Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10498 |
| ensemblid | ENSG00000142453.13 |
| hgncid | 23393 |
| symbol | CARM1 |
| name | coactivator associated arginine methyltransferase 1 |
| refseq_nuc | NM_199141.2 |
| refseq_prot | NP_954592.1 |
| ensembl_nuc | ENST00000327064.9 |
| ensembl_prot | ENSP00000325690.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 10871553 |
| end | 10923075 |
| strand | + |
| ver | v1.2 |
| region | chr19:10871553-10923075 |
| region5000 | chr19:10866553-10928075 |
| regionname0 | CARM1_chr19_10871553_10923075 |
| regionname5000 | CARM1_chr19_10866553_10928075 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 608 | 350 | 80 | 64 | 153 | 11 | 40 | 121 | CARM1_chr19_10866553_10928075 | CARM1 | MAAAA others(603): Show |
chr19 | 10866553 | 10928075 |
| a0002 | 0/0 | 609 | 3 | 1 | 0 | 1 | 1 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | MAAAA others(604): Show |
chr19 | 10866553 | 10928075 |
| a0003 | 0/0 | 608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | MAAAA others(603): Show |
chr19 | 10866553 | 10928075 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1824 | 338 | 75 | 64 | 151 | 11 | 35 | CARM1_chr19_10866553_10928075 | CARM1 | ATGGC others(1819): Show |
chr19 | 10866553 | 10928075 | ||
| a0001c0002 | 0/0 | 1824 | 4 | 0 | 0 | 0 | 0 | 4 | CARM1_chr19_10866553_10928075 | CARM1 | ATGGC others(1819): Show |
chr19 | 10866553 | 10928075 | ||
| a0001c0004 | 0/0 | 1824 | 2 | 2 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | ATGGC others(1819): Show |
chr19 | 10866553 | 10928075 | ||
| a0001c0005 | 0/0 | 1824 | 2 | 2 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | ATGGC others(1819): Show |
chr19 | 10866553 | 10928075 | ||
| a0001c0006 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | ATGGC others(1819): Show |
chr19 | 10866553 | 10928075 | ||
| a0001c0008 | 0/0 | 1824 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | ATGGC others(1819): Show |
chr19 | 10866553 | 10928075 | ||
| a0001c0009 | 0/0 | 1824 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | ATGGC others(1819): Show |
chr19 | 10866553 | 10928075 | ||
| a0001c0010 | 0/0 | 1824 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | ATGGC others(1819): Show |
chr19 | 10866553 | 10928075 | ||
| a0002c0003 | 0/0 | 1827 | 3 | 1 | 0 | 1 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | ATGGC others(1822): Show |
chr19 | 10866553 | 10928075 | ||
| a0003c0007 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | ATGGC others(1819): Show |
chr19 | 10866553 | 10928075 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3295 | 167 | 46 | 36 | 58 | 4 | 21 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0002 | 0/0 | 3295 | 146 | 25 | 22 | 82 | 5 | 12 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0003 | 0/0 | 3296 | 7 | 0 | 3 | 0 | 2 | 2 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3291): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0004 | 0/0 | 3296 | 4 | 1 | 1 | 2 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3291): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0005 | 0/0 | 3295 | 3 | 0 | 0 | 3 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0006 | 0/0 | 3295 | 2 | 0 | 0 | 2 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0007 | 0/0 | 3235 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3230): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0008 | 0/0 | 3296 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3291): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0010 | 0/0 | 3295 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0011 | 0/0 | 3295 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0012 | 0/0 | 3295 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0014 | 0/0 | 3295 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0016 | 0/0 | 3295 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0018 | 0/0 | 3295 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0001t0020 | 0/0 | 3337 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3332): Show |
chr19 | 10866553 | 10928075 |
| a0001c0002t0001 | 0/0 | 3295 | 3 | 0 | 0 | 0 | 0 | 3 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0002t0015 | 0/0 | 3295 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0004t0002 | 0/0 | 3295 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0004t0019 | 0/0 | 3307 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3302): Show |
chr19 | 10866553 | 10928075 |
| a0001c0005t0002 | 0/0 | 3295 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0005t0013 | 0/0 | 3295 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0006t0017 | 0/0 | 3295 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0008t0001 | 0/0 | 3295 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0009t0001 | 0/0 | 3295 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0001c0010t0009 | 0/0 | 3295 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| a0002c0003t0001 | 0/0 | 3298 | 3 | 1 | 0 | 1 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3293): Show |
chr19 | 10866553 | 10928075 |
| a0003c0007t0002 | 0/0 | 3295 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | CTCGG others(3290): Show |
chr19 | 10866553 | 10928075 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0011g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0014g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0016g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0018g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0001t0020g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0002t0015g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0004t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0004t0019g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0005t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0005t0013g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0006t0017g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0008t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0009t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0001c0010t0009g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0002c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0002c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0002c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| a0003c0007t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0045 | EUR | GBR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0095 | EUR | GBR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | GBR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | FIN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | FIN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00423 | hp2 | a0001 | c0001 | t0010 | g0043 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01081 | hp1 | a0001 | c0001 | t0016 | g0274 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0080 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0289 | EUR | IBS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | IBS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0036 | EUR | IBS | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG01981 | hp2 | a0001 | c0001 | t0020 | g0277 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0168 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0169 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02698 | hp2 | a0001 | c0002 | t0015 | g0093 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0114 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02896 | hp2 | a0003 | c0007 | t0002 | g0070 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02970 | hp2 | a0001 | c0005 | t0002 | g0090 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03130 | hp1 | a0001 | c0006 | t0017 | g0342 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03453 | hp1 | a0001 | c0004 | t0019 | g0020 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03486 | hp2 | a0001 | c0001 | t0018 | g0239 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03669 | hp2 | a0001 | c0010 | t0009 | g0244 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | STU | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | BEB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | BEB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | BEB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | STU | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | STU | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | BEB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | STU | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | STU | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | STU | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | STU | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | STU | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0094 | AFR | YRI | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | YRI | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | CHB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | YRI | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | YRI | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18972 | hp1 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18973 | hp1 | a0001 | c0008 | t0001 | g0009 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18987 | hp1 | a0001 | c0009 | t0001 | g0234 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18987 | hp2 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0188 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19030 | hp2 | a0001 | c0005 | t0013 | g0096 | AFR | LWK | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | LWK | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0134 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19088 | hp1 | a0001 | c0001 | t0014 | g0210 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | YRI | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | YRI | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0083 | AFR | ASW | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA20129 | hp2 | a0001 | c0004 | t0002 | g0069 | AFR | ASW | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0035 | EUR | TSI | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | USA | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | USA | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0196 | REF | REF | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0207 | REF | REF | CARM1_chr19_10866553_10928075 | CARM1 | chr19 | 10866553 | 10928075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10871708 | A | AGCG | 1 | a0002 | 3 | HG00140.hp1 NA18522.hp1 NA18972.hp1 |
disruptive_inframe_insertion | MODERATE | c.20_22dupCGG | p.Ala7dup | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 173/3295 | 23/1827 | 8/608 | INFO_REALIGN_3_PRIME | chr19 | 10871708 | ||
| chr19:10919879 | T | G | 1 | a0003 | 1 | HG02896.hp2 | missense_variant&splice_region_variant | MODERATE | c.1109T>G | p.Ile370Arg | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/16 | 1259/3295 | 1109/1827 | 370/608 | chr19 | 10919879 | |||
| chr19:10919898 | C | G | 1 | a0003 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1128C>G | p.Phe376Leu | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/16 | 1278/3295 | 1128/1827 | 376/608 | chr19 | 10919898 | |||
| chr19:10919901 | C | G | 1 | a0003 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1131C>G | p.His377Gln | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/16 | 1281/3295 | 1131/1827 | 377/608 | chr19 | 10919901 | |||
| chr19:10919902 | A | G | 1 | a0003 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1132A>G | p.Met378Val | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/16 | 1282/3295 | 1132/1827 | 378/608 | chr19 | 10919902 | |||
| chr19:10919903 | T | A | 1 | a0003 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1133T>A | p.Met378Lys | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/16 | 1283/3295 | 1133/1827 | 378/608 | chr19 | 10919903 | |||
| chr19:10919905 | C | G | 1 | a0003 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1135C>G | p.Leu379Val | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/16 | 1285/3295 | 1135/1827 | 379/608 | chr19 | 10919905 | |||
| chr19:10919914 | G | A | 1 | a0003 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1144G>A | p.Gly382Arg | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/16 | 1294/3295 | 1144/1827 | 382/608 | chr19 | 10919914 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10908112 | G | A | 1 | a0001c0002 | 4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
synonymous_variant | LOW | c.420G>A | p.Arg140Arg | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 3/16 | 570/3295 | 420/1827 | 140/608 | chr19 | 10908112 | |||
| chr19:10912222 | G | A | 1 | a0001c0006 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.597G>A | p.Ser199Ser | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/16 | 747/3295 | 597/1827 | 199/608 | chr19 | 10912222 | |||
| chr19:10913885 | G | A | 1 | a0001c0004 | 2 | HG03453.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.678G>A | p.Val226Val | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/16 | 828/3295 | 678/1827 | 226/608 | chr19 | 10913885 | |||
| chr19:10919883 | A | G | 1 | a0003c0007 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.1113A>G | p.Glu371Glu | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/16 | 1263/3295 | 1113/1827 | 371/608 | chr19 | 10919883 | |||
| chr19:10919913 | A | C | 1 | a0003c0007 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.1143A>C | p.Ser381Ser | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/16 | 1293/3295 | 1143/1827 | 381/608 | chr19 | 10919913 | |||
| chr19:10920662 | G | A | 1 | a0001c0008 | 1 | NA18973.hp1 | synonymous_variant | LOW | c.1338G>A | p.Gln446Gln | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 12/16 | 1488/3295 | 1338/1827 | 446/608 | chr19 | 10920662 | |||
| chr19:10920906 | G | A | 2 | a0001c0002 a0001c0005 |
6 | HG02698.hp2 HG02738.hp2 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.1497G>A | p.Thr499Thr | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 13/16 | 1647/3295 | 1497/1827 | 499/608 | chr19 | 10920906 | |||
| chr19:10921691 | C | T | 1 | a0001c0010 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.1761C>T | p.Gly587Gly | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 1911/3295 | 1761/1827 | 587/608 | chr19 | 10921691 | |||
| chr19:10921712 | G | A | 1 | a0001c0009 | 1 | NA18987.hp1 | synonymous_variant | LOW | c.1782G>A | p.Ala594Ala | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 1932/3295 | 1782/1827 | 594/608 | chr19 | 10921712 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10871571 | T | TGCGGCGG others(35): Show |
1 | a0001c0001t0020 | 1 | HG01981.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121_-80dupTAGCGGC others(35): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 79 | INFO_REALIGN_3_PRIME | chr19 | 10871571 | |||||
| chr19:10871579 | C | CG | 2 | a0001c0001t0004 a0001c0001t0008 |
5 | HG01175.hp2 HG02145.hp1 HG02615.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-122dupG | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 121 | INFO_REALIGN_3_PRIME | chr19 | 10871579 | |||||
| chr19:10871580 | GGTAGCGG others(53): Show |
G | 1 | a0001c0001t0007 | 1 | NA19062.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121_-62delTAGCGGC others(53): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 62 | INFO_REALIGN_3_PRIME | chr19 | 10871580 | |||||
| chr19:10871583 | AGCGGCAG others(2): Show |
A | 2 | a0001c0002t0001 a0001c0002t0015 |
4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-114_-106delAGCGGC others(3): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 106 | INFO_REALIGN_3_PRIME | chr19 | 10871583 | |||||
| chr19:10871583 | AGCGGCAG others(5): Show |
A | 1 | a0001c0001t0001 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-114_-103delAGCGGC others(6): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 103 | INFO_REALIGN_3_PRIME | chr19 | 10871583 | |||||
| chr19:10871589 | A | AGCG | 1 | a0001c0001t0001 | 33 | HG00323.hp1 HG00558.hp1 HG00621.hp1 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-66_-64dupGGC | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 63 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871589 | A | AGCGGCG | 2 | a0001c0001t0001 a0001c0005t0013 |
