Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1108 |
| ensemblid | ENSG00000111642.16 |
| hgncid | 1919 |
| symbol | CHD4 |
| name | chromodomain helicase DNA binding protein 4 |
| refseq_nuc | NM_001273.5 |
| refseq_prot | NP_001264.2 |
| ensembl_nuc | ENST00000544040.7 |
| ensembl_prot | ENSP00000440542.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 6570082 |
| end | 6607379 |
| strand | - |
| ver | v1.2 |
| region | chr12:6570082-6607379 |
| region5000 | chr12:6565082-6612379 |
| regionname0 | CHD4_chr12_6570082_6607379 |
| regionname5000 | CHD4_chr12_6565082_6612379 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1912 | 205 | 74 | 31 | 74 | 5 | 20 | 50 | CHD4_chr12_6565082_6612379 | CHD4 | MASGL others(1907): Show |
chr12 | 6565082 | 6612379 |
| a0002 | 1/0 | 1912 | 156 | 9 | 39 | 83 | 7 | 17 | 63 | CHD4_chr12_6565082_6612379 | CHD4 | MASGL others(1907): Show |
chr12 | 6565082 | 6612379 |
| a0003 | 0/0 | 1912 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | MASGL others(1907): Show |
chr12 | 6565082 | 6612379 |
| a0004 | 0/0 | 1912 | 4 | 0 | 0 | 3 | 0 | 1 | 3 | CHD4_chr12_6565082_6612379 | CHD4 | MASGL others(1907): Show |
chr12 | 6565082 | 6612379 |
| a0005 | 0/0 | 1912 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | MASGL others(1907): Show |
chr12 | 6565082 | 6612379 |
| a0006 | 0/0 | 1912 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | MASGL others(1907): Show |
chr12 | 6565082 | 6612379 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 5736 | 114 | 65 | 17 | 21 | 2 | 8 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0001c0003 | 0/0 | 5736 | 65 | 0 | 10 | 49 | 0 | 6 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0001c0004 | 0/0 | 5736 | 22 | 8 | 3 | 2 | 3 | 6 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0001c0013 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0001c0014 | 0/0 | 5736 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0001c0016 | 0/0 | 5736 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0001c0017 | 0/0 | 5736 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0002c0001 | 1/0 | 5736 | 136 | 9 | 28 | 76 | 6 | 16 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0002c0005 | 0/0 | 5736 | 15 | 0 | 10 | 4 | 1 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0002c0008 | 0/0 | 5736 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0002c0009 | 0/0 | 5736 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0002c0010 | 0/0 | 5736 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0002c0012 | 0/0 | 5736 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0003c0006 | 0/0 | 5736 | 7 | 7 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0004c0007 | 0/0 | 5736 | 4 | 0 | 0 | 3 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0005c0011 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 | ||
| a0006c0015 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | ATGGC others(5731): Show |
chr12 | 6565082 | 6612379 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 6491 | 77 | 33 | 15 | 19 | 2 | 7 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0001c0002t0002 | 0/0 | 6491 | 34 | 30 | 2 | 1 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0001c0002t0003 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6488): Show |
chr12 | 6565082 | 6612379 |
| a0001c0002t0004 | 0/0 | 6493 | 2 | 2 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6488): Show |
chr12 | 6565082 | 6612379 |
| a0001c0003t0001 | 0/0 | 6491 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0001c0003t0002 | 0/0 | 6491 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0001c0003t0003 | 0/0 | 6493 | 61 | 0 | 10 | 46 | 0 | 5 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6488): Show |
chr12 | 6565082 | 6612379 |
| a0001c0003t0005 | 0/0 | 6491 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0001c0004t0002 | 0/0 | 6491 | 21 | 7 | 3 | 2 | 3 | 6 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0001c0004t0006 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0001c0013t0002 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0001c0014t0001 | 0/0 | 6491 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0001c0016t0003 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6488): Show |
chr12 | 6565082 | 6612379 |
| a0001c0017t0003 | 0/0 | 6493 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6488): Show |
chr12 | 6565082 | 6612379 |
| a0002c0001t0001 | 1/0 | 6491 | 134 | 9 | 27 | 75 | 6 | 16 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0002c0001t0007 | 0/0 | 6491 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0002c0001t0008 | 0/0 | 6491 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0002c0005t0001 | 0/0 | 6491 | 15 | 0 | 10 | 4 | 1 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0002c0008t0001 | 0/0 | 6491 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0002c0009t0001 | 0/0 | 6491 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0002c0010t0001 | 0/0 | 6491 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0002c0012t0001 | 0/0 | 6491 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0003c0006t0002 | 0/0 | 6491 | 7 | 7 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0004c0007t0001 | 0/0 | 6491 | 4 | 0 | 0 | 3 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0005c0011t0001 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| a0006c0015t0002 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | CCCCC others(6486): Show |
chr12 | 6565082 | 6612379 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0034 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0002t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0002 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0003t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0004t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0013t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0014t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0016t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0001c0017t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0001 | 1/0 | 18 | 2 | 1 | 12 | 1 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0003 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0007 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0001t0008g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0005t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0005t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0005t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0005t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0005t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0005t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0005t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0005t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0008t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0009t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0010t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0002c0012t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0003c0006t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0003c0006t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0003c0006t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0003c0006t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0003c0006t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0003c0006t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0003c0006t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0004c0007t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0004c0007t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0004c0007t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0004c0007t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0005c0011t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| a0006c0015t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0002 | g0014 | EUR | GBR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00099 | hp2 | a0002 | c0001 | t0001 | g0156 | EUR | GBR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | GBR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00140 | hp2 | a0002 | c0001 | t0001 | g0206 | EUR | GBR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00280 | hp1 | a0002 | c0005 | t0001 | g0023 | EUR | FIN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0258 | EUR | FIN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00323 | hp1 | a0001 | c0004 | t0002 | g0065 | EUR | FIN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0126 | EUR | FIN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00408 | hp1 | a0002 | c0001 | t0001 | g0290 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0182 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0079 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00544 | hp1 | a0001 | c0003 | t0003 | g0091 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0217 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00558 | hp1 | a0001 | c0003 | t0003 | g0115 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00558 | hp2 | a0002 | c0001 | t0001 | g0158 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0216 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00609 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00621 | hp2 | a0001 | c0003 | t0003 | g0020 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00639 | hp1 | a0002 | c0001 | t0001 | g0157 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0207 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00673 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | CHS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00733 | hp1 | a0001 | c0004 | t0002 | g0062 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00733 | hp2 | a0002 | c0001 | t0001 | g0205 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0170 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0213 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0007 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0024 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0161 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01081 | hp2 | a0002 | c0001 | t0001 | g0031 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01099 | hp2 | a0002 | c0001 | t0001 | g0199 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01106 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01106 | hp2 | a0002 | c0005 | t0001 | g0006 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01109 | hp1 | a0002 | c0005 | t0001 | g0169 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01109 | hp2 | a0001 | c0014 | t0001 | g0255 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01167 | hp1 | a0002 | c0001 | t0001 | g0200 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0081 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01175 | hp2 | a0001 | c0004 | t0002 | g0067 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01192 | hp1 | a0002 | c0005 | t0001 | g0178 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0279 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01243 | hp1 | a0001 | c0003 | t0003 | g0114 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01255 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01257 | hp1 | a0002 | c0005 | t0001 | g0127 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01257 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01258 | hp1 | a0001 | c0003 | t0003 | g0002 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01258 | hp2 | a0002 | c0001 | t0001 | g0024 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0288 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01346 | hp1 | a0001 | c0004 | t0002 | g0063 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0256 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01358 | hp1 | a0001 | c0003 | t0003 | g0002 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01433 | hp1 | a0002 | c0001 | t0008 | g0172 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0195 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0105 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01496 | hp2 | a0002 | c0005 | t0001 | g0152 | AMR | CLM | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0153 | EUR | IBS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01515 | hp2 | a0002 | c0001 | t0001 | g0190 | EUR | IBS | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0247 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0225 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01891 | hp2 | a0003 | c0006 | t0002 | g0043 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01928 | hp1 | a0002 | c0005 | t0001 | g0181 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01928 | hp2 | a0002 | c0001 | t0001 | g0214 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0002 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01943 | hp1 | a0002 | c0005 | t0001 | g0006 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01943 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01952 | hp1 | a0001 | c0003 | t0003 | g0112 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0265 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01975 | hp1 | a0002 | c0005 | t0001 | g0155 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0208 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0212 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01993 | hp1 | a0001 | c0003 | t0003 | g0002 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02004 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02004 | hp2 | a0001 | c0003 | t0003 | g0107 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02027 | hp1 | a0001 | c0003 | t0003 | g0094 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02027 | hp2 | a0001 | c0004 | t0002 | g0066 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02040 | hp1 | a0001 | c0003 | t0003 | g0005 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0180 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0293 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0287 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02074 | hp1 | a0002 | c0001 | t0001 | g0174 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0261 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0019 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02129 