Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84103 |
| ensemblid | ENSG00000138813.10 |
| hgncid | 25274 |
| symbol | C4orf17 |
| name | chromosome 4 open reading frame 17 |
| refseq_nuc | NM_032149.3 |
| refseq_prot | NP_115525.2 |
| ensembl_nuc | ENST00000326581.9 |
| ensembl_prot | ENSP00000322582.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 99511021 |
| end | 99542303 |
| strand | + |
| ver | v1.2 |
| region | chr4:99511021-99542303 |
| region5000 | chr4:99506021-99547303 |
| regionname0 | C4orf17_chr4_99511021_99542303 |
| regionname5000 | C4orf17_chr4_99506021_99547303 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 359 | 177 | 9 | 46 | 106 | 5 | 9 | 89 | C4orf17_chr4_99506021_99547303 | C4orf17 | MNLNP others(354): Show |
chr4 | 99506021 | 99547303 |
| a0002 | 0/0 | 359 | 86 | 37 | 8 | 33 | 0 | 8 | 30 | C4orf17_chr4_99506021_99547303 | C4orf17 | MNLNP others(354): Show |
chr4 | 99506021 | 99547303 |
| a0003 | 0/0 | 359 | 75 | 22 | 12 | 25 | 1 | 15 | 22 | C4orf17_chr4_99506021_99547303 | C4orf17 | MNLNP others(354): Show |
chr4 | 99506021 | 99547303 |
| a0004 | 0/0 | 359 | 29 | 11 | 5 | 8 | 0 | 5 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | MNLNP others(354): Show |
chr4 | 99506021 | 99547303 |
| a0005 | 0/0 | 355 | 18 | 17 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | MNLNP others(350): Show |
chr4 | 99506021 | 99547303 |
| a0006 | 0/0 | 359 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | MNLNP others(354): Show |
chr4 | 99506021 | 99547303 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1077 | 176 | 9 | 46 | 106 | 5 | 9 | C4orf17_chr4_99506021_99547303 | C4orf17 | ATGAA others(1072): Show |
chr4 | 99506021 | 99547303 | ||
| a0001c0011 | 0/1 | 1077 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | ATGAA others(1072): Show |
chr4 | 99506021 | 99547303 | ||
| a0002c0003 | 0/0 | 1077 | 43 | 9 | 1 | 32 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | ATGAA others(1072): Show |
chr4 | 99506021 | 99547303 | ||
| a0002c0004 | 0/0 | 1077 | 36 | 21 | 7 | 1 | 0 | 7 | C4orf17_chr4_99506021_99547303 | C4orf17 | ATGAA others(1072): Show |
chr4 | 99506021 | 99547303 | ||
| a0002c0007 | 0/0 | 1077 | 4 | 4 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | ATGAA others(1072): Show |
chr4 | 99506021 | 99547303 | ||
| a0002c0009 | 0/0 | 1077 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | ATGAA others(1072): Show |
chr4 | 99506021 | 99547303 | ||
| a0003c0002 | 0/0 | 1077 | 72 | 19 | 12 | 25 | 1 | 15 | C4orf17_chr4_99506021_99547303 | C4orf17 | ATGAA others(1072): Show |
chr4 | 99506021 | 99547303 | ||
| a0003c0008 | 0/0 | 1077 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | ATGAA others(1072): Show |
chr4 | 99506021 | 99547303 | ||
| a0004c0005 | 0/0 | 1077 | 29 | 11 | 5 | 8 | 0 | 5 | C4orf17_chr4_99506021_99547303 | C4orf17 | ATGAA others(1072): Show |
chr4 | 99506021 | 99547303 | ||
| a0005c0006 | 0/0 | 1065 | 18 | 17 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | ATGAA others(1060): Show |
chr4 | 99506021 | 99547303 | ||
| a0006c0010 | 0/0 | 1077 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | ATGAA others(1072): Show |
chr4 | 99506021 | 99547303 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1619 | 176 | 9 | 46 | 106 | 5 | 9 | C4orf17_chr4_99506021_99547303 | C4orf17 | AACAT others(1614): Show |
chr4 | 99506021 | 99547303 |
| a0001c0011t0001 | 0/1 | 1619 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | AACAT others(1614): Show |
chr4 | 99506021 | 99547303 |
| a0002c0003t0001 | 0/0 | 1619 | 43 | 9 | 1 | 32 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | AACAT others(1614): Show |
chr4 | 99506021 | 99547303 |
| a0002c0004t0001 | 0/0 | 1619 | 36 | 21 | 7 | 1 | 0 | 7 | C4orf17_chr4_99506021_99547303 | C4orf17 | AACAT others(1614): Show |
chr4 | 99506021 | 99547303 |
| a0002c0007t0001 | 0/0 | 1619 | 4 | 4 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | AACAT others(1614): Show |
chr4 | 99506021 | 99547303 |
| a0002c0009t0001 | 0/0 | 1619 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | AACAT others(1614): Show |
chr4 | 99506021 | 99547303 |
| a0003c0002t0001 | 0/0 | 1619 | 72 | 19 | 12 | 25 | 1 | 15 | C4orf17_chr4_99506021_99547303 | C4orf17 | AACAT others(1614): Show |
chr4 | 99506021 | 99547303 |
| a0003c0008t0001 | 0/0 | 1619 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | AACAT others(1614): Show |
chr4 | 99506021 | 99547303 |
| a0004c0005t0001 | 0/0 | 1619 | 29 | 11 | 5 | 8 | 0 | 5 | C4orf17_chr4_99506021_99547303 | C4orf17 | AACAT others(1614): Show |
chr4 | 99506021 | 99547303 |
| a0005c0006t0001 | 0/0 | 1607 | 18 | 17 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | AACAT others(1602): Show |
chr4 | 99506021 | 99547303 |
| a0006c0010t0001 | 0/0 | 1619 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | AACAT others(1614): Show |
chr4 | 99506021 | 99547303 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 0 | 0 | 17 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0187 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0001c0011t0001g0025 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0007t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0007t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0007t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0007t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0009t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0002c0009t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0004 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0008t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0008t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0003c0008t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0004c0005t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0005c0006t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| a0006c0010t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0003 | c0002 | t0001 | g0176 | EUR | GBR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00438 | hp2 | a0004 | c0005 | t0001 | g0063 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00544 | hp1 | a0004 | c0005 | t0001 | g0057 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00558 | hp1 | a0004 | c0005 | t0001 | g0015 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00558 | hp2 | a0002 | c0003 | t0001 | g0282 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0039 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00639 | hp2 | a0002 | c0004 | t0001 | g0043 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00733 | hp1 | a0004 | c0005 | t0001 | g0058 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00741 | hp1 | a0003 | c0002 | t0001 | g0075 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01070 | hp1 | a0002 | c0004 | t0001 | g0036 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01070 | hp2 | a0002 | c0003 | t0001 | g0283 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01071 | hp2 | a0002 | c0004 | t0001 | g0036 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01074 | hp1 | a0002 | c0004 | t0001 | g0229 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01106 | hp1 | a0003 | c0002 | t0001 | g0183 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01106 | hp2 | a0003 | c0002 | t0001 | g0191 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01109 | hp1 | a0004 | c0005 | t0001 | g0047 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01167 | hp1 | a0003 | c0002 | t0001 | g0193 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01167 | hp2 | a0003 | c0002 | t0001 | g0208 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01168 | hp2 | a0004 | c0005 | t0001 | g0044 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01169 | hp2 | a0003 | c0002 | t0001 | g0184 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01192 | hp1 | a0003 | c0002 | t0001 | g0030 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01192 | hp2 | a0004 | c0005 | t0001 | g0050 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01243 | hp1 | a0002 | c0004 | t0001 | g0040 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01243 | hp2 | a0004 | c0005 | t0001 | g0052 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01255 | hp2 | a0003 | c0002 | t0001 | g0198 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01257 | hp1 | a0002 | c0004 | t0001 | g0042 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01361 | hp1 | a0003 | c0002 | t0001 | g0195 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01361 | hp2 | a0002 | c0004 | t0001 | g0041 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01884 | hp1 | a0003 | c0002 | t0001 | g0004 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01884 | hp2 | a0005 | c0006 | t0001 | g0254 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01891 | hp2 | a0004 | c0005 | t0001 | g0014 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01934 | hp1 | a0003 | c0002 | t0001 | g0010 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01975 | hp2 | a0005 | c0006 | t0001 | g0250 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02015 | hp1 | a0003 | c0002 | t0001 | g0181 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02027 | hp2 | a0003 | c0002 | t0001 | g0005 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02040 | hp1 | a0003 | c0002 | t0001 | g0006 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02055 | hp1 | a0004 | c0005 | t0001 | g0048 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02055 | hp2 | a0003 | c0002 | t0001 | g0200 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02056 | hp2 | a0004 | c0005 | t0001 | g0055 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02071 | hp2 | a0004 | c0005 | t0001 | g0015 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02083 | hp1 | a0004 | c0005 | t0001 | g0062 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0288 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02132 | hp2 | a0004 | c0005 | t0001 | g0061 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02145 | hp2 | a0002 | c0007 | t0001 | g0292 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02148 | hp1 | a0003 | c0002 | t0001 | g0188 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02257 | hp2 | a0002 | c0004 | t0001 | g0303 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02258 | hp1 | a0005 | c0006 | t0001 | g0037 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02258 | hp2 | a0003 | c0002 | t0001 | g0074 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02280 | hp1 | a0002 | c0004 | t0001 | g0071 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02280 | hp2 | a0002 | c0004 | t0001 | g0237 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02451 | hp1 | a0003 | c0002 | t0001 | g0004 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02451 | hp2 | a0004 | c0005 | t0001 | g0228 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02602 | hp1 | a0003 | c0002 | t0001 | g0004 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02602 | hp2 | a0004 | c0005 | t0001 | g0059 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02615 | hp1 | a0005 | c0006 | t0001 | g0251 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02615 | hp2 | a0003 | c0008 | t0001 | g0097 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02622 | hp1 | a0003 | c0002 | t0001 | g0203 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02622 | hp2 | a0005 | c0006 | t0001 | g0252 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0230 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02630 | hp2 | a0002 | c0004 | t0001 | g0243 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02647 | hp1 | a0002 | c0009 | t0001 | g0021 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02698 | hp2 | a0003 | c0002 | t0001 | g0209 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02717 | hp1 | a0003 | c0002 | t0001 | g0175 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02723 | hp2 | a0002 | c0009 | t0001 | g0021 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02735 | hp1 | a0002 | c0004 | t0001 | g0238 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02735 | hp2 | a0003 | c0002 | t0001 | g0305 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02738 | hp1 | a0003 | c0002 | t0001 | g0201 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02738 | hp2 | a0003 | c0002 | t0001 | g0178 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0269 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02809 | hp2 | a0005 | c0006 | t0001 | g0037 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02818 | hp1 | a0002 | c0004 | t0001 | g0236 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02818 | hp2 | a0003 | c0002 | t0001 | g0196 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02886 | hp1 | a0003 | c0002 | t0001 | g0185 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02886 | hp2 | a0004 | c0005 | t0001 | g0046 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02895 | hp2 | a0003 | c0002 | t0001 | g0029 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02896 | hp1 | a0002 | c0004 | t0001 | g0070 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02896 | hp2 | a0002 | c0004 | t0001 | g0011 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02897 | hp1 | a0002 | c0004 | t0001 | g0011 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02897 | hp2 | a0003 | c0002 | t0001 | g0029 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02922 | hp1 | a0005 | c0006 | t0001 | g0259 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0108 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02965 | hp1 | a0005 | c0006 | t0001 | g0260 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02965 | hp2 | a0004 | c0005 | t0001 | g0054 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02970 | hp1 | a0003 | c0002 | t0001 | g0179 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02970 | hp2 | a0002 | c0009 | t0001 | g0267 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02976 | hp1 | a0003 | c0002 | t0001 | g0004 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02976 | hp2 | a0002 | c0007 | t0001 | g0301 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03017 | hp1 | a0003 | c0002 | t0001 | g0210 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03017 | hp2 | a0003 | c0002 | t0001 | g0180 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03041 | hp1 | a0005 | c0006 | t0001 | g0038 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0291 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03098 | hp1 | a0003 | c0002 | t0001 | g0263 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03098 | hp2 | a0002 | c0004 | t0001 | g0224 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03130 | hp1 | a0002 | c0004 | t0001 | g0011 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03130 | hp2 | a0005 | c0006 | t0001 | g0038 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03139 | hp1 | a0003 | c0008 | t0001 | g0098 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03139 | hp2 | a0004 | c0005 | t0001 | g0045 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03195 | hp1 | a0002 | c0004 | t0001 | g0173 