Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9685 |
| ensemblid | ENSG00000113282.14 |
| hgncid | 23186 |
| symbol | CLINT1 |
| name | clathrin interactor 1 |
| refseq_nuc | NM_014666.4 |
| refseq_prot | NP_055481.1 |
| ensembl_nuc | ENST00000411809.7 |
| ensembl_prot | ENSP00000388340.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 157785747 |
| end | 157859145 |
| strand | - |
| ver | v1.2 |
| region | chr5:157785747-157859145 |
| region5000 | chr5:157780747-157864145 |
| regionname0 | CLINT1_chr5_157785747_157859145 |
| regionname5000 | CLINT1_chr5_157780747_157864145 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 625 | 337 | 90 | 59 | 141 | 16 | 29 | 107 | CLINT1_chr5_157780747_157864145 | CLINT1 | MLNMW others(620): Show |
chr5 | 157780747 | 157864145 |
| a0002 | 0/0 | 625 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | MLNMW others(620): Show |
chr5 | 157780747 | 157864145 |
| a0003 | 0/0 | 625 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | MLNMW others(620): Show |
chr5 | 157780747 | 157864145 |
| a0004 | 0/0 | 625 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | MLNMW others(620): Show |
chr5 | 157780747 | 157864145 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1875 | 321 | 74 | 59 | 141 | 16 | 29 | CLINT1_chr5_157780747_157864145 | CLINT1 | ATGTT others(1870): Show |
chr5 | 157780747 | 157864145 | ||
| a0001c0002 | 0/0 | 1875 | 13 | 13 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | ATGTT others(1870): Show |
chr5 | 157780747 | 157864145 | ||
| a0001c0004 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | ATGTT others(1870): Show |
chr5 | 157780747 | 157864145 | ||
| a0001c0006 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | ATGTT others(1870): Show |
chr5 | 157780747 | 157864145 | ||
| a0001c0008 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | ATGTT others(1870): Show |
chr5 | 157780747 | 157864145 | ||
| a0002c0005 | 0/0 | 1875 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | ATGTT others(1870): Show |
chr5 | 157780747 | 157864145 | ||
| a0003c0003 | 0/0 | 1875 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | ATGTT others(1870): Show |
chr5 | 157780747 | 157864145 | ||
| a0004c0007 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | ATGTT others(1870): Show |
chr5 | 157780747 | 157864145 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3952 | 122 | 32 | 32 | 35 | 7 | 14 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0001t0002 | 0/0 | 3952 | 104 | 9 | 19 | 60 | 7 | 9 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0001t0003 | 0/0 | 3952 | 52 | 21 | 2 | 24 | 0 | 5 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0001t0004 | 0/0 | 3952 | 28 | 7 | 5 | 13 | 2 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0001t0005 | 0/0 | 3950 | 6 | 0 | 0 | 6 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3945): Show |
chr5 | 157780747 | 157864145 |
| a0001c0001t0006 | 0/0 | 3952 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0001t0007 | 0/0 | 3952 | 2 | 2 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0001t0008 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0001t0009 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0001t0010 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0001t0011 | 0/0 | 3952 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0001t0012 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0002t0003 | 0/0 | 3952 | 13 | 13 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0004t0003 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0006t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0001c0008t0002 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0002c0005t0001 | 0/0 | 3952 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0003c0003t0001 | 0/0 | 3952 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| a0004c0007t0003 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | GCGTC others(3947): Show |
chr5 | 157780747 | 157864145 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0171 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0009g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0010g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0011g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0001t0012g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0004t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0006t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0001c0008t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0002c0005t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0003c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| a0004c0007t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | GBR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | GBR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0167 | EUR | GBR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0114 | EUR | FIN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0299 | EUR | FIN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00609 | hp2 | a0001 | c0001 | t0008 | g0263 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0104 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0158 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01192 | hp2 | a0001 | c0001 | t0011 | g0061 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0102 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01433 | hp1 | a0002 | c0005 | t0001 | g0210 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0151 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0178 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0177 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0145 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0101 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CDX | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CDX | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02257 | hp1 | a0001 | c0006 | t0001 | g0325 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0053 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0331 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0056 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0294 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0076 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0054 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0052 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0058 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02922 | hp1 | a0001 | c0004 | t0003 | g0072 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0081 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0057 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0073 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0080 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0330 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03195 | hp2 | a0001 | c0008 | t0002 | g0193 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0099 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0324 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0074 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CHB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | CHB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18975 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18981 | hp1 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | LWK | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | LWK | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19084 | hp2 | a0004 | c0007 | t0003 | g0031 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0055 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0075 | AFR | ASW | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ASW | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | TSI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | TSI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0332 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | USA | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | USA | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | USA | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | USA | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0328 | AFR | LWK | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0220 | REF | REF | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0171 | REF | REF | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:157787812 | A | G | 1 | a0002 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.1712T>C | p.Met571Thr | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1887/3952 | 1712/1878 | 571/625 | chr5 | 157787812 | |||
| chr5:157791783 | T | C | 1 | a0004 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.1300A>G | p.Met434Val | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/12 | 1475/3952 | 1300/1878 | 434/625 | chr5 | 157791783 | |||
| chr5:157791912 | C | T | 1 | a0003 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1171G>A | p.Glu391Lys | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/12 | 1346/3952 | 1171/1878 | 391/625 | chr5 | 157791912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:157787664 | G | A | 1 | a0001c0006 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1860C>T | p.Phe620Phe | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 2035/3952 | 1860/1878 | 620/625 | chr5 | 157787664 | |||
| chr5:157789370 | C | T | 1 | a0001c0004 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.1524G>A | p.Gln508Gln | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/12 | 1699/3952 | 1524/1878 | 508/625 | chr5 | 157789370 | |||
| chr5:157809711 | C | G | 1 | a0001c0002 | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
synonymous_variant | LOW | c.612G>C | p.Leu204Leu | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/12 | 787/3952 | 612/1878 | 204/625 | chr5 | 157809711 | |||
| chr5:157816791 | G | A | 1 | a0001c0008 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.186C>T | p.Asn62Asn | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/12 | 361/3952 | 186/1878 | 62/625 | chr5 | 157816791 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:157785918 | G | A | 1 | a0001c0001t0011 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1728C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1728 | chr5 | 157785918 | ||||||
| chr5:157786168 | T | C | 1 | a0001c0001t0010 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1478A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1478 | chr5 | 157786168 | ||||||
| chr5:157786366 | A | T | 1 | a0001c0001t0010 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1280T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1280 | chr5 | 157786366 | ||||||
| chr5:157786380 | CAT | C | 1 | a0001c0001t0005 | 6 | NA18962.hp2 NA18981.hp1 NA18998.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1264_*1265delAT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1264 | chr5 | 157786380 | ||||||
| chr5:157786489 | A | G | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(2): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1157T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1157 | chr5 | 157786489 | ||||||
| chr5:157787179 | A | G | 2 | a0001c0001t0004 a0001c0001t0005 |
34 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*467T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 467 | chr5 | 157787179 | ||||||
| chr5:157787237 | C | T | 1 | a0001c0001t0009 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 409 | chr5 | 157787237 | ||||||
| chr5:157787345 | C | G | 1 | a0001c0001t0008 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 301 | chr5 | 157787345 | ||||||
| chr5:157787426 | T | C | 5 | a0001c0001t0003 a0001c0001t0011 a0001c0002t0003 others(2): Show |
68 | HG00597.hp1 HG01109.hp2 HG01192.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*220A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 220 | chr5 | 157787426 | ||||||
| chr5:157787460 | T | C | 1 | a0001c0001t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 186 | chr5 | 157787460 | ||||||
| chr5:157859012 | C | T | 1 | a0001c0001t0006 | 2 | NA18966.hp1 NA18975.hp2 |
5_prime_UTR_variant | MODIFIER | c.-42G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/12 | 42 | chr5 | 157859012 | ||||||
| chr5:157859096 | G | C | 1 | a0001c0001t0007 | 2 | HG02109.hp2 HG02572.hp2 |
5_prime_UTR_variant | MODIFIER | c.-126C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/12 | 126 | chr5 | 157859096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:157788001 | C | T | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1532-9G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788001 | |||||||
| chr5:157788019 | C | T | 67 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(64): Show |
68 | HG00597.hp1 HG01109.hp2 HG01192.hp2 others(65): Show |
intron_variant | MODIFIER | c.1532-27G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788019 | |||||||
| chr5:157788342 | T | C | 1 | a0001c0001t0003g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1532-350A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788342 | |||||||
| chr5:157788405 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1532-413T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788405 | |||||||
| chr5:157788520 | T | A | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1532-528A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788520 | |||||||
| chr5:157788705 | C | T | 72 | a0001c0001t0001g0234 a0001c0001t0001g0257 a0001c0001t0001g0258 others(69): Show |
73 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.1531+658G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788705 | |||||||
| chr5:157788706 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1531+657C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788706 | |||||||
| chr5:157788817 | A | C | 7 | a0001c0001t0001g0079 a0001c0001t0001g0272 a0001c0001t0001g0287 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1531+546T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788817 | |||||||
| chr5:157788913 | G | A | 3 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0094 |
3 | HG01109.hp2 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1531+450C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788913 | |||||||
| chr5:157788968 | GA | G | 128 | a0001c0001t0001g0270 a0001c0001t0001g0276 a0001c0001t0001g0278 others(125): Show |
131 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1531+394delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788968 | |||||||
| chr5:157788968 | GAAAAAAA others(2): Show |
G | 48 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(45): Show |
49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.1531+386_1531+394d others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788968 | |||||||
| chr5:157788968 | GAAAAAAA others(3): Show |
G | 20 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0047 others(17): Show |
20 | HG01109.hp2 HG02451.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.1531+385_1531+394d others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788968 | |||||||
| chr5:157789169 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1531+194A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157789169 | |||||||
| chr5:157789181 | T | C | 47 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(44): Show |
48 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.1531+182A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157789181 | |||||||
| chr5:157789323 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1531+40C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157789323 | |||||||
| chr5:157789360 | T | C | 1 | a0001c0001t0002g0180 | 1 | NA18612.hp2 | splice_region_variant&intron_variant | LOW | c.1531+3A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157789360 | |||||||
| chr5:157789927 | G | A | 67 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(64): Show |
68 | HG00597.hp1 HG01109.hp2 HG01192.hp2 others(65): Show |
intron_variant | MODIFIER | c.1381-414C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157789927 | |||||||
| chr5:157790031 | T | G | 13 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0054 others(10): Show |
13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1381-518A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790031 | |||||||
| chr5:157790188 | G | C | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1381-675C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790188 | |||||||
| chr5:157790543 | C | A | 1 | a0001c0001t0001g0231 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1381-1030G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790543 | |||||||
| chr5:157790546 | A | C | 1 | a0001c0001t0002g0114 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1381-1033T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790546 | |||||||
| chr5:157790861 | G | A | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1380+842C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790861 | |||||||
| chr5:157790958 | A | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1380+745T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790958 | |||||||
| chr5:157791002 | A | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1380+701T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791002 | |||||||
| chr5:157791032 | G | A | 228 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(225): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1380+671C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791032 | |||||||
| chr5:157791051 | T | G | 48 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(45): Show |
49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.1380+652A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791051 | |||||||
| chr5:157791086 | T | C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1380+617A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791086 | |||||||
| chr5:157791246 | G | T | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1380+457C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791246 | |||||||
| chr5:157791367 | T | C | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1380+336A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791367 | |||||||
| chr5:157791371 | T | G | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1380+332A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791371 | |||||||
| chr5:157791410 | G | T | 83 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(80): Show |
86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1380+293C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791410 | |||||||
| chr5:157791560 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1380+143G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791560 | |||||||
| chr5:157791576 | C | A | 4 | a0001c0001t0002g0085 a0001c0001t0002g0191 a0001c0001t0002g0192 others(1): Show |
4 | HG02970.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380+127G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791576 | |||||||
| chr5:157791582 | CAT | C | 4 | a0001c0001t0002g0085 a0001c0001t0002g0191 a0001c0001t0002g0192 others(1): Show |
4 | HG02970.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380+119_1380+120d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791582 | |||||||
| chr5:157792093 | C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1088-98G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792093 | |||||||
| chr5:157792243 | T | C | 1 | a0001c0001t0009g0328 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1088-248A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792243 | |||||||
| chr5:157792255 | T | TA | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1088-261dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792255 | |||||||
| chr5:157792289 | T | G | 1 | a0001c0001t0003g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1088-294A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792289 | |||||||
| chr5:157792314 | G | A | 4 | a0001c0001t0001g0269 a0001c0001t0001g0290 a0001c0001t0001g0299 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088-319C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792314 | |||||||
| chr5:157792416 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1088-421G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792416 | |||||||
| chr5:157792472 | C | T | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1088-477G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792472 | |||||||
| chr5:157792473 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1088-478C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792473 | |||||||
| chr5:157792486 | T | G | 13 | a0001c0001t0002g0086 a0001c0001t0002g0194 a0001c0001t0002g0195 others(10): Show |
13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1088-491A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792486 | |||||||
| chr5:157792642 | A | G | 13 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0054 others(10): Show |
13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1088-647T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792642 | |||||||
| chr5:157792738 | T | C | 1 | a0001c0001t0002g0172 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1088-743A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792738 | |||||||
| chr5:157792949 | C | T | 13 | a0001c0001t0002g0086 a0001c0001t0002g0194 a0001c0001t0002g0195 others(10): Show |
13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1088-954G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792949 | |||||||
| chr5:157793082 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1088-1087A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793082 | |||||||
| chr5:157793214 | CT | C | 75 | a0001c0001t0001g0235 a0001c0001t0001g0241 a0001c0001t0001g0242 others(72): Show |