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02129 | hp2 | a0002 | c0001 | t0001 | g0192 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02135 | hp1 | a0002 | c0001 | t0001 | g0191 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0028 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0253 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0277 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02148 | hp1 | a0002 | c0001 | t0001 | g0203 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02148 | hp2 | a0002 | c0001 | t0001 | g0171 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | CDX | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | CDX | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02165 | hp1 | a0002 | c0001 | t0001 | g0211 | EAS | CDX | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | CDX | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02257 | hp2 | a0002 | c0001 | t0001 | g0007 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02258 | hp1 | a0002 | c0001 | t0001 | g0202 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02273 | hp1 | a0002 | c0005 | t0001 | g0006 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02273 | hp2 | a0002 | c0001 | t0001 | g0193 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02280 | hp2 | a0001 | c0004 | t0002 | g0015 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02293 | hp2 | a0002 | c0005 | t0001 | g0006 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02300 | hp1 | a0002 | c0009 | t0001 | g0147 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02523 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | KHV | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0266 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02572 | hp2 | a0002 | c0001 | t0001 | g0204 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0276 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02602 | hp2 | a0002 | c0001 | t0001 | g0177 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0054 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0051 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02622 | hp2 | a0003 | c0006 | t0002 | g0044 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0250 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0280 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02683 | hp1 | a0001 | c0004 | t0002 | g0068 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02683 | hp2 | a0002 | c0001 | t0001 | g0201 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02723 | hp2 | a0005 | c0011 | t0001 | g0163 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0198 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02735 | hp2 | a0002 | c0001 | t0001 | g0160 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0240 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0291 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02818 | hp1 | a0001 | c0004 | t0002 | g0072 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0252 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02895 | hp1 | a0003 | c0006 | t0002 | g0048 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0056 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02896 | hp1 | a0003 | c0006 | t0002 | g0047 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02897 | hp1 | a0003 | c0006 | t0002 | g0042 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0264 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0082 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0249 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02976 | hp2 | a0001 | c0004 | t0002 | g0073 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0242 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03017 | hp2 | a0001 | c0004 | t0002 | g0075 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0040 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0060 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0248 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0078 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03195 | hp2 | a0002 | c0001 | t0001 | g0007 | AFR | ESN | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0059 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03225 | hp1 | a0001 | c0004 | t0002 | g0074 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0226 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0274 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03239 | hp2 | a0002 | c0001 | t0001 | g0285 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03453 | hp1 | a0001 | c0013 | t0002 | g0053 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0267 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03491 | hp1 | a0001 | c0004 | t0002 | g0278 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03491 | hp2 | a0002 | c0001 | t0001 | g0209 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0210 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03492 | hp2 | a0002 | c0001 | t0001 | g0029 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03540 | hp1 | a0003 | c0006 | t0002 | g0046 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03540 | hp2 | a0001 | c0004 | t0006 | g0039 | AFR | GWD | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0055 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0140 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03654 | hp2 | a0004 | c0007 | t0001 | g0143 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03669 | hp2 | a0002 | c0010 | t0001 | g0194 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0286 | SAS | STU | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0292 | SAS | STU | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0275 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03704 | hp2 | a0001 | c0003 | t0003 | g0108 | SAS | PJL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03834 | hp1 | a0001 | c0003 | t0003 | g0010 | SAS | BEB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | BEB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0289 | SAS | BEB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0077 | SAS | BEB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0235 | SAS | BEB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0185 | SAS | BEB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0028 | SAS | STU | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG04115 | hp2 | a0001 | c0003 | t0003 | g0111 | SAS | STU | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG04184 | hp1 | a0001 | c0003 | t0003 | g0109 | SAS | BEB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG04184 | hp2 | a0001 | c0004 | t0002 | g0295 | SAS | BEB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG04199 | hp1 | a0001 | c0004 | t0002 | g0076 | SAS | STU | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG04199 | hp2 | a0001 | c0003 | t0003 | g0110 | SAS | STU | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG04204 | hp1 | a0001 | c0004 | t0002 | g0064 | SAS | STU | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0162 | SAS | STU | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | YRI | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | YRI | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | CHB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18612 | hp2 | a0001 | c0003 | t0003 | g0020 | EAS | CHB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18906 | hp1 | a0001 | c0004 | t0002 | g0071 | AFR | YRI | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | YRI | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18939 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18940 | hp1 | a0001 | c0003 | t0003 | g0122 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18940 | hp2 | a0002 | c0001 | t0001 | g0215 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18941 | hp1 | a0001 | c0003 | t0003 | g0098 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18941 | hp2 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0168 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0219 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18946 | hp1 | a0001 | c0003 | t0003 | g0086 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18946 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18951 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18954 | hp1 | a0001 | c0003 | t0003 | g0119 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18959 | hp2 | a0001 | c0003 | t0003 | g0087 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18960 | hp1 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18964 | hp2 | a0004 | c0007 | t0001 | g0144 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18965 | hp2 | a0002 | c0001 | t0001 | g0196 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18967 | hp2 | a0001 | c0003 | t0005 | g0095 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18968 | hp1 | a0001 | c0003 | t0005 | g0104 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0150 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18969 | hp1 | a0001 | c0003 | t0003 | g0093 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18969 | hp2 | a0002 | c0001 | t0001 | g0175 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18970 | hp2 | a0001 | c0003 | t0003 | g0100 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18971 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18972 | hp1 | a0001 | c0003 | t0003 | g0121 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18972 | hp2 | a0002 | c0001 | t0001 | g0186 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18973 | hp1 | a0001 | c0003 | t0003 | g0103 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18973 | hp2 | a0002 | c0001 | t0001 | g0148 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18974 | hp2 | a0001 | c0003 | t0003 | g0089 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18977 | hp1 | a0001 | c0003 | t0003 | g0018 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18977 | hp2 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18978 | hp1 | a0002 | c0001 | t0001 | g0294 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18978 | hp2 | a0001 | c0003 | t0003 | g0283 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18981 | hp1 | a0001 | c0003 | t0002 | g0096 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18981 | hp2 | a0002 | c0001 | t0001 | g0221 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18982 | hp1 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18982 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18987 | hp1 | a0001 | c0003 | t0003 | g0118 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18987 | hp2 | a0002 | c0001 | t0001 | g0222 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18989 | hp1 | a0001 | c0003 | t0003 | g0017 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18989 | hp2 | a0002 | c0001 | t0001 | g0173 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18990 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18992 | hp1 | a0001 | c0003 | t0003 | g0101 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18992 | hp2 | a0002 | c0005 | t0001 | g0154 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18995 | hp1 | a0002 | c0001 | t0001 | g0273 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18995 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18997 | hp1 | a0001 | c0003 | t0003 | g0018 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18997 | hp2 | a0002 | c0001 | t0001 | g0164 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18998 | hp2 | a0002 | c0012 | t0001 | g0188 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18999 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18999 | hp2 | a0002 | c0001 | t0001 | g0176 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19000 | hp1 | a0002 | c0001 | t0001 | g0220 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19000 | hp2 | a0001 | c0003 | t0003 | g0116 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19003 | hp1 | a0002 | c0001 | t0001 | g0149 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19003 | hp2 | a0001 | c0003 | t0003 | g0092 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19004 | hp1 | a0001 | c0003 | t0003 | g0282 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0224 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0183 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19009 | hp1 | a0002 | c0005 | t0001 | g0184 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19010 | hp1 | a0002 | c0001 | t0001 | g0166 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19010 | hp2 | a0001 | c0003 | t0003 | g0102 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19012 | hp1 | a0001 | c0003 | t0003 | g0123 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19012 | hp2 | a0002 | c0005 | t0001 | g0023 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19030 | hp1 | a0001 | c0004 | t0002 | g0069 | AFR | LWK | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0052 | AFR | LWK | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | LWK | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | LWK | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19054 | hp1 | a0001 | c0003 | t0003 | g0120 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0189 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19060 | hp1 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19060 | hp2 | a0001 | c0003 | t0003 | g0113 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19062 | hp1 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19062 | hp2 | a0001 | c0003 | t0003 | g0019 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19063 | hp1 | a0001 | c0004 | t0002 | g0070 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19063 | hp2 | a0001 | c0003 | t0003 | g0117 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19065 | hp1 | a0001 | c0016 | t0003 | g0099 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19065 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0165 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0218 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19070 | hp1 | a0001 | c0003 | t0003 | g0124 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0223 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19074 | hp2 | a0002 | c0001 | t0007 | g0159 