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03195 | hp2 | a0002 | c0007 | t0001 | g0281 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0275 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0107 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03225 | hp2 | a0002 | c0004 | t0001 | g0239 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03453 | hp1 | a0005 | c0006 | t0001 | g0258 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0234 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03486 | hp1 | a0002 | c0007 | t0001 | g0297 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03486 | hp2 | a0005 | c0006 | t0001 | g0069 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03490 | hp2 | a0003 | c0002 | t0001 | g0064 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03491 | hp1 | a0002 | c0004 | t0001 | g0245 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03492 | hp1 | a0002 | c0004 | t0001 | g0244 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03516 | hp1 | a0005 | c0006 | t0001 | g0262 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03516 | hp2 | a0002 | c0004 | t0001 | g0233 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03540 | hp1 | a0003 | c0002 | t0001 | g0004 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03540 | hp2 | a0004 | c0005 | t0001 | g0051 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03579 | hp1 | a0002 | c0003 | t0001 | g0302 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03579 | hp2 | a0003 | c0002 | t0001 | g0110 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03654 | hp1 | a0003 | c0002 | t0001 | g0182 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03669 | hp1 | a0003 | c0002 | t0001 | g0031 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03669 | hp2 | a0002 | c0004 | t0001 | g0265 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03688 | hp1 | a0003 | c0002 | t0001 | g0186 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03688 | hp2 | a0002 | c0004 | t0001 | g0246 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03704 | hp2 | a0002 | c0004 | t0001 | g0247 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03834 | hp1 | a0004 | c0005 | t0001 | g0066 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03834 | hp2 | a0006 | c0010 | t0001 | g0225 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03927 | hp2 | a0003 | c0002 | t0001 | g0030 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03942 | hp1 | a0003 | c0002 | t0001 | g0197 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03942 | hp2 | a0004 | c0005 | t0001 | g0067 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG04115 | hp2 | a0003 | c0002 | t0001 | g0005 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG04184 | hp2 | a0003 | c0002 | t0001 | g0189 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG04228 | hp1 | a0002 | c0004 | t0001 | g0235 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG04228 | hp2 | a0002 | c0003 | t0001 | g0279 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18906 | hp1 | a0003 | c0002 | t0001 | g0204 | AFR | YRI | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18906 | hp2 | a0004 | c0005 | t0001 | g0014 | AFR | YRI | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18940 | hp2 | a0002 | c0003 | t0001 | g0273 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18941 | hp1 | a0002 | c0003 | t0001 | g0300 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18944 | hp1 | a0003 | c0002 | t0001 | g0202 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18946 | hp1 | a0003 | c0002 | t0001 | g0009 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18947 | hp1 | a0004 | c0005 | t0001 | g0065 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18947 | hp2 | a0002 | c0003 | t0001 | g0274 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18948 | hp1 | a0003 | c0002 | t0001 | g0190 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0289 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0277 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18956 | hp1 | a0002 | c0003 | t0001 | g0290 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18956 | hp2 | a0003 | c0002 | t0001 | g0009 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18959 | hp1 | a0003 | c0002 | t0001 | g0194 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18960 | hp1 | a0003 | c0002 | t0001 | g0005 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18960 | hp2 | a0002 | c0003 | t0001 | g0268 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18961 | hp1 | a0003 | c0002 | t0001 | g0172 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18965 | hp1 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18965 | hp2 | a0003 | c0002 | t0001 | g0068 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18967 | hp2 | a0003 | c0002 | t0001 | g0177 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18969 | hp1 | a0003 | c0002 | t0001 | g0006 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18972 | hp1 | a0002 | c0003 | t0001 | g0278 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18975 | hp2 | a0003 | c0002 | t0001 | g0006 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18976 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18976 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18978 | hp1 | a0002 | c0003 | t0001 | g0280 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18979 | hp2 | a0003 | c0002 | t0001 | g0205 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18986 | hp1 | a0002 | c0003 | t0001 | g0296 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18987 | hp1 | a0002 | c0004 | t0001 | g0248 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18987 | hp2 | a0002 | c0003 | t0001 | g0293 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18988 | hp2 | a0002 | c0003 | t0001 | g0285 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18991 | hp1 | a0003 | c0002 | t0001 | g0207 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18993 | hp2 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18994 | hp2 | a0003 | c0002 | t0001 | g0010 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0272 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19001 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19003 | hp1 | a0003 | c0002 | t0001 | g0032 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19004 | hp2 | a0002 | c0003 | t0001 | g0294 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19010 | hp1 | a0003 | c0002 | t0001 | g0032 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19012 | hp1 | a0003 | c0002 | t0001 | g0009 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19030 | hp1 | a0002 | c0004 | t0001 | g0240 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19030 | hp2 | a0005 | c0006 | t0001 | g0253 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0101 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19054 | hp2 | a0002 | c0003 | t0001 | g0270 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19058 | hp1 | a0002 | c0003 | t0001 | g0295 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19060 | hp1 | a0003 | c0002 | t0001 | g0010 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19062 | hp1 | a0003 | c0002 | t0001 | g0006 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19065 | hp2 | a0002 | c0003 | t0001 | g0298 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19066 | hp2 | a0002 | c0003 | t0001 | g0276 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19077 | hp2 | a0003 | c0002 | t0001 | g0031 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19079 | hp2 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19080 | hp1 | a0003 | c0002 | t0001 | g0005 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19081 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19083 | hp2 | a0002 | c0003 | t0001 | g0287 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19086 | hp1 | a0002 | c0003 | t0001 | g0072 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19087 | hp2 | a0002 | c0003 | t0001 | g0073 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19089 | hp2 | a0002 | c0003 | t0001 | g0299 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19090 | hp1 | a0003 | c0002 | t0001 | g0206 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19240 | hp1 | a0004 | c0005 | t0001 | g0049 | AFR | YRI | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA19240 | hp2 | a0005 | c0006 | t0001 | g0255 | AFR | YRI | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0284 | AFR | ASW | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA20129 | hp2 | a0005 | c0006 | t0001 | g0261 | AFR | ASW | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA20905 | hp1 | a0004 | c0005 | t0001 | g0060 | SAS | GIH | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA20905 | hp2 | a0004 | c0005 | t0001 | g0056 | SAS | GIH | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG01123 | hp2 | a0003 | c0002 | t0001 | g0199 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02109 | hp1 | a0002 | c0004 | t0001 | g0249 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0286 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02486 | hp1 | a0005 | c0006 | t0001 | g0257 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02486 | hp2 | a0004 | c0005 | t0001 | g0226 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02559 | hp1 | a0003 | c0002 | t0001 | g0109 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG02559 | hp2 | a0005 | c0006 | t0001 | g0256 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03471 | hp1 | a0002 | c0004 | t0001 | g0231 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG03471 | hp2 | a0003 | c0002 | t0001 | g0111 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG06807 | hp1 | a0002 | c0004 | t0001 | g0241 | AFR | USA | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| HG06807 | hp2 | a0003 | c0008 | t0001 | g0099 | AFR | USA | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA20300 | hp1 | a0003 | c0002 | t0001 | g0192 | AFR | USA | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0271 | AFR | USA | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA21309 | hp1 | a0002 | c0004 | t0001 | g0242 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| NA21309 | hp2 | a0004 | c0005 | t0001 | g0053 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| homoSapiens | chm13v2 | a0001 | c0011 | t0001 | g0025 | REF | REF | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0187 | REF | REF | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:99522563 | G | A | 2 | a0003 a0004 |
104 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(101): Show |
missense_variant | MODERATE | c.191G>A | p.Gly64Glu | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/9 | 536/1619 | 191/1080 | 64/359 | chr4 | 99522563 | |||
| chr4:99522625 | T | C | 5 | a0002 a0003 a0004 others(2): Show |
209 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(206): Show |
missense_variant | MODERATE | c.253T>C | p.Ser85Pro | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/9 | 598/1619 | 253/1080 | 85/359 | chr4 | 99522625 | |||
| chr4:99522643 | G | A | 1 | a0003 | 75 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(72): Show |
missense_variant | MODERATE | c.271G>A | p.Glu91Lys | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/9 | 616/1619 | 271/1080 | 91/359 | chr4 | 99522643 | |||
| chr4:99529881 | TCAGGGAT others(5): Show |
T | 1 | a0005 | 18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
disruptive_inframe_deletion | MODERATE | c.470_481delCAGGGATG others(4): Show |
p.Ser157_Ser161delin others(4): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/9 | 815/1619 | 470/1080 | 157/359 | chr4 | 99529881 | |||
| chr4:99529894 | G | A | 1 | a0005 | 18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
missense_variant | MODERATE | c.482G>A | p.Ser161Asn | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/9 | 827/1619 | 482/1080 | 161/359 | chr4 | 99529894 | |||
| chr4:99542101 | C | T | 1 | a0006 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1072C>T | p.Arg358Trp | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 9/9 | 1417/1619 | 1072/1080 | 358/359 | chr4 | 99542101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:99522627 | C | G | 2 | a0002c0009 a0003c0002 |
75 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(72): Show |
synonymous_variant | LOW | c.255C>G | p.Ser85Ser | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/9 | 600/1619 | 255/1080 | 85/359 | chr4 | 99522627 | |||
| chr4:99522696 | A | G | 3 | a0002c0003 a0002c0007 a0002c0009 |
50 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(47): Show |
synonymous_variant | LOW | c.324A>G | p.Pro108Pro | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/9 | 669/1619 | 324/1080 | 108/359 | chr4 | 99522696 | |||
| chr4:99539356 | G | A | 1 | a0002c0007 | 4 | HG02145.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.822G>A | p.Gly274Gly | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/9 | 1167/1619 | 822/1080 | 274/359 | chr4 | 99539356 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:99511423 | C | CT | 43 | a0001c0001t0001g0266 a0001c0001t0001g0304 a0002c0003t0001g0012 others(40): Show |
48 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.-94+162dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99511423 | ||||||
| chr4:99511423 | CT | C | 30 | a0002c0004t0001g0070 a0002c0004t0001g0071 a0003c0002t0001g0064 others(27): Show |
32 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-94+162delT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99511423 | ||||||
| chr4:99511426 | T | C | 4 | a0002c0004t0001g0040 a0002c0004t0001g0041 a0002c0004t0001g0042 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+154T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511426 | |||||||
| chr4:99511555 | C | G | 4 | a0002c0004t0001g0040 a0002c0004t0001g0041 a0002c0004t0001g0042 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+283C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511555 | |||||||
| chr4:99511684 | G | A | 41 | a0001c0001t0001g0266 a0002c0003t0001g0012 a0002c0003t0001g0013 others(38): Show |
46 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.-94+412G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511684 | |||||||
| chr4:99511703 | A | G | 1 | a0002c0004t0001g0265 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-94+431A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511703 | |||||||
| chr4:99511866 | T | C | 2 | a0003c0002t0001g0074 a0003c0002t0001g0075 |
2 | HG00741.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-94+594T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511866 | |||||||
| chr4:99511887 | A | C | 1 | a0001c0001t0001g0264 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-94+615A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511887 | |||||||
| chr4:99511972 | G | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(26): Show |
61 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-94+700G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511972 | |||||||
