Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100506658 |
| ensemblid | ENSG00000197822.12 |
| hgncid | 8104 |
| symbol | OCLN |
| name | occludin |
| refseq_nuc | NM_001205254.2 |
| refseq_prot | NP_001192183.1 |
| ensembl_nuc | ENST00000396442.7 |
| ensembl_prot | ENSP00000379719.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 69492790 |
| end | 69558104 |
| strand | + |
| ver | v1.2 |
| region | chr5:69492790-69558104 |
| region5000 | chr5:69487790-69563104 |
| regionname0 | OCLN_chr5_69492790_69558104 |
| regionname5000 | OCLN_chr5_69487790_69563104 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 522 | 281 | 69 | 63 | 115 | 4 | 28 | 97 | OCLN_chr5_69487790_69563104 | OCLN | MSSRP others(517): Show |
chr5 | 69487790 | 69563104 |
| a0002 | 0/0 | 522 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | MSSRP others(517): Show |
chr5 | 69487790 | 69563104 |
| a0003 | 0/0 | 522 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | MSSRP others(517): Show |
chr5 | 69487790 | 69563104 |
| a0004 | 0/0 | 522 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | MSSRP others(517): Show |
chr5 | 69487790 | 69563104 |
| a0005 | 0/0 | 522 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | MSSRP others(517): Show |
chr5 | 69487790 | 69563104 |
| a0006 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | MSSRP others(517): Show |
chr5 | 69487790 | 69563104 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1566 | 275 | 68 | 60 | 114 | 3 | 28 | OCLN_chr5_69487790_69563104 | OCLN | ATGTC others(1561): Show |
chr5 | 69487790 | 69563104 | ||
| a0001c0002 | 0/0 | 1566 | 4 | 0 | 3 | 0 | 1 | 0 | OCLN_chr5_69487790_69563104 | OCLN | ATGTC others(1561): Show |
chr5 | 69487790 | 69563104 | ||
| a0001c0007 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | ATGTC others(1561): Show |
chr5 | 69487790 | 69563104 | ||
| a0001c0008 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | ATGTC others(1561): Show |
chr5 | 69487790 | 69563104 | ||
| a0002c0003 | 0/0 | 1566 | 3 | 3 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | ATGTC others(1561): Show |
chr5 | 69487790 | 69563104 | ||
| a0002c0004 | 0/0 | 1566 | 2 | 2 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | ATGTC others(1561): Show |
chr5 | 69487790 | 69563104 | ||
| a0003c0005 | 0/0 | 1566 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | ATGTC others(1561): Show |
chr5 | 69487790 | 69563104 | ||
| a0004c0006 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | ATGTC others(1561): Show |
chr5 | 69487790 | 69563104 | ||
| a0005c0009 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | ATGTC others(1561): Show |
chr5 | 69487790 | 69563104 | ||
| a0006c0010 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | ATGTC others(1561): Show |
chr5 | 69487790 | 69563104 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6180 | 93 | 9 | 15 | 56 | 1 | 12 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0002 | 0/1 | 6178 | 60 | 31 | 11 | 6 | 1 | 10 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6173): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0003 | 1/0 | 6181 | 50 | 9 | 14 | 25 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6176): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0004 | 0/0 | 6182 | 8 | 4 | 4 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6177): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0005 | 0/0 | 6183 | 7 | 6 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6178): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0006 | 0/0 | 6178 | 5 | 0 | 1 | 4 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6173): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0007 | 0/0 | 6179 | 2 | 0 | 2 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6174): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0008 | 0/0 | 6180 | 5 | 0 | 1 | 3 | 1 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0009 | 0/0 | 6182 | 3 | 2 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6177): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0010 | 0/0 | 6180 | 5 | 0 | 0 | 5 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0011 | 0/0 | 6178 | 4 | 0 | 4 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6173): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0012 | 0/0 | 6179 | 3 | 1 | 0 | 1 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6174): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0013 | 0/0 | 6180 | 3 | 0 | 0 | 3 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0015 | 0/0 | 6184 | 3 | 3 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6179): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0016 | 0/0 | 6180 | 2 | 0 | 0 | 0 | 0 | 2 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0017 | 0/0 | 6181 | 2 | 0 | 0 | 1 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6176): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0018 | 0/0 | 6184 | 2 | 1 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6179): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0019 | 0/0 | 6181 | 2 | 0 | 0 | 2 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6176): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0020 | 0/0 | 6180 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0021 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0022 | 0/0 | 6179 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6174): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0023 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0024 | 0/0 | 6178 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6173): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0025 | 0/0 | 6180 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0027 | 0/0 | 6180 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0028 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0029 | 0/0 | 6178 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6173): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0030 | 0/0 | 6179 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6174): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0032 | 0/0 | 6181 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6176): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0033 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6176): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0034 | 0/0 | 6181 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6176): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0037 | 0/0 | 6177 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6172): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0038 | 0/0 | 6179 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6174): Show |
chr5 | 69487790 | 69563104 |
| a0001c0001t0039 | 0/0 | 6184 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6179): Show |
chr5 | 69487790 | 69563104 |
| a0001c0002t0007 | 0/0 | 6179 | 3 | 0 | 2 | 0 | 1 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6174): Show |
chr5 | 69487790 | 69563104 |
| a0001c0002t0031 | 0/0 | 6180 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0001c0007t0036 | 0/0 | 6184 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6179): Show |
chr5 | 69487790 | 69563104 |
| a0001c0008t0035 | 0/0 | 6182 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6177): Show |
chr5 | 69487790 | 69563104 |
| a0002c0003t0014 | 0/0 | 6184 | 3 | 3 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6179): Show |
chr5 | 69487790 | 69563104 |
| a0002c0004t0009 | 0/0 | 6182 | 2 | 2 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6177): Show |
chr5 | 69487790 | 69563104 |
| a0003c0005t0026 | 0/0 | 6180 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| a0004c0006t0003 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6176): Show |
chr5 | 69487790 | 69563104 |
| a0005c0009t0005 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6178): Show |
chr5 | 69487790 | 69563104 |
| a0006c0010t0001 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | AGTCC others(6175): Show |
chr5 | 69487790 | 69563104 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0002 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0007g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0009g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0010g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0010g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0010g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0010g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0011g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0011g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0011g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0012g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0012g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0013g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0013g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0013g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0015g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0015g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0016g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0016g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0017g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0017g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0018g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0018g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0019g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0019g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0020g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0021g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0022g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0023g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0024g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0025g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0027g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0028g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0029g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0030g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0032g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0033g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0034g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0037g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0038g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0001t0039g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0002t0007g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0002t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0002t0031g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0007t0036g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0001c0008t0035g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0002c0003t0014g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0002c0003t0014g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0002c0003t0014g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0002c0004t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0002c0004t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0003c0005t0026g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0004c0006t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0005c0009t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| a0006c0010t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00099 | hp2 | a0001 | c0002 | t0007 | g0007 | EUR | GBR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0254 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00733 | hp1 | a0003 | c0005 | t0026 | g0200 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00733 | hp2 | a0001 | c0001 | t0037 | g0062 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG00741 | hp2 | a0001 | c0001 | t0018 | g0192 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01074 | hp1 | a0001 | c0001 | t0011 | g0119 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0265 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01099 | hp2 | a0001 | c0001 | t0020 | g0106 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0079 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0015 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01168 | hp2 | a0001 | c0001 | t0038 | g0105 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01175 | hp1 | a0001 | c0001 | t0011 | g0177 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01175 | hp2 | a0001 | c0002 | t0031 | g0174 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01192 | hp1 | a0001 | c0002 | t0007 | g0007 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01192 | hp2 | a0001 | c0001 | t0011 | g0013 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0110 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01243 | hp2 | a0001 | c0001 | t0027 | g0215 | AMR | PUR | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0100 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01257 | hp1 | a0001 | c0002 | t0007 | g0114 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01261 | hp1 | a0001 | c0001 | t0008 | g0063 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0118 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01884 | hp1 | a0001 | c0007 | t0036 | g0262 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01891 | hp2 | a0002 | c0003 | t0014 | g0109 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01928 | hp1 | a0001 | c0001 | t0029 | g0068 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01934 | hp1 | a0001 | c0001 | t0011 | g0013 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0113 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0230 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | KHV | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02074 | hp2 | a0001 | c0001 | t0013 | g0162 | EAS | KHV | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | KHV | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02145 | hp2 | a0001 | c0001 | t0033 | g0242 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0018 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02280 | hp2 | a0001 | c0001 | t0018 | g0197 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0112 | AMR | PEL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02451 | hp2 | a0002 | c0004 | t0009 | g0207 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02615 | hp1 | a0002 | c0003 | t0014 | g0097 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02683 | hp2 | a0001 | c0001 | t0016 | g0166 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02735 | hp1 | a0001 | c0001 | t0025 | g0133 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02738 | hp1 | a0001 | c0001 | t0017 | g0191 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02886 | hp2 | a0002 | c0003 | t0014 | g0021 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02965 | hp2 | a0001 | c0001 | t0039 | g0198 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0260 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03098 | hp2 | a0004 | c0006 | t0003 | g0201 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0264 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03225 | hp2 | a0001 | c0001 | t0015 | g0018 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03453 | hp1 | a0002 | c0004 | t0009 | g0078 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03490 | hp2 | a0001 | c0001 | t0012 | g0151 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03516 | hp1 | a0005 | c0009 | t0005 | g0196 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ESN | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0081 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03834 | hp2 | a0001 | c0001 | t0016 | g0102 | SAS | BEB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | BEB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0251 | SAS | STU | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | STU | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | STU | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18747 | hp1 | a0001 | c0001 | t0008 | g0046 | EAS | CHB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18747 | hp2 | a0001 | c0001 | t0028 | g0089 | EAS | CHB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0263 | AFR | YRI | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18950 | hp2 | a0001 | c0001 | t0010 | g0148 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18957 | hp1 | a0001 | c0001 | t0012 | g0132 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18957 | hp2 | a0001 | c0001 | t0008 | g0042 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18959 | hp1 | a0001 | c0001 | t0021 | g0146 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18959 | hp2 | a0001 | c0001 | t0010 | g0023 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18961 | hp2 | a0001 | c0001 | t0006 | g0253 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18962 | hp2 | a0001 | c0001 | t0019 | g0244 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18965 | hp2 | a0001 | c0001 | t0006 | g0261 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18967 | hp2 | a0001 | c0001 | t0023 | g0073 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18968 | hp1 | a0001 | c0001 | t0019 | g0035 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18981 | hp1 | a0001 | c0001 | t0030 | g0057 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18993 | hp1 | a0001 | c0001 | t0006 | g0256 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18995 | hp1 | a0001 | c0001 | t0013 | g0183 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA18997 | hp2 | a0001 | c0001 | t0032 | g0006 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19000 | hp1 | a0001 | c0001 | t0034 | g0076 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19000 | hp2 | a0001 | c0008 | t0035 | g0033 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19005 | hp1 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19009 | hp1 | a0001 | c0001 | t0022 | g0070 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19009 | hp2 | a0001 | c0001 | t0017 | g0131 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19011 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | LWK | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | LWK | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19056 | hp2 | a0006 | c0010 | t0001 | g0082 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19058 | hp2 | a0001 | c0001 | t0024 | g0233 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19076 | hp2 | a0001 | c0001 | t0006 | g0084 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19079 | hp2 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0255 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19091 | hp1 | a0001 | c0001 | t0013 | g0028 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | YRI | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0199 | AFR | ASW | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | ASW | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0115 | EUR | TSI | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA20752 | hp2 | a0001 | c0001 | t0008 | g0045 | EUR | TSI | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | USA | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | USA | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | USA | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | LWK | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | LWK | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0250 | REF | REF | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0002 | REF | REF | OCLN_chr5_69487790_69563104 | OCLN | chr5 | 69487790 | 69563104 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:69509202 | A | G | 1 | a0006 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.112A>G | p.Met38Val | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/9 | 291/6181 | 112/1569 | 38/522 | chr5 | 69509202 | |||