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19076 | hp1 | a0001 | c0003 | t0003 | g0088 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19076 | hp2 | a0002 | c0001 | t0001 | g0151 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19077 | hp1 | a0002 | c0001 | t0001 | g0197 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19077 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19080 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19080 | hp2 | a0001 | c0003 | t0003 | g0281 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19081 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19081 | hp2 | a0001 | c0017 | t0003 | g0296 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19082 | hp1 | a0001 | c0003 | t0003 | g0106 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19082 | hp2 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19083 | hp1 | a0001 | c0003 | t0003 | g0284 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0167 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19084 | hp1 | a0004 | c0007 | t0001 | g0146 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19085 | hp1 | a0002 | c0008 | t0001 | g0036 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19085 | hp2 | a0002 | c0005 | t0001 | g0179 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19087 | hp1 | a0002 | c0008 | t0001 | g0036 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19087 | hp2 | a0001 | c0003 | t0003 | g0097 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19088 | hp2 | a0004 | c0007 | t0001 | g0145 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19091 | hp1 | a0001 | c0003 | t0003 | g0017 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19091 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19240 | hp1 | a0001 | c0004 | t0002 | g0015 | AFR | YRI | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA19240 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | YRI | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0057 | AFR | ASW | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | ASW | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA20752 | hp1 | a0001 | c0004 | t0002 | g0014 | EUR | TSI | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0031 | EUR | TSI | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02109 | hp1 | a0003 | c0006 | t0002 | g0045 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0083 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02486 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG02559 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | ACB | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0085 | AFR | MSL | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG06807 | hp1 | a0002 | c0001 | t0001 | g0125 | AFR | USA | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | USA | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18955 | hp1 | a0001 | c0003 | t0003 | g0090 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA18955 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA21309 | hp1 | a0006 | c0015 | t0002 | g0049 | AFR | LWK | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| NA21309 | hp2 | a0002 | c0001 | t0001 | g0187 | AFR | LWK | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0034 | REF | REF | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0001 | g0001 | REF | REF | CHD4_chr12_6565082_6612379 | CHD4 | chr12 | 6565082 | 6612379 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6578884 | G | A | 2 | a0003 a0006 |
8 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
missense_variant | MODERATE | c.4943C>T | p.Ser1648Leu | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 34/40 | 5101/6491 | 4943/5739 | 1648/1912 | chr12 | 6578884 | |||
| chr12:6581703 | G | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.4627C>T | p.Pro1543Ser | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 31/40 | 4785/6491 | 4627/5739 | 1543/1912 | chr12 | 6581703 | |||
| chr12:6601978 | A | C | 1 | a0004 | 4 | HG03654.hp2 NA18964.hp2 NA19084.hp1 others(1): Show |
missense_variant | MODERATE | c.420T>G | p.Asp140Glu | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 4/40 | 578/6491 | 420/5739 | 140/1912 | chr12 | 6601978 | |||
| chr12:6601981 | C | A | 3 | a0001 a0003 a0006 |
212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
missense_variant | MODERATE | c.417G>T | p.Glu139Asp | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 4/40 | 575/6491 | 417/5739 | 139/1912 | chr12 | 6601981 | |||
| chr12:6601984 | C | A | 1 | a0006 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.414G>T | p.Glu138Asp | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 4/40 | 572/6491 | 414/5739 | 138/1912 | chr12 | 6601984 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6573177 | G | C | 1 | a0002c0010 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.5454C>G | p.Leu1818Leu | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/40 | 5612/6491 | 5454/5739 | 1818/1912 | chr12 | 6573177 | |||
| chr12:6581743 | C | T | 1 | a0002c0005 | 15 | HG00280.hp1 HG01106.hp2 HG01109.hp1 others(12): Show |
synonymous_variant | LOW | c.4587G>A | p.Lys1529Lys | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 31/40 | 4745/6491 | 4587/5739 | 1529/1912 | chr12 | 6581743 | |||
| chr12:6582242 | C | T | 1 | a0001c0016 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.4410G>A | p.Pro1470Pro | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 30/40 | 4568/6491 | 4410/5739 | 1470/1912 | chr12 | 6582242 | |||
| chr12:6591919 | T | C | 1 | a0002c0008 | 2 | NA19085.hp1 NA19087.hp1 |
synonymous_variant | LOW | c.3087A>G | p.Ala1029Ala | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 20/40 | 3245/6491 | 3087/5739 | 1029/1912 | chr12 | 6591919 | |||
| chr12:6596119 | G | A | 1 | a0001c0017 | 1 | NA19081.hp2 | synonymous_variant | LOW | c.1911C>T | p.His637His | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 13/40 | 2069/6491 | 1911/5739 | 637/1912 | chr12 | 6596119 | |||
| chr12:6597938 | C | T | 1 | a0002c0009 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.1848G>A | p.Gly616Gly | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/40 | 2006/6491 | 1848/5739 | 616/1912 | chr12 | 6597938 | |||
| chr12:6597986 | G | A | 1 | a0001c0014 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1800C>T | p.Asn600Asn | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/40 | 1958/6491 | 1800/5739 | 600/1912 | chr12 | 6597986 | |||
| chr12:6598360 | G | A | 1 | a0001c0004 | 22 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(19): Show |
synonymous_variant | LOW | c.1548C>T | p.Pro516Pro | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 11/40 | 1706/6491 | 1548/5739 | 516/1912 | chr12 | 6598360 | |||
| chr12:6599893 | G | A | 1 | a0001c0004 | 22 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(19): Show |
synonymous_variant | LOW | c.1362C>T | p.Val454Val | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/40 | 1520/6491 | 1362/5739 | 454/1912 | chr12 | 6599893 | |||
| chr12:6600322 | G | A | 1 | a0002c0012 | 1 | NA18998.hp2 | synonymous_variant | LOW | c.1137C>T | p.Gly379Gly | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 9/40 | 1295/6491 | 1137/5739 | 379/1912 | chr12 | 6600322 | |||
| chr12:6601455 | C | T | 1 | a0001c0013 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.633G>A | p.Glu211Glu | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 6/40 | 791/6491 | 633/5739 | 211/1912 | chr12 | 6601455 | |||
| chr12:6606361 | G | A | 3 | a0001c0003 a0001c0016 a0001c0017 |
67 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(64): Show |
synonymous_variant | LOW | c.13C>T | p.Leu5Leu | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/40 | 171/6491 | 13/5739 | 5/1912 | chr12 | 6606361 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6570157 | C | CTT | 5 | a0001c0002t0003 a0001c0002t0004 a0001c0003t0003 others(2): Show |
66 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*517_*518dupAA | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 40/40 | 518 | chr12 | 6570157 | ||||||
| chr12:6570197 | T | G | 1 | a0002c0001t0008 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479A>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 40/40 | 479 | chr12 | 6570197 | ||||||
| chr12:6570257 | C | T | 1 | a0002c0001t0007 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*419G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 40/40 | 419 | chr12 | 6570257 | ||||||
| chr12:6570577 | G | A | 5 | a0001c0002t0003 a0001c0003t0003 a0001c0003t0005 others(2): Show |
66 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*99C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 40/40 | 99 | chr12 | 6570577 | ||||||
| chr12:6606427 | A | G | 13 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(10): Show |
134 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
5_prime_UTR_variant | MODIFIER | c.-54T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/40 | 54 | chr12 | 6606427 | ||||||
| chr12:6607344 | C | G | 1 | a0001c0004t0006 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-123G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 1/40 | 971 | chr12 | 6607344 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6570710 | G | A | 6 | a0001c0002t0001g0268 a0001c0002t0002g0008 a0001c0002t0002g0077 others(3): Show |
8 | HG01168.hp2 HG02155.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.5722-17C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 39/39 | chr12 | 6570710 | |||||||
| chr12:6570815 | A | G | 1 | a0001c0002t0002g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5721+54T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 39/39 | chr12 | 6570815 | |||||||
| chr12:6571152 | G | A | 1 | a0002c0001t0001g0211 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5558-120C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6571152 | |||||||
| chr12:6571372 | C | T | 6 | a0001c0002t0001g0268 a0001c0002t0002g0008 a0001c0002t0002g0077 others(3): Show |
8 | HG01168.hp2 HG02155.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.5558-340G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6571372 | |||||||
| chr12:6571472 | G | A | 1 | a0001c0002t0002g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5558-440C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6571472 | |||||||
| chr12:6571524 | T | C | 1 | a0002c0001t0001g0192 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.5558-492A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6571524 | |||||||
| chr12:6571548 | G | A | 1 | a0001c0002t0002g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5558-516C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6571548 | |||||||
| chr12:6571686 | C | T | 7 | a0001c0002t0001g0037 a0001c0002t0001g0263 a0001c0002t0001g0264 others(4): Show |
8 | HG01952.hp2 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.5558-654G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6571686 | |||||||
| chr12:6571687 | G | A | 1 | a0002c0001t0001g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.5558-655C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6571687 | |||||||
| chr12:6571731 | C | CG | 116 | a0001c0002t0001g0037 a0001c0002t0001g0225 a0001c0002t0001g0259 others(113): Show |
142 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.5558-700dupC | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6571731 | |||||||
| chr12:6571912 | G | C | 1 | a0001c0002t0001g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5558-880C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6571912 | |||||||
| chr12:6571942 | CAA | C | 5 | a0001c0002t0002g0008 a0001c0002t0002g0077 a0001c0002t0002g0078 others(2): Show |
7 | HG01168.hp2 HG02155.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.5558-912_5558-911d others(4): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6571942 | |||||||
| chr12:6571964 | A | C | 4 | a0001c0002t0002g0008 a0001c0002t0002g0077 a0001c0002t0002g0080 others(1): Show |
6 | HG01168.hp2 HG02155.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.5558-932T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6571964 | |||||||
| chr12:6572043 | C | T | 117 | a0001c0002t0001g0037 a0001c0002t0001g0225 a0001c0002t0001g0259 others(114): Show |
143 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.5558-1011G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572043 | |||||||
| chr12:6572082 | C | T | 2 | a0001c0002t0001g0021 a0001c0002t0001g0129 |
3 | HG02559.hp1 HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.5557+992G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572082 | |||||||
| chr12:6572150 | G | A | 1 | a0002c0001t0001g0288 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5557+924C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572150 | |||||||
| chr12:6572429 | A | C | 1 | a0001c0002t0001g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.5557+645T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572429 | |||||||
| chr12:6572502 | C | T | 53 | a0001c0002t0003g0079 a0001c0002t0004g0051 a0001c0002t0004g0052 others(50): Show |
68 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.5557+572G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572502 | |||||||
| chr12:6572539 | T | A | 1 | a0001c0013t0002g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5557+535A>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572539 | |||||||
| chr12:6572620 | A | G | 55 | a0001c0002t0001g0037 a0001c0002t0001g0225 a0001c0002t0001g0259 others(52): Show |
66 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.5557+454T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572620 | |||||||
| chr12:6572654 | TC | T | 118 | a0001c0002t0001g0037 a0001c0002t0001g0225 a0001c0002t0001g0259 others(115): Show |
144 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.5557+419delG | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572654 | |||||||
| chr12:6572697 | A | G | 51 | a0001c0002t0003g0079 a0001c0003t0003g0002 a0001c0003t0003g0005 others(48): Show |
66 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.5557+377T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572697 | |||||||
| chr12:6572702 | C | T | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG01175.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.5557+372G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572702 | |||||||
