Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1047 |
| ensemblid | ENSG00000153132.13 |
| hgncid | 2060 |
| symbol | CLGN |
| name | calmegin |
| refseq_nuc | NM_004362.3 |
| refseq_prot | NP_004353.1 |
| ensembl_nuc | ENST00000325617.10 |
| ensembl_prot | ENSP00000326699.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 140388453 |
| end | 140427648 |
| strand | - |
| ver | v1.2 |
| region | chr4:140388453-140427648 |
| region5000 | chr4:140383453-140432648 |
| regionname0 | CLGN_chr4_140388453_140427648 |
| regionname5000 | CLGN_chr4_140383453_140432648 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 610 | 278 | 75 | 56 | 107 | 9 | 30 | 85 | CLGN_chr4_140383453_140432648 | CLGN | MHFQA others(605): Show |
chr4 | 140383453 | 140432648 |
| a0002 | 0/0 | 610 | 57 | 4 | 12 | 34 | 1 | 6 | 26 | CLGN_chr4_140383453_140432648 | CLGN | MHFQA others(605): Show |
chr4 | 140383453 | 140432648 |
| a0003 | 0/1 | 610 | 14 | 11 | 1 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | MHFQA others(605): Show |
chr4 | 140383453 | 140432648 |
| a0004 | 0/0 | 610 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | MHFQA others(605): Show |
chr4 | 140383453 | 140432648 |
| a0005 | 0/0 | 610 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CLGN_chr4_140383453_140432648 | CLGN | MHFQA others(605): Show |
chr4 | 140383453 | 140432648 |
| a0006 | 0/0 | 607 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CLGN_chr4_140383453_140432648 | CLGN | MHFQA others(602): Show |
chr4 | 140383453 | 140432648 |
| a0007 | 0/0 | 610 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | MHFQA others(605): Show |
chr4 | 140383453 | 140432648 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1830 | 272 | 71 | 54 | 107 | 9 | 30 | CLGN_chr4_140383453_140432648 | CLGN | ATGCA others(1825): Show |
chr4 | 140383453 | 140432648 | ||
| a0001c0006 | 0/0 | 1830 | 3 | 3 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | ATGCA others(1825): Show |
chr4 | 140383453 | 140432648 | ||
| a0001c0007 | 0/0 | 1830 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | ATGCA others(1825): Show |
chr4 | 140383453 | 140432648 | ||
| a0001c0010 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | ATGCA others(1825): Show |
chr4 | 140383453 | 140432648 | ||
| a0002c0002 | 0/0 | 1830 | 52 | 4 | 10 | 34 | 1 | 3 | CLGN_chr4_140383453_140432648 | CLGN | ATGCA others(1825): Show |
chr4 | 140383453 | 140432648 | ||
| a0002c0004 | 0/0 | 1830 | 5 | 0 | 2 | 0 | 0 | 3 | CLGN_chr4_140383453_140432648 | CLGN | ATGCA others(1825): Show |
chr4 | 140383453 | 140432648 | ||
| a0003c0003 | 0/1 | 1830 | 14 | 11 | 1 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | ATGCA others(1825): Show |
chr4 | 140383453 | 140432648 | ||
| a0004c0005 | 0/0 | 1830 | 4 | 0 | 3 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | ATGCA others(1825): Show |
chr4 | 140383453 | 140432648 | ||
| a0005c0008 | 0/0 | 1830 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | ATGCA others(1825): Show |
chr4 | 140383453 | 140432648 | ||
| a0006c0009 | 0/0 | 1830 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | ATGCA others(1825): Show |
chr4 | 140383453 | 140432648 | ||
| a0007c0011 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | ATGCA others(1825): Show |
chr4 | 140383453 | 140432648 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2725 | 199 | 65 | 39 | 63 | 6 | 25 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0001c0001t0002 | 0/0 | 2725 | 64 | 3 | 15 | 41 | 3 | 2 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0001c0001t0004 | 0/0 | 2725 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0001c0001t0005 | 0/0 | 2725 | 3 | 0 | 0 | 0 | 0 | 3 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0001c0001t0006 | 0/0 | 2725 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0001c0001t0007 | 0/0 | 2725 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0001c0001t0008 | 0/0 | 2725 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0001c0006t0001 | 0/0 | 2725 | 3 | 3 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0001c0007t0001 | 0/0 | 2725 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0001c0010t0001 | 0/0 | 2725 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0002c0002t0001 | 0/0 | 2725 | 52 | 4 | 10 | 34 | 1 | 3 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0002c0004t0001 | 0/0 | 2725 | 5 | 0 | 2 | 0 | 0 | 3 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0003c0003t0001 | 0/0 | 2725 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0003c0003t0003 | 0/1 | 2725 | 9 | 7 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0003c0003t0004 | 0/0 | 2725 | 4 | 4 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0004c0005t0001 | 0/0 | 2725 | 4 | 0 | 3 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0005c0008t0001 | 0/0 | 2725 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0006c0009t0001 | 0/0 | 2725 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| a0007c0011t0001 | 0/0 | 2725 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | AGTAG others(2720): Show |
chr4 | 140383453 | 140432648 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 1 | 2 | 5 | 0 | 3 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0004 | 0/0 | 7 | 2 | 5 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0005g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0001t0008g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0006t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0006t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0006t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0007t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0001c0010t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0002c0004t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0003c0003t0003g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0003c0003t0003g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0003c0003t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0003c0003t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0003c0003t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0003c0003t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0003c0003t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0003c0003t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0004c0005t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0004c0005t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0005c0008t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0006c0009t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0006c0009t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| a0007c0011t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0201 | EUR | GBR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0065 | EUR | FIN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | FIN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00642 | hp2 | a0002 | c0004 | t0001 | g0219 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | CHS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00738 | hp2 | a0004 | c0005 | t0001 | g0026 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01070 | hp1 | a0002 | c0004 | t0001 | g0250 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01106 | hp2 | a0003 | c0003 | t0003 | g0007 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01168 | hp1 | a0004 | c0005 | t0001 | g0025 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01169 | hp1 | a0004 | c0005 | t0001 | g0025 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0236 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01256 | hp1 | a0001 | c0007 | t0001 | g0030 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01258 | hp2 | a0001 | c0007 | t0001 | g0030 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0235 | EUR | IBS | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0213 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0230 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0267 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | CDX | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CDX | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02165 | hp2 | a0001 | c0001 | t0008 | g0070 | EAS | CDX | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02258 | hp1 | a0003 | c0003 | t0004 | g0039 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0254 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0214 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0188 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02717 | hp2 | a0003 | c0003 | t0003 | g0239 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02896 | hp1 | a0003 | c0003 | t0003 | g0007 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02896 | hp2 | a0001 | c0006 | t0001 | g0198 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02897 | hp1 | a0003 | c0003 | t0003 | g0007 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0089 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0046 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03139 | hp1 | a0001 | c0006 | t0001 | g0203 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03195 | hp2 | a0003 | c0003 | t0003 | g0007 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0020 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03490 | hp1 | a0002 | c0004 | t0001 | g0128 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03491 | hp2 | a0005 | c0008 | t0001 | g0035 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03492 | hp1 | a0005 | c0008 | t0001 | g0035 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03540 | hp2 | a0003 | c0003 | t0004 | g0087 | AFR | GWD | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0261 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03710 | hp1 | a0002 | c0004 | t0001 | g0212 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0247 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0225 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0020 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG04204 | hp1 | a0006 | c0009 | t0001 | g0232 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG04228 | hp1 | a0006 | c0009 | t0001 | g0211 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | STU | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | CHB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | YRI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0266 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19043 | hp2 | a0003 | c0003 | t0003 | g0200 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19067 | hp1 | a0007 | c0011 | t0001 | g0258 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19240 | hp1 | a0001 | c0010 | t0001 | g0196 | AFR | YRI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ASW | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA20129 | hp2 | a0003 | c0003 | t0003 | g0202 | AFR | ASW | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | TSI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA20752 | hp2 | a0004 | c0005 | t0001 | g0026 | EUR | TSI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | GIH | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA20905 | hp2 | a0002 | c0004 | t0001 | g0234 | SAS | GIH | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0229 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02109 | hp1 | a0003 | c0003 | t0004 | g0088 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02486 | hp1 | a0001 | c0006 | t0001 | g0197 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0189 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG03471 | hp2 | a0003 | c0003 | t0003 | g0007 | AFR | MSL | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | USA | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA21309 | hp1 | a0003 | c0003 | t0004 | g0039 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0003 | g0199 | REF | REF | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0208 | REF | REF | CLGN_chr4_140383453_140432648 | CLGN | chr4 | 140383453 | 140432648 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:140389235 | G | A | 1 | a0006 | 2 | HG04204.hp1 HG04228.hp1 |
stop_gained | HIGH | c.1822C>T | p.Arg608* | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 15/15 | 1943/2725 | 1822/1833 | 608/610 | chr4 | 140389235 | |||
| chr4:140393998 | T | G | 1 | a0005 | 2 | HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.1193A>C | p.Glu398Ala | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/15 | 1314/2725 | 1193/1833 | 398/610 | chr4 | 140393998 | |||
| chr4:140395914 | G | A | 3 | a0002 a0006 a0007 |
60 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(57): Show |
missense_variant | MODERATE | c.1054C>T | p.Arg352Trp | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/15 | 1175/2725 | 1054/1833 | 352/610 | chr4 | 140395914 | |||
| chr4:140398867 | C | T | 1 | a0003 | 13 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(10): Show |
missense_variant | MODERATE | c.868G>A | p.Val290Ile | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/15 | 989/2725 | 868/1833 | 290/610 | chr4 | 140398867 | |||
| chr4:140398927 | G | A | 1 | a0004 | 4 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
missense_variant | MODERATE | c.808C>T | p.Pro270Ser | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/15 | 929/2725 | 808/1833 | 270/610 | chr4 | 140398927 | |||
| chr4:140402008 | C | A | 1 | a0003 | 13 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(10): Show |
missense_variant | MODERATE | c.478G>T | p.Ala160Ser | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/15 | 599/2725 | 478/1833 | 160/610 | chr4 | 140402008 | |||
| chr4:140405970 | T | C | 1 | a0007 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.391A>G | p.Ile131Val | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/15 | 512/2725 | 391/1833 | 131/610 | chr4 | 140405970 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:140392346 | G | A | 1 | a0001c0007 | 2 | HG01256.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.1524C>T | p.Thr508Thr | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/15 | 1645/2725 | 1524/1833 | 508/610 | chr4 | 140392346 | |||
| chr4:140394000 | G | A | 1 | a0001c0010 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.1191C>T | p.Phe397Phe | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/15 | 1312/2725 | 1191/1833 | 397/610 | chr4 | 140394000 | |||
| chr4:140398976 | G | A | 1 | a0002c0004 | 5 | HG00642.hp2 HG01070.hp1 HG03490.hp1 others(2): Show |
synonymous_variant | LOW | c.759C>T | p.Leu253Leu | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/15 | 880/2725 | 759/1833 | 253/610 | chr4 | 140398976 | |||
