Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80817 |
| ensemblid | ENSG00000164118.13 |
| hgncid | 29356 |
| symbol | CEP44 |
| name | centrosomal protein 44 |
| refseq_nuc | NM_001040157.3 |
| refseq_prot | NP_001035247.1 |
| ensembl_nuc | ENST00000503780.6 |
| ensembl_prot | ENSP00000423153.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 174283911 |
| end | 174320328 |
| strand | + |
| ver | v1.2 |
| region | chr4:174283911-174320328 |
| region5000 | chr4:174278911-174325328 |
| regionname0 | CEP44_chr4_174283911_174320328 |
| regionname5000 | CEP44_chr4_174278911_174325328 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 390 | 255 | 42 | 45 | 142 | 5 | 19 | 112 | CEP44_chr4_174278911_174325328 | CEP44 | MATGD others(385): Show |
chr4 | 174278911 | 174325328 |
| a0002 | 0/0 | 390 | 125 | 40 | 30 | 27 | 9 | 19 | 19 | CEP44_chr4_174278911_174325328 | CEP44 | MATGD others(385): Show |
chr4 | 174278911 | 174325328 |
| a0003 | 0/0 | 390 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | MATGD others(385): Show |
chr4 | 174278911 | 174325328 |
| a0004 | 0/0 | 390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | MATGD others(385): Show |
chr4 | 174278911 | 174325328 |
| a0005 | 0/0 | 390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | MATGD others(385): Show |
chr4 | 174278911 | 174325328 |
| a0006 | 0/0 | 390 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | MATGD others(385): Show |
chr4 | 174278911 | 174325328 |
| a0007 | 0/0 | 390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | MATGD others(385): Show |
chr4 | 174278911 | 174325328 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1170 | 132 | 14 | 21 | 85 | 2 | 10 | CEP44_chr4_174278911_174325328 | CEP44 | ATGGC others(1165): Show |
chr4 | 174278911 | 174325328 | ||
| a0001c0003 | 1/1 | 1170 | 120 | 28 | 24 | 54 | 3 | 9 | CEP44_chr4_174278911_174325328 | CEP44 | ATGGC others(1165): Show |
chr4 | 174278911 | 174325328 | ||
| a0001c0005 | 0/0 | 1170 | 3 | 0 | 0 | 3 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | ATGGC others(1165): Show |
chr4 | 174278911 | 174325328 | ||
| a0002c0002 | 0/0 | 1170 | 124 | 40 | 30 | 27 | 8 | 19 | CEP44_chr4_174278911_174325328 | CEP44 | ATGGC others(1165): Show |
chr4 | 174278911 | 174325328 | ||
| a0002c0008 | 0/0 | 1170 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | ATGGC others(1165): Show |
chr4 | 174278911 | 174325328 | ||
| a0003c0004 | 0/0 | 1170 | 4 | 3 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | ATGGC others(1165): Show |
chr4 | 174278911 | 174325328 | ||
| a0004c0010 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | ATGGC others(1165): Show |
chr4 | 174278911 | 174325328 | ||
| a0005c0007 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | ATGGC others(1165): Show |
chr4 | 174278911 | 174325328 | ||
| a0006c0009 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | ATGGC others(1165): Show |
chr4 | 174278911 | 174325328 | ||
| a0007c0006 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | ATGGC others(1165): Show |
chr4 | 174278911 | 174325328 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4298 | 120 | 14 | 20 | 75 | 2 | 9 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0001c0001t0005 | 0/0 | 4295 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0001c0001t0008 | 0/0 | 4298 | 5 | 0 | 0 | 5 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0001c0001t0014 | 0/0 | 4298 | 2 | 0 | 0 | 2 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0001c0001t0016 | 0/0 | 4298 | 2 | 0 | 0 | 2 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0001c0001t0026 | 0/0 | 4298 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0001c0001t0031 | 0/0 | 4298 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0001c0003t0002 | 1/1 | 4298 | 105 | 28 | 11 | 52 | 3 | 9 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0001c0003t0007 | 0/0 | 4303 | 10 | 0 | 10 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4298): Show |
chr4 | 174278911 | 174325328 |
| a0001c0003t0011 | 0/0 | 4298 | 3 | 0 | 3 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0001c0003t0027 | 0/0 | 4298 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0001c0003t0029 | 0/0 | 4298 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0001c0005t0002 | 0/0 | 4298 | 2 | 0 | 0 | 2 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0001c0005t0018 | 0/0 | 4298 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0003 | 0/0 | 4291 | 33 | 2 | 15 | 2 | 6 | 8 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4286): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0004 | 0/0 | 4295 | 30 | 5 | 0 | 23 | 0 | 2 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0005 | 0/0 | 4295 | 28 | 13 | 8 | 2 | 0 | 5 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0006 | 0/0 | 4295 | 8 | 8 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0009 | 0/0 | 4295 | 5 | 0 | 2 | 0 | 1 | 2 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0010 | 0/0 | 4294 | 3 | 3 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4289): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0012 | 0/0 | 4295 | 2 | 2 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0013 | 0/0 | 4295 | 3 | 2 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0015 | 0/0 | 4291 | 2 | 0 | 2 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4286): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0017 | 0/0 | 4295 | 2 | 2 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0019 | 0/0 | 4295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0020 | 0/0 | 4291 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4286): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0021 | 0/0 | 4295 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0022 | 0/0 | 4295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0023 | 0/0 | 4295 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0024 | 0/0 | 4291 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4286): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0025 | 0/0 | 4295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0002t0030 | 0/0 | 4295 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0002c0008t0004 | 0/0 | 4295 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0003c0004t0006 | 0/0 | 4295 | 4 | 3 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| a0004c0010t0010 | 0/0 | 4294 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4289): Show |
chr4 | 174278911 | 174325328 |
| a0005c0007t0028 | 0/0 | 4298 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0006c0009t0002 | 0/0 | 4298 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4293): Show |
chr4 | 174278911 | 174325328 |
| a0007c0006t0012 | 0/0 | 4295 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | AGAGA others(4290): Show |
chr4 | 174278911 | 174325328 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 1 | 6 | 10 | 0 | 2 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0016 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0008g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0014g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0014g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0016g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0016g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0026g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0001t0031g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0002 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0007g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0007g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0007g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0007g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0007g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0011g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0011g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0011g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0027g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0003t0029g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0005t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0005t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0001c0005t0018g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0004 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0009 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0009g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0009g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0009g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0009g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0010g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0012g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0012g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0013g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0013g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0013g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0015g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0017g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0019g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0020g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0021g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0022g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0023g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0024g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0025g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0002t0030g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0002c0008t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0003c0004t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0003c0004t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0003c0004t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0003c0004t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0004c0010t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0005c0007t0028g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0006c0009t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| a0007c0006t0012g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0003 | g0036 | EUR | GBR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00140 | hp1 | a0001 | c0003 | t0002 | g0220 | EUR | GBR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00140 | hp2 | a0002 | c0002 | t0003 | g0004 | EUR | GBR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0018 | EUR | FIN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0276 | EUR | FIN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00323 | hp2 | a0002 | c0008 | t0004 | g0064 | EUR | FIN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00408 | hp2 | a0001 | c0003 | t0002 | g0224 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00423 | hp2 | a0001 | c0001 | t0031 | g0003 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0217 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00544 | hp2 | a0002 | c0002 | t0003 | g0189 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0267 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00609 | hp1 | a0002 | c0002 | t0004 | g0087 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00621 | hp2 | a0002 | c0002 | t0004 | g0084 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00639 | hp1 | a0002 | c0002 | t0005 | g0198 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0042 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0257 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00642 | hp2 | a0001 | c0003 | t0007 | g0007 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00673 | hp1 | a0002 | c0002 | t0004 | g0088 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00733 | hp1 | a0002 | c0002 | t0013 | g0091 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0268 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00738 | hp2 | a0002 | c0002 | t0024 | g0004 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00741 | hp1 | a0002 | c0002 | t0009 | g0097 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0174 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01069 | hp1 | a0002 | c0002 | t0005 | g0009 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01069 | hp2 | a0001 | c0003 | t0002 | g0251 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01070 | hp1 | a0001 | c0003 | t0007 | g0046 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01070 | hp2 | a0002 | c0002 | t0015 | g0004 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01071 | hp1 | a0002 | c0002 | t0015 | g0004 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01074 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01074 | hp2 | a0001 | c0003 | t0011 | g0243 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01081 | hp1 | a0002 | c0002 | t0003 | g0190 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01099 | hp1 | a0002 | c0002 | t0005 | g0166 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0237 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0038 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01109 | hp1 | a0003 | c0004 | t0006 | g0049 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01109 | hp2 | a0002 | c0002 | t0003 | g0036 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01167 | hp1 | a0002 | c0002 | t0005 | g0201 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01168 | hp1 | a0002 | c0002 | t0003 | g0018 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01168 | hp2 | a0001 | c0003 | t0011 | g0245 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01169 | hp1 | a0001 | c0003 | t0011 | g0244 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0159 | AMR | PUR | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01255 | hp1 | a0002 | c0002 | t0023 | g0171 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01255 | hp2 | a0002 | c0002 | t0003 | g0183 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01256 | hp1 | a0002 | c0002 | t0005 | g0165 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01256 | hp2 | a0001 | c0003 | t0002 | g0041 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01257 | hp1 | a0002 | c0002 | t0005 | g0197 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0261 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01346 | hp1 | a0001 | c0003 | t0007 | g0007 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01346 | hp2 | a0002 | c0002 | t0003 | g0181 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0192 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01361 | hp1 | a0002 | c0002 | t0003 | g0175 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0262 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01433 | hp1 | a0002 | c0002 | t0003 | g0018 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01433 | hp2 | a0002 | c0002 | t0005 | g0009 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01496 | hp1 | a0001 | c0003 | t0007 | g0248 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01515 | hp1 | a0002 | c0002 | t0003 | g0004 | EUR | IBS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0188 | EUR | IBS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01516 | hp1 | a0002 | c0002 | t0009 | g0092 | EUR | IBS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01516 | hp2 | a0002 | c0002 | t0020 | g0037 | EUR | IBS | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01884 | hp1 | a0002 | c0002 | t0004 | g0073 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01884 | hp2 | a0002 | c0002 | t0012 | g0095 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0042 