| chr4:99511990 | C | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0100 a0002c0003t0001g0101 others(3): Show |
7 | HG00735.hp1 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-94+718C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511990 | |||||||
| chr4:99512139 | A | T | 4 | a0002c0004t0001g0040 a0002c0004t0001g0041 a0002c0004t0001g0042 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-850A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512139 | |||||||
| chr4:99512195 | C | T | 19 | a0002c0004t0001g0070 a0002c0004t0001g0071 a0003c0002t0001g0263 others(16): Show |
21 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-93-794C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512195 | |||||||
| chr4:99512196 | G | A | 1 | a0002c0003t0001g0302 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-93-793G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512196 | |||||||
| chr4:99512327 | G | A | 4 | a0002c0004t0001g0040 a0002c0004t0001g0041 a0002c0004t0001g0042 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-662G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512327 | |||||||
| chr4:99512345 | G | C | 1 | a0002c0004t0001g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-93-644G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512345 | |||||||
| chr4:99512352 | C | T | 24 | a0001c0001t0001g0232 a0002c0004t0001g0011 a0002c0004t0001g0229 others(21): Show |
26 | HG01074.hp1 HG01346.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-93-637C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512352 | |||||||
| chr4:99512380 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-93-609C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512380 | |||||||
| chr4:99512451 | C | A | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG01261.hp2 HG01358.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-538C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512451 | |||||||
| chr4:99512579 | A | C | 4 | a0002c0004t0001g0040 a0002c0004t0001g0041 a0002c0004t0001g0042 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-410A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512579 | |||||||
| chr4:99512638 | GTCA | G | 23 | a0001c0001t0001g0232 a0002c0004t0001g0011 a0002c0004t0001g0229 others(20): Show |
25 | HG01074.hp1 HG01346.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-93-346_-93-344del others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99512638 | ||||||
| chr4:99512812 | T | A | 1 | a0002c0004t0001g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-93-177T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512812 | |||||||
| chr4:99512870 | C | A | 1 | a0001c0001t0001g0266 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-93-119C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512870 | |||||||
| chr4:99512904 | C | T | 1 | a0004c0005t0001g0226 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-93-85C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512904 | |||||||
| chr4:99513288 | C | T | 1 | a0002c0003t0001g0302 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.127+80C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513288 | |||||||
| chr4:99513402 | C | T | 24 | a0001c0001t0001g0232 a0002c0004t0001g0011 a0002c0004t0001g0229 others(21): Show |
26 | HG01074.hp1 HG01346.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.127+194C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513402 | |||||||
| chr4:99513453 | G | C | 1 | a0002c0004t0001g0229 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.127+245G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513453 | |||||||
| chr4:99513512 | G | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
292 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.127+304G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513512 | |||||||
| chr4:99513629 | C | G | 16 | a0003c0002t0001g0263 a0005c0006t0001g0037 a0005c0006t0001g0038 others(13): Show |
18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.127+421C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513629 | |||||||
| chr4:99513642 | C | T | 41 | a0001c0001t0001g0266 a0002c0003t0001g0012 a0002c0003t0001g0013 others(38): Show |
46 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.127+434C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513642 | |||||||
| chr4:99513668 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.127+460C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513668 | |||||||
| chr4:99513795 | C | T | 31 | a0001c0001t0001g0028 a0001c0001t0001g0142 a0001c0001t0001g0143 others(28): Show |
32 | HG00140.hp2 HG00408.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.127+587C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513795 | |||||||
| chr4:99513915 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(26): Show |
61 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.127+707C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513915 | |||||||
| chr4:99513929 | A | T | 3 | a0001c0001t0001g0304 a0002c0003t0001g0302 a0002c0004t0001g0303 |
3 | HG02145.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.127+721A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513929 | |||||||
| chr4:99513931 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.127+723A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513931 | |||||||
| chr4:99514202 | A | G | 4 | a0002c0004t0001g0040 a0002c0004t0001g0041 a0002c0004t0001g0042 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+994A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514202 | |||||||
| chr4:99514408 | G | GA | 28 | a0001c0001t0001g0304 a0002c0003t0001g0107 a0002c0003t0001g0302 others(25): Show |
31 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+1207dupA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99514408 | ||||||
| chr4:99514435 | G | T | 41 | a0001c0001t0001g0266 a0002c0003t0001g0012 a0002c0003t0001g0013 others(38): Show |
46 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.127+1227G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514435 | |||||||
| chr4:99514474 | T | G | 2 | a0002c0004t0001g0230 a0002c0004t0001g0231 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.127+1266T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514474 | |||||||
| chr4:99514583 | T | A | 4 | a0002c0004t0001g0040 a0002c0004t0001g0041 a0002c0004t0001g0042 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+1375T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514583 | |||||||
| chr4:99514642 | A | G | 1 | a0002c0003t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127+1434A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514642 | |||||||
| chr4:99514669 | G | A | 28 | a0001c0001t0001g0304 a0002c0003t0001g0107 a0002c0003t0001g0302 others(25): Show |
31 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+1461G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514669 | |||||||
| chr4:99514745 | C | T | 1 | a0002c0007t0001g0301 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127+1537C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514745 | |||||||
| chr4:99514894 | T | C | 28 | a0001c0001t0001g0304 a0002c0003t0001g0107 a0002c0003t0001g0302 others(25): Show |
31 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+1686T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514894 | |||||||
| chr4:99514910 | C | T | 28 | a0001c0001t0001g0304 a0002c0003t0001g0107 a0002c0003t0001g0302 others(25): Show |
31 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+1702C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514910 | |||||||
| chr4:99514997 | C | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(26): Show |
61 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.127+1789C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514997 | |||||||
| chr4:99515075 | T | A | 28 | a0001c0001t0001g0304 a0002c0003t0001g0107 a0002c0003t0001g0302 others(25): Show |
31 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+1867T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515075 | |||||||
| chr4:99515180 | T | C | 3 | a0003c0008t0001g0097 a0003c0008t0001g0098 a0003c0008t0001g0099 |
3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.127+1972T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515180 | |||||||
| chr4:99515197 | A | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(26): Show |
61 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.127+1989A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515197 | |||||||
| chr4:99515220 | C | A | 1 | a0004c0005t0001g0226 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127+2012C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515220 | |||||||
| chr4:99515262 | C | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(72): Show |
88 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.127+2054C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515262 | |||||||
| chr4:99515356 | C | T | 1 | a0002c0004t0001g0249 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.127+2148C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515356 | |||||||
| chr4:99515560 | G | A | 1 | a0003c0002t0001g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.127+2352G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515560 | |||||||
| chr4:99515788 | A | T | 1 | a0002c0003t0001g0300 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.127+2580A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515788 | |||||||
| chr4:99515887 | T | C | 26 | a0002c0003t0001g0107 a0002c0004t0001g0040 a0002c0004t0001g0041 others(23): Show |
29 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.127+2679T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515887 | |||||||
| chr4:99515949 | C | G | 1 | a0002c0003t0001g0299 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.127+2741C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515949 | |||||||
| chr4:99516068 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.127+2860C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516068 | |||||||
| chr4:99516279 | T | C | 22 | a0002c0003t0001g0107 a0002c0004t0001g0070 a0002c0004t0001g0071 others(19): Show |
25 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.127+3071T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516279 | |||||||
| chr4:99516310 | A | G | 1 | a0004c0005t0001g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.127+3102A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516310 | |||||||
| chr4:99516396 | T | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(72): Show |
88 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.127+3188T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516396 | |||||||
| chr4:99516404 | G | A | 2 | a0003c0002t0001g0009 a0003c0002t0001g0172 |
4 | NA18946.hp1 NA18956.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+3196G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516404 | |||||||
| chr4:99516407 | A | C | 1 | a0003c0002t0001g0111 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.127+3199A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516407 | |||||||
| chr4:99516479 | G | A | 2 | a0001c0001t0001g0112 a0002c0004t0001g0108 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.127+3271G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516479 | |||||||
| chr4:99516522 | G | A | 1 | a0004c0005t0001g0044 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.127+3314G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516522 | |||||||
| chr4:99516644 | A | G | 26 | a0002c0003t0001g0107 a0002c0004t0001g0040 a0002c0004t0001g0041 others(23): Show |
29 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.127+3436A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516644 | |||||||
| chr4:99516730 | G | A | 4 | a0002c0004t0001g0040 a0002c0004t0001g0041 a0002c0004t0001g0042 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+3522G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516730 | |||||||
| chr4:99516943 | C | T | 1 | a0004c0005t0001g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.127+3735C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516943 | |||||||
| chr4:99516983 | G | GA | 12 | a0004c0005t0001g0014 a0004c0005t0001g0045 a0004c0005t0001g0046 others(9): Show |
13 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.127+3778dupA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99516983 | ||||||
| chr4:99517028 | G | A | 1 | a0002c0004t0001g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.127+3820G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517028 | |||||||
| chr4:99517041 | G | A | 1 | a0004c0005t0001g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.127+3833G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517041 | |||||||
| chr4:99517172 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(67): Show |
106 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.127+3964C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517172 | |||||||
| chr4:99517329 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
274 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.127+4121A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517329 | |||||||
| chr4:99517500 | C | T | 2 | a0002c0003t0001g0101 a0002c0003t0001g0302 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.127+4292C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517500 | |||||||
| chr4:99517543 | CTCTCTTT others(7): Show |
C | 27 | a0003c0002t0001g0064 a0004c0005t0001g0014 a0004c0005t0001g0015 others(24): Show |
29 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.127+4344_127+4357d others(16): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99517543 | ||||||
| chr4:99517578 | T | TA | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
244 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.127+4376dupA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99517578 | ||||||
| chr4:99517888 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.128-4612G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517888 | |||||||
| chr4:99517919 | C | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.128-4581C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517919 | |||||||
| chr4:99517952 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.128-4548A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517952 | |||||||
| chr4:99517995 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
250 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.128-4505C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517995 | |||||||
| chr4:99518159 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.128-4341C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518159 | |||||||
| chr4:99518194 | C | T | 1 | a0003c0002t0001g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.128-4306C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518194 | |||||||
| chr4:99518249 | T | G | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG00280.hp1 HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.128-4251T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518249 | |||||||