| chr4:140400496 | A | G | 1 | a0001c0006 | 3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.555T>C | p.Cys185Cys | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/15 | 676/2725 | 555/1833 | 185/610 | chr4 | 140400496 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:140388548 | A | G | 1 | a0003c0003t0003 | 8 | HG01106.hp2 HG02717.hp2 HG02896.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*676T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 15/15 | 676 | chr4 | 140388548 | ||||||
| chr4:140388603 | C | T | 1 | a0001c0001t0005 | 3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*621G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 15/15 | 621 | chr4 | 140388603 | ||||||
| chr4:140388946 | A | G | 1 | a0001c0001t0008 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 15/15 | 278 | chr4 | 140388946 | ||||||
| chr4:140389072 | T | G | 4 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(1): Show |
71 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*152A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 15/15 | 152 | chr4 | 140389072 | ||||||
| chr4:140427594 | G | T | 2 | a0001c0001t0002 a0001c0001t0008 |
65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
5_prime_UTR_variant | MODIFIER | c.-67C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/15 | 14516 | chr4 | 140427594 | ||||||
| chr4:140427632 | G | C | 1 | a0001c0001t0006 | 2 | HG02074.hp1 NA18965.hp1 |
5_prime_UTR_variant | MODIFIER | c.-105C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/15 | 14554 | chr4 | 140427632 | ||||||
| chr4:140427633 | C | T | 1 | a0001c0001t0007 | 1 | HG03130.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/15 | 14555 | chr4 | 140427633 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:140389353 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753-49T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389353 | |||||||
| chr4:140389424 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1753-120T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389424 | |||||||
| chr4:140389500 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1753-196A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389500 | |||||||
| chr4:140389505 | A | T | 1 | a0001c0006t0001g0197 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1753-201T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389505 | |||||||
| chr4:140389515 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1753-211C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389515 | |||||||
| chr4:140389547 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0010t0001g0196 |
3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1753-243G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389547 | |||||||
| chr4:140389694 | C | T | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1753-390G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389694 | |||||||
| chr4:140389702 | A | G | 1 | a0001c0001t0002g0063 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1753-398T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389702 | |||||||
| chr4:140389739 | A | G | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1753-435T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389739 | |||||||
| chr4:140389869 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1753-565A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140389869 | |||||||
| chr4:140390008 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1752+620T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390008 | |||||||
| chr4:140390048 | T | C | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1752+580A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390048 | |||||||
| chr4:140390074 | T | A | 1 | a0002c0002t0001g0236 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1752+554A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390074 | |||||||
| chr4:140390081 | C | CA | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752+546dupT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390081 | |||||||
| chr4:140390115 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
7 | HG01891.hp1 HG02622.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752+513T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390115 | |||||||
| chr4:140390132 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1752+496C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390132 | |||||||
| chr4:140390384 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1752+244A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390384 | |||||||
| chr4:140390553 | T | C | 9 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(6): Show |
14 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1752+75A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390553 | |||||||
| chr4:140390596 | C | T | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1752+32G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 14/14 | chr4 | 140390596 | |||||||
| chr4:140390806 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1652-78A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140390806 | |||||||
| chr4:140390809 | G | A | 1 | a0002c0002t0001g0253 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1652-81C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140390809 | |||||||
| chr4:140390966 | G | A | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1652-238C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140390966 | |||||||
| chr4:140391096 | A | G | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1652-368T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391096 | |||||||
| chr4:140391238 | T | C | 12 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(9): Show |
13 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1652-510A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391238 | |||||||
| chr4:140391505 | G | GTA | 12 | a0001c0001t0001g0231 a0001c0001t0001g0243 a0001c0001t0001g0252 others(9): Show |
12 | HG00673.hp1 HG01123.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651+712_1651+713d others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391505 | |||||||
| chr4:140391722 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1651+497C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391722 | |||||||
| chr4:140391891 | C | T | 3 | a0002c0002t0001g0226 a0002c0002t0001g0235 a0002c0002t0001g0251 |
3 | HG01175.hp1 HG01261.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1651+328G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391891 | |||||||
| chr4:140391936 | A | C | 1 | a0003c0003t0004g0039 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1651+283T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391936 | |||||||
| chr4:140391961 | C | T | 1 | a0002c0004t0001g0212 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1651+258G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 13/14 | chr4 | 140391961 | |||||||
| chr4:140392427 | T | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0244 |
2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1492-49A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 12/14 | chr4 | 140392427 | |||||||
| chr4:140392429 | A | G | 1 | a0003c0003t0003g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1492-51T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 12/14 | chr4 | 140392429 | |||||||
| chr4:140392554 | G | GA | 4 | a0001c0001t0002g0019 a0001c0001t0002g0073 a0001c0001t0002g0074 others(1): Show |
5 | HG01433.hp1 HG01928.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1491+31dupT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 12/14 | chr4 | 140392554 | |||||||
| chr4:140392719 | C | T | 1 | a0003c0003t0001g0201 | 1 | HG00140.hp2 | splice_region_variant&intron_variant | LOW | c.1366-8G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140392719 | |||||||
| chr4:140392876 | A | G | 8 | a0003c0003t0001g0201 a0003c0003t0003g0007 a0003c0003t0003g0200 others(5): Show |
13 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1366-165T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140392876 | |||||||
| chr4:140392902 | G | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
157 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1366-191C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140392902 | |||||||
| chr4:140393040 | A | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-329T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393040 | |||||||
| chr4:140393147 | A | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0194 |
4 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-436T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393147 | |||||||
| chr4:140393178 | T | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1366-467A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393178 | |||||||
| chr4:140393216 | C | T | 47 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(44): Show |
65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.1366-505G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393216 | |||||||
| chr4:140393268 | G | A | 3 | a0001c0001t0001g0184 a0001c0001t0006g0267 a0003c0003t0004g0039 |
4 | HG02074.hp1 HG02258.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-557C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393268 | |||||||
| chr4:140393394 | G | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1365+432C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393394 | |||||||
| chr4:140393447 | G | T | 2 | a0001c0001t0002g0018 a0001c0001t0002g0072 |
3 | NA18948.hp1 NA18983.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1365+379C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393447 | |||||||
| chr4:140393568 | A | G | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1365+258T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393568 | |||||||
| chr4:140393609 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1365+217A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 11/14 | chr4 | 140393609 | |||||||
| chr4:140394102 | A | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0181 a0001c0001t0001g0182 |
4 | HG01070.hp2 HG01071.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-61T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394102 | |||||||
| chr4:140394136 | C | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1150-95G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394136 | |||||||
| chr4:140394148 | AAG | A | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1150-109_1150-108d others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394148 | |||||||
| chr4:140394227 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1150-186A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394227 | |||||||
| chr4:140394233 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1150-192G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394233 | |||||||
| chr4:140394234 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1150-193C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394234 | |||||||
| chr4:140394364 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0224 |
2 | HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1150-323T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394364 | |||||||
| chr4:140394587 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1150-546A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394587 | |||||||
| chr4:140394849 | A | G | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1150-808T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394849 | |||||||
| chr4:140394885 | T | C | 7 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0049 others(4): Show |
11 | HG01975.hp2 HG01978.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.1150-844A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394885 | |||||||
| chr4:140394914 | G | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0181 a0001c0001t0001g0182 |
4 | HG01070.hp2 HG01071.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-873C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394914 | |||||||
| chr4:140394915 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0133 a0001c0001t0001g0155 others(1): Show |
5 | HG00140.hp1 HG01106.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1150-874G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394915 | |||||||
| chr4:140394928 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1150-887G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140394928 | |||||||
| chr4:140395006 | G | A | 1 | a0001c0010t0001g0196 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1149+813C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395006 | |||||||
| chr4:140395011 | C | T | 5 | a0003c0003t0001g0201 a0003c0003t0003g0007 a0003c0003t0003g0200 others(2): Show |
9 | HG00140.hp2 HG01106.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1149+808G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395011 | |||||||
| chr4:140395034 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1149+785C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395034 | |||||||
| chr4:140395067 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1149+752G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395067 | |||||||
| chr4:140395145 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1149+674A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395145 | |||||||
| chr4:140395159 | G | GT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
163 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.1149+659dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395159 | |||||||
| chr4:140395167 | G | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(253): Show |
342 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.1149+652C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395167 | |||||||
| chr4:140395292 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1149+527C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395292 | |||||||
| chr4:140395413 | T | C | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1149+406A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395413 | |||||||
| chr4:140395483 | A | G | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1149+336T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395483 | |||||||
| chr4:140395609 | A | G | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1149+210T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395609 | |||||||
| chr4:140395654 | T | C | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1149+165A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395654 | |||||||
| chr4:140395729 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1149+90G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 10/14 | chr4 | 140395729 | |||||||