| chr5:69509542 | C | T | 1 | a0005 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.452C>T | p.Ala151Val | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/9 | 631/6181 | 452/1569 | 151/522 | chr5 | 69509542 | |||
| chr5:69534724 | G | A | 1 | a0002 | 2 | HG02451.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.922G>A | p.Val308Met | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/9 | 1101/6181 | 922/1569 | 308/522 | chr5 | 69534724 | |||
| chr5:69534724 | G | C | 1 | a0002 | 3 | HG01891.hp2 HG02615.hp1 HG02886.hp2 |
missense_variant | MODERATE | c.922G>C | p.Val308Leu | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/9 | 1101/6181 | 922/1569 | 308/522 | chr5 | 69534724 | |||
| chr5:69534806 | G | A | 2 | a0003 a0004 |
2 | HG00733.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.1004G>A | p.Arg335Gln | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/9 | 1183/6181 | 1004/1569 | 335/522 | chr5 | 69534806 | |||
| chr5:69548052 | G | A | 1 | a0003 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.1376G>A | p.Arg459His | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/9 | 1555/6181 | 1376/1569 | 459/522 | chr5 | 69548052 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:69509711 | A | G | 1 | a0001c0008 | 1 | NA19000.hp2 | synonymous_variant | LOW | c.621A>G | p.Leu207Leu | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/9 | 800/6181 | 621/1569 | 207/522 | chr5 | 69509711 | |||
| chr5:69509789 | G | A | 1 | a0001c0002 | 4 | HG00099.hp2 HG01175.hp2 HG01192.hp1 others(1): Show |
synonymous_variant | LOW | c.699G>A | p.Leu233Leu | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/9 | 878/6181 | 699/1569 | 233/522 | chr5 | 69509789 | |||
| chr5:69547975 | G | A | 1 | a0001c0007 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1299G>A | p.Lys433Lys | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/9 | 1478/6181 | 1299/1569 | 433/522 | chr5 | 69547975 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:69492819 | C | T | 1 | a0001c0001t0039 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-150C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/9 | 11426 | chr5 | 69492819 | ||||||
| chr5:69553979 | C | T | 2 | a0001c0001t0010 a0001c0001t0019 |
7 | NA18950.hp2 NA18959.hp2 NA18962.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*308C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 308 | chr5 | 69553979 | ||||||
| chr5:69554017 | G | C | 1 | a0001c0001t0020 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*346G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 346 | chr5 | 69554017 | ||||||
| chr5:69554102 | A | G | 1 | a0001c0001t0015 | 3 | HG02258.hp1 HG03041.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*431A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 431 | chr5 | 69554102 | ||||||
| chr5:69554940 | AT | A | 4 | a0001c0001t0012 a0001c0001t0021 a0001c0001t0022 others(1): Show |
6 | HG03490.hp2 NA18957.hp1 NA18959.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1284delT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1284 | INFO_REALIGN_3_PRIME | chr5 | 69554940 | |||||
| chr5:69554958 | G | A | 1 | a0001c0001t0024 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1287G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1287 | chr5 | 69554958 | ||||||
| chr5:69554960 | CAG | C | 3 | a0001c0001t0011 a0001c0001t0037 a0001c0001t0038 |
6 | HG00733.hp2 HG01074.hp1 HG01168.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1292_*1293delAG | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1292 | INFO_REALIGN_3_PRIME | chr5 | 69554960 | |||||
| chr5:69555095 | G | C | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(15): Show |
131 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1424G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1424 | chr5 | 69555095 | ||||||
| chr5:69555139 | G | T | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(15): Show |
131 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1468G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1468 | chr5 | 69555139 | ||||||
| chr5:69555236 | A | AGT | 7 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0018 others(4): Show |
18 | HG00741.hp2 HG01074.hp2 HG01884.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1588_*1589dupGT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1590 | INFO_REALIGN_3_PRIME | chr5 | 69555236 | |||||
| chr5:69555236 | AGT | A | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(22): Show |
196 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*1588_*1589delGT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1588 | INFO_REALIGN_3_PRIME | chr5 | 69555236 | |||||
| chr5:69555261 | A | AT | 13 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0017 others(10): Show |
23 | HG00741.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1609dupT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1610 | INFO_REALIGN_3_PRIME | chr5 | 69555261 | |||||
| chr5:69555261 | AT | A | 7 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(4): Show |
73 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1609delT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1609 | INFO_REALIGN_3_PRIME | chr5 | 69555261 | |||||
| chr5:69555306 | C | T | 1 | a0001c0001t0028 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1635C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1635 | chr5 | 69555306 | ||||||
| chr5:69555318 | C | T | 1 | a0001c0001t0013 | 3 | HG02074.hp2 NA18995.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1647C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1647 | chr5 | 69555318 | ||||||
| chr5:69555380 | C | T | 1 | a0001c0001t0006 | 5 | HG00642.hp2 NA18961.hp2 NA18965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1709C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1709 | chr5 | 69555380 | ||||||
| chr5:69555381 | G | A | 1 | a0001c0001t0016 | 2 | HG02683.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1710G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1710 | chr5 | 69555381 | ||||||
| chr5:69555386 | C | G | 1 | a0001c0001t0034 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1715C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1715 | chr5 | 69555386 | ||||||
| chr5:69555412 | C | T | 1 | a0001c0001t0027 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1741C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1741 | chr5 | 69555412 | ||||||
| chr5:69555517 | C | T | 4 | a0001c0001t0005 a0001c0001t0018 a0002c0003t0014 others(1): Show |
13 | HG00741.hp2 HG01074.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1846C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 1846 | chr5 | 69555517 | ||||||
| chr5:69555714 | G | A | 1 | a0001c0001t0025 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2043G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 2043 | chr5 | 69555714 | ||||||
| chr5:69555994 | C | T | 1 | a0001c0001t0033 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2323C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 2323 | chr5 | 69555994 | ||||||
| chr5:69556457 | C | G | 1 | a0003c0005t0026 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2786C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 2786 | chr5 | 69556457 | ||||||
| chr5:69556664 | G | T | 3 | a0001c0001t0005 a0001c0001t0018 a0005c0009t0005 |
10 | HG00741.hp2 HG01074.hp2 HG02055.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2993G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 2993 | chr5 | 69556664 | ||||||
| chr5:69556707 | T | C | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(32): Show |
227 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*3036T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 3036 | chr5 | 69556707 | ||||||
| chr5:69557203 | A | G | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(15): Show |
131 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*3532A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 3532 | chr5 | 69557203 | ||||||
| chr5:69557336 | T | TA | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(15): Show |
131 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*3669dupA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 3670 | INFO_REALIGN_3_PRIME | chr5 | 69557336 | |||||
| chr5:69557347 | T | G | 1 | a0001c0001t0029 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3676T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 3676 | chr5 | 69557347 | ||||||
| chr5:69557631 | G | C | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(15): Show |
131 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*3960G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 3960 | chr5 | 69557631 | ||||||
| chr5:69557659 | A | G | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(15): Show |
131 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*3988A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 3988 | chr5 | 69557659 | ||||||
| chr5:69557817 | T | G | 1 | a0001c0001t0032 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4146T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 4146 | chr5 | 69557817 | ||||||
| chr5:69557845 | T | A | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(15): Show |
131 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*4174T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 4174 | chr5 | 69557845 | ||||||
| chr5:69558050 | C | T | 7 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(4): Show |
72 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*4379C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 4379 | chr5 | 69558050 | ||||||
| chr5:69558080 | A | G | 1 | a0001c0001t0015 | 3 | HG02258.hp1 HG03041.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4409A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 9/9 | 4409 | chr5 | 69558080 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:69492957 | G | C | 1 | a0001c0001t0002g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-69+57G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69492957 | |||||||
| chr5:69492986 | C | T | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(200): Show |
215 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.-69+86C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69492986 | |||||||
| chr5:69493028 | C | T | 5 | a0001c0001t0005g0019 a0001c0001t0005g0263 a0001c0001t0005g0264 others(2): Show |
6 | HG01074.hp2 HG03195.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69+128C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69493028 | |||||||
| chr5:69493132 | C | T | 21 | a0001c0001t0001g0259 a0001c0001t0002g0017 a0001c0001t0002g0245 others(18): Show |
23 | HG00642.hp2 HG01070.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.-69+232C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69493132 | |||||||
| chr5:69493205 | T | C | 2 | a0001c0001t0003g0022 a0002c0003t0014g0021 |
2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-69+305T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69493205 | |||||||
| chr5:69493212 | G | A | 1 | a0002c0004t0009g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-69+312G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69493212 | |||||||
| chr5:69493341 | G | A | 3 | a0001c0001t0009g0079 a0001c0001t0009g0080 a0001c0001t0009g0081 |
3 | HG01109.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-69+441G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69493341 | |||||||
| chr5:69493354 | C | T | 1 | a0002c0004t0009g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-69+454C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69493354 | |||||||
| chr5:69493420 | C | G | 1 | a0001c0001t0033g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-69+520C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69493420 | |||||||
| chr5:69493848 | C | G | 42 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0235 others(39): Show |
44 | HG00438.hp2 HG01167.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.-69+948C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69493848 | |||||||
| chr5:69493863 | G | C | 2 | a0001c0001t0003g0205 a0001c0001t0003g0206 |
2 | NA18939.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.-69+963G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69493863 | |||||||
| chr5:69493871 | G | C | 11 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
11 | HG00423.hp1 HG02080.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.-69+971G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69493871 | |||||||
| chr5:69493914 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-69+1014C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69493914 | |||||||
| chr5:69494084 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18962.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-69+1184C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69494084 | |||||||
| chr5:69494185 | TTG | T | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.-69+1305_-69+1306d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69494185 | ||||||
| chr5:69494189 | G | C | 134 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(131): Show |
142 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-69+1289G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69494189 | |||||||
| chr5:69494428 | C | T | 6 | a0001c0001t0005g0019 a0001c0001t0005g0263 a0001c0001t0005g0264 others(3): Show |
7 | HG01074.hp2 HG02280.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69+1528C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69494428 | |||||||
| chr5:69494468 | A | G | 2 | a0001c0001t0002g0240 a0001c0001t0002g0241 |
2 | HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-69+1568A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69494468 | |||||||
| chr5:69494613 | G | T | 41 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0235 others(38): Show |
43 | HG00438.hp2 HG01167.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-69+1713G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69494613 | |||||||
| chr5:69494729 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0003g0001 others(12): Show |
20 | HG00738.hp1 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-69+1829G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69494729 | |||||||
| chr5:69494903 | C | T | 1 | a0005c0009t0005g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-69+2003C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69494903 | |||||||
| chr5:69495072 | G | C | 2 | a0001c0001t0019g0035 a0001c0001t0019g0244 |
2 | NA18962.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-69+2172G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69495072 | |||||||
| chr5:69495087 | C | G | 1 | a0001c0001t0003g0077 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-69+2187C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69495087 | |||||||
| chr5:69495345 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-69+2445A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69495345 | |||||||
| chr5:69495572 | A | C | 1 | a0001c0001t0001g0194 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-69+2672A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69495572 | |||||||
| chr5:69495822 | C | T | 1 | a0001c0001t0002g0239 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-69+2922C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69495822 | |||||||
| chr5:69495984 | TA | T | 4 | a0001c0001t0012g0199 a0001c0001t0033g0242 a0003c0005t0026g0200 others(1): Show |
4 | HG00733.hp1 HG02145.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69+3089delA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69495984 | ||||||
| chr5:69496031 | T | C | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | NA18961.hp1 NA18979.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69+3131T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69496031 | |||||||
| chr5:69496033 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-69+3133C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69496033 | |||||||
| chr5:69496036 | A | G | 2 | a0001c0001t0003g0205 a0001c0001t0003g0206 |
2 | NA18939.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.-69+3136A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69496036 | |||||||
| chr5:69496239 | C | T | 7 | a0001c0001t0005g0019 a0001c0001t0005g0263 a0001c0001t0005g0264 others(4): Show |
8 | HG00741.hp2 HG01074.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-69+3339C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69496239 | |||||||
| chr5:69496240 | A | C | 1 | a0001c0001t0017g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-69+3340A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69496240 | |||||||
| chr5:69496559 | T | C | 6 | a0001c0001t0005g0019 a0001c0001t0005g0263 a0001c0001t0005g0264 others(3): Show |
7 | HG01074.hp2 HG02280.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69+3659T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69496559 | |||||||
| chr5:69496561 | C | CT | 13 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(10): Show |
13 | HG00438.hp1 HG00741.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.-69+3682dupT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69496561 | ||||||
| chr5:69496561 | C | CTT | 37 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0235 others(34): Show |
39 | HG00438.hp2 HG01167.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.-69+3681_-69+3682d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69496561 | ||||||
| chr5:69496561 | CT | C | 17 | a0001c0001t0001g0038 a0001c0001t0001g0101 a0001c0001t0001g0103 others(14): Show |
18 | HG01070.hp1 HG01081.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.-69+3682delT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69496561 | ||||||
| chr5:69496589 | G | A | 1 | a0002c0004t0009g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-69+3689G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69496589 | |||||||
| chr5:69496591 | T | G | 204 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(201): Show |
216 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.-69+3691T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69496591 | |||||||
| chr5:69496714 | T | C | 42 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0235 others(39): Show |
44 | HG00438.hp2 HG01167.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.-69+3814T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69496714 | |||||||
| chr5:69496778 | A | T | 1 | a0001c0001t0002g0245 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-69+3878A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69496778 | |||||||
| chr5:69497101 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-69+4201A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69497101 | |||||||
| chr5:69497135 | G | A | 1 | a0001c0001t0020g0106 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-69+4235G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69497135 | |||||||
| chr5:69497238 | AT | A | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.-69+4350delT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69497238 | ||||||
| chr5:69497247 | T | C | 1 | a0001c0001t0020g0106 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-69+4347T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69497247 | |||||||
| chr5:69497364 | C | G | 1 | a0001c0001t0003g0075 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-69+4464C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69497364 | |||||||
| chr5:69497377 | T | A | 1 | a0001c0001t0005g0263 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-69+4477T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69497377 | |||||||
