 | G | A | 1 | a0001c0001t0003g0068 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.197-8861G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152712881 | |||||||
| chr6:152712893 | TTATA | T | 28 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(25): Show |
57 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.197-8843_197-8840d others(6): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152712893 | ||||||
| chr6:152712964 | A | T | 1 | a0001c0001t0003g0027 | 3 | HG02258.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.197-8778A>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152712964 | |||||||
| chr6:152713020 | G | T | 76 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(73): Show |
169 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.197-8722G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713020 | |||||||
| chr6:152713113 | T | C | 42 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(39): Show |
101 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.197-8629T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713113 | |||||||
| chr6:152713133 | T | C | 2 | a0003c0003t0001g0011 a0003c0003t0014g0011 |
6 | HG00323.hp2 HG00735.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-8609T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713133 | |||||||
| chr6:152713370 | T | G | 1 | a0001c0001t0035g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-8372T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713370 | |||||||
| chr6:152713415 | A | G | 76 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(73): Show |
169 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.197-8327A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713415 | |||||||
| chr6:152713496 | A | G | 1 | a0003c0003t0001g0156 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.197-8246A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713496 | |||||||
| chr6:152713612 | C | T | 1 | a0001c0001t0002g0037 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.197-8130C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713612 | |||||||
| chr6:152713663 | A | C | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.197-8079A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713663 | |||||||
| chr6:152713766 | C | G | 1 | a0001c0001t0016g0031 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.197-7976C>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713766 | |||||||
| chr6:152713784 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.197-7958C>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713784 | |||||||
| chr6:152713873 | G | A | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.197-7869G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713873 | |||||||
| chr6:152713947 | T | C | 1 | a0001c0001t0003g0069 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.197-7795T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713947 | |||||||
| chr6:152713966 | G | A | 2 | a0001c0001t0012g0130 a0001c0001t0024g0129 |
2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.197-7776G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713966 | |||||||
| chr6:152713972 | G | C | 1 | a0001c0001t0017g0158 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.197-7770G>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713972 | |||||||
| chr6:152713982 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.197-7760A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713982 | |||||||
| chr6:152713986 | C | T | 44 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(41): Show |
103 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.197-7756C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152713986 | |||||||
| chr6:152714126 | C | T | 4 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(1): Show |
8 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-7616C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714126 | |||||||
| chr6:152714257 | GA | G | 44 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(41): Show |
103 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.197-7484delA | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714257 | |||||||
| chr6:152714305 | CT | C | 51 | a0001c0001t0001g0075 a0001c0001t0002g0009 a0001c0001t0002g0023 others(48): Show |
121 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.197-7421delT | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152714305 | ||||||
| chr6:152714305 | CTT | C | 7 | a0001c0001t0003g0072 a0001c0001t0007g0071 a0001c0001t0007g0124 others(4): Show |
7 | HG01081.hp2 HG01123.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-7422_197-7421d others(4): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152714305 | ||||||
| chr6:152714305 | CTTT | C | 32 | a0001c0001t0002g0070 a0001c0001t0003g0127 a0001c0001t0003g0128 others(29): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.197-7423_197-7421d others(5): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152714305 | ||||||
| chr6:152714308 | T | TC | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0152 |
3 | HG01261.hp2 NA18955.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.197-7434_197-7433i others(3): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714308 | |||||||
| chr6:152714309 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(64): Show |
172 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.197-7433T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714309 | |||||||
| chr6:152714310 | T | C | 1 | a0001c0001t0002g0149 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.197-7432T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714310 | |||||||
| chr6:152714472 | C | A | 32 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(29): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.197-7270C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714472 | |||||||
| chr6:152714537 | T | G | 7 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0087 others(4): Show |
7 | HG02083.hp2 HG02155.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-7205T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714537 | |||||||