| chr4:140396066 | G | A | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.998+26C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 9/14 | chr4 | 140396066 | |||||||
| chr4:140396510 | T | C | 3 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0010t0001g0196 |
3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.885-305A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396510 | |||||||
| chr4:140396646 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.885-441A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396646 | |||||||
| chr4:140396750 | G | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0172 |
2 | NA18998.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.885-545C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396750 | |||||||
| chr4:140396862 | C | CAT | 8 | a0001c0001t0001g0231 a0001c0001t0001g0242 a0001c0001t0001g0243 others(5): Show |
9 | HG01168.hp2 HG01256.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.885-659_885-658dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396862 | |||||||
| chr4:140396862 | CATATATA others(7): Show |
C | 5 | a0003c0003t0003g0007 a0003c0003t0003g0202 a0003c0003t0003g0239 others(2): Show |
9 | HG01106.hp2 HG02109.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.885-671_885-658del others(14): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396862 | |||||||
| chr4:140396874 | C | CAT | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.885-671_885-670dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396874 | |||||||
| chr4:140396874 | C | CATAT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0029 others(2): Show |
6 | HG00639.hp2 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.885-673_885-670dup others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396874 | |||||||
| chr4:140396874 | C | T | 2 | a0001c0006t0001g0203 a0003c0003t0001g0201 |
2 | HG00140.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.885-669G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396874 | |||||||
| chr4:140396875 | ATATATAT others(9): Show |
A | 2 | a0001c0001t0004g0188 a0001c0001t0004g0189 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.885-686_885-671del others(16): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396875 | |||||||
| chr4:140396876 | T | C | 2 | a0001c0006t0001g0203 a0003c0003t0001g0201 |
2 | HG00140.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.885-671A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396876 | |||||||
| chr4:140396878 | T | C | 1 | a0001c0006t0001g0203 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.885-673A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396878 | |||||||
| chr4:140396884 | T | C | 1 | a0001c0006t0001g0197 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.885-679A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396884 | |||||||
| chr4:140396886 | T | C | 1 | a0001c0006t0001g0197 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.885-681A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396886 | |||||||
| chr4:140396889 | A | ATATG | 9 | a0001c0001t0001g0021 a0001c0001t0001g0098 a0001c0001t0001g0099 others(6): Show |
10 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.885-685_885-684ins others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396889 | |||||||
| chr4:140396889 | A | G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0194 others(3): Show |
7 | HG01243.hp2 HG01496.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.885-684T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396889 | |||||||
| chr4:140396890 | T | C | 5 | a0003c0003t0003g0007 a0003c0003t0003g0202 a0003c0003t0003g0239 others(2): Show |
9 | HG01106.hp2 HG02109.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.885-685A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396890 | |||||||
| chr4:140396890 | T | TATAC | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.885-686_885-685ins others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396890 | |||||||
| chr4:140396891 | G | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0240 others(14): Show |
26 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.885-686C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396891 | |||||||
| chr4:140396891 | G | GTA | 53 | a0001c0001t0001g0015 a0001c0001t0001g0102 a0001c0001t0001g0209 others(50): Show |
63 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.885-688_885-687dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396891 | |||||||
| chr4:140396891 | G | GTATA | 8 | a0002c0002t0001g0002 a0002c0002t0001g0016 a0002c0002t0001g0045 others(5): Show |
11 | HG00738.hp1 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.885-690_885-687dup others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396891 | |||||||
| chr4:140396891 | G | GTATATAT others(13): Show |
2 | a0001c0001t0001g0224 a0002c0002t0001g0228 |
2 | HG03209.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.885-687_885-686ins others(20): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396891 | |||||||
| chr4:140396893 | A | G | 11 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0105 others(8): Show |
13 | HG01192.hp2 HG01243.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.885-688T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396893 | |||||||
| chr4:140396895 | A | G | 1 | a0001c0010t0001g0196 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.885-690T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396895 | |||||||
| chr4:140396897 | A | G | 2 | a0001c0001t0001g0193 a0001c0006t0001g0203 |
2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.885-692T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396897 | |||||||
| chr4:140396897 | ATATATAT others(3): Show |
A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0194 |
4 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.885-702_885-693del others(10): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396897 | |||||||
| chr4:140396898 | T | C | 1 | a0003c0003t0004g0039 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.885-693A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396898 | |||||||
| chr4:140396899 | A | G | 2 | a0001c0001t0001g0193 a0001c0006t0001g0203 |
2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.885-694T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396899 | |||||||
| chr4:140396901 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.885-696T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396901 | |||||||
| chr4:140396903 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.885-698T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396903 | |||||||
| chr4:140396904 | TATGTATA others(15): Show |
T | 1 | a0003c0003t0004g0039 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.885-721_885-700del others(22): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396904 | |||||||
| chr4:140396905 | A | ATATG | 3 | a0001c0001t0001g0032 a0001c0001t0001g0148 a0002c0004t0001g0234 |
4 | HG01070.hp2 HG01071.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.885-701_885-700ins others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396905 | |||||||
| chr4:140396905 | A | ATG | 4 | a0001c0001t0002g0008 a0001c0001t0002g0059 a0001c0001t0002g0061 others(1): Show |
7 | HG01975.hp2 HG01978.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.885-702_885-701dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396905 | |||||||
| chr4:140396905 | A | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
13 | HG01891.hp1 HG02040.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.885-700T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396905 | |||||||
| chr4:140396907 | G | A | 22 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0032 others(19): Show |
28 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.885-702C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396907 | |||||||
| chr4:140396907 | G | GTA | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.885-704_885-703dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396907 | |||||||
| chr4:140396907 | G | GTATA | 14 | a0001c0001t0001g0022 a0001c0001t0001g0105 a0001c0001t0001g0109 others(11): Show |
17 | HG00438.hp1 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.885-706_885-703dup others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396907 | |||||||
| chr4:140396907 | G | GTATATAT others(11): Show |
3 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0069 |
5 | NA18986.hp1 NA18999.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.885-703_885-702ins others(18): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396907 | |||||||
| chr4:140396922 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0194 |
4 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.885-717A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396922 | |||||||
| chr4:140396922 | TAC | T | 3 | a0003c0003t0003g0007 a0003c0003t0003g0202 a0003c0003t0003g0239 |
6 | HG01106.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.885-719_885-718del others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396922 | |||||||
| chr4:140396922 | TACAC | T | 4 | a0003c0003t0001g0201 a0003c0003t0003g0200 a0003c0003t0004g0087 others(1): Show |
4 | HG00140.hp2 HG02109.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.885-721_885-718del others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396922 | |||||||
| chr4:140396924 | C | T | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0003c0003t0003g0007 |
3 | HG02486.hp1 HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.885-719G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396924 | |||||||
| chr4:140396926 | C | T | 7 | a0001c0001t0001g0086 a0001c0001t0001g0248 a0001c0006t0001g0197 others(4): Show |
11 | HG01106.hp2 HG02300.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.885-721G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396926 | |||||||
| chr4:140396943 | A | T | 1 | a0001c0001t0001g0154 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.885-738T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140396943 | |||||||
| chr4:140397068 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.885-863G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397068 | |||||||
| chr4:140397114 | A | G | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.885-909T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397114 | |||||||
| chr4:140397128 | T | A | 17 | a0002c0002t0001g0002 a0002c0002t0001g0041 a0002c0002t0001g0044 others(14): Show |
27 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.885-923A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397128 | |||||||
| chr4:140397454 | G | C | 1 | a0001c0001t0002g0069 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.885-1249C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397454 | |||||||
| chr4:140397458 | GT | G | 14 | a0001c0001t0001g0215 a0001c0001t0001g0218 a0001c0001t0002g0064 others(11): Show |
19 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.885-1254delA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397458 | |||||||
| chr4:140397632 | G | A | 9 | a0001c0001t0001g0224 a0003c0003t0001g0201 a0003c0003t0003g0007 others(6): Show |
14 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.884+1219C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397632 | |||||||
| chr4:140397745 | A | T | 1 | a0001c0001t0002g0069 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.884+1106T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397745 | |||||||
| chr4:140397779 | C | G | 4 | a0003c0003t0003g0007 a0003c0003t0003g0200 a0003c0003t0003g0202 others(1): Show |
8 | HG01106.hp2 HG02717.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.884+1072G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397779 | |||||||
| chr4:140397860 | C | T | 2 | a0001c0001t0001g0184 a0003c0003t0004g0039 |
3 | HG02258.hp1 NA18965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.884+991G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397860 | |||||||
| chr4:140397861 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.884+990C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397861 | |||||||
| chr4:140397890 | C | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0057 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.884+961G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140397890 | |||||||
| chr4:140398229 | T | C | 3 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0010t0001g0196 |
3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.884+622A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398229 | |||||||
| chr4:140398257 | C | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0126 |
2 | HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.884+594G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398257 | |||||||
| chr4:140398263 | C | CT | 62 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0023 others(59): Show |
83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.884+587dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398263 | |||||||
| chr4:140398263 | C | CTT | 14 | a0001c0001t0001g0113 a0001c0001t0001g0171 a0001c0001t0002g0017 others(11): Show |
20 | HG01106.hp2 HG02109.hp1 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.884+586_884+587dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398263 | |||||||
| chr4:140398263 | C | CTTT | 6 | a0001c0001t0002g0049 a0001c0001t0002g0054 a0001c0001t0002g0062 others(3): Show |
6 | HG00558.hp2 HG02717.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.884+585_884+587dup others(3): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398263 | |||||||
| chr4:140398263 | CT | C | 30 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0034 others(27): Show |
36 | HG00280.hp2 HG00639.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.884+587delA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398263 | |||||||
| chr4:140398308 | C | T | 8 | a0003c0003t0001g0201 a0003c0003t0003g0007 a0003c0003t0003g0200 others(5): Show |
13 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.884+543G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398308 | |||||||
| chr4:140398343 | C | T | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.884+508G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398343 | |||||||
| chr4:140398418 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.884+433G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398418 | |||||||
| chr4:140398431 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0181 a0001c0001t0001g0182 |
4 | HG01070.hp2 HG01071.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.884+420C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398431 | |||||||