| chr12:6572724 | G | A | 1 | a0002c0001t0001g0183 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.5557+350C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572724 | |||||||
| chr12:6572856 | G | A | 1 | a0001c0002t0001g0227 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5557+218C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572856 | |||||||
| chr12:6572875 | T | TA | 9 | a0001c0002t0001g0037 a0001c0002t0001g0263 a0001c0002t0001g0264 others(6): Show |
11 | HG01952.hp2 HG02055.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.5557+198dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 38/39 | chr12 | 6572875 | |||||||
| chr12:6573368 | A | G | 4 | a0001c0003t0003g0018 a0001c0003t0003g0106 a0001c0003t0003g0113 others(1): Show |
5 | NA18977.hp1 NA18997.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.5362-99T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6573368 | |||||||
| chr12:6573845 | A | G | 108 | a0001c0002t0001g0037 a0001c0002t0001g0225 a0001c0002t0001g0259 others(105): Show |
134 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.5362-576T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6573845 | |||||||
| chr12:6573916 | CAA | C | 48 | a0001c0002t0001g0225 a0001c0002t0001g0259 a0001c0002t0001g0268 others(45): Show |
58 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.5362-649_5362-648d others(4): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6573916 | |||||||
| chr12:6573979 | C | T | 1 | a0001c0002t0001g0249 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5362-710G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6573979 | |||||||
| chr12:6574029 | A | G | 1 | a0001c0002t0002g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5362-760T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6574029 | |||||||
| chr12:6574121 | G | A | 117 | a0001c0002t0001g0037 a0001c0002t0001g0225 a0001c0002t0001g0259 others(114): Show |
143 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.5362-852C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6574121 | |||||||
| chr12:6574160 | T | C | 1 | a0001c0004t0002g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5362-891A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6574160 | |||||||
| chr12:6574321 | CAT | C | 1 | a0001c0002t0002g0008 | 3 | HG02809.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5362-1054_5362-105 others(6): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6574321 | |||||||
| chr12:6574479 | CTTAAT | C | 6 | a0002c0001t0001g0012 a0002c0001t0001g0022 a0002c0001t0001g0165 others(3): Show |
9 | HG00438.hp1 NA18944.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.5362-1215_5362-121 others(9): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6574479 | |||||||
| chr12:6574528 | A | G | 8 | a0003c0006t0002g0042 a0003c0006t0002g0043 a0003c0006t0002g0044 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.5362-1259T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6574528 | |||||||
| chr12:6574645 | T | A | 1 | a0001c0004t0002g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5362-1376A>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6574645 | |||||||
| chr12:6574654 | T | G | 23 | a0001c0002t0001g0021 a0001c0002t0001g0129 a0001c0002t0001g0225 others(20): Show |
30 | HG01192.hp2 HG01884.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.5362-1385A>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6574654 | |||||||
| chr12:6575219 | G | A | 2 | a0001c0002t0001g0245 a0001c0002t0001g0246 |
2 | HG01175.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.5362-1950C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6575219 | |||||||
| chr12:6575314 | G | A | 10 | a0001c0002t0001g0139 a0001c0002t0001g0247 a0001c0002t0001g0248 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.5362-2045C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6575314 | |||||||
| chr12:6575449 | C | CA | 42 | a0001c0002t0001g0037 a0001c0002t0001g0129 a0001c0002t0001g0137 others(39): Show |
56 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.5362-2181dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6575449 | |||||||
| chr12:6575512 | T | G | 2 | a0001c0004t0002g0075 a0001c0004t0002g0076 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5362-2243A>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6575512 | |||||||
| chr12:6575600 | C | G | 1 | a0002c0001t0001g0288 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5361+2185G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6575600 | |||||||
| chr12:6575748 | C | G | 1 | a0002c0001t0001g0195 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5361+2037G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6575748 | |||||||
| chr12:6575897 | C | T | 1 | a0001c0002t0001g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5361+1888G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6575897 | |||||||
| chr12:6575957 | C | T | 14 | a0001c0002t0001g0225 a0001c0002t0002g0004 a0001c0002t0002g0050 others(11): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.5361+1828G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6575957 | |||||||
| chr12:6576022 | G | A | 51 | a0001c0002t0003g0079 a0001c0003t0003g0002 a0001c0003t0003g0005 others(48): Show |
66 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.5361+1763C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576022 | |||||||
| chr12:6576049 | CT | C | 9 | a0001c0002t0001g0139 a0001c0002t0001g0247 a0001c0002t0001g0250 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.5361+1735delA | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576049 | |||||||
| chr12:6576096 | C | T | 1 | a0001c0002t0001g0033 | 2 | HG01891.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.5361+1689G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576096 | |||||||
| chr12:6576103 | T | A | 101 | a0001c0002t0001g0225 a0001c0002t0001g0259 a0001c0002t0001g0268 others(98): Show |
126 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.5361+1682A>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576103 | |||||||
| chr12:6576103 | T | C | 1 | a0002c0001t0001g0161 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5361+1682A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576103 | |||||||
| chr12:6576220 | G | A | 1 | a0001c0002t0004g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5361+1565C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576220 | |||||||
| chr12:6576229 | C | G | 1 | a0002c0001t0001g0222 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.5361+1556G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576229 | |||||||
| chr12:6576408 | A | G | 1 | a0001c0013t0002g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5361+1377T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576408 | |||||||
| chr12:6576439 | T | C | 48 | a0001c0002t0001g0225 a0001c0002t0001g0259 a0001c0002t0001g0268 others(45): Show |
58 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.5361+1346A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576439 | |||||||
| chr12:6576487 | G | C | 1 | a0001c0002t0001g0132 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5361+1298C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576487 | |||||||
| chr12:6576502 | A | C | 3 | a0001c0003t0003g0105 a0001c0003t0003g0107 a0001c0003t0003g0112 |
3 | HG01496.hp1 HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.5361+1283T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576502 | |||||||
| chr12:6576633 | G | C | 5 | a0001c0002t0002g0004 a0001c0002t0002g0057 a0001c0002t0002g0058 others(2): Show |
8 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.5361+1152C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576633 | |||||||
| chr12:6576674 | C | T | 1 | a0002c0001t0001g0287 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.5361+1111G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576674 | |||||||
| chr12:6576921 | G | A | 1 | a0002c0005t0001g0155 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5361+864C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576921 | |||||||
| chr12:6576941 | CT | C | 50 | a0001c0002t0001g0225 a0001c0002t0001g0259 a0001c0002t0001g0268 others(47): Show |
60 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.5361+843delA | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6576941 | |||||||
| chr12:6577030 | G | A | 1 | a0002c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5361+755C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6577030 | |||||||
| chr12:6577203 | C | T | 1 | a0001c0002t0001g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5361+582G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6577203 | |||||||
| chr12:6577265 | C | CA | 39 | a0001c0002t0001g0034 a0001c0002t0001g0038 a0001c0002t0001g0126 others(36): Show |
40 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.5361+519dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6577265 | |||||||
| chr12:6577294 | C | T | 3 | a0002c0001t0001g0024 a0002c0001t0001g0153 a0002c0001t0001g0171 |
4 | HG01071.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.5361+491G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6577294 | |||||||
| chr12:6577417 | C | CA | 68 | a0001c0002t0001g0037 a0001c0002t0001g0233 a0001c0002t0001g0263 others(65): Show |
87 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.5361+367dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6577417 | |||||||
| chr12:6577417 | C | CAA | 12 | a0001c0003t0003g0090 a0001c0003t0003g0094 a0001c0003t0003g0102 others(9): Show |
12 | HG02027.hp1 HG02148.hp1 HG04184.hp1 others(9): Show |
intron_variant | MODIFIER | c.5361+366_5361+367d others(4): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6577417 | |||||||
| chr12:6577417 | CA | C | 12 | a0001c0002t0001g0032 a0001c0002t0001g0226 a0001c0002t0001g0227 others(9): Show |
13 | HG00558.hp2 HG00639.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.5361+367delT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6577417 | |||||||
| chr12:6577417 | CAA | C | 53 | a0001c0002t0001g0225 a0001c0002t0001g0259 a0001c0002t0002g0004 others(50): Show |
63 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.5361+366_5361+367d others(4): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6577417 | |||||||
| chr12:6577417 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0258 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5361+358_5361+367d others(12): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6577417 | |||||||
| chr12:6577696 | G | A | 1 | a0002c0001t0001g0216 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.5361+89C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6577696 | |||||||
| chr12:6577758 | G | A | 1 | a0002c0009t0001g0147 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5361+27C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 37/39 | chr12 | 6577758 | |||||||
| chr12:6577971 | T | C | 2 | a0002c0001t0001g0196 a0002c0001t0001g0197 |
2 | NA18965.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.5229-54A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 36/39 | chr12 | 6577971 | |||||||
| chr12:6578592 | G | A | 1 | a0002c0001t0001g0198 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4982-46C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 34/39 | chr12 | 6578592 | |||||||
| chr12:6579042 | TGGTGGCT others(128): Show |
T | 47 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(44): Show |
57 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.4910-260_4910-126d others(2): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579042 | |||||||
| chr12:6579180 | T | A | 1 | a0001c0002t0001g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4910-263A>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579180 | |||||||
| chr12:6579275 | C | T | 7 | a0001c0002t0001g0037 a0001c0002t0001g0263 a0001c0002t0001g0264 others(4): Show |
8 | HG01952.hp2 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4910-358G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579275 | |||||||
| chr12:6579351 | G | A | 47 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(44): Show |
57 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.4910-434C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579351 | |||||||
| chr12:6579546 | T | C | 1 | a0001c0002t0004g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4910-629A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579546 | |||||||
| chr12:6579568 | G | A | 1 | a0001c0002t0002g0056 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4910-651C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579568 | |||||||
| chr12:6579588 | C | CA | 47 | a0001c0002t0001g0034 a0001c0002t0001g0038 a0001c0002t0001g0126 others(44): Show |
48 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.4910-672dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579588 | |||||||
| chr12:6579600 | A | C | 1 | a0002c0001t0001g0294 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.4910-683T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579600 | |||||||
| chr12:6579680 | G | C | 20 | a0001c0004t0002g0014 a0001c0004t0002g0015 a0001c0004t0002g0062 others(17): Show |
22 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.4910-763C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579680 | |||||||
| chr12:6579750 | C | CA | 37 | a0001c0002t0001g0233 a0001c0002t0001g0259 a0001c0002t0001g0268 others(34): Show |
42 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.4910-834dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579750 | |||||||
| chr12:6579778 | C | T | 1 | a0002c0001t0001g0207 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4910-861G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579778 | |||||||
| chr12:6579807 | C | A | 232 | a0001c0002t0001g0021 a0001c0002t0001g0032 a0001c0002t0001g0033 others(229): Show |
276 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.4910-890G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579807 | |||||||
| chr12:6579852 | G | A | 1 | a0001c0002t0001g0251 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4910-935C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579852 | |||||||