20 | HG01070.hp2 HG01081.hp2 HG01109.hp1 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-69_-64dupGGCGGC | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 63 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871589 | A | AGCGGCGG others(2): Show |
2 | a0001c0001t0001 a0001c0001t0008 |
7 | HG02145.hp1 HG02280.hp2 HG03579.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-72_-64dupGGCGGCGG others(1): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 63 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871589 | A | AGCGGCGG others(5): Show |
2 | a0001c0001t0001 a0001c0001t0002 |
3 | HG03453.hp2 HG03710.hp2 NA18941.hp1 |
5_prime_UTR_variant | MODIFIER | c.-75_-64dupGGCGGCGG others(4): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 63 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871589 | A | AGCGGCGG others(14): Show |
2 | a0001c0001t0001 a0001c0001t0002 |
3 | HG02080.hp1 HG04184.hp2 HG04204.hp1 |
5_prime_UTR_variant | MODIFIER | c.-84_-64dupGGCGGCGG others(13): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 63 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871589 | A | AGCGGCGG others(17): Show |
1 | a0001c0001t0001 | 1 | HG00408.hp1 | 5_prime_UTR_variant | MODIFIER | c.-87_-64dupGGCGGCGG others(16): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 63 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871589 | A | G | 1 | a0001c0001t0001 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-114A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 114 | chr19 | 10871589 | ||||||
| chr19:10871589 | AGCG | A | 1 | a0001c0001t0001 | 13 | HG00597.hp2 HG02257.hp1 HG02572.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-66_-64delGGC | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 64 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871589 | AGCGGCG | A | 1 | a0001c0001t0001 | 13 | HG00099.hp2 HG01358.hp1 HG02258.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-69_-64delGGCGGC | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 64 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871589 | AGCGGCGG others(2): Show |
A | 2 | a0001c0001t0001 a0001c0001t0016 |
3 | HG01081.hp1 NA18952.hp1 NA19089.hp1 |
5_prime_UTR_variant | MODIFIER | c.-72_-64delGGCGGCGG others(1): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 64 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871589 | AGCGGCGG others(5): Show |
A | 1 | a0001c0001t0001 | 4 | HG03139.hp2 NA18970.hp1 NA18981.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-75_-64delGGCGGCGG others(4): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 64 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871589 | AGCGGCGG others(8): Show |
A | 1 | a0001c0001t0001 | 2 | HG01070.hp1 HG01071.hp1 |
5_prime_UTR_variant | MODIFIER | c.-78_-64delGGCGGCGG others(7): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 64 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871589 | AGCGGCGG others(11): Show |
A | 1 | a0001c0001t0001 | 4 | HG00741.hp2 HG01074.hp1 HG01168.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-81_-64delGGCGGCGG others(10): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 64 | INFO_REALIGN_3_PRIME | chr19 | 10871589 | |||||
| chr19:10871592 | G | A | 3 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0011 |
4 | HG00621.hp2 NA18957.hp1 NA18987.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-111G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 111 | chr19 | 10871592 | ||||||
| chr19:10871598 | G | GGCGGCGG others(14): Show |
1 | a0001c0001t0002 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-85_-84insTGCGGCGG others(13): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 84 | INFO_REALIGN_3_PRIME | chr19 | 10871598 | |||||
| chr19:10871601 | G | GGCGGCGG others(8): Show |
1 | a0001c0001t0002 | 6 | HG00323.hp2 HG00733.hp2 HG01109.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-88_-87insTGCGGCGG others(7): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 87 | INFO_REALIGN_3_PRIME | chr19 | 10871601 | |||||
| chr19:10871601 | GGCGGCGG others(32): Show |
G | 1 | a0001c0001t0001 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-90_-52delGGCGGCGG others(31): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 52 | INFO_REALIGN_3_PRIME | chr19 | 10871601 | |||||
| chr19:10871604 | G | GGCGGCGG others(17): Show |
1 | a0001c0001t0002 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-76_-75insTGCGGCGG others(16): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 75 | INFO_REALIGN_3_PRIME | chr19 | 10871604 | |||||
| chr19:10871604 | G | GGCGGCGG others(14): Show |
1 | a0001c0001t0002 | 3 | HG02630.hp1 HG02735.hp2 HG03041.hp1 |
5_prime_UTR_variant | MODIFIER | c.-79_-78insTGCGGCGG others(13): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 78 | INFO_REALIGN_3_PRIME | chr19 | 10871604 | |||||
| chr19:10871604 | G | GGCGGCGG others(11): Show |
2 | a0001c0001t0004 a0001c0001t0006 |
3 | HG02071.hp1 HG02135.hp1 HG02615.hp1 |
5_prime_UTR_variant | MODIFIER | c.-82_-81insTGCGGCGG others(10): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 81 | INFO_REALIGN_3_PRIME | chr19 | 10871604 | |||||
| chr19:10871604 | G | GGCGGCGG others(8): Show |
1 | a0001c0001t0002 | 8 | HG01255.hp2 HG01516.hp1 HG01934.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-85_-84insTGCGGCGG others(7): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 84 | INFO_REALIGN_3_PRIME | chr19 | 10871604 | |||||
| chr19:10871607 | GGCGGCGG others(26): Show |
G | 1 | a0001c0001t0001 | 1 | NA18957.hp1 | 5_prime_UTR_variant | MODIFIER | c.-84_-52delGGCGGCGG others(25): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 52 | INFO_REALIGN_3_PRIME | chr19 | 10871607 | |||||
| chr19:10871610 | G | GGCGGCGG others(2): Show |
1 | a0001c0001t0002 | 3 | HG01069.hp2 HG01071.hp2 HG01358.hp2 |
5_prime_UTR_variant | MODIFIER | c.-85_-84insTGCGGCGG others(1): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 84 | INFO_REALIGN_3_PRIME | chr19 | 10871610 | |||||
| chr19:10871619 | GGCGGCGG others(14): Show |
G | 6 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(3): Show |
19 | HG00438.hp1 HG02040.hp1 HG02074.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-72_-52delGGCGGCGG others(13): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 52 | INFO_REALIGN_3_PRIME | chr19 | 10871619 | |||||
| chr19:10871622 | GGCGGCGG others(11): Show |
G | 2 | a0001c0001t0002 a0002c0003t0001 |
9 | HG00140.hp1 HG02717.hp2 HG02895.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-69_-52delGGCGGCAG others(10): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 52 | INFO_REALIGN_3_PRIME | chr19 | 10871622 | |||||
| chr19:10871625 | GGCGGCGG others(8): Show |
G | 2 | a0001c0001t0002 a0001c0001t0003 |
9 | HG01261.hp1 HG02015.hp1 HG02451.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-66_-52delGGCAGCGG others(7): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 52 | INFO_REALIGN_3_PRIME | chr19 | 10871625 | |||||
| chr19:10871628 | GGCGGCGG others(5): Show |
G | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(4): Show |
87 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(84): Show |
5_prime_UTR_variant | MODIFIER | c.-63_-52delAGCGGCGG others(4): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 52 | INFO_REALIGN_3_PRIME | chr19 | 10871628 | |||||
| chr19:10871631 | G | A | 1 | a0001c0001t0001 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 72 | chr19 | 10871631 | ||||||
| chr19:10871631 | GGCGGCGG others(2): Show |
G | 4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0011 others(1): Show |
16 | HG00621.hp2 HG00639.hp1 HG01069.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-63_-55delAGCGGCGG others(1): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 55 | INFO_REALIGN_3_PRIME | chr19 | 10871631 | |||||
| chr19:10871634 | GGCGGCA | G | 2 | a0001c0001t0002 a0003c0007t0002 |
4 | HG01099.hp2 HG02809.hp2 HG02896.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-63_-58delAGCGGC | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 58 | INFO_REALIGN_3_PRIME | chr19 | 10871634 | |||||