| chr4:140398639 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.884+212T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398639 | |||||||
| chr4:140398667 | A | G | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.884+184T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398667 | |||||||
| chr4:140398744 | T | C | 3 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0010t0001g0196 |
3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.884+107A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398744 | |||||||
| chr4:140398782 | C | G | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.884+69G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 8/14 | chr4 | 140398782 | |||||||
| chr4:140399210 | A | G | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.695-170T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399210 | |||||||
| chr4:140399311 | C | G | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.695-271G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399311 | |||||||
| chr4:140399314 | A | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0194 |
4 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-274T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399314 | |||||||
| chr4:140399319 | G | A | 1 | a0001c0001t0004g0189 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.695-279C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399319 | |||||||
| chr4:140399530 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0010t0001g0196 |
3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.695-490T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399530 | |||||||
| chr4:140399546 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-506C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399546 | |||||||
| chr4:140399553 | G | A | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.695-513C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399553 | |||||||
| chr4:140399586 | C | T | 2 | a0006c0009t0001g0211 a0006c0009t0001g0232 |
2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.695-546G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399586 | |||||||
| chr4:140399587 | C | A | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.695-547G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399587 | |||||||
| chr4:140399620 | T | G | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.695-580A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399620 | |||||||
| chr4:140399679 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0172 |
2 | NA18998.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.695-639A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399679 | |||||||
| chr4:140399975 | G | A | 4 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0113 others(1): Show |
4 | HG01261.hp2 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+382C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399975 | |||||||
| chr4:140399981 | G | A | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.694+376C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140399981 | |||||||
| chr4:140400028 | T | G | 3 | a0001c0001t0002g0047 a0001c0001t0002g0053 a0001c0001t0002g0065 |
3 | HG00323.hp1 HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.694+329A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400028 | |||||||
| chr4:140400045 | T | C | 1 | a0002c0002t0001g0238 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.694+312A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400045 | |||||||
| chr4:140400227 | T | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0194 |
4 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+130A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400227 | |||||||
| chr4:140400246 | T | C | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.694+111A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400246 | |||||||
| chr4:140400271 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.694+86T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400271 | |||||||
| chr4:140400308 | A | T | 2 | a0001c0001t0004g0188 a0001c0001t0004g0189 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.694+49T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 7/14 | chr4 | 140400308 | |||||||
| chr4:140400578 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.502-29C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400578 | |||||||
| chr4:140400652 | G | C | 1 | a0002c0002t0001g0261 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.502-103C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400652 | |||||||
| chr4:140400663 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.502-114T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400663 | |||||||
| chr4:140400730 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.502-181A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400730 | |||||||
| chr4:140400860 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.502-311C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400860 | |||||||
| chr4:140400998 | A | G | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.502-449T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140400998 | |||||||
| chr4:140401045 | C | T | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.502-496G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401045 | |||||||
| chr4:140401082 | C | T | 61 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(58): Show |
80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.502-533G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401082 | |||||||
| chr4:140401225 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.502-676T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401225 | |||||||
| chr4:140401265 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.502-716G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401265 | |||||||
| chr4:140401382 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.501+603A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401382 | |||||||
| chr4:140401534 | A | G | 5 | a0002c0004t0001g0128 a0002c0004t0001g0212 a0002c0004t0001g0219 others(2): Show |
5 | HG00642.hp2 HG01070.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+451T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401534 | |||||||
| chr4:140401639 | A | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.501+346T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401639 | |||||||
| chr4:140401909 | A | T | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+76T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 6/14 | chr4 | 140401909 | |||||||
| chr4:140402088 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.420-22G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402088 | |||||||
| chr4:140402115 | G | A | 11 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(8): Show |
16 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.420-49C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402115 | |||||||
| chr4:140402153 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.420-87A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402153 | |||||||
| chr4:140402511 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.420-445A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402511 | |||||||
| chr4:140402686 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.420-620A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402686 | |||||||
| chr4:140402714 | GT | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.420-649delA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402714 | |||||||
| chr4:140402781 | C | T | 1 | a0002c0002t0001g0247 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.420-715G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402781 | |||||||
| chr4:140402832 | G | A | 1 | a0001c0001t0001g0033 | 2 | NA19007.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.420-766C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402832 | |||||||
| chr4:140402945 | A | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG03490.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.420-879T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140402945 | |||||||
| chr4:140403037 | G | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0010t0001g0196 |
3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.420-971C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403037 | |||||||
| chr4:140403155 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0049 a0001c0001t0002g0062 |
4 | NA19004.hp1 NA19058.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.420-1089C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403155 | |||||||
| chr4:140403219 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.420-1153G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403219 | |||||||
| chr4:140403266 | A | C | 3 | a0002c0002t0001g0016 a0002c0002t0001g0225 a0002c0002t0001g0247 |
5 | HG00738.hp1 HG01255.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.420-1200T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403266 | |||||||
| chr4:140403345 | C | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0010t0001g0196 |
3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.420-1279G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403345 | |||||||
| chr4:140403408 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0010t0001g0196 |
3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.420-1342C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403408 | |||||||
| chr4:140403416 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.420-1350A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403416 | |||||||
| chr4:140403534 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0010t0001g0196 |
3 | HG02559.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.420-1468G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403534 | |||||||
| chr4:140403562 | C | T | 1 | a0002c0002t0001g0229 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.420-1496G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403562 | |||||||
| chr4:140403687 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.420-1621T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403687 | |||||||
| chr4:140403719 | C | T | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.420-1653G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140403719 | |||||||
| chr4:140404057 | A | G | 13 | a0001c0001t0005g0020 a0001c0001t0005g0089 a0001c0006t0001g0197 others(10): Show |
19 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.419+1885T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404057 | |||||||
| chr4:140404095 | A | T | 3 | a0001c0001t0001g0242 a0002c0002t0001g0225 a0002c0002t0001g0247 |
3 | HG02602.hp2 HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.419+1847T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404095 | |||||||
| chr4:140404099 | T | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0166 a0001c0001t0005g0020 others(1): Show |
5 | HG01071.hp2 HG03017.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.419+1843A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404099 | |||||||
| chr4:140404163 | G | A | 5 | a0003c0003t0001g0201 a0003c0003t0003g0007 a0003c0003t0003g0200 others(2): Show |
9 | HG00140.hp2 HG01106.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.419+1779C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404163 | |||||||
| chr4:140404255 | G | A | 10 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 others(7): Show |
15 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.419+1687C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404255 | |||||||
| chr4:140404283 | C | T | 47 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(44): Show |
65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.419+1659G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404283 | |||||||
| chr4:140404284 | A | G | 47 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(44): Show |
65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.419+1658T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404284 | |||||||
| chr4:140404328 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0205 |
2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.419+1614G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404328 | |||||||
| chr4:140404378 | G | C | 16 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0001t0005g0020 others(13): Show |
22 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.419+1564C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404378 | |||||||
| chr4:140404584 | A | G | 72 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(69): Show |
93 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.419+1358T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404584 | |||||||
| chr4:140404655 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.419+1287G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404655 | |||||||
| chr4:140404663 | C | CT | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.419+1278dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404663 | |||||||
| chr4:140404693 | C | T | 2 | a0001c0001t0004g0188 a0001c0001t0004g0189 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.419+1249G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404693 | |||||||
| chr4:140404773 | G | A | 3 | a0001c0001t0002g0058 a0001c0001t0002g0066 a0001c0001t0002g0084 |
3 | NA18975.hp1 NA18992.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.419+1169C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404773 | |||||||
| chr4:140404813 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0190 a0001c0001t0001g0191 |
4 | HG02698.hp2 HG03017.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.419+1129G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404813 | |||||||
| chr4:140404911 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.419+1031G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404911 | |||||||
| chr4:140404935 | CAT | C | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.419+1005_419+1006d others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140404935 | |||||||
| chr4:140405138 | ATTGT | A | 4 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0113 others(1): Show |
4 | HG01261.hp2 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.419+800_419+803del others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405138 | |||||||
| chr4:140405169 | T | A | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.419+773A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405169 | |||||||
| chr4:140405171 | TTA | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.419+769_419+770del others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405171 | |||||||