| chr12:6579928 | C | T | 2 | a0001c0002t0001g0248 a0001c0002t0001g0253 |
2 | HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.4910-1011G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6579928 | |||||||
| chr12:6580043 | G | A | 47 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(44): Show |
57 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.4909+1001C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580043 | |||||||
| chr12:6580055 | C | CA | 6 | a0001c0002t0001g0253 a0001c0002t0002g0279 a0001c0003t0002g0096 others(3): Show |
6 | HG01192.hp2 HG02074.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.4909+988dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580055 | |||||||
| chr12:6580055 | CA | C | 102 | a0001c0002t0001g0037 a0001c0002t0001g0242 a0001c0002t0001g0263 others(99): Show |
124 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.4909+988delT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580055 | |||||||
| chr12:6580055 | CAA | C | 5 | a0001c0003t0003g0017 a0001c0003t0003g0108 a0001c0003t0003g0120 others(2): Show |
6 | HG03225.hp1 HG03704.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.4909+987_4909+988d others(4): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580055 | |||||||
| chr12:6580229 | A | AAAC | 3 | a0001c0002t0001g0229 a0003c0006t0002g0043 a0003c0006t0002g0045 |
3 | HG00738.hp1 HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.4909+812_4909+814d others(5): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580229 | |||||||
| chr12:6580229 | A | AAACAAC | 6 | a0003c0006t0002g0042 a0003c0006t0002g0044 a0003c0006t0002g0046 others(3): Show |
6 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.4909+809_4909+814d others(8): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580229 | |||||||
| chr12:6580229 | AAAC | A | 7 | a0001c0002t0001g0037 a0001c0002t0001g0263 a0001c0002t0001g0264 others(4): Show |
8 | HG01952.hp2 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4909+812_4909+814d others(5): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580229 | |||||||
| chr12:6580229 | AAACAACA others(2): Show |
A | 28 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0016 others(25): Show |
33 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.4909+806_4909+814d others(11): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580229 | |||||||
| chr12:6580232 | C | A | 59 | a0001c0002t0001g0268 a0001c0002t0002g0008 a0001c0002t0002g0077 others(56): Show |
76 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.4909+812G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580232 | |||||||
| chr12:6580241 | C | A | 27 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0016 others(24): Show |
32 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.4909+803G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580241 | |||||||
| chr12:6580303 | C | T | 1 | a0002c0001t0001g0030 | 2 | NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.4909+741G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580303 | |||||||
| chr12:6580339 | T | C | 1 | a0002c0001t0001g0161 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4909+705A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580339 | |||||||
| chr12:6580377 | G | A | 5 | a0001c0003t0003g0105 a0001c0003t0003g0107 a0001c0003t0003g0112 others(2): Show |
5 | HG00558.hp1 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.4909+667C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580377 | |||||||
| chr12:6580377 | G | T | 1 | a0001c0002t0004g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4909+667C>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580377 | |||||||
| chr12:6580398 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4909+646C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580398 | |||||||
| chr12:6580445 | G | A | 8 | a0003c0006t0002g0042 a0003c0006t0002g0043 a0003c0006t0002g0044 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.4909+599C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580445 | |||||||
| chr12:6580446 | C | T | 1 | a0001c0002t0001g0262 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.4909+598G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580446 | |||||||
| chr12:6580519 | C | A | 28 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0016 others(25): Show |
33 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.4909+525G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580519 | |||||||
| chr12:6580520 | A | T | 28 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0016 others(25): Show |
33 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.4909+524T>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580520 | |||||||
| chr12:6580639 | G | A | 47 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(44): Show |
57 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.4909+405C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580639 | |||||||
| chr12:6580704 | G | GA | 25 | a0001c0002t0001g0021 a0001c0002t0001g0134 a0001c0002t0001g0231 others(22): Show |
30 | HG01109.hp1 HG01175.hp1 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.4909+339dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580704 | |||||||
| chr12:6580704 | G | GAAAAAAA others(3): Show |
3 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0082 |
5 | HG02451.hp1 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4909+330_4909+339d others(12): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580704 | |||||||
| chr12:6580704 | G | GAAAAAAA others(4): Show |
3 | a0001c0002t0002g0083 a0001c0002t0002g0279 a0001c0002t0002g0280 |
3 | HG01192.hp2 HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.4909+329_4909+339d others(13): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580704 | |||||||
| chr12:6580704 | G | GAAAAAAA others(5): Show |
1 | a0001c0004t0002g0067 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4909+328_4909+339d others(14): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580704 | |||||||
| chr12:6580704 | G | GAAAAAAA others(8): Show |
1 | a0001c0004t0002g0075 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4909+325_4909+339d others(17): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580704 | |||||||
| chr12:6580704 | G | GAAAAAAA others(10): Show |
1 | a0001c0004t0002g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4909+323_4909+339d others(19): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580704 | |||||||
| chr12:6580704 | G | GGAAAAAA others(8): Show |
1 | a0001c0002t0004g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4909+339_4909+340i others(17): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580704 | |||||||
| chr12:6580704 | GA | G | 54 | a0001c0002t0001g0037 a0001c0002t0001g0241 a0001c0002t0001g0263 others(51): Show |
69 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.4909+339delT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580704 | |||||||
| chr12:6580710 | A | AAAAAAAA others(5): Show |
6 | a0001c0004t0002g0014 a0001c0004t0002g0062 a0001c0004t0002g0063 others(3): Show |
7 | HG00099.hp1 HG00733.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.4909+333_4909+334i others(14): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580710 | |||||||
| chr12:6580710 | A | AAAAAAAC others(5): Show |
1 | a0001c0004t0002g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4909+333_4909+334i others(14): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580710 | |||||||
| chr12:6580711 | A | AAAAAAAA others(4): Show |
1 | a0001c0004t0002g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4909+332_4909+333i others(13): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580711 | |||||||
| chr12:6580713 | A | AAAACAAA others(5): Show |
1 | a0001c0004t0002g0066 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4909+330_4909+331i others(14): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580713 | |||||||
| chr12:6580714 | A | AAAAAAAA others(5): Show |
2 | a0001c0004t0002g0064 a0001c0004t0002g0065 |
2 | HG00323.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.4909+329_4909+330i others(14): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580714 | |||||||
| chr12:6580715 | A | AAAAAAAC others(5): Show |
7 | a0001c0002t0002g0085 a0001c0004t0002g0015 a0001c0004t0002g0070 others(4): Show |
8 | HG02280.hp2 HG02818.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.4909+328_4909+329i others(14): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580715 | |||||||
| chr12:6580727 | A | AAAAAAAG | 6 | a0001c0002t0001g0268 a0001c0002t0002g0055 a0001c0002t0002g0057 others(3): Show |
6 | HG02145.hp2 HG03453.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.4909+316_4909+317i others(9): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580727 | |||||||
| chr12:6580727 | A | AAAAAAG | 13 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0050 others(10): Show |
18 | HG01168.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.4909+316_4909+317i others(8): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580727 | |||||||
| chr12:6580739 | T | G | 1 | a0001c0002t0001g0131 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4909+305A>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580739 | |||||||
| chr12:6580964 | G | A | 8 | a0003c0006t0002g0042 a0003c0006t0002g0043 a0003c0006t0002g0044 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.4909+80C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6580964 | |||||||
| chr12:6581016 | C | CA | 52 | a0001c0002t0003g0079 a0001c0002t0004g0051 a0001c0003t0003g0002 others(49): Show |
67 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.4909+27dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6581016 | |||||||
| chr12:6581020 | C | A | 52 | a0001c0002t0003g0079 a0001c0002t0004g0051 a0001c0003t0003g0002 others(49): Show |
67 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.4909+24G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6581020 | |||||||
| chr12:6581024 | A | C | 28 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0016 others(25): Show |
33 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.4909+20T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 33/39 | chr12 | 6581024 | |||||||
| chr12:6581487 | G | A | 1 | a0001c0002t0001g0258 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4682-99C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 31/39 | chr12 | 6581487 | |||||||
| chr12:6581517 | G | A | 1 | a0002c0001t0001g0224 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4682-129C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 31/39 | chr12 | 6581517 | |||||||
| chr12:6581984 | G | A | 13 | a0001c0002t0002g0004 a0001c0002t0002g0050 a0001c0002t0002g0054 others(10): Show |
16 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.4515+153C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 30/39 | chr12 | 6581984 | |||||||
| chr12:6582286 | G | A | 47 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(44): Show |
57 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(54): Show |
splice_region_variant&intron_variant | LOW | c.4371-5C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 29/39 | chr12 | 6582286 | |||||||
| chr12:6582318 | C | T | 1 | a0001c0002t0002g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4371-37G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 29/39 | chr12 | 6582318 | |||||||
| chr12:6582393 | G | A | 52 | a0001c0002t0003g0079 a0001c0002t0004g0051 a0001c0003t0003g0002 others(49): Show |
67 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.4371-112C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 29/39 | chr12 | 6582393 | |||||||
| chr12:6582412 | G | A | 1 | a0002c0001t0001g0261 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4371-131C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 29/39 | chr12 | 6582412 | |||||||
| chr12:6583551 | T | G | 2 | a0001c0003t0003g0089 a0001c0003t0003g0090 |
2 | NA18955.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.3880-173A>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6583551 | |||||||
| chr12:6583740 | G | A | 1 | a0002c0005t0001g0154 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3880-362C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6583740 | |||||||
| chr12:6583807 | C | T | 1 | a0001c0002t0003g0079 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3880-429G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6583807 | |||||||
| chr12:6583846 | A | T | 1 | a0001c0002t0001g0258 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3880-468T>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6583846 | |||||||
| chr12:6583882 | G | A | 1 | a0001c0002t0001g0292 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3880-504C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6583882 | |||||||
| chr12:6584366 | A | G | 7 | a0001c0002t0001g0037 a0001c0002t0001g0263 a0001c0002t0001g0264 others(4): Show |
8 | HG01952.hp2 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3880-988T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6584366 | |||||||
| chr12:6584410 | A | T | 1 | a0001c0004t0002g0072 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3880-1032T>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6584410 | |||||||
| chr12:6584482 | C | G | 1 | a0003c0006t0002g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3880-1104G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6584482 | |||||||
| chr12:6584547 | G | A | 53 | a0001c0002t0003g0079 a0001c0002t0004g0051 a0001c0002t0004g0052 others(50): Show |
68 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.3880-1169C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6584547 | |||||||
| chr12:6584621 | C | T | 1 | a0002c0001t0001g0261 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3880-1243G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6584621 | |||||||
| chr12:6585041 | G | T | 1 | a0002c0001t0001g0222 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3880-1663C>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585041 | |||||||
| chr12:6585108 | G | A | 8 | a0003c0006t0002g0042 a0003c0006t0002g0043 a0003c0006t0002g0044 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.3880-1730C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585108 | |||||||