76 | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.1088-1220delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793214 | |||||||
| chr5:157793405 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1088-1410A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793405 | |||||||
| chr5:157793420 | G | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1088-1425C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793420 | |||||||
| chr5:157793492 | C | T | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1087+1406G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793492 | |||||||
| chr5:157793577 | G | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1087+1321C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793577 | |||||||
| chr5:157793620 | A | T | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1087+1278T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793620 | |||||||
| chr5:157793711 | T | C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1087+1187A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793711 | |||||||
| chr5:157793869 | T | G | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1087+1029A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793869 | |||||||
| chr5:157793957 | C | G | 3 | a0001c0001t0002g0111 a0001c0001t0002g0114 a0001c0001t0002g0167 |
3 | HG00140.hp2 HG00323.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1087+941G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793957 | |||||||
| chr5:157793963 | C | T | 3 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG01243.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1087+935G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793963 | |||||||
| chr5:157794095 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1087+803T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157794095 | |||||||
| chr5:157794141 | T | C | 2 | a0001c0001t0003g0208 a0001c0001t0004g0107 |
2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1087+757A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157794141 | |||||||
| chr5:157794354 | G | GT | 13 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0054 others(10): Show |
13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1087+543dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157794354 | |||||||
| chr5:157794481 | A | G | 13 | a0001c0001t0002g0086 a0001c0001t0002g0194 a0001c0001t0002g0195 others(10): Show |
13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1087+417T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157794481 | |||||||
| chr5:157794654 | C | A | 1 | a0001c0001t0002g0204 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1087+244G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157794654 | |||||||
| chr5:157795238 | A | G | 69 | a0001c0001t0001g0288 a0001c0001t0002g0040 a0001c0001t0003g0001 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.1013-266T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795238 | |||||||
| chr5:157795666 | GGGGCAAA others(2): Show |
G | 13 | a0001c0001t0002g0086 a0001c0001t0002g0194 a0001c0001t0002g0195 others(10): Show |
13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-703_1013-695d others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795666 | |||||||
| chr5:157795683 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1013-711A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795683 | |||||||
| chr5:157795765 | T | C | 1 | a0001c0001t0003g0020 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1013-793A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795765 | |||||||
| chr5:157795786 | T | C | 47 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(44): Show |
48 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.1013-814A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795786 | |||||||
| chr5:157795904 | A | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1013-932T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795904 | |||||||
| chr5:157795984 | T | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1013-1012A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795984 | |||||||
| chr5:157796002 | G | C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1013-1030C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796002 | |||||||
| chr5:157796110 | C | T | 2 | a0001c0001t0003g0028 a0001c0001t0003g0029 |
2 | NA18990.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1013-1138G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796110 | |||||||
| chr5:157796171 | A | G | 1 | a0001c0001t0008g0263 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1013-1199T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796171 | |||||||
| chr5:157796225 | G | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1013-1253C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796225 | |||||||
| chr5:157796428 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1013-1456G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796428 | |||||||
| chr5:157796778 | A | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1013-1806T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796778 | |||||||
| chr5:157796795 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1013-1823T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796795 | |||||||
| chr5:157796807 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-1835A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796807 | |||||||
| chr5:157796887 | C | CAT | 9 | a0001c0001t0002g0093 a0001c0001t0002g0127 a0001c0001t0002g0173 others(6): Show |
9 | HG00741.hp2 HG02040.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.1013-1917_1013-191 others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796887 | |||||||
| chr5:157796887 | CAT | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0275 a0001c0001t0001g0303 others(25): Show |
29 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1013-1917_1013-191 others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796887 | |||||||
| chr5:157797006 | G | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1013-2034C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797006 | |||||||
| chr5:157797170 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1013-2198A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797170 | |||||||
| chr5:157797204 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1013-2232G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797204 | |||||||
| chr5:157797361 | A | G | 208 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1013-2389T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797361 | |||||||
| chr5:157797472 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1013-2500C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797472 | |||||||
| chr5:157797544 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1013-2572G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797544 | |||||||
| chr5:157797823 | T | C | 1 | a0001c0001t0002g0123 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1013-2851A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797823 | |||||||
| chr5:157797872 | T | C | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1013-2900A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797872 | |||||||
| chr5:157798095 | G | A | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1013-3123C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798095 | |||||||
| chr5:157798187 | T | C | 138 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(135): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1013-3215A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798187 | |||||||
| chr5:157798204 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3232T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798204 | |||||||
| chr5:157798205 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3233C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798205 | |||||||
| chr5:157798206 | C | A | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3234G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798206 | |||||||
| chr5:157798207 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3235T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798207 | |||||||
| chr5:157798213 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3241G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798213 | |||||||
| chr5:157798214 | C | G | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3242G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798214 | |||||||
| chr5:157798215 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3243T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798215 | |||||||
| chr5:157798221 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3249G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798221 | |||||||
| chr5:157798222 | T | G | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3250A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798222 | |||||||
| chr5:157798223 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3251A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798223 | |||||||
| chr5:157798224 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3252G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798224 | |||||||
| chr5:157798478 | G | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1013-3506C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798478 | |||||||
| chr5:157798803 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1013-3831G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798803 | |||||||
| chr5:157799076 | C | T | 5 | a0001c0001t0003g0019 a0001c0001t0003g0022 a0001c0001t0003g0028 others(2): Show |
5 | NA18945.hp2 NA18951.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-4104G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799076 | |||||||
| chr5:157799221 | C | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(82): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1013-4249G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799221 | |||||||
| chr5:157799405 | G | A | 1 | a0001c0001t0002g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1012+4245C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799405 | |||||||
| chr5:157799417 | C | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(18): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1012+4233G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799417 | |||||||
| chr5:157799418 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1012+4232G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799418 | |||||||
| chr5:157799463 | T | C | 5 | a0001c0001t0004g0099 a0001c0001t0004g0102 a0001c0001t0004g0104 others(2): Show |
5 | HG01099.hp1 HG01358.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1012+4187A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799463 | |||||||
| chr5:157799573 | T | C | 4 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0057 others(1): Show |
4 | HG02886.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+4077A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799573 | |||||||
| chr5:157799605 | T | C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1012+4045A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799605 | |||||||
| chr5:157799968 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1012+3682A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799968 | |||||||
| chr5:157800009 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+3641A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800009 | |||||||
| chr5:157800323 | T | G | 33 | a0001c0001t0004g0004 a0001c0001t0004g0082 a0001c0001t0004g0084 others(30): Show |
34 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1012+3327A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800323 | |||||||
| chr5:157800368 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0261 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1012+3282G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800368 | |||||||
| chr5:157800461 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+3189G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800461 | |||||||
| chr5:157800715 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1012+2935A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800715 | |||||||
| chr5:157800771 | T | C | 48 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(45): Show |
49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.1012+2879A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800771 | |||||||
| chr5:157801165 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1012+2485C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801165 | |||||||
| chr5:157801224 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+2426A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801224 | |||||||
| chr5:157801271 | C | T | 13 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0054 others(10): Show |
13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1012+2379G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801271 | |||||||
| chr5:157801330 | A | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+2320T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801330 | |||||||
| chr5:157801504 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1012+2146G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801504 | |||||||
| chr5:157801591 | G | T | 1 | a0001c0001t0002g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1012+2059C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801591 | |||||||
| chr5:157801894 | T | A | 2 | a0001c0001t0003g0066 a0001c0001t0003g0077 |
2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1012+1756A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801894 | |||||||
| chr5:157801898 | GT | G | 69 | a0001c0001t0001g0232 a0001c0001t0001g0253 a0001c0001t0002g0040 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.1012+1751delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801898 | |||||||
| chr5:157801936 | T | C | 208 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1012+1714A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801936 | |||||||
| chr5:157801983 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1012+1667G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801983 | |||||||
| chr5:157801997 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+1653G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801997 | |||||||
| chr5:157802086 | G | T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1012+1564C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802086 | |||||||
| chr5:157802542 | CT | C | 68 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+1107delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802542 | |||||||
| chr5:157802544 | T | C | 1 | a0001c0001t0002g0108 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1012+1106A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802544 | |||||||
| chr5:157802631 | C | T | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1012+1019G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802631 | |||||||
| chr5:157802638 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1012+1012G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802638 | |||||||
| chr5:157802653 | C | A | 1 | a0001c0001t0004g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1012+997G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802653 | |||||||
| chr5:157802979 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1012+671G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802979 | |||||||
| chr5:157803185 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+465G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157803185 | |||||||
| chr5:157803486 | A | C | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1012+164T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157803486 | |||||||
| chr5:157803524 | C | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+126G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157803524 | |||||||
| chr5:157803636 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1012+14T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157803636 | |||||||
| chr5:157803826 | T | G | 1 | a0001c0001t0002g0314 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.943-107A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157803826 | |||||||
| chr5:157804037 | T | TA | 6 | a0001c0001t0001g0250 a0001c0001t0001g0255 a0001c0001t0001g0261 others(3): Show |
6 | HG01981.hp2 HG02738.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-319dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804037 | |||||||
| chr5:157804037 | TA | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0079 others(8): Show |
11 | HG02004.hp1 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.943-319delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804037 | |||||||
| chr5:157804037 | TAA | T | 124 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(121): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.943-320_943-319del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804037 | |||||||
| chr5:157804037 | TAAAAAAA others(2): Show |
T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.943-327_943-319del others(9): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804037 | |||||||
| chr5:157804104 | T | C | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.943-385A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804104 | |||||||
| chr5:157804322 | C | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.943-603G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804322 | |||||||
| chr5:157804454 | T | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0308 others(9): Show |
13 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.943-735A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804454 | |||||||
| chr5:157804782 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.943-1063G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804782 | |||||||
| chr5:157804806 | A | T | 1 | a0001c0001t0004g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.942+1060T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804806 | |||||||
| chr5:157804868 | G | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.942+998C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804868 | |||||||
| chr5:157804921 | C | A | 5 | a0001c0001t0001g0275 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.942+945G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804921 | |||||||
| chr5:157804931 | A | AAAAAAG | 134 | a0001c0001t0001g0255 a0001c0001t0002g0002 a0001c0001t0002g0003 others(131): Show |
138 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.942+929_942+934dup others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804931 | |||||||
| chr5:157804931 | AAAAAAG | A | 4 | a0001c0001t0002g0085 a0001c0001t0002g0191 a0001c0001t0002g0192 others(1): Show |
4 | HG02970.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.942+929_942+934del others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804931 | |||||||
| chr5:157805296 | T | A | 1 | a0001c0001t0001g0265 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.942+570A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157805296 | |||||||
| chr5:157805634 | A | G | 208 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.942+232T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157805634 | |||||||
| chr5:157805671 | C | G | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.942+195G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157805671 | |||||||
| chr5:157805713 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.942+153A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157805713 | |||||||
| chr5:157805756 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.942+110G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157805756 | |||||||
| chr5:157806149 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.696-37C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806149 | |||||||
| chr5:157806281 | A | G | 281 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(278): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.696-169T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806281 | |||||||
| chr5:157806298 | G | C | 1 | a0001c0001t0001g0326 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.696-186C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806298 | |||||||
| chr5:157806365 | T | C | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.696-253A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806365 | |||||||
| chr5:157806398 | T | TTTTG | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-287_696-286ins others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806398 | |||||||
| chr5:157806493 | GA | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-382delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806493 | |||||||
| chr5:157806513 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-401G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806513 | |||||||
| chr5:157806530 | T | C | 3 | a0001c0001t0001g0309 a0001c0001t0001g0316 a0001c0001t0001g0319 |
3 | HG01123.hp2 HG01168.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.696-418A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806530 | |||||||
| chr5:157806850 | G | T | 7 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0056 others(4): Show |
7 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.696-738C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806850 | |||||||
| chr5:157806963 | G | A | 13 | a0001c0001t0002g0086 a0001c0001t0002g0194 a0001c0001t0002g0195 others(10): Show |
13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.696-851C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806963 | |||||||