| chr4:99518301 | C | T | 1 | a0002c0004t0001g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.128-4199C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518301 | |||||||
| chr4:99518485 | TA | T | 8 | a0002c0003t0001g0274 a0002c0004t0001g0239 a0003c0002t0001g0064 others(5): Show |
9 | HG00438.hp2 HG01167.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.128-3981delA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAA | T | 8 | a0001c0001t0001g0174 a0001c0001t0001g0216 a0002c0003t0001g0275 others(5): Show |
8 | HG00733.hp2 HG02109.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-3982_128-3981d others(4): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAA | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0117 a0001c0001t0001g0118 others(8): Show |
12 | HG01243.hp2 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.128-3983_128-3981d others(5): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAA | T | 22 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(19): Show |
23 | HG00558.hp2 HG00621.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.128-3985_128-3981d others(7): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAAA | T | 8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0124 others(5): Show |
8 | HG00639.hp1 HG01175.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-3986_128-3981d others(8): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAAAA | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0078 others(25): Show |
40 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.128-3987_128-3981d others(9): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAAAA others(1): Show |
T | 18 | a0001c0001t0001g0024 a0001c0001t0001g0080 a0001c0001t0001g0112 others(15): Show |
19 | HG00639.hp2 HG01099.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.128-3988_128-3981d others(10): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAAAA others(2): Show |
T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(41): Show |
76 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.128-3989_128-3981d others(11): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAAAA others(3): Show |
T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0086 others(19): Show |
25 | HG00280.hp1 HG00280.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.128-3990_128-3981d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAAAA others(4): Show |
T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0091 a0001c0001t0001g0092 others(7): Show |
13 | HG01070.hp1 HG01071.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.128-3991_128-3981d others(13): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAAAA others(5): Show |
T | 5 | a0001c0001t0001g0093 a0002c0004t0001g0071 a0002c0004t0001g0303 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-3992_128-3981d others(14): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAAAA others(6): Show |
T | 1 | a0005c0006t0001g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.128-3993_128-3981d others(15): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAAAA others(7): Show |
T | 6 | a0005c0006t0001g0038 a0005c0006t0001g0254 a0005c0006t0001g0255 others(3): Show |
7 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-3994_128-3981d others(16): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAAAA others(8): Show |
T | 1 | a0005c0006t0001g0260 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.128-3995_128-3981d others(17): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518485 | TAAAAAAA others(9): Show |
T | 3 | a0002c0003t0001g0107 a0005c0006t0001g0261 a0005c0006t0001g0262 |
3 | HG03225.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.128-3996_128-3981d others(18): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | ||||||
| chr4:99518503 | AAAAAAAA others(10): Show |
A | 1 | a0005c0006t0001g0259 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.128-3995_128-3979d others(19): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518503 | ||||||
| chr4:99518504 | AAAAAAAA others(9): Show |
A | 1 | a0005c0006t0001g0250 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.128-3994_128-3979d others(18): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518504 | ||||||
| chr4:99518505 | AAAAAAAA others(8): Show |
A | 3 | a0002c0003t0001g0302 a0002c0009t0001g0021 a0005c0006t0001g0037 |
4 | HG02258.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-3993_128-3979d others(17): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518505 | ||||||
| chr4:99518505 | AAAAAAAA others(10): Show |
A | 1 | a0002c0009t0001g0021 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.128-3993_128-3977d others(19): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518505 | ||||||
| chr4:99518506 | A | ATATATAT others(4): Show |
1 | a0002c0004t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.128-3994_128-3993i others(13): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518506 | |||||||
| chr4:99518506 | A | T | 1 | a0002c0003t0001g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.128-3994A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518506 | |||||||
| chr4:99518507 | AAAAAAAA others(6): Show |
A | 1 | a0002c0004t0001g0224 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.128-3991_128-3979d others(15): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518507 | ||||||
| chr4:99518507 | AAAAAAAA others(8): Show |
A | 2 | a0002c0003t0001g0101 a0002c0004t0001g0173 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.128-3991_128-3977d others(17): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518507 | ||||||
| chr4:99518507 | AAAAAAAA others(12): Show |
A | 1 | a0002c0009t0001g0267 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.128-3991_128-3973d others(21): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518507 | ||||||
| chr4:99518508 | A | AT | 3 | a0002c0004t0001g0229 a0002c0004t0001g0234 a0002c0004t0001g0235 |
3 | HG01074.hp1 HG03453.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.128-3992_128-3991i others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518508 | |||||||
| chr4:99518508 | A | T | 7 | a0002c0003t0001g0269 a0002c0003t0001g0271 a0002c0003t0001g0272 others(4): Show |
7 | HG02809.hp1 HG02818.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-3992A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518508 | |||||||
| chr4:99518508 | AAAAAAAA others(5): Show |
A | 2 | a0002c0004t0001g0011 a0005c0006t0001g0069 |
2 | HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.128-3990_128-3979d others(14): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518508 | ||||||
| chr4:99518508 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0076 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.128-3990_128-3977d others(16): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518508 | ||||||
| chr4:99518509 | AAAAAAAA others(4): Show |
A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0143 a0002c0004t0001g0011 others(2): Show |
6 | HG02071.hp1 HG02735.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-3989_128-3979d others(13): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518509 | ||||||
| chr4:99518510 | A | T | 19 | a0002c0003t0001g0072 a0002c0003t0001g0268 a0002c0003t0001g0269 others(16): Show |
19 | HG01074.hp1 HG01243.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-3990A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518510 | |||||||
| chr4:99518510 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0115 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-3988_128-3979d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518510 | ||||||
| chr4:99518511 | AAAAAAAA others(2): Show |
A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0116 a0001c0001t0001g0144 others(3): Show |
7 | HG01975.hp1 HG02451.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-3987_128-3979d others(11): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518511 | ||||||
| chr4:99518512 | A | T | 35 | a0002c0003t0001g0039 a0002c0003t0001g0072 a0002c0003t0001g0268 others(32): Show |
35 | HG00639.hp2 HG01070.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.128-3988A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518512 | |||||||
| chr4:99518512 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0100 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.128-3986_128-3977d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518512 | ||||||
| chr4:99518514 | A | AT | 9 | a0003c0002t0001g0005 a0003c0002t0001g0031 a0003c0002t0001g0175 others(6): Show |
9 | HG02015.hp1 HG02056.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.128-3986_128-3985i others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518514 | |||||||
| chr4:99518514 | A | ATATATAT others(4): Show |
1 | a0003c0008t0001g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.128-3986_128-3985i others(13): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518514 | |||||||
| chr4:99518514 | A | T | 49 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0216 others(46): Show |
51 | HG00621.hp1 HG00639.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.128-3986A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518514 | |||||||
| chr4:99518516 | A | AT | 7 | a0003c0002t0001g0004 a0003c0002t0001g0006 a0003c0002t0001g0029 others(4): Show |
7 | HG00733.hp1 HG02602.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-3984_128-3983i others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518516 | |||||||
| chr4:99518516 | A | ATAT | 3 | a0003c0002t0001g0004 a0003c0002t0001g0179 a0003c0002t0001g0185 |
4 | HG01884.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-3984_128-3983i others(5): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518516 | |||||||
| chr4:99518516 | A | T | 88 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0120 others(85): Show |
94 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-3984A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518516 | |||||||
| chr4:99518518 | A | AATATATA others(3): Show |
1 | a0003c0002t0001g0189 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.128-3964_128-3955d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518518 | ||||||
| chr4:99518518 | A | AT | 3 | a0003c0002t0001g0006 a0003c0002t0001g0178 a0003c0002t0001g0305 |
4 | HG02040.hp1 HG02735.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-3982_128-3981i others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518518 | |||||||
| chr4:99518518 | A | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0022 others(152): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.128-3982A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518518 | |||||||
| chr4:99518538 | T | G | 2 | a0003c0002t0001g0175 a0004c0005t0001g0065 |
2 | HG02717.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.128-3962T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518538 | |||||||
| chr4:99518540 | T | G | 7 | a0001c0001t0001g0120 a0002c0004t0001g0233 a0003c0002t0001g0030 others(4): Show |
9 | HG01192.hp1 HG02056.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-3960T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518540 | |||||||
| chr4:99518542 | T | G | 20 | a0001c0001t0001g0104 a0001c0001t0001g0113 a0001c0001t0001g0120 others(17): Show |
22 | HG00140.hp1 HG00544.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.128-3958T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518542 | |||||||
| chr4:99518542 | T | TAGAGAGA others(7): Show |
1 | a0002c0004t0001g0265 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.128-3957_128-3956i others(16): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518542 | ||||||
| chr4:99518544 | T | G | 47 | a0001c0001t0001g0100 a0001c0001t0001g0104 a0001c0001t0001g0113 others(44): Show |
50 | HG00140.hp1 HG00544.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-3956T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518544 | |||||||
| chr4:99518544 | T | TAGAG | 4 | a0002c0004t0001g0236 a0003c0002t0001g0185 a0004c0005t0001g0060 others(1): Show |
4 | HG02132.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-3919_128-3916d others(6): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | ||||||
| chr4:99518544 | T | TAGAGAGA others(3): Show |
1 | a0003c0008t0001g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.128-3925_128-3916d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | ||||||
| chr4:99518544 | T | TATATAGA others(3): Show |
2 | a0003c0002t0001g0200 a0003c0002t0001g0201 |
2 | HG02055.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.128-3955_128-3954i others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | ||||||
| chr4:99518544 | T | TATATATA others(9): Show |
1 | a0003c0008t0001g0099 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.128-3955_128-3954i others(18): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | ||||||
| chr4:99518544 | T | TATATATA others(5): Show |
1 | a0003c0002t0001g0207 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.128-3955_128-3954i others(14): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | ||||||
| chr4:99518544 | TAGAG | T | 9 | a0001c0001t0001g0148 a0002c0004t0001g0036 a0002c0004t0001g0108 others(6): Show |
10 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.128-3919_128-3916d others(6): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | ||||||
| chr4:99518544 | TAGAGAG | T | 11 | a0001c0001t0001g0076 a0001c0001t0001g0093 a0002c0004t0001g0241 others(8): Show |
12 | HG01168.hp2 HG01975.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.128-3921_128-3916d others(8): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | ||||||
| chr4:99518544 | TAGAGAGA others(1): Show |
T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(13): Show |
20 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.128-3923_128-3916d others(10): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | ||||||
| chr4:99518544 | TAGAGAGA others(3): Show |
T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(18): Show |
50 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-3925_128-3916d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | ||||||
| chr4:99518544 | TAGAGAGA others(5): Show |
T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0079 a0001c0001t0001g0304 others(2): Show |
6 | HG00408.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-3927_128-3916d others(14): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | ||||||
| chr4:99518546 | G | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0024 others(128): Show |
157 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.128-3954G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518546 | |||||||
| chr4:99518548 | G | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0024 others(85): Show |
110 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.128-3952G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518548 | |||||||
| chr4:99518550 | G | T | 53 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0112 others(50): Show |
62 | HG00140.hp2 HG00558.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.128-3950G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518550 | |||||||