| chr5:69497385 | A | AT | 116 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(113): Show |
123 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-69+4506dupT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69497385 | ||||||
| chr5:69497385 | A | ATT | 16 | a0001c0001t0001g0092 a0001c0001t0001g0175 a0001c0001t0001g0176 others(13): Show |
17 | HG00423.hp1 HG00438.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-69+4505_-69+4506d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69497385 | ||||||
| chr5:69497385 | AT | A | 9 | a0001c0001t0002g0036 a0001c0001t0002g0210 a0001c0001t0002g0211 others(6): Show |
9 | HG00741.hp2 HG01943.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-69+4506delT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69497385 | ||||||
| chr5:69497526 | T | G | 5 | a0001c0001t0003g0041 a0001c0001t0003g0069 a0001c0001t0008g0040 others(2): Show |
5 | NA18957.hp2 NA18984.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.-69+4626T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69497526 | |||||||
| chr5:69497627 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-69+4727C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69497627 | |||||||
| chr5:69497779 | G | A | 1 | a0001c0001t0039g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-69+4879G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69497779 | |||||||
| chr5:69497783 | A | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02735.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-69+4883A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69497783 | |||||||
| chr5:69498081 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-69+5181G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69498081 | |||||||
| chr5:69498107 | G | A | 118 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(115): Show |
125 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-69+5207G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69498107 | |||||||
| chr5:69498110 | C | T | 1 | a0001c0001t0007g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-69+5210C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69498110 | |||||||
| chr5:69498143 | A | T | 200 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(197): Show |
212 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.-69+5243A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69498143 | |||||||
| chr5:69498181 | A | G | 7 | a0001c0001t0002g0036 a0001c0001t0002g0039 a0001c0001t0002g0064 others(4): Show |
7 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69+5281A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69498181 | |||||||
| chr5:69498258 | C | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18962.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-69+5358C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69498258 | |||||||
| chr5:69498664 | G | T | 1 | a0001c0001t0033g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-68-5513G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69498664 | |||||||
| chr5:69498866 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68-5311A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69498866 | |||||||
| chr5:69498868 | A | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68-5309A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69498868 | |||||||
| chr5:69499140 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-68-5037G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499140 | |||||||
| chr5:69499370 | T | C | 1 | a0001c0001t0020g0106 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-68-4807T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499370 | |||||||
| chr5:69499625 | G | A | 2 | a0001c0001t0004g0112 a0001c0001t0004g0113 |
2 | HG02004.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-68-4552G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499625 | |||||||
| chr5:69499645 | C | T | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-68-4532C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499645 | |||||||
| chr5:69499663 | C | T | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-68-4514C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499663 | |||||||
| chr5:69499671 | T | G | 61 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(58): Show |
65 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.-68-4506T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499671 | |||||||
| chr5:69499790 | T | A | 3 | a0001c0001t0015g0018 a0001c0001t0015g0260 a0001c0007t0036g0262 |
4 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68-4387T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499790 | |||||||
| chr5:69499860 | C | G | 1 | a0004c0006t0003g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-68-4317C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499860 | |||||||
| chr5:69499876 | C | T | 1 | a0001c0001t0008g0063 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-68-4301C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499876 | |||||||
| chr5:69499930 | C | T | 1 | a0001c0001t0033g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-68-4247C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499930 | |||||||
| chr5:69499931 | G | T | 1 | a0002c0004t0009g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-68-4246G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499931 | |||||||
| chr5:69499991 | G | C | 25 | a0001c0001t0002g0017 a0001c0001t0002g0098 a0001c0001t0002g0099 others(22): Show |
27 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-68-4186G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69499991 | |||||||
| chr5:69500125 | C | T | 1 | a0005c0009t0005g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-68-4052C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69500125 | |||||||
| chr5:69500264 | G | T | 1 | a0001c0001t0016g0166 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-68-3913G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69500264 | |||||||
| chr5:69500359 | A | G | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0004g0011 others(2): Show |
6 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-68-3818A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69500359 | |||||||
| chr5:69500402 | T | C | 2 | a0001c0001t0004g0100 a0001c0001t0004g0118 |
2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-68-3775T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69500402 | |||||||
| chr5:69500403 | C | CT | 154 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0083 others(151): Show |
160 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.-68-3760dupT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69500403 | ||||||
| chr5:69500451 | A | T | 1 | a0002c0004t0009g0207 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-68-3726A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69500451 | |||||||
| chr5:69500732 | G | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-68-3445G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69500732 | |||||||
| chr5:69501340 | G | C | 2 | a0001c0001t0008g0045 a0001c0001t0008g0063 |
2 | HG01261.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-68-2837G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69501340 | |||||||
| chr5:69501404 | T | C | 2 | a0001c0001t0003g0071 a0001c0001t0003g0072 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-68-2773T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69501404 | |||||||
| chr5:69501490 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-68-2687C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69501490 | |||||||
| chr5:69501631 | G | GA | 8 | a0001c0001t0005g0019 a0001c0001t0005g0230 a0001c0001t0005g0263 others(5): Show |
9 | HG00741.hp2 HG01074.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-68-2533dupA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69501631 | ||||||
| chr5:69501631 | GA | G | 110 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(107): Show |
116 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-68-2533delA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 69501631 | ||||||
| chr5:69501713 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-68-2464A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69501713 | |||||||
| chr5:69502227 | A | T | 2 | a0001c0001t0015g0018 a0001c0001t0015g0260 |
3 | HG02258.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-68-1950A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69502227 | |||||||
| chr5:69502236 | T | G | 1 | a0001c0001t0006g0084 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-68-1941T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69502236 | |||||||
| chr5:69502265 | T | A | 1 | a0001c0001t0002g0014 | 2 | HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-68-1912T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69502265 | |||||||
| chr5:69502286 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-68-1891G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69502286 | |||||||
| chr5:69502291 | G | A | 17 | a0001c0001t0002g0017 a0001c0001t0002g0098 a0001c0001t0002g0099 others(14): Show |
19 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-68-1886G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69502291 | |||||||
| chr5:69502314 | A | AT | 198 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(195): Show |
209 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.-68-1863_-68-1862i others(3): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69502314 | |||||||
| chr5:69503175 | G | A | 3 | a0001c0001t0012g0199 a0003c0005t0026g0200 a0004c0006t0003g0201 |
3 | HG00733.hp1 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-68-1002G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 1/8 | chr5 | 69503175 | |||||||
| chr5:69504465 | A | G | 1 | a0001c0001t0006g0256 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.50+171A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69504465 | |||||||
| chr5:69504644 | T | C | 3 | a0001c0001t0015g0018 a0001c0001t0015g0260 a0001c0007t0036g0262 |
4 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.50+350T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69504644 | |||||||
| chr5:69504675 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.50+381G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69504675 | |||||||
| chr5:69504814 | A | G | 1 | a0001c0001t0039g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.50+520A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69504814 | |||||||
| chr5:69504940 | C | T | 1 | a0001c0001t0003g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.50+646C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69504940 | |||||||
| chr5:69504949 | G | A | 1 | a0001c0001t0008g0046 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.50+655G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69504949 | |||||||
| chr5:69505034 | G | A | 1 | a0001c0002t0007g0114 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.50+740G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69505034 | |||||||
| chr5:69505044 | G | A | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.50+750G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69505044 | |||||||
| chr5:69505158 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.50+864G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69505158 | |||||||
| chr5:69505246 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.50+952G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69505246 | |||||||
| chr5:69505331 | A | G | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.50+1037A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69505331 | |||||||
| chr5:69505691 | A | G | 1 | a0002c0003t0014g0097 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.50+1397A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69505691 | |||||||
| chr5:69505999 | T | C | 1 | a0001c0001t0023g0073 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.50+1705T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69505999 | |||||||
| chr5:69506506 | A | G | 1 | a0001c0001t0003g0003 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.50+2212A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69506506 | |||||||
| chr5:69506527 | C | T | 1 | a0001c0001t0039g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.50+2233C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69506527 | |||||||
| chr5:69506539 | C | T | 132 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(129): Show |
139 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.50+2245C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69506539 | |||||||
| chr5:69506879 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.51-2262T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69506879 | |||||||
| chr5:69507160 | A | T | 1 | a0001c0001t0001g0236 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.51-1981A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69507160 | |||||||
| chr5:69507208 | C | A | 1 | a0001c0001t0002g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.51-1933C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69507208 | |||||||
| chr5:69507669 | G | A | 1 | a0001c0001t0013g0183 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.51-1472G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69507669 | |||||||
| chr5:69508265 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0178 |
2 | HG01952.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.51-876A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69508265 | |||||||
| chr5:69508300 | C | T | 3 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0074 |
3 | HG01168.hp1 HG01169.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.51-841C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69508300 | |||||||
| chr5:69508326 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.51-815C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69508326 | |||||||
| chr5:69508745 | C | A | 1 | a0001c0001t0002g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.51-396C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69508745 | |||||||
| chr5:69508826 | T | A | 1 | a0001c0001t0002g0014 | 2 | HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.51-315T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69508826 | |||||||
| chr5:69508917 | T | C | 28 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 others(25): Show |
29 | HG01167.hp1 HG01243.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.51-224T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69508917 | |||||||
| chr5:69508945 | C | A | 1 | a0001c0001t0004g0112 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.51-196C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69508945 | |||||||
| chr5:69508998 | T | C | 8 | a0001c0001t0005g0019 a0001c0001t0005g0230 a0001c0001t0005g0263 others(5): Show |
9 | HG00741.hp2 HG01074.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.51-143T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 2/8 | chr5 | 69508998 | |||||||
| chr5:69510107 | C | T | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.729+288C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69510107 | |||||||
| chr5:69510212 | TCACA | T | 6 | a0001c0001t0005g0019 a0001c0001t0005g0263 a0001c0001t0005g0264 others(3): Show |
7 | HG01074.hp2 HG02280.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.729+396_729+399del others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr5 | 69510212 | ||||||
| chr5:69510572 | A | T | 1 | a0001c0001t0007g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.729+753A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69510572 | |||||||
| chr5:69510600 | C | T | 58 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(55): Show |
62 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.729+781C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69510600 | |||||||
| chr5:69510915 | A | G | 1 | a0001c0001t0010g0255 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.729+1096A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69510915 | |||||||
| chr5:69510980 | G | A | 1 | a0001c0001t0027g0215 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.729+1161G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69510980 | |||||||
| chr5:69511070 | T | C | 1 | a0001c0001t0002g0214 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.729+1251T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69511070 | |||||||
| chr5:69511138 | G | A | 133 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(130): Show |
140 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.729+1319G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69511138 | |||||||
| chr5:69511241 | A | AT | 123 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(120): Show |
130 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.729+1437dupT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr5 | 69511241 | ||||||
| chr5:69511241 | A | ATT | 15 | a0001c0001t0001g0091 a0001c0001t0001g0155 a0001c0001t0001g0156 others(12): Show |
15 | HG01255.hp1 HG02055.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.729+1436_729+1437d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr5 | 69511241 | ||||||
| chr5:69511373 | T | C | 181 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(178): Show |
190 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.729+1554T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69511373 | |||||||
| chr5:69511527 | T | A | 3 | a0002c0003t0014g0021 a0002c0003t0014g0097 a0002c0003t0014g0109 |
3 | HG01891.hp2 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.729+1708T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69511527 | |||||||
| chr5:69511544 | T | A | 3 | a0002c0003t0014g0021 a0002c0003t0014g0097 a0002c0003t0014g0109 |
3 | HG01891.hp2 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.729+1725T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69511544 | |||||||
| chr5:69511590 | A | T | 197 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(194): Show |
208 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.729+1771A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69511590 | |||||||
| chr5:69511763 | G | A | 1 | a0002c0003t0014g0097 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.729+1944G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69511763 | |||||||
| chr5:69512023 | CA | C | 9 | a0001c0001t0002g0065 a0001c0001t0003g0030 a0001c0001t0003g0032 others(6): Show |
9 | HG01168.hp1 HG01257.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.730-1903delA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr5 | 69512023 | ||||||
| chr5:69512036 | A | AAG | 195 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(192): Show |
206 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.730-1911_730-1910i others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr5 | 69512036 | ||||||
| chr5:69512348 | C | T | 1 | a0001c0001t0013g0162 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.730-1600C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69512348 | |||||||
| chr5:69512485 | G | A | 1 | a0001c0001t0004g0011 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.730-1463G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69512485 | |||||||
| chr5:69512595 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.730-1353G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69512595 | |||||||
| chr5:69512674 | A | G | 197 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(194): Show |
208 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.730-1274A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69512674 | |||||||