| chr5:157806963 | GGA | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.696-853_696-852del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806963 | |||||||
| chr5:157806963 | GGAGA | G | 4 | a0001c0001t0002g0093 a0001c0001t0002g0174 a0001c0001t0004g0104 others(1): Show |
4 | HG01099.hp1 HG02040.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-855_696-852del others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806963 | |||||||
| chr5:157806963 | GGAGAGA | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-857_696-852del others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806963 | |||||||
| chr5:157807088 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.696-976T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807088 | |||||||
| chr5:157807114 | A | AACTATGA others(2): Show |
233 | a0001c0001t0001g0008 a0001c0001t0001g0275 a0001c0001t0001g0303 others(230): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.696-1003_696-1002i others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807114 | |||||||
| chr5:157807237 | A | C | 51 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(48): Show |
52 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.696-1125T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807237 | |||||||
| chr5:157807411 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.696-1299A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807411 | |||||||
| chr5:157807415 | C | G | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.696-1303G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807415 | |||||||
| chr5:157807469 | G | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.696-1357C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807469 | |||||||
| chr5:157807498 | T | C | 4 | a0001c0001t0002g0085 a0001c0001t0002g0191 a0001c0001t0002g0192 others(1): Show |
4 | HG02970.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1386A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807498 | |||||||
| chr5:157807500 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG00280.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.696-1388C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807500 | |||||||
| chr5:157807507 | A | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-1395T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807507 | |||||||
| chr5:157807716 | G | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-1604C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807716 | |||||||
| chr5:157807742 | G | A | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.696-1630C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807742 | |||||||
| chr5:157807863 | G | A | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.696-1751C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807863 | |||||||
| chr5:157807879 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.695+1749T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807879 | |||||||
| chr5:157807931 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG00280.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.695+1697C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807931 | |||||||
| chr5:157808050 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.695+1578A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157808050 | |||||||
| chr5:157808105 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.695+1523T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157808105 | |||||||
| chr5:157808108 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.695+1520G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157808108 | |||||||
| chr5:157808364 | C | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(82): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.695+1264G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157808364 | |||||||
| chr5:157808520 | G | C | 1 | a0001c0001t0001g0266 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.695+1108C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157808520 | |||||||
| chr5:157809116 | T | C | 69 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.695+512A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809116 | |||||||
| chr5:157809181 | A | T | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.695+447T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809181 | |||||||
| chr5:157809214 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.695+414T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809214 | |||||||
| chr5:157809228 | G | A | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.695+400C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809228 | |||||||
| chr5:157809497 | T | TA | 123 | a0001c0001t0001g0276 a0001c0001t0002g0002 a0001c0001t0002g0003 others(120): Show |
127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.695+130dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809497 | |||||||
| chr5:157809497 | TA | T | 70 | a0001c0001t0001g0221 a0001c0001t0002g0040 a0001c0001t0003g0001 others(67): Show |
71 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.695+130delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809497 | |||||||
| chr5:157809498 | A | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0228 a0001c0001t0001g0229 |
4 | NA18941.hp1 NA19062.hp2 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.695+130T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809498 | |||||||
| chr5:157809574 | G | A | 7 | a0001c0001t0001g0270 a0001c0001t0001g0276 a0001c0001t0001g0278 others(4): Show |
7 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.695+54C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809574 | |||||||
| chr5:157809605 | C | T | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.695+23G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809605 | |||||||
| chr5:157809841 | G | A | 3 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0094 |
3 | HG01109.hp2 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.518-36C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157809841 | |||||||
| chr5:157810253 | A | G | 13 | a0001c0001t0002g0083 a0001c0001t0002g0090 a0001c0001t0002g0092 others(10): Show |
13 | HG01952.hp1 HG02074.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.518-448T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810253 | |||||||
| chr5:157810427 | T | C | 233 | a0001c0001t0001g0008 a0001c0001t0001g0275 a0001c0001t0001g0303 others(230): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.518-622A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810427 | |||||||
| chr5:157810446 | G | C | 1 | a0001c0001t0002g0016 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.518-641C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810446 | |||||||
| chr5:157810450 | A | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.518-645T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810450 | |||||||
| chr5:157810515 | G | A | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.518-710C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810515 | |||||||
| chr5:157810633 | T | C | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.518-828A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810633 | |||||||
| chr5:157810633 | T | G | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.518-828A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810633 | |||||||
| chr5:157810865 | T | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(18): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.518-1060A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810865 | |||||||
| chr5:157810878 | T | C | 2 | a0001c0001t0002g0131 a0001c0001t0010g0330 |
2 | HG03130.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.518-1073A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810878 | |||||||
| chr5:157810879 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.518-1074A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810879 | |||||||
| chr5:157811049 | A | T | 12 | a0001c0001t0002g0003 a0001c0001t0002g0110 a0001c0001t0002g0117 others(9): Show |
13 | HG00597.hp2 HG02027.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.518-1244T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811049 | |||||||
| chr5:157811073 | T | C | 4 | a0001c0001t0004g0141 a0001c0001t0004g0143 a0001c0001t0004g0186 others(1): Show |
4 | NA18940.hp2 NA18943.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-1268A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811073 | |||||||
| chr5:157811105 | C | G | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG01070.hp2 HG01169.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-1300G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811105 | |||||||
| chr5:157811105 | C | T | 69 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.518-1300G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811105 | |||||||
| chr5:157811264 | G | A | 1 | a0001c0001t0004g0185 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.518-1459C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811264 | |||||||
| chr5:157811388 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.518-1583G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811388 | |||||||
| chr5:157811529 | CA | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0299 a0001c0001t0001g0306 others(32): Show |
36 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.517+1533delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811529 | |||||||
| chr5:157811529 | CAA | C | 54 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(51): Show |
55 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.517+1532_517+1533d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811529 | |||||||
| chr5:157811749 | A | G | 1 | a0001c0001t0003g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.517+1314T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811749 | |||||||
| chr5:157811921 | C | T | 2 | a0001c0001t0002g0191 a0001c0008t0002g0193 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.517+1142G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811921 | |||||||
| chr5:157811934 | T | C | 13 | a0001c0001t0002g0086 a0001c0001t0002g0194 a0001c0001t0002g0195 others(10): Show |
13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.517+1129A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811934 | |||||||
| chr5:157811973 | A | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.517+1090T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811973 | |||||||
| chr5:157812023 | T | TAAAAAAA | 63 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(60): Show |
64 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.517+1033_517+1039d others(9): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812023 | |||||||
| chr5:157812112 | G | C | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.517+951C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812112 | |||||||
| chr5:157812149 | A | AAGCAG | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.517+909_517+913dup others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812149 | |||||||
| chr5:157812258 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517+805C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812258 | |||||||
| chr5:157812288 | T | A | 5 | a0001c0002t0003g0053 a0001c0002t0003g0056 a0001c0002t0003g0073 others(2): Show |
5 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+775A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812288 | |||||||
| chr5:157812289 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG01496.hp1 HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.517+774C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812289 | |||||||
| chr5:157812400 | C | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.517+663G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812400 | |||||||
| chr5:157812593 | T | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0248 |
3 | HG00438.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.517+470A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812593 | |||||||
| chr5:157812663 | G | C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.517+400C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812663 | |||||||
| chr5:157812777 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.517+286A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812777 | |||||||
| chr5:157813472 | G | T | 1 | a0001c0001t0002g0182 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.353-245C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813472 | |||||||
| chr5:157813478 | T | G | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.353-251A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813478 | |||||||
| chr5:157813534 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.353-307A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813534 | |||||||
| chr5:157813657 | C | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.353-430G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813657 | |||||||
| chr5:157813663 | G | T | 1 | a0001c0001t0002g0120 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.353-436C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813663 | |||||||
| chr5:157813745 | T | C | 1 | a0001c0001t0007g0331 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.352+440A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813745 | |||||||
| chr5:157813772 | A | G | 1 | a0001c0001t0002g0091 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.352+413T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813772 | |||||||
| chr5:157814143 | A | G | 2 | a0001c0001t0003g0208 a0001c0004t0003g0072 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.352+42T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157814143 | |||||||
| chr5:157814297 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
splice_region_variant&intron_variant | LOW | c.244-4G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814297 | |||||||
| chr5:157814359 | TA | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.244-67delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814359 | |||||||
| chr5:157814513 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.244-220A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814513 | |||||||
| chr5:157814571 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.244-278G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814571 | |||||||
| chr5:157814681 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.244-388A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814681 | |||||||
| chr5:157814777 | C | G | 1 | a0001c0001t0002g0183 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.244-484G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814777 | |||||||
| chr5:157814804 | G | A | 136 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(133): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.244-511C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814804 | |||||||
| chr5:157814988 | G | A | 1 | a0001c0001t0002g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.244-695C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814988 | |||||||
| chr5:157815030 | CA | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0223 a0001c0001t0001g0244 others(4): Show |
8 | HG00280.hp1 HG00323.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.244-738delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815030 | |||||||
| chr5:157815078 | A | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.244-785T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815078 | |||||||
| chr5:157815104 | T | C | 5 | a0001c0001t0001g0275 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-811A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815104 | |||||||
| chr5:157815120 | T | TAC | 38 | a0001c0001t0001g0222 a0001c0001t0001g0232 a0001c0001t0001g0253 others(35): Show |
38 | HG01070.hp2 HG01081.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.244-829_244-828dup others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | |||||||
| chr5:157815120 | T | TACAC | 4 | a0001c0001t0002g0085 a0001c0001t0002g0192 a0001c0002t0003g0054 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-831_244-828dup others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | |||||||
| chr5:157815120 | T | TACACAC | 29 | a0001c0001t0002g0090 a0001c0001t0002g0109 a0001c0001t0002g0116 others(26): Show |
30 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.244-833_244-828dup others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | |||||||
| chr5:157815120 | T | TACACACA others(1): Show |
6 | a0001c0001t0005g0098 a0001c0001t0005g0100 a0001c0001t0005g0103 others(3): Show |
6 | NA18962.hp2 NA18981.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-835_244-828dup others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | |||||||
| chr5:157815120 | T | TACACACA others(3): Show |
1 | a0001c0001t0004g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.244-837_244-828dup others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | |||||||
| chr5:157815120 | T | TACACACA others(5): Show |
1 | a0001c0001t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.244-839_244-828dup others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | |||||||
| chr5:157815120 | T | TACACACA others(7): Show |
1 | a0001c0001t0004g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244-841_244-828dup others(14): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | |||||||
| chr5:157815120 | TAC | T | 13 | a0001c0001t0001g0275 a0001c0001t0001g0303 a0001c0001t0001g0304 others(10): Show |
13 | HG01243.hp1 HG01243.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.244-829_244-828del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | |||||||
| chr5:157815168 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.244-875G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815168 | |||||||
| chr5:157815262 | T | G | 1 | a0001c0001t0003g0046 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.244-969A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815262 | |||||||
| chr5:157815297 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.244-1004A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815297 | |||||||
| chr5:157815345 | T | C | 3 | a0001c0001t0002g0135 a0001c0001t0002g0180 a0001c0001t0002g0181 |
3 | NA18612.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.244-1052A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815345 | |||||||
| chr5:157815379 | G | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.244-1086C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815379 | |||||||
| chr5:157815414 | G | GA | 136 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(133): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.244-1122dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815414 | |||||||
| chr5:157815457 | A | G | 208 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.244-1164T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815457 | |||||||
| chr5:157815463 | T | C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.244-1170A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815463 | |||||||
| chr5:157815904 | A | C | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.243+830T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815904 | |||||||
| chr5:157815911 | A | T | 273 | a0001c0001t0001g0008 a0001c0001t0001g0079 a0001c0001t0001g0266 others(270): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.243+823T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815911 | |||||||
| chr5:157815980 | T | C | 208 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.243+754A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815980 | |||||||
| chr5:157816455 | C | G | 3 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0001c0001t0001g0243 |
3 | HG01981.hp1 HG02004.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.243+279G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157816455 | |||||||
| chr5:157817007 | C | T | 1 | a0001c0001t0002g0126 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.147-177G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 2/11 | chr5 | 157817007 | |||||||
| chr5:157817094 | T | C | 13 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0054 others(10): Show |
13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.147-264A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 2/11 | chr5 | 157817094 | |||||||
| chr5:157817132 | T | C | 1 | a0001c0001t0003g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147-302A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 2/11 | chr5 | 157817132 | |||||||
| chr5:157817341 | T | C | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG01070.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.146+102A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 2/11 | chr5 | 157817341 | |||||||
| chr5:157817398 | A | T | 1 | a0001c0001t0003g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.146+45T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 2/11 | chr5 | 157817398 | |||||||
| chr5:157817587 | T | G | 1 | a0001c0001t0003g0043 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.42-40A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157817587 | |||||||
| chr5:157817592 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.42-45A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157817592 | |||||||
| chr5:157817613 | A | G | 13 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0054 others(10): Show |
13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-66T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157817613 | |||||||
| chr5:157817622 | A | G | 13 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0054 others(10): Show |