| chr19:10871637 | G | A | 1 | a0001c0001t0001 | 2 | HG01884.hp2 HG01952.hp1 |
5_prime_UTR_variant | MODIFIER | c.-66G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 66 | chr19 | 10871637 | ||||||
| chr19:10871637 | G | GGCGGCGG others(11): Show |
1 | a0001c0001t0002 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-64_-63insGGCGGCGG others(10): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 63 | INFO_REALIGN_3_PRIME | chr19 | 10871637 | |||||
| chr19:10871637 | G | GGCGGCGG others(17): Show |
1 | a0001c0001t0002 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-64_-63insGGCGGCGG others(16): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 63 | INFO_REALIGN_3_PRIME | chr19 | 10871637 | |||||
| chr19:10871637 | G | GGCGGCGG others(26): Show |
1 | a0001c0001t0001 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64_-63insGGCGGCGG others(25): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 63 | INFO_REALIGN_3_PRIME | chr19 | 10871637 | |||||
| chr19:10871639 | CAGCGGCG others(4): Show |
C | 1 | a0001c0001t0001 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63_-53delAGCGGCGG others(3): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 53 | chr19 | 10871639 | ||||||
| chr19:10871640 | A | G | 2 | a0001c0001t0001 a0001c0004t0019 |
6 | HG02559.hp2 HG02615.hp2 HG03453.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-63A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 63 | chr19 | 10871640 | ||||||
| chr19:10871640 | AGCG | A | 4 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0015 others(1): Show |
9 | HG02523.hp1 HG02523.hp2 HG02698.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-54_-52delGGC | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 52 | INFO_REALIGN_3_PRIME | chr19 | 10871640 | |||||
| chr19:10871643 | G | A | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(12): Show |
172 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
5_prime_UTR_variant | MODIFIER | c.-60G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 60 | chr19 | 10871643 | ||||||
| chr19:10871643 | G | GGCGGCGG others(5): Show |
1 | a0001c0004t0019 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52_-51insGGCAGCGG others(4): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/16 | 51 | INFO_REALIGN_3_PRIME | chr19 | 10871643 | |||||
| chr19:10921764 | G | A | 1 | a0001c0010t0009 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 7 | chr19 | 10921764 | ||||||
| chr19:10921825 | C | T | 1 | a0001c0001t0018 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*68C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 68 | chr19 | 10921825 | ||||||
| chr19:10921907 | G | A | 1 | a0001c0001t0010 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 150 | chr19 | 10921907 | ||||||
| chr19:10922001 | G | A | 1 | a0001c0001t0005 | 3 | NA18995.hp2 NA19081.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*244G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 244 | chr19 | 10922001 | ||||||
| chr19:10922198 | T | C | 1 | a0001c0001t0011 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*441T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 441 | chr19 | 10922198 | ||||||
| chr19:10922203 | A | T | 1 | a0001c0001t0011 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*446A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 446 | chr19 | 10922203 | ||||||
| chr19:10922268 | G | A | 1 | a0001c0001t0014 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*511G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 511 | chr19 | 10922268 | ||||||
| chr19:10922308 | C | T | 1 | a0001c0006t0017 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*551C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 551 | chr19 | 10922308 | ||||||
| chr19:10922329 | C | T | 1 | a0001c0005t0013 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*572C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 572 | chr19 | 10922329 | ||||||
| chr19:10922471 | G | A | 2 | a0001c0001t0012 a0001c0004t0019 |
2 | HG03453.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*714G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 714 | chr19 | 10922471 | ||||||
| chr19:10922489 | T | TA | 1 | a0001c0001t0003 | 7 | HG00738.hp1 HG01168.hp2 HG01243.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*733dupA | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 734 | INFO_REALIGN_3_PRIME | chr19 | 10922489 | |||||
| chr19:10922665 | G | A | 1 | a0001c0002t0015 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*908G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 908 | chr19 | 10922665 | ||||||
| chr19:10922852 | G | A | 1 | a0001c0001t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1095G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 1095 | chr19 | 10922852 | ||||||
| chr19:10922893 | G | A | 1 | a0001c0001t0012 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1136G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 1136 | chr19 | 10922893 | ||||||
| chr19:10922944 | G | A | 1 | a0001c0001t0016 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1187G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 1187 | chr19 | 10922944 | ||||||
| chr19:10923007 | G | T | 1 | a0001c0001t0006 | 2 | HG02071.hp1 HG02135.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1250G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 16/16 | 1250 | chr19 | 10923007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:10872125 | G | A | 1 | a0001c0001t0002g0011 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.220+203G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10872125 | |||||||
| chr19:10872151 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.220+229G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10872151 | |||||||
| chr19:10872321 | C | T | 1 | a0001c0006t0017g0342 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.220+399C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10872321 | |||||||
| chr19:10872445 | C | A | 1 | a0001c0001t0002g0013 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.220+523C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10872445 | |||||||
| chr19:10872468 | G | C | 1 | a0001c0001t0008g0014 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.220+546G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10872468 | |||||||
| chr19:10872543 | C | G | 1 | a0001c0001t0002g0341 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.220+621C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10872543 | |||||||
| chr19:10872684 | TG | T | 5 | a0001c0001t0001g0019 a0001c0001t0002g0016 a0001c0001t0002g0017 others(2): Show |
5 | NA18972.hp1 NA18986.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+768delG | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10872684 | ||||||
| chr19:10872816 | C | G | 1 | a0001c0001t0001g0340 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.220+894C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10872816 | |||||||
| chr19:10873179 | G | A | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220+1257G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873179 | |||||||
| chr19:10873313 | T | A | 2 | a0001c0001t0002g0038 a0001c0001t0002g0242 |
2 | HG02257.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.220+1391T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873313 | |||||||
| chr19:10873350 | G | A | 1 | a0001c0001t0002g0021 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.220+1428G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873350 | |||||||
| chr19:10873351 | A | G | 1 | a0001c0001t0002g0021 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.220+1429A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873351 | |||||||
| chr19:10873624 | G | GT | 74 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(71): Show |
79 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.220+1735dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10873624 | ||||||
| chr19:10873624 | G | GTT | 23 | a0001c0001t0001g0012 a0001c0001t0001g0317 a0001c0001t0001g0318 others(20): Show |