| chr5:69512700 | G | A | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.730-1248G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69512700 | |||||||
| chr5:69512747 | T | A | 2 | a0001c0001t0001g0231 a0001c0001t0002g0004 |
3 | HG00438.hp2 NA18951.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.730-1201T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69512747 | |||||||
| chr5:69513007 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.730-941C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69513007 | |||||||
| chr5:69513021 | G | A | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.730-927G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69513021 | |||||||
| chr5:69513113 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.730-835C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69513113 | |||||||
| chr5:69513389 | T | C | 3 | a0002c0003t0014g0021 a0002c0003t0014g0097 a0002c0003t0014g0109 |
3 | HG01891.hp2 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.730-559T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69513389 | |||||||
| chr5:69513469 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.730-479G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69513469 | |||||||
| chr5:69513607 | G | C | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0004g0011 others(2): Show |
6 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-341G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69513607 | |||||||
| chr5:69513614 | A | G | 1 | a0001c0001t0006g0254 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.730-334A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69513614 | |||||||
| chr5:69513625 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.730-323C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69513625 | |||||||
| chr5:69513683 | G | GATAGTTC others(324): Show |
1 | a0005c0009t0005g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.730-256_730-255ins others(331): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr5 | 69513683 | ||||||
| chr5:69513940 | C | G | 1 | a0001c0001t0001g0038 | 1 | NA18966.hp1 | splice_region_variant&intron_variant | LOW | c.730-8C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 3/8 | chr5 | 69513940 | |||||||
| chr5:69514327 | T | G | 5 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
5 | HG02080.hp2 HG04204.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+218T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69514327 | |||||||
| chr5:69514350 | T | TA | 3 | a0001c0001t0004g0011 a0001c0001t0004g0163 a0001c0001t0004g0179 |
4 | HG01891.hp1 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+248dupA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69514350 | ||||||
| chr5:69514373 | T | C | 1 | a0001c0001t0003g0005 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.891+264T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69514373 | |||||||
| chr5:69514427 | G | T | 1 | a0001c0001t0002g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.891+318G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69514427 | |||||||
| chr5:69514474 | G | A | 1 | a0001c0001t0039g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.891+365G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69514474 | |||||||
| chr5:69514886 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.891+777T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69514886 | |||||||
| chr5:69515126 | T | C | 8 | a0001c0001t0002g0245 a0001c0001t0012g0199 a0001c0001t0033g0242 others(5): Show |
8 | HG00733.hp1 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.891+1017T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515126 | |||||||
| chr5:69515131 | C | G | 1 | a0001c0001t0002g0245 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.891+1022C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515131 | |||||||
| chr5:69515131 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.891+1022C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515131 | |||||||
| chr5:69515148 | G | C | 1 | a0001c0001t0015g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.891+1039G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515148 | |||||||
| chr5:69515171 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.891+1062C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515171 | |||||||
| chr5:69515176 | G | GGACGGGG others(296): Show |
2 | a0001c0001t0015g0018 a0001c0001t0015g0260 |
3 | HG02258.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.891+1324_891+1325i others(305): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515176 | ||||||
| chr5:69515179 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0003g0054 |
2 | HG00609.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.891+1070C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515179 | |||||||
| chr5:69515180 | GGGGCGGC others(198): Show |
G | 1 | a0001c0001t0002g0245 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.891+1090_891+1294d others(2): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515180 | ||||||
| chr5:69515193 | G | A | 1 | a0002c0003t0014g0021 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.891+1084G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515193 | |||||||
| chr5:69515239 | C | G | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1130C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515239 | |||||||
| chr5:69515246 | A | C | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1137A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515246 | |||||||
| chr5:69515254 | G | A | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1145G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515254 | |||||||
| chr5:69515257 | T | C | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1148T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515257 | |||||||
| chr5:69515258 | G | A | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1149G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515258 | |||||||
| chr5:69515275 | G | A | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1166G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515275 | |||||||
| chr5:69515291 | C | T | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1182C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515291 | |||||||
| chr5:69515298 | T | C | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1189T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515298 | |||||||
| chr5:69515303 | G | A | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1194G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515303 | |||||||
| chr5:69515306 | T | C | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1197T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515306 | |||||||
| chr5:69515366 | G | C | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1257G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515366 | |||||||
| chr5:69515381 | A | G | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1272A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515381 | |||||||
| chr5:69515385 | A | G | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1276A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515385 | |||||||
| chr5:69515397 | C | T | 2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.891+1288C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515397 | |||||||
| chr5:69515402 | A | G | 3 | a0001c0001t0002g0245 a0001c0001t0003g0054 a0001c0007t0036g0262 |
3 | HG00609.hp1 HG01884.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.891+1293A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515402 | |||||||
| chr5:69515418 | T | C | 3 | a0001c0001t0002g0245 a0001c0001t0003g0054 a0001c0007t0036g0262 |
3 | HG00609.hp1 HG01884.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.891+1309T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515418 | |||||||
| chr5:69515430 | A | G | 4 | a0001c0001t0003g0054 a0001c0001t0005g0230 a0001c0001t0018g0192 others(1): Show |
4 | HG00609.hp1 HG00741.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+1321A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515430 | |||||||
| chr5:69515446 | CGGGCAGA others(72): Show |
C | 1 | a0001c0001t0002g0245 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.891+1340_891+1418d others(81): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515446 | ||||||
| chr5:69515450 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.891+1341C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515450 | |||||||
| chr5:69515451 | A | G | 1 | a0001c0001t0003g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.891+1342A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515451 | |||||||
| chr5:69515453 | A | G | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1344A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515453 | |||||||
| chr5:69515459 | T | TGACCCCC others(3): Show |
1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.891+1350_891+1351i others(12): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515459 | |||||||
| chr5:69515463 | C | G | 1 | a0001c0001t0003g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.891+1354C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515463 | |||||||
| chr5:69515466 | T | C | 2 | a0001c0001t0003g0054 a0001c0007t0036g0262 |
2 | HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.891+1357T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515466 | |||||||
| chr5:69515467 | T | C | 1 | a0001c0001t0003g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.891+1358T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515467 | |||||||
| chr5:69515470 | CAGTAGGG others(17): Show |
C | 1 | a0001c0001t0003g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.891+1362_891+1385d others(26): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515470 | |||||||
| chr5:69515473 | T | A | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.891+1364T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515473 | |||||||
| chr5:69515474 | A | C | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.891+1365A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515474 | |||||||
| chr5:69515483 | C | T | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.891+1374C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515483 | |||||||
| chr5:69515486 | G | C | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.891+1377G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515486 | |||||||
| chr5:69515488 | A | G | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.891+1379A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515488 | |||||||
| chr5:69515494 | G | C | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.891+1385G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515494 | |||||||
| chr5:69515496 | C | A | 1 | a0001c0001t0003g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.891+1387C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515496 | |||||||
| chr5:69515499 | T | C | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.891+1390T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515499 | |||||||
| chr5:69515508 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.891+1399G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515508 | |||||||
| chr5:69515516 | C | T | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.891+1407C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515516 | |||||||
| chr5:69515528 | C | A | 1 | a0001c0001t0002g0245 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.891+1419C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515528 | |||||||
| chr5:69515528 | C | CGGGGGGC others(41): Show |
1 | a0001c0001t0006g0084 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.891+1436_891+1437i others(50): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515528 | ||||||
| chr5:69515528 | C | CGGGGGGC others(92): Show |
1 | a0001c0002t0007g0007 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.891+1498_891+1499i others(101): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515528 | ||||||
| chr5:69515528 | C | CGGGGGGC others(93): Show |
1 | a0001c0001t0008g0063 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.891+1469_891+1470i others(102): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515528 | ||||||
| chr5:69515528 | C | CGGGGGGG others(95): Show |
1 | a0001c0001t0011g0013 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.891+1425_891+1426i others(104): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515528 | ||||||
| chr5:69515539 | C | CCACCCCC others(91): Show |
1 | a0001c0001t0004g0179 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.891+1431_891+1432i others(100): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCA others(40): Show |
7 | a0001c0001t0002g0252 a0001c0001t0006g0253 a0001c0001t0006g0254 others(4): Show |
7 | HG00642.hp2 HG03927.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+1436_891+1437i others(49): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(90): Show |
2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18962.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.891+1437_891+1438i others(99): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(91): Show |
1 | a0001c0001t0002g0248 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.891+1486_891+1487i others(100): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(91): Show |
44 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(41): Show |
46 | HG00099.hp2 HG00733.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.891+1498_891+1499i others(100): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(91): Show |
99 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0083 others(96): Show |
102 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.891+1498_891+1499i others(100): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(92): Show |
7 | a0001c0001t0001g0012 a0001c0001t0001g0157 a0001c0001t0001g0168 others(4): Show |
8 | HG01070.hp2 HG01071.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.891+1498_891+1499i others(101): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(91): Show |
4 | a0001c0001t0001g0181 a0001c0001t0004g0100 a0001c0001t0004g0118 others(1): Show |
4 | HG01099.hp2 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+1498_891+1499i others(100): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(92): Show |
1 | a0001c0001t0005g0230 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.891+1487_891+1488i others(101): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(93): Show |
1 | a0001c0001t0001g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.891+1487_891+1488i others(102): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(91): Show |
45 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0048 others(42): Show |
48 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.891+1469_891+1470i others(100): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(91): Show |
8 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0024 others(5): Show |
11 | HG00738.hp1 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.891+1469_891+1470i others(100): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(92): Show |
1 | a0001c0001t0003g0032 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.891+1469_891+1470i others(101): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(92): Show |
1 | a0001c0001t0003g0243 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.891+1438_891+1439i others(101): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(92): Show |
1 | a0001c0002t0031g0174 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.891+1438_891+1439i others(101): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(92): Show |
7 | a0001c0001t0001g0147 a0001c0001t0010g0148 a0001c0001t0011g0177 others(4): Show |
7 | HG01175.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+1438_891+1439i others(101): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(92): Show |
10 | a0001c0001t0001g0231 a0001c0001t0002g0004 a0001c0001t0002g0064 others(7): Show |
11 | HG00438.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+1438_891+1439i others(101): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(93): Show |
1 | a0001c0001t0024g0233 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.891+1438_891+1439i others(102): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(92): Show |
1 | a0001c0001t0003g0001 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.891+1438_891+1439i others(101): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(93): Show |
1 | a0001c0001t0001g0026 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.891+1438_891+1439i others(102): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(93): Show |
2 | a0001c0001t0003g0208 a0001c0001t0003g0209 |
2 | HG03669.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.891+1438_891+1439i others(102): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(94): Show |
2 | a0001c0001t0002g0020 a0001c0001t0002g0232 |
2 | HG03704.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.891+1438_891+1439i others(103): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(95): Show |
1 | a0001c0001t0002g0036 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.891+1438_891+1439i others(104): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515539 | C | CCCCCCCC others(96): Show |
1 | a0001c0001t0002g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.891+1438_891+1439i others(105): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515539 | ||||||
| chr5:69515540 | C | CCCCCCCC others(140): Show |
3 | a0001c0001t0002g0258 a0001c0001t0015g0018 a0001c0001t0015g0260 |
4 | HG01256.hp2 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+1498_891+1499i others(149): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515540 | ||||||
| chr5:69515567 | C | CGGCTGGC others(88): Show |
5 | a0001c0001t0005g0019 a0001c0001t0005g0263 a0001c0001t0005g0264 others(2): Show |
6 | HG01074.hp2 HG03195.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.891+1498_891+1499i others(97): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515567 | ||||||
| chr5:69515575 | C | T | 1 | a0001c0001t0006g0254 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.891+1466C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515575 | |||||||
| chr5:69515579 | C | CGGGGGGC others(91): Show |
3 | a0001c0001t0001g0165 a0001c0001t0004g0011 a0001c0001t0004g0163 |
4 | HG02818.hp1 HG02976.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+1498_891+1499i others(100): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515579 | ||||||
| chr5:69515579 | C | CGGGGGGC others(92): Show |
1 | a0001c0001t0001g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.891+1498_891+1499i others(101): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515579 | ||||||
| chr5:69515579 | C | CGGGGGGC others(93): Show |
1 | a0001c0001t0017g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.891+1498_891+1499i others(102): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515579 | ||||||
| chr5:69515579 | C | T | 1 | a0001c0001t0004g0179 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.891+1470C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515579 | |||||||
| chr5:69515657 | G | A | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.891+1548G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515657 | |||||||
| chr5:69515672 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.891+1563C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515672 | |||||||
| chr5:69515734 | C | T | 3 | a0001c0001t0009g0079 a0001c0001t0009g0080 a0001c0001t0009g0081 |