| chr12:6585138 | A | C | 47 | a0001c0002t0003g0079 a0001c0003t0003g0002 a0001c0003t0003g0005 others(44): Show |
62 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.3880-1760T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585138 | |||||||
| chr12:6585308 | G | A | 1 | a0002c0001t0001g0217 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3880-1930C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585308 | |||||||
| chr12:6585334 | G | A | 2 | a0001c0003t0003g0093 a0001c0003t0003g0281 |
2 | NA18969.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.3880-1956C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585334 | |||||||
| chr12:6585388 | G | A | 1 | a0001c0003t0003g0123 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3879+1996C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585388 | |||||||
| chr12:6585489 | A | G | 48 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(45): Show |
58 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.3879+1895T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585489 | |||||||
| chr12:6585714 | G | A | 1 | a0001c0002t0002g0280 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3879+1670C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585714 | |||||||
| chr12:6585767 | C | T | 2 | a0001c0002t0002g0040 a0001c0002t0002g0041 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3879+1617G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585767 | |||||||
| chr12:6585788 | C | CA | 6 | a0001c0002t0001g0237 a0001c0002t0001g0239 a0001c0003t0002g0096 others(3): Show |
6 | HG00423.hp1 HG02027.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.3879+1595dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585788 | |||||||
| chr12:6585788 | CAA | C | 47 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(44): Show |
57 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3879+1594_3879+159 others(6): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585788 | |||||||
| chr12:6585800 | A | C | 1 | a0002c0005t0001g0154 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3879+1584T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585800 | |||||||
| chr12:6585802 | C | A | 8 | a0003c0006t0002g0042 a0003c0006t0002g0043 a0003c0006t0002g0044 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.3879+1582G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585802 | |||||||
| chr12:6585824 | G | A | 6 | a0003c0006t0002g0042 a0003c0006t0002g0044 a0003c0006t0002g0046 others(3): Show |
6 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3879+1560C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585824 | |||||||
| chr12:6585873 | G | A | 1 | a0002c0001t0001g0165 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3879+1511C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585873 | |||||||
| chr12:6585878 | A | G | 5 | a0001c0003t0003g0100 a0001c0003t0003g0101 a0001c0003t0003g0102 others(2): Show |
5 | NA18970.hp2 NA18992.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.3879+1506T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585878 | |||||||
| chr12:6585895 | C | T | 1 | a0001c0003t0003g0112 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3879+1489G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585895 | |||||||
| chr12:6585933 | A | C | 1 | a0001c0002t0001g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3879+1451T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585933 | |||||||
| chr12:6585957 | G | A | 1 | a0001c0004t0002g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3879+1427C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585957 | |||||||
| chr12:6585967 | G | A | 3 | a0001c0002t0002g0077 a0001c0002t0002g0080 a0001c0002t0002g0081 |
3 | HG01168.hp2 HG02155.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3879+1417C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585967 | |||||||
| chr12:6585977 | G | C | 3 | a0001c0002t0002g0077 a0001c0002t0002g0080 a0001c0002t0002g0081 |
3 | HG01168.hp2 HG02155.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3879+1407C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6585977 | |||||||
| chr12:6586108 | A | T | 1 | a0001c0002t0001g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3879+1276T>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6586108 | |||||||
| chr12:6586112 | T | C | 100 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(97): Show |
125 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.3879+1272A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6586112 | |||||||
| chr12:6586137 | G | A | 12 | a0001c0003t0003g0002 a0001c0003t0003g0005 a0001c0003t0003g0019 others(9): Show |
23 | HG00621.hp2 HG00673.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.3879+1247C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6586137 | |||||||
| chr12:6586277 | G | A | 2 | a0002c0001t0001g0025 a0002c0001t0001g0164 |
3 | NA18997.hp2 NA18998.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.3879+1107C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6586277 | |||||||
| chr12:6586322 | A | G | 1 | a0002c0001t0001g0168 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3879+1062T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6586322 | |||||||
| chr12:6586419 | C | A | 48 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(45): Show |
58 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.3879+965G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6586419 | |||||||
| chr12:6586621 | A | G | 100 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(97): Show |
125 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.3879+763T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6586621 | |||||||
| chr12:6586705 | G | GT | 11 | a0001c0002t0001g0253 a0002c0001t0001g0167 a0002c0001t0001g0222 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.3879+678dupA | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6586705 | |||||||
| chr12:6586711 | T | C | 1 | a0002c0001t0001g0261 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3879+673A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6586711 | |||||||
| chr12:6586822 | C | T | 51 | a0001c0002t0003g0079 a0001c0003t0003g0002 a0001c0003t0003g0005 others(48): Show |
66 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.3879+562G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6586822 | |||||||
| chr12:6586931 | C | G | 1 | a0001c0002t0002g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3879+453G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6586931 | |||||||
| chr12:6587040 | T | C | 4 | a0001c0003t0003g0108 a0001c0003t0003g0109 a0001c0003t0003g0110 others(1): Show |
4 | HG03704.hp2 HG04115.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.3879+344A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6587040 | |||||||
| chr12:6587177 | T | C | 2 | a0002c0001t0001g0196 a0002c0001t0001g0197 |
2 | NA18965.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.3879+207A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6587177 | |||||||
| chr12:6587281 | T | C | 7 | a0001c0002t0001g0037 a0001c0002t0001g0263 a0001c0002t0001g0264 others(4): Show |
8 | HG01952.hp2 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3879+103A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 25/39 | chr12 | 6587281 | |||||||
| chr12:6587611 | T | G | 1 | a0001c0002t0001g0270 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3704-52A>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 24/39 | chr12 | 6587611 | |||||||
| chr12:6587690 | C | T | 8 | a0001c0002t0001g0032 a0001c0002t0001g0225 a0001c0002t0001g0226 others(5): Show |
9 | HG00738.hp1 HG01167.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.3703+22G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 24/39 | chr12 | 6587690 | |||||||
| chr12:6588088 | T | G | 2 | a0001c0004t0002g0075 a0001c0004t0002g0076 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3466-139A>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 23/39 | chr12 | 6588088 | |||||||
| chr12:6588114 | C | G | 1 | a0001c0002t0004g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3466-165G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 23/39 | chr12 | 6588114 | |||||||
| chr12:6588128 | T | C | 1 | a0002c0001t0001g0207 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3465+170A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 23/39 | chr12 | 6588128 | |||||||
| chr12:6588160 | A | G | 1 | a0001c0002t0001g0239 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3465+138T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 23/39 | chr12 | 6588160 | |||||||
| chr12:6588187 | G | A | 33 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0038 others(30): Show |
35 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.3465+111C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 23/39 | chr12 | 6588187 | |||||||
| chr12:6588676 | A | G | 99 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(96): Show |
124 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.3341-254T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6588676 | |||||||
| chr12:6588786 | A | C | 1 | a0001c0003t0003g0090 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3341-364T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6588786 | |||||||
| chr12:6588795 | T | C | 1 | a0002c0001t0001g0274 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3341-373A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6588795 | |||||||
| chr12:6588846 | G | A | 52 | a0001c0002t0003g0079 a0001c0003t0003g0002 a0001c0003t0003g0005 others(49): Show |
67 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.3341-424C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6588846 | |||||||
| chr12:6589046 | G | A | 1 | a0001c0004t0002g0067 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3341-624C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6589046 | |||||||
| chr12:6589063 | C | T | 15 | a0002c0001t0001g0011 a0002c0001t0001g0012 a0002c0001t0001g0022 others(12): Show |
21 | HG00438.hp1 HG03688.hp1 NA18944.hp1 others(18): Show |
intron_variant | MODIFIER | c.3341-641G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6589063 | |||||||
| chr12:6589220 | G | A | 1 | a0001c0013t0002g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3341-798C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6589220 | |||||||
| chr12:6589351 | T | C | 1 | a0002c0001t0001g0288 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3341-929A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6589351 | |||||||
| chr12:6589487 | G | A | 1 | a0002c0001t0001g0165 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3341-1065C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6589487 | |||||||
| chr12:6589507 | G | A | 6 | a0001c0002t0002g0004 a0001c0002t0002g0056 a0001c0002t0002g0057 others(3): Show |
9 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.3341-1085C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6589507 | |||||||
| chr12:6589565 | G | A | 1 | a0001c0002t0001g0253 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3341-1143C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6589565 | |||||||
| chr12:6589765 | C | CA | 6 | a0001c0002t0002g0008 a0001c0002t0002g0050 a0001c0002t0002g0077 others(3): Show |
8 | HG01168.hp2 HG02055.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.3341-1344dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6589765 | |||||||
| chr12:6589805 | G | A | 1 | a0001c0002t0004g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3341-1383C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6589805 | |||||||
| chr12:6590005 | C | G | 40 | a0002c0001t0001g0003 a0002c0001t0001g0029 a0002c0001t0001g0030 others(37): Show |
49 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.3340+1461G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590005 | |||||||
| chr12:6590075 | G | A | 1 | a0002c0001t0001g0287 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3340+1391C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590075 | |||||||
| chr12:6590127 | G | A | 1 | a0001c0013t0002g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3340+1339C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590127 | |||||||
| chr12:6590131 | T | C | 7 | a0001c0002t0001g0139 a0001c0002t0001g0247 a0001c0002t0001g0250 others(4): Show |
7 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.3340+1335A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590131 | |||||||
| chr12:6590204 | G | GA | 100 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(97): Show |
125 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.3340+1261dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590204 | |||||||
| chr12:6590279 | C | T | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0234 |
3 | HG02056.hp1 HG02132.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.3340+1187G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590279 | |||||||
| chr12:6590313 | G | C | 1 | a0001c0002t0001g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3340+1153C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590313 | |||||||
| chr12:6590381 | T | C | 47 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(44): Show |
57 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3340+1085A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590381 | |||||||
| chr12:6590395 | T | C | 5 | a0001c0002t0002g0008 a0001c0002t0002g0077 a0001c0002t0002g0078 others(2): Show |
7 | HG01168.hp2 HG02155.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3340+1071A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590395 | |||||||
| chr12:6590488 | G | A | 13 | a0001c0002t0002g0004 a0001c0002t0002g0050 a0001c0002t0002g0054 others(10): Show |
16 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3340+978C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590488 | |||||||
| chr12:6590597 | T | C | 1 | a0001c0004t0002g0064 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3340+869A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590597 | |||||||
| chr12:6590668 | T | G | 1 | a0002c0001t0001g0166 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3340+798A>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590668 | |||||||