23 | HG01070.hp2 HG01081.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.220+1734_220+1735d others(4): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10873624 | ||||||
| chr19:10873624 | G | GTTT | 6 | a0001c0001t0001g0019 a0001c0001t0001g0336 a0001c0001t0001g0337 others(3): Show |
6 | HG01943.hp1 HG02258.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+1733_220+1735d others(5): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10873624 | ||||||
| chr19:10873624 | GT | G | 52 | a0001c0001t0001g0022 a0001c0001t0001g0146 a0001c0001t0001g0148 others(49): Show |
53 | HG00408.hp2 HG00639.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.220+1735delT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10873624 | ||||||
| chr19:10873624 | GTT | G | 19 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(16): Show |
19 | HG00140.hp1 HG00323.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.220+1734_220+1735d others(4): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10873624 | ||||||
| chr19:10873624 | GTTT | G | 30 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0002g0016 others(27): Show |
30 | HG00438.hp1 HG01175.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.220+1733_220+1735d others(5): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10873624 | ||||||
| chr19:10873624 | GTTTT | G | 42 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0024 others(39): Show |
45 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.220+1732_220+1735d others(6): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10873624 | ||||||
| chr19:10873624 | GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0028 |
2 | HG02080.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.220+1724_220+1735d others(14): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10873624 | ||||||
| chr19:10873624 | GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0002g0025 a0001c0001t0007g0026 |
2 | NA19062.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.220+1723_220+1735d others(15): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10873624 | ||||||
| chr19:10873630 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.220+1708T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873630 | |||||||
| chr19:10873631 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.220+1709T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873631 | |||||||
| chr19:10873641 | T | G | 1 | a0001c0001t0002g0024 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.220+1719T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873641 | |||||||
| chr19:10873657 | T | G | 1 | a0001c0001t0002g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.220+1735T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873657 | |||||||
| chr19:10873709 | G | A | 4 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+1787G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873709 | |||||||
| chr19:10873791 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.220+1869C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873791 | |||||||
| chr19:10873846 | A | G | 5 | a0001c0001t0002g0065 a0001c0001t0002g0091 a0001c0001t0002g0092 others(2): Show |
5 | NA18946.hp2 NA18985.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+1924A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873846 | |||||||
| chr19:10873860 | T | G | 2 | a0001c0001t0002g0115 a0001c0001t0002g0116 |
2 | HG02074.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.220+1938T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873860 | |||||||
| chr19:10873886 | G | A | 1 | a0002c0003t0001g0094 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.220+1964G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873886 | |||||||
| chr19:10873931 | G | T | 1 | a0001c0001t0002g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.220+2009G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873931 | |||||||
| chr19:10873955 | T | C | 1 | a0002c0003t0001g0095 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.220+2033T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873955 | |||||||
| chr19:10873959 | G | A | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220+2037G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10873959 | |||||||
| chr19:10874139 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.220+2217A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874139 | |||||||
| chr19:10874160 | T | C | 9 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
9 | NA18747.hp2 NA18948.hp1 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+2238T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874160 | |||||||
| chr19:10874279 | ACATTCCT others(123): Show |
A | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220+2360_220+2489d others(2): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10874279 | ||||||
| chr19:10874381 | A | T | 1 | a0001c0001t0004g0133 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.220+2459A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874381 | |||||||
| chr19:10874382 | T | A | 1 | a0001c0001t0004g0133 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.220+2460T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874382 | |||||||
| chr19:10874464 | C | T | 2 | a0001c0001t0002g0089 a0001c0005t0002g0090 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.220+2542C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874464 | |||||||
| chr19:10874476 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220+2554C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874476 | |||||||
| chr19:10874679 | A | C | 1 | a0001c0001t0011g0015 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.220+2757A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874679 | |||||||
| chr19:10874682 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.220+2760G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874682 | |||||||
| chr19:10874686 | C | T | 84 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(81): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.220+2764C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874686 | |||||||
| chr19:10874737 | C | A | 1 | a0001c0001t0002g0167 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.220+2815C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874737 | |||||||
| chr19:10874813 | G | A | 187 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(184): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.220+2891G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874813 | |||||||
| chr19:10874851 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.220+2929G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10874851 | |||||||
| chr19:10875016 | C | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02965.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.220+3094C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875016 | |||||||
| chr19:10875023 | G | GA | 7 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(4): Show |
7 | HG01978.hp1 HG02109.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+3116dupA | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10875023 | ||||||
| chr19:10875023 | GA | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0335 a0001c0001t0002g0191 others(3): Show |
6 | HG02698.hp2 NA18957.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+3116delA | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10875023 | ||||||
| chr19:10875335 | T | A | 1 | a0001c0001t0011g0015 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.220+3413T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875335 | |||||||
| chr19:10875342 | T | A | 3 | a0001c0001t0002g0242 a0001c0004t0002g0069 a0001c0004t0019g0020 |
3 | HG02257.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220+3420T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875342 | |||||||
| chr19:10875374 | C | G | 1 | a0001c0002t0015g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.220+3452C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875374 | |||||||