3 | HG01109.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.891+1625C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515734 | |||||||
| chr5:69515746 | G | A | 1 | a0001c0001t0005g0230 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.891+1637G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515746 | |||||||
| chr5:69515800 | G | A | 3 | a0001c0001t0012g0199 a0002c0004t0009g0078 a0002c0004t0009g0207 |
3 | HG02451.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891+1691G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515800 | |||||||
| chr5:69515857 | C | CG | 9 | a0001c0001t0001g0048 a0001c0001t0001g0123 a0001c0001t0001g0124 others(6): Show |
9 | HG00738.hp2 HG01978.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.891+1752dupG | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69515857 | ||||||
| chr5:69515986 | G | A | 3 | a0001c0001t0012g0199 a0002c0004t0009g0078 a0002c0004t0009g0207 |
3 | HG02451.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891+1877G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69515986 | |||||||
| chr5:69516089 | C | CG | 5 | a0001c0001t0001g0187 a0001c0001t0002g0217 a0001c0001t0003g0024 others(2): Show |
5 | HG02004.hp2 HG02145.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+1984dupG | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69516089 | ||||||
| chr5:69516181 | C | T | 3 | a0001c0001t0012g0199 a0002c0004t0009g0078 a0002c0004t0009g0207 |
3 | HG02451.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891+2072C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69516181 | |||||||
| chr5:69516240 | A | T | 6 | a0001c0001t0005g0019 a0001c0001t0005g0263 a0001c0001t0005g0264 others(3): Show |
7 | HG01074.hp2 HG02280.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+2131A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69516240 | |||||||
| chr5:69516252 | T | C | 3 | a0001c0001t0012g0199 a0002c0004t0009g0078 a0002c0004t0009g0207 |
3 | HG02451.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891+2143T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69516252 | |||||||
| chr5:69516279 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.891+2170G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69516279 | |||||||
| chr5:69516341 | A | T | 4 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0002g0115 others(1): Show |
4 | HG01081.hp1 HG01978.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+2232A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69516341 | |||||||
| chr5:69516406 | A | C | 1 | a0001c0001t0001g0090 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.891+2297A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69516406 | |||||||
| chr5:69516494 | AGGGAGAG others(10): Show |
A | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.891+2398_891+2414d others(19): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69516494 | ||||||
| chr5:69516509 | G | A | 3 | a0001c0001t0012g0199 a0002c0004t0009g0078 a0002c0004t0009g0207 |
3 | HG02451.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891+2400G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69516509 | |||||||
| chr5:69517259 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02735.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.891+3150C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517259 | |||||||
| chr5:69517295 | AAT | A | 33 | a0001c0001t0001g0085 a0001c0001t0001g0091 a0001c0001t0001g0152 others(30): Show |
34 | HG00438.hp1 HG00609.hp2 HG02027.hp2 others(31): Show |
intron_variant | MODIFIER | c.891+3205_891+3206d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69517295 | ||||||
| chr5:69517312 | A | G | 26 | a0001c0001t0002g0017 a0001c0001t0002g0098 a0001c0001t0002g0099 others(23): Show |
28 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.891+3203A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517312 | |||||||
| chr5:69517313 | TA | T | 2 | a0001c0001t0003g0005 a0002c0003t0014g0021 |
3 | HG01167.hp2 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.891+3205delA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517313 | |||||||
| chr5:69517314 | A | T | 8 | a0001c0001t0001g0026 a0001c0001t0002g0016 a0001c0001t0002g0064 others(5): Show |
8 | HG01257.hp2 HG01258.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.891+3205A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517314 | |||||||
| chr5:69517314 | AT | A | 13 | a0001c0001t0001g0124 a0001c0001t0001g0128 a0001c0001t0001g0187 others(10): Show |
13 | HG01891.hp2 HG01943.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.891+3219delT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69517314 | ||||||
| chr5:69517314 | ATT | A | 137 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(134): Show |
146 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.891+3218_891+3219d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69517314 | ||||||
| chr5:69517315 | T | TA | 7 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
8 | HG00438.hp2 HG00733.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.891+3206_891+3207i others(3): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517315 | |||||||
| chr5:69517316 | T | A | 8 | a0001c0001t0003g0047 a0001c0001t0003g0061 a0001c0001t0003g0069 others(5): Show |
8 | HG02280.hp2 HG03516.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.891+3207T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517316 | |||||||
| chr5:69517317 | T | A | 3 | a0001c0001t0001g0195 a0001c0001t0002g0125 a0001c0001t0003g0050 |
3 | HG02451.hp1 HG03710.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.891+3208T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517317 | |||||||
| chr5:69517318 | T | A | 34 | a0001c0001t0001g0086 a0001c0001t0001g0126 a0001c0001t0001g0127 others(31): Show |
36 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.891+3209T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517318 | |||||||
| chr5:69517319 | T | A | 1 | a0001c0001t0007g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.891+3210T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517319 | |||||||
| chr5:69517320 | T | A | 26 | a0001c0001t0001g0086 a0001c0001t0002g0017 a0001c0001t0002g0098 others(23): Show |
28 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.891+3211T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517320 | |||||||
| chr5:69517397 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.891+3288G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517397 | |||||||
| chr5:69517404 | G | A | 1 | a0001c0001t0033g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.891+3295G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517404 | |||||||
| chr5:69517799 | T | C | 130 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(127): Show |
137 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.891+3690T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517799 | |||||||
| chr5:69517799 | T | TC | 3 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0017g0191 |
3 | HG02738.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.891+3693dupC | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69517799 | ||||||
| chr5:69517834 | T | C | 1 | a0001c0001t0001g0012 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.891+3725T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517834 | |||||||
| chr5:69517839 | T | C | 1 | a0001c0001t0002g0016 | 2 | NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.891+3730T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517839 | |||||||
| chr5:69517905 | T | C | 9 | a0001c0001t0005g0019 a0001c0001t0005g0230 a0001c0001t0005g0263 others(6): Show |
10 | HG00741.hp2 HG01074.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.891+3796T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69517905 | |||||||
| chr5:69518171 | A | G | 1 | a0001c0001t0003g0060 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.891+4062A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69518171 | |||||||
| chr5:69518504 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.891+4395C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69518504 | |||||||
| chr5:69518596 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.891+4487C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69518596 | |||||||
| chr5:69518952 | G | C | 196 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(193): Show |
207 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.891+4843G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69518952 | |||||||
| chr5:69519077 | G | A | 59 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(56): Show |
63 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.891+4968G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69519077 | |||||||
| chr5:69519253 | C | A | 3 | a0001c0001t0002g0216 a0001c0001t0002g0240 a0001c0001t0002g0241 |
3 | HG02486.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.891+5144C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69519253 | |||||||
| chr5:69519293 | G | A | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.891+5184G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69519293 | |||||||
| chr5:69519473 | C | A | 1 | a0001c0001t0013g0162 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.891+5364C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69519473 | |||||||
| chr5:69519722 | T | A | 1 | a0001c0001t0006g0084 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.891+5613T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69519722 | |||||||
| chr5:69519771 | A | G | 2 | a0001c0001t0015g0018 a0001c0001t0015g0260 |
3 | HG02258.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.891+5662A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69519771 | |||||||
| chr5:69519999 | G | A | 3 | a0001c0001t0012g0199 a0002c0004t0009g0078 a0002c0004t0009g0207 |
3 | HG02451.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891+5890G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69519999 | |||||||
| chr5:69520045 | C | T | 1 | a0001c0001t0012g0151 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.891+5936C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69520045 | |||||||
| chr5:69520118 | G | T | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.891+6009G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69520118 | |||||||
| chr5:69520158 | C | T | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.891+6049C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69520158 | |||||||
| chr5:69520233 | A | G | 5 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(2): Show |
5 | NA18961.hp1 NA18979.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+6124A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69520233 | |||||||
| chr5:69520353 | C | T | 1 | a0003c0005t0026g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.891+6244C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69520353 | |||||||
| chr5:69520533 | A | G | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.891+6424A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69520533 | |||||||
| chr5:69520689 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0160 |
2 | NA18964.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.891+6580A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69520689 | |||||||
| chr5:69520725 | C | T | 58 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(55): Show |
62 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.891+6616C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69520725 | |||||||
| chr5:69520812 | A | G | 2 | a0001c0001t0002g0015 a0001c0001t0007g0015 |
2 | HG01167.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.891+6703A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69520812 | |||||||
| chr5:69520891 | A | G | 1 | a0001c0001t0006g0084 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.891+6782A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69520891 | |||||||
| chr5:69521194 | G | A | 1 | a0001c0001t0003g0003 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.891+7085G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69521194 | |||||||
| chr5:69521250 | A | G | 2 | a0002c0004t0009g0078 a0002c0004t0009g0207 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.891+7141A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69521250 | |||||||
| chr5:69521388 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.891+7279G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69521388 | |||||||
| chr5:69521712 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.891+7603G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69521712 | |||||||
| chr5:69521769 | T | A | 3 | a0001c0001t0009g0079 a0001c0001t0009g0080 a0001c0001t0009g0081 |
3 | HG01109.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.891+7660T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69521769 | |||||||
| chr5:69521913 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.891+7804G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69521913 | |||||||
| chr5:69522051 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.891+7942G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522051 | |||||||
| chr5:69522081 | G | T | 1 | a0001c0001t0003g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.891+7972G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522081 | |||||||
| chr5:69522506 | TAAAAATT others(34): Show |
T | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8398_891+8438d others(43): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522506 | |||||||
| chr5:69522551 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8442C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522551 | |||||||
| chr5:69522552 | C | A | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8443C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522552 | |||||||
| chr5:69522553 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8444A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522553 | |||||||
| chr5:69522557 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8448C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522557 | |||||||
| chr5:69522558 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8449A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522558 | |||||||
| chr5:69522561 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8452T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522561 | |||||||
| chr5:69522568 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8459T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522568 | |||||||
| chr5:69522570 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8461T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522570 | |||||||
| chr5:69522572 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8463T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522572 | |||||||
| chr5:69522575 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8466T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522575 | |||||||
| chr5:69522577 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8468T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522577 | |||||||
| chr5:69522580 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8471T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522580 | |||||||
| chr5:69522582 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8473T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522582 | |||||||
| chr5:69522584 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8475T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522584 | |||||||
| chr5:69522589 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8480T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522589 | |||||||
| chr5:69522590 | C | CAACAACG others(39): Show |
1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8481_891+8482i others(48): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522590 | |||||||
| chr5:69522591 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8482C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522591 | |||||||
| chr5:69522625 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.891+8516A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522625 | |||||||
| chr5:69522735 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.891+8626T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522735 | |||||||
| chr5:69522808 | G | C | 1 | a0001c0001t0003g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.891+8699G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522808 | |||||||
| chr5:69522874 | G | A | 3 | a0002c0003t0014g0021 a0002c0003t0014g0097 a0002c0003t0014g0109 |
3 | HG01891.hp2 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.891+8765G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522874 | |||||||
| chr5:69522879 | G | A | 1 | a0001c0001t0012g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.891+8770G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522879 | |||||||
| chr5:69522894 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0019g0035 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.891+8787_891+8797d others(13): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69522894 | ||||||
| chr5:69522894 | C | CTTTTTTT others(5): Show |
13 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0121 others(10): Show |
14 | HG01074.hp2 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.891+8786_891+8797d others(14): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69522894 | ||||||
| chr5:69522894 | C | CTTTTTTT others(6): Show |
170 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(167): Show |
180 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.891+8797_891+8798i others(15): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69522894 | ||||||
| chr5:69522894 | C | CTTTTTTT others(7): Show |
12 | a0001c0001t0001g0096 a0001c0001t0001g0153 a0001c0001t0001g0186 others(9): Show |
12 | HG01175.hp1 HG02451.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.891+8797_891+8798i others(16): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69522894 | ||||||
| chr5:69522928 | A | C | 1 | a0001c0001t0003g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.891+8819A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69522928 | |||||||
| chr5:69524108 | C | T | 119 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(116): Show |
125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.891+9999C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69524108 | |||||||
| chr5:69524403 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.892-10291G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69524403 | |||||||
| chr5:69524521 | G | T | 196 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(193): Show |
207 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.892-10173G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69524521 | |||||||
| chr5:69524841 | C | T | 1 | a0001c0001t0029g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.892-9853C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69524841 | |||||||
| chr5:69525302 | C | T | 58 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(55): Show |
62 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.892-9392C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69525302 | |||||||
| chr5:69525326 | G | A | 7 | a0001c0001t0001g0231 a0001c0001t0002g0004 a0001c0001t0002g0016 others(4): Show |
9 | HG00438.hp2 HG03669.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.892-9368G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69525326 | |||||||
| chr5:69525356 | A | G | 3 | a0001c0001t0012g0199 a0002c0004t0009g0078 a0002c0004t0009g0207 |
3 | HG02451.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.892-9338A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69525356 | |||||||
