Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80319 |
| ensemblid | ENSG00000168772.12 |
| hgncid | 24593 |
| symbol | CXXC4 |
| name | CXXC finger protein 4 |
| refseq_nuc | NM_025212.4 |
| refseq_prot | NP_079488.2 |
| ensembl_nuc | ENST00000394767.3 |
| ensembl_prot | ENSP00000378248.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 104468308 |
| end | 104494894 |
| strand | - |
| ver | v1.2 |
| region | chr4:104468308-104494894 |
| region5000 | chr4:104463308-104499894 |
| regionname0 | CXXC4_chr4_104468308_104494894 |
| regionname5000 | CXXC4_chr4_104463308_104499894 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 367 | 302 | 82 | 58 | 119 | 8 | 33 | 94 | CXXC4_chr4_104463308_104499894 | CXXC4 | MNTNV others(362): Show |
chr4 | 104463308 | 104499894 |
| a0002 | 0/0 | 195 | 20 | 4 | 7 | 6 | 0 | 3 | 4 | CXXC4_chr4_104463308_104499894 | CXXC4 | MNTNV others(190): Show |
chr4 | 104463308 | 104499894 |
| a0003 | 0/0 | 367 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | CXXC4_chr4_104463308_104499894 | CXXC4 | MNTNV others(362): Show |
chr4 | 104463308 | 104499894 |
| a0004 | 0/0 | 367 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | MNTNV others(362): Show |
chr4 | 104463308 | 104499894 |
| a0005 | 0/0 | 367 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | MNTNV others(362): Show |
chr4 | 104463308 | 104499894 |
| a0006 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | MNTNV others(356): Show |
chr4 | 104463308 | 104499894 |
| a0007 | 0/0 | 367 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | MNTNV others(362): Show |
chr4 | 104463308 | 104499894 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1101 | 300 | 81 | 57 | 119 | 8 | 33 | CXXC4_chr4_104463308_104499894 | CXXC4 | ATGAA others(1096): Show |
chr4 | 104463308 | 104499894 | ||
| a0001c0005 | 0/0 | 1101 | 2 | 1 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | ATGAA others(1096): Show |
chr4 | 104463308 | 104499894 | ||
| a0002c0002 | 0/0 | 1102 | 20 | 4 | 7 | 6 | 0 | 3 | CXXC4_chr4_104463308_104499894 | CXXC4 | ATGAA others(1097): Show |
chr4 | 104463308 | 104499894 | ||
| a0003c0003 | 0/0 | 1101 | 5 | 0 | 0 | 5 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | ATGAA others(1096): Show |
chr4 | 104463308 | 104499894 | ||
| a0004c0004 | 0/0 | 1101 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | ATGAA others(1096): Show |
chr4 | 104463308 | 104499894 | ||
| a0005c0007 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | ATGAA others(1096): Show |
chr4 | 104463308 | 104499894 | ||
| a0006c0008 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | ATGAA others(1078): Show |
chr4 | 104463308 | 104499894 | ||
| a0007c0006 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | ATGAA others(1096): Show |
chr4 | 104463308 | 104499894 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5569 | 91 | 4 | 18 | 53 | 2 | 12 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5564): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0002 | 0/0 | 5572 | 56 | 9 | 16 | 19 | 3 | 9 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0003 | 0/0 | 5570 | 40 | 18 | 1 | 20 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5565): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0004 | 0/0 | 5573 | 25 | 1 | 6 | 17 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5568): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0005 | 0/0 | 5571 | 4 | 1 | 0 | 1 | 0 | 2 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0006 | 0/0 | 5571 | 7 | 6 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0007 | 0/0 | 5571 | 8 | 6 | 1 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0008 | 0/0 | 5572 | 6 | 6 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0009 | 0/0 | 5573 | 6 | 0 | 1 | 1 | 2 | 2 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5568): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0010 | 0/0 | 5572 | 3 | 3 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0011 | 0/0 | 5572 | 4 | 3 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0012 | 0/0 | 5572 | 3 | 3 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0013 | 0/0 | 5573 | 4 | 0 | 1 | 0 | 1 | 2 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5568): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0014 | 0/0 | 5570 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5565): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0015 | 0/0 | 5568 | 4 | 0 | 4 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5563): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0016 | 0/0 | 5569 | 3 | 2 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5564): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0017 | 0/0 | 5570 | 2 | 1 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5565): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0018 | 0/0 | 5570 | 3 | 0 | 0 | 3 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5565): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0019 | 0/0 | 5572 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0020 | 0/0 | 5573 | 2 | 1 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5568): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0021 | 0/0 | 5568 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5563): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0022 | 0/0 | 5572 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0023 | 0/0 | 5569 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5564): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0024 | 0/0 | 5569 | 2 | 0 | 2 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5564): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0026 | 0/0 | 5571 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0028 | 0/0 | 5571 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0029 | 0/0 | 5571 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0030 | 0/0 | 5574 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5569): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0031 | 0/0 | 5571 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0032 | 0/0 | 5571 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0033 | 0/0 | 5571 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0034 | 0/0 | 5572 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0035 | 0/0 | 5572 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0036 | 0/0 | 5573 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5568): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0037 | 0/0 | 5572 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0038 | 0/0 | 5573 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5568): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0040 | 0/0 | 5573 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5568): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0042 | 0/0 | 5572 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0043 | 0/0 | 5571 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0045 | 0/0 | 5572 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0001c0001t0046 | 0/0 | 5569 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5564): Show |
chr4 | 104463308 | 104499894 |
| a0001c0005t0005 | 0/0 | 5571 | 2 | 1 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0002c0002t0001 | 0/0 | 5570 | 8 | 0 | 1 | 5 | 0 | 2 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5565): Show |
chr4 | 104463308 | 104499894 |
| a0002c0002t0002 | 0/0 | 5573 | 4 | 0 | 3 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5568): Show |
chr4 | 104463308 | 104499894 |
| a0002c0002t0004 | 0/0 | 5574 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5569): Show |
chr4 | 104463308 | 104499894 |
| a0002c0002t0006 | 0/0 | 5572 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0002c0002t0010 | 0/0 | 5573 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5568): Show |
chr4 | 104463308 | 104499894 |
| a0002c0002t0012 | 0/0 | 5573 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5568): Show |
chr4 | 104463308 | 104499894 |
| a0002c0002t0017 | 0/0 | 5571 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0002c0002t0027 | 0/0 | 5573 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5568): Show |
chr4 | 104463308 | 104499894 |
| a0002c0002t0039 | 0/0 | 5575 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5570): Show |
chr4 | 104463308 | 104499894 |
| a0002c0002t0044 | 0/0 | 5570 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5565): Show |
chr4 | 104463308 | 104499894 |
| a0003c0003t0005 | 0/0 | 5571 | 3 | 0 | 0 | 3 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5566): Show |
chr4 | 104463308 | 104499894 |
| a0003c0003t0025 | 0/0 | 5572 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0003c0003t0041 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5564): Show |
chr4 | 104463308 | 104499894 |
| a0004c0004t0014 | 0/0 | 5570 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5565): Show |
chr4 | 104463308 | 104499894 |
| a0005c0007t0002 | 0/0 | 5572 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5567): Show |
chr4 | 104463308 | 104499894 |
| a0006c0008t0004 | 0/0 | 5555 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5550): Show |
chr4 | 104463308 | 104499894 |
| a0007c0006t0001 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | GCACA others(5564): Show |