| chr4:99518552 | G | T | 21 | a0001c0001t0001g0027 a0001c0001t0001g0093 a0001c0001t0001g0116 others(18): Show |
23 | HG00140.hp2 HG01070.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.128-3948G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518552 | |||||||
| chr4:99518554 | G | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0088 others(18): Show |
25 | HG01081.hp2 HG02486.hp1 HG02523.hp1 others(22): Show |
intron_variant | MODIFIER | c.128-3946G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518554 | |||||||
| chr4:99518556 | G | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(21): Show |
47 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-3944G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518556 | |||||||
| chr4:99518558 | G | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0079 others(5): Show |
10 | HG00408.hp1 HG00544.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-3942G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518558 | |||||||
| chr4:99518560 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.128-3940G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518560 | |||||||
| chr4:99518566 | G | C | 1 | a0002c0009t0001g0267 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.128-3934G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518566 | |||||||
| chr4:99518573 | AGAGAGAG others(9): Show |
A | 2 | a0002c0003t0001g0269 a0002c0003t0001g0270 |
2 | HG02809.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.128-3922_128-3907d others(18): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518573 | ||||||
| chr4:99518574 | G | C | 1 | a0002c0009t0001g0021 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.128-3926G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518574 | |||||||
| chr4:99518575 | AGAGAGAG others(7): Show |
A | 1 | a0002c0003t0001g0273 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.128-3920_128-3907d others(16): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518575 | ||||||
| chr4:99518576 | G | C | 1 | a0002c0009t0001g0021 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.128-3924G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518576 | |||||||
| chr4:99518577 | AGAGAGAG others(5): Show |
A | 1 | a0002c0003t0001g0300 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.128-3918_128-3907d others(14): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518577 | ||||||
| chr4:99518578 | G | C | 1 | a0002c0009t0001g0267 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.128-3922G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518578 | |||||||
| chr4:99518579 | AGAGAGGG others(3): Show |
A | 1 | a0002c0003t0001g0272 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.128-3916_128-3907d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518579 | ||||||
| chr4:99518581 | AGAGGGAG others(1): Show |
A | 4 | a0002c0003t0001g0101 a0002c0003t0001g0107 a0002c0003t0001g0302 others(1): Show |
4 | HG02723.hp2 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-3915_128-3908d others(10): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518581 | ||||||
| chr4:99518582 | G | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0100 a0002c0004t0001g0070 others(17): Show |
23 | HG00735.hp1 HG01884.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.128-3918G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518582 | |||||||
| chr4:99518583 | AGGGAGG | A | 29 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0039 others(26): Show |
34 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.128-3915_128-3910d others(8): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518583 | ||||||
| chr4:99518585 | G | A | 6 | a0002c0003t0001g0072 a0002c0003t0001g0268 a0002c0003t0001g0275 others(3): Show |
6 | HG02145.hp2 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-3915G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518585 | |||||||
| chr4:99518589 | G | A | 7 | a0002c0003t0001g0072 a0002c0003t0001g0268 a0002c0003t0001g0275 others(4): Show |
7 | HG02145.hp2 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-3911G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518589 | |||||||
| chr4:99518730 | C | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
195 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.128-3770C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518730 | |||||||
| chr4:99518753 | A | T | 1 | a0003c0002t0001g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.128-3747A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518753 | |||||||
| chr4:99518757 | G | A | 4 | a0002c0004t0001g0040 a0002c0004t0001g0041 a0002c0004t0001g0042 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-3743G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518757 | |||||||
| chr4:99518757 | G | GTC | 27 | a0002c0004t0001g0011 a0002c0004t0001g0036 a0002c0004t0001g0108 others(24): Show |
30 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.128-3741_128-3740d others(4): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518757 | ||||||
| chr4:99518879 | T | C | 4 | a0003c0002t0001g0109 a0003c0002t0001g0110 a0003c0002t0001g0111 others(1): Show |
4 | HG02559.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-3621T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518879 | |||||||
| chr4:99518922 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
195 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.128-3578T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518922 | |||||||
| chr4:99518955 | G | A | 2 | a0002c0009t0001g0021 a0002c0009t0001g0267 |
3 | HG02647.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.128-3545G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518955 | |||||||
| chr4:99519489 | T | C | 44 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0039 others(41): Show |
50 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.128-3011T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519489 | |||||||
| chr4:99519602 | T | G | 2 | a0002c0004t0001g0173 a0002c0004t0001g0224 |
2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.128-2898T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519602 | |||||||
| chr4:99519622 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.128-2878G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519622 | |||||||
| chr4:99519687 | G | T | 5 | a0004c0005t0001g0015 a0004c0005t0001g0055 a0004c0005t0001g0057 others(2): Show |
6 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-2813G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519687 | |||||||
| chr4:99519688 | A | T | 1 | a0002c0003t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.128-2812A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519688 | |||||||
| chr4:99519762 | T | A | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG01261.hp2 HG01358.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-2738T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519762 | |||||||
| chr4:99519794 | G | C | 1 | a0002c0004t0001g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.128-2706G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519794 | |||||||
| chr4:99519826 | G | A | 1 | a0002c0003t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-2674G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519826 | |||||||
| chr4:99520089 | A | AT | 93 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(90): Show |
109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.128-2393dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99520089 | ||||||
| chr4:99520089 | A | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(27): Show |
62 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.128-2411A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520089 | |||||||
| chr4:99520089 | AT | A | 44 | a0001c0001t0001g0020 a0001c0001t0001g0100 a0002c0003t0001g0012 others(41): Show |
51 | HG00558.hp2 HG00621.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.128-2393delT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99520089 | ||||||
| chr4:99520092 | T | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(27): Show |
62 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.128-2408T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520092 | |||||||
| chr4:99520096 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.128-2404T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520096 | |||||||
| chr4:99520101 | T | C | 26 | a0004c0005t0001g0014 a0004c0005t0001g0015 a0004c0005t0001g0044 others(23): Show |
28 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.128-2399T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520101 | |||||||
| chr4:99520175 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(27): Show |
62 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.128-2325C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520175 | |||||||
| chr4:99520235 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.128-2265G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520235 | |||||||
| chr4:99520256 | A | AT | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
244 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.128-2234dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99520256 | ||||||
| chr4:99520297 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.128-2203G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520297 | |||||||
| chr4:99520308 | G | A | 8 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0113 others(5): Show |
9 | HG00639.hp1 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-2192G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520308 | |||||||
| chr4:99520337 | C | T | 1 | a0002c0004t0001g0265 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.128-2163C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520337 | |||||||
| chr4:99520371 | A | C | 1 | a0005c0006t0001g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.128-2129A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520371 | |||||||
| chr4:99520649 | A | G | 4 | a0002c0004t0001g0040 a0002c0004t0001g0041 a0002c0004t0001g0042 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-1851A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520649 | |||||||
| chr4:99520729 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
245 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.128-1771A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520729 | |||||||
| chr4:99520840 | T | C | 2 | a0003c0002t0001g0186 a0003c0002t0001g0209 |
2 | HG02698.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.128-1660T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520840 | |||||||
| chr4:99520924 | T | C | 7 | a0002c0004t0001g0238 a0002c0004t0001g0244 a0002c0004t0001g0245 others(4): Show |
7 | HG02735.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-1576T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520924 | |||||||
| chr4:99520947 | T | A | 1 | a0004c0005t0001g0060 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.128-1553T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520947 | |||||||
| chr4:99521004 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0095 |
3 | NA18961.hp2 NA19075.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.128-1496G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521004 | |||||||
| chr4:99521101 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0131 |
2 | NA18969.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.128-1399C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521101 | |||||||
| chr4:99521200 | C | T | 1 | a0003c0002t0001g0032 | 2 | NA19003.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.128-1300C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521200 | |||||||
| chr4:99521215 | T | C | 2 | a0002c0009t0001g0021 a0002c0009t0001g0267 |
3 | HG02647.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.128-1285T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521215 | |||||||
| chr4:99521332 | A | G | 1 | a0004c0005t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.128-1168A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521332 | |||||||
| chr4:99521374 | C | CA | 29 | a0001c0001t0001g0232 a0002c0003t0001g0275 a0002c0004t0001g0234 others(26): Show |
31 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.128-1115dupA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99521374 | ||||||
| chr4:99521386 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
312 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.128-1114G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521386 | |||||||
| chr4:99521421 | T | C | 1 | a0002c0003t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.128-1079T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521421 | |||||||
| chr4:99521539 | T | G | 2 | a0002c0009t0001g0021 a0002c0009t0001g0267 |
3 | HG02647.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.128-961T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521539 | |||||||
| chr4:99521559 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
309 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.128-941A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521559 | |||||||
| chr4:99521683 | C | T | 27 | a0002c0004t0001g0011 a0002c0004t0001g0036 a0002c0004t0001g0108 others(24): Show |
30 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.128-817C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521683 | |||||||
| chr4:99521728 | A | G | 28 | a0001c0001t0001g0161 a0001c0001t0001g0167 a0004c0005t0001g0014 others(25): Show |
30 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.128-772A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521728 | |||||||
| chr4:99521774 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.128-726C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521774 | |||||||
| chr4:99521784 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.128-716C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521784 | |||||||
| chr4:99521804 | A | G | 7 | a0003c0002t0001g0183 a0003c0002t0001g0184 a0003c0002t0001g0192 others(4): Show |
7 | HG01106.hp1 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-696A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521804 | |||||||
| chr4:99521853 | G | T | 62 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0039 others(59): Show |
70 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-647G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521853 | |||||||
| chr4:99521910 | G | C | 1 | a0004c0005t0001g0065 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.128-590G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521910 | |||||||
| chr4:99521914 | G | A | 4 | a0002c0004t0001g0040 a0002c0004t0001g0041 a0002c0004t0001g0042 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-586G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521914 | |||||||
| chr4:99521986 | A | G | 60 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0039 others(57): Show |
67 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.128-514A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521986 | |||||||