| chr19:10875573 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.220+3651C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875573 | |||||||
| chr19:10875585 | C | T | 1 | a0001c0001t0003g0063 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.220+3663C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875585 | |||||||
| chr19:10875625 | C | T | 7 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(4): Show |
7 | HG02559.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+3703C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875625 | |||||||
| chr19:10875646 | C | G | 2 | a0001c0004t0002g0069 a0001c0004t0019g0020 |
2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220+3724C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875646 | |||||||
| chr19:10875666 | T | C | 1 | a0001c0001t0002g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.220+3744T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875666 | |||||||
| chr19:10875670 | C | T | 62 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(59): Show |
62 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.220+3748C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875670 | |||||||
| chr19:10875715 | T | C | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220+3793T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875715 | |||||||
| chr19:10875717 | C | G | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220+3795C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875717 | |||||||
| chr19:10875823 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0237 a0001c0001t0001g0238 others(7): Show |
11 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+3901A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875823 | |||||||
| chr19:10875927 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.220+4005C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875927 | |||||||
| chr19:10875995 | G | A | 81 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(78): Show |
84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.220+4073G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10875995 | |||||||
| chr19:10876047 | T | G | 1 | a0001c0001t0011g0015 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.220+4125T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876047 | |||||||
| chr19:10876122 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0193 a0001c0001t0001g0194 others(3): Show |
7 | NA18941.hp1 NA18962.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+4200G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876122 | |||||||
| chr19:10876173 | C | A | 84 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(81): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.220+4251C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876173 | |||||||
| chr19:10876233 | C | T | 84 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(81): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.220+4311C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876233 | |||||||
| chr19:10876321 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.220+4399C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876321 | |||||||
| chr19:10876337 | A | G | 256 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(253): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.220+4415A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876337 | |||||||
| chr19:10876408 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.220+4486C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876408 | |||||||
| chr19:10876429 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.220+4507G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876429 | |||||||
| chr19:10876728 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.220+4806C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876728 | |||||||
| chr19:10876816 | G | A | 4 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(1): Show |
4 | HG02717.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+4894G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876816 | |||||||
| chr19:10876908 | G | A | 1 | a0001c0005t0013g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+4986G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876908 | |||||||
| chr19:10876917 | G | T | 1 | a0001c0001t0011g0015 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.220+4995G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876917 | |||||||
| chr19:10876985 | G | T | 1 | a0001c0001t0002g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.220+5063G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10876985 | |||||||
| chr19:10877078 | C | T | 1 | a0001c0001t0002g0155 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.220+5156C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10877078 | |||||||
| chr19:10877300 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.220+5378G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10877300 | |||||||
| chr19:10877395 | C | T | 4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0308 others(1): Show |
4 | HG00597.hp2 HG03710.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+5473C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10877395 | |||||||
| chr19:10878142 | G | T | 1 | a0001c0001t0003g0062 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.220+6220G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10878142 | |||||||
| chr19:10878178 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.220+6256G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10878178 | |||||||
| chr19:10878296 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.220+6374G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10878296 | |||||||
| chr19:10878807 | C | CT | 14 | a0001c0001t0001g0292 a0001c0001t0001g0307 a0001c0001t0001g0339 others(11): Show |
14 | HG00741.hp2 HG01934.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+6900dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10878807 | ||||||
| chr19:10878957 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG00642.hp1 HG00738.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.220+7035C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10878957 | |||||||
| chr19:10879236 | C | T | 1 | a0001c0004t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.220+7314C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10879236 | |||||||
| chr19:10879316 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.220+7394T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10879316 | |||||||
| chr19:10879621 | G | T | 1 | a0001c0004t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.220+7699G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10879621 | |||||||
| chr19:10879653 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
13 | HG00733.hp1 HG01192.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.220+7731C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10879653 | |||||||
| chr19:10879716 | T | G | 1 | a0001c0001t0002g0117 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.220+7794T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10879716 | |||||||
| chr19:10879862 | G | C | 1 | a0001c0001t0002g0011 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.220+7940G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10879862 | |||||||
| chr19:10879891 | C | T | 3 | a0001c0001t0002g0242 a0001c0004t0002g0069 a0001c0004t0019g0020 |
3 | HG02257.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220+7969C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10879891 | |||||||
| chr19:10880062 | T | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02965.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.220+8140T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10880062 | |||||||
| chr19:10880295 | G | T | 1 | a0001c0001t0001g0215 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.220+8373G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10880295 | |||||||
| chr19:10880390 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0064 |
2 | HG00140.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.220+8468G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10880390 | |||||||