chr4 | 104463308 | 104499894 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 33 | 1 | 3 | 22 | 1 | 5 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0004 | 1/0 | 11 | 1 | 2 | 6 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0002 | 0/0 | 13 | 3 | 1 | 9 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0005 | 0/0 | 9 | 1 | 6 | 1 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0003 | 0/0 | 11 | 0 | 3 | 7 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0006g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0006g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0007g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0008g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0009g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0009g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0009g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0010g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0010g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0011g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0012g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0013g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0013g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0013g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0014g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0015g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0016g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0016g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0017g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0017g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0018g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0018g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0019g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0020g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0020g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0021g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0021g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0022g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0022g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0023g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0023g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0024g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0024g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0026g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0028g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0029g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0030g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0031g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0032g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0033g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0034g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0035g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0036g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0037g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0038g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0040g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0042g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0043g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0045g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0001t0046g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0001c0005t0005g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0001g0010 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0010g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0012g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0017g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0027g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0039g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0002c0002t0044g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0003c0003t0005g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0003c0003t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0003c0003t0025g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0003c0003t0041g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0004c0004t0014g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0005c0007t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0006c0008t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| a0007c0006t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00099 | hp2 | a0001 | c0001 | t0013 | g0128 | EUR | GBR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00140 | hp1 | a0001 | c0001 | t0009 | g0039 | EUR | GBR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0039 | EUR | GBR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CHS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0137 | EAS | CHS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0155 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | CHS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00735 | hp1 | a0001 | c0005 | t0005 | g0045 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG00738 | hp2 | a0001 | c0001 | t0042 | g0156 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01069 | hp1 | a0001 | c0001 | t0015 | g0009 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01070 | hp1 | a0001 | c0001 | t0017 | g0121 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01070 | hp2 | a0001 | c0001 | t0037 | g0119 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01071 | hp1 | a0001 | c0001 | t0015 | g0009 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01071 | hp2 | a0001 | c0001 | t0013 | g0038 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01109 | hp1 | a0001 | c0001 | t0016 | g0023 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01167 | hp1 | a0005 | c0007 | t0002 | g0118 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01175 | hp1 | a0001 | c0001 | t0020 | g0153 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01192 | hp1 | a0001 | c0001 | t0011 | g0017 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0161 | AMR | PUR | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01255 | hp1 | a0001 | c0001 | t0015 | g0009 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0091 | AMR | CLM | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | IBS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0162 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01891 | hp2 | a0001 | c0001 | t0033 | g0186 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01928 | hp1 | a0002 | c0002 | t0004 | g0046 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01928 | hp2 | a0001 | c0001 | t0024 | g0146 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01934 | hp2 | a0001 | c0001 | t0015 | g0009 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0124 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01993 | hp1 | a0001 | c0001 | t0024 | g0111 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02055 | hp1 | a0001 | c0001 | t0021 | g0168 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02055 | hp2 | a0001 | c0001 | t0023 | g0152 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02080 | hp1 | a0001 | c0001 | t0018 | g0036 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02080 | hp2 | a0003 | c0003 | t0005 | g0188 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02083 | hp2 | a0001 | c0001 | t0040 | g0129 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02145 | hp2 | a0002 | c0002 | t0027 | g0180 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02148 | hp2 | a0002 | c0002 | t0039 | g0086 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | CDX | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | CDX | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | CDX | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0125 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0080 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02300 | hp1 | a0002 | c0002 | t0006 | g0165 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0150 | AMR | PEL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02451 | hp1 | a0001 | c0001 | t0020 | g0052 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0031 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0017 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02630 | hp2 | a0001 | c0005 | t0005 | g0045 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02647 | hp1 | a0002 | c0002 | t0010 | g0099 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02647 | hp2 | a0004 | c0004 | t0014 | g0029 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02717 | hp1 | a0001 | c0001 | t0023 | g0122 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0072 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02738 | hp1 | a0001 | c0001 | t0013 | g0151 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02809 | hp1 | a0001 | c0001 | t0011 | g0172 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0183 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02922 | hp1 | a0004 | c0004 | t0014 | g0029 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02970 | hp2 | a0001 | c0001 | t0029 | g0174 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0018 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02976 | hp2 | a0001 | c0001 | t0021 | g0169 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03130 | hp1 | a0001 | c0001 | t0019 | g0044 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0181 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0031 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0023 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03225 | hp2 | a0001 | c0001 | t0045 | g0093 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03453 | hp2 | a0001 | c0001 | t0016 | g0064 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0017 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03710 | hp1 | a0001 | c0001 | t0035 | g0061 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03710 | hp2 | a0001 | c0001 | t0046 | g0147 | SAS | PJL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | BEB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0185 | SAS | BEB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03927 | hp1 | a0002 | c0002 | t0044 | g0097 | SAS | BEB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | BEB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03942 | hp1 | a0001 | c0001 | t0009 | g0158 | SAS | BEB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG04115 | hp1 | a0001 | c0001 | t0030 | g0058 | SAS | STU | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG04115 | hp2 | a0001 | c0001 | t0034 | g0127 | SAS | STU | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0022 | SAS | BEB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | STU | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG04204 | hp2 | a0001 | c0001 | t0013 | g0038 | SAS | STU | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | STU | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | STU | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18522 | hp1 | a0001 | c0001 | t0017 | g0074 | AFR | YRI | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18522 | hp2 | a0001 | c0001 | t0022 | g0175 | AFR | YRI | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18906 | hp1 | a0001 | c0001 | t0031 | g0102 | AFR | YRI | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | YRI | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18953 | hp1 | a0006 | c0008 | t0004 | g0065 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18956 | hp2 | a0001 | c0001 | t0043 | g0110 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18965 | hp2 | a0001 | c0001 | t0038 | g0059 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18974 | hp1 | a0003 | c0003 | t0025 | g0187 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18977 | hp1 | a0003 | c0003 | t0041 | g0189 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18998 | hp1 | a0001 | c0001 | t0036 | g0055 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19000 | hp1 | a0001 | c0001 | t0018 | g0108 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19000 | hp2 | a0001 | c0001 | t0018 | g0036 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19003 | hp1 | a0003 | c0003 | t0005 | g0032 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19006 | hp1 | a0001 | c0001 | t0009 | g0022 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19030 | hp1 | a0002 | c0002 | t0017 | g0073 | AFR | LWK | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19030 | hp2 | a0002 | c0002 | t0012 | g0087 | AFR | LWK | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19043 | hp1 | a0001 | c0001 | t0022 | g0176 | AFR | LWK | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | LWK | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19074 | hp1 | a0007 | c0006 | t0001 | g0100 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19074 | hp2 | a0001 | c0001 | t0007 | g0130 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19079 | hp2 | a0003 | c0003 | t0005 | g0032 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0095 | AFR | ASW | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ASW | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0113 | EUR | TSI | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | TSI | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | GIH | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0079 | SAS | GIH | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0163 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02486 | hp1 | a0001 | c0001 | t0019 | g0044 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02559 | hp1 | a0001 | c0001 | t0012 | g0062 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0148 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0182 | AFR | MSL | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG06807 | hp1 | a0001 | c0001 | t0026 | g0173 | AFR | USA | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | USA | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0092 | AFR | USA | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | USA | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA21309 | hp1 | a0001 | c0001 | t0032 | g0090 | AFR | LWK | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| NA21309 | hp2 | a0001 | c0001 | t0028 | g0063 | AFR | LWK | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | CXXC4_chr4_104463308_104499894 | CXXC4 | chr4 | 104463308 | 104499894 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:104490832 | C | T | 1 | a0005 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.971G>A | p.Ser324Asn | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/3 | 1422/5569 | 971/1104 | 324/367 | chr4 | 104490832 | |||
| chr4:104491297 | C | G | 1 | a0003 | 5 | HG02080.hp2 NA18974.hp1 NA18977.hp1 others(2): Show |
missense_variant | MODERATE | c.506G>C | p.Ser169Thr | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/3 | 957/5569 | 506/1104 | 169/367 | chr4 | 104491297 | |||
| chr4:104491333 | C | G | 1 | a0007 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.470G>C | p.Gly157Ala | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/3 | 921/5569 | 470/1104 | 157/367 | chr4 | 104491333 | |||
| chr4:104491452 | A | AC | 1 | a0002 | 20 | HG01099.hp1 HG01243.hp1 HG01928.hp1 others(17): Show |
frameshift_variant | HIGH | c.350dupG | p.Gly118fs | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/3 | 801/5569 | 350/1104 | 117/367 | chr4 | 104491452 | |||
| chr4:104491453 | C | G | 1 | a0004 | 2 | HG02647.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.350G>C | p.Gly117Ala | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/3 | 801/5569 | 350/1104 | 117/367 | chr4 | 104491453 | |||
| chr4:104491455 | CCCCCCGC others(11): Show |
C | 1 | a0006 | 1 | NA18953.hp1 | disruptive_inframe_deletion | MODERATE | c.330_347delCGGGGGCG others(10): Show |
p.Gly111_Gly116del | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/3 | 798/5569 | 330/1104 | 110/367 | chr4 | 104491455 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:104490822 | C | T | 1 | a0001c0005 | 2 | HG00735.hp1 HG02630.hp2 |
synonymous_variant | LOW | c.981G>A | p.Arg327Arg | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/3 | 1432/5569 | 981/1104 | 327/367 | chr4 | 104490822 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:104468392 | A | AC | 2 | a0001c0001t0017 a0002c0002t0017 |
3 | HG01070.hp1 NA18522.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3929dupG | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3929 | chr4 | 104468392 | ||||||
| chr4:104468393 | C | CT | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
206 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*3928dupA | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3928 | chr4 | 104468393 | ||||||
| chr4:104468393 | C | CTT | 4 | a0001c0001t0013 a0001c0001t0037 a0001c0001t0043 others(1): Show |
7 | HG00099.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3927_*3928dupAA | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3928 | chr4 | 104468393 | ||||||
| chr4:104468427 | C | G | 1 | a0001c0001t0038 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3895G>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3895 | chr4 | 104468427 | ||||||
| chr4:104468469 | G | A | 1 | a0002c0002t0044 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3853C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3853 | chr4 | 104468469 | ||||||
| chr4:104468647 | G | A | 1 | a0001c0001t0028 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3675C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3675 | chr4 | 104468647 | ||||||
| chr4:104468700 | T | TA | 8 | a0001c0001t0004 a0001c0001t0030 a0001c0001t0036 others(5): Show |
32 | HG00673.hp2 HG01169.hp2 HG01346.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3621dupT | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3621 | chr4 | 104468700 | ||||||
| chr4:104468700 | TA | T | 30 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(27): Show |
101 | HG00621.hp2 HG00673.hp1 HG00735.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3621delT | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3621 | chr4 | 104468700 | ||||||
| chr4:104468716 | G | T | 1 | a0001c0001t0036 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3606C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3606 | chr4 | 104468716 | ||||||
| chr4:104468717 | A | G | 2 | a0001c0001t0026 a0001c0001t0029 |
2 | HG02970.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3605T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3605 | chr4 | 104468717 | ||||||
| chr4:104468808 | A | G | 1 | a0001c0001t0011 | 4 | HG01192.hp1 HG02572.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3514T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3514 | chr4 | 104468808 | ||||||
| chr4:104469008 | T | C | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(47): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*3314A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3314 | chr4 | 104469008 | ||||||