| chr5:69525588 | C | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0172 a0001c0001t0001g0173 others(1): Show |
4 | HG01071.hp1 HG01074.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-9106C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69525588 | |||||||
| chr5:69525693 | T | A | 2 | a0001c0001t0010g0023 a0001c0001t0010g0025 |
2 | NA18959.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.892-9001T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69525693 | |||||||
| chr5:69525926 | G | A | 12 | a0001c0001t0005g0019 a0001c0001t0005g0230 a0001c0001t0005g0263 others(9): Show |
13 | HG00741.hp2 HG01074.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.892-8768G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69525926 | |||||||
| chr5:69526205 | C | T | 1 | a0001c0001t0013g0183 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.892-8489C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69526205 | |||||||
| chr5:69526399 | G | T | 1 | a0001c0001t0007g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.892-8295G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69526399 | |||||||
| chr5:69526554 | C | CCAGAGCT others(13): Show |
116 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(113): Show |
122 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.892-8139_892-8120d others(22): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69526554 | ||||||
| chr5:69526575 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.892-8119G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69526575 | |||||||
| chr5:69526632 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.892-8062A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69526632 | |||||||
| chr5:69526666 | G | GA | 4 | a0001c0001t0001g0128 a0001c0001t0001g0187 a0001c0001t0012g0132 others(1): Show |
4 | NA18957.hp1 NA18967.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-8022dupA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69526666 | ||||||
| chr5:69526871 | G | C | 1 | a0001c0001t0025g0133 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.892-7823G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69526871 | |||||||
| chr5:69527048 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.892-7646C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69527048 | |||||||
| chr5:69527207 | A | T | 2 | a0001c0001t0016g0102 a0001c0001t0016g0166 |
2 | HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.892-7487A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69527207 | |||||||
| chr5:69527599 | C | T | 1 | a0001c0001t0005g0230 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.892-7095C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69527599 | |||||||
| chr5:69527695 | G | T | 1 | a0001c0001t0005g0230 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.892-6999G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69527695 | |||||||
| chr5:69527913 | T | C | 1 | a0006c0010t0001g0082 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.892-6781T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69527913 | |||||||
| chr5:69528116 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.892-6578A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69528116 | |||||||
| chr5:69528360 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.892-6334A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69528360 | |||||||
| chr5:69528411 | A | ACATGGTG others(2): Show |
197 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(194): Show |
208 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.892-6283_892-6282i others(11): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69528411 | |||||||
| chr5:69528483 | T | C | 197 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(194): Show |
208 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.892-6211T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69528483 | |||||||
| chr5:69528823 | C | G | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.892-5871C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69528823 | |||||||
| chr5:69528843 | A | G | 4 | a0001c0001t0033g0242 a0001c0001t0039g0198 a0002c0004t0009g0078 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-5851A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69528843 | |||||||
| chr5:69529038 | G | A | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.892-5656G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69529038 | |||||||
| chr5:69529059 | A | G | 61 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(58): Show |
65 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.892-5635A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69529059 | |||||||
| chr5:69529193 | A | G | 1 | a0001c0001t0027g0215 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.892-5501A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69529193 | |||||||
| chr5:69529267 | A | G | 1 | a0001c0001t0002g0017 | 2 | HG01070.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.892-5427A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69529267 | |||||||
| chr5:69529518 | C | A | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.892-5176C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69529518 | |||||||
| chr5:69529668 | A | G | 28 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 others(25): Show |
29 | HG01167.hp1 HG01243.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.892-5026A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69529668 | |||||||
| chr5:69529830 | C | T | 1 | a0004c0006t0003g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.892-4864C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69529830 | |||||||
| chr5:69529858 | C | A | 1 | a0001c0001t0002g0016 | 2 | NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.892-4836C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69529858 | |||||||
| chr5:69529944 | T | C | 1 | a0001c0001t0003g0051 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.892-4750T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69529944 | |||||||
| chr5:69530214 | C | A | 54 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(51): Show |
57 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.892-4480C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69530214 | |||||||
| chr5:69530419 | C | T | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.892-4275C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69530419 | |||||||
| chr5:69530420 | G | A | 1 | a0002c0003t0014g0109 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.892-4274G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69530420 | |||||||
| chr5:69530485 | T | A | 1 | a0001c0001t0003g0051 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.892-4209T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69530485 | |||||||
| chr5:69530961 | G | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0172 a0001c0001t0001g0173 others(1): Show |
4 | HG01071.hp1 HG01074.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-3733G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69530961 | |||||||
| chr5:69530970 | A | G | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.892-3724A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69530970 | |||||||
| chr5:69531164 | C | G | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.892-3530C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69531164 | |||||||
| chr5:69532081 | C | T | 19 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 others(16): Show |
20 | HG01167.hp1 HG02145.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.892-2613C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532081 | |||||||
| chr5:69532198 | A | C | 2 | a0002c0004t0009g0078 a0002c0004t0009g0207 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.892-2496A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532198 | |||||||
| chr5:69532299 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.892-2395A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532299 | |||||||
| chr5:69532359 | C | T | 2 | a0001c0001t0002g0248 a0001c0001t0007g0110 |
2 | HG01243.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.892-2335C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532359 | |||||||
| chr5:69532430 | G | A | 5 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0074 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-2264G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532430 | |||||||
| chr5:69532469 | A | G | 59 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(56): Show |
63 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.892-2225A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532469 | |||||||
| chr5:69532494 | T | C | 1 | a0001c0001t0016g0102 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.892-2200T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532494 | |||||||
| chr5:69532545 | T | C | 1 | a0001c0001t0002g0017 | 2 | HG01070.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.892-2149T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532545 | |||||||
| chr5:69532693 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.892-2001C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532693 | |||||||
| chr5:69532703 | C | T | 1 | a0001c0001t0021g0146 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.892-1991C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532703 | |||||||
| chr5:69532971 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.892-1723A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532971 | |||||||
| chr5:69532974 | A | AT | 25 | a0001c0001t0002g0017 a0001c0001t0002g0098 a0001c0001t0002g0099 others(22): Show |
27 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.892-1720_892-1719i others(3): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532974 | |||||||
| chr5:69532976 | T | A | 194 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(191): Show |
205 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.892-1718T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532976 | |||||||
| chr5:69532978 | T | A | 2 | a0001c0001t0001g0176 a0001c0001t0005g0230 |
2 | HG02055.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.892-1716T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69532978 | |||||||
| chr5:69532999 | A | ATG | 5 | a0001c0001t0001g0120 a0001c0001t0001g0153 a0001c0001t0001g0190 others(2): Show |
5 | HG00438.hp1 HG01243.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-1671_892-1670d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69532999 | ||||||
| chr5:69532999 | A | ATGTG | 44 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0087 others(41): Show |
44 | HG00423.hp1 HG00642.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.892-1673_892-1670d others(6): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69532999 | ||||||
| chr5:69532999 | A | ATGTGTG | 77 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0085 others(74): Show |
83 | HG00423.hp2 HG00609.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.892-1675_892-1670d others(8): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69532999 | ||||||
| chr5:69532999 | A | ATGTGTGT others(1): Show |
20 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0104 others(17): Show |
22 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.892-1677_892-1670d others(10): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69532999 | ||||||
| chr5:69532999 | A | ATGTGTGT others(3): Show |
18 | a0001c0001t0002g0211 a0001c0001t0002g0213 a0001c0001t0002g0214 others(15): Show |
19 | HG01109.hp2 HG01256.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.892-1679_892-1670d others(12): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69532999 | ||||||
| chr5:69532999 | A | ATGTGTGT others(5): Show |
3 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0241 |
3 | HG02486.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.892-1681_892-1670d others(14): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69532999 | ||||||
| chr5:69532999 | ATG | A | 12 | a0001c0001t0001g0231 a0001c0001t0002g0004 a0001c0001t0002g0016 others(9): Show |
14 | HG00438.hp2 HG00733.hp1 HG03098.hp2 others(11): Show |
intron_variant | MODIFIER | c.892-1671_892-1670d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69532999 | ||||||
| chr5:69533012 | T | TGTGTGTG others(1): Show |
18 | a0001c0001t0002g0017 a0001c0001t0002g0098 a0001c0001t0002g0099 others(15): Show |
20 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.892-1675_892-1674i others(10): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69533012 | ||||||
| chr5:69533013 | G | GTGTGTGC others(1): Show |
6 | a0001c0001t0002g0252 a0001c0001t0006g0084 a0001c0001t0006g0253 others(3): Show |
6 | HG00642.hp2 HG03927.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-1675_892-1674i others(10): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69533013 | ||||||
| chr5:69533037 | ATG | A | 4 | a0001c0001t0001g0083 a0001c0001t0001g0138 a0001c0001t0003g0137 others(1): Show |
4 | HG02135.hp1 NA18747.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-1655_892-1654d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69533037 | ||||||
| chr5:69533038 | T | C | 26 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 others(23): Show |
27 | HG01167.hp1 HG02055.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.892-1656T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533038 | |||||||
| chr5:69533039 | G | A | 192 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(189): Show |
203 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.892-1655G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533039 | |||||||
| chr5:69533046 | T | C | 1 | a0004c0006t0003g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.892-1648T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533046 | |||||||
| chr5:69533068 | T | C | 6 | a0001c0001t0002g0258 a0001c0001t0015g0018 a0001c0001t0015g0260 others(3): Show |
7 | HG01256.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-1626T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533068 | |||||||
| chr5:69533076 | C | T | 7 | a0001c0001t0002g0067 a0001c0001t0002g0258 a0001c0001t0015g0018 others(4): Show |
8 | HG01256.hp2 HG01884.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-1618C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533076 | |||||||
| chr5:69533076 | CAT | C | 25 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0093 others(22): Show |
26 | HG00423.hp2 HG01496.hp1 HG02135.hp1 others(23): Show |
intron_variant | MODIFIER | c.892-1606_892-1605d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69533076 | ||||||
| chr5:69533088 | T | C | 13 | a0001c0001t0002g0014 a0001c0001t0002g0223 a0001c0001t0002g0248 others(10): Show |
15 | HG01074.hp2 HG01243.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.892-1606T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533088 | |||||||
| chr5:69533090 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.892-1604C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533090 | |||||||
| chr5:69533092 | CACACACA others(19): Show |
C | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.892-1576_892-1551d others(28): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69533092 | ||||||
| chr5:69533106 | C | T | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.892-1588C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533106 | |||||||
| chr5:69533108 | C | CACAT | 7 | a0001c0001t0002g0252 a0001c0001t0006g0084 a0001c0001t0006g0253 others(4): Show |
7 | HG00642.hp2 HG03927.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-1585_892-1584i others(6): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69533108 | ||||||
| chr5:69533108 | C | CAT | 50 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0098 others(47): Show |
52 | HG00099.hp2 HG00741.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.892-1576_892-1575d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69533108 | ||||||
| chr5:69533108 | C | T | 133 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(130): Show |
141 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.892-1586C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533108 | |||||||
| chr5:69533118 | T | TAC | 7 | a0001c0001t0001g0140 a0001c0001t0001g0185 a0001c0001t0001g0189 others(4): Show |
7 | HG01070.hp1 HG01243.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-1560_892-1559d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69533118 | ||||||
| chr5:69533134 | C | CAT | 2 | a0001c0001t0001g0231 a0001c0001t0002g0004 |
3 | HG00438.hp2 NA18951.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.892-1552_892-1551d others(4): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69533134 | ||||||
| chr5:69533136 | T | C | 3 | a0001c0001t0003g0022 a0001c0001t0003g0058 a0001c0001t0003g0059 |
3 | HG01884.hp2 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.892-1558T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533136 | |||||||
| chr5:69533252 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.892-1442G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533252 | |||||||
| chr5:69533256 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0155 |
2 | HG02080.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.892-1438C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533256 | |||||||
| chr5:69533380 | C | T | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.892-1314C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533380 | |||||||
| chr5:69533487 | GT | G | 3 | a0002c0003t0014g0021 a0002c0003t0014g0097 a0002c0003t0014g0109 |
3 | HG01891.hp2 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.892-1206delT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533487 | |||||||
| chr5:69533489 | G | C | 3 | a0002c0003t0014g0021 a0002c0003t0014g0097 a0002c0003t0014g0109 |
3 | HG01891.hp2 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.892-1205G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533489 | |||||||
| chr5:69533491 | G | A | 3 | a0002c0003t0014g0021 a0002c0003t0014g0097 a0002c0003t0014g0109 |
3 | HG01891.hp2 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.892-1203G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533491 | |||||||
| chr5:69533492 | T | C | 3 | a0002c0003t0014g0021 a0002c0003t0014g0097 a0002c0003t0014g0109 |
3 | HG01891.hp2 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.892-1202T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533492 | |||||||
| chr5:69533593 | G | A | 196 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(193): Show |
207 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.892-1101G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533593 | |||||||
| chr5:69533794 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.892-900A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533794 | |||||||
| chr5:69533903 | A | G | 1 | a0001c0001t0039g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.892-791A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69533903 | |||||||
| chr5:69534210 | A | T | 133 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(130): Show |
140 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.892-484A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69534210 | |||||||
| chr5:69534313 | C | T | 1 | a0003c0005t0026g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.892-381C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69534313 | |||||||
| chr5:69534321 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.892-373C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69534321 | |||||||