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01934 | hp2 | a0001 | c0003 | t0007 | g0010 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01943 | hp1 | a0001 | c0003 | t0002 | g0266 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01952 | hp1 | a0002 | c0002 | t0005 | g0009 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01952 | hp2 | a0001 | c0003 | t0007 | g0007 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01978 | hp1 | a0001 | c0003 | t0007 | g0256 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01978 | hp2 | a0001 | c0003 | t0002 | g0041 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01981 | hp2 | a0002 | c0002 | t0009 | g0027 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01993 | hp1 | a0001 | c0003 | t0007 | g0255 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02004 | hp1 | a0002 | c0002 | t0003 | g0037 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02027 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0269 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02055 | hp2 | a0002 | c0002 | t0004 | g0090 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02056 | hp1 | a0001 | c0003 | t0002 | g0213 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02056 | hp2 | a0002 | c0002 | t0004 | g0079 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02071 | hp1 | a0001 | c0003 | t0027 | g0221 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02083 | hp1 | a0002 | c0002 | t0004 | g0014 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02129 | hp1 | a0001 | c0003 | t0002 | g0223 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02129 | hp2 | a0001 | c0003 | t0029 | g0222 | EAS | KHV | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02145 | hp2 | a0003 | c0004 | t0006 | g0047 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02148 | hp2 | a0001 | c0003 | t0007 | g0010 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02155 | hp1 | a0002 | c0002 | t0004 | g0077 | EAS | CDX | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0271 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0185 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02273 | hp2 | a0002 | c0002 | t0003 | g0191 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02280 | hp1 | a0002 | c0002 | t0017 | g0021 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02293 | hp1 | a0001 | c0003 | t0007 | g0007 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0179 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0216 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02602 | hp2 | a0002 | c0002 | t0003 | g0180 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02615 | hp2 | a0002 | c0002 | t0005 | g0168 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02622 | hp1 | a0002 | c0002 | t0006 | g0099 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02630 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02630 | hp2 | a0002 | c0002 | t0010 | g0020 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02647 | hp1 | a0002 | c0002 | t0005 | g0163 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02647 | hp2 | a0002 | c0002 | t0010 | g0020 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02698 | hp1 | a0001 | c0003 | t0002 | g0002 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0254 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0232 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02723 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02723 | hp2 | a0002 | c0002 | t0005 | g0063 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02735 | hp1 | a0002 | c0002 | t0005 | g0200 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02735 | hp2 | a0002 | c0002 | t0003 | g0184 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02738 | hp1 | a0001 | c0003 | t0002 | g0010 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0278 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02809 | hp2 | a0002 | c0002 | t0012 | g0094 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02886 | hp1 | a0002 | c0002 | t0025 | g0170 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02886 | hp2 | a0002 | c0002 | t0006 | g0193 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02895 | hp1 | a0001 | c0003 | t0002 | g0234 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0250 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0233 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02896 | hp2 | a0002 | c0002 | t0006 | g0101 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02922 | hp1 | a0002 | c0002 | t0006 | g0061 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02922 | hp2 | a0002 | c0002 | t0017 | g0021 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0083 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02976 | hp1 | a0001 | c0003 | t0002 | g0241 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03017 | hp1 | a0001 | c0003 | t0002 | g0249 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0186 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03041 | hp1 | a0002 | c0002 | t0005 | g0160 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0230 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03098 | hp1 | a0001 | c0003 | t0002 | g0273 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03098 | hp2 | a0002 | c0002 | t0005 | g0161 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03130 | hp1 | a0002 | c0002 | t0005 | g0017 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0274 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0240 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03139 | hp2 | a0002 | c0002 | t0005 | g0017 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03195 | hp1 | a0001 | c0003 | t0002 | g0242 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0239 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03209 | hp1 | a0002 | c0002 | t0005 | g0169 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03209 | hp2 | a0003 | c0004 | t0006 | g0050 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03225 | hp1 | a0002 | c0002 | t0005 | g0279 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0231 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0252 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03239 | hp2 | a0002 | c0002 | t0005 | g0009 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03486 | hp1 | a0002 | c0002 | t0013 | g0085 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03486 | hp2 | a0002 | c0002 | t0005 | g0164 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03490 | hp2 | a0002 | c0002 | t0003 | g0178 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03492 | hp1 | a0002 | c0002 | t0004 | g0081 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0272 | AFR | ESN | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0019 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03540 | hp2 | a0002 | c0002 | t0005 | g0167 | AFR | GWD | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03579 | hp1 | a0002 | c0002 | t0019 | g0096 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03579 | hp2 | a0002 | c0002 | t0022 | g0172 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03654 | hp1 | a0002 | c0002 | t0009 | g0027 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03654 | hp2 | a0002 | c0002 | t0030 | g0069 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03669 | hp1 | a0002 | c0002 | t0021 | g0199 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03669 | hp2 | a0002 | c0002 | t0003 | g0187 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03688 | hp1 | a0002 | c0002 | t0005 | g0204 | SAS | STU | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0013 | SAS | STU | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03710 | hp1 | a0002 | c0002 | t0004 | g0089 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03927 | hp2 | a0002 | c0002 | t0005 | g0203 | SAS | BEB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03942 | hp1 | a0002 | c0002 | t0003 | g0038 | SAS | BEB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03942 | hp2 | a0001 | c0003 | t0002 | g0260 | SAS | BEB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG04115 | hp1 | a0002 | c0002 | t0005 | g0009 | SAS | STU | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG04115 | hp2 | a0002 | c0002 | t0009 | g0098 | SAS | STU | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0176 | SAS | BEB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG04184 | hp2 | a0001 | c0001 | t0026 | g0125 | SAS | BEB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0007 | SAS | STU | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG04228 | hp2 | a0001 | c0003 | t0002 | g0007 | SAS | STU | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18522 | hp2 | a0002 | c0002 | t0005 | g0017 | AFR | YRI | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | CHB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18747 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | CHB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18747 | hp2 | a0002 | c0002 | t0004 | g0075 | EAS | CHB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0019 | AFR | YRI | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18939 | hp2 | a0001 | c0003 | t0002 | g0208 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0218 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18942 | hp1 | a0001 | c0003 | t0002 | g0226 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18943 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18945 | hp2 | a0001 | c0003 | t0002 | g0040 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18947 | hp1 | a0002 | c0002 | t0004 | g0067 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18949 | hp2 | a0001 | c0005 | t0018 | g0264 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0177 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18957 | hp1 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18957 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18962 | hp1 | a0002 | c0002 | t0004 | g0070 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18966 | hp1 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18966 | hp2 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18967 | hp1 | a0001 | c0001 | t0016 | g0149 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18967 | hp2 | a0001 | c0003 | t0002 | g0247 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18968 | hp2 | a0001 | c0001 | t0014 | g0065 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18969 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18970 | hp1 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18970 | hp2 | a0001 | c0005 | t0002 | g0258 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18972 | hp1 | a0001 | c0003 | t0002 | g0253 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18973 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18974 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18975 | hp2 | a0002 | c0002 | t0004 | g0014 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18977 | hp1 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18977 | hp2 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18979 | hp1 | a0001 | c0003 | t0002 | g0013 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18979 | hp2 | a0002 | c0002 | t0004 | g0086 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18980 | hp1 | a0006 | c0009 | t0002 | g0265 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18982 | hp1 | a0002 | c0002 | t0005 | g0205 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18982 | hp2 | a0001 | c0001 | t0016 | g0028 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18983 | hp2 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18986 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18987 | hp1 | a0002 | c0002 | t0004 | g0072 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18989 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18989 | hp2 | a0002 | c0002 | t0004 | g0014 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18990 | hp2 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18992 | hp2 | a0001 | c0003 | t0002 | g0228 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18994 | hp2 | a0001 | c0001 | t0008 | g0114 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18999 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19000 | hp2 | a0002 | c0002 | t0005 | g0202 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19002 | hp2 | a0001 | c0005 | t0002 | g0013 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19003 | hp1 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19006 | hp1 | a0001 | c0003 | t0002 | g0214 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19007 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19009 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19010 | hp2 | a0001 | c0003 | t0002 | g0225 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0270 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19012 | hp1 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19030 | hp1 | a0003 | c0004 | t0006 | g0048 | AFR | LWK | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19030 | hp2 | a0002 | c0002 | t0006 | g0196 | AFR | LWK | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19043 | hp1 | a0002 | c0002 | t0004 | g0068 | AFR | LWK | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19043 | hp2 | a0002 | c0002 | t0010 | g0043 | AFR | LWK | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19054 | hp1 | a0002 | c0002 | t0004 | g0026 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19055 | hp1 | a0001 | c0001 | t0008 | g0112 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19055 | hp2 | a0001 | c0003 | t0002 | g0227 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19057 | hp2 | a0001 | c0003 | t0002 | g0040 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19059 | hp1 | a0002 | c0002 | t0004 | g0080 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19063 | hp1 | a0001 | c0003 | t0002 | g0211 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19064 | hp2 | a0001 | c0003 | t0002 | g0013 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19066 | hp2 | a0002 | c0002 | t0004 | g0076 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19067 | hp2 | a0001 | c0003 | t0002 | g0210 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19068 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19070 | hp1 | a0002 | c0002 | t0004 | g0071 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19072 | hp1 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19072 | hp2 | a0001 | c0003 | t0002 | g0209 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19077 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19081 | hp2 | a0001 | c0003 | t0002 | g0219 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19082 | hp1 | a0001 | c0003 | t0002 | g0215 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19083 | hp1 | a0001 | c0003 | t0002 | g0212 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19084 | hp2 | a0002 | c0002 | t0004 | g0026 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19085 | hp1 | a0001 | c0003 | t0002 | g0277 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19086 | hp1 | a0001 | c0003 | t0002 | g0246 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19087 | hp1 | a0002 | c0002 | t0004 | g0078 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19090 | hp2 | a0001 | c0001 | t0008 | g0105 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19091 | hp1 | a0001 | c0001 | t0014 | g0028 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19091 | hp2 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0263 | AFR | YRI | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA19240 | hp2 | a0007 | c0006 | t0012 | g0102 | AFR | YRI | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA20129 | hp1 | a0002 | c0002 | t0006 | g0052 | AFR | ASW | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA20129 | hp2 | a0002 | c0002 | t0013 | g0082 | AFR | ASW | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA20752 | hp1 | a0002 | c0002 | t0003 | g0004 | EUR | TSI | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0275 | EUR | TSI | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | GIH | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0182 | SAS | GIH | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG01123 | hp2 | a0001 | c0003 | t0002 | g0019 | AMR | CLM | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02109 | hp2 | a0002 | c0002 | t0004 | g0074 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02486 | hp1 | a0004 | c0010 | t0010 | g0044 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02486 | hp2 | a0002 | c0002 | t0005 | g0162 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG02559 | hp2 | a0002 | c0002 | t0006 | g0051 | AFR | ACB | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0259 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG03471 | hp2 | a0002 | c0002 | t0006 | g0100 | AFR | MSL | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG06807 | hp1 | a0005 | c0007 | t0028 | g0045 | AFR | USA | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0229 | AFR | USA | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA21309 | hp1 | a0002 | c0002 | t0003 | g0173 | AFR | LWK | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| NA21309 | hp2 | a0001 | c0003 | t0002 | g0235 | AFR | LWK | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0002 | g0236 | REF | REF | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0238 | REF | REF | CEP44_chr4_174278911_174325328 | CEP44 | chr4 | 174278911 | 174325328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:174299153 | G | A | 1 | a0007 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.32G>A | p.Arg11Gln | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/12 | 212/4298 | 32/1173 | 11/390 | chr4 | 174299153 | |||
| chr4:174302163 | C | T | 1 | a0004 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.214C>T | p.Arg72Cys | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/12 | 394/4298 | 214/1173 | 72/390 | chr4 | 174302163 | |||
| chr4:174303815 | T | C | 1 | a0003 | 4 | HG01109.hp1 HG02145.hp2 HG03209.hp2 others(1): Show |
missense_variant | MODERATE | c.350T>C | p.Met117Thr | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 5/12 | 530/4298 | 350/1173 | 117/390 | chr4 | 174303815 | |||
| chr4:174303820 | A | C | 1 | a0007 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.355A>C | p.Lys119Gln | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 5/12 | 535/4298 | 355/1173 | 119/390 | chr4 | 174303820 | |||
| chr4:174304301 | G | A | 5 | a0002 a0003 a0004 others(2): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
missense_variant | MODERATE | c.439G>A | p.Gly147Ser | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/12 | 619/4298 | 439/1173 | 147/390 | chr4 | 174304301 | |||
| chr4:174316559 | G | C | 1 | a0006 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.1116G>C | p.Met372Ile | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 11/12 | 1296/4298 | 1116/1173 | 372/390 | chr4 | 174316559 | |||
| chr4:174317369 | A | G | 1 | a0005 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1159A>G | p.Asn387Asp | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1339/4298 | 1159/1173 | 387/390 | chr4 | 174317369 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:174308760 | A | G | 1 | a0001c0005 | 3 | NA18949.hp2 NA18970.hp2 NA19002.hp2 |
synonymous_variant | LOW | c.579A>G | p.Pro193Pro | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/12 | 759/4298 | 579/1173 | 193/390 | chr4 | 174308760 | |||
| chr4:174316257 | T | C | 7 | a0001c0001 a0002c0002 a0002c0008 others(4): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
synonymous_variant | LOW | c.1053T>C | p.Thr351Thr | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 10/12 | 1233/4298 | 1053/1173 | 351/390 | chr4 | 174316257 | |||
| chr4:174317357 | C | T | 1 | a0002c0008 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.1147C>T | p.Leu383Leu | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1327/4298 | 1147/1173 | 383/390 | chr4 | 174317357 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:174297978 | T | A | 1 | a0001c0001t0014 | 2 | NA18968.hp2 NA19091.hp1 |
5_prime_UTR_variant | MODIFIER | c.-135T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/12 | 1144 | chr4 | 174297978 | ||||||
| chr4:174298001 | G | A | 1 | a0001c0005t0018 | 1 | NA18949.hp2 | 5_prime_UTR_variant | MODIFIER | c.-112G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/12 | 1121 | chr4 | 174298001 | ||||||
| chr4:174317634 | C | G | 1 | a0001c0001t0031 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*251C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 251 | chr4 | 174317634 | ||||||
| chr4:174317874 | G | A | 1 | a0002c0002t0015 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*491G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 491 | chr4 | 174317874 | ||||||
| chr4:174317917 | T | A | 1 | a0002c0002t0019 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*534T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 534 | chr4 | 174317917 | ||||||
| chr4:174318127 | G | C | 12 | a0001c0001t0005 a0002c0002t0003 a0002c0002t0005 others(9): Show |
74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*744G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 744 | chr4 | 174318127 | ||||||
| chr4:174318167 | G | A | 12 | a0001c0001t0005 a0002c0002t0003 a0002c0002t0005 others(9): Show |
74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*784G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 784 | chr4 | 174318167 | ||||||
| chr4:174318221 | G | A | 6 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0014 others(3): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*838G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 838 | chr4 | 174318221 | ||||||
| chr4:174318243 | A | G | 1 | a0002c0002t0025 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*860A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 860 | chr4 | 174318243 | ||||||
| chr4:174318256 | T | A | 2 | a0001c0001t0014 a0001c0001t0016 |
4 | NA18967.hp1 NA18968.hp2 NA18982.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*873T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 873 | chr4 | 174318256 | ||||||
| chr4:174318322 | G | A | 1 | a0001c0001t0008 | 5 | NA18994.hp2 NA19002.hp1 NA19055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*939G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 939 | chr4 | 174318322 | ||||||
| chr4:174318324 | C | T | 1 | a0002c0002t0024 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*941C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 941 | chr4 | 174318324 | ||||||
| chr4:174318503 | TTAC | T | 23 | a0001c0001t0005 a0002c0002t0003 a0002c0002t0004 others(20): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1126_*1128delCTA | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1126 | INFO_REALIGN_3_PRIME | chr4 | 174318503 | |||||
| chr4:174318538 | A | G | 1 | a0001c0003t0029 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1155A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1155 | chr4 | 174318538 | ||||||
| chr4:174318576 | A | C | 4 | a0002c0002t0004 a0002c0002t0013 a0002c0002t0030 others(1): Show |
35 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1193A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1193 | chr4 | 174318576 | ||||||
| chr4:174318628 | G | A | 1 | a0002c0002t0020 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1245G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1245 | chr4 | 174318628 | ||||||
| chr4:174318684 | A | G | 1 | a0002c0002t0023 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1301A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1301 | chr4 | 174318684 | ||||||
| chr4:174318686 | A | G | 1 | a0002c0002t0013 | 3 | HG00733.hp1 HG03486.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1303A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1303 | chr4 | 174318686 | ||||||
| chr4:174318802 | C | T | 4 | a0002c0002t0004 a0002c0002t0013 a0002c0002t0030 others(1): Show |
35 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1419C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1419 | chr4 | 174318802 | ||||||
| chr4:174318846 | A | G | 24 | a0001c0001t0005 a0002c0002t0003 a0002c0002t0004 others(21): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1463A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1463 | chr4 | 174318846 | ||||||
| chr4:174319064 | G | A | 1 | a0001c0003t0011 | 3 | HG01074.hp2 HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1681G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1681 | chr4 | 174319064 | ||||||
| chr4:174319075 | C | CTAGAT | 1 | a0001c0003t0007 | 10 | HG00642.hp2 HG01070.hp1 HG01346.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1694_*1698dupAGAT others(1): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1699 | INFO_REALIGN_3_PRIME | chr4 | 174319075 | |||||
| chr4:174319122 | C | G | 1 | a0002c0002t0022 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1739C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1739 | chr4 | 174319122 | ||||||
| chr4:174319367 | T | C | 3 | a0002c0002t0009 a0002c0002t0017 a0002c0002t0019 |
8 | HG00741.hp1 HG01516.hp1 HG01981.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1984T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 1984 | chr4 | 174319367 | ||||||
| chr4:174319455 | C | G | 8 | a0002c0002t0004 a0002c0002t0009 a0002c0002t0012 others(5): Show |
44 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2072C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 2072 | chr4 | 174319455 | ||||||
| chr4:174319693 | A | G | 1 | a0002c0002t0019 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2310A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 2310 | chr4 | 174319693 | ||||||
| chr4:174319778 | TTATC | T | 4 | a0002c0002t0003 a0002c0002t0015 a0002c0002t0020 others(1): Show |
37 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2398_*2401delTCTA | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 2398 | INFO_REALIGN_3_PRIME | chr4 | 174319778 | |||||
| chr4:174319794 | AT | A | 2 | a0002c0002t0010 a0004c0010t0010 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2416delT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 2416 | INFO_REALIGN_3_PRIME | chr4 | 174319794 | |||||
| chr4:174319977 | A | T | 5 | a0002c0002t0003 a0002c0002t0015 a0002c0002t0020 others(2): Show |
38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2594A>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 2594 | chr4 | 174319977 | ||||||
| chr4:174319981 | C | A | 1 | a0001c0003t0027 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2598C>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 2598 | chr4 | 174319981 | ||||||
| chr4:174320026 | A | G | 1 | a0001c0001t0026 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2643A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 2643 | chr4 | 174320026 | ||||||
| chr4:174320044 | C | G | 1 | a0002c0002t0030 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2661C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 2661 | chr4 | 174320044 | ||||||
| chr4:174320051 | C | G | 1 | a0002c0002t0021 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2668C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 2668 | chr4 | 174320051 | ||||||
| chr4:174320227 | A | G | 3 | a0002c0002t0009 a0002c0002t0017 a0002c0002t0019 |
8 | HG00741.hp1 HG01516.hp1 HG01981.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2844A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 2844 | chr4 | 174320227 | ||||||
| chr4:174320325 | G | A | 4 | a0002c0002t0004 a0002c0002t0013 a0002c0002t0030 others(1): Show |
35 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2942G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 12/12 | 2942 | chr4 | 174320325 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:174284072 | A | T | 1 | a0002c0002t0005g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-148+129A>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174284072 | |||||||
| chr4:174284324 | G | C | 3 | a0002c0002t0010g0020 a0002c0002t0010g0043 a0004c0010t0010g0044 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-148+381G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174284324 | |||||||
| chr4:174284441 | C | T | 1 | a0001c0003t0002g0278 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-148+498C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174284441 | |||||||
| chr4:174284730 | GCCTTTCT others(4): Show |
G | 1 | a0001c0003t0002g0277 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-148+796_-148+806d others(13): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174284730 | ||||||
| chr4:174285007 | T | G | 1 | a0002c0002t0017g0021 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-148+1064T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174285007 | |||||||
| chr4:174285017 | A | T | 1 | a0001c0003t0002g0042 | 2 | HG00639.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.-148+1074A>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174285017 | |||||||
| chr4:174285038 | T | A | 1 | a0005c0007t0028g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-148+1095T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174285038 | |||||||
| chr4:174285216 | A | T | 1 | a0002c0002t0017g0021 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-148+1273A>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174285216 | |||||||
| chr4:174285254 | G | A | 1 | a0001c0003t0007g0046 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-148+1311G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174285254 | |||||||
| chr4:174285259 | T | G | 4 | a0003c0004t0006g0047 a0003c0004t0006g0048 a0003c0004t0006g0049 others(1): Show |
4 | HG01109.hp1 HG02145.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-148+1316T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174285259 | |||||||
| chr4:174285373 | G | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(197): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.-148+1430G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174285373 | |||||||
| chr4:174285695 | G | C | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-148+1752G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174285695 | |||||||
| chr4:174285762 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-148+1819C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174285762 | |||||||
| chr4:174286050 | G | A | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-148+2107G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174286050 | |||||||
| chr4:174286264 | T | G | 1 | a0002c0002t0017g0021 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-148+2321T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174286264 | |||||||
| chr4:174286429 | T | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0053 others(7): Show |