| chr4:104469307 | G | A | 6 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0014 others(3): Show |
16 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3015C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 3015 | chr4 | 104469307 | ||||||
| chr4:104469360 | C | T | 1 | a0001c0001t0008 | 6 | HG01884.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2962G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 2962 | chr4 | 104469360 | ||||||
| chr4:104469437 | A | T | 1 | a0001c0001t0035 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2885T>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 2885 | chr4 | 104469437 | ||||||
| chr4:104469438 | T | C | 1 | a0001c0001t0029 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2884A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 2884 | chr4 | 104469438 | ||||||
| chr4:104469693 | T | C | 1 | a0001c0001t0024 | 2 | HG01928.hp2 HG01993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2629A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 2629 | chr4 | 104469693 | ||||||
| chr4:104470020 | G | C | 6 | a0001c0001t0005 a0001c0001t0033 a0001c0005t0005 others(3): Show |
12 | HG00621.hp2 HG00735.hp1 HG01891.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2302C>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 2302 | chr4 | 104470020 | ||||||
| chr4:104470167 | G | GA | 20 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(17): Show |
49 | HG00621.hp2 HG00735.hp1 HG01192.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2154dupT | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 2154 | chr4 | 104470167 | ||||||
| chr4:104470167 | GA | G | 2 | a0001c0001t0015 a0001c0001t0021 |
6 | HG01069.hp1 HG01071.hp1 HG01255.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2154delT | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 2154 | chr4 | 104470167 | ||||||
| chr4:104470182 | A | AAC | 3 | a0001c0001t0009 a0001c0001t0042 a0002c0002t0039 |
8 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2139_*2140insGT | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 2139 | chr4 | 104470182 | ||||||
| chr4:104470182 | A | AC | 17 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(14): Show |
111 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2139dupG | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 2139 | chr4 | 104470182 | ||||||
| chr4:104470245 | A | G | 2 | a0001c0001t0011 a0001c0001t0032 |
5 | HG01192.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2077T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 2077 | chr4 | 104470245 | ||||||
| chr4:104470530 | C | T | 2 | a0001c0001t0011 a0001c0001t0032 |
5 | HG01192.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1792G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 1792 | chr4 | 104470530 | ||||||
| chr4:104470548 | A | G | 2 | a0001c0001t0011 a0001c0001t0032 |
5 | HG01192.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1774T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 1774 | chr4 | 104470548 | ||||||
| chr4:104470842 | G | T | 30 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(27): Show |
101 | HG00621.hp2 HG00673.hp1 HG00735.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1480C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 1480 | chr4 | 104470842 | ||||||
| chr4:104470865 | C | T | 13 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(10): Show |
29 | HG00621.hp2 HG00735.hp1 HG01884.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1457G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 1457 | chr4 | 104470865 | ||||||
| chr4:104471112 | G | T | 1 | a0001c0001t0016 | 3 | HG01109.hp1 HG03209.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1210C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 1210 | chr4 | 104471112 | ||||||
| chr4:104471174 | T | C | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(17): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1148A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 1148 | chr4 | 104471174 | ||||||
| chr4:104471234 | G | A | 1 | a0001c0001t0034 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1088C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 1088 | chr4 | 104471234 | ||||||
| chr4:104471328 | A | G | 1 | a0001c0001t0019 | 2 | HG02486.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*994T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 994 | chr4 | 104471328 | ||||||
| chr4:104471355 | T | C | 1 | a0001c0001t0033 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*967A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 967 | chr4 | 104471355 | ||||||
| chr4:104471436 | G | A | 1 | a0001c0001t0040 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*886C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 886 | chr4 | 104471436 | ||||||
| chr4:104471522 | C | T | 1 | a0001c0001t0034 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*800G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 800 | chr4 | 104471522 | ||||||
| chr4:104472163 | T | C | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(16): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*159A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 159 | chr4 | 104472163 | ||||||
| chr4:104472172 | C | CT | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(27): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*149dupA | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 149 | chr4 | 104472172 | ||||||
| chr4:104472172 | C | CTT | 14 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0011 others(11): Show |
28 | HG01175.hp1 HG01192.hp1 HG01884.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*148_*149dupAA | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 149 | chr4 | 104472172 | ||||||
| chr4:104472204 | A | G | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(47): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*118T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 3/3 | 118 | chr4 | 104472204 | ||||||
| chr4:104491883 | G | A | 1 | a0001c0001t0045 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/3 | 81 | chr4 | 104491883 | ||||||
| chr4:104492028 | T | G | 1 | a0001c0001t0046 | 1 | HG03710.hp2 | 5_prime_UTR_variant | MODIFIER | c.-226A>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/3 | 226 | chr4 | 104492028 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:104472438 | T | C | 2 | a0001c0001t0011g0017 a0001c0001t0011g0172 |
4 | HG01192.hp1 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-72A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104472438 | |||||||
| chr4:104472509 | G | T | 2 | a0001c0001t0026g0173 a0001c0001t0029g0174 |
2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1060-143C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104472509 | |||||||
| chr4:104472580 | T | C | 3 | a0001c0001t0003g0088 a0001c0001t0016g0023 a0001c0001t0016g0064 |
4 | HG01109.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-214A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104472580 | |||||||
| chr4:104472607 | T | C | 8 | a0001c0001t0008g0018 a0001c0001t0008g0095 a0001c0001t0008g0162 others(5): Show |
11 | HG01884.hp2 HG02486.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1060-241A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104472607 | |||||||
| chr4:104472626 | C | A | 32 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(29): Show |
50 | HG00673.hp1 HG01070.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1060-260G>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104472626 | |||||||
| chr4:104472693 | C | G | 1 | a0002c0002t0006g0165 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1060-327G>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104472693 | |||||||
| chr4:104472757 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1060-391G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104472757 | |||||||
| chr4:104472770 | T | A | 1 | a0001c0001t0031g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1060-404A>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104472770 | |||||||
| chr4:104472791 | C | T | 1 | a0001c0001t0032g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1060-425G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104472791 | |||||||
| chr4:104472950 | G | A | 1 | a0001c0001t0012g0092 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1060-584C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104472950 | |||||||
| chr4:104472964 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1060-598A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104472964 | |||||||
| chr4:104473057 | A | T | 2 | a0001c0001t0006g0012 a0001c0001t0006g0019 |
7 | HG01975.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-691T>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104473057 | |||||||
| chr4:104473135 | C | CTTAAA | 22 | a0001c0001t0005g0079 a0001c0001t0005g0137 a0001c0001t0005g0177 others(19): Show |
29 | HG00621.hp2 HG00735.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1060-770_1060-769i others(7): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104473135 | |||||||
| chr4:104473141 | GAAT | G | 31 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(28): Show |
49 | HG00673.hp1 HG01070.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1060-778_1060-776d others(5): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104473141 | |||||||