13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-75T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157817622 | |||||||
| chr5:157817747 | T | C | 1 | a0001c0001t0003g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.42-200A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157817747 | |||||||
| chr5:157818161 | G | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-614C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818161 | |||||||
| chr5:157818169 | G | C | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-622C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818169 | |||||||
| chr5:157818203 | A | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.42-656T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818203 | |||||||
| chr5:157818465 | T | C | 7 | a0001c0001t0001g0270 a0001c0001t0001g0276 a0001c0001t0001g0278 others(4): Show |
7 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-918A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818465 | |||||||
| chr5:157818466 | C | CCAA | 7 | a0001c0001t0001g0270 a0001c0001t0001g0276 a0001c0001t0001g0278 others(4): Show |
7 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-920_42-919insTT others(1): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818466 | |||||||
| chr5:157818467 | T | A | 7 | a0001c0001t0001g0270 a0001c0001t0001g0276 a0001c0001t0001g0278 others(4): Show |
7 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-920A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818467 | |||||||
| chr5:157818467 | T | TA | 52 | a0001c0001t0001g0079 a0001c0001t0001g0222 a0001c0001t0001g0223 others(49): Show |
52 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.42-921dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818467 | |||||||
| chr5:157818467 | TA | T | 13 | a0001c0001t0001g0221 a0001c0001t0001g0244 a0001c0001t0001g0246 others(10): Show |
13 | HG01070.hp1 HG01192.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-921delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818467 | |||||||
| chr5:157818604 | G | A | 11 | a0001c0001t0004g0004 a0001c0001t0004g0084 a0001c0001t0004g0140 others(8): Show |
12 | NA18940.hp2 NA18942.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.42-1057C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818604 | |||||||
| chr5:157818680 | C | G | 13 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0054 others(10): Show |
13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-1133G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818680 | |||||||
| chr5:157818682 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0231 a0001c0001t0001g0232 others(4): Show |
8 | HG00438.hp1 NA18954.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.42-1135T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818682 | |||||||
| chr5:157818739 | C | T | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-1192G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818739 | |||||||
| chr5:157818769 | C | T | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-1222G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818769 | |||||||
| chr5:157818913 | G | A | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-1366C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818913 | |||||||
| chr5:157819034 | G | A | 1 | a0001c0001t0003g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.42-1487C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819034 | |||||||
| chr5:157819207 | C | G | 122 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(119): Show |
126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.42-1660G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819207 | |||||||
| chr5:157819241 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-1694A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819241 | |||||||
| chr5:157819474 | C | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-1927G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819474 | |||||||
| chr5:157819487 | A | T | 2 | a0001c0001t0003g0208 a0001c0004t0003g0072 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.42-1940T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819487 | |||||||
| chr5:157819498 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.42-1951A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819498 | |||||||
| chr5:157819692 | C | T | 3 | a0001c0001t0001g0309 a0001c0001t0001g0316 a0001c0001t0001g0319 |
3 | HG01123.hp2 HG01168.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.42-2145G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819692 | |||||||
| chr5:157819923 | G | A | 1 | a0001c0001t0002g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.42-2376C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819923 | |||||||
| chr5:157819964 | G | T | 33 | a0001c0001t0004g0004 a0001c0001t0004g0082 a0001c0001t0004g0084 others(30): Show |
34 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.42-2417C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819964 | |||||||
| chr5:157820131 | AC | A | 3 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0094 |
3 | HG01109.hp2 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-2585delG | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820131 | |||||||
| chr5:157820152 | G | A | 207 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(204): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.42-2605C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820152 | |||||||
| chr5:157820264 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-2717G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820264 | |||||||
| chr5:157820301 | T | A | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-2754A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820301 | |||||||
| chr5:157820333 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.42-2786G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820333 | |||||||
| chr5:157820346 | C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42-2799G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820346 | |||||||
| chr5:157820504 | A | C | 1 | a0001c0001t0002g0040 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.42-2957T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820504 | |||||||
| chr5:157820571 | T | G | 1 | a0001c0001t0002g0314 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.42-3024A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820571 | |||||||
| chr5:157820779 | T | A | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.42-3232A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820779 | |||||||
| chr5:157820856 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-3309G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820856 | |||||||
| chr5:157820926 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.42-3379T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820926 | |||||||
| chr5:157820996 | C | A | 1 | a0001c0001t0002g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.42-3449G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820996 | |||||||
| chr5:157821070 | G | T | 5 | a0001c0001t0001g0272 a0001c0001t0001g0287 a0001c0001t0001g0288 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-3523C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821070 | |||||||
| chr5:157821104 | C | A | 1 | a0001c0001t0003g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.42-3557G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821104 | |||||||
| chr5:157821187 | AG | A | 69 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.42-3641delC | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821187 | |||||||
| chr5:157821237 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0248 |
3 | HG00438.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.42-3690A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821237 | |||||||
| chr5:157821386 | G | GA | 208 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.42-3840dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821386 | |||||||
| chr5:157821422 | A | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-3875T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821422 | |||||||
| chr5:157821492 | A | G | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-3945T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821492 | |||||||
| chr5:157821540 | T | A | 13 | a0001c0001t0002g0086 a0001c0001t0002g0194 a0001c0001t0002g0195 others(10): Show |
13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.42-3993A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821540 | |||||||
| chr5:157821620 | T | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0226 |
3 | HG02257.hp2 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.42-4073A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821620 | |||||||
| chr5:157821681 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-4134A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821681 | |||||||
| chr5:157821683 | G | T | 1 | a0001c0002t0003g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.42-4136C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821683 | |||||||
| chr5:157821839 | G | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0308 others(15): Show |
19 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.42-4292C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821839 | |||||||
| chr5:157821999 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-4452A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821999 | |||||||
| chr5:157822040 | A | G | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-4493T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822040 | |||||||
| chr5:157822053 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.42-4506A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822053 | |||||||
| chr5:157822065 | G | A | 23 | a0001c0001t0004g0004 a0001c0001t0004g0082 a0001c0001t0004g0084 others(20): Show |
24 | HG01099.hp1 HG01358.hp2 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.42-4518C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822065 | |||||||
| chr5:157822141 | T | A | 1 | a0001c0001t0002g0109 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.42-4594A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822141 | |||||||
| chr5:157822156 | C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42-4609G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822156 | |||||||
| chr5:157822200 | A | G | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-4653T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822200 | |||||||
| chr5:157822212 | CT | C | 69 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.42-4666delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822212 | |||||||
| chr5:157822336 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.42-4789A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822336 | |||||||
| chr5:157822497 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-4950G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822497 | |||||||
| chr5:157822513 | T | C | 1 | a0001c0001t0003g0059 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.42-4966A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822513 | |||||||
| chr5:157822737 | A | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-5190T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822737 | |||||||
| chr5:157822770 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.42-5223G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822770 | |||||||
| chr5:157823126 | T | C | 1 | a0004c0007t0003g0031 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.42-5579A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823126 | |||||||
| chr5:157823156 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.42-5609C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823156 | |||||||
| chr5:157823181 | G | C | 1 | a0001c0001t0002g0314 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.42-5634C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823181 | |||||||
| chr5:157823254 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-5707A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823254 | |||||||
| chr5:157823418 | T | G | 1 | a0001c0001t0003g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.42-5871A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823418 | |||||||
| chr5:157823419 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.42-5872C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823419 | |||||||
| chr5:157823456 | G | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-5909C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823456 | |||||||
| chr5:157823549 | T | A | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.42-6002A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823549 | |||||||
| chr5:157823780 | C | T | 5 | a0001c0001t0001g0272 a0001c0001t0001g0287 a0001c0001t0001g0288 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-6233G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823780 | |||||||
| chr5:157823782 | G | A | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-6235C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823782 | |||||||
| chr5:157823841 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-6294G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823841 | |||||||
| chr5:157823880 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-6333A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823880 | |||||||
| chr5:157823887 | C | T | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-6340G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823887 | |||||||
| chr5:157823905 | G | A | 1 | a0001c0001t0002g0189 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.42-6358C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823905 | |||||||
| chr5:157823918 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-6371G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823918 | |||||||
| chr5:157823920 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-6373A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823920 | |||||||
| chr5:157824074 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.42-6527G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824074 | |||||||
| chr5:157824129 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.42-6582A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824129 | |||||||
| chr5:157824293 | G | A | 69 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.42-6746C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824293 | |||||||
| chr5:157824356 | G | A | 1 | a0001c0001t0002g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.42-6809C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824356 | |||||||
| chr5:157824410 | C | T | 4 | a0001c0002t0003g0054 a0001c0002t0003g0055 a0001c0002t0003g0057 others(1): Show |
4 | HG02886.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-6863G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824410 | |||||||
| chr5:157824557 | A | G | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-7010T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824557 | |||||||
| chr5:157824572 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0164 |
3 | HG03834.hp1 NA19004.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.42-7025A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824572 | |||||||
| chr5:157824600 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.42-7053A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824600 | |||||||
| chr5:157824626 | G | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-7079C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824626 | |||||||
| chr5:157824652 | T | G | 136 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(133): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.42-7105A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824652 | |||||||
| chr5:157824779 | T | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-7232A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824779 | |||||||
| chr5:157824833 | A | G | 136 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(133): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.42-7286T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824833 | |||||||
| chr5:157825153 | G | A | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.42-7606C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157825153 | |||||||
| chr5:157825205 | A | G | 2 | a0001c0001t0003g0026 a0001c0001t0003g0067 |
2 | HG00597.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.42-7658T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157825205 | |||||||
| chr5:157825387 | A | G | 3 | a0001c0001t0002g0135 a0001c0001t0002g0180 a0001c0001t0002g0181 |
3 | NA18612.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.42-7840T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157825387 | |||||||
| chr5:157825814 | C | T | 5 | a0001c0001t0001g0275 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-8267G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157825814 | |||||||
| chr5:157825931 | T | C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-8384A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157825931 | |||||||
| chr5:157826176 | G | A | 1 | a0001c0002t0003g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.42-8629C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826176 | |||||||
| chr5:157826326 | T | C | 3 | a0001c0001t0002g0135 a0001c0001t0002g0180 a0001c0001t0002g0181 |
3 | NA18612.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.42-8779A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826326 | |||||||
| chr5:157826395 | T | C | 51 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(48): Show |
52 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.42-8848A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826395 | |||||||
| chr5:157826425 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.42-8878T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826425 | |||||||
| chr5:157826515 | A | AT | 180 | a0001c0001t0001g0008 a0001c0001t0001g0255 a0001c0001t0001g0275 others(177): Show |
185 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.42-8969dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826515 | |||||||
| chr5:157826630 | ACATG | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.42-9087_42-9084del others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826630 | |||||||
| chr5:157826638 | G | C | 1 | a0001c0001t0002g0122 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.42-9091C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826638 | |||||||
| chr5:157826638 | G | T | 136 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(133): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.42-9091C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826638 | |||||||
| chr5:157827035 | T | C | 1 | a0001c0001t0002g0152 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.42-9488A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827035 | |||||||
| chr5:157827223 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.42-9676T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827223 | |||||||
| chr5:157827266 | C | T | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.42-9719G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827266 | |||||||
| chr5:157827314 | T | C | 3 | a0001c0001t0001g0250 a0001c0001t0001g0261 a0001c0001t0001g0264 |
3 | HG02559.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.42-9767A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827314 | |||||||
| chr5:157827544 | C | T | 1 | a0001c0001t0002g0005 | 2 | HG00280.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.42-9997G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827544 | |||||||
| chr5:157827562 | A | C | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-10015T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827562 | |||||||
| chr5:157827773 | T | G | 1 | a0001c0001t0001g0323 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.42-10226A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827773 | |||||||
| chr5:157827797 | A | T | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-10250T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827797 | |||||||
| chr5:157827979 | T | C | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.42-10432A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827979 | |||||||
| chr5:157827987 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.42-10440G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827987 | |||||||
| chr5:157827993 | A | G | 69 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.42-10446T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827993 | |||||||
| chr5:157828447 | A | C | 33 | a0001c0001t0004g0004 a0001c0001t0004g0082 a0001c0001t0004g0084 others(30): Show |
34 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.42-10900T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828447 | |||||||
| chr5:157828475 | G | A | 208 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(205): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.42-10928C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828475 | |||||||
| chr5:157828503 | A | G | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-10956T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828503 | |||||||
| chr5:157828583 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-11036C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828583 | |||||||
| chr5:157828719 | T | C | 1 | a0001c0001t0006g0010 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.42-11172A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828719 | |||||||
| chr5:157828892 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-11345G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828892 | |||||||