15 | HG01106.hp1 HG02015.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.-148+2486T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174286429 | |||||||
| chr4:174286481 | G | C | 22 | a0001c0003t0002g0005 a0001c0003t0002g0006 a0001c0003t0002g0011 others(19): Show |
36 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.-148+2538G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174286481 | |||||||
| chr4:174286668 | C | G | 10 | a0002c0002t0005g0009 a0002c0002t0005g0197 a0002c0002t0005g0198 others(7): Show |
14 | HG00639.hp1 HG01069.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.-148+2725C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174286668 | |||||||
| chr4:174286827 | G | A | 1 | a0002c0002t0017g0021 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-148+2884G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174286827 | |||||||
| chr4:174286988 | T | G | 1 | a0002c0002t0006g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-148+3045T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174286988 | |||||||
| chr4:174287054 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-148+3111T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174287054 | |||||||
| chr4:174287220 | A | G | 2 | a0001c0003t0002g0275 a0001c0003t0002g0276 |
2 | HG00323.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-148+3277A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174287220 | |||||||
| chr4:174287439 | G | A | 1 | a0002c0002t0005g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-148+3496G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174287439 | |||||||
| chr4:174287581 | A | G | 10 | a0002c0002t0005g0009 a0002c0002t0005g0197 a0002c0002t0005g0198 others(7): Show |
14 | HG00639.hp1 HG01069.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.-148+3638A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174287581 | |||||||
| chr4:174287623 | A | G | 1 | a0002c0002t0006g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-148+3680A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174287623 | |||||||
| chr4:174287777 | T | C | 1 | a0002c0008t0004g0064 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-148+3834T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174287777 | |||||||
| chr4:174288221 | T | C | 1 | a0001c0001t0008g0023 | 2 | NA19002.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-148+4278T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174288221 | |||||||
| chr4:174288223 | C | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0194 a0001c0001t0001g0195 |
4 | HG01891.hp1 HG02615.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-148+4280C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174288223 | |||||||
| chr4:174288299 | A | G | 1 | a0002c0002t0006g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-148+4356A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174288299 | |||||||
| chr4:174288336 | C | T | 3 | a0001c0003t0002g0272 a0001c0003t0002g0273 a0001c0003t0002g0274 |
3 | HG03098.hp1 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-148+4393C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174288336 | |||||||
| chr4:174288781 | C | T | 62 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(59): Show |
77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-148+4838C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174288781 | |||||||
| chr4:174288791 | G | A | 1 | a0001c0001t0014g0065 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-148+4848G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174288791 | |||||||
| chr4:174288988 | A | G | 1 | a0002c0002t0006g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-148+5045A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174288988 | |||||||
| chr4:174289061 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-148+5118T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174289061 | |||||||
| chr4:174289090 | T | C | 1 | a0002c0002t0006g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-148+5147T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174289090 | |||||||
| chr4:174289295 | CT | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(117): Show |
168 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.-148+5368delT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174289295 | ||||||
| chr4:174289295 | CTT | C | 9 | a0001c0001t0001g0093 a0002c0002t0005g0160 a0002c0002t0005g0161 others(6): Show |
10 | HG01109.hp1 HG01516.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-148+5367_-148+536 others(6): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174289295 | ||||||
| chr4:174289295 | CTTT | C | 30 | a0002c0002t0004g0014 a0002c0002t0004g0024 a0002c0002t0004g0025 others(27): Show |
35 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.-148+5366_-148+536 others(7): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174289295 | ||||||
| chr4:174289297 | T | C | 1 | a0002c0002t0003g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-148+5354T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174289297 | |||||||
| chr4:174289439 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-148+5496A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174289439 | |||||||
| chr4:174289463 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-148+5520A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174289463 | |||||||
| chr4:174289472 | T | C | 1 | a0001c0003t0002g0229 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-148+5529T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174289472 | |||||||
| chr4:174289696 | A | G | 2 | a0001c0003t0002g0042 a0001c0003t0002g0271 |
3 | HG00639.hp2 HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-148+5753A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174289696 | |||||||
| chr4:174289812 | T | C | 6 | a0001c0003t0002g0230 a0001c0003t0002g0231 a0001c0003t0002g0232 others(3): Show |
6 | HG02717.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-148+5869T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174289812 | |||||||
| chr4:174289905 | C | T | 3 | a0002c0002t0010g0020 a0002c0002t0010g0043 a0004c0010t0010g0044 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-148+5962C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174289905 | |||||||
| chr4:174289914 | C | T | 1 | a0002c0002t0005g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-148+5971C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174289914 | |||||||
| chr4:174290036 | T | A | 77 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(74): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-148+6093T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290036 | |||||||
| chr4:174290057 | T | C | 7 | a0002c0002t0009g0027 a0002c0002t0009g0092 a0002c0002t0009g0097 others(4): Show |
8 | HG00741.hp1 HG01516.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-148+6114T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290057 | |||||||
| chr4:174290112 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-148+6169C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290112 | |||||||
| chr4:174290138 | G | A | 1 | a0002c0002t0004g0067 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-148+6195G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290138 | |||||||
| chr4:174290243 | T | C | 62 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(59): Show |
77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-148+6300T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290243 | |||||||
| chr4:174290320 | T | C | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-148+6377T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290320 | |||||||
| chr4:174290428 | T | TAAATTTG others(306): Show |
1 | a0002c0002t0022g0172 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-148+6494_-148+649 others(317): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174290428 | ||||||
| chr4:174290428 | T | TAAATTTG others(306): Show |
24 | a0002c0002t0003g0004 a0002c0002t0003g0036 a0002c0002t0003g0037 others(21): Show |
30 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.-148+6494_-148+649 others(317): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174290428 | ||||||
| chr4:174290428 | T | TAAATTTG others(307): Show |
5 | a0002c0002t0003g0018 a0002c0002t0003g0173 a0002c0002t0003g0174 others(2): Show |
7 | HG00280.hp1 HG00741.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-148+6494_-148+649 others(318): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174290428 | ||||||
| chr4:174290447 | T | G | 4 | a0002c0002t0006g0099 a0002c0002t0006g0100 a0002c0002t0006g0101 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-148+6504T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290447 | |||||||
| chr4:174290583 | A | G | 3 | a0002c0002t0010g0020 a0002c0002t0010g0043 a0004c0010t0010g0044 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-148+6640A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290583 | |||||||
| chr4:174290615 | G | C | 2 | a0002c0002t0012g0094 a0002c0002t0012g0095 |
2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-148+6672G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290615 | |||||||
| chr4:174290627 | C | G | 1 | a0001c0003t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-148+6684C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290627 | |||||||
| chr4:174290869 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-148+6926A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290869 | |||||||
| chr4:174290889 | A | G | 1 | a0002c0002t0023g0171 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-148+6946A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290889 | |||||||
| chr4:174290901 | C | T | 1 | a0002c0002t0006g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-148+6958C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290901 | |||||||
| chr4:174290926 | C | T | 1 | a0001c0003t0002g0234 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-148+6983C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290926 | |||||||
| chr4:174290939 | A | G | 30 | a0002c0002t0004g0014 a0002c0002t0004g0024 a0002c0002t0004g0025 others(27): Show |
35 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.-148+6996A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174290939 | |||||||
| chr4:174291027 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-147-6939G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174291027 | |||||||
| chr4:174291190 | T | G | 1 | a0007c0006t0012g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-147-6776T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174291190 | |||||||
| chr4:174291226 | CTT | C | 14 | a0002c0002t0006g0061 a0002c0002t0006g0099 a0002c0002t0006g0100 others(11): Show |
15 | HG00741.hp1 HG01516.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-147-6739_-147-673 others(6): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174291226 | |||||||
| chr4:174291351 | T | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(87): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-147-6615T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174291351 | |||||||
| chr4:174291381 | C | A | 4 | a0003c0004t0006g0047 a0003c0004t0006g0048 a0003c0004t0006g0049 others(1): Show |
4 | HG01109.hp1 HG02145.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147-6585C>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174291381 | |||||||
| chr4:174291410 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-147-6556C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174291410 | |||||||
| chr4:174291782 | C | CTTTTTTT others(1): Show |
5 | a0002c0002t0004g0024 a0002c0002t0004g0070 a0002c0002t0004g0071 others(2): Show |
6 | HG00323.hp2 HG03654.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.-147-6180_-147-617 others(12): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174291782 | ||||||
| chr4:174291782 | C | CTTTTTTT others(2): Show |
10 | a0002c0002t0004g0025 a0002c0002t0004g0067 a0002c0002t0004g0072 others(7): Show |
11 | HG01884.hp1 HG02056.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-147-6180_-147-617 others(13): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174291782 | ||||||
| chr4:174291782 | C | CTTTTTTT others(3): Show |
8 | a0002c0002t0004g0026 a0002c0002t0004g0080 a0002c0002t0004g0081 others(5): Show |
9 | HG00621.hp2 HG02970.hp1 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-147-6180_-147-617 others(14): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174291782 | ||||||
| chr4:174291782 | C | CTTTTTTT others(4): Show |
4 | a0002c0002t0004g0087 a0002c0002t0004g0088 a0002c0002t0004g0089 others(1): Show |
4 | HG00609.hp1 HG00673.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147-6180_-147-617 others(15): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174291782 | ||||||
| chr4:174291782 | C | CTTTTTTT others(5): Show |
1 | a0002c0002t0013g0091 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-147-6180_-147-617 others(16): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174291782 | ||||||
| chr4:174291782 | C | CTTTTTTT others(10): Show |
1 | a0005c0007t0028g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-147-6180_-147-617 others(21): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174291782 | ||||||
| chr4:174291787 | C | CT | 28 | a0001c0001t0001g0194 a0001c0003t0002g0002 a0001c0003t0002g0005 others(25): Show |
33 | HG00597.hp1 HG00741.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.-147-6154dupT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174291787 | ||||||
| chr4:174291787 | C | CTT | 18 | a0002c0002t0003g0179 a0002c0002t0005g0009 a0002c0002t0005g0169 others(15): Show |
20 | HG00639.hp1 HG01069.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-147-6155_-147-615 others(6): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174291787 | ||||||
| chr4:174291787 | C | CTTT | 44 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(41): Show |
53 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.-147-6156_-147-615 others(7): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174291787 | ||||||
| chr4:174291787 | C | CTTTT | 6 | a0002c0002t0003g0004 a0002c0002t0003g0036 a0002c0002t0003g0038 others(3): Show |
7 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.-147-6157_-147-615 others(8): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174291787 | ||||||
| chr4:174291787 | C | T | 30 | a0002c0002t0004g0024 a0002c0002t0004g0025 a0002c0002t0004g0026 others(27): Show |
33 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.-147-6179C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174291787 | |||||||
| chr4:174291787 | CT | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(77): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-147-6154delT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174291787 | ||||||
| chr4:174291970 | T | C | 1 | a0001c0003t0002g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-147-5996T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174291970 | |||||||
| chr4:174292067 | C | A | 1 | a0002c0002t0005g0162 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-147-5899C>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174292067 | |||||||
| chr4:174292148 | T | A | 7 | a0001c0003t0002g0006 a0001c0003t0002g0208 a0001c0003t0002g0209 others(4): Show |
12 | HG02027.hp2 HG02056.hp1 NA18939.hp2 others(9): Show |