| chr19:10880513 | A | AT | 28 | a0001c0001t0001g0012 a0001c0001t0001g0214 a0001c0001t0001g0217 others(25): Show |
28 | HG00621.hp2 HG00741.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.220+8612dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10880513 | ||||||
| chr19:10880513 | AT | A | 63 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0165 others(60): Show |
63 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.220+8612delT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10880513 | ||||||
| chr19:10880558 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.220+8636T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10880558 | |||||||
| chr19:10880566 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.220+8644C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10880566 | |||||||
| chr19:10880567 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.220+8645G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10880567 | |||||||
| chr19:10880600 | T | TACCTTGG others(123): Show |
1 | a0001c0001t0001g0267 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.220+8679_220+8808d others(132): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10880600 | ||||||
| chr19:10880657 | A | G | 1 | a0001c0001t0001g0019 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.220+8735A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10880657 | |||||||
| chr19:10880683 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.220+8761T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10880683 | |||||||
| chr19:10880729 | CAGTTTTG others(201): Show |
C | 1 | a0001c0002t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.220+8808_220+9015d others(2): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10880729 | |||||||
| chr19:10880831 | CCCTGGAG others(123): Show |
C | 3 | a0001c0001t0001g0211 a0001c0001t0001g0265 a0001c0001t0001g0267 |
3 | HG01884.hp1 HG01952.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.220+8911_220+9040d others(2): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10880831 | ||||||
| chr19:10880943 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.220+9021G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10880943 | |||||||
| chr19:10880974 | G | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0304 |
2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.220+9052G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10880974 | |||||||
| chr19:10881011 | A | T | 1 | a0001c0001t0002g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.220+9089A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10881011 | |||||||
| chr19:10881151 | G | A | 75 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(72): Show |
78 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.220+9229G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10881151 | |||||||
| chr19:10881696 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.220+9774C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10881696 | |||||||
| chr19:10881757 | T | C | 1 | a0001c0001t0001g0019 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.220+9835T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10881757 | |||||||
| chr19:10881767 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.220+9845G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10881767 | |||||||
| chr19:10881793 | C | T | 2 | a0002c0003t0001g0094 a0002c0003t0001g0095 |
2 | HG00140.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.220+9871C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10881793 | |||||||
| chr19:10881935 | G | A | 2 | a0001c0004t0002g0069 a0001c0004t0019g0020 |
2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220+10013G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10881935 | |||||||
| chr19:10882039 | C | G | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220+10117C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882039 | |||||||
| chr19:10882048 | G | A | 68 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(65): Show |
71 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.220+10126G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882048 | |||||||
| chr19:10882107 | G | T | 1 | a0001c0001t0002g0127 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.220+10185G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882107 | |||||||
| chr19:10882123 | G | C | 1 | a0001c0001t0002g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.220+10201G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882123 | |||||||
| chr19:10882276 | G | A | 1 | a0001c0001t0008g0014 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.220+10354G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882276 | |||||||
| chr19:10882358 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.220+10436G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882358 | |||||||
| chr19:10882534 | C | CT | 48 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0211 others(45): Show |
49 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.220+10637dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10882534 | ||||||
| chr19:10882534 | C | CTT | 125 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(122): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.220+10636_220+1063 others(6): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10882534 | ||||||
| chr19:10882534 | C | CTTT | 23 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0054 others(20): Show |
23 | HG00673.hp1 HG02071.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.220+10635_220+1063 others(7): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10882534 | ||||||
| chr19:10882619 | G | A | 75 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(72): Show |
78 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.220+10697G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882619 | |||||||
| chr19:10882741 | C | A | 2 | a0001c0001t0001g0160 a0002c0003t0001g0018 |
2 | NA18971.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.220+10819C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882741 | |||||||
| chr19:10882743 | T | C | 1 | a0001c0001t0002g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.220+10821T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882743 | |||||||
| chr19:10882752 | G | T | 1 | a0001c0001t0001g0302 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.220+10830G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882752 | |||||||
| chr19:10882761 | C | G | 1 | a0001c0005t0013g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+10839C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882761 | |||||||
| chr19:10882967 | A | T | 69 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(66): Show |
69 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.220+11045A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10882967 | |||||||
| chr19:10883079 | C | G | 4 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+11157C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10883079 | |||||||
| chr19:10883141 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.220+11219C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10883141 | |||||||
| chr19:10883347 | C | G | 71 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(68): Show |
71 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.220+11425C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10883347 | |||||||
| chr19:10883412 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.220+11490C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10883412 | |||||||
| chr19:10883497 | C | T | 1 | a0001c0001t0008g0014 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.220+11575C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10883497 | |||||||
| chr19:10883500 | A | C | 5 | a0001c0001t0001g0146 a0001c0001t0002g0147 a0001c0001t0002g0189 others(2): Show |
5 | NA18947.hp2 NA18956.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+11578A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10883500 | |||||||