| chr5:157828927 | T | TA | 111 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0215 others(108): Show |
113 | HG00140.hp1 HG00597.hp1 HG00741.hp1 others(110): Show |
intron_variant | MODIFIER | c.42-11381dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828927 | |||||||
| chr5:157828927 | T | TAA | 9 | a0001c0001t0003g0041 a0001c0001t0003g0044 a0001c0001t0003g0045 others(6): Show |
9 | HG01981.hp2 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.42-11382_42-11381d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828927 | |||||||
| chr5:157828927 | TA | T | 12 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(9): Show |
12 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.42-11381delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828927 | |||||||
| chr5:157829039 | T | C | 1 | a0001c0001t0002g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.42-11492A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829039 | |||||||
| chr5:157829062 | A | G | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-11515T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829062 | |||||||
| chr5:157829102 | AAAC | A | 9 | a0001c0001t0002g0003 a0001c0001t0002g0110 a0001c0001t0002g0117 others(6): Show |
10 | HG02027.hp1 HG02056.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.42-11558_42-11556d others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829102 | |||||||
| chr5:157829116 | G | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-11569C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829116 | |||||||
| chr5:157829618 | G | T | 1 | a0001c0002t0003g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.42-12071C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829618 | |||||||
| chr5:157829672 | C | T | 135 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(132): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.42-12125G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829672 | |||||||
| chr5:157829689 | A | AT | 21 | a0001c0001t0001g0214 a0001c0001t0001g0224 a0001c0001t0001g0226 others(18): Show |
21 | HG00423.hp1 HG00544.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.42-12143dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | |||||||
| chr5:157829689 | ATT | A | 12 | a0001c0001t0002g0087 a0001c0001t0002g0106 a0001c0001t0002g0112 others(9): Show |
12 | HG01106.hp1 HG02145.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.42-12144_42-12143d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | |||||||
| chr5:157829689 | ATTT | A | 131 | a0001c0001t0001g0306 a0001c0001t0001g0309 a0001c0001t0001g0310 others(128): Show |
135 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.42-12145_42-12143d others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | |||||||
| chr5:157829689 | ATTTT | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0308 a0001c0001t0001g0311 others(12): Show |
16 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.42-12146_42-12143d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | |||||||
| chr5:157829689 | ATTTTTTT others(1): Show |
A | 18 | a0001c0001t0003g0023 a0001c0001t0003g0039 a0001c0001t0003g0208 others(15): Show |
18 | HG02451.hp2 HG02615.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.42-12150_42-12143d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | |||||||
| chr5:157829689 | ATTTTTTT others(2): Show |
A | 49 | a0001c0001t0002g0040 a0001c0001t0003g0019 a0001c0001t0003g0020 others(46): Show |
49 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.42-12151_42-12143d others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | |||||||
| chr5:157829689 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0003g0001 | 2 | NA18974.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.42-12152_42-12143d others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | |||||||
| chr5:157829795 | GC | G | 69 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.42-12249delG | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829795 | |||||||
| chr5:157829839 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.42-12292G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829839 | |||||||
| chr5:157829873 | A | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-12326T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829873 | |||||||
| chr5:157830001 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-12454A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830001 | |||||||
| chr5:157830025 | TAC | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-12480_42-12479d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830025 | |||||||
| chr5:157830091 | G | A | 1 | a0001c0001t0006g0009 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.42-12544C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830091 | |||||||
| chr5:157830185 | T | G | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-12638A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830185 | |||||||
| chr5:157830232 | T | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-12685A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830232 | |||||||
| chr5:157830288 | C | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-12741G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830288 | |||||||
| chr5:157830320 | G | C | 1 | a0001c0001t0002g0127 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.42-12773C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830320 | |||||||
| chr5:157830533 | T | C | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42-12986A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830533 | |||||||
| chr5:157830616 | C | T | 135 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(132): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.42-13069G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830616 | |||||||
| chr5:157830743 | C | CCTCCCTC others(5): Show |
2 | a0001c0001t0003g0032 a0001c0001t0003g0034 |
2 | HG02602.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.42-13208_42-13197d others(14): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830743 | |||||||
| chr5:157830746 | C | CCCTCTCT others(4): Show |
1 | a0001c0001t0003g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.42-13200_42-13199i others(13): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830746 | |||||||
| chr5:157830747 | C | CCT | 29 | a0001c0001t0001g0216 a0001c0001t0001g0310 a0001c0001t0001g0317 others(26): Show |
30 | HG00140.hp1 HG01192.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.42-13202_42-13201d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830747 | |||||||
| chr5:157830747 | C | CCTCT | 2 | a0001c0001t0001g0008 a0001c0001t0001g0321 |
3 | HG00280.hp1 HG01433.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.42-13204_42-13201d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830747 | |||||||
| chr5:157830749 | T | TCTCTCTC others(3): Show |
5 | a0001c0001t0003g0019 a0001c0001t0003g0026 a0001c0001t0003g0027 others(2): Show |
5 | HG02056.hp1 HG03098.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-13203_42-13202i others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830749 | |||||||
| chr5:157830751 | T | C | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-13204A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830751 | |||||||
| chr5:157830751 | T | TCTCTCTC others(1): Show |
3 | a0001c0001t0003g0028 a0001c0001t0003g0062 a0001c0001t0003g0064 |
3 | HG03516.hp2 NA19065.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.42-13205_42-13204i others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830751 | |||||||
| chr5:157830753 | T | TCTCTCC | 6 | a0001c0001t0003g0060 a0001c0001t0003g0065 a0001c0001t0003g0066 others(3): Show |
6 | HG01109.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13207_42-13206i others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830753 | |||||||
| chr5:157830755 | T | TCTCC | 7 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0077 others(4): Show |
7 | HG02615.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-13209_42-13208i others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830755 | |||||||
| chr5:157830757 | C | CCT | 14 | a0001c0001t0001g0213 a0001c0001t0001g0247 a0001c0001t0001g0248 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.42-13212_42-13211d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | |||||||
| chr5:157830757 | C | CCTCT | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0254 others(5): Show |
8 | HG00323.hp2 HG00423.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-13214_42-13211d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | |||||||
| chr5:157830757 | C | CT | 5 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0259 others(2): Show |
5 | HG00609.hp1 HG02145.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-13211_42-13210i others(3): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | |||||||
| chr5:157830757 | C | CTCT | 3 | a0001c0001t0001g0223 a0001c0001t0001g0289 a0001c0001t0002g0178 |
3 | HG01496.hp1 HG01516.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.42-13211_42-13210i others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | |||||||
| chr5:157830757 | C | T | 61 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0306 others(58): Show |
62 | HG00280.hp1 HG00597.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-13210G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | |||||||
| chr5:157830757 | CCT | C | 22 | a0001c0001t0002g0017 a0001c0001t0002g0083 a0001c0001t0002g0092 others(19): Show |
22 | HG00621.hp2 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-13212_42-13211d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | |||||||
| chr5:157830757 | CCTCT | C | 14 | a0001c0001t0001g0266 a0001c0001t0004g0099 a0001c0001t0004g0101 others(11): Show |
14 | HG01358.hp2 HG01981.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.42-13214_42-13211d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | |||||||
| chr5:157830757 | CCTCTCT | C | 25 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0286 others(22): Show |
26 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.42-13216_42-13211d others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | |||||||
| chr5:157830757 | CCTCTCTC others(1): Show |
C | 5 | a0001c0001t0001g0249 a0001c0001t0004g0141 a0001c0001t0004g0187 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-13218_42-13211d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | |||||||
| chr5:157830757 | CCTCTCTC others(3): Show |
C | 7 | a0001c0001t0001g0275 a0001c0001t0001g0303 a0001c0001t0001g0304 others(4): Show |
7 | HG00741.hp1 HG01106.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-13220_42-13211d others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | |||||||
| chr5:157830759 | T | C | 16 | a0001c0001t0003g0035 a0001c0001t0003g0037 a0001c0001t0003g0044 others(13): Show |
16 | HG00597.hp1 HG02135.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.42-13212A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830759 | |||||||
| chr5:157830761 | T | C | 1 | a0001c0001t0003g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.42-13214A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830761 | |||||||
| chr5:157830763 | T | C | 2 | a0001c0001t0002g0191 a0001c0008t0002g0193 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.42-13216A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830763 | |||||||
| chr5:157830780 | CTCTCTCT others(15): Show |
C | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-13255_42-13234d others(24): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830780 | |||||||
| chr5:157830782 | CTCTCTCT others(9): Show |
C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0165 |
3 | NA18965.hp1 NA19004.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.42-13251_42-13236d others(18): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830782 | |||||||
| chr5:157830784 | CTCTCTCT others(9): Show |
C | 1 | a0001c0001t0002g0164 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.42-13253_42-13238d others(18): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830784 | |||||||
| chr5:157830790 | C | A | 6 | a0001c0001t0005g0100 a0001c0001t0005g0103 a0001c0001t0005g0146 others(3): Show |
6 | HG02257.hp1 NA18981.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13243G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830790 | |||||||
| chr5:157830792 | C | A | 25 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0214 others(22): Show |
25 | HG00423.hp2 HG01168.hp1 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.42-13245G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830792 | |||||||
| chr5:157830792 | C | CTATATAT others(3): Show |
1 | a0001c0001t0003g0048 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.42-13246_42-13245i others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830792 | |||||||
| chr5:157830792 | CTCTCTA | C | 4 | a0001c0001t0002g0122 a0001c0001t0002g0197 a0001c0001t0002g0200 others(1): Show |
4 | HG01099.hp2 HG03130.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-13251_42-13246d others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830792 | |||||||
| chr5:157830794 | C | A | 50 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0214 others(47): Show |
51 | HG00423.hp2 HG00639.hp1 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.42-13247G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830794 | |||||||
| chr5:157830794 | C | CTA | 10 | a0001c0001t0001g0239 a0001c0001t0001g0255 a0001c0001t0001g0270 others(7): Show |
10 | HG00099.hp1 HG01256.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.42-13248_42-13247i others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830794 | |||||||
| chr5:157830794 | C | CTATATA | 3 | a0001c0001t0002g0106 a0001c0001t0003g0068 a0001c0002t0003g0056 |
3 | HG02145.hp1 HG02615.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.42-13248_42-13247i others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830794 | |||||||
| chr5:157830794 | CTCTA | C | 4 | a0001c0001t0001g0252 a0001c0001t0004g0104 a0001c0001t0004g0145 others(1): Show |
4 | HG01099.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-13251_42-13248d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830794 | |||||||
| chr5:157830796 | C | A | 109 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(106): Show |
111 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.42-13249G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | C | CTATA | 6 | a0001c0001t0001g0273 a0001c0001t0001g0285 a0001c0001t0003g0067 others(3): Show |
6 | HG00597.hp1 HG01192.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13253_42-13250d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | C | CTATATA | 7 | a0001c0001t0003g0001 a0001c0001t0003g0020 a0001c0001t0003g0042 others(4): Show |
7 | HG02451.hp2 HG02809.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-13255_42-13250d others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | C | CTATATAT others(1): Show |
4 | a0001c0001t0003g0035 a0001c0001t0003g0037 a0001c0001t0003g0044 others(1): Show |
4 | HG02135.hp1 HG02486.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-13257_42-13250d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | C | CTATATAT others(3): Show |
3 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0004c0007t0003g0031 |
3 | HG02970.hp1 HG03540.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.42-13259_42-13250d others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | C | CTCTA | 6 | a0001c0001t0001g0271 a0001c0001t0001g0283 a0001c0001t0001g0322 others(3): Show |
6 | HG01192.hp1 HG03486.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13250_42-13249i others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | C | CTCTATA | 5 | a0001c0001t0001g0250 a0001c0001t0002g0040 a0001c0001t0003g0001 others(2): Show |
5 | HG00140.hp1 HG03225.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-13250_42-13249i others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | C | CTCTCTA | 6 | a0001c0001t0001g0261 a0001c0001t0003g0021 a0001c0001t0003g0033 others(3): Show |
6 | HG02129.hp2 NA18951.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13250_42-13249i others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | C | CTCTCTAT others(1): Show |
4 | a0001c0001t0001g0274 a0001c0001t0001g0284 a0001c0001t0003g0036 others(1): Show |
4 | HG00438.hp2 HG02523.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-13250_42-13249i others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | C | CTCTCTAT others(3): Show |
1 | a0001c0008t0002g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.42-13250_42-13249i others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | C | CTCTCTCT others(3): Show |
1 | a0001c0001t0001g0313 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.42-13250_42-13249i others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | C | CTCTCTCT others(5): Show |
1 | a0001c0001t0003g0041 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.42-13250_42-13249i others(14): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830796 | CTA | C | 31 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0013 others(28): Show |
33 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.42-13251_42-13250d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | |||||||
| chr5:157830798 | A | C | 60 | a0001c0001t0001g0079 a0001c0001t0001g0215 a0001c0001t0001g0218 others(57): Show |
60 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.42-13251T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830798 | |||||||
| chr5:157830800 | A | C | 32 | a0001c0001t0001g0215 a0001c0001t0001g0246 a0001c0001t0001g0247 others(29): Show |
32 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.42-13253T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830800 | |||||||
| chr5:157830802 | A | C | 6 | a0001c0001t0001g0215 a0001c0001t0001g0280 a0001c0001t0002g0087 others(3): Show |
6 | HG02165.hp2 HG04204.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13255T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830802 | |||||||
| chr5:157830835 | G | A | 1 | a0001c0002t0003g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42-13288C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830835 | |||||||
| chr5:157830852 | T | A | 2 | a0001c0001t0002g0090 a0001c0001t0002g0109 |
2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.42-13305A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830852 | |||||||
| chr5:157831047 | AAAAC | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-13504_42-13501d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831047 | |||||||
| chr5:157831063 | A | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.42-13516T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831063 | |||||||
| chr5:157831065 | A | C | 140 | a0001c0001t0001g0006 a0001c0001t0001g0227 a0001c0001t0001g0228 others(137): Show |
145 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.42-13518T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831065 | |||||||
| chr5:157831190 | CT | C | 70 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(67): Show |
71 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.42-13644delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831190 | |||||||
| chr5:157831495 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.42-13948A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831495 | |||||||
| chr5:157831506 | A | G | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-13959T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831506 | |||||||
| chr5:157831605 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.42-14058A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831605 | |||||||
| chr5:157831651 | A | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-14104T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831651 | |||||||
| chr5:157831693 | C | CT | 68 | a0001c0001t0001g0222 a0001c0001t0001g0235 a0001c0001t0001g0250 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-14147dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831693 | |||||||
| chr5:157831693 | C | CTT | 18 | a0001c0001t0003g0024 a0001c0001t0003g0046 a0001c0001t0003g0051 others(15): Show |
18 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.42-14148_42-14147d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831693 | |||||||
| chr5:157831693 | CT | C | 84 | a0001c0001t0001g0212 a0001c0001t0001g0268 a0001c0001t0001g0301 others(81): Show |
87 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.42-14147delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831693 | |||||||
| chr5:157831733 | C | T | 3 | a0001c0001t0002g0123 a0001c0001t0002g0153 a0001c0001t0002g0154 |
3 | HG00621.hp2 NA18964.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.42-14186G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831733 | |||||||
| chr5:157831739 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.42-14192C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831739 | |||||||
| chr5:157831804 | A | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-14257T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831804 | |||||||
| chr5:157831816 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-14269A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831816 | |||||||
| chr5:157831881 | G | A | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42-14334C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831881 | |||||||
| chr5:157832019 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.42-14472C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832019 | |||||||
| chr5:157832057 | G | A | 5 | a0001c0001t0001g0275 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-14510C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832057 | |||||||