| chr4:99522197 | T | TAGAAGGT others(23): Show |
1 | a0001c0001t0001g0162 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.128-301_128-272dup others(30): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99522197 | ||||||
| chr4:99522250 | C | T | 62 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0039 others(59): Show |
70 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-250C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99522250 | |||||||
| chr4:99522301 | A | G | 2 | a0002c0009t0001g0021 a0002c0009t0001g0267 |
3 | HG02647.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.128-199A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99522301 | |||||||
| chr4:99522347 | A | AT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(142): Show |
201 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.128-142dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99522347 | ||||||
| chr4:99522347 | A | ATT | 9 | a0002c0003t0001g0101 a0002c0003t0001g0107 a0002c0003t0001g0302 others(6): Show |
10 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.128-143_128-142dup others(2): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99522347 | ||||||
| chr4:99522347 | A | ATTT | 18 | a0002c0004t0001g0070 a0002c0004t0001g0071 a0005c0006t0001g0037 others(15): Show |
20 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.128-144_128-142dup others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99522347 | ||||||
| chr4:99522357 | TTGGTTTA others(5): Show |
T | 39 | a0002c0003t0001g0012 a0002c0003t0001g0013 a0002c0003t0001g0039 others(36): Show |
44 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.128-141_128-130del others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99522357 | ||||||
| chr4:99522370 | T | C | 18 | a0002c0004t0001g0070 a0002c0004t0001g0071 a0005c0006t0001g0037 others(15): Show |
20 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.128-130T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99522370 | |||||||
| chr4:99522404 | A | G | 86 | a0001c0001t0001g0161 a0001c0001t0001g0167 a0003c0002t0001g0004 others(83): Show |
106 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.128-96A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99522404 | |||||||
| chr4:99522778 | A | G | 2 | a0002c0003t0001g0101 a0002c0003t0001g0302 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.337+69A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99522778 | |||||||
| chr4:99522869 | A | G | 27 | a0002c0004t0001g0011 a0002c0004t0001g0036 a0002c0004t0001g0108 others(24): Show |
30 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.337+160A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99522869 | |||||||
| chr4:99523021 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(141): Show |
188 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.337+312T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523021 | |||||||
| chr4:99523062 | T | TGAAATTG others(937): Show |
1 | a0002c0004t0001g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.337+364_337+365ins others(944): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99523062 | ||||||
| chr4:99523206 | A | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(66): Show |
106 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.337+497A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523206 | |||||||
| chr4:99523250 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.337+541G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523250 | |||||||
| chr4:99523278 | T | TAG | 51 | a0001c0001t0001g0020 a0001c0001t0001g0100 a0002c0003t0001g0107 others(48): Show |
57 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.337+570_337+571ins others(2): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99523278 | ||||||
| chr4:99523527 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
300 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(297): Show |
intron_variant | MODIFIER | c.337+818T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523527 | |||||||
| chr4:99523528 | G | A | 2 | a0002c0004t0001g0011 a0002c0004t0001g0241 |
4 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+819G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523528 | |||||||
| chr4:99523610 | A | G | 88 | a0001c0001t0001g0304 a0002c0003t0001g0276 a0002c0003t0001g0302 others(85): Show |
108 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.337+901A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523610 | |||||||
| chr4:99523681 | T | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0100 a0001c0001t0001g0304 others(8): Show |
12 | HG00639.hp2 HG00735.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.338-840T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523681 | |||||||
| chr4:99523755 | T | C | 1 | a0002c0004t0001g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.338-766T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523755 | |||||||
| chr4:99523775 | C | T | 1 | a0002c0003t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.338-746C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523775 | |||||||
| chr4:99523885 | T | C | 1 | a0002c0003t0001g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.338-636T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523885 | |||||||
| chr4:99523906 | T | C | 19 | a0002c0003t0001g0101 a0002c0004t0001g0041 a0002c0004t0001g0042 others(16): Show |
21 | HG00639.hp2 HG01257.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.338-615T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523906 | |||||||
| chr4:99523907 | T | C | 2 | a0005c0006t0001g0037 a0005c0006t0001g0253 |
3 | HG02258.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.338-614T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523907 | |||||||
| chr4:99523974 | T | C | 1 | a0004c0005t0001g0050 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.338-547T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523974 | |||||||
| chr4:99523975 | A | C | 1 | a0002c0003t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.338-546A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523975 | |||||||
| chr4:99523976 | C | CT | 16 | a0001c0001t0001g0003 a0001c0001t0001g0146 a0001c0001t0001g0152 others(13): Show |
16 | HG01071.hp1 HG01109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.338-524dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99523976 | ||||||
| chr4:99523976 | CT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
141 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.338-524delT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99523976 | ||||||
| chr4:99523976 | CTT | C | 44 | a0001c0001t0001g0171 a0002c0004t0001g0040 a0003c0008t0001g0097 others(41): Show |
48 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.338-525_338-524del others(2): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99523976 | ||||||
| chr4:99524010 | T | C | 16 | a0005c0006t0001g0037 a0005c0006t0001g0038 a0005c0006t0001g0069 others(13): Show |
18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.338-511T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524010 | |||||||
| chr4:99524081 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0089 others(78): Show |
97 | HG00558.hp2 HG00621.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.338-440G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524081 | |||||||
| chr4:99524092 | G | A | 1 | a0002c0003t0001g0272 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.338-429G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524092 | |||||||
| chr4:99524125 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
213 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.338-396G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524125 | |||||||
| chr4:99524136 | C | T | 1 | a0002c0004t0001g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.338-385C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524136 | |||||||
| chr4:99524140 | C | T | 16 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(13): Show |
16 | HG00741.hp1 HG01106.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.338-381C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524140 | |||||||
| chr4:99524192 | A | G | 1 | a0004c0005t0001g0065 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.338-329A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524192 | |||||||
| chr4:99524202 | C | T | 32 | a0001c0001t0001g0113 a0002c0003t0001g0101 a0002c0003t0001g0283 others(29): Show |
33 | HG00438.hp2 HG00558.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.338-319C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524202 | |||||||
| chr4:99524227 | C | T | 1 | a0002c0003t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.338-294C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524227 | |||||||
| chr4:99524241 | T | A | 1 | a0001c0001t0001g0020 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.338-280T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524241 | |||||||
| chr4:99524291 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.338-230C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524291 | |||||||
| chr4:99524432 | T | TC | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
289 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(286): Show |
intron_variant | MODIFIER | c.338-89_338-88insC | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524432 | |||||||
| chr4:99524472 | A | G | 1 | a0003c0002t0001g0305 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.338-49A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524472 | |||||||
| chr4:99524606 | GCTAT | G | 69 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(66): Show |
85 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.402+26_402+29delCT others(2): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99524606 | ||||||
| chr4:99524629 | A | G | 56 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(53): Show |
70 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.402+44A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99524629 | |||||||
| chr4:99524704 | A | T | 6 | a0001c0001t0001g0146 a0001c0001t0001g0152 a0001c0001t0001g0158 others(3): Show |
6 | HG01071.hp1 HG02300.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+119A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99524704 | |||||||
| chr4:99524733 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.402+148A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99524733 | |||||||
| chr4:99524809 | C | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0116 others(5): Show |
9 | HG00639.hp1 HG00733.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+224C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99524809 | |||||||
| chr4:99525022 | C | A | 2 | a0002c0003t0001g0101 a0002c0003t0001g0302 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.402+437C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525022 | |||||||
| chr4:99525154 | G | C | 1 | a0003c0002t0001g0189 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.402+569G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525154 | |||||||
| chr4:99525282 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.402+697C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525282 | |||||||
| chr4:99525286 | C | T | 1 | a0004c0005t0001g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.402+701C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525286 | |||||||
| chr4:99525302 | T | A | 15 | a0001c0001t0001g0020 a0002c0003t0001g0271 a0002c0003t0001g0275 others(12): Show |
22 | HG01192.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.402+717T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525302 | |||||||
| chr4:99525322 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(54): Show |
71 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.402+737C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525322 | |||||||
| chr4:99525795 | CA | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0090 a0001c0001t0001g0124 others(3): Show |
7 | HG00639.hp1 HG02896.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.402+1224delA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99525795 | ||||||
| chr4:99525976 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.402+1391C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525976 | |||||||
| chr4:99526076 | C | T | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.402+1491C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526076 | |||||||
| chr4:99526096 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.402+1511G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526096 | |||||||
| chr4:99526111 | A | G | 2 | a0003c0002t0001g0184 a0003c0002t0001g0193 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.402+1526A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526111 | |||||||
| chr4:99526164 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.402+1579C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526164 | |||||||
| chr4:99526298 | T | C | 1 | a0002c0003t0001g0302 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.402+1713T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526298 | |||||||
| chr4:99526362 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.402+1777A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526362 | |||||||
| chr4:99526458 | G | A | 72 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(69): Show |
88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.402+1873G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526458 | |||||||
| chr4:99526643 | T | C | 3 | a0002c0004t0001g0036 a0002c0004t0001g0173 a0002c0004t0001g0224 |
4 | HG01070.hp1 HG01071.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+2058T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526643 | |||||||
| chr4:99526651 | C | CT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(107): Show |
163 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.402+2080dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99526651 | ||||||
| chr4:99526651 | C | CTT | 19 | a0002c0004t0001g0233 a0003c0002t0001g0206 a0004c0005t0001g0051 others(16): Show |
21 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.402+2079_402+2080d others(4): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99526651 | ||||||
| chr4:99526740 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0304 a0002c0003t0001g0107 |
3 | HG00735.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.402+2155T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526740 | |||||||
| chr4:99526848 | C | T | 1 | a0004c0005t0001g0065 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.402+2263C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526848 | |||||||
| chr4:99526913 | T | C | 2 | a0002c0004t0001g0011 a0002c0004t0001g0241 |
4 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+2328T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526913 | |||||||
| chr4:99526964 | T | G | 72 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(69): Show |
88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.402+2379T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526964 | |||||||