| chr12:6590699 | C | T | 100 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(97): Show |
125 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.3340+767G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590699 | |||||||
| chr12:6590849 | G | A | 1 | a0001c0004t0002g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3340+617C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590849 | |||||||
| chr12:6590851 | G | A | 1 | a0001c0002t0001g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3340+615C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590851 | |||||||
| chr12:6590919 | T | TC | 8 | a0003c0006t0002g0042 a0003c0006t0002g0043 a0003c0006t0002g0044 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.3340+546dupG | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590919 | |||||||
| chr12:6590980 | G | A | 47 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(44): Show |
57 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3340+486C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6590980 | |||||||
| chr12:6591122 | C | CA | 85 | a0001c0002t0001g0037 a0001c0002t0001g0038 a0001c0002t0001g0132 others(82): Show |
92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.3340+343dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6591122 | |||||||
| chr12:6591122 | C | CAA | 22 | a0001c0002t0001g0035 a0001c0002t0001g0134 a0001c0002t0001g0139 others(19): Show |
23 | HG00140.hp2 HG01109.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.3340+342_3340+343d others(4): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6591122 | |||||||
| chr12:6591122 | CA | C | 47 | a0001c0002t0002g0004 a0001c0002t0002g0054 a0001c0002t0002g0055 others(44): Show |
57 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.3340+343delT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6591122 | |||||||
| chr12:6591135 | A | C | 1 | a0001c0002t0002g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3340+331T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6591135 | |||||||
| chr12:6591143 | A | AC | 3 | a0001c0002t0001g0268 a0001c0002t0002g0059 a0001c0002t0002g0081 |
3 | HG01168.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3340+322_3340+323i others(3): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6591143 | |||||||
| chr12:6591143 | A | C | 16 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0050 others(13): Show |
21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3340+323T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6591143 | |||||||
| chr12:6591147 | A | C | 1 | a0002c0001t0001g0274 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3340+319T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6591147 | |||||||
| chr12:6591445 | A | C | 2 | a0001c0002t0001g0247 a0001c0002t0001g0257 |
2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3340+21T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6591445 | |||||||
| chr12:6591445 | A | G | 3 | a0002c0001t0001g0218 a0002c0001t0001g0219 a0002c0001t0001g0220 |
3 | NA18944.hp2 NA19000.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.3340+21T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 22/39 | chr12 | 6591445 | |||||||
| chr12:6591614 | G | A | 1 | a0001c0002t0002g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3223-31C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 21/39 | chr12 | 6591614 | |||||||
| chr12:6591622 | T | G | 1 | a0002c0001t0001g0207 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3223-39A>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 21/39 | chr12 | 6591622 | |||||||
| chr12:6592609 | G | A | 1 | a0001c0002t0002g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2775-43C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 18/39 | chr12 | 6592609 | |||||||
| chr12:6592613 | G | T | 1 | a0002c0001t0001g0294 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2775-47C>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 18/39 | chr12 | 6592613 | |||||||
| chr12:6592984 | G | A | 3 | a0003c0006t0002g0042 a0003c0006t0002g0047 a0003c0006t0002g0048 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2652+107C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 17/39 | chr12 | 6592984 | |||||||
| chr12:6592988 | ATTTTCCC others(20): Show |
A | 1 | a0001c0002t0001g0033 | 2 | HG01891.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2652+76_2652+102de others(28): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 17/39 | chr12 | 6592988 | |||||||
| chr12:6593335 | C | T | 7 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0016 others(4): Show |
10 | HG01192.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2514+81G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 16/39 | chr12 | 6593335 | |||||||
| chr12:6593393 | G | A | 7 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0016 others(4): Show |
10 | HG01192.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2514+23C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 16/39 | chr12 | 6593393 | |||||||
| chr12:6593649 | G | GGCCCCAG others(9): Show |
1 | a0001c0002t0004g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2314-49_2314-34dup others(16): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 15/39 | chr12 | 6593649 | |||||||
| chr12:6593997 | G | A | 1 | a0002c0005t0001g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2314-381C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 15/39 | chr12 | 6593997 | |||||||
| chr12:6594005 | T | C | 1 | a0001c0004t0002g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2314-389A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 15/39 | chr12 | 6594005 | |||||||
| chr12:6594006 | T | C | 27 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0016 others(24): Show |
32 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.2314-390A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 15/39 | chr12 | 6594006 | |||||||
| chr12:6594132 | G | A | 2 | a0001c0002t0001g0021 a0001c0002t0001g0129 |
3 | HG02559.hp1 HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2313+327C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 15/39 | chr12 | 6594132 | |||||||
| chr12:6594245 | C | A | 1 | a0001c0004t0002g0295 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2313+214G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 15/39 | chr12 | 6594245 | |||||||
| chr12:6594358 | G | A | 1 | a0001c0003t0003g0094 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2313+101C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 15/39 | chr12 | 6594358 | |||||||
| chr12:6594381 | A | C | 5 | a0001c0002t0002g0008 a0001c0002t0002g0077 a0001c0002t0002g0078 others(2): Show |
7 | HG01168.hp2 HG02155.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2313+78T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 15/39 | chr12 | 6594381 | |||||||
| chr12:6594429 | C | A | 2 | a0001c0002t0001g0266 a0001c0002t0001g0267 |
2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2313+30G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 15/39 | chr12 | 6594429 | |||||||
| chr12:6594886 | G | A | 1 | a0002c0001t0001g0208 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2122-236C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 14/39 | chr12 | 6594886 | |||||||
| chr12:6595003 | C | G | 13 | a0001c0004t0002g0014 a0001c0004t0002g0062 a0001c0004t0002g0063 others(10): Show |
14 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.2121+331G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 14/39 | chr12 | 6595003 | |||||||
| chr12:6595047 | T | A | 100 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(97): Show |
125 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.2121+287A>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 14/39 | chr12 | 6595047 | |||||||
| chr12:6595181 | G | C | 2 | a0002c0005t0001g0179 a0002c0005t0001g0184 |
2 | NA19009.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2121+153C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 14/39 | chr12 | 6595181 | |||||||
| chr12:6595267 | T | A | 1 | a0002c0001t0001g0180 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2121+67A>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 14/39 | chr12 | 6595267 | |||||||
| chr12:6595285 | G | A | 1 | a0001c0002t0002g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2121+49C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 14/39 | chr12 | 6595285 | |||||||
| chr12:6595788 | C | CA | 70 | a0001c0002t0001g0244 a0001c0002t0001g0245 a0001c0002t0001g0246 others(67): Show |
85 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2024+217dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 13/39 | chr12 | 6595788 | |||||||
| chr12:6595788 | CA | C | 47 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(44): Show |
55 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2024+217delT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 13/39 | chr12 | 6595788 | |||||||
| chr12:6595956 | CA | C | 8 | a0001c0002t0001g0263 a0001c0003t0003g0086 a0001c0003t0003g0087 others(5): Show |
8 | HG02897.hp2 HG03491.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.2024+49delT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 13/39 | chr12 | 6595956 | |||||||
| chr12:6596214 | C | T | 27 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0016 others(24): Show |
32 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1893-77G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596214 | |||||||
| chr12:6596229 | A | C | 13 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0001g0231 others(10): Show |
14 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1893-92T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596229 | |||||||
| chr12:6596478 | G | A | 1 | a0001c0004t0002g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1893-341C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596478 | |||||||
| chr12:6596486 | T | TA | 7 | a0001c0002t0001g0133 a0001c0002t0001g0134 a0001c0003t0005g0095 others(4): Show |
7 | HG00597.hp1 HG01168.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1893-350dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596486 | |||||||
| chr12:6596486 | TA | T | 5 | a0001c0002t0001g0021 a0001c0002t0001g0129 a0002c0001t0001g0148 others(2): Show |
6 | HG02559.hp1 HG02622.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1893-350delT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596486 | |||||||
| chr12:6596522 | G | A | 1 | a0002c0001t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1893-385C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596522 | |||||||
| chr12:6596528 | G | A | 1 | a0001c0004t0002g0070 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1893-391C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596528 | |||||||
| chr12:6596771 | G | T | 33 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0038 others(30): Show |
35 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1893-634C>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596771 | |||||||
| chr12:6596778 | C | T | 7 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0016 others(4): Show |
10 | HG01192.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1893-641G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596778 | |||||||
| chr12:6596781 | C | A | 1 | a0001c0002t0001g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1893-644G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596781 | |||||||
| chr12:6596787 | G | A | 2 | a0002c0001t0001g0209 a0002c0001t0001g0210 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1893-650C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596787 | |||||||
| chr12:6596964 | A | C | 53 | a0001c0002t0003g0079 a0001c0002t0004g0051 a0001c0002t0004g0052 others(50): Show |
68 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1893-827T>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596964 | |||||||
| chr12:6596998 | G | A | 18 | a0001c0002t0001g0135 a0002c0001t0001g0003 a0002c0001t0001g0030 others(15): Show |
25 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1893-861C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6596998 | |||||||
| chr12:6597046 | G | C | 53 | a0001c0002t0003g0079 a0001c0002t0004g0051 a0001c0002t0004g0052 others(50): Show |
68 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1892+848C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597046 | |||||||
| chr12:6597094 | C | T | 1 | a0001c0002t0001g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1892+800G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597094 | |||||||
| chr12:6597113 | C | CA | 48 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(45): Show |
58 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1892+780dupT | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597113 | |||||||
| chr12:6597209 | G | A | 1 | a0001c0002t0002g0081 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1892+685C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597209 | |||||||
| chr12:6597315 | G | A | 100 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(97): Show |
125 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1892+579C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597315 | |||||||
| chr12:6597364 | G | C | 1 | a0002c0012t0001g0188 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1892+530C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597364 | |||||||
| chr12:6597423 | G | A | 2 | a0001c0002t0002g0040 a0001c0002t0002g0041 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1892+471C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597423 | |||||||
| chr12:6597578 | G | A | 100 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(97): Show |
125 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1892+316C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597578 | |||||||
| chr12:6597671 | C | G | 7 | a0001c0002t0001g0259 a0001c0002t0002g0009 a0001c0002t0002g0016 others(4): Show |
10 | HG01192.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1892+223G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597671 | |||||||
| chr12:6597722 | C | T | 8 | a0003c0006t0002g0042 a0003c0006t0002g0043 a0003c0006t0002g0044 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1892+172G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597722 | |||||||