| chr5:157832067 | A | G | 1 | a0001c0006t0001g0325 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.42-14520T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832067 | |||||||
| chr5:157832505 | T | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(18): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-14958A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832505 | |||||||
| chr5:157832585 | TATCTTCT others(8): Show |
T | 1 | a0001c0006t0001g0325 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.42-15053_42-15039d others(17): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832585 | |||||||
| chr5:157832805 | G | A | 9 | a0001c0001t0002g0003 a0001c0001t0002g0110 a0001c0001t0002g0117 others(6): Show |
10 | HG02027.hp1 HG02056.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.42-15258C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832805 | |||||||
| chr5:157832822 | G | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.42-15275C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832822 | |||||||
| chr5:157833007 | G | T | 153 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(150): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.42-15460C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833007 | |||||||
| chr5:157833081 | T | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-15534A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833081 | |||||||
| chr5:157833167 | A | AAC | 13 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0054 others(10): Show |
13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-15621_42-15620i others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833167 | |||||||
| chr5:157833168 | C | A | 13 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0054 others(10): Show |
13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-15621G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833168 | |||||||
| chr5:157833209 | G | A | 13 | a0001c0002t0003g0052 a0001c0002t0003g0053 a0001c0002t0003g0054 others(10): Show |
13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-15662C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833209 | |||||||
| chr5:157833248 | A | C | 1 | a0001c0001t0004g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.42-15701T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833248 | |||||||
| chr5:157833307 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-15760A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833307 | |||||||
| chr5:157833400 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42-15853A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833400 | |||||||
| chr5:157833569 | T | C | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-16022A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833569 | |||||||
| chr5:157833601 | C | T | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG01070.hp2 HG01169.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-16054G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833601 | |||||||
| chr5:157833752 | C | A | 4 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0063 others(1): Show |
4 | HG01884.hp2 HG02109.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-16205G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833752 | |||||||
| chr5:157833889 | C | T | 1 | a0001c0002t0003g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42-16342G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833889 | |||||||
| chr5:157833895 | T | A | 1 | a0001c0001t0003g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.42-16348A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833895 | |||||||
| chr5:157833934 | C | T | 2 | a0001c0001t0003g0023 a0001c0001t0003g0211 |
2 | HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.42-16387G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833934 | |||||||
| chr5:157834070 | G | A | 48 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(45): Show |
49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.42-16523C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834070 | |||||||
| chr5:157834162 | G | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-16615C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834162 | |||||||
| chr5:157834184 | T | C | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-16637A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834184 | |||||||
| chr5:157834216 | G | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-16669C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834216 | |||||||
| chr5:157834290 | G | A | 3 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0094 |
3 | HG01109.hp2 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-16743C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834290 | |||||||
| chr5:157834294 | G | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-16747C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834294 | |||||||
| chr5:157834359 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-16812G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834359 | |||||||
| chr5:157834363 | T | TAA | 66 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(63): Show |
67 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.42-16818_42-16817d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834363 | |||||||
| chr5:157834454 | A | C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-16907T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834454 | |||||||
| chr5:157834650 | T | C | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-17103A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834650 | |||||||
| chr5:157834674 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.42-17127G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834674 | |||||||
| chr5:157834747 | C | A | 2 | a0001c0001t0004g0105 a0001c0001t0004g0107 |
2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.42-17200G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834747 | |||||||
| chr5:157834835 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.42-17288C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834835 | |||||||
| chr5:157835179 | T | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-17632A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835179 | |||||||
| chr5:157835506 | C | A | 1 | a0001c0002t0003g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42-17959G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835506 | |||||||
| chr5:157835754 | T | C | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG01070.hp2 HG01169.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-18207A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835754 | |||||||
| chr5:157835755 | G | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.42-18208C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835755 | |||||||
| chr5:157835780 | A | G | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-18233T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835780 | |||||||
| chr5:157835808 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.42-18261G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835808 | |||||||
| chr5:157835949 | A | G | 2 | a0001c0001t0001g0250 a0001c0001t0001g0261 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.42-18402T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835949 | |||||||
| chr5:157836012 | C | A | 5 | a0001c0001t0001g0275 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-18465G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157836012 | |||||||
| chr5:157836347 | T | A | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-18800A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157836347 | |||||||
| chr5:157836385 | T | C | 19 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0308 others(16): Show |
20 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-18838A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157836385 | |||||||
| chr5:157836909 | T | G | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-19362A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157836909 | |||||||
| chr5:157837077 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.42-19530T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837077 | |||||||
| chr5:157837110 | C | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0275 a0001c0001t0001g0303 others(27): Show |
31 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.42-19563G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837110 | |||||||
| chr5:157837348 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.42-19801C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837348 | |||||||
| chr5:157837411 | T | TAC | 16 | a0001c0001t0001g0007 a0001c0001t0001g0213 a0001c0001t0001g0231 others(13): Show |
17 | HG00609.hp2 HG01071.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.42-19866_42-19865d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837411 | |||||||
| chr5:157837411 | T | TACAC | 3 | a0001c0001t0001g0248 a0001c0001t0001g0274 a0001c0001t0001g0298 |
3 | HG00438.hp1 HG00438.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.42-19868_42-19865d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837411 | |||||||
| chr5:157837411 | TACAC | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(19): Show |
23 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.42-19868_42-19865d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837411 | |||||||
| chr5:157837415 | C | CAA | 4 | a0001c0001t0002g0126 a0001c0001t0002g0161 a0001c0001t0002g0169 others(1): Show |
4 | HG03831.hp2 NA18939.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-19869_42-19868i others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837415 | |||||||
| chr5:157837415 | C | T | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-19868G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837415 | |||||||
| chr5:157837417 | C | A | 197 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(194): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.42-19870G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837417 | |||||||
| chr5:157837417 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(19): Show |
23 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.42-19870G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837417 | |||||||
| chr5:157837419 | C | T | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-19872G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837419 | |||||||
| chr5:157837499 | G | C | 1 | a0001c0001t0001g0313 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.42-19952C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837499 | |||||||
| chr5:157837647 | T | C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-20100A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837647 | |||||||
| chr5:157837649 | C | CTT | 14 | a0001c0001t0002g0086 a0001c0001t0002g0192 a0001c0001t0002g0194 others(11): Show |
14 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.42-20104_42-20103d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | |||||||
| chr5:157837649 | C | CTTT | 87 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(84): Show |
90 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.42-20105_42-20103d others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | |||||||
| chr5:157837649 | C | CTTTT | 34 | a0001c0001t0002g0122 a0001c0001t0002g0207 a0001c0001t0004g0004 others(31): Show |
35 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.42-20106_42-20103d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | |||||||
| chr5:157837649 | C | CTTTTTTT others(1): Show |
18 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0308 others(15): Show |
19 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.42-20110_42-20103d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | |||||||
| chr5:157837649 | C | CTTTTTTT others(2): Show |
58 | a0001c0001t0001g0307 a0001c0001t0001g0322 a0001c0001t0002g0040 others(55): Show |
59 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.42-20111_42-20103d others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | |||||||
| chr5:157837649 | C | CTTTTTTT others(3): Show |
15 | a0001c0001t0003g0041 a0001c0001t0003g0044 a0001c0001t0003g0045 others(12): Show |
15 | HG02145.hp2 HG02486.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.42-20112_42-20103d others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | |||||||
| chr5:157837649 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-20103_42-20102i others(17): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | |||||||
| chr5:157837649 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-20102G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | |||||||
| chr5:157837791 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(18): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-20244C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837791 | |||||||
| chr5:157837833 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.42-20286C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837833 | |||||||
| chr5:157837883 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(18): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-20336G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837883 | |||||||
| chr5:157837892 | T | C | 8 | a0001c0001t0003g0060 a0001c0001t0003g0064 a0001c0001t0003g0065 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-20345A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837892 | |||||||
| chr5:157837953 | C | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0177 a0001c0001t0002g0178 |
4 | HG00280.hp2 HG01358.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-20406G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837953 | |||||||
| chr5:157838025 | T | C | 1 | a0001c0001t0003g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.42-20478A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838025 | |||||||
| chr5:157838026 | A | G | 48 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(45): Show |
49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.42-20479T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838026 | |||||||
| chr5:157838055 | T | C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-20508A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838055 | |||||||
| chr5:157838073 | C | T | 1 | a0001c0001t0002g0190 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.42-20526G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838073 | |||||||
| chr5:157838122 | G | GT | 55 | a0001c0001t0001g0219 a0001c0001t0001g0233 a0001c0001t0001g0269 others(52): Show |
56 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.42-20576dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838122 | |||||||
| chr5:157838122 | G | T | 1 | a0001c0001t0004g0140 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.42-20575C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838122 | |||||||
| chr5:157838122 | GT | G | 67 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(64): Show |
68 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.42-20576delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838122 | |||||||
| chr5:157838192 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.42-20645C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838192 | |||||||
| chr5:157838279 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.41+20651G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838279 | |||||||
| chr5:157838324 | C | T | 1 | a0001c0001t0004g0082 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.41+20606G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838324 | |||||||
| chr5:157838403 | G | T | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+20527C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838403 | |||||||
| chr5:157838491 | T | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.41+20439A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838491 | |||||||
| chr5:157838501 | G | A | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+20429C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838501 | |||||||
| chr5:157838591 | G | C | 1 | a0001c0001t0001g0295 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.41+20339C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838591 | |||||||
| chr5:157838599 | A | G | 329 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(326): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.41+20331T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838599 | |||||||
| chr5:157838677 | A | G | 228 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(225): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.41+20253T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838677 | |||||||
| chr5:157838872 | T | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(18): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+20058A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838872 | |||||||
| chr5:157838993 | G | C | 32 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(29): Show |
33 | HG00140.hp1 HG00597.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.41+19937C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838993 | |||||||
| chr5:157839004 | G | A | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41+19926C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839004 | |||||||
| chr5:157839107 | T | C | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG01070.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.41+19823A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839107 | |||||||
| chr5:157839114 | A | C | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41+19816T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839114 | |||||||
| chr5:157839184 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.41+19746C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839184 | |||||||
| chr5:157839331 | C | T | 2 | a0001c0002t0003g0080 a0001c0002t0003g0081 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.41+19599G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839331 | |||||||
| chr5:157839426 | C | T | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+19504G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839426 | |||||||
| chr5:157839427 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.41+19503G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839427 | |||||||
| chr5:157839467 | A | G | 207 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(204): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.41+19463T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839467 | |||||||
| chr5:157839526 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.41+19404A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839526 | |||||||
| chr5:157839575 | C | T | 207 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(204): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.41+19355G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839575 | |||||||
| chr5:157839588 | G | A | 228 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(225): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.41+19342C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839588 | |||||||
| chr5:157839609 | T | TA | 53 | a0001c0001t0001g0243 a0001c0001t0001g0249 a0001c0001t0002g0040 others(50): Show |
54 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(51): Show |
intron_variant | MODIFIER | c.41+19320dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839609 | |||||||
| chr5:157839614 | A | T | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+19316T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839614 | |||||||
| chr5:157839618 | A | C | 6 | a0001c0001t0002g0087 a0001c0001t0002g0172 a0001c0002t0003g0053 others(3): Show |
6 | HG02165.hp2 HG02451.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+19312T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839618 | |||||||
| chr5:157839626 | C | A | 6 | a0001c0001t0001g0275 a0001c0001t0001g0292 a0001c0001t0001g0303 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+19304G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839626 | |||||||
| chr5:157839626 | C | CA | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+19303dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839626 | |||||||
| chr5:157839635 | A | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(18): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+19295T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839635 | |||||||
| chr5:157839651 | T | C | 51 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(48): Show |
52 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.41+19279A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839651 | |||||||
| chr5:157839670 | A | T | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41+19260T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839670 | |||||||
| chr5:157839692 | G | A | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+19238C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839692 | |||||||
| chr5:157839720 | A | AATCT | 61 | a0001c0001t0001g0213 a0001c0001t0001g0227 a0001c0001t0001g0231 others(58): Show |
62 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+19206_41+19209d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | |||||||
| chr5:157839720 | A | AATCTATC others(1): Show |
26 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0212 others(23): Show |
26 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.41+19202_41+19209d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | |||||||
| chr5:157839720 | A | AATCTATC others(5): Show |
8 | a0001c0001t0001g0079 a0001c0001t0001g0226 a0001c0001t0001g0266 others(5): Show |