| chr6:152714614 | T | C | 1 | a0001c0001t0015g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.197-7128T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714614 | |||||||
| chr6:152714646 | C | T | 44 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(41): Show |
103 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.197-7096C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714646 | |||||||
| chr6:152714673 | G | A | 32 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(29): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.197-7069G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714673 | |||||||
| chr6:152714742 | G | A | 32 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(29): Show |
66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.197-7000G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714742 | |||||||
| chr6:152714793 | C | CAT | 3 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0035g0126 |
3 | HG02109.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.197-6939_197-6938d others(4): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152714793 | ||||||
| chr6:152714795 | T | C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
6 | NA18950.hp2 NA18956.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-6947T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714795 | |||||||
| chr6:152714818 | T | C | 76 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(73): Show |
169 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.197-6924T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714818 | |||||||
| chr6:152714835 | G | A | 1 | a0001c0001t0014g0113 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.197-6907G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714835 | |||||||
| chr6:152714853 | C | T | 1 | a0001c0001t0003g0080 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.197-6889C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152714853 | |||||||
| chr6:152715224 | T | C | 1 | a0001c0001t0003g0073 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.197-6518T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152715224 | |||||||
| chr6:152715241 | C | T | 1 | a0001c0001t0003g0079 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.197-6501C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152715241 | |||||||
| chr6:152715242 | G | A | 22 | a0002c0002t0003g0052 a0002c0002t0004g0003 a0002c0002t0004g0028 others(19): Show |
51 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.197-6500G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152715242 | |||||||
| chr6:152715243 | C | T | 21 | a0002c0002t0003g0052 a0002c0002t0004g0003 a0002c0002t0004g0028 others(18): Show |
50 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.197-6499C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152715243 | |||||||
| chr6:152715380 | T | C | 3 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0035g0126 |
3 | HG02109.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.197-6362T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152715380 | |||||||
| chr6:152715440 | CA | C | 44 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(41): Show |
103 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.197-6297delA | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152715440 | ||||||
| chr6:152715454 | C | A | 1 | a0001c0001t0001g0109 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.197-6288C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152715454 | |||||||
| chr6:152715493 | A | G | 1 | a0003c0003t0001g0148 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.197-6249A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152715493 | |||||||
| chr6:152715571 | T | TAA | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(160): Show |
382 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.197-6170_197-6169i others(4): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152715571 | ||||||
| chr6:152715757 | A | C | 1 | a0001c0001t0030g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.197-5985A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152715757 | |||||||
| chr6:152715767 | A | C | 25 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0004g0134 others(22): Show |
54 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.197-5975A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152715767 | |||||||
| chr6:152715873 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.197-5869G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152715873 | |||||||
| chr6:152716009 | T | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(160): Show |
382 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.197-5733T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152716009 | |||||||
| chr6:152716013 | G | GTT | 1 | a0002c0002t0011g0029 | 3 | HG01109.hp2 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.197-5728_197-5727d others(4): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152716013 | ||||||
| chr6:152716152 | G | A | 6 | a0001c0001t0003g0027 a0001c0001t0005g0006 a0001c0001t0005g0055 others(3): Show |
23 | HG01358.hp2 HG01975.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.197-5590G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152716152 | |||||||
| chr6:152716163 | C | T | 75 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(72): Show |
168 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.197-5579C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152716163 | |||||||
| chr6:152716239 | G | A | 1 | a0001c0001t0002g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.197-5503G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152716239 | |||||||
| chr6:152716261 | A | C | 1 | a0001c0001t0002g0095 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.197-5481A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152716261 | |||||||
| chr6:152716278 | C | T | 2 | a0001c0001t0003g0060 a0001c0001t0003g0078 |
2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.197-5464C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152716278 | |||||||
| chr6:152716282 | A | T | 1 | a0001c0001t0003g0027 | 3 | HG02258.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.197-5460A>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152716282 | |||||||