| chr12:6597790 | C | A | 1 | a0001c0003t0003g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1892+104G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597790 | |||||||
| chr12:6597805 | T | G | 7 | a0001c0002t0001g0037 a0001c0002t0001g0263 a0001c0002t0001g0264 others(4): Show |
8 | HG01952.hp2 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1892+89A>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597805 | |||||||
| chr12:6597816 | G | A | 53 | a0001c0002t0003g0079 a0001c0002t0004g0051 a0001c0002t0004g0052 others(50): Show |
68 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1892+78C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 12/39 | chr12 | 6597816 | |||||||
| chr12:6598147 | C | T | 2 | a0001c0002t0002g0040 a0001c0002t0002g0041 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1687-48G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 11/39 | chr12 | 6598147 | |||||||
| chr12:6598219 | T | C | 8 | a0003c0006t0002g0042 a0003c0006t0002g0043 a0003c0006t0002g0044 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1686+3A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 11/39 | chr12 | 6598219 | |||||||
| chr12:6598430 | G | A | 2 | a0001c0002t0001g0136 a0001c0002t0001g0256 |
2 | HG01346.hp2 HG01361.hp2 |
splice_region_variant&intron_variant | LOW | c.1483-5C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6598430 | |||||||
| chr12:6598463 | C | T | 8 | a0001c0002t0001g0032 a0001c0002t0001g0225 a0001c0002t0001g0226 others(5): Show |
9 | HG00738.hp1 HG01167.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1483-38G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6598463 | |||||||
| chr12:6598558 | C | G | 5 | a0001c0002t0002g0008 a0001c0002t0002g0077 a0001c0002t0002g0078 others(2): Show |
7 | HG01168.hp2 HG02155.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483-133G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6598558 | |||||||
| chr12:6598576 | C | T | 1 | a0001c0002t0004g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1483-151G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6598576 | |||||||
| chr12:6598582 | G | A | 1 | a0001c0004t0002g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1483-157C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6598582 | |||||||
| chr12:6598780 | G | A | 1 | a0001c0002t0001g0257 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1483-355C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6598780 | |||||||
| chr12:6598855 | A | T | 1 | a0001c0002t0001g0033 | 2 | HG01891.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1483-430T>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6598855 | |||||||
| chr12:6598977 | T | C | 1 | a0001c0002t0001g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1483-552A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6598977 | |||||||
| chr12:6599452 | T | A | 1 | a0002c0001t0001g0031 | 2 | HG01081.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1482+321A>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6599452 | |||||||
| chr12:6599593 | T | A | 1 | a0001c0002t0001g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1482+180A>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6599593 | |||||||
| chr12:6599647 | A | T | 13 | a0001c0004t0002g0014 a0001c0004t0002g0062 a0001c0004t0002g0063 others(10): Show |
14 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1482+126T>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6599647 | |||||||
| chr12:6599732 | C | T | 20 | a0001c0004t0002g0014 a0001c0004t0002g0015 a0001c0004t0002g0062 others(17): Show |
22 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1482+41G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 10/39 | chr12 | 6599732 | |||||||
| chr12:6600116 | C | A | 1 | a0002c0001t0001g0217 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1242+101G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 9/39 | chr12 | 6600116 | |||||||
| chr12:6600150 | C | T | 13 | a0001c0002t0003g0079 a0001c0003t0003g0010 a0001c0003t0003g0086 others(10): Show |
15 | HG00423.hp2 HG00544.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.1242+67G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 9/39 | chr12 | 6600150 | |||||||
| chr12:6600163 | T | C | 1 | a0002c0001t0001g0223 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1242+54A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 9/39 | chr12 | 6600163 | |||||||
| chr12:6600481 | T | A | 6 | a0002c0001t0001g0218 a0002c0001t0001g0219 a0002c0001t0001g0220 others(3): Show |
6 | NA18944.hp2 NA18981.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063+53A>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 8/39 | chr12 | 6600481 | |||||||
| chr12:6600699 | C | CGTTTCAA others(15): Show |
1 | a0002c0001t0001g0189 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.928-31_928-30insTC others(20): Show |
CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 7/39 | chr12 | 6600699 | |||||||
| chr12:6600724 | G | A | 1 | a0002c0001t0001g0224 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.928-55C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 7/39 | chr12 | 6600724 | |||||||
| chr12:6600779 | G | A | 49 | a0002c0001t0001g0003 a0002c0001t0001g0007 a0002c0001t0001g0029 others(46): Show |
61 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.928-110C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 7/39 | chr12 | 6600779 | |||||||
| chr12:6601271 | A | G | 9 | a0001c0002t0001g0032 a0001c0002t0001g0225 a0001c0002t0001g0226 others(6): Show |
10 | HG00738.hp1 HG01167.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.799+18T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 6/39 | chr12 | 6601271 | |||||||
| chr12:6601957 | C | T | 2 | a0001c0004t0002g0062 a0001c0004t0002g0063 |
2 | HG00733.hp1 HG01346.hp1 |
splice_region_variant&intron_variant | LOW | c.438+3G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 4/39 | chr12 | 6601957 | |||||||
| chr12:6602285 | A | G | 2 | a0001c0002t0001g0141 a0001c0002t0001g0142 |
2 | HG02071.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.222+91T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 3/39 | chr12 | 6602285 | |||||||
| chr12:6602590 | C | T | 1 | a0002c0001t0001g0140 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.101-93G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6602590 | |||||||
| chr12:6602919 | T | C | 1 | a0001c0002t0001g0258 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.101-422A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6602919 | |||||||
| chr12:6603041 | C | T | 1 | a0001c0002t0002g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.101-544G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6603041 | |||||||
| chr12:6603155 | C | G | 1 | a0001c0002t0001g0139 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.101-658G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6603155 | |||||||
| chr12:6603190 | C | T | 1 | a0002c0001t0001g0138 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.101-693G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6603190 | |||||||
| chr12:6603550 | G | C | 1 | a0001c0002t0004g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.101-1053C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6603550 | |||||||
| chr12:6603566 | C | CG | 61 | a0001c0002t0001g0126 a0001c0002t0001g0130 a0001c0002t0001g0131 others(58): Show |
76 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.101-1070dupC | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6603566 | |||||||
| chr12:6603569 | G | C | 1 | a0002c0008t0001g0036 | 2 | NA19085.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.101-1072C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6603569 | |||||||
| chr12:6603593 | C | T | 20 | a0001c0004t0002g0014 a0001c0004t0002g0015 a0001c0004t0002g0062 others(17): Show |
22 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.101-1096G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6603593 | |||||||
| chr12:6603814 | G | A | 34 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0008 others(31): Show |
41 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.101-1317C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6603814 | |||||||
| chr12:6603823 | C | T | 1 | a0001c0002t0004g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.101-1326G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6603823 | |||||||
| chr12:6604049 | G | A | 2 | a0001c0002t0002g0084 a0001c0002t0002g0085 |
2 | HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.101-1552C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6604049 | |||||||
| chr12:6604072 | C | T | 2 | a0001c0002t0001g0021 a0001c0002t0001g0129 |
3 | HG02559.hp1 HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.101-1575G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6604072 | |||||||
| chr12:6604248 | T | G | 2 | a0001c0002t0002g0040 a0001c0002t0002g0041 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.101-1751A>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6604248 | |||||||
| chr12:6604284 | A | G | 109 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(106): Show |
134 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.101-1787T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6604284 | |||||||
| chr12:6604298 | C | T | 1 | a0002c0001t0001g0128 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.101-1801G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6604298 | |||||||
| chr12:6604470 | C | A | 48 | a0001c0002t0001g0259 a0001c0002t0001g0268 a0001c0002t0002g0004 others(45): Show |
58 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.100+1804G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6604470 | |||||||
| chr12:6604626 | A | G | 1 | a0002c0005t0001g0127 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.100+1648T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6604626 | |||||||
| chr12:6604900 | T | C | 1 | a0001c0002t0001g0260 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.100+1374A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6604900 | |||||||
| chr12:6604925 | G | A | 12 | a0001c0003t0003g0002 a0001c0003t0003g0005 a0001c0003t0003g0019 others(9): Show |
23 | HG00621.hp2 HG00673.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.100+1349C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6604925 | |||||||
| chr12:6604940 | A | G | 53 | a0001c0002t0004g0051 a0001c0002t0004g0052 a0001c0003t0002g0096 others(50): Show |
68 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.100+1334T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6604940 | |||||||
| chr12:6604963 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.100+1311G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6604963 | |||||||
| chr12:6605172 | T | A | 1 | a0001c0003t0003g0124 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.100+1102A>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6605172 | |||||||
| chr12:6605272 | G | A | 1 | a0002c0001t0001g0261 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100+1002C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6605272 | |||||||
| chr12:6605470 | G | A | 1 | a0001c0002t0001g0262 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.100+804C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6605470 | |||||||
| chr12:6605502 | T | C | 117 | a0001c0002t0001g0037 a0001c0002t0001g0263 a0001c0002t0001g0264 others(114): Show |
143 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.100+772A>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6605502 | |||||||
| chr12:6605505 | C | A | 5 | a0001c0002t0001g0038 a0001c0002t0001g0269 a0001c0002t0001g0270 others(2): Show |
6 | HG00438.hp2 HG00673.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+769G>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6605505 | |||||||
| chr12:6605511 | G | A | 2 | a0002c0001t0001g0273 a0002c0001t0001g0294 |
2 | NA18978.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.100+763C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6605511 | |||||||
| chr12:6605740 | G | A | 1 | a0002c0001t0001g0274 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.100+534C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6605740 | |||||||
| chr12:6605812 | A | G | 2 | a0002c0001t0001g0125 a0002c0001t0001g0285 |
2 | HG03239.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.100+462T>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6605812 | |||||||
| chr12:6605873 | C | G | 9 | a0001c0002t0002g0050 a0003c0006t0002g0042 a0003c0006t0002g0043 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.100+401G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6605873 | |||||||
| chr12:6606256 | C | T | 51 | a0001c0003t0002g0096 a0001c0003t0003g0002 a0001c0003t0003g0005 others(48): Show |
66 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.100+18G>A | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 2/39 | chr12 | 6606256 | |||||||
| chr12:6606464 | G | C | 1 | a0001c0002t0001g0276 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-78-13C>G | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 1/39 | chr12 | 6606464 | |||||||
| chr12:6606814 | T | TG | 18 | a0001c0002t0001g0291 a0001c0002t0001g0292 a0001c0002t0001g0293 others(15): Show |
18 | HG00408.hp1 HG01192.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-78-364dupC | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 1/39 | chr12 | 6606814 | |||||||
| chr12:6606906 | C | G | 2 | a0001c0002t0002g0040 a0001c0002t0002g0041 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-79+394G>C | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 1/39 | chr12 | 6606906 | |||||||
| chr12:6607055 | G | A | 1 | a0001c0002t0002g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-79+245C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 1/39 | chr12 | 6607055 | |||||||
| chr12:6607091 | G | A | 1 | a0001c0004t0002g0295 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-79+209C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 1/39 | chr12 | 6607091 | |||||||
| chr12:6607168 | G | A | 1 | a0001c0017t0003g0296 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-79+132C>T | CHD4 | ENSG00000111642.16 | transcript | ENST00000544040.7 | protein_coding | 1/39 | chr12 | 6607168 |