8 | HG02257.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.41+19198_41+19209d others(14): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | |||||||
| chr5:157839720 | A | AATCTATC others(9): Show |
2 | a0001c0001t0001g0310 a0001c0001t0007g0331 |
2 | HG01928.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+19194_41+19209d others(18): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | |||||||
| chr5:157839720 | A | AATCTATC others(13): Show |
1 | a0001c0001t0001g0319 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.41+19190_41+19209d others(22): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | |||||||
| chr5:157839720 | AATCT | A | 17 | a0001c0001t0001g0219 a0001c0001t0001g0225 a0001c0001t0001g0242 others(14): Show |
17 | HG00099.hp2 HG00621.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.41+19206_41+19209d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | |||||||
| chr5:157839720 | AATCTATC others(1): Show |
A | 12 | a0001c0001t0002g0083 a0001c0001t0002g0093 a0001c0001t0002g0106 others(9): Show |
12 | HG01433.hp1 HG02040.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.41+19202_41+19209d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | |||||||
| chr5:157839720 | AATCTATC others(5): Show |
A | 76 | a0001c0001t0001g0244 a0001c0001t0002g0002 a0001c0001t0002g0003 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.41+19198_41+19209d others(14): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | |||||||
| chr5:157839720 | AATCTATC others(9): Show |
A | 64 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(61): Show |
65 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(62): Show |
intron_variant | MODIFIER | c.41+19194_41+19209d others(18): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | |||||||
| chr5:157839720 | AATCTATC others(13): Show |
A | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.41+19190_41+19209d others(22): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | |||||||
| chr5:157839722 | T | TCTAC | 3 | a0001c0001t0001g0269 a0001c0001t0001g0290 a0001c0001t0001g0299 |
3 | HG00323.hp2 HG01346.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.41+19207_41+19208i others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839722 | |||||||
| chr5:157839960 | C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.41+18970G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839960 | |||||||
| chr5:157840015 | G | A | 2 | a0001c0001t0003g0094 a0002c0005t0001g0210 |
2 | HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.41+18915C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840015 | |||||||
| chr5:157840019 | C | A | 4 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(1): Show |
4 | HG00621.hp1 NA18961.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+18911G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840019 | |||||||
| chr5:157840073 | T | C | 1 | a0003c0003t0001g0324 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.41+18857A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840073 | |||||||
| chr5:157840114 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.41+18816C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840114 | |||||||
| chr5:157840166 | A | G | 207 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(204): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.41+18764T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840166 | |||||||
| chr5:157840176 | C | T | 13 | a0001c0001t0002g0086 a0001c0001t0002g0194 a0001c0001t0002g0195 others(10): Show |
13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.41+18754G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840176 | |||||||
| chr5:157840192 | C | CA | 10 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0248 others(7): Show |
10 | HG00438.hp1 HG00438.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.41+18737dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840192 | |||||||
| chr5:157840192 | C | CAAA | 106 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(103): Show |
110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.41+18735_41+18737d others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840192 | |||||||
| chr5:157840192 | C | CAAAA | 39 | a0001c0001t0002g0088 a0001c0001t0002g0106 a0001c0001t0002g0111 others(36): Show |
39 | HG00140.hp2 HG00609.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.41+18734_41+18737d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840192 | |||||||
| chr5:157840192 | CA | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0301 a0001c0001t0001g0306 others(24): Show |
28 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.41+18737delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840192 | |||||||
| chr5:157840192 | CAA | C | 44 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(41): Show |
45 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.41+18736_41+18737d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840192 | |||||||
| chr5:157840250 | T | TA | 35 | a0001c0001t0001g0216 a0001c0001t0002g0122 a0001c0001t0002g0168 others(32): Show |
36 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.41+18679dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840250 | |||||||
| chr5:157840739 | T | TA | 52 | a0001c0001t0002g0040 a0001c0001t0002g0169 a0001c0001t0003g0001 others(49): Show |
53 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(50): Show |
intron_variant | MODIFIER | c.41+18190dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840739 | |||||||
| chr5:157840835 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0221 |
2 | HG01257.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.41+18095C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840835 | |||||||
| chr5:157840953 | T | G | 135 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(132): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.41+17977A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840953 | |||||||
| chr5:157841132 | G | A | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+17798C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841132 | |||||||
| chr5:157841133 | G | A | 1 | a0001c0001t0002g0170 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.41+17797C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841133 | |||||||
| chr5:157841158 | C | T | 1 | a0001c0001t0003g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.41+17772G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841158 | |||||||
| chr5:157841250 | A | G | 1 | a0001c0001t0002g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.41+17680T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841250 | |||||||
| chr5:157841347 | C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.41+17583G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841347 | |||||||
| chr5:157841374 | TGGCCAAC others(42): Show |
T | 1 | a0001c0001t0007g0332 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.41+17507_41+17555d others(51): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841374 | |||||||
| chr5:157841696 | T | C | 5 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG01070.hp2 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+17234A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841696 | |||||||
| chr5:157841786 | T | C | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.41+17144A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841786 | |||||||
| chr5:157841845 | A | G | 7 | a0001c0001t0001g0270 a0001c0001t0001g0276 a0001c0001t0001g0278 others(4): Show |
7 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.41+17085T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841845 | |||||||
| chr5:157841909 | C | G | 69 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.41+17021G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841909 | |||||||
| chr5:157841931 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.41+16999C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841931 | |||||||
| chr5:157842080 | T | C | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+16850A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157842080 | |||||||
| chr5:157842409 | C | A | 50 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(47): Show |
51 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.41+16521G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157842409 | |||||||
| chr5:157842713 | C | A | 36 | a0001c0001t0002g0085 a0001c0001t0002g0191 a0001c0001t0002g0192 others(33): Show |
37 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.41+16217G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157842713 | |||||||
| chr5:157842825 | G | A | 2 | a0001c0001t0003g0208 a0001c0004t0003g0072 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.41+16105C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157842825 | |||||||
| chr5:157842930 | A | G | 48 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(45): Show |
49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.41+16000T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157842930 | |||||||
| chr5:157843575 | G | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.41+15355C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157843575 | |||||||
| chr5:157843741 | A | G | 18 | a0001c0001t0001g0269 a0001c0001t0001g0271 a0001c0001t0001g0273 others(15): Show |
18 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(15): Show |
intron_variant | MODIFIER | c.41+15189T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157843741 | |||||||
| chr5:157843852 | C | T | 84 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(81): Show |
87 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.41+15078G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157843852 | |||||||
| chr5:157843867 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.41+15063C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157843867 | |||||||
| chr5:157843902 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.41+15028A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157843902 | |||||||
| chr5:157844011 | A | G | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+14919T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844011 | |||||||
| chr5:157844075 | A | C | 5 | a0001c0001t0001g0275 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+14855T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844075 | |||||||
| chr5:157844132 | T | C | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+14798A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844132 | |||||||
| chr5:157844222 | A | C | 1 | a0001c0001t0003g0062 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.41+14708T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844222 | |||||||
| chr5:157844680 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.41+14250C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844680 | |||||||
| chr5:157844825 | T | G | 1 | a0001c0001t0002g0123 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.41+14105A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844825 | |||||||
| chr5:157844854 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.41+14076A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844854 | |||||||
| chr5:157844897 | T | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+14033A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844897 | |||||||
| chr5:157844927 | C | T | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+14003G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844927 | |||||||
| chr5:157845097 | C | T | 19 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0308 others(16): Show |
20 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.41+13833G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845097 | |||||||
| chr5:157845124 | G | A | 1 | a0001c0001t0003g0037 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.41+13806C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845124 | |||||||
| chr5:157845210 | G | A | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+13720C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845210 | |||||||
| chr5:157845266 | T | C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+13664A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845266 | |||||||
| chr5:157845327 | C | T | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+13603G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845327 | |||||||
| chr5:157845328 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.41+13602C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845328 | |||||||
| chr5:157845445 | C | T | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+13485G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845445 | |||||||
| chr5:157845455 | G | A | 207 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(204): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.41+13475C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845455 | |||||||
| chr5:157845553 | A | AT | 31 | a0001c0001t0001g0214 a0001c0001t0001g0232 a0001c0001t0001g0259 others(28): Show |
31 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.41+13376dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845553 | |||||||
| chr5:157845591 | G | A | 1 | a0001c0001t0009g0328 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.41+13339C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845591 | |||||||
| chr5:157845638 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.41+13292C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845638 | |||||||
| chr5:157845741 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.41+13189T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845741 | |||||||
| chr5:157845776 | G | A | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.41+13154C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845776 | |||||||
| chr5:157845779 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.41+13151G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845779 | |||||||
| chr5:157845823 | G | A | 1 | a0001c0001t0004g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41+13107C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845823 | |||||||
| chr5:157845845 | T | C | 1 | a0001c0001t0003g0038 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.41+13085A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845845 | |||||||
| chr5:157845850 | G | A | 2 | a0001c0001t0002g0192 a0001c0001t0010g0330 |
2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.41+13080C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845850 | |||||||
| chr5:157845852 | C | A | 1 | a0001c0001t0002g0108 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.41+13078G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845852 | |||||||
| chr5:157845932 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.41+12998C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845932 | |||||||
| chr5:157846380 | CACA | C | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+12547_41+12549d others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846380 | |||||||
| chr5:157846599 | T | A | 1 | a0001c0001t0001g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.41+12331A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846599 | |||||||
| chr5:157846603 | A | G | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41+12327T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846603 | |||||||
| chr5:157846629 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.41+12301T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846629 | |||||||
| chr5:157846651 | A | G | 1 | a0001c0002t0003g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.41+12279T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846651 | |||||||
| chr5:157846653 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.41+12277G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846653 | |||||||
| chr5:157846655 | G | C | 1 | a0001c0001t0002g0087 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.41+12275C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846655 | |||||||
| chr5:157846673 | C | G | 1 | a0001c0001t0002g0204 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.41+12257G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846673 | |||||||
| chr5:157846681 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.41+12249C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846681 | |||||||
| chr5:157846836 | T | C | 51 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(48): Show |
52 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.41+12094A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846836 | |||||||
| chr5:157846977 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.41+11953T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846977 | |||||||
| chr5:157847046 | G | A | 5 | a0001c0001t0001g0275 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+11884C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847046 | |||||||
| chr5:157847095 | AT | A | 6 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(3): Show |
6 | HG01081.hp1 HG01106.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+11834delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847095 | |||||||
| chr5:157847180 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.41+11750G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847180 | |||||||
| chr5:157847389 | T | C | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+11541A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847389 | |||||||
| chr5:157847460 | G | A | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+11470C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847460 | |||||||
| chr5:157847477 | C | G | 1 | a0001c0001t0002g0125 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.41+11453G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847477 | |||||||
| chr5:157847510 | C | CA | 14 | a0001c0001t0002g0086 a0001c0001t0002g0194 a0001c0001t0002g0195 others(11): Show |
14 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.41+11419dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847510 | |||||||
| chr5:157847562 | T | A | 1 | a0001c0001t0011g0061 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.41+11368A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847562 | |||||||
| chr5:157847581 | C | T | 135 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(132): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.41+11349G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847581 | |||||||
| chr5:157847801 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.41+11129T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847801 | |||||||
| chr5:157847811 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+11119T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847811 | |||||||
| chr5:157847906 | G | C | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41+11024C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847906 | |||||||
| chr5:157848063 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.41+10867A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848063 | |||||||
| chr5:157848065 | C | T | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+10865G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848065 | |||||||
| chr5:157848289 | G | C | 123 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.41+10641C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848289 | |||||||
| chr5:157848348 | C | A | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+10582G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848348 | |||||||
| chr5:157848408 | A | T | 7 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0002g0085 others(4): Show |
7 | HG02109.hp2 HG02572.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+10522T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848408 | |||||||
| chr5:157848411 | T | A | 1 | a0001c0001t0002g0108 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.41+10519A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848411 | |||||||
| chr5:157848428 | G | A | 123 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.41+10502C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848428 | |||||||
| chr5:157848488 | G | A | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+10442C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848488 | |||||||
| chr5:157848597 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.41+10333C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848597 | |||||||
| chr5:157848773 | T | C | 2 | a0001c0001t0006g0009 a0001c0001t0006g0010 |
2 | NA18966.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.41+10157A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848773 | |||||||
| chr5:157848810 | C | T | 3 | a0001c0001t0002g0085 a0001c0001t0002g0191 a0001c0008t0002g0193 |
3 | HG03139.hp2 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.41+10120G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848810 | |||||||
| chr5:157848811 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.41+10119C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848811 | |||||||
| chr5:157848818 | C | T | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+10112G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848818 | |||||||
| chr5:157848848 | G | C | 1 | a0001c0001t0002g0124 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.41+10082C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848848 | |||||||
| chr5:157848863 | C | T | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+10067G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848863 | |||||||
| chr5:157849111 | A | G | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+9819T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849111 | |||||||