| chr4:140405172 | TA | T | 25 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0032 others(22): Show |
30 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.419+769delT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405172 | |||||||
| chr4:140405173 | A | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.419+769T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405173 | |||||||
| chr4:140405177 | T | A | 1 | a0002c0004t0001g0128 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.419+765A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405177 | |||||||
| chr4:140405178 | T | A | 1 | a0003c0003t0003g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.419+764A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405178 | |||||||
| chr4:140405178 | T | TTA | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.419+763_419+764ins others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405178 | |||||||
| chr4:140405179 | A | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(7): Show |
15 | HG00642.hp2 HG02572.hp2 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.419+763T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405179 | |||||||
| chr4:140405183 | T | TA | 13 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(10): Show |
18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.419+758_419+759ins others(1): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405183 | |||||||
| chr4:140405184 | T | A | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.419+758A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405184 | |||||||
| chr4:140405185 | T | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0246 |
4 | HG02280.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.419+757A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405185 | |||||||
| chr4:140405190 | T | A | 61 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(58): Show |
81 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.419+752A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405190 | |||||||
| chr4:140405191 | A | AT | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
158 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.419+750dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405191 | |||||||
| chr4:140405191 | A | T | 3 | a0001c0001t0001g0215 a0001c0001t0005g0020 a0001c0001t0005g0089 |
4 | HG02615.hp1 HG03017.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.419+751T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405191 | |||||||
| chr4:140405197 | T | A | 1 | a0001c0001t0001g0205 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.419+745A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405197 | |||||||
| chr4:140405329 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0150 |
3 | HG00438.hp2 HG02027.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.419+613G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405329 | |||||||
| chr4:140405333 | C | T | 13 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(10): Show |
18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.419+609G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405333 | |||||||
| chr4:140405345 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.419+597G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405345 | |||||||
| chr4:140405426 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.419+516A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405426 | |||||||
| chr4:140405430 | C | T | 13 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(10): Show |
18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.419+512G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405430 | |||||||
| chr4:140405533 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.419+409T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405533 | |||||||
| chr4:140405629 | T | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.419+313A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 5/14 | chr4 | 140405629 | |||||||
| chr4:140406126 | T | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.278-43A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406126 | |||||||
| chr4:140406252 | C | CT | 8 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(5): Show |
9 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.278-170dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406252 | |||||||
| chr4:140406252 | C | CTT | 5 | a0003c0003t0001g0201 a0003c0003t0003g0007 a0003c0003t0003g0200 others(2): Show |
9 | HG00140.hp2 HG01106.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.278-171_278-170dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406252 | |||||||
| chr4:140406441 | C | T | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.278-358G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406441 | |||||||
| chr4:140406612 | T | C | 1 | a0003c0003t0003g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.278-529A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406612 | |||||||
| chr4:140406623 | G | A | 1 | a0003c0003t0004g0039 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.278-540C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406623 | |||||||
| chr4:140406742 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.278-659A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406742 | |||||||
| chr4:140406925 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-842G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406925 | |||||||
| chr4:140406953 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.278-870A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140406953 | |||||||
| chr4:140407047 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.278-964T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407047 | |||||||
| chr4:140407058 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-975A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407058 | |||||||
| chr4:140407209 | G | A | 3 | a0002c0002t0001g0016 a0002c0002t0001g0225 a0002c0002t0001g0247 |
5 | HG00738.hp1 HG01255.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-1126C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407209 | |||||||
| chr4:140407227 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.278-1144A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407227 | |||||||
| chr4:140407328 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.278-1245G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407328 | |||||||
| chr4:140407374 | G | A | 25 | a0002c0002t0001g0016 a0002c0002t0001g0042 a0002c0002t0001g0213 others(22): Show |
28 | HG00642.hp2 HG00673.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.278-1291C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407374 | |||||||
| chr4:140407494 | A | C | 2 | a0001c0001t0001g0205 a0001c0010t0001g0196 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.278-1411T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407494 | |||||||
| chr4:140407497 | C | T | 59 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(56): Show |
78 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.278-1414G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407497 | |||||||
| chr4:140407586 | C | CA | 28 | a0001c0001t0001g0038 a0001c0001t0001g0102 a0001c0001t0001g0150 others(25): Show |
35 | HG00639.hp1 HG00673.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.278-1504dupT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407586 | |||||||
| chr4:140407586 | C | CAAA | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-1506_278-1504d others(5): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407586 | |||||||
| chr4:140407586 | CA | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
154 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.278-1504delT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407586 | |||||||
| chr4:140407757 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.278-1674C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407757 | |||||||
| chr4:140407789 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.278-1706A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407789 | |||||||
| chr4:140407935 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-1852A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407935 | |||||||
| chr4:140407950 | T | A | 3 | a0002c0002t0001g0044 a0002c0002t0001g0255 a0002c0002t0001g0263 |
4 | NA18971.hp2 NA18997.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-1867A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407950 | |||||||
| chr4:140407960 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.277+1877T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407960 | |||||||
| chr4:140407997 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0218 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.277+1840T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140407997 | |||||||
| chr4:140408363 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.277+1474C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408363 | |||||||
| chr4:140408458 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.277+1379A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408458 | |||||||
| chr4:140408631 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.277+1206G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408631 | |||||||
| chr4:140408668 | A | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+1169T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408668 | |||||||
| chr4:140408757 | T | A | 59 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(56): Show |
78 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.277+1080A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408757 | |||||||
| chr4:140408827 | G | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
5 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+1010C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408827 | |||||||
| chr4:140408860 | C | CAT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
173 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.277+975_277+976dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | |||||||
| chr4:140408860 | C | CATAT | 18 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0094 others(15): Show |
21 | HG00280.hp2 HG00558.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.277+973_277+976dup others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | |||||||
| chr4:140408860 | C | CATATAT | 6 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(3): Show |
6 | HG02132.hp1 HG02630.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+971_277+976dup others(6): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | |||||||
| chr4:140408860 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0086 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.277+967_277+976dup others(10): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | |||||||
| chr4:140408860 | CATAT | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.277+973_277+976del others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | |||||||
| chr4:140408860 | CATATATA others(1): Show |
C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(12): Show |
24 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.277+969_277+976del others(8): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408860 | |||||||
| chr4:140408882 | T | TAC | 3 | a0001c0001t0002g0051 a0001c0001t0002g0055 a0001c0001t0002g0057 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.277+954_277+955ins others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408882 | |||||||
| chr4:140408884 | T | C | 5 | a0001c0001t0002g0051 a0001c0001t0002g0055 a0001c0001t0002g0057 others(2): Show |
5 | HG00438.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.277+953A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408884 | |||||||
| chr4:140408884 | T | TAC | 4 | a0001c0001t0001g0176 a0001c0001t0001g0209 a0001c0001t0002g0059 others(1): Show |
4 | HG01975.hp1 HG01975.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+951_277+952dup others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408884 | |||||||
| chr4:140408884 | T | TACAC | 40 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(37): Show |
58 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.277+949_277+952dup others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140408884 | |||||||
| chr4:140409036 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.277+801T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409036 | |||||||
| chr4:140409225 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.277+612A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409225 | |||||||
| chr4:140409372 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0145 a0001c0001t0001g0146 |
4 | NA18966.hp2 NA18982.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+465G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409372 | |||||||
| chr4:140409417 | G | A | 61 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(58): Show |
80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.277+420C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409417 | |||||||
| chr4:140409498 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.277+339T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409498 | |||||||
| chr4:140409519 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+318G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409519 | |||||||
| chr4:140409556 | TG | T | 8 | a0001c0001t0001g0102 a0001c0001t0001g0217 a0001c0001t0001g0220 others(5): Show |
8 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+280delC | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409556 | |||||||
| chr4:140409557 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+280C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409557 | |||||||
| chr4:140409809 | A | G | 6 | a0001c0001t0001g0231 a0001c0001t0001g0242 a0001c0001t0001g0243 others(3): Show |
6 | HG01168.hp2 HG01256.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+28T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 4/14 | chr4 | 140409809 | |||||||
| chr4:140409984 | T | A | 10 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(7): Show |
15 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.219-89A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 3/14 | chr4 | 140409984 | |||||||
| chr4:140410172 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.219-277C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 3/14 | chr4 | 140410172 | |||||||
| chr4:140410341 | C | T | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.218+212G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 3/14 | chr4 | 140410341 | |||||||