intron_variant | MODIFIER | c.-147-5818T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174292148 | |||||||
| chr4:174292250 | A | G | 1 | a0002c0002t0004g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-147-5716A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174292250 | |||||||
| chr4:174292714 | G | T | 62 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(59): Show |
77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-147-5252G>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174292714 | |||||||
| chr4:174292780 | A | G | 77 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(74): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-147-5186A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174292780 | |||||||
| chr4:174292824 | T | C | 1 | a0002c0002t0023g0171 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-147-5142T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174292824 | |||||||
| chr4:174292921 | T | C | 1 | a0001c0003t0002g0237 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-147-5045T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174292921 | |||||||
| chr4:174293056 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-147-4910G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174293056 | |||||||
| chr4:174293215 | C | A | 1 | a0002c0002t0005g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-147-4751C>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174293215 | |||||||
| chr4:174293215 | C | T | 4 | a0002c0002t0006g0099 a0002c0002t0006g0100 a0002c0002t0006g0101 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147-4751C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174293215 | |||||||
| chr4:174293687 | G | T | 9 | a0001c0001t0001g0034 a0001c0003t0002g0006 a0001c0003t0002g0208 others(6): Show |
15 | HG01081.hp2 HG02027.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.-147-4279G>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174293687 | |||||||
| chr4:174293957 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(280): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.-147-4009A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174293957 | |||||||
| chr4:174294046 | CT | C | 11 | a0001c0001t0001g0053 a0001c0001t0001g0103 a0001c0003t0002g0208 others(8): Show |
11 | HG02300.hp1 HG02559.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.-147-3904delT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174294046 | ||||||
| chr4:174294184 | C | A | 2 | a0002c0002t0004g0081 a0002c0002t0030g0069 |
2 | HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-147-3782C>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294184 | |||||||
| chr4:174294197 | G | A | 1 | a0001c0003t0002g0241 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-147-3769G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294197 | |||||||
| chr4:174294215 | G | A | 8 | a0002c0002t0005g0160 a0002c0002t0005g0161 a0002c0002t0005g0163 others(5): Show |
8 | HG01109.hp1 HG02145.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-147-3751G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294215 | |||||||
| chr4:174294250 | C | T | 1 | a0002c0002t0005g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-147-3716C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294250 | |||||||
| chr4:174294251 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-147-3715G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294251 | |||||||
| chr4:174294410 | C | G | 1 | a0002c0002t0003g0192 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-147-3556C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294410 | |||||||
| chr4:174294410 | C | T | 1 | a0007c0006t0012g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-147-3556C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294410 | |||||||
| chr4:174294433 | G | A | 1 | a0001c0001t0008g0105 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-147-3533G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294433 | |||||||
| chr4:174294458 | T | C | 1 | a0001c0003t0002g0214 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-147-3508T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294458 | |||||||
| chr4:174294526 | G | A | 1 | a0001c0003t0002g0215 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-147-3440G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294526 | |||||||
| chr4:174294539 | G | A | 1 | a0002c0002t0005g0197 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-147-3427G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294539 | |||||||
| chr4:174294631 | C | T | 1 | a0002c0002t0005g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-147-3335C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294631 | |||||||
| chr4:174294650 | G | A | 3 | a0001c0001t0001g0106 a0001c0003t0002g0040 a0001c0003t0002g0227 |
4 | NA18945.hp2 NA19055.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147-3316G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294650 | |||||||
| chr4:174294667 | G | C | 14 | a0002c0002t0006g0061 a0002c0002t0006g0099 a0002c0002t0006g0100 others(11): Show |
15 | HG00741.hp1 HG01516.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-147-3299G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294667 | |||||||
| chr4:174294715 | C | T | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-147-3251C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294715 | |||||||
| chr4:174294716 | G | A | 1 | a0001c0001t0008g0105 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-147-3250G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294716 | |||||||
| chr4:174294725 | A | AC | 17 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0141 others(14): Show |
19 | HG00544.hp1 HG02056.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-147-3239dupC | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174294725 | ||||||
| chr4:174294727 | CA | C | 3 | a0002c0002t0010g0020 a0002c0002t0010g0043 a0004c0010t0010g0044 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147-3238delA | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294727 | |||||||
| chr4:174294728 | A | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(194): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-147-3238A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294728 | |||||||
| chr4:174294746 | G | A | 1 | a0002c0002t0006g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-147-3220G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294746 | |||||||
| chr4:174294749 | C | T | 30 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(27): Show |
38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.-147-3217C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294749 | |||||||
| chr4:174294765 | C | T | 8 | a0002c0002t0009g0027 a0002c0002t0009g0092 a0002c0002t0009g0097 others(5): Show |
9 | HG00741.hp1 HG01516.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147-3201C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294765 | |||||||
| chr4:174294777 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-147-3189C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294777 | |||||||
| chr4:174294781 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-147-3185C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294781 | |||||||
| chr4:174294787 | G | A | 1 | a0002c0002t0006g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-147-3179G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294787 | |||||||
| chr4:174294799 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-147-3167G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294799 | |||||||
| chr4:174294810 | C | T | 1 | a0001c0003t0002g0278 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-147-3156C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294810 | |||||||
| chr4:174294827 | G | A | 1 | a0001c0003t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-147-3139G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294827 | |||||||
| chr4:174294833 | G | T | 8 | a0002c0002t0009g0027 a0002c0002t0009g0092 a0002c0002t0009g0097 others(5): Show |
9 | HG00741.hp1 HG01516.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147-3133G>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294833 | |||||||
| chr4:174294834 | A | G | 3 | a0002c0002t0010g0020 a0002c0002t0010g0043 a0004c0010t0010g0044 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147-3132A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294834 | |||||||
| chr4:174294844 | G | A | 31 | a0002c0002t0004g0014 a0002c0002t0004g0024 a0002c0002t0004g0025 others(28): Show |
36 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.-147-3122G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294844 | |||||||
| chr4:174294875 | C | T | 6 | a0002c0002t0006g0061 a0002c0002t0006g0099 a0002c0002t0006g0100 others(3): Show |
6 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-3091C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294875 | |||||||
| chr4:174294879 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-147-3087C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294879 | |||||||
| chr4:174294884 | C | T | 1 | a0002c0002t0006g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-147-3082C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294884 | |||||||
| chr4:174294939 | C | T | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-147-3027C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294939 | |||||||
| chr4:174294956 | A | G | 1 | a0002c0002t0005g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-147-3010A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294956 | |||||||
| chr4:174294961 | ACGGCTGG others(91): Show |
A | 10 | a0002c0002t0005g0017 a0002c0002t0005g0162 a0002c0002t0005g0165 others(7): Show |
12 | HG01099.hp1 HG01255.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.-147-2992_-147-289 others(102): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174294961 | ||||||
| chr4:174294975 | G | T | 1 | a0002c0002t0005g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-147-2991G>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174294975 | |||||||
| chr4:174295013 | G | T | 1 | a0002c0002t0006g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-147-2953G>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295013 | |||||||
| chr4:174295023 | C | T | 2 | a0001c0001t0001g0132 a0002c0002t0017g0021 |
3 | HG00280.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-147-2943C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295023 | |||||||
| chr4:174295061 | G | A | 1 | a0002c0002t0017g0021 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-147-2905G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295061 | |||||||
| chr4:174295122 | G | A | 3 | a0002c0002t0010g0020 a0002c0002t0010g0043 a0004c0010t0010g0044 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147-2844G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295122 | |||||||
| chr4:174295122 | G | C | 1 | a0001c0003t0002g0242 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-147-2844G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295122 | |||||||
| chr4:174295124 | G | A | 1 | a0001c0003t0002g0041 | 2 | HG01256.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-147-2842G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295124 | |||||||
| chr4:174295150 | T | TGGGGTGG others(33): Show |
1 | a0002c0002t0005g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-147-2799_-147-276 others(44): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174295150 | ||||||
| chr4:174295220 | A | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0148 |
3 | NA18974.hp2 NA18980.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-147-2746A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295220 | |||||||
| chr4:174295237 | G | C | 5 | a0001c0003t0002g0275 a0001c0003t0002g0276 a0001c0003t0011g0243 others(2): Show |
5 | HG00323.hp1 HG01074.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147-2729G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295237 | |||||||
| chr4:174295270 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-147-2696C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295270 | |||||||
| chr4:174295276 | G | A | 1 | a0002c0002t0004g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-147-2690G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295276 | |||||||
| chr4:174295307 | C | T | 1 | a0001c0003t0002g0226 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-147-2659C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295307 | |||||||
| chr4:174295446 | C | T | 2 | a0002c0002t0012g0094 a0002c0002t0012g0095 |
2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-147-2520C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295446 | |||||||
| chr4:174295475 | C | T | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-147-2491C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295475 | |||||||
| chr4:174295486 | C | T | 4 | a0002c0002t0006g0099 a0002c0002t0006g0100 a0002c0002t0006g0101 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147-2480C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295486 | |||||||
| chr4:174295528 | C | T | 1 | a0002c0002t0004g0014 | 3 | HG02083.hp1 NA18975.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-147-2438C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295528 | |||||||
| chr4:174295532 | C | T | 62 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(59): Show |
77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-147-2434C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295532 | |||||||
| chr4:174295563 | G | T | 1 | a0001c0003t0002g0019 | 3 | HG01123.hp2 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-147-2403G>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295563 | |||||||
| chr4:174295580 | C | CG | 17 | a0001c0001t0001g0054 a0001c0001t0001g0104 a0001c0001t0001g0108 others(14): Show |
17 | HG01099.hp2 HG01884.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.-147-2382dupG | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174295580 | ||||||
| chr4:174295593 | G | A | 5 | a0001c0003t0002g0216 a0001c0003t0002g0230 a0001c0003t0002g0231 others(2): Show |
5 | HG01496.hp1 HG02602.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147-2373G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295593 | |||||||
| chr4:174295603 | T | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0062 others(23): Show |
33 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.-147-2363T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295603 | |||||||
| chr4:174295637 | G | A | 3 | a0002c0002t0006g0099 a0002c0002t0006g0100 a0002c0002t0006g0193 |
3 | HG02622.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-147-2329G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295637 | |||||||
| chr4:174295762 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-147-2204A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295762 | |||||||
| chr4:174295860 | G | A | 2 | a0001c0003t0002g0237 a0001c0003t0002g0249 |
2 | HG01099.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-147-2106G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295860 | |||||||
| chr4:174295910 | T | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147-2056T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174295910 | |||||||
| chr4:174296017 | C | G | 1 | a0007c0006t0012g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-147-1949C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296017 | |||||||