| chr6:152716409 | C | T | 1 | a0002c0002t0010g0165 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.197-5333C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152716409 | |||||||
| chr6:152716445 | T | A | 2 | a0003c0003t0001g0011 a0003c0003t0014g0011 |
6 | HG00323.hp2 HG00735.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-5297T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152716445 | |||||||
| chr6:152716653 | CT | C | 5 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0017g0158 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-5087delT | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152716653 | ||||||
| chr6:152716655 | T | G | 42 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(39): Show |
101 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.197-5087T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152716655 | |||||||
| chr6:152716742 | G | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(1): Show |
8 | HG02257.hp2 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-5000G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152716742 | |||||||
| chr6:152717112 | C | T | 1 | a0003c0003t0001g0147 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.197-4630C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717112 | |||||||
| chr6:152717174 | GA | G | 39 | a0001c0001t0001g0075 a0001c0001t0002g0065 a0001c0001t0002g0070 others(36): Show |
97 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.197-4559delA | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152717174 | ||||||
| chr6:152717188 | T | C | 16 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0002g0004 others(13): Show |
47 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.197-4554T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717188 | |||||||
| chr6:152717195 | A | C | 1 | a0002c0002t0010g0164 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.197-4547A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717195 | |||||||
| chr6:152717197 | C | A | 1 | a0002c0002t0010g0164 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.197-4545C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717197 | |||||||
| chr6:152717198 | A | C | 1 | a0002c0002t0010g0164 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.197-4544A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717198 | |||||||
| chr6:152717280 | G | A | 1 | a0002c0002t0004g0162 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.197-4462G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717280 | |||||||
| chr6:152717470 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(53): Show |
132 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.197-4272C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717470 | |||||||
| chr6:152717555 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.197-4187A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717555 | |||||||
| chr6:152717599 | C | T | 132 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(129): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.197-4143C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717599 | |||||||
| chr6:152717702 | T | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(113): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.197-4040T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717702 | |||||||
| chr6:152717755 | G | A | 30 | a0001c0001t0003g0021 a0001c0001t0003g0044 a0001c0001t0003g0132 others(27): Show |
62 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.197-3987G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717755 | |||||||
| chr6:152717786 | T | G | 1 | a0003c0003t0001g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.197-3956T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717786 | |||||||
| chr6:152717837 | TAAAC | T | 24 | a0001c0001t0004g0107 a0001c0001t0004g0131 a0001c0001t0004g0134 others(21): Show |
52 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.197-3901_197-3898d others(6): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152717837 | ||||||
| chr6:152717875 | G | T | 25 | a0001c0001t0004g0107 a0001c0001t0004g0131 a0001c0001t0004g0134 others(22): Show |
53 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.197-3867G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717875 | |||||||
| chr6:152717886 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.197-3856G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717886 | |||||||
| chr6:152717888 | T | G | 3 | a0003c0003t0001g0144 a0003c0003t0001g0154 a0003c0003t0001g0156 |
3 | HG00140.hp1 HG00733.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.197-3854T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717888 | |||||||
| chr6:152717944 | G | A | 25 | a0001c0001t0004g0107 a0001c0001t0004g0131 a0001c0001t0004g0134 others(22): Show |
53 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.197-3798G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152717944 | |||||||
| chr6:152718210 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.197-3532T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152718210 | |||||||
| chr6:152718300 | C | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(55): Show |
134 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.197-3442C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152718300 | |||||||
| chr6:152718308 | C | A | 28 | a0001c0001t0004g0107 a0001c0001t0004g0131 a0001c0001t0004g0134 others(25): Show |
56 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.197-3434C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152718308 | |||||||
| chr6:152718314 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.197-3428T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152718314 | |||||||
| chr6:152718361 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.197-3381A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152718361 | |||||||
| chr6:152718498 | G | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0020 others(28): Show |
76 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.197-3244G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152718498 | |||||||