| chr5:157849159 | TAC | T | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG01070.hp2 HG01169.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+9769_41+9770del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849159 | |||||||
| chr5:157849208 | A | G | 1 | a0001c0001t0011g0061 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.41+9722T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849208 | |||||||
| chr5:157849362 | G | A | 71 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(68): Show |
72 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(69): Show |
intron_variant | MODIFIER | c.41+9568C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849362 | |||||||
| chr5:157849492 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.41+9438G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849492 | |||||||
| chr5:157849537 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.41+9393G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849537 | |||||||
| chr5:157849901 | A | T | 1 | a0001c0001t0002g0083 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.41+9029T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849901 | |||||||
| chr5:157849978 | A | C | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+8952T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849978 | |||||||
| chr5:157849988 | G | T | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41+8942C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849988 | |||||||
| chr5:157849993 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41+8937C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849993 | |||||||
| chr5:157850010 | T | C | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41+8920A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850010 | |||||||
| chr5:157850028 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.41+8902G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850028 | |||||||
| chr5:157850043 | A | G | 4 | a0001c0001t0001g0270 a0001c0001t0001g0276 a0001c0001t0001g0296 others(1): Show |
4 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+8887T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850043 | |||||||
| chr5:157850323 | T | C | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG00099.hp2 HG01496.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+8607A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850323 | |||||||
| chr5:157850344 | A | G | 195 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.41+8586T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850344 | |||||||
| chr5:157850440 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.41+8490C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850440 | |||||||
| chr5:157850565 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.41+8365G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850565 | |||||||
| chr5:157850579 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.41+8351G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850579 | |||||||
| chr5:157850612 | C | CA | 34 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0307 others(31): Show |
34 | HG00597.hp2 HG00741.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.41+8317dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850612 | |||||||
| chr5:157850612 | CA | C | 175 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0079 others(172): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.41+8317delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850612 | |||||||
| chr5:157850612 | CAA | C | 18 | a0001c0001t0001g0213 a0001c0001t0001g0270 a0001c0001t0001g0329 others(15): Show |
18 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.41+8316_41+8317del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850612 | |||||||
| chr5:157850650 | A | T | 3 | a0001c0001t0002g0135 a0001c0001t0002g0180 a0001c0001t0002g0181 |
3 | NA18612.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.41+8280T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850650 | |||||||
| chr5:157850726 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.41+8204T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850726 | |||||||
| chr5:157850804 | A | T | 195 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.41+8126T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850804 | |||||||
| chr5:157851123 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+7807C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851123 | |||||||
| chr5:157851138 | GCAAA | G | 68 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(65): Show |
69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+7788_41+7791del others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851138 | |||||||
| chr5:157851271 | C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.41+7659G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851271 | |||||||
| chr5:157851279 | C | T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.41+7651G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851279 | |||||||
| chr5:157851323 | A | G | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41+7607T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851323 | |||||||
| chr5:157851418 | G | A | 3 | a0001c0001t0004g0104 a0001c0001t0004g0145 a0001c0001t0004g0151 |
3 | HG01099.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.41+7512C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851418 | |||||||
| chr5:157851572 | CAGCTACT others(15): Show |
C | 48 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(45): Show |
49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.41+7336_41+7357del others(22): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851572 | |||||||
| chr5:157851680 | C | T | 123 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.41+7250G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851680 | |||||||
| chr5:157851686 | C | CA | 83 | a0001c0001t0001g0012 a0001c0001t0001g0265 a0001c0001t0002g0040 others(80): Show |
84 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.41+7243dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851686 | |||||||
| chr5:157851782 | T | C | 4 | a0001c0001t0001g0269 a0001c0001t0001g0290 a0001c0001t0001g0299 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+7148A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851782 | |||||||
| chr5:157851832 | G | C | 1 | a0001c0006t0001g0325 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41+7098C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851832 | |||||||
| chr5:157851940 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.41+6990T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851940 | |||||||
| chr5:157851976 | A | G | 1 | a0001c0001t0006g0009 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.41+6954T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851976 | |||||||
| chr5:157852047 | G | T | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+6883C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852047 | |||||||
| chr5:157852200 | T | A | 3 | a0001c0001t0002g0135 a0001c0001t0002g0180 a0001c0001t0002g0181 |
3 | NA18612.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.41+6730A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852200 | |||||||
| chr5:157852206 | T | C | 2 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
2 | HG00423.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.41+6724A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852206 | |||||||
| chr5:157852235 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.41+6695G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852235 | |||||||
| chr5:157852471 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0228 a0001c0001t0001g0229 |
4 | NA18941.hp1 NA19062.hp2 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+6459A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852471 | |||||||
| chr5:157852478 | A | G | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+6452T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852478 | |||||||
| chr5:157852500 | C | T | 2 | a0001c0001t0004g0096 a0001c0001t0004g0158 |
2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.41+6430G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852500 | |||||||
| chr5:157852554 | A | C | 1 | a0001c0001t0001g0266 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.41+6376T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852554 | |||||||
| chr5:157852561 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.41+6369T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852561 | |||||||
| chr5:157852675 | C | T | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+6255G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852675 | |||||||
| chr5:157852752 | C | G | 228 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(225): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.41+6178G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852752 | |||||||
| chr5:157852820 | T | C | 33 | a0001c0001t0004g0004 a0001c0001t0004g0082 a0001c0001t0004g0084 others(30): Show |
34 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.41+6110A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852820 | |||||||
| chr5:157852896 | C | T | 2 | a0001c0001t0003g0021 a0001c0001t0003g0059 |
2 | HG02129.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.41+6034G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852896 | |||||||
| chr5:157853111 | G | T | 97 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(94): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.41+5819C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853111 | |||||||
| chr5:157853123 | A | G | 247 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(244): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.41+5807T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853123 | |||||||
| chr5:157853173 | C | G | 2 | a0001c0001t0002g0136 a0001c0001t0002g0157 |
2 | NA19066.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.41+5757G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853173 | |||||||
| chr5:157853282 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.41+5648C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853282 | |||||||
| chr5:157853353 | GA | G | 69 | a0001c0001t0001g0291 a0001c0001t0002g0040 a0001c0001t0003g0001 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.41+5576delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853353 | |||||||
| chr5:157853388 | A | G | 69 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(66): Show |
70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.41+5542T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853388 | |||||||
| chr5:157853404 | A | G | 1 | a0001c0001t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.41+5526T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853404 | |||||||
| chr5:157853423 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.41+5507A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853423 | |||||||
| chr5:157853550 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41+5380C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853550 | |||||||
| chr5:157853722 | A | G | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41+5208T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853722 | |||||||
| chr5:157853777 | C | CA | 38 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0229 others(35): Show |
39 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.41+5152dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853777 | |||||||
| chr5:157853777 | CA | C | 113 | a0001c0001t0001g0231 a0001c0001t0001g0269 a0001c0001t0001g0303 others(110): Show |
115 | HG00597.hp1 HG00621.hp2 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.41+5152delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853777 | |||||||
| chr5:157853777 | CAA | C | 9 | a0001c0001t0003g0020 a0001c0001t0003g0042 a0001c0001t0003g0043 others(6): Show |
9 | HG01517.hp2 HG02735.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.41+5151_41+5152del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853777 | |||||||
| chr5:157853777 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.41+5142_41+5152del others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853777 | |||||||
| chr5:157853793 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.41+5137T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853793 | |||||||
| chr5:157853796 | A | G | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41+5134T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853796 | |||||||
| chr5:157853905 | T | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0084 a0001c0001t0004g0140 others(8): Show |
12 | NA18940.hp2 NA18942.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.41+5025A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853905 | |||||||
| chr5:157854025 | A | G | 1 | a0001c0001t0002g0144 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.41+4905T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854025 | |||||||
| chr5:157854050 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(18): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+4880T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854050 | |||||||
| chr5:157854279 | C | T | 1 | a0001c0001t0007g0331 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41+4651G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854279 | |||||||
| chr5:157854313 | A | G | 1 | a0001c0002t0003g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.41+4617T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854313 | |||||||
| chr5:157854401 | T | C | 1 | a0001c0001t0003g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.41+4529A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854401 | |||||||
| chr5:157854714 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.41+4216G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854714 | |||||||
| chr5:157855141 | C | CG | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.41+3788dupC | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855141 | |||||||
| chr5:157855142 | G | GGA | 8 | a0001c0001t0001g0212 a0001c0001t0001g0275 a0001c0001t0001g0301 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.41+3787_41+3788ins others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855142 | |||||||
| chr5:157855157 | C | CG | 89 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(86): Show |
92 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.41+3772dupC | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855157 | |||||||
| chr5:157855157 | C | CGG | 75 | a0001c0001t0001g0007 a0001c0001t0001g0079 a0001c0001t0001g0230 others(72): Show |
76 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.41+3771_41+3772dup others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855157 | |||||||
| chr5:157855157 | C | CGGG | 34 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0213 others(31): Show |
35 | HG00099.hp2 HG00438.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.41+3770_41+3772dup others(3): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855157 | |||||||
| chr5:157855157 | C | CGGGG | 30 | a0001c0001t0001g0011 a0001c0001t0001g0212 a0001c0001t0002g0040 others(27): Show |
31 | HG00140.hp1 HG01884.hp2 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.41+3769_41+3772dup others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855157 | |||||||
| chr5:157855161 | G | GGC | 21 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(18): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+3768_41+3769ins others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855161 | |||||||
| chr5:157855166 | G | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(18): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+3764C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855166 | |||||||
| chr5:157855169 | C | T | 1 | a0001c0001t0003g0019 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.41+3761G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855169 | |||||||
| chr5:157855231 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG00280.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.41+3699C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855231 | |||||||
| chr5:157855279 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.41+3651G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855279 | |||||||
| chr5:157855399 | T | C | 3 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG01243.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.41+3531A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855399 | |||||||
| chr5:157855406 | T | C | 1 | a0001c0006t0001g0325 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41+3524A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855406 | |||||||
| chr5:157855495 | C | T | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+3435G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855495 | |||||||
| chr5:157855648 | T | C | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | NA18991.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.41+3282A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855648 | |||||||
| chr5:157855928 | C | A | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+3002G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855928 | |||||||
| chr5:157856144 | C | T | 1 | a0001c0001t0002g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.41+2786G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856144 | |||||||
| chr5:157856244 | C | T | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 |
3 | HG01070.hp2 HG01169.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.41+2686G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856244 | |||||||
| chr5:157856440 | T | C | 4 | a0001c0001t0002g0085 a0001c0001t0002g0191 a0001c0001t0002g0192 others(1): Show |
4 | HG02970.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+2490A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856440 | |||||||
| chr5:157856489 | G | A | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+2441C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856489 | |||||||
| chr5:157856772 | A | G | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+2158T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856772 | |||||||
| chr5:157856868 | G | A | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+2062C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856868 | |||||||
| chr5:157857067 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.41+1863G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857067 | |||||||
| chr5:157857117 | C | T | 3 | a0001c0001t0002g0086 a0001c0001t0002g0194 a0001c0001t0002g0195 |
3 | HG00735.hp2 HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.41+1813G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857117 | |||||||
| chr5:157857170 | C | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0306 a0001c0001t0001g0307 others(18): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+1760G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857170 | |||||||
| chr5:157857224 | C | CA | 14 | a0001c0001t0002g0194 a0001c0001t0002g0195 a0001c0001t0002g0196 others(11): Show |
14 | HG00609.hp1 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.41+1705dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857224 | |||||||
| chr5:157857224 | CA | C | 129 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(126): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.41+1705delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857224 | |||||||
| chr5:157857224 | CAA | C | 64 | a0001c0001t0002g0040 a0001c0001t0003g0001 a0001c0001t0003g0019 others(61): Show |
65 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.41+1704_41+1705del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857224 | |||||||
| chr5:157857296 | A | C | 6 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(3): Show |
6 | HG01081.hp1 HG01106.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+1634T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857296 | |||||||
| chr5:157857323 | G | A | 1 | a0001c0001t0003g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.41+1607C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857323 | |||||||
| chr5:157857368 | G | A | 1 | a0001c0001t0009g0328 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.41+1562C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857368 | |||||||
| chr5:157857417 | T | C | 1 | a0001c0001t0003g0209 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.41+1513A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857417 | |||||||
| chr5:157857598 | T | A | 1 | a0001c0001t0001g0329 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.41+1332A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857598 | |||||||
| chr5:157858177 | C | A | 1 | a0002c0005t0001g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+753G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858177 | |||||||
| chr5:157858206 | T | G | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+724A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858206 | |||||||
| chr5:157858294 | G | C | 1 | a0001c0001t0003g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.41+636C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858294 | |||||||
| chr5:157858542 | C | T | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(54): Show |
59 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.41+388G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858542 | |||||||
| chr5:157858720 | G | A | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.41+210C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858720 | |||||||
| chr5:157858862 | G | C | 1 | a0001c0001t0010g0330 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+68C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858862 |