| chr4:104473168 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0015g0009 |
6 | HG01069.hp1 HG01071.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-802C>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104473168 | |||||||
| chr4:104473178 | T | C | 1 | a0001c0001t0005g0079 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1060-812A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104473178 | |||||||
| chr4:104473193 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1060-827G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104473193 | |||||||
| chr4:104473369 | T | C | 10 | a0001c0001t0005g0079 a0001c0001t0005g0137 a0001c0001t0005g0177 others(7): Show |
12 | HG00621.hp2 HG00735.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1060-1003A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104473369 | |||||||
| chr4:104473390 | T | A | 1 | a0001c0001t0004g0060 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1060-1024A>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104473390 | |||||||
| chr4:104473468 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1060-1102A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104473468 | |||||||
| chr4:104473790 | A | ATTG | 144 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0013 others(141): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1060-1425_1060-142 others(7): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104473790 | |||||||
| chr4:104474149 | A | G | 10 | a0001c0001t0005g0079 a0001c0001t0005g0137 a0001c0001t0005g0177 others(7): Show |
12 | HG00621.hp2 HG00735.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1060-1783T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104474149 | |||||||
| chr4:104474163 | C | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0048 a0002c0002t0002g0096 |
4 | HG00558.hp2 NA18946.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-1797G>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104474163 | |||||||
| chr4:104474459 | C | T | 1 | a0001c0001t0042g0156 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1060-2093G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104474459 | |||||||
| chr4:104474494 | T | C | 1 | a0001c0001t0003g0166 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1060-2128A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104474494 | |||||||
| chr4:104474580 | C | T | 2 | a0001c0001t0021g0168 a0001c0001t0021g0169 |
2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1060-2214G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104474580 | |||||||
| chr4:104474877 | T | C | 1 | a0001c0001t0002g0082 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1060-2511A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104474877 | |||||||
| chr4:104475462 | G | A | 2 | a0001c0001t0022g0175 a0001c0001t0022g0176 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1060-3096C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104475462 | |||||||
| chr4:104475483 | T | C | 1 | a0001c0001t0031g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1060-3117A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104475483 | |||||||
| chr4:104475554 | G | T | 1 | a0001c0001t0003g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1060-3188C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104475554 | |||||||
| chr4:104475602 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1060-3236A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104475602 | |||||||
| chr4:104475826 | C | G | 1 | a0001c0001t0001g0035 | 2 | HG01258.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1060-3460G>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104475826 | |||||||
| chr4:104476049 | T | TCTAGTCT others(14): Show |
1 | a0001c0001t0035g0061 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1060-3684_1060-368 others(25): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104476049 | |||||||
| chr4:104476251 | A | G | 1 | a0001c0001t0003g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1060-3885T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104476251 | |||||||
| chr4:104476252 | CA | C | 4 | a0001c0001t0008g0018 a0001c0001t0008g0095 a0001c0001t0008g0162 others(1): Show |
6 | HG01884.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-3887delT | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104476252 | |||||||
| chr4:104476274 | T | C | 133 | a0001c0001t0001g0078 a0001c0001t0002g0002 a0001c0001t0002g0005 others(130): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1060-3908A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104476274 | |||||||
| chr4:104476463 | A | C | 1 | a0001c0001t0002g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1060-4097T>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104476463 | |||||||
| chr4:104476652 | ATAAC | A | 20 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(17): Show |
37 | HG00673.hp1 HG01243.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1060-4290_1060-428 others(8): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104476652 | |||||||
| chr4:104476911 | T | C | 78 | a0001c0001t0001g0078 a0001c0001t0002g0002 a0001c0001t0002g0005 others(75): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1060-4545A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104476911 | |||||||
| chr4:104476982 | T | C | 3 | a0001c0001t0017g0074 a0001c0001t0017g0121 a0002c0002t0017g0073 |
3 | HG01070.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1060-4616A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104476982 | |||||||
| chr4:104477077 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1060-4711T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477077 | |||||||
| chr4:104477127 | A | G | 2 | a0001c0001t0026g0173 a0001c0001t0029g0174 |
2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1060-4761T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477127 | |||||||
| chr4:104477302 | C | T | 1 | a0001c0001t0045g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1060-4936G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477302 | |||||||
| chr4:104477316 | G | A | 1 | a0001c0001t0031g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1060-4950C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477316 | |||||||
| chr4:104477398 | T | C | 4 | a0001c0001t0012g0062 a0001c0001t0012g0092 a0001c0001t0012g0148 others(1): Show |
4 | HG02559.hp1 HG03471.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-5032A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477398 | |||||||
| chr4:104477405 | C | T | 1 | a0001c0001t0001g0014 | 3 | HG01167.hp2 HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1060-5039G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477405 | |||||||
| chr4:104477588 | CAT | C | 28 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(25): Show |
45 | HG00673.hp1 HG01070.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.1060-5224_1060-522 others(6): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477588 | |||||||
| chr4:104477670 | T | A | 12 | a0001c0001t0005g0079 a0001c0001t0005g0137 a0001c0001t0005g0177 others(9): Show |
14 | HG00621.hp2 HG00735.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1060-5304A>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477670 | |||||||
| chr4:104477670 | T | C | 1 | a0001c0001t0003g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1060-5304A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477670 | |||||||
| chr4:104477783 | A | T | 1 | a0001c0001t0003g0051 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1060-5417T>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477783 | |||||||
| chr4:104477821 | C | T | 1 | a0001c0001t0012g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1060-5455G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477821 | |||||||
| chr4:104477987 | A | C | 10 | a0001c0001t0005g0079 a0001c0001t0005g0137 a0001c0001t0005g0177 others(7): Show |
12 | HG00621.hp2 HG00735.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1060-5621T>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477987 | |||||||
| chr4:104477999 | G | C | 1 | a0001c0001t0001g0159 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1060-5633C>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104477999 | |||||||
| chr4:104478117 | G | A | 2 | a0001c0001t0012g0092 a0002c0002t0012g0087 |
2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1060-5751C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478117 | |||||||
| chr4:104478128 | G | A | 1 | a0001c0001t0003g0051 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1060-5762C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478128 | |||||||
| chr4:104478129 | A | G | 1 | a0001c0001t0003g0051 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1060-5763T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478129 | |||||||
| chr4:104478130 | G | A | 1 | a0001c0001t0003g0051 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1060-5764C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478130 | |||||||
| chr4:104478167 | C | T | 1 | a0001c0001t0018g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1060-5801G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478167 | |||||||
| chr4:104478178 | G | C | 3 | a0001c0001t0011g0017 a0001c0001t0011g0172 a0001c0001t0032g0090 |
5 | HG01192.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-5812C>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478178 | |||||||