| chr4:140410843 | CAG | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0096 a0001c0001t0001g0167 others(2): Show |
6 | HG02155.hp2 NA18991.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-219_145-218del others(2): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140410843 | |||||||
| chr4:140411196 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0170 |
2 | NA18992.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.145-570T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411196 | |||||||
| chr4:140411245 | T | C | 2 | a0001c0001t0002g0011 a0001c0001t0002g0050 |
4 | HG02523.hp1 NA18961.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-619A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411245 | |||||||
| chr4:140411303 | A | G | 1 | a0003c0003t0003g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.145-677T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411303 | |||||||
| chr4:140411408 | G | C | 4 | a0002c0002t0001g0043 a0002c0002t0001g0210 a0002c0002t0001g0254 others(1): Show |
5 | HG02258.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.145-782C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411408 | |||||||
| chr4:140411484 | T | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
5 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-858A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411484 | |||||||
| chr4:140411889 | C | T | 2 | a0002c0002t0001g0227 a0002c0002t0001g0228 |
2 | NA18986.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.144+1046G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140411889 | |||||||
| chr4:140412125 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.144+810C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412125 | |||||||
| chr4:140412150 | G | C | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.144+785C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412150 | |||||||
| chr4:140412262 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.144+673G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412262 | |||||||
| chr4:140412321 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.144+614G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412321 | |||||||
| chr4:140412649 | A | T | 3 | a0001c0006t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0203 |
3 | HG02486.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.144+286T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412649 | |||||||
| chr4:140412873 | G | A | 1 | a0001c0006t0001g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.144+62C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 2/14 | chr4 | 140412873 | |||||||
| chr4:140413348 | A | C | 1 | a0002c0002t0001g0260 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-9-261T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413348 | |||||||
| chr4:140413363 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-9-276G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413363 | |||||||
| chr4:140413497 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-410C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413497 | |||||||
| chr4:140413498 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-411A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413498 | |||||||
| chr4:140413574 | C | G | 8 | a0001c0001t0001g0102 a0001c0001t0001g0217 a0001c0001t0001g0220 others(5): Show |
8 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-487G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413574 | |||||||
| chr4:140413588 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9-501C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413588 | |||||||
| chr4:140413661 | C | T | 47 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(44): Show |
65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.-9-574G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413661 | |||||||
| chr4:140413664 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-577G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413664 | |||||||
| chr4:140413694 | T | A | 1 | a0001c0001t0002g0067 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-9-607A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413694 | |||||||
| chr4:140413707 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG01358.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-9-620G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413707 | |||||||
| chr4:140413708 | G | A | 10 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(7): Show |
15 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-621C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413708 | |||||||
| chr4:140413794 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-9-707A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413794 | |||||||
| chr4:140413863 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-9-776T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413863 | |||||||
| chr4:140413949 | A | G | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-9-862T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413949 | |||||||
| chr4:140413950 | C | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-9-863G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413950 | |||||||
| chr4:140413951 | G | A | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-864C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413951 | |||||||
| chr4:140413995 | C | T | 1 | a0002c0004t0001g0128 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-9-908G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140413995 | |||||||
| chr4:140414003 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-9-916C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414003 | |||||||
| chr4:140414131 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-9-1044A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414131 | |||||||
| chr4:140414142 | G | A | 1 | a0001c0006t0001g0203 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9-1055C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414142 | |||||||
| chr4:140414166 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-9-1079T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414166 | |||||||
| chr4:140414275 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1188G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414275 | |||||||
| chr4:140414290 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(4): Show |
11 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-1203G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414290 | |||||||
| chr4:140414387 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.-9-1300A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414387 | |||||||
| chr4:140414388 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1301C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414388 | |||||||
| chr4:140414413 | G | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
5 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1326C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414413 | |||||||
| chr4:140414459 | T | A | 18 | a0001c0001t0001g0102 a0001c0001t0001g0209 a0001c0001t0001g0217 others(15): Show |
18 | HG00639.hp1 HG01109.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9-1372A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414459 | |||||||
| chr4:140414510 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-9-1423G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414510 | |||||||
| chr4:140414592 | G | A | 10 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(7): Show |
15 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-1505C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414592 | |||||||
| chr4:140414717 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-1630G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414717 | |||||||
| chr4:140414735 | A | G | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-1648T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414735 | |||||||
| chr4:140414745 | G | T | 1 | a0001c0001t0002g0073 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-9-1658C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414745 | |||||||
| chr4:140414787 | C | T | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-1700G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414787 | |||||||
| chr4:140414797 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1710G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414797 | |||||||
| chr4:140414830 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-9-1743C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414830 | |||||||
| chr4:140414895 | T | C | 10 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(7): Show |
15 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-1808A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140414895 | |||||||
| chr4:140415129 | C | A | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-2042G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415129 | |||||||
| chr4:140415224 | A | C | 2 | a0001c0001t0002g0058 a0001c0001t0002g0084 |
2 | NA18975.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-9-2137T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415224 | |||||||
| chr4:140415236 | C | G | 2 | a0006c0009t0001g0211 a0006c0009t0001g0232 |
2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-9-2149G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415236 | |||||||
| chr4:140415493 | A | G | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-2406T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415493 | |||||||
| chr4:140415588 | T | A | 2 | a0001c0001t0004g0188 a0001c0001t0004g0189 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-9-2501A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415588 | |||||||
| chr4:140415742 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-9-2655T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415742 | |||||||
| chr4:140415758 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-9-2671A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415758 | |||||||
| chr4:140415847 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-9-2760C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415847 | |||||||
| chr4:140415865 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-2778G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415865 | |||||||
| chr4:140415892 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-9-2805T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415892 | |||||||
| chr4:140415919 | C | T | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-2832G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415919 | |||||||
| chr4:140415921 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-9-2834G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415921 | |||||||
| chr4:140415944 | C | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-2857G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415944 | |||||||
| chr4:140415954 | A | G | 10 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(7): Show |
15 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-2867T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415954 | |||||||
| chr4:140415972 | G | A | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-2885C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140415972 | |||||||
| chr4:140416059 | G | A | 62 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(59): Show |
81 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-9-2972C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416059 | |||||||
| chr4:140416070 | A | T | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-2983T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416070 | |||||||
| chr4:140416136 | A | G | 44 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(41): Show |
62 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.-9-3049T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416136 | |||||||
| chr4:140416190 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-9-3103C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416190 | |||||||
| chr4:140416210 | A | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0057 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-9-3123T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416210 | |||||||
| chr4:140416332 | G | A | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-3245C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416332 | |||||||
| chr4:140416407 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9-3320G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416407 | |||||||
| chr4:140416409 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9-3322T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416409 | |||||||
| chr4:140416472 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-3385T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416472 | |||||||
| chr4:140416479 | A | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0093 others(9): Show |
21 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9-3392T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416479 | |||||||
| chr4:140416496 | G | A | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-3409C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416496 | |||||||
| chr4:140416528 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.-9-3441A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416528 | |||||||
| chr4:140416578 | A | G | 13 | a0001c0001t0001g0100 a0001c0001t0001g0205 a0001c0006t0001g0197 others(10): Show |
18 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-3491T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416578 | |||||||
| chr4:140416612 | C | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.-9-3525G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416612 | |||||||
| chr4:140416629 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3542T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416629 | |||||||
| chr4:140416674 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3587C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416674 | |||||||
| chr4:140416685 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3598T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416685 | |||||||
| chr4:140416712 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3625G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416712 | |||||||
| chr4:140416754 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3667A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416754 | |||||||
| chr4:140416764 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3677C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416764 | |||||||