| chr4:99527010 | G | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
290 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(287): Show |
intron_variant | MODIFIER | c.402+2425G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527010 | |||||||
| chr4:99527065 | C | G | 73 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(70): Show |
89 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.402+2480C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527065 | |||||||
| chr4:99527104 | C | T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
14 | HG01074.hp2 HG01255.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.402+2519C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527104 | |||||||
| chr4:99527383 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0161 a0001c0001t0001g0167 |
3 | HG01099.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.403-2432A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527383 | |||||||
| chr4:99527501 | G | C | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.403-2314G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527501 | |||||||
| chr4:99527575 | C | T | 1 | a0002c0004t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.403-2240C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527575 | |||||||
| chr4:99527584 | C | T | 1 | a0002c0004t0001g0248 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.403-2231C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527584 | |||||||
| chr4:99527588 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(70): Show |
109 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.403-2227C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527588 | |||||||
| chr4:99527667 | C | T | 78 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(75): Show |
96 | HG00544.hp1 HG00558.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.403-2148C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527667 | |||||||
| chr4:99527702 | C | T | 1 | a0002c0003t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.403-2113C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527702 | |||||||
| chr4:99527713 | C | G | 1 | a0002c0003t0001g0286 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.403-2102C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527713 | |||||||
| chr4:99527820 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.403-1995G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527820 | |||||||
| chr4:99527933 | C | G | 1 | a0003c0002t0001g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.403-1882C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527933 | |||||||
| chr4:99528195 | T | C | 1 | a0004c0005t0001g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.403-1620T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528195 | |||||||
| chr4:99528208 | TAAAAG | T | 61 | a0001c0001t0001g0078 a0001c0001t0001g0113 a0002c0003t0001g0101 others(58): Show |
76 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.403-1604_403-1600d others(7): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99528208 | ||||||
| chr4:99528212 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.403-1603A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528212 | |||||||
| chr4:99528256 | G | C | 1 | a0002c0003t0001g0302 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.403-1559G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528256 | |||||||
| chr4:99528352 | CTCTT | C | 3 | a0003c0008t0001g0097 a0003c0008t0001g0098 a0003c0008t0001g0099 |
3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.403-1459_403-1456d others(6): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99528352 | ||||||
| chr4:99528532 | T | G | 16 | a0005c0006t0001g0037 a0005c0006t0001g0038 a0005c0006t0001g0069 others(13): Show |
18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.403-1283T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528532 | |||||||
| chr4:99528543 | C | G | 16 | a0005c0006t0001g0037 a0005c0006t0001g0038 a0005c0006t0001g0069 others(13): Show |
18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.403-1272C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528543 | |||||||
| chr4:99528578 | A | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(70): Show |
109 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.403-1237A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528578 | |||||||
| chr4:99528709 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.403-1106G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528709 | |||||||
| chr4:99528794 | C | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0139 |
2 | HG01346.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.403-1021C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528794 | |||||||
| chr4:99528794 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.403-1021C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528794 | |||||||
| chr4:99528816 | C | A | 72 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(69): Show |
88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.403-999C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528816 | |||||||
| chr4:99528840 | T | C | 73 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(70): Show |
89 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.403-975T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528840 | |||||||
| chr4:99528922 | AT | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0304 a0002c0003t0001g0107 |
3 | HG00735.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.403-890delT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99528922 | ||||||
| chr4:99529099 | A | G | 1 | a0004c0005t0001g0226 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.403-716A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99529099 | |||||||
| chr4:99529536 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.403-279A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99529536 | |||||||
| chr4:99529555 | C | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0022 others(142): Show |
182 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(179): Show |
intron_variant | MODIFIER | c.403-260C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99529555 | |||||||
| chr4:99529616 | A | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(55): Show |
72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.403-199A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99529616 | |||||||
| chr4:99529800 | A | G | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.403-15A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99529800 | |||||||
| chr4:99529970 | G | A | 55 | a0001c0001t0001g0078 a0001c0001t0001g0113 a0002c0003t0001g0276 others(52): Show |
70 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.546+12G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99529970 | |||||||
| chr4:99530036 | A | T | 1 | a0003c0002t0001g0199 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.546+78A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530036 | |||||||
| chr4:99530040 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+82C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530040 | |||||||
| chr4:99530210 | C | A | 1 | a0002c0003t0001g0302 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.546+252C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530210 | |||||||
| chr4:99530218 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
291 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+260A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530218 | |||||||
| chr4:99530230 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+272C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530230 | |||||||
| chr4:99530238 | C | T | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.546+280C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530238 | |||||||
| chr4:99530265 | A | G | 8 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0116 others(5): Show |
9 | HG00639.hp1 HG00733.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+307A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530265 | |||||||
| chr4:99530299 | T | C | 1 | a0004c0005t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.546+341T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530299 | |||||||
| chr4:99530360 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+402C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530360 | |||||||
| chr4:99530452 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(70): Show |
109 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.546+494G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530452 | |||||||
| chr4:99530527 | A | AT | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+575dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99530527 | ||||||
| chr4:99530624 | C | T | 2 | a0002c0004t0001g0042 a0002c0004t0001g0043 |
2 | HG00639.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.546+666C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530624 | |||||||
| chr4:99530663 | A | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+705A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530663 | |||||||
| chr4:99530784 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(70): Show |
109 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.546+826A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530784 | |||||||
| chr4:99530792 | AGAATAAA others(2): Show |
A | 3 | a0004c0005t0001g0014 a0004c0005t0001g0045 a0004c0005t0001g0048 |
4 | HG01891.hp2 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+838_546+846del others(9): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99530792 | ||||||
| chr4:99530978 | C | T | 1 | a0005c0006t0001g0250 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.546+1020C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530978 | |||||||
| chr4:99531005 | G | T | 16 | a0005c0006t0001g0037 a0005c0006t0001g0038 a0005c0006t0001g0069 others(13): Show |
18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.546+1047G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531005 | |||||||
| chr4:99531122 | G | GT | 72 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(69): Show |
88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.546+1173dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99531122 | ||||||
| chr4:99531122 | GT | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(95): Show |
141 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.546+1173delT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99531122 | ||||||
| chr4:99531191 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.546+1233T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531191 | |||||||
| chr4:99531224 | A | G | 1 | a0002c0003t0001g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.546+1266A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531224 | |||||||
| chr4:99531290 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.546+1332C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531290 | |||||||
| chr4:99531506 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.546+1548G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531506 | |||||||
| chr4:99531555 | A | G | 8 | a0002c0004t0001g0040 a0003c0002t0001g0183 a0003c0002t0001g0184 others(5): Show |
8 | HG01106.hp1 HG01123.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+1597A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531555 | |||||||
| chr4:99531630 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.546+1672C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531630 | |||||||
| chr4:99531729 | C | G | 2 | a0001c0001t0001g0100 a0002c0003t0001g0107 |
2 | HG00735.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.546+1771C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531729 | |||||||
| chr4:99531804 | C | T | 3 | a0003c0008t0001g0097 a0003c0008t0001g0098 a0003c0008t0001g0099 |
3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.546+1846C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531804 | |||||||
| chr4:99531854 | C | CA | 161 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0022 others(158): Show |
200 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(197): Show |
intron_variant | MODIFIER | c.546+1903dupA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99531854 | ||||||
| chr4:99531854 | C | CAA | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(54): Show |
91 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.546+1902_546+1903d others(4): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99531854 | ||||||
| chr4:99531887 | T | C | 2 | a0002c0004t0001g0173 a0002c0004t0001g0224 |
2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.546+1929T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531887 | |||||||
| chr4:99532067 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.546+2109A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532067 | |||||||
| chr4:99532080 | T | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(55): Show |
72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.546+2122T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532080 | |||||||
| chr4:99532304 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(55): Show |
72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.546+2346T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532304 | |||||||
| chr4:99532348 | C | T | 2 | a0002c0004t0001g0246 a0003c0002t0001g0182 |
2 | HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.546+2390C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532348 | |||||||
| chr4:99532419 | G | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(51): Show |
67 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.546+2461G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532419 | |||||||
| chr4:99532589 | C | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
294 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(291): Show |
intron_variant | MODIFIER | c.546+2631C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532589 | |||||||
| chr4:99532611 | G | A | 72 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(69): Show |
88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.546+2653G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532611 | |||||||
| chr4:99532768 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.546+2810G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532768 | |||||||
| chr4:99533496 | A | C | 1 | a0002c0004t0001g0070 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.546+3538A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99533496 | |||||||
| chr4:99533582 | G | T | 1 | a0002c0003t0001g0302 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.546+3624G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99533582 | |||||||
| chr4:99533808 | CG | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+3853delG | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99533808 | ||||||
| chr4:99534002 | G | A | 61 | a0001c0001t0001g0078 a0001c0001t0001g0113 a0002c0003t0001g0101 others(58): Show |