| chr4:104478179 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1060-5813G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478179 | |||||||
| chr4:104478457 | G | T | 1 | a0001c0001t0002g0028 | 2 | HG00609.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1060-6091C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478457 | |||||||
| chr4:104478479 | A | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0115 |
3 | HG01074.hp1 HG01358.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1060-6113T>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478479 | |||||||
| chr4:104478555 | C | T | 13 | a0001c0001t0002g0126 a0001c0001t0002g0135 a0001c0001t0003g0006 others(10): Show |
23 | HG00673.hp1 HG02056.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.1060-6189G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478555 | |||||||
| chr4:104478632 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1060-6266C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478632 | |||||||
| chr4:104478717 | A | C | 2 | a0001c0001t0026g0173 a0001c0001t0029g0174 |
2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1060-6351T>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478717 | |||||||
| chr4:104478900 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1060-6534A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478900 | |||||||
| chr4:104478933 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1060-6567A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478933 | |||||||
| chr4:104478980 | T | C | 3 | a0001c0001t0011g0017 a0001c0001t0011g0172 a0001c0001t0032g0090 |
5 | HG01192.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-6614A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104478980 | |||||||
| chr4:104479187 | C | T | 143 | a0001c0001t0001g0078 a0001c0001t0002g0002 a0001c0001t0002g0005 others(140): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1060-6821G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104479187 | |||||||
| chr4:104479349 | C | T | 11 | a0001c0001t0008g0018 a0001c0001t0008g0095 a0001c0001t0008g0162 others(8): Show |
16 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1060-6983G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104479349 | |||||||
| chr4:104479691 | T | G | 1 | a0002c0002t0002g0150 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1060-7325A>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104479691 | |||||||
| chr4:104479736 | CTTCT | C | 12 | a0001c0001t0005g0079 a0001c0001t0005g0137 a0001c0001t0005g0177 others(9): Show |
14 | HG00621.hp2 HG00735.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1060-7374_1060-737 others(8): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104479736 | |||||||
| chr4:104479771 | TTCCC | T | 1 | a0001c0001t0008g0018 | 3 | HG02809.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1060-7409_1060-740 others(8): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104479771 | |||||||
| chr4:104480109 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1060-7743C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104480109 | |||||||
| chr4:104480250 | A | C | 1 | a0001c0001t0004g0091 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1060-7884T>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104480250 | |||||||
| chr4:104480460 | C | G | 57 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(54): Show |
86 | HG00673.hp1 HG01070.hp1 HG01192.hp1 others(83): Show |
intron_variant | MODIFIER | c.1060-8094G>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104480460 | |||||||
| chr4:104480557 | G | T | 56 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(53): Show |
85 | HG00673.hp1 HG01070.hp1 HG01192.hp1 others(82): Show |
intron_variant | MODIFIER | c.1060-8191C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104480557 | |||||||
| chr4:104480620 | GA | G | 54 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(51): Show |
82 | HG00673.hp1 HG01070.hp1 HG01192.hp1 others(79): Show |
intron_variant | MODIFIER | c.1060-8255delT | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104480620 | |||||||
| chr4:104480719 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1060-8353C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104480719 | |||||||
| chr4:104480767 | C | T | 57 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(54): Show |
86 | HG00673.hp1 HG01070.hp1 HG01192.hp1 others(83): Show |
intron_variant | MODIFIER | c.1060-8401G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104480767 | |||||||
| chr4:104480846 | TTCCC | T | 4 | a0001c0001t0003g0190 a0001c0001t0007g0080 a0001c0001t0007g0125 others(1): Show |
4 | HG00673.hp1 HG02258.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-8484_1060-848 others(8): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104480846 | |||||||
| chr4:104480864 | CCCTT | C | 12 | a0001c0001t0008g0018 a0001c0001t0008g0095 a0001c0001t0008g0162 others(9): Show |
19 | HG01192.hp1 HG01884.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1060-8502_1060-849 others(8): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104480864 | |||||||
| chr4:104481066 | A | T | 1 | a0002c0002t0001g0094 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1060-8700T>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481066 | |||||||
| chr4:104481092 | C | G | 3 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0036g0055 |
3 | NA18943.hp1 NA18998.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1060-8726G>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481092 | |||||||
| chr4:104481184 | A | C | 1 | a0001c0001t0031g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1060-8818T>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481184 | |||||||
| chr4:104481250 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1060-8884G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481250 | |||||||
| chr4:104481361 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0106 |
2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1060-8995G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481361 | |||||||
| chr4:104481363 | C | T | 1 | a0001c0001t0021g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1060-8997G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481363 | |||||||
| chr4:104481449 | C | T | 2 | a0001c0001t0004g0056 a0001c0001t0036g0055 |
2 | NA18998.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1060-9083G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481449 | |||||||
| chr4:104481489 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1060-9123G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481489 | |||||||
| chr4:104481544 | G | GA | 8 | a0001c0001t0012g0062 a0001c0001t0012g0092 a0001c0001t0012g0148 others(5): Show |
8 | HG02145.hp2 HG02559.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1060-9179dupT | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481544 | |||||||
| chr4:104481695 | T | C | 4 | a0001c0001t0002g0015 a0001c0001t0002g0075 a0001c0001t0002g0170 others(1): Show |
6 | HG00642.hp2 HG00733.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+9049A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481695 | |||||||
| chr4:104481709 | C | T | 1 | a0001c0001t0007g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1059+9035G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481709 | |||||||
| chr4:104481803 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1059+8941C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481803 | |||||||
| chr4:104481848 | G | A | 3 | a0001c0001t0011g0017 a0001c0001t0011g0172 a0001c0001t0032g0090 |
5 | HG01192.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+8896C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481848 | |||||||
| chr4:104481972 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1059+8772G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104481972 | |||||||
| chr4:104482078 | A | C | 1 | a0001c0001t0023g0122 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1059+8666T>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104482078 | |||||||
| chr4:104482178 | T | A | 57 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(54): Show |
86 | HG00673.hp1 HG01070.hp1 HG01192.hp1 others(83): Show |
intron_variant | MODIFIER | c.1059+8566A>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104482178 | |||||||
| chr4:104482337 | A | C | 1 | a0001c0001t0020g0153 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1059+8407T>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104482337 | |||||||
| chr4:104482337 | A | G | 1 | a0001c0001t0022g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1059+8407T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104482337 | |||||||
| chr4:104482377 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1059+8367A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104482377 | |||||||
| chr4:104482534 | A | G | 1 | a0001c0001t0031g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1059+8210T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104482534 | |||||||
| chr4:104482569 | T | A | 144 | a0001c0001t0001g0078 a0001c0001t0002g0002 a0001c0001t0002g0005 others(141): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1059+8175A>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104482569 | |||||||