| chr4:174296326 | T | C | 62 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(59): Show |
77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-147-1640T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296326 | |||||||
| chr4:174296451 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-147-1515T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296451 | |||||||
| chr4:174296522 | C | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(86): Show |
130 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-147-1444C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296522 | |||||||
| chr4:174296631 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0194 a0001c0001t0001g0195 |
4 | HG01891.hp1 HG02615.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147-1335G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296631 | |||||||
| chr4:174296645 | A | G | 2 | a0002c0002t0012g0094 a0002c0002t0012g0095 |
2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-147-1321A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296645 | |||||||
| chr4:174296737 | A | C | 1 | a0001c0003t0002g0225 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-147-1229A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296737 | |||||||
| chr4:174296763 | A | AT | 113 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0033 others(110): Show |
157 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.-147-1182dupT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174296763 | ||||||
| chr4:174296763 | A | ATT | 54 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0003t0002g0214 others(51): Show |
67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.-147-1183_-147-118 others(6): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174296763 | ||||||
| chr4:174296763 | AT | A | 9 | a0001c0001t0001g0111 a0001c0001t0001g0145 a0002c0002t0004g0068 others(6): Show |
10 | HG00741.hp1 HG01516.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.-147-1182delT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174296763 | ||||||
| chr4:174296852 | T | C | 6 | a0001c0003t0002g0230 a0001c0003t0002g0231 a0001c0003t0002g0232 others(3): Show |
6 | HG02717.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-147-1114T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296852 | |||||||
| chr4:174296862 | G | A | 1 | a0001c0003t0002g0252 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-147-1104G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296862 | |||||||
| chr4:174296905 | A | G | 1 | a0001c0003t0002g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-147-1061A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296905 | |||||||
| chr4:174296923 | G | A | 1 | a0001c0003t0002g0217 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-147-1043G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296923 | |||||||
| chr4:174296991 | T | A | 1 | a0002c0002t0005g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-147-975T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174296991 | |||||||
| chr4:174297038 | C | A | 1 | a0002c0002t0012g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-147-928C>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174297038 | |||||||
| chr4:174297473 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-147-493C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174297473 | |||||||
| chr4:174297626 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-147-340C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174297626 | |||||||
| chr4:174297651 | A | AGT | 23 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0109 others(20): Show |
29 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-147-282_-147-281d others(4): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174297651 | ||||||
| chr4:174297651 | A | AGTGT | 56 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(53): Show |
90 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-147-284_-147-281d others(6): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174297651 | ||||||
| chr4:174297651 | A | AGTGTGT | 18 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(15): Show |
26 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.-147-286_-147-281d others(8): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174297651 | ||||||
| chr4:174297651 | A | AGTGTGTG others(1): Show |
5 | a0001c0001t0001g0113 a0001c0001t0001g0148 a0001c0001t0008g0112 others(2): Show |
6 | HG01074.hp2 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-288_-147-281d others(10): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174297651 | ||||||
| chr4:174297651 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0120 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-147-290_-147-281d others(12): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174297651 | ||||||
| chr4:174297651 | AGT | A | 44 | a0001c0003t0002g0013 a0001c0003t0002g0220 a0001c0003t0002g0228 others(41): Show |
52 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-147-282_-147-281d others(4): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174297651 | ||||||
| chr4:174297651 | AGTGT | A | 27 | a0001c0001t0005g0268 a0001c0003t0002g0041 a0001c0003t0002g0249 others(24): Show |
34 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.-147-284_-147-281d others(6): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174297651 | ||||||
| chr4:174297651 | AGTGTGT | A | 33 | a0001c0003t0002g0232 a0001c0003t0002g0233 a0001c0003t0002g0234 others(30): Show |
41 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.-147-286_-147-281d others(8): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174297651 | ||||||
| chr4:174297651 | AGTGTGTG others(1): Show |
A | 6 | a0002c0002t0003g0191 a0002c0002t0006g0099 a0002c0002t0006g0100 others(3): Show |
6 | HG02273.hp2 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147-288_-147-281d others(10): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174297651 | ||||||
| chr4:174297651 | AGTGTGTG others(3): Show |
A | 1 | a0002c0002t0006g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-147-290_-147-281d others(12): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174297651 | ||||||
| chr4:174297651 | AGTGTGTG others(5): Show |
A | 6 | a0002c0002t0004g0026 a0002c0002t0004g0072 a0002c0002t0004g0077 others(3): Show |
7 | HG00621.hp2 HG02155.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-147-292_-147-281d others(14): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 174297651 | ||||||
| chr4:174297951 | C | G | 1 | a0002c0002t0005g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-147-15C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 1/11 | chr4 | 174297951 | |||||||
| chr4:174298097 | C | T | 1 | a0001c0003t0002g0263 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-51+35C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298097 | |||||||
| chr4:174298112 | T | C | 1 | a0001c0003t0027g0221 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-51+50T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298112 | |||||||
| chr4:174298126 | T | C | 31 | a0002c0002t0004g0014 a0002c0002t0004g0024 a0002c0002t0004g0025 others(28): Show |
36 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.-51+64T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298126 | |||||||
| chr4:174298170 | A | AT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(87): Show |
136 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-51+131dupT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 174298170 | ||||||
| chr4:174298170 | A | ATT | 62 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0116 others(59): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-51+130_-51+131dup others(2): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 174298170 | ||||||
| chr4:174298170 | A | ATTT | 10 | a0002c0002t0003g0038 a0002c0002t0003g0159 a0002c0002t0003g0174 others(7): Show |
11 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51+129_-51+131dup others(3): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 174298170 | ||||||
| chr4:174298170 | AT | A | 34 | a0001c0003t0002g0005 a0001c0003t0002g0006 a0001c0003t0002g0011 others(31): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-51+131delT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 174298170 | ||||||
| chr4:174298207 | G | A | 1 | a0002c0002t0006g0100 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-51+145G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298207 | |||||||
| chr4:174298215 | G | A | 3 | a0002c0002t0010g0020 a0002c0002t0010g0043 a0004c0010t0010g0044 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+153G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298215 | |||||||
| chr4:174298254 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(86): Show |
130 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-51+192C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298254 | |||||||
| chr4:174298321 | G | A | 14 | a0002c0002t0006g0061 a0002c0002t0006g0099 a0002c0002t0006g0100 others(11): Show |
15 | HG00741.hp1 HG01516.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-51+259G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298321 | |||||||
| chr4:174298376 | C | T | 1 | a0002c0002t0005g0017 | 3 | HG03130.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-51+314C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298376 | |||||||
| chr4:174298403 | C | T | 3 | a0002c0002t0010g0020 a0002c0002t0010g0043 a0004c0010t0010g0044 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+341C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298403 | |||||||
| chr4:174298411 | C | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(87): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-51+349C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298411 | |||||||
| chr4:174298418 | G | A | 1 | a0002c0002t0004g0078 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-51+356G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298418 | |||||||
| chr4:174298427 | G | A | 1 | a0002c0002t0004g0078 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-51+365G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298427 | |||||||
| chr4:174298477 | G | A | 3 | a0002c0002t0010g0020 a0002c0002t0010g0043 a0004c0010t0010g0044 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+415G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298477 | |||||||
| chr4:174298481 | T | G | 1 | a0001c0003t0007g0255 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-51+419T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298481 | |||||||
| chr4:174298533 | A | G | 1 | a0002c0002t0004g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-51+471A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298533 | |||||||
| chr4:174298662 | G | A | 63 | a0001c0001t0005g0268 a0002c0002t0003g0004 a0002c0002t0003g0018 others(60): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-50-410G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | chr4 | 174298662 | |||||||
| chr4:174298779 | T | TAA | 8 | a0002c0002t0009g0027 a0002c0002t0009g0092 a0002c0002t0009g0097 others(5): Show |
9 | HG00741.hp1 HG01516.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50-285_-50-284dup others(2): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 174298779 | ||||||
| chr4:174299308 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.89+98G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174299308 | |||||||
| chr4:174299484 | A | C | 10 | a0002c0002t0006g0051 a0002c0002t0006g0052 a0002c0002t0009g0027 others(7): Show |
11 | HG00741.hp1 HG01516.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.89+274A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174299484 | |||||||
| chr4:174299714 | T | C | 1 | a0001c0003t0002g0263 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.89+504T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174299714 | |||||||
| chr4:174299965 | C | G | 2 | a0002c0002t0003g0177 a0002c0002t0003g0189 |
2 | HG00544.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.89+755C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174299965 | |||||||
| chr4:174300395 | A | T | 2 | a0002c0002t0005g0200 a0002c0002t0021g0199 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.89+1185A>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174300395 | |||||||
| chr4:174300722 | C | G | 2 | a0002c0002t0012g0094 a0002c0002t0012g0095 |
2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90-1317C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174300722 | |||||||
| chr4:174300919 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.90-1120A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174300919 | |||||||
| chr4:174301108 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.90-931A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174301108 | |||||||
| chr4:174301149 | A | G | 1 | a0004c0010t0010g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.90-890A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174301149 | |||||||
| chr4:174301251 | C | T | 6 | a0001c0003t0002g0230 a0001c0003t0002g0231 a0001c0003t0002g0232 others(3): Show |
6 | HG02717.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.90-788C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174301251 | |||||||
| chr4:174301437 | G | A | 1 | a0001c0003t0002g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90-602G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174301437 | |||||||
| chr4:174301459 | A | T | 5 | a0002c0002t0009g0027 a0002c0002t0009g0092 a0002c0002t0009g0097 others(2): Show |
6 | HG00741.hp1 HG01516.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.90-580A>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174301459 | |||||||
| chr4:174301579 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | NA18992.hp1 NA19000.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.90-460G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174301579 | |||||||
| chr4:174301671 | A | G | 2 | a0002c0002t0012g0094 a0002c0002t0012g0095 |
2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90-368A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174301671 | |||||||
| chr4:174301698 | A | C | 3 | a0002c0002t0005g0162 a0002c0002t0005g0168 a0002c0002t0025g0170 |
3 | HG02486.hp2 HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.90-341A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174301698 | |||||||
| chr4:174301859 | T | G | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.90-180T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 3/11 | chr4 | 174301859 | |||||||
| chr4:174302284 | A | C | 1 | a0001c0003t0002g0266 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.237+98A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174302284 | |||||||
| chr4:174302330 | T | C | 1 | a0002c0002t0017g0021 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.237+144T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174302330 | |||||||
| chr4:174302458 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(280): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.237+272A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174302458 | |||||||
| chr4:174302485 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.237+299G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174302485 | |||||||
| chr4:174302783 | A | AT | 13 | a0001c0001t0001g0031 a0001c0001t0001g0158 a0001c0001t0016g0149 others(10): Show |