| chr5:69534438 | C | G | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.892-256C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69534438 | |||||||
| chr5:69534668 | A | G | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.892-26A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | chr5 | 69534668 | |||||||
| chr5:69534901 | G | GGTTTTTG others(2): Show |
59 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(56): Show |
63 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1037+70_1037+71ins others(9): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69534901 | ||||||
| chr5:69535273 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1037+434C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69535273 | |||||||
| chr5:69535556 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0134 |
2 | HG00738.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1037+717G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69535556 | |||||||
| chr5:69535720 | C | T | 5 | a0001c0001t0002g0211 a0001c0001t0002g0213 a0001c0001t0002g0227 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037+881C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69535720 | |||||||
| chr5:69535826 | T | C | 3 | a0001c0001t0009g0079 a0001c0001t0009g0080 a0001c0001t0009g0081 |
3 | HG01109.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1037+987T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69535826 | |||||||
| chr5:69535847 | G | C | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1037+1008G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69535847 | |||||||
| chr5:69535852 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0172 a0001c0001t0001g0173 others(1): Show |
4 | HG01071.hp1 HG01074.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037+1013C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69535852 | |||||||
| chr5:69535929 | G | A | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1037+1090G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69535929 | |||||||
| chr5:69536032 | G | A | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1037+1193G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536032 | |||||||
| chr5:69536041 | C | T | 27 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 others(24): Show |
28 | HG01167.hp1 HG02055.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.1037+1202C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536041 | |||||||
| chr5:69536042 | G | A | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1037+1203G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536042 | |||||||
| chr5:69536105 | G | A | 2 | a0002c0004t0009g0078 a0002c0004t0009g0207 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1037+1266G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536105 | |||||||
| chr5:69536439 | G | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0003g0001 others(24): Show |
32 | HG00738.hp1 HG01256.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.1037+1600G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536439 | |||||||
| chr5:69536563 | C | G | 1 | a0001c0001t0002g0245 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1037+1724C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536563 | |||||||
| chr5:69536622 | G | T | 1 | a0001c0001t0002g0227 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1037+1783G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536622 | |||||||
| chr5:69536647 | C | T | 1 | a0004c0006t0003g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1037+1808C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536647 | |||||||
| chr5:69536690 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1037+1851C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536690 | |||||||
| chr5:69536691 | G | A | 3 | a0001c0001t0009g0079 a0001c0001t0009g0080 a0001c0001t0009g0081 |
3 | HG01109.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1037+1852G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536691 | |||||||
| chr5:69536823 | C | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0219 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1037+1984C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536823 | |||||||
| chr5:69536898 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1037+2059G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536898 | |||||||
| chr5:69536916 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1037+2077C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69536916 | |||||||
| chr5:69537189 | C | CT | 101 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(98): Show |
107 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.1037+2372dupT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69537189 | ||||||
| chr5:69537189 | C | CTT | 24 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0111 others(21): Show |
24 | HG00423.hp2 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1037+2371_1037+237 others(6): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69537189 | ||||||
| chr5:69537189 | CTTTTTTT others(2): Show |
C | 32 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 others(29): Show |
34 | HG00733.hp1 HG01167.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.1037+2364_1037+237 others(13): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69537189 | ||||||
| chr5:69537273 | C | T | 4 | a0001c0001t0001g0181 a0001c0001t0004g0100 a0001c0001t0004g0118 others(1): Show |
4 | HG01099.hp2 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037+2434C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69537273 | |||||||
| chr5:69537399 | A | G | 1 | a0002c0004t0009g0207 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1037+2560A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69537399 | |||||||
| chr5:69537414 | G | T | 1 | a0001c0001t0003g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1037+2575G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69537414 | |||||||
| chr5:69537452 | T | C | 58 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(55): Show |
62 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.1037+2613T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69537452 | |||||||
| chr5:69537614 | T | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0121 a0001c0001t0001g0158 others(2): Show |
6 | NA18939.hp2 NA18940.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.1037+2775T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69537614 | |||||||
| chr5:69537778 | A | AAC | 61 | a0001c0001t0001g0111 a0001c0001t0002g0014 a0001c0001t0002g0015 others(58): Show |
65 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.1037+2959_1037+296 others(6): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69537778 | ||||||
| chr5:69537876 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0219 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1037+3037G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69537876 | |||||||
| chr5:69538009 | CT | C | 196 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(193): Show |
207 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.1037+3182delT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69538009 | ||||||
| chr5:69538454 | C | T | 1 | a0001c0001t0016g0166 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1037+3615C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69538454 | |||||||
| chr5:69538527 | C | T | 1 | a0001c0001t0003g0051 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1037+3688C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69538527 | |||||||
| chr5:69538588 | G | A | 1 | a0001c0001t0005g0230 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1037+3749G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69538588 | |||||||
| chr5:69538629 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1037+3790A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69538629 | |||||||
| chr5:69538652 | C | T | 4 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0053 others(1): Show |
4 | HG02559.hp2 HG02647.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037+3813C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69538652 | |||||||
| chr5:69538819 | G | A | 4 | a0002c0004t0009g0078 a0002c0004t0009g0207 a0003c0005t0026g0200 others(1): Show |
4 | HG00733.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037+3980G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69538819 | |||||||
| chr5:69538913 | T | G | 63 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0017 others(60): Show |
67 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1037+4074T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69538913 | |||||||
| chr5:69539042 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0154 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1037+4203A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539042 | |||||||
| chr5:69539140 | C | T | 7 | a0001c0001t0005g0019 a0001c0001t0005g0263 a0001c0001t0005g0264 others(4): Show |
8 | HG01074.hp2 HG02280.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1037+4301C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539140 | |||||||
| chr5:69539157 | T | C | 4 | a0001c0001t0002g0258 a0001c0001t0015g0018 a0001c0001t0015g0260 others(1): Show |
5 | HG01256.hp2 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037+4318T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539157 | |||||||
| chr5:69539287 | T | G | 2 | a0001c0001t0001g0231 a0001c0001t0002g0004 |
3 | HG00438.hp2 NA18951.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1037+4448T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539287 | |||||||
| chr5:69539391 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1037+4552A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539391 | |||||||
| chr5:69539481 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1037+4642G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539481 | |||||||
| chr5:69539568 | A | C | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1037+4729A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539568 | |||||||
| chr5:69539586 | A | T | 1 | a0001c0001t0002g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1037+4747A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539586 | |||||||
| chr5:69539617 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1037+4778C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539617 | |||||||
| chr5:69539651 | T | C | 197 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(194): Show |
208 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1037+4812T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539651 | |||||||
| chr5:69539681 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1037+4842C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539681 | |||||||
| chr5:69539772 | A | T | 1 | a0001c0001t0003g0027 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1037+4933A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539772 | |||||||
| chr5:69539773 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1037+4934G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539773 | |||||||
| chr5:69539935 | A | G | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1038-4969A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69539935 | |||||||
| chr5:69540151 | G | A | 133 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(130): Show |
140 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1038-4753G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69540151 | |||||||
| chr5:69540169 | C | T | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038-4735C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69540169 | |||||||
| chr5:69540263 | A | G | 1 | a0001c0001t0003g0075 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1038-4641A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69540263 | |||||||
| chr5:69540305 | G | A | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038-4599G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69540305 | |||||||
| chr5:69540378 | T | G | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038-4526T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69540378 | |||||||
| chr5:69540396 | G | A | 119 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(116): Show |
125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1038-4508G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69540396 | |||||||
| chr5:69540454 | C | T | 1 | a0003c0005t0026g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1038-4450C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69540454 | |||||||
| chr5:69540556 | C | G | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038-4348C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69540556 | |||||||
| chr5:69540565 | A | G | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038-4339A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69540565 | |||||||
| chr5:69540616 | A | G | 4 | a0002c0004t0009g0078 a0002c0004t0009g0207 a0003c0005t0026g0200 others(1): Show |
4 | HG00733.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038-4288A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69540616 | |||||||
| chr5:69540867 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1038-4037C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69540867 | |||||||
| chr5:69541179 | C | T | 1 | a0001c0001t0027g0215 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1038-3725C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69541179 | |||||||
| chr5:69541221 | C | T | 4 | a0002c0004t0009g0078 a0002c0004t0009g0207 a0003c0005t0026g0200 others(1): Show |
4 | HG00733.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038-3683C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69541221 | |||||||
| chr5:69541307 | A | C | 4 | a0002c0004t0009g0078 a0002c0004t0009g0207 a0003c0005t0026g0200 others(1): Show |
4 | HG00733.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038-3597A>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69541307 | |||||||
| chr5:69541394 | C | T | 1 | a0001c0001t0003g0060 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1038-3510C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69541394 | |||||||
| chr5:69541810 | T | A | 1 | a0001c0001t0024g0233 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1038-3094T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69541810 | |||||||
| chr5:69541871 | G | A | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038-3033G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69541871 | |||||||
| chr5:69542069 | C | T | 1 | a0001c0001t0017g0131 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1038-2835C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69542069 | |||||||
| chr5:69542192 | G | GT | 24 | a0001c0001t0002g0017 a0001c0001t0002g0098 a0001c0001t0002g0099 others(21): Show |
26 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1038-2704dupT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69542192 | ||||||
| chr5:69542201 | G | T | 26 | a0001c0001t0002g0017 a0001c0001t0002g0098 a0001c0001t0002g0099 others(23): Show |
28 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1038-2703G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69542201 | |||||||
| chr5:69542259 | G | T | 25 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 others(22): Show |
26 | HG01167.hp1 HG02055.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.1038-2645G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69542259 | |||||||
| chr5:69542274 | C | T | 2 | a0001c0001t0015g0018 a0001c0001t0015g0260 |
3 | HG02258.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1038-2630C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69542274 | |||||||
| chr5:69542375 | A | T | 1 | a0001c0001t0005g0230 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1038-2529A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69542375 | |||||||
| chr5:69542598 | A | G | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038-2306A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69542598 | |||||||
| chr5:69543082 | C | T | 3 | a0001c0001t0039g0198 a0003c0005t0026g0200 a0004c0006t0003g0201 |
3 | HG00733.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1038-1822C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69543082 | |||||||
| chr5:69543111 | C | G | 120 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(117): Show |
126 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1038-1793C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69543111 | |||||||
| chr5:69543130 | C | T | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038-1774C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69543130 | |||||||
| chr5:69543131 | A | G | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038-1773A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69543131 | |||||||
| chr5:69543220 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1038-1684A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69543220 | |||||||
| chr5:69543284 | T | A | 4 | a0001c0001t0033g0242 a0001c0001t0039g0198 a0003c0005t0026g0200 others(1): Show |
4 | HG00733.hp1 HG02145.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038-1620T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69543284 | |||||||
| chr5:69543368 | G | C | 1 | a0001c0001t0018g0192 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1038-1536G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69543368 | |||||||
| chr5:69543490 | T | C | 1 | a0001c0001t0002g0004 | 2 | NA18951.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1038-1414T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69543490 | |||||||
| chr5:69543523 | A | AT | 5 | a0001c0001t0001g0094 a0001c0001t0002g0258 a0001c0001t0015g0018 others(2): Show |
6 | HG01256.hp2 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038-1367dupT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69543523 | ||||||
| chr5:69543813 | G | C | 1 | a0001c0001t0006g0253 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1038-1091G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69543813 | |||||||
| chr5:69544023 | C | T | 1 | a0001c0001t0003g0208 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1038-881C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69544023 | |||||||
| chr5:69544077 | T | C | 1 | a0002c0004t0009g0207 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1038-827T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69544077 | |||||||
| chr5:69544374 | A | G | 2 | a0001c0001t0033g0242 a0001c0001t0039g0198 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1038-530A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69544374 | |||||||
| chr5:69544469 | T | C | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1038-435T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69544469 | |||||||
| chr5:69544561 | G | C | 1 | a0001c0001t0005g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1038-343G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69544561 | |||||||
| chr5:69544754 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1038-150G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69544754 | |||||||
| chr5:69544812 | G | A | 1 | a0001c0001t0012g0151 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1038-92G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69544812 | |||||||
| chr5:69544829 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1038-75A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 5/8 | chr5 | 69544829 | |||||||
| chr5:69545150 | C | T | 1 | a0001c0001t0016g0102 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1253+31C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69545150 | |||||||
| chr5:69545431 | C | T | 4 | a0001c0001t0017g0131 a0001c0001t0025g0133 a0003c0005t0026g0200 others(1): Show |