| chr4:104482752 | C | T | 1 | a0002c0002t0044g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1059+7992G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104482752 | |||||||
| chr4:104482776 | A | G | 2 | a0001c0001t0003g0030 a0001c0001t0003g0043 |
4 | HG01884.hp1 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+7968T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104482776 | |||||||
| chr4:104482844 | C | T | 1 | a0001c0001t0031g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1059+7900G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104482844 | |||||||
| chr4:104483218 | T | G | 2 | a0001c0001t0023g0122 a0001c0001t0023g0152 |
2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1059+7526A>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104483218 | |||||||
| chr4:104483327 | C | A | 1 | a0002c0002t0006g0165 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1059+7417G>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104483327 | |||||||
| chr4:104483336 | C | T | 2 | a0001c0001t0014g0031 a0004c0004t0014g0029 |
4 | HG02451.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+7408G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104483336 | |||||||
| chr4:104483521 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1059+7223A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104483521 | |||||||
| chr4:104483582 | A | G | 1 | a0002c0002t0006g0165 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1059+7162T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104483582 | |||||||
| chr4:104483713 | C | T | 1 | a0001c0001t0010g0181 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1059+7031G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104483713 | |||||||
| chr4:104483727 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1059+7017G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104483727 | |||||||
| chr4:104483889 | T | C | 30 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(27): Show |
47 | HG00673.hp1 HG01070.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.1059+6855A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104483889 | |||||||
| chr4:104484079 | C | T | 12 | a0001c0001t0005g0079 a0001c0001t0005g0137 a0001c0001t0005g0177 others(9): Show |
14 | HG00621.hp2 HG00735.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059+6665G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104484079 | |||||||
| chr4:104484083 | A | G | 124 | a0001c0001t0001g0078 a0001c0001t0002g0002 a0001c0001t0002g0005 others(121): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1059+6661T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104484083 | |||||||
| chr4:104484145 | T | C | 2 | a0001c0001t0021g0168 a0001c0001t0021g0169 |
2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1059+6599A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104484145 | |||||||
| chr4:104484471 | A | C | 4 | a0001c0001t0010g0072 a0001c0001t0010g0181 a0001c0001t0019g0044 others(1): Show |
5 | HG02486.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+6273T>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104484471 | |||||||
| chr4:104484537 | A | G | 87 | a0001c0001t0001g0078 a0001c0001t0002g0002 a0001c0001t0002g0005 others(84): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1059+6207T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104484537 | |||||||
| chr4:104484541 | A | G | 144 | a0001c0001t0001g0078 a0001c0001t0002g0002 a0001c0001t0002g0005 others(141): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1059+6203T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104484541 | |||||||
| chr4:104484689 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1059+6055A>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104484689 | |||||||
| chr4:104485542 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1059+5202G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104485542 | |||||||
| chr4:104485943 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1059+4801C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104485943 | |||||||
| chr4:104486011 | T | G | 2 | a0001c0001t0012g0092 a0002c0002t0012g0087 |
2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1059+4733A>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486011 | |||||||
| chr4:104486069 | C | T | 7 | a0001c0001t0002g0015 a0001c0001t0002g0075 a0001c0001t0002g0154 others(4): Show |
9 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+4675G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486069 | |||||||
| chr4:104486466 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1059+4278G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486466 | |||||||
| chr4:104486535 | C | T | 22 | a0001c0001t0006g0012 a0001c0001t0006g0019 a0001c0001t0008g0018 others(19): Show |
32 | HG01884.hp2 HG01975.hp2 HG02300.hp1 others(29): Show |
intron_variant | MODIFIER | c.1059+4209G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486535 | |||||||
| chr4:104486546 | C | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0068 a0001c0001t0001g0071 others(1): Show |
5 | HG02129.hp1 NA18943.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+4198G>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486546 | |||||||
| chr4:104486718 | T | C | 85 | a0001c0001t0001g0078 a0001c0001t0002g0002 a0001c0001t0002g0005 others(82): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1059+4026A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486718 | |||||||
| chr4:104486719 | T | C | 1 | a0001c0001t0004g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1059+4025A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486719 | |||||||
| chr4:104486734 | C | T | 3 | a0001c0001t0010g0072 a0001c0001t0010g0181 a0002c0002t0010g0099 |
3 | HG02647.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1059+4010G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486734 | |||||||
| chr4:104486759 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0138 a0001c0001t0001g0159 |
3 | NA18982.hp1 NA19068.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1059+3985A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486759 | |||||||
| chr4:104486832 | T | A | 1 | a0001c0001t0004g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1059+3912A>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486832 | |||||||
| chr4:104486834 | C | A | 1 | a0001c0001t0004g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1059+3910G>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486834 | |||||||
| chr4:104486836 | T | A | 1 | a0001c0001t0004g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1059+3908A>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486836 | |||||||
| chr4:104486837 | C | T | 1 | a0001c0001t0004g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1059+3907G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486837 | |||||||
| chr4:104486842 | G | T | 1 | a0001c0001t0004g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1059+3902C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486842 | |||||||
| chr4:104486846 | G | T | 1 | a0001c0001t0004g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1059+3898C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486846 | |||||||
| chr4:104486847 | G | T | 1 | a0001c0001t0004g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1059+3897C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486847 | |||||||
| chr4:104486936 | G | A | 2 | a0001c0001t0002g0132 a0001c0001t0002g0135 |
2 | HG02486.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1059+3808C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104486936 | |||||||
| chr4:104487077 | G | A | 4 | a0001c0001t0006g0012 a0001c0001t0006g0019 a0001c0001t0045g0093 others(1): Show |
9 | HG01975.hp2 HG02300.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+3667C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104487077 | |||||||
| chr4:104487190 | T | C | 1 | a0001c0001t0004g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1059+3554A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104487190 | |||||||
| chr4:104487251 | G | C | 1 | a0001c0001t0002g0134 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1059+3493C>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104487251 | |||||||
| chr4:104487263 | G | A | 3 | a0001c0001t0011g0017 a0001c0001t0011g0172 a0001c0001t0032g0090 |
5 | HG01192.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+3481C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104487263 | |||||||
| chr4:104487401 | T | C | 1 | a0002c0002t0027g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1059+3343A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104487401 | |||||||
| chr4:104487435 | C | G | 1 | a0001c0001t0016g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1059+3309G>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104487435 | |||||||
| chr4:104487512 | G | C | 1 | a0001c0001t0005g0177 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1059+3232C>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104487512 | |||||||
| chr4:104487576 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1059+3168G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104487576 | |||||||
| chr4:104487952 | G | T | 1 | a0001c0001t0032g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1059+2792C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104487952 | |||||||
| chr4:104488202 | C | T | 1 | a0002c0002t0006g0165 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1059+2542G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104488202 | |||||||