15 | HG00741.hp1 HG01109.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.237+613dupT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 174302783 | ||||||
| chr4:174302844 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.237+658G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174302844 | |||||||
| chr4:174302867 | G | A | 9 | a0002c0002t0004g0068 a0002c0002t0004g0073 a0002c0002t0004g0074 others(6): Show |
9 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.237+681G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174302867 | |||||||
| chr4:174302893 | G | A | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.237+707G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174302893 | |||||||
| chr4:174302933 | G | A | 1 | a0001c0003t0002g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.237+747G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174302933 | |||||||
| chr4:174302963 | T | C | 1 | a0002c0002t0006g0099 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.238-740T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174302963 | |||||||
| chr4:174303069 | C | T | 1 | a0002c0002t0004g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.238-634C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174303069 | |||||||
| chr4:174303254 | G | T | 5 | a0002c0002t0009g0027 a0002c0002t0009g0092 a0002c0002t0009g0097 others(2): Show |
6 | HG00741.hp1 HG01516.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-449G>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174303254 | |||||||
| chr4:174303262 | GTGTTTTT others(8): Show |
G | 37 | a0002c0002t0004g0014 a0002c0002t0004g0024 a0002c0002t0004g0025 others(34): Show |
43 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.238-439_238-425del others(15): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 174303262 | ||||||
| chr4:174303279 | A | C | 37 | a0002c0002t0004g0014 a0002c0002t0004g0024 a0002c0002t0004g0025 others(34): Show |
43 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.238-424A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174303279 | |||||||
| chr4:174303299 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.238-404A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174303299 | |||||||
| chr4:174303334 | G | A | 1 | a0002c0002t0005g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.238-369G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174303334 | |||||||
| chr4:174303551 | C | T | 2 | a0002c0002t0003g0037 a0002c0002t0020g0037 |
2 | HG01516.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.238-152C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174303551 | |||||||
| chr4:174303587 | G | T | 1 | a0001c0003t0002g0257 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.238-116G>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174303587 | |||||||
| chr4:174303631 | G | C | 1 | a0001c0003t0029g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.238-72G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 4/11 | chr4 | 174303631 | |||||||
| chr4:174303856 | T | G | 1 | a0002c0002t0005g0163 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.384+7T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 5/11 | chr4 | 174303856 | |||||||
| chr4:174303915 | A | G | 4 | a0002c0002t0004g0024 a0002c0002t0004g0025 a0002c0002t0004g0067 others(1): Show |
6 | NA18947.hp1 NA18957.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.384+66A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 5/11 | chr4 | 174303915 | |||||||
| chr4:174304511 | A | G | 1 | a0002c0002t0005g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.507+142A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174304511 | |||||||
| chr4:174304569 | A | C | 13 | a0001c0003t0002g0012 a0001c0003t0002g0019 a0001c0003t0002g0241 others(10): Show |
18 | HG01123.hp2 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.507+200A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174304569 | |||||||
| chr4:174304799 | TG | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0194 a0001c0001t0001g0195 |
4 | HG01891.hp1 HG02615.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+432delG | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 174304799 | ||||||
| chr4:174304813 | C | T | 1 | a0002c0002t0003g0188 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.507+444C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174304813 | |||||||
| chr4:174305154 | T | G | 1 | a0002c0002t0004g0088 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.507+785T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174305154 | |||||||
| chr4:174305369 | G | A | 1 | a0001c0003t0007g0256 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.507+1000G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174305369 | |||||||
| chr4:174305374 | A | G | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.507+1005A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174305374 | |||||||
| chr4:174305395 | A | G | 2 | a0002c0002t0003g0182 a0002c0002t0003g0187 |
2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.507+1026A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174305395 | |||||||
| chr4:174305435 | C | A | 1 | a0002c0002t0006g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.507+1066C>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174305435 | |||||||
| chr4:174305463 | T | C | 1 | a0002c0002t0021g0199 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.507+1094T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174305463 | |||||||
| chr4:174305479 | C | T | 3 | a0002c0002t0010g0020 a0002c0002t0010g0043 a0004c0010t0010g0044 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+1110C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174305479 | |||||||
| chr4:174305701 | C | T | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.507+1332C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174305701 | |||||||
| chr4:174305721 | A | G | 1 | a0002c0002t0003g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.507+1352A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174305721 | |||||||
| chr4:174305812 | T | G | 1 | a0001c0005t0018g0264 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.507+1443T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174305812 | |||||||
| chr4:174306021 | A | G | 6 | a0002c0002t0005g0160 a0002c0002t0005g0161 a0003c0004t0006g0047 others(3): Show |
6 | HG01109.hp1 HG02145.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+1652A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174306021 | |||||||
| chr4:174306122 | C | T | 11 | a0001c0001t0005g0268 a0002c0002t0005g0009 a0002c0002t0005g0197 others(8): Show |
15 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.507+1753C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174306122 | |||||||
| chr4:174306520 | C | T | 1 | a0002c0002t0003g0185 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.507+2151C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174306520 | |||||||
| chr4:174306521 | G | A | 2 | a0001c0003t0002g0275 a0001c0003t0002g0276 |
2 | HG00323.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.507+2152G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174306521 | |||||||
| chr4:174306768 | G | C | 6 | a0002c0002t0006g0061 a0002c0002t0006g0099 a0002c0002t0006g0100 others(3): Show |
6 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.508-1921G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174306768 | |||||||
| chr4:174306892 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(87): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.508-1797A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174306892 | |||||||
| chr4:174307030 | G | A | 1 | a0002c0002t0006g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.508-1659G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174307030 | |||||||
| chr4:174307248 | T | C | 1 | a0002c0002t0003g0192 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.508-1441T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174307248 | |||||||
| chr4:174307249 | A | G | 1 | a0001c0001t0026g0125 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.508-1440A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174307249 | |||||||
| chr4:174307274 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.508-1415A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174307274 | |||||||
| chr4:174307293 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.508-1396C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174307293 | |||||||
| chr4:174307398 | T | C | 2 | a0002c0002t0005g0160 a0002c0002t0005g0161 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.508-1291T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174307398 | |||||||
| chr4:174307433 | T | C | 4 | a0001c0001t0008g0023 a0001c0001t0008g0105 a0001c0001t0008g0112 others(1): Show |
5 | NA18994.hp2 NA19002.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-1256T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174307433 | |||||||
| chr4:174307581 | G | A | 1 | a0007c0006t0012g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.508-1108G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174307581 | |||||||
| chr4:174307737 | T | A | 38 | a0002c0002t0004g0014 a0002c0002t0004g0024 a0002c0002t0004g0025 others(35): Show |
44 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.508-952T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174307737 | |||||||
| chr4:174307765 | GA | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(149): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.508-917delA | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 174307765 | ||||||
| chr4:174307935 | A | T | 1 | a0001c0003t0002g0219 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.508-754A>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174307935 | |||||||
| chr4:174307967 | G | A | 1 | a0002c0002t0017g0021 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.508-722G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174307967 | |||||||
| chr4:174308233 | C | T | 6 | a0002c0002t0005g0160 a0002c0002t0005g0161 a0003c0004t0006g0047 others(3): Show |
6 | HG01109.hp1 HG02145.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-456C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174308233 | |||||||
| chr4:174308310 | G | A | 30 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(27): Show |
38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.508-379G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 6/11 | chr4 | 174308310 | |||||||
| chr4:174308935 | T | C | 1 | a0002c0002t0005g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.678+76T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174308935 | |||||||
| chr4:174309116 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.678+257A>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174309116 | |||||||
| chr4:174309122 | C | G | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.678+263C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174309122 | |||||||
| chr4:174309191 | G | C | 39 | a0001c0001t0001g0141 a0002c0002t0004g0014 a0002c0002t0004g0024 others(36): Show |
45 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.678+332G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174309191 | |||||||
| chr4:174309215 | T | A | 2 | a0001c0001t0008g0105 a0001c0001t0008g0112 |
2 | NA19055.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.678+356T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174309215 | |||||||
| chr4:174309322 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.678+463C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174309322 | |||||||
| chr4:174309390 | T | C | 4 | a0002c0002t0006g0099 a0002c0002t0006g0100 a0002c0002t0006g0101 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-460T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174309390 | |||||||
| chr4:174309441 | T | G | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.679-409T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174309441 | |||||||
| chr4:174309519 | G | A | 1 | a0001c0003t0002g0260 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.679-331G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174309519 | |||||||
| chr4:174309735 | C | G | 2 | a0002c0002t0006g0051 a0002c0002t0006g0052 |
2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.679-115C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174309735 | |||||||
| chr4:174309745 | G | A | 38 | a0002c0002t0004g0014 a0002c0002t0004g0024 a0002c0002t0004g0025 others(35): Show |
44 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.679-105G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174309745 | |||||||
| chr4:174309769 | C | T | 6 | a0001c0003t0002g0230 a0001c0003t0002g0231 a0001c0003t0002g0232 others(3): Show |
6 | HG02717.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.679-81C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 7/11 | chr4 | 174309769 | |||||||
| chr4:174310100 | A | C | 8 | a0002c0002t0005g0160 a0002c0002t0005g0161 a0002c0002t0005g0163 others(5): Show |
8 | HG01109.hp1 HG02145.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.885+44A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 8/11 | chr4 | 174310100 | |||||||
| chr4:174310103 | G | GT | 26 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0062 others(23): Show |
33 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.885+56dupT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 174310103 | ||||||
| chr4:174310143 | C | G | 1 | a0002c0002t0003g0184 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.885+87C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 8/11 | chr4 | 174310143 | |||||||
| chr4:174310196 | T | C | 7 | a0002c0002t0009g0027 a0002c0002t0009g0092 a0002c0002t0009g0097 others(4): Show |
8 | HG00741.hp1 HG01516.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.885+140T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 8/11 | chr4 | 174310196 | |||||||
| chr4:174310206 | T | C | 2 | a0002c0002t0005g0160 a0002c0002t0005g0161 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.885+150T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 8/11 | chr4 | 174310206 | |||||||
| chr4:174310362 | T | A | 2 | a0002c0002t0005g0160 a0002c0002t0005g0161 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.885+306T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 8/11 | chr4 | 174310362 | |||||||
| chr4:174310559 | C | G | 1 | a0002c0002t0017g0021 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.886-224C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 8/11 | chr4 | 174310559 | |||||||
| chr4:174311148 | T | C | 1 | a0002c0002t0006g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.961+290T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174311148 | |||||||
| chr4:174311218 | A | G | 63 | a0001c0001t0005g0268 a0002c0002t0003g0004 a0002c0002t0003g0018 others(60): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.961+360A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174311218 | |||||||
| chr4:174311308 | C | G | 6 | a0001c0003t0002g0230 a0001c0003t0002g0231 a0001c0003t0002g0232 others(3): Show |
6 | HG02717.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.961+450C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174311308 | |||||||
| chr4:174311366 | G | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