76 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.547-3667G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534002 | |||||||
| chr4:99534010 | T | C | 1 | a0002c0003t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.547-3659T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534010 | |||||||
| chr4:99534012 | T | G | 4 | a0002c0007t0001g0281 a0002c0007t0001g0292 a0002c0007t0001g0297 others(1): Show |
4 | HG02145.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-3657T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534012 | |||||||
| chr4:99534044 | T | C | 1 | a0003c0002t0001g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.547-3625T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534044 | |||||||
| chr4:99534347 | A | G | 1 | a0002c0003t0001g0302 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.547-3322A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534347 | |||||||
| chr4:99534413 | C | T | 15 | a0001c0001t0001g0020 a0002c0003t0001g0271 a0002c0003t0001g0275 others(12): Show |
22 | HG01192.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.547-3256C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534413 | |||||||
| chr4:99534719 | C | T | 1 | a0002c0003t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.547-2950C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534719 | |||||||
| chr4:99534837 | G | A | 1 | a0003c0002t0001g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.547-2832G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534837 | |||||||
| chr4:99534925 | A | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.547-2744A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534925 | |||||||
| chr4:99535033 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0304 a0002c0003t0001g0107 |
3 | HG00735.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.547-2636C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535033 | |||||||
| chr4:99535075 | C | T | 54 | a0001c0001t0001g0113 a0002c0003t0001g0276 a0002c0004t0001g0011 others(51): Show |
69 | HG00544.hp1 HG00741.hp1 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.547-2594C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535075 | |||||||
| chr4:99535122 | C | T | 38 | a0002c0003t0001g0276 a0002c0004t0001g0229 a0002c0004t0001g0230 others(35): Show |
50 | HG00544.hp1 HG00741.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.547-2547C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535122 | |||||||
| chr4:99535151 | C | T | 1 | a0004c0005t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.547-2518C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535151 | |||||||
| chr4:99535180 | G | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01516.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.547-2489G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535180 | |||||||
| chr4:99535280 | C | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0116 others(5): Show |
9 | HG00639.hp1 HG00733.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.547-2389C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535280 | |||||||
| chr4:99535311 | G | A | 4 | a0003c0002t0001g0109 a0003c0002t0001g0110 a0003c0002t0001g0111 others(1): Show |
4 | HG02559.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-2358G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535311 | |||||||
| chr4:99535330 | T | TTTTCCAA others(21): Show |
1 | a0001c0001t0001g0082 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.547-2337_547-2310d others(30): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99535330 | ||||||
| chr4:99535408 | C | G | 3 | a0002c0004t0001g0036 a0002c0004t0001g0173 a0002c0004t0001g0224 |
4 | HG01070.hp1 HG01071.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-2261C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535408 | |||||||
| chr4:99535417 | C | T | 3 | a0003c0008t0001g0097 a0003c0008t0001g0098 a0003c0008t0001g0099 |
3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.547-2252C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535417 | |||||||
| chr4:99535592 | A | G | 16 | a0005c0006t0001g0037 a0005c0006t0001g0038 a0005c0006t0001g0069 others(13): Show |
18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.547-2077A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535592 | |||||||
| chr4:99535677 | C | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(55): Show |
72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.547-1992C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535677 | |||||||
| chr4:99535744 | A | T | 6 | a0001c0001t0001g0142 a0001c0001t0001g0154 a0003c0002t0001g0186 others(3): Show |
6 | HG00140.hp2 HG01168.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-1925A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535744 | |||||||
| chr4:99535845 | T | C | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.547-1824T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535845 | |||||||
| chr4:99535960 | A | ACAGT | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.547-1706_547-1705i others(6): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99535960 | ||||||
| chr4:99536119 | G | A | 1 | a0003c0002t0001g0109 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.547-1550G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536119 | |||||||
| chr4:99536187 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.547-1482C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536187 | |||||||
| chr4:99536215 | C | A | 3 | a0003c0008t0001g0097 a0003c0008t0001g0098 a0003c0008t0001g0099 |
3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.547-1454C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536215 | |||||||
| chr4:99536275 | C | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(55): Show |
72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.547-1394C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536275 | |||||||
| chr4:99536471 | A | G | 1 | a0002c0004t0001g0070 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.547-1198A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536471 | |||||||
| chr4:99536529 | G | T | 3 | a0003c0008t0001g0097 a0003c0008t0001g0098 a0003c0008t0001g0099 |
3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.547-1140G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536529 | |||||||
| chr4:99536533 | C | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0022 others(142): Show |
182 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(179): Show |
intron_variant | MODIFIER | c.547-1136C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536533 | |||||||
| chr4:99536684 | T | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.547-985T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536684 | |||||||
| chr4:99536690 | A | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0148 |
2 | HG01081.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.547-979A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536690 | |||||||
| chr4:99536783 | G | A | 1 | a0004c0005t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.547-886G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536783 | |||||||
| chr4:99536988 | C | G | 1 | a0002c0003t0001g0277 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.547-681C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536988 | |||||||
| chr4:99537008 | C | T | 1 | a0003c0002t0001g0064 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.547-661C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537008 | |||||||
| chr4:99537245 | TG | T | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.547-423delG | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537245 | |||||||
| chr4:99537267 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.547-402G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537267 | |||||||
| chr4:99537291 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.547-378A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537291 | |||||||
| chr4:99537404 | G | T | 51 | a0001c0001t0001g0113 a0002c0003t0001g0276 a0002c0004t0001g0011 others(48): Show |
65 | HG00544.hp1 HG00741.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.547-265G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537404 | |||||||
| chr4:99537506 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.547-163G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537506 | |||||||
| chr4:99537564 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(55): Show |
72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.547-105T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537564 | |||||||
| chr4:99537616 | A | G | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.547-53A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537616 | |||||||
| chr4:99537836 | T | C | 3 | a0002c0004t0001g0244 a0002c0004t0001g0245 a0002c0004t0001g0265 |
3 | HG03491.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.628+86T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99537836 | |||||||
| chr4:99537871 | C | T | 72 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(69): Show |
88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.628+121C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99537871 | |||||||
| chr4:99538189 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.628+439C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538189 | |||||||
| chr4:99538398 | G | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(55): Show |
72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.628+648G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538398 | |||||||
| chr4:99538516 | T | G | 1 | a0004c0005t0001g0226 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.629-647T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538516 | |||||||
| chr4:99538538 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.629-625C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538538 | |||||||
| chr4:99538595 | C | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(55): Show |
72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.629-568C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538595 | |||||||
| chr4:99538605 | T | C | 72 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(69): Show |
88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.629-558T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538605 | |||||||
| chr4:99538698 | A | G | 72 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(69): Show |
88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.629-465A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538698 | |||||||
| chr4:99538709 | A | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0022 others(142): Show |
182 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(179): Show |
intron_variant | MODIFIER | c.629-454A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538709 | |||||||
| chr4:99539374 | A | G | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
splice_region_variant&intron_variant | LOW | c.836+4A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99539374 | |||||||
| chr4:99539396 | A | C | 1 | a0004c0005t0001g0226 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.836+26A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99539396 | |||||||
| chr4:99539681 | T | C | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.836+311T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99539681 | |||||||
| chr4:99539854 | C | T | 1 | a0002c0004t0001g0248 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.836+484C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99539854 | |||||||
| chr4:99539867 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.836+497A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99539867 | |||||||
| chr4:99540010 | T | A | 3 | a0003c0008t0001g0097 a0003c0008t0001g0098 a0003c0008t0001g0099 |
3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.837-402T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99540010 | |||||||
| chr4:99540065 | A | G | 1 | a0003c0002t0001g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.837-347A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99540065 | |||||||
| chr4:99540114 | A | G | 1 | a0002c0003t0001g0302 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.837-298A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99540114 | |||||||
| chr4:99540553 | A | C | 1 | a0004c0005t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.880+98A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540553 | |||||||
| chr4:99540712 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(54): Show |
71 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.880+257G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540712 | |||||||
| chr4:99540875 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.880+420G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540875 | |||||||
| chr4:99540900 | A | C | 3 | a0003c0008t0001g0097 a0003c0008t0001g0098 a0003c0008t0001g0099 |
3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880+445A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540900 | |||||||
| chr4:99540928 | C | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0116 others(5): Show |
9 | HG00639.hp1 HG00733.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.880+473C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540928 | |||||||
| chr4:99540980 | A | G | 72 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0112 others(69): Show |
88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.880+525A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540980 | |||||||
| chr4:99541235 | C | T | 1 | a0004c0005t0001g0063 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.881-675C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541235 | |||||||
| chr4:99541262 | T | C | 8 | a0005c0006t0001g0037 a0005c0006t0001g0250 a0005c0006t0001g0252 others(5): Show |
9 | HG01975.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.881-648T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541262 | |||||||
| chr4:99541277 | A | G | 3 | a0003c0008t0001g0097 a0003c0008t0001g0098 a0003c0008t0001g0099 |
3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.881-633A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541277 | |||||||
| chr4:99541451 | A | G | 1 | a0002c0003t0001g0302 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.881-459A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541451 | |||||||
| chr4:99541537 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0094 others(55): Show |
72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.881-373T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541537 | |||||||
| chr4:99541566 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(127): Show |
160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.881-344C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541566 | |||||||
| chr4:99541764 | G | A | 1 | a0002c0004t0001g0041 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.881-146G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541764 |