| chr4:104488240 | G | C | 2 | a0001c0001t0011g0017 a0001c0001t0011g0172 |
4 | HG01192.hp1 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+2504C>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104488240 | |||||||
| chr4:104488353 | T | C | 1 | a0001c0001t0031g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1059+2391A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104488353 | |||||||
| chr4:104488497 | T | C | 131 | a0001c0001t0001g0078 a0001c0001t0002g0002 a0001c0001t0002g0005 others(128): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1059+2247A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104488497 | |||||||
| chr4:104488530 | C | G | 12 | a0001c0001t0005g0079 a0001c0001t0005g0137 a0001c0001t0005g0177 others(9): Show |
14 | HG00621.hp2 HG00735.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059+2214G>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104488530 | |||||||
| chr4:104488539 | T | G | 33 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(30): Show |
51 | HG00673.hp1 HG01070.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.1059+2205A>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104488539 | |||||||
| chr4:104488592 | T | C | 4 | a0001c0001t0008g0018 a0001c0001t0008g0095 a0001c0001t0008g0162 others(1): Show |
6 | HG01884.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+2152A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104488592 | |||||||
| chr4:104488610 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1059+2134G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104488610 | |||||||
| chr4:104488686 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1059+2058C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104488686 | |||||||
| chr4:104489239 | C | T | 23 | a0001c0001t0006g0012 a0001c0001t0006g0019 a0001c0001t0008g0018 others(20): Show |
33 | HG01884.hp2 HG01975.hp2 HG02300.hp1 others(30): Show |
intron_variant | MODIFIER | c.1059+1505G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104489239 | |||||||
| chr4:104489341 | G | T | 1 | a0001c0001t0008g0095 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1059+1403C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104489341 | |||||||
| chr4:104489353 | A | C | 107 | a0001c0001t0001g0078 a0001c0001t0002g0002 a0001c0001t0002g0005 others(104): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1059+1391T>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104489353 | |||||||
| chr4:104489891 | C | A | 1 | a0001c0001t0016g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1059+853G>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104489891 | |||||||
| chr4:104490025 | A | G | 36 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0011 others(33): Show |
55 | HG00673.hp1 HG01070.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.1059+719T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104490025 | |||||||
| chr4:104490252 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1059+492A>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104490252 | |||||||
| chr4:104490462 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1059+282G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104490462 | |||||||
| chr4:104490475 | A | G | 8 | a0001c0001t0008g0018 a0001c0001t0008g0095 a0001c0001t0008g0162 others(5): Show |
11 | HG01884.hp2 HG02486.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1059+269T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104490475 | |||||||
| chr4:104490529 | ACTCT | A | 3 | a0001c0001t0007g0016 a0001c0001t0007g0080 a0001c0001t0007g0163 |
5 | HG02109.hp1 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+211_1059+214d others(6): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104490529 | |||||||
| chr4:104490537 | T | G | 11 | a0001c0001t0008g0018 a0001c0001t0008g0095 a0001c0001t0008g0162 others(8): Show |
16 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1059+207A>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 2/2 | chr4 | 104490537 | |||||||
| chr4:104492084 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-257-25G>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104492084 | |||||||
| chr4:104492311 | A | C | 1 | a0001c0001t0006g0019 | 3 | HG02622.hp1 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-257-252T>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104492311 | |||||||
| chr4:104492485 | T | A | 1 | a0001c0001t0004g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-257-426A>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104492485 | |||||||
| chr4:104492754 | A | T | 1 | a0001c0001t0004g0085 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-257-695T>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104492754 | |||||||
| chr4:104492767 | A | C | 1 | a0001c0001t0002g0149 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-257-708T>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104492767 | |||||||
| chr4:104492918 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-257-859C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104492918 | |||||||
| chr4:104492977 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-257-918C>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104492977 | |||||||
| chr4:104493048 | A | AG | 20 | a0001c0001t0001g0067 a0001c0001t0001g0138 a0001c0001t0002g0047 others(17): Show |
29 | HG00673.hp2 HG01192.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.-257-990dupC | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104493048 | |||||||
| chr4:104493049 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-257-990C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104493049 | |||||||
| chr4:104493065 | C | T | 120 | a0001c0001t0001g0178 a0001c0001t0002g0002 a0001c0001t0002g0005 others(117): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.-257-1006G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104493065 | |||||||
| chr4:104493540 | G | A | 1 | a0001c0001t0012g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-258+1161C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104493540 | |||||||
| chr4:104493760 | C | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0138 a0001c0001t0001g0159 others(1): Show |
4 | NA18951.hp2 NA18982.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.-258+941G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104493760 | |||||||
| chr4:104493840 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-258+861T>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104493840 | |||||||
| chr4:104494029 | G | A | 42 | a0001c0001t0001g0078 a0001c0001t0002g0005 a0001c0001t0002g0013 others(39): Show |
57 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-258+672C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494029 | |||||||
| chr4:104494067 | C | G | 3 | a0001c0001t0007g0016 a0001c0001t0007g0080 a0001c0001t0007g0163 |
5 | HG02109.hp1 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-258+634G>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494067 | |||||||
| chr4:104494173 | G | C | 1 | a0001c0001t0001g0040 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-258+528C>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494173 | |||||||
| chr4:104494243 | C | T | 8 | a0001c0001t0005g0079 a0001c0001t0005g0137 a0001c0001t0005g0185 others(5): Show |
9 | HG00621.hp2 HG00735.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-258+458G>A | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494243 | |||||||
| chr4:104494658 | TG | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0034 others(78): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-258+42delC | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494658 | |||||||
| chr4:104494658 | TGG | T | 46 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0026 others(43): Show |
92 | HG00558.hp2 HG00639.hp2 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.-258+41_-258+42del others(2): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494658 | |||||||
| chr4:104494662 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-258+39C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494662 | |||||||
| chr4:104494662 | G | GA | 4 | a0001c0001t0003g0043 a0001c0001t0003g0160 a0001c0001t0003g0161 others(1): Show |
5 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-258+38_-258+39ins others(1): Show |
CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494662 | |||||||
| chr4:104494663 | G | A | 36 | a0001c0001t0001g0178 a0001c0001t0002g0170 a0001c0001t0002g0171 others(33): Show |
51 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.-258+38C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494663 | |||||||
| chr4:104494664 | G | A | 2 | a0001c0001t0006g0012 a0001c0001t0006g0019 |
7 | HG01975.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-258+37C>T | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494664 | |||||||
| chr4:104494669 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-258+32C>G | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494669 | |||||||
| chr4:104494672 | T | G | 9 | a0001c0001t0002g0192 a0001c0001t0003g0190 a0001c0001t0003g0191 others(6): Show |
10 | HG00673.hp1 HG00735.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-258+29A>C | CXXC4 | ENSG00000168772.12 | transcript | ENST00000394767.3 | protein_coding | 1/2 | chr4 | 104494672 |