5 | HG02040.hp1 HG02080.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.961+508G>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174311366 | |||||||
| chr4:174311481 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.961+623A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174311481 | |||||||
| chr4:174311552 | G | A | 283 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(280): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.961+694G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174311552 | |||||||
| chr4:174311727 | C | T | 1 | a0002c0002t0005g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.961+869C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174311727 | |||||||
| chr4:174311770 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.961+912G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174311770 | |||||||
| chr4:174311813 | T | C | 1 | a0002c0002t0006g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.961+955T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174311813 | |||||||
| chr4:174312078 | C | T | 1 | a0002c0002t0004g0076 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.961+1220C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312078 | |||||||
| chr4:174312113 | G | T | 1 | a0002c0002t0004g0088 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.961+1255G>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312113 | |||||||
| chr4:174312244 | T | A | 1 | a0002c0002t0006g0101 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.961+1386T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312244 | |||||||
| chr4:174312268 | T | G | 6 | a0002c0002t0009g0027 a0002c0002t0009g0092 a0002c0002t0009g0097 others(3): Show |
8 | HG00741.hp1 HG01516.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.961+1410T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312268 | |||||||
| chr4:174312281 | T | A | 1 | a0001c0001t0001g0093 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.961+1423T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312281 | |||||||
| chr4:174312413 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.961+1555C>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312413 | |||||||
| chr4:174312636 | A | G | 6 | a0002c0002t0006g0061 a0002c0002t0006g0099 a0002c0002t0006g0100 others(3): Show |
6 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.961+1778A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312636 | |||||||
| chr4:174312692 | G | A | 1 | a0002c0002t0017g0021 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.961+1834G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312692 | |||||||
| chr4:174312718 | A | G | 1 | a0002c0002t0003g0183 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.961+1860A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312718 | |||||||
| chr4:174312764 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.961+1906C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312764 | |||||||
| chr4:174312771 | C | A | 1 | a0001c0001t0001g0093 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.961+1913C>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312771 | |||||||
| chr4:174312792 | A | T | 1 | a0001c0003t0002g0219 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.961+1934A>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312792 | |||||||
| chr4:174312855 | T | C | 38 | a0002c0002t0004g0014 a0002c0002t0004g0024 a0002c0002t0004g0025 others(35): Show |
44 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.961+1997T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312855 | |||||||
| chr4:174312926 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.961+2068G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312926 | |||||||
| chr4:174312979 | G | A | 123 | a0001c0001t0005g0268 a0001c0003t0002g0012 a0001c0003t0002g0019 others(120): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.961+2121G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312979 | |||||||
| chr4:174312992 | T | C | 3 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0148 |
3 | NA18974.hp2 NA18980.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.961+2134T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174312992 | |||||||
| chr4:174313030 | C | T | 1 | a0002c0002t0006g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.961+2172C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174313030 | |||||||
| chr4:174313099 | T | A | 1 | a0002c0002t0005g0201 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.961+2241T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174313099 | |||||||
| chr4:174313161 | TG | T | 13 | a0001c0003t0002g0012 a0001c0003t0002g0019 a0001c0003t0002g0241 others(10): Show |
18 | HG01123.hp2 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.961+2304delG | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174313161 | |||||||
| chr4:174313163 | T | A | 13 | a0001c0003t0002g0012 a0001c0003t0002g0019 a0001c0003t0002g0241 others(10): Show |
18 | HG01123.hp2 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.961+2305T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174313163 | |||||||
| chr4:174313177 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.961+2319G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174313177 | |||||||
| chr4:174313278 | C | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(87): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.961+2420C>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174313278 | |||||||
| chr4:174313295 | A | G | 39 | a0001c0003t0002g0261 a0002c0002t0004g0014 a0002c0002t0004g0024 others(36): Show |
45 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.961+2437A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174313295 | |||||||
| chr4:174313377 | A | C | 2 | a0002c0002t0005g0160 a0002c0002t0005g0161 |
2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.961+2519A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174313377 | |||||||
| chr4:174313381 | G | GA | 40 | a0001c0003t0002g0212 a0002c0002t0003g0174 a0002c0002t0004g0014 others(37): Show |
47 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.961+2537dupA | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 174313381 | ||||||
| chr4:174313381 | GA | G | 6 | a0001c0001t0005g0268 a0002c0002t0005g0017 a0002c0002t0006g0099 others(3): Show |
8 | HG00738.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.961+2537delA | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 174313381 | ||||||
| chr4:174313395 | AG | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(86): Show |
127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.961+2539delG | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 174313395 | ||||||
| chr4:174313396 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0054 |
2 | NA18991.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.961+2538G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174313396 | |||||||
| chr4:174313539 | A | G | 1 | a0001c0003t0002g0218 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.962-2627A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174313539 | |||||||
| chr4:174313611 | A | T | 1 | a0002c0002t0005g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.962-2555A>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174313611 | |||||||
| chr4:174314006 | C | A | 1 | a0002c0002t0006g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.962-2160C>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174314006 | |||||||
| chr4:174314097 | G | A | 1 | a0001c0003t0002g0269 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.962-2069G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174314097 | |||||||
| chr4:174314216 | T | A | 2 | a0002c0002t0003g0182 a0002c0002t0003g0187 |
2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.962-1950T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174314216 | |||||||
| chr4:174314520 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.962-1646A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174314520 | |||||||
| chr4:174314639 | G | C | 5 | a0002c0002t0009g0027 a0002c0002t0009g0092 a0002c0002t0009g0097 others(2): Show |
6 | HG00741.hp1 HG01516.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.962-1527G>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174314639 | |||||||
| chr4:174314639 | G | GC | 6 | a0001c0003t0002g0230 a0001c0003t0002g0231 a0001c0003t0002g0232 others(3): Show |
6 | HG02717.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.962-1522dupC | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 174314639 | ||||||
| chr4:174314788 | C | T | 1 | a0002c0002t0022g0172 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.962-1378C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174314788 | |||||||
| chr4:174314952 | A | C | 3 | a0002c0002t0004g0073 a0002c0002t0004g0083 a0002c0002t0004g0090 |
3 | HG01884.hp1 HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.962-1214A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174314952 | |||||||
| chr4:174315032 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.962-1134A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315032 | |||||||
| chr4:174315112 | A | G | 111 | a0001c0001t0005g0268 a0002c0002t0003g0004 a0002c0002t0003g0018 others(108): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.962-1054A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315112 | |||||||
| chr4:174315165 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0106 a0001c0001t0001g0128 others(1): Show |
6 | HG03927.hp1 NA18990.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.962-1001A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315165 | |||||||
| chr4:174315215 | A | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(198): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.962-951A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315215 | |||||||
| chr4:174315227 | G | A | 30 | a0002c0002t0004g0014 a0002c0002t0004g0024 a0002c0002t0004g0025 others(27): Show |
35 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.962-939G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315227 | |||||||
| chr4:174315232 | A | AT | 10 | a0001c0003t0002g0247 a0001c0003t0007g0256 a0001c0003t0029g0222 others(7): Show |
10 | HG01978.hp1 HG02129.hp2 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.962-919dupT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 174315232 | ||||||
| chr4:174315232 | AT | A | 46 | a0001c0001t0001g0123 a0001c0003t0002g0230 a0001c0003t0002g0231 others(43): Show |
53 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.962-919delT | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 174315232 | ||||||
| chr4:174315249 | C | T | 40 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(37): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.962-917C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315249 | |||||||
| chr4:174315267 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.962-899A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315267 | |||||||
| chr4:174315655 | T | A | 3 | a0002c0002t0010g0020 a0002c0002t0010g0043 a0004c0010t0010g0044 |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.962-511T>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315655 | |||||||
| chr4:174315698 | G | A | 62 | a0001c0001t0005g0268 a0002c0002t0003g0004 a0002c0002t0003g0018 others(59): Show |
77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.962-468G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315698 | |||||||
| chr4:174315704 | G | A | 1 | a0005c0007t0028g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.962-462G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315704 | |||||||
| chr4:174315707 | A | G | 1 | a0005c0007t0028g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.962-459A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315707 | |||||||
| chr4:174315710 | T | G | 1 | a0005c0007t0028g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.962-456T>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315710 | |||||||
| chr4:174315802 | C | T | 1 | a0007c0006t0012g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.962-364C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315802 | |||||||
| chr4:174315811 | T | C | 1 | a0002c0002t0005g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.962-355T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174315811 | |||||||
| chr4:174315840 | CA | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(169): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.962-307delA | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 174315840 | ||||||
| chr4:174315840 | CAA | C | 11 | a0001c0001t0001g0093 a0001c0003t0002g0276 a0001c0003t0011g0245 others(8): Show |
13 | HG00323.hp1 HG00741.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.962-308_962-307del others(2): Show |
CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 174315840 | ||||||
| chr4:174316050 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.962-116C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174316050 | |||||||
| chr4:174316057 | C | A | 30 | a0002c0002t0003g0004 a0002c0002t0003g0018 a0002c0002t0003g0036 others(27): Show |
38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.962-109C>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174316057 | |||||||
| chr4:174316129 | A | G | 1 | a0001c0003t0002g0224 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.962-37A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 9/11 | chr4 | 174316129 | |||||||
| chr4:174316385 | C | T | 39 | a0002c0002t0004g0014 a0002c0002t0004g0024 a0002c0002t0004g0025 others(36): Show |
44 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1086+95C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 10/11 | chr4 | 174316385 | |||||||
| chr4:174316418 | G | A | 1 | a0002c0002t0017g0021 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1087-112G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 10/11 | chr4 | 174316418 | |||||||
| chr4:174316460 | A | C | 1 | a0005c0007t0028g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1087-70A>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 10/11 | chr4 | 174316460 | |||||||
| chr4:174316725 | A | T | 2 | a0001c0003t0002g0259 a0001c0003t0002g0269 |
2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1124+158A>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 11/11 | chr4 | 174316725 | |||||||
| chr4:174316727 | A | G | 1 | a0002c0002t0012g0095 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1124+160A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 11/11 | chr4 | 174316727 | |||||||
| chr4:174316817 | G | A | 2 | a0001c0003t0002g0042 a0001c0003t0002g0271 |
3 | HG00639.hp2 HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1124+250G>A | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 11/11 | chr4 | 174316817 | |||||||
| chr4:174317089 | T | C | 1 | a0002c0002t0006g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1125-246T>C | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 11/11 | chr4 | 174317089 | |||||||
| chr4:174317122 | A | G | 1 | a0002c0002t0005g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1125-213A>G | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 11/11 | chr4 | 174317122 | |||||||
| chr4:174317159 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(198): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1125-176C>T | CEP44 | ENSG00000164118.13 | transcript | ENST00000503780.6 | protein_coding | 11/11 | chr4 | 174317159 |