| chr4:140416784 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3697C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416784 | |||||||
| chr4:140416785 | C | G | 3 | a0001c0001t0001g0100 a0001c0001t0005g0020 a0001c0001t0005g0089 |
4 | HG02818.hp1 HG03017.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-3698G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416785 | |||||||
| chr4:140416814 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3727T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416814 | |||||||
| chr4:140416816 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-3729A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416816 | |||||||
| chr4:140416880 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3793T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416880 | |||||||
| chr4:140416895 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3808T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416895 | |||||||
| chr4:140416921 | C | T | 1 | a0003c0003t0004g0039 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-9-3834G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416921 | |||||||
| chr4:140416923 | T | C | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-3836A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416923 | |||||||
| chr4:140416962 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3875G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416962 | |||||||
| chr4:140416968 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3881A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416968 | |||||||
| chr4:140416982 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-9-3895G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140416982 | |||||||
| chr4:140417007 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-3920C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417007 | |||||||
| chr4:140417031 | C | G | 61 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(58): Show |
80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-9-3944G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417031 | |||||||
| chr4:140417116 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-9-4029A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417116 | |||||||
| chr4:140417138 | C | T | 1 | a0001c0006t0001g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-9-4051G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417138 | |||||||
| chr4:140417148 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-9-4061G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417148 | |||||||
| chr4:140417150 | A | G | 1 | a0002c0004t0001g0128 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-9-4063T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417150 | |||||||
| chr4:140417268 | G | A | 59 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(56): Show |
78 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.-9-4181C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417268 | |||||||
| chr4:140417378 | T | G | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-4291A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417378 | |||||||
| chr4:140417410 | T | A | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-4323A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417410 | |||||||
| chr4:140417426 | C | T | 1 | a0001c0006t0001g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-9-4339G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417426 | |||||||
| chr4:140417444 | A | C | 1 | a0001c0001t0002g0073 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-9-4357T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417444 | |||||||
| chr4:140417456 | T | C | 6 | a0001c0001t0002g0019 a0001c0001t0002g0052 a0001c0001t0002g0073 others(3): Show |
8 | HG01346.hp2 HG01433.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-4369A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417456 | |||||||
| chr4:140417466 | C | CA | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-4380dupT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417466 | |||||||
| chr4:140417757 | G | T | 10 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(7): Show |
15 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-4670C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417757 | |||||||
| chr4:140417823 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-9-4736G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417823 | |||||||
| chr4:140417965 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9-4878G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140417965 | |||||||
| chr4:140418071 | T | C | 2 | a0001c0001t0001g0205 a0001c0010t0001g0196 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-9-4984A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418071 | |||||||
| chr4:140418136 | A | G | 12 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(9): Show |
13 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-5049T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418136 | |||||||
| chr4:140418224 | C | T | 1 | a0001c0006t0001g0203 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9-5137G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418224 | |||||||
| chr4:140418412 | A | G | 15 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(12): Show |
24 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-9-5325T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418412 | |||||||
| chr4:140418539 | G | A | 1 | a0003c0003t0004g0039 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-9-5452C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418539 | |||||||
| chr4:140418572 | T | C | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-5485A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418572 | |||||||
| chr4:140418680 | A | G | 1 | a0004c0005t0001g0025 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-9-5593T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418680 | |||||||
| chr4:140418727 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-9-5640T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418727 | |||||||
| chr4:140418741 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-5654A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418741 | |||||||
| chr4:140418745 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-9-5658T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418745 | |||||||
| chr4:140418767 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-5680T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418767 | |||||||
| chr4:140418795 | C | T | 2 | a0001c0001t0001g0217 a0002c0002t0001g0259 |
2 | HG00639.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-9-5708G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418795 | |||||||
| chr4:140418818 | G | A | 1 | a0001c0010t0001g0196 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-9-5731C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418818 | |||||||
| chr4:140418868 | A | T | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-9-5781T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418868 | |||||||
| chr4:140418916 | C | T | 1 | a0001c0001t0005g0020 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-9-5829G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418916 | |||||||
| chr4:140418931 | T | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-9-5844A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140418931 | |||||||
| chr4:140419181 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-9-6094A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419181 | |||||||
| chr4:140419197 | C | A | 12 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(9): Show |
13 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-6110G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419197 | |||||||
| chr4:140419213 | G | GA | 11 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0170 others(8): Show |
11 | HG01168.hp2 HG01175.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-6127dupT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419213 | |||||||
| chr4:140419238 | G | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-6151C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419238 | |||||||
| chr4:140419239 | T | A | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-6152A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419239 | |||||||
| chr4:140419259 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-9-6172G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419259 | |||||||
| chr4:140419423 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-6336C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419423 | |||||||
| chr4:140419444 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-9-6357G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419444 | |||||||
| chr4:140419532 | T | C | 1 | a0001c0006t0001g0203 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9-6445A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419532 | |||||||
| chr4:140419795 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 |
7 | HG02572.hp2 HG02970.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-6708C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419795 | |||||||
| chr4:140419858 | C | A | 1 | a0001c0001t0001g0125 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-9-6771G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419858 | |||||||
| chr4:140419875 | T | C | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-6788A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140419875 | |||||||
| chr4:140420096 | T | C | 3 | a0001c0001t0001g0105 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG01192.hp2 HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-7009A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420096 | |||||||
| chr4:140420114 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.-9-7027G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420114 | |||||||
| chr4:140420158 | A | G | 12 | a0001c0001t0001g0205 a0001c0006t0001g0197 a0001c0006t0001g0198 others(9): Show |
17 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-7071T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420158 | |||||||
| chr4:140420343 | T | A | 1 | a0003c0003t0003g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-10+7194A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420343 | |||||||
| chr4:140420363 | T | C | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+7174A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420363 | |||||||
| chr4:140420380 | T | A | 10 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0018 others(7): Show |
17 | HG00408.hp2 HG02074.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10+7157A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420380 | |||||||
| chr4:140420553 | T | TA | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
156 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-10+6983_-10+6984i others(3): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420553 | |||||||
| chr4:140420554 | T | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
169 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-10+6983A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420554 | |||||||
| chr4:140420554 | TA | T | 12 | a0001c0001t0001g0231 a0001c0001t0001g0248 a0001c0001t0002g0055 others(9): Show |
13 | HG01123.hp1 HG01168.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.-10+6982delT | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420554 | |||||||
| chr4:140420555 | A | T | 9 | a0001c0001t0001g0205 a0001c0001t0004g0188 a0001c0001t0004g0189 others(6): Show |
9 | HG00140.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10+6982T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420555 | |||||||
| chr4:140420556 | A | T | 3 | a0001c0001t0004g0188 a0001c0001t0004g0189 a0001c0006t0001g0203 |
3 | HG02630.hp1 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10+6981T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420556 | |||||||
| chr4:140420616 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-10+6921A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420616 | |||||||
| chr4:140420742 | C | T | 2 | a0001c0001t0004g0188 a0001c0001t0004g0189 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10+6795G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420742 | |||||||
| chr4:140420768 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-10+6769C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420768 | |||||||
| chr4:140420820 | G | T | 2 | a0001c0001t0001g0092 a0002c0004t0001g0128 |
2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-10+6717C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140420820 | |||||||
| chr4:140421044 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-10+6493T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421044 | |||||||
| chr4:140421279 | T | G | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+6258A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421279 | |||||||
| chr4:140421283 | C | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(12): Show |
24 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-10+6254G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421283 | |||||||
| chr4:140421316 | C | A | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+6221G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421316 | |||||||
| chr4:140421361 | T | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG03490.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-10+6176A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421361 | |||||||
| chr4:140421362 | G | T | 1 | a0002c0002t0001g0226 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-10+6175C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421362 | |||||||
| chr4:140421379 | T | G | 2 | a0001c0001t0004g0188 a0001c0001t0004g0189 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10+6158A>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421379 | |||||||
| chr4:140421413 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-10+6124T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421413 | |||||||
| chr4:140421425 | G | C | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-10+6112C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421425 | |||||||
| chr4:140421469 | T | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
9 | NA18939.hp1 NA18943.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+6068A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421469 | |||||||
| chr4:140421598 | A | AT | 15 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(12): Show |