| chr6:152718511 | G | T | 11 | a0001c0001t0007g0033 a0001c0001t0007g0061 a0001c0001t0007g0071 others(8): Show |
13 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.197-3231G>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152718511 | |||||||
| chr6:152718702 | G | A | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.197-3040G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152718702 | |||||||
| chr6:152719052 | T | A | 2 | a0005c0007t0001g0135 a0005c0007t0001g0136 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.197-2690T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152719052 | |||||||
| chr6:152719056 | C | T | 1 | a0001c0001t0022g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.197-2686C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152719056 | |||||||
| chr6:152719173 | A | G | 1 | a0001c0001t0002g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.197-2569A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152719173 | |||||||
| chr6:152719214 | T | C | 1 | a0001c0001t0024g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.197-2528T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152719214 | |||||||
| chr6:152719412 | G | A | 27 | a0001c0001t0004g0107 a0001c0001t0004g0131 a0001c0001t0004g0134 others(24): Show |
55 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.197-2330G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152719412 | |||||||
| chr6:152719604 | T | C | 27 | a0001c0001t0004g0107 a0001c0001t0004g0131 a0001c0001t0004g0134 others(24): Show |
55 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.197-2138T>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152719604 | |||||||
| chr6:152719648 | C | T | 1 | a0001c0001t0035g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-2094C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152719648 | |||||||
| chr6:152720014 | C | A | 4 | a0001c0001t0003g0030 a0001c0001t0003g0034 a0001c0001t0009g0034 others(1): Show |
6 | NA18942.hp2 NA18971.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-1728C>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720014 | |||||||
| chr6:152720185 | ATG | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0103 |
3 | HG02922.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.197-1553_197-1552d others(4): Show |
MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 152720185 | ||||||
| chr6:152720226 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.197-1516A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720226 | |||||||
| chr6:152720299 | T | G | 2 | a0001c0001t0012g0041 a0001c0001t0012g0130 |
3 | HG01099.hp2 HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.197-1443T>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720299 | |||||||
| chr6:152720329 | C | T | 28 | a0001c0001t0004g0107 a0001c0001t0004g0131 a0001c0001t0004g0134 others(25): Show |
56 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.197-1413C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720329 | |||||||
| chr6:152720411 | G | A | 1 | a0001c0001t0035g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.197-1331G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720411 | |||||||
| chr6:152720487 | A | G | 2 | a0001c0001t0017g0158 a0001c0001t0026g0058 |
2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.197-1255A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720487 | |||||||
| chr6:152720638 | A | C | 6 | a0001c0001t0007g0033 a0001c0001t0007g0061 a0001c0001t0007g0071 others(3): Show |
7 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-1104A>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720638 | |||||||
| chr6:152720754 | G | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0020 others(28): Show |
76 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.197-988G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720754 | |||||||
| chr6:152720760 | T | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(60): Show |
143 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.197-982T>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720760 | |||||||
| chr6:152720786 | G | A | 2 | a0001c0001t0003g0127 a0001c0001t0003g0128 |
2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.197-956G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720786 | |||||||
| chr6:152720849 | A | G | 3 | a0001c0001t0024g0129 a0001c0001t0025g0133 a0001c0001t0026g0058 |
3 | HG01081.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.197-893A>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720849 | |||||||
| chr6:152720865 | G | A | 3 | a0001c0001t0024g0129 a0001c0001t0025g0133 a0001c0001t0026g0058 |
3 | HG01081.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.197-877G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720865 | |||||||
| chr6:152720869 | C | T | 2 | a0001c0001t0003g0127 a0001c0001t0003g0128 |
2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.197-873C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720869 | |||||||
| chr6:152720958 | C | G | 3 | a0001c0001t0024g0129 a0001c0001t0025g0133 a0001c0001t0026g0058 |
3 | HG01081.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.197-784C>G | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152720958 | |||||||
| chr6:152721068 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(69): Show |
154 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.197-674G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152721068 | |||||||
| chr6:152721193 | G | C | 6 | a0001c0001t0007g0033 a0001c0001t0007g0061 a0001c0001t0007g0071 others(3): Show |
7 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-549G>C | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152721193 | |||||||
| chr6:152721512 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.197-230C>T | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152721512 | |||||||
| chr6:152721522 | G | A | 27 | a0001c0001t0004g0107 a0001c0001t0004g0131 a0001c0001t0004g0134 others(24): Show |
55 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.197-220G>A | MYCT1 | ENSG00000120279.7 | transcript | ENST00000367245.6 | protein_coding | 1/1 | chr6 | 152721522 |