4 | HG00733.hp1 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1253+312C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69545431 | |||||||
| chr5:69545472 | G | A | 1 | a0001c0001t0024g0233 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1253+353G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69545472 | |||||||
| chr5:69545498 | G | A | 128 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(125): Show |
135 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1253+379G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69545498 | |||||||
| chr5:69545526 | G | A | 4 | a0001c0001t0017g0131 a0001c0001t0025g0133 a0003c0005t0026g0200 others(1): Show |
4 | HG00733.hp1 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1253+407G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69545526 | |||||||
| chr5:69545631 | T | C | 3 | a0002c0003t0014g0021 a0002c0003t0014g0097 a0002c0003t0014g0109 |
3 | HG01891.hp2 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1253+512T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69545631 | |||||||
| chr5:69545745 | C | CT | 28 | a0001c0001t0002g0017 a0001c0001t0002g0098 a0001c0001t0002g0099 others(25): Show |
30 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1253+637dupT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr5 | 69545745 | ||||||
| chr5:69545755 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1253+636T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69545755 | |||||||
| chr5:69545843 | A | G | 1 | a0001c0001t0039g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1253+724A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69545843 | |||||||
| chr5:69545925 | C | T | 3 | a0002c0003t0014g0021 a0002c0003t0014g0097 a0002c0003t0014g0109 |
3 | HG01891.hp2 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1253+806C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69545925 | |||||||
| chr5:69546075 | G | A | 2 | a0001c0001t0003g0205 a0001c0001t0003g0206 |
2 | NA18939.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1253+956G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69546075 | |||||||
| chr5:69546222 | A | G | 3 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0074 |
3 | HG01168.hp1 HG01169.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1253+1103A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69546222 | |||||||
| chr5:69546486 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1253+1367A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69546486 | |||||||
| chr5:69546511 | T | G | 57 | a0001c0001t0001g0181 a0001c0001t0002g0014 a0001c0001t0002g0015 others(54): Show |
60 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1253+1392T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69546511 | |||||||
| chr5:69546613 | G | A | 4 | a0001c0001t0002g0258 a0001c0001t0015g0018 a0001c0001t0015g0260 others(1): Show |
5 | HG01256.hp2 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254-1317G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69546613 | |||||||
| chr5:69546961 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1254-969C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69546961 | |||||||
| chr5:69546962 | G | A | 2 | a0001c0001t0015g0018 a0001c0001t0015g0260 |
3 | HG02258.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1254-968G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69546962 | |||||||
| chr5:69547002 | A | G | 30 | a0001c0001t0001g0181 a0001c0001t0002g0017 a0001c0001t0002g0098 others(27): Show |
32 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1254-928A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69547002 | |||||||
| chr5:69547049 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0160 |
2 | NA18964.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1254-881C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69547049 | |||||||
| chr5:69547143 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0160 |
2 | NA18964.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1254-787C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69547143 | |||||||
| chr5:69547157 | CA | C | 4 | a0001c0001t0001g0181 a0001c0001t0003g0220 a0001c0001t0017g0131 others(1): Show |
4 | HG01981.hp1 HG02723.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254-766delA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr5 | 69547157 | ||||||
| chr5:69547249 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0012g0132 |
2 | NA18957.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1254-681G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69547249 | |||||||
| chr5:69547301 | G | T | 1 | a0001c0001t0015g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1254-629G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69547301 | |||||||
| chr5:69547348 | G | A | 5 | a0001c0001t0001g0123 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG00642.hp1 HG00738.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254-582G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69547348 | |||||||
| chr5:69547440 | A | G | 2 | a0001c0001t0017g0131 a0001c0001t0025g0133 |
2 | HG02735.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1254-490A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69547440 | |||||||
| chr5:69547569 | C | CA | 56 | a0001c0001t0001g0123 a0001c0001t0001g0187 a0001c0001t0002g0014 others(53): Show |
60 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.1254-345dupA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr5 | 69547569 | ||||||
| chr5:69547569 | CA | C | 7 | a0001c0001t0001g0169 a0001c0001t0001g0181 a0001c0001t0002g0125 others(4): Show |
7 | HG01981.hp1 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254-345delA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr5 | 69547569 | ||||||
| chr5:69547638 | G | A | 25 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 others(22): Show |
26 | HG01167.hp1 HG02055.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.1254-292G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69547638 | |||||||
| chr5:69547798 | A | G | 6 | a0001c0001t0001g0181 a0001c0001t0003g0220 a0001c0001t0017g0131 others(3): Show |
6 | HG01981.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1254-132A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69547798 | |||||||
| chr5:69547901 | A | T | 1 | a0003c0005t0026g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1254-29A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 6/8 | chr5 | 69547901 | |||||||
| chr5:69548173 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0160 |
2 | NA18964.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1425+72A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69548173 | |||||||
| chr5:69548315 | G | GT | 9 | a0001c0001t0001g0181 a0001c0001t0002g0240 a0001c0001t0003g0032 others(6): Show |
9 | HG01981.hp1 HG02074.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1425+230dupT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69548315 | ||||||
| chr5:69548375 | G | A | 5 | a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0186 others(2): Show |
5 | NA18959.hp1 NA18995.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.1425+274G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69548375 | |||||||
| chr5:69548387 | C | A | 4 | a0001c0001t0001g0181 a0001c0001t0003g0220 a0001c0001t0017g0131 others(1): Show |
4 | HG01981.hp1 HG02723.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1425+286C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69548387 | |||||||
| chr5:69548460 | C | T | 6 | a0001c0001t0001g0181 a0001c0001t0003g0220 a0001c0001t0017g0131 others(3): Show |
6 | HG01981.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1425+359C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69548460 | |||||||
| chr5:69548462 | T | C | 222 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(219): Show |
235 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1425+361T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69548462 | |||||||
| chr5:69548538 | T | C | 115 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(112): Show |
121 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1425+437T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69548538 | |||||||
| chr5:69548600 | G | A | 26 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 others(23): Show |
27 | HG01167.hp1 HG02055.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1425+499G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69548600 | |||||||
| chr5:69548718 | G | A | 6 | a0001c0001t0001g0181 a0001c0001t0003g0220 a0001c0001t0017g0131 others(3): Show |
6 | HG01981.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1425+617G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69548718 | |||||||
| chr5:69548884 | T | C | 7 | a0001c0001t0001g0181 a0001c0001t0003g0220 a0001c0001t0017g0131 others(4): Show |
7 | HG01981.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1425+783T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69548884 | |||||||
| chr5:69549060 | G | A | 2 | a0002c0004t0009g0078 a0002c0004t0009g0207 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1425+959G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549060 | |||||||
| chr5:69549105 | C | T | 5 | a0001c0001t0001g0181 a0001c0001t0003g0220 a0001c0001t0017g0131 others(2): Show |
5 | HG01981.hp1 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1425+1004C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549105 | |||||||
| chr5:69549166 | TA | T | 186 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(183): Show |
197 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.1425+1081delA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69549166 | ||||||
| chr5:69549224 | T | C | 197 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(194): Show |
208 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1425+1123T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549224 | |||||||
| chr5:69549263 | C | T | 5 | a0001c0001t0001g0181 a0001c0001t0003g0220 a0001c0001t0017g0131 others(2): Show |
5 | HG01981.hp1 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1425+1162C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549263 | |||||||
| chr5:69549295 | C | T | 1 | a0001c0001t0010g0149 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1425+1194C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549295 | |||||||
| chr5:69549298 | G | A | 1 | a0001c0001t0017g0131 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1425+1197G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549298 | |||||||
| chr5:69549340 | C | A | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1425+1239C>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549340 | |||||||
| chr5:69549340 | C | CA | 15 | a0001c0001t0001g0181 a0001c0001t0002g0217 a0001c0001t0002g0224 others(12): Show |
15 | HG00733.hp1 HG01243.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.1425+1262dupA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69549340 | ||||||
| chr5:69549340 | CA | C | 94 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(91): Show |
101 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1425+1262delA | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69549340 | ||||||
| chr5:69549340 | CAA | C | 36 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0087 others(33): Show |
36 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1425+1261_1425+126 others(6): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69549340 | ||||||
| chr5:69549368 | TTAAG | T | 5 | a0001c0001t0001g0181 a0001c0001t0003g0220 a0001c0001t0017g0131 others(2): Show |
5 | HG01981.hp1 HG02145.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1425+1271_1425+127 others(8): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69549368 | ||||||
| chr5:69549508 | A | G | 3 | a0001c0002t0007g0007 a0001c0002t0007g0114 a0001c0002t0031g0174 |
4 | HG00099.hp2 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1425+1407A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549508 | |||||||
| chr5:69549565 | T | G | 4 | a0002c0004t0009g0078 a0002c0004t0009g0207 a0003c0005t0026g0200 others(1): Show |
4 | HG00733.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1425+1464T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549565 | |||||||
| chr5:69549721 | C | T | 2 | a0001c0001t0016g0102 a0001c0001t0016g0166 |
2 | HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1425+1620C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549721 | |||||||
| chr5:69549727 | T | A | 3 | a0001c0001t0001g0181 a0001c0001t0017g0131 a0001c0001t0025g0133 |
3 | HG01981.hp1 HG02735.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1425+1626T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549727 | |||||||
| chr5:69549852 | G | C | 3 | a0001c0001t0001g0181 a0001c0001t0017g0131 a0001c0001t0025g0133 |
3 | HG01981.hp1 HG02735.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1426-1692G>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549852 | |||||||
| chr5:69549962 | G | T | 3 | a0001c0001t0001g0181 a0001c0001t0017g0131 a0001c0001t0025g0133 |
3 | HG01981.hp1 HG02735.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1426-1582G>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69549962 | |||||||
| chr5:69549979 | GT | G | 7 | a0001c0001t0003g0220 a0001c0001t0006g0084 a0001c0001t0006g0253 others(4): Show |
7 | HG00642.hp2 HG02723.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1426-1554delT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69549979 | ||||||
| chr5:69550188 | AT | A | 174 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(171): Show |
185 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1426-1335delT | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69550188 | ||||||
| chr5:69550188 | ATT | A | 15 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0142 others(12): Show |
16 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1426-1336_1426-133 others(6): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69550188 | ||||||
| chr5:69550259 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1426-1285T>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69550259 | |||||||
| chr5:69550443 | T | C | 3 | a0001c0001t0001g0181 a0001c0001t0017g0131 a0001c0001t0025g0133 |
3 | HG01981.hp1 HG02735.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1426-1101T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69550443 | |||||||
| chr5:69550478 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1426-1066C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69550478 | |||||||
| chr5:69550483 | T | C | 3 | a0001c0001t0001g0181 a0001c0001t0017g0131 a0001c0001t0025g0133 |
3 | HG01981.hp1 HG02735.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1426-1061T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69550483 | |||||||
| chr5:69550563 | T | C | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1426-981T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69550563 | |||||||
| chr5:69550575 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1426-969C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69550575 | |||||||
| chr5:69550686 | T | C | 1 | a0001c0001t0007g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1426-858T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69550686 | |||||||
| chr5:69550707 | T | G | 2 | a0001c0001t0001g0138 a0001c0001t0003g0137 |
2 | HG02135.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1426-837T>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69550707 | |||||||
| chr5:69550721 | T | C | 2 | a0003c0005t0026g0200 a0004c0006t0003g0201 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1426-823T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69550721 | |||||||
| chr5:69551033 | C | T | 1 | a0001c0001t0039g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1426-511C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69551033 | |||||||
| chr5:69551044 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1426-500A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69551044 | |||||||
| chr5:69551221 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1426-323C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69551221 | |||||||
| chr5:69551254 | A | G | 7 | a0001c0001t0001g0181 a0001c0001t0002g0247 a0001c0001t0017g0131 others(4): Show |
7 | HG00733.hp1 HG01981.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1426-290A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69551254 | |||||||
| chr5:69551434 | A | G | 1 | a0001c0001t0018g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1426-110A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69551434 | |||||||
| chr5:69551535 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1426-9C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 7/8 | chr5 | 69551535 | |||||||
| chr5:69551768 | T | C | 1 | a0001c0001t0008g0046 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1467+183T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69551768 | |||||||
| chr5:69551771 | T | C | 1 | a0001c0007t0036g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1467+186T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69551771 | |||||||
| chr5:69552043 | A | T | 2 | a0001c0001t0015g0018 a0001c0001t0015g0260 |
3 | HG02258.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1467+458A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552043 | |||||||
| chr5:69552119 | G | A | 2 | a0002c0004t0009g0078 a0002c0004t0009g0207 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1467+534G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552119 | |||||||
| chr5:69552174 | C | T | 1 | a0001c0001t0008g0046 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1467+589C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552174 | |||||||
| chr5:69552397 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | NA18966.hp1 NA18968.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1467+812A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552397 | |||||||
| chr5:69552399 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | NA18966.hp1 NA18968.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1467+814A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552399 | |||||||
| chr5:69552456 | C | T | 1 | a0001c0001t0013g0162 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1467+871C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552456 | |||||||
| chr5:69552482 | A | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | NA18962.hp1 NA18966.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1467+897A>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552482 | |||||||
| chr5:69552573 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1467+988T>C | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552573 | |||||||
| chr5:69552588 | C | G | 155 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(152): Show |
162 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1468-982C>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552588 | |||||||
| chr5:69552616 | G | A | 21 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 others(18): Show |
22 | HG01167.hp1 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1468-954G>A | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552616 | |||||||
| chr5:69552706 | A | G | 1 | a0001c0001t0002g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1468-864A>G | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552706 | |||||||
| chr5:69552846 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1468-724C>T | OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 8/8 | chr5 | 69552846 |