24 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-10+5938dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421598 | |||||||
| chr4:140421603 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-10+5934G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421603 | |||||||
| chr4:140421697 | C | T | 1 | a0002c0002t0001g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-10+5840G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421697 | |||||||
| chr4:140421722 | G | A | 3 | a0002c0002t0001g0016 a0002c0002t0001g0225 a0002c0002t0001g0247 |
5 | HG00738.hp1 HG01255.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+5815C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421722 | |||||||
| chr4:140421862 | C | A | 1 | a0002c0002t0001g0264 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-10+5675G>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421862 | |||||||
| chr4:140421978 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-10+5559G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421978 | |||||||
| chr4:140421979 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
147 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.-10+5558T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140421979 | |||||||
| chr4:140422303 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-10+5234G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140422303 | |||||||
| chr4:140422772 | T | C | 2 | a0001c0001t0001g0205 a0001c0010t0001g0196 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-10+4765A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140422772 | |||||||
| chr4:140422840 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
5 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+4697G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140422840 | |||||||
| chr4:140422928 | T | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(10): Show |
22 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-10+4609A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140422928 | |||||||
| chr4:140422931 | C | G | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+4606G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140422931 | |||||||
| chr4:140423043 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-10+4494A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423043 | |||||||
| chr4:140423078 | G | A | 60 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0104 others(57): Show |
80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-10+4459C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423078 | |||||||
| chr4:140423262 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-10+4275T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423262 | |||||||
| chr4:140423334 | G | A | 2 | a0003c0003t0003g0007 a0003c0003t0003g0202 |
6 | HG01106.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+4203C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423334 | |||||||
| chr4:140423398 | G | T | 2 | a0002c0002t0001g0257 a0007c0011t0001g0258 |
2 | NA18963.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-10+4139C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423398 | |||||||
| chr4:140423580 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
7 | HG01891.hp1 HG02622.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+3957C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423580 | |||||||
| chr4:140423888 | A | T | 48 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(45): Show |
67 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10+3649T>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423888 | |||||||
| chr4:140423957 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10+3580G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140423957 | |||||||
| chr4:140424257 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-10+3280T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424257 | |||||||
| chr4:140424300 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0118 others(7): Show |
17 | HG00558.hp1 HG01358.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10+3237G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424300 | |||||||
| chr4:140424337 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0186 |
3 | HG02155.hp2 NA19007.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-10+3200C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424337 | |||||||
| chr4:140424450 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-10+3087G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424450 | |||||||
| chr4:140424454 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10+3083C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424454 | |||||||
| chr4:140424989 | C | G | 1 | a0003c0003t0004g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-10+2548G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140424989 | |||||||
| chr4:140425114 | T | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.-10+2423A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425114 | |||||||
| chr4:140425204 | T | C | 2 | a0001c0001t0004g0188 a0001c0001t0004g0189 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10+2333A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425204 | |||||||
| chr4:140425348 | G | A | 15 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(12): Show |
24 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-10+2189C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425348 | |||||||
| chr4:140425427 | A | AGGGTGTG others(1): Show |
3 | a0001c0001t0002g0012 a0001c0001t0002g0047 a0001c0001t0002g0076 |
5 | HG01192.hp1 NA18986.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+2102_-10+2109d others(10): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425427 | |||||||
| chr4:140425429 | G | GGT | 35 | a0001c0001t0001g0015 a0001c0001t0001g0103 a0001c0001t0001g0104 others(32): Show |
42 | HG00673.hp1 HG00673.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.-10+2106_-10+2107d others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | |||||||
| chr4:140425429 | G | GGTGT | 26 | a0001c0001t0001g0102 a0001c0001t0001g0209 a0001c0001t0001g0217 others(23): Show |
38 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.-10+2104_-10+2107d others(6): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | |||||||
| chr4:140425429 | G | GGTGTGT | 9 | a0001c0001t0001g0215 a0001c0001t0004g0188 a0002c0002t0001g0213 others(6): Show |
9 | HG01952.hp1 HG02300.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10+2102_-10+2107d others(8): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | |||||||
| chr4:140425429 | G | GGTGTGTG others(3): Show |
33 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(30): Show |
50 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-10+2107_-10+2108i others(12): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | |||||||
| chr4:140425429 | G | GGTGTGTG others(5): Show |
4 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 others(1): Show |
4 | HG01346.hp2 HG02523.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+2107_-10+2108i others(14): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | |||||||
| chr4:140425429 | G | GGTGTGTG others(4): Show |
1 | a0001c0001t0002g0048 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-10+2107_-10+2108i others(13): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | |||||||
| chr4:140425429 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0205 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-10+2098_-10+2107d others(12): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | |||||||
| chr4:140425429 | GGT | G | 5 | a0001c0001t0001g0252 a0001c0001t0005g0020 a0001c0001t0005g0089 others(2): Show |
6 | HG01070.hp1 HG01256.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+2106_-10+2107d others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | |||||||
| chr4:140425429 | GGTGT | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(2): Show |
9 | HG02109.hp1 HG02572.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+2104_-10+2107d others(6): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | |||||||
| chr4:140425429 | GGTGTGTG others(5): Show |
G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-10+2096_-10+2107d others(14): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425429 | |||||||
| chr4:140425431 | T | TGTGTGG | 4 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(1): Show |
4 | HG00408.hp2 HG00558.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+2105_-10+2106i others(8): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425431 | |||||||
| chr4:140425444 | G | GTGTC | 6 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0115 others(3): Show |
6 | HG00323.hp2 HG01175.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+2092_-10+2093i others(6): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425444 | |||||||
| chr4:140425446 | G | GTC | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
154 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.-10+2090_-10+2091i others(4): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425446 | |||||||
| chr4:140425448 | G | C | 2 | a0001c0001t0001g0034 a0005c0008t0001g0035 |
4 | HG01074.hp1 HG02559.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+2089C>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425448 | |||||||
| chr4:140425622 | C | CT | 22 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0038 others(19): Show |
27 | HG00323.hp2 HG01175.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-10+1914dupA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425622 | |||||||
| chr4:140425622 | CT | C | 8 | a0001c0001t0001g0036 a0001c0001t0002g0084 a0001c0001t0002g0085 others(5): Show |
9 | HG02109.hp1 HG02258.hp2 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+1914delA | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425622 | |||||||
| chr4:140425622 | CTTT | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(7): Show |
18 | HG00140.hp2 HG01106.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-10+1912_-10+1914d others(5): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425622 | |||||||
| chr4:140425622 | CTTTTTTT others(1): Show |
C | 14 | a0002c0002t0001g0002 a0002c0002t0001g0044 a0002c0002t0001g0045 others(11): Show |
23 | HG00408.hp1 HG00597.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.-10+1907_-10+1914d others(10): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425622 | |||||||
| chr4:140425645 | T | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(12): Show |
24 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-10+1892A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425645 | |||||||
| chr4:140425694 | T | A | 2 | a0001c0001t0001g0205 a0001c0010t0001g0196 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-10+1843A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425694 | |||||||
| chr4:140425775 | C | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(10): Show |
22 | HG00140.hp2 HG01106.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-10+1762G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425775 | |||||||
| chr4:140425876 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-10+1661C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140425876 | |||||||
| chr4:140426074 | A | G | 15 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0204 others(12): Show |
24 | HG00140.hp2 HG01106.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-10+1463T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426074 | |||||||
| chr4:140426115 | G | A | 2 | a0001c0001t0004g0188 a0001c0001t0004g0189 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-10+1422C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426115 | |||||||
| chr4:140426369 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
330 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-10+1168G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426369 | |||||||
| chr4:140426867 | T | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0190 a0001c0001t0001g0191 |
4 | HG02698.hp2 HG03017.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+670A>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426867 | |||||||
| chr4:140426894 | G | T | 1 | a0001c0006t0001g0197 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-10+643C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426894 | |||||||
| chr4:140426962 | C | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0089 |
3 | HG03017.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-10+575G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140426962 | |||||||
| chr4:140427103 | A | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
330 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-10+434T>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427103 | |||||||
| chr4:140427118 | C | CG | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
324 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(321): Show |
intron_variant | MODIFIER | c.-10+418dupC | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427118 | |||||||
| chr4:140427122 | C | G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
6 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+415G>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427122 | |||||||
| chr4:140427123 | T | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
6 | HG01243.hp2 HG01496.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+414A>G | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427123 | |||||||
| chr4:140427177 | C | T | 1 | a0001c0010t0001g0196 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-10+360G>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427177 | |||||||
| chr4:140427283 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
332 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(329): Show |
intron_variant | MODIFIER | c.-10+254T>C | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427283 | |||||||
| chr4:140427351 | G | T | 2 | a0003c0003t0004g0087 a0003c0003t0004g0088 |
2 | HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+186C>A | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427351 | |||||||
| chr4:140427408 | G | A | 65 | a0001c0001t0001g0015 a0001c0001t0001g0209 a0001c0001t0001g0215 others(62): Show |
81 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.-10+129C>T | CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427408 | |||||||
| chr4:140427448 | GGGGGAAG others(4): Show |
G | 1 | a0001c0001t0001g0086 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10+78_-10+88delGC others(9): Show |
CLGN | ENSG00000153132.13 | transcript | ENST00000325617.10 | protein_coding | 1/14 | chr4 | 140427448 |