| chr19:10883536 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.220+11614C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10883536 | |||||||
| chr19:10883553 | C | T | 1 | a0001c0006t0017g0342 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.220+11631C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10883553 | |||||||
| chr19:10883726 | T | A | 7 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(4): Show |
7 | HG00738.hp1 HG01168.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+11804T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10883726 | |||||||
| chr19:10883727 | A | T | 1 | a0001c0001t0001g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.220+11805A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10883727 | |||||||
| chr19:10883878 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.220+11956C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10883878 | |||||||
| chr19:10884013 | G | GT | 63 | a0001c0001t0001g0164 a0001c0001t0001g0209 a0001c0001t0001g0217 others(60): Show |
63 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.220+12108dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10884013 | ||||||
| chr19:10884013 | G | GTT | 54 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(51): Show |
57 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.220+12107_220+1210 others(6): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10884013 | ||||||
| chr19:10884013 | G | GTTT | 14 | a0001c0001t0002g0030 a0001c0001t0002g0033 a0001c0001t0002g0060 others(11): Show |
14 | HG01175.hp2 HG01192.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+12106_220+1210 others(7): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10884013 | ||||||
| chr19:10884019 | T | G | 1 | a0001c0001t0002g0315 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.220+12097T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884019 | |||||||
| chr19:10884027 | T | G | 2 | a0002c0003t0001g0094 a0002c0003t0001g0095 |
2 | HG00140.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.220+12105T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884027 | |||||||
| chr19:10884031 | C | T | 1 | a0001c0001t0002g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.220+12109C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884031 | |||||||
| chr19:10884032 | G | T | 1 | a0001c0001t0002g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.220+12110G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884032 | |||||||
| chr19:10884038 | T | C | 2 | a0001c0001t0002g0089 a0001c0005t0002g0090 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.220+12116T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884038 | |||||||
| chr19:10884060 | G | A | 5 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(2): Show |
5 | HG01934.hp1 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+12138G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884060 | |||||||
| chr19:10884134 | G | A | 2 | a0001c0001t0002g0089 a0001c0005t0002g0090 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.220+12212G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884134 | |||||||
| chr19:10884341 | C | CA | 14 | a0001c0001t0001g0232 a0001c0001t0001g0278 a0001c0001t0001g0304 others(11): Show |
14 | HG01109.hp2 HG01175.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+12434dupA | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10884341 | ||||||
| chr19:10884352 | A | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0313 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.220+12430A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884352 | |||||||
| chr19:10884381 | C | G | 1 | a0001c0001t0001g0299 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.220+12459C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884381 | |||||||
| chr19:10884589 | G | C | 2 | a0001c0001t0002g0089 a0001c0005t0002g0090 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.220+12667G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884589 | |||||||
| chr19:10884713 | A | T | 1 | a0001c0004t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.220+12791A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884713 | |||||||
| chr19:10884714 | T | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0237 a0001c0001t0001g0238 others(5): Show |
9 | HG01109.hp1 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+12792T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884714 | |||||||
| chr19:10884726 | A | T | 1 | a0001c0001t0002g0091 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.220+12804A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884726 | |||||||
| chr19:10884766 | G | A | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220+12844G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884766 | |||||||
| chr19:10884829 | C | T | 2 | a0001c0001t0002g0089 a0001c0005t0002g0090 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.220+12907C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10884829 | |||||||
| chr19:10885010 | ATTTAT | A | 4 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+13093_220+1309 others(9): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10885010 | ||||||
| chr19:10885165 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.220+13243C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10885165 | |||||||
| chr19:10885534 | A | T | 1 | a0001c0005t0013g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+13612A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10885534 | |||||||
| chr19:10885715 | C | T | 75 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(72): Show |
78 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.220+13793C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10885715 | |||||||
| chr19:10885774 | C | A | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220+13852C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10885774 | |||||||
| chr19:10885790 | G | C | 1 | a0001c0001t0006g0169 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.220+13868G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10885790 | |||||||
| chr19:10885847 | G | GC | 70 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(67): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.220+13931dupC | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10885847 | ||||||
| chr19:10885851 | CCCACAGG others(6): Show |
C | 6 | a0001c0001t0002g0037 a0001c0001t0002g0066 a0001c0001t0002g0072 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+13931_220+1394 others(17): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10885851 | ||||||
| chr19:10885888 | AT | A | 79 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(76): Show |
79 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.220+13992delT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10885888 | ||||||
| chr19:10885889 | T | TTTC | 5 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0078 others(2): Show |
6 | HG01256.hp2 HG01258.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+13969_220+1397 others(7): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10885889 | ||||||
| chr19:10885890 | T | TTC | 52 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(49): Show |
54 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.220+13969_220+1397 others(6): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10885890 | ||||||
| chr19:10885891 | T | TC | 35 | a0001c0001t0001g0002 a0001c0001t0001g0156 a0001c0001t0001g0157 others(32): Show |
37 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.220+13969_220+1397 others(5): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10885891 | |||||||
| chr19:10885892 | T | C | 167 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): Show |
173 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.220+13970T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10885892 | |||||||
| chr19:10885893 | T | C | 79 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(76): Show |
79 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.220+13971T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10885893 | |||||||
| chr19:10885894 | T | C | 2 | a0001c0001t0002g0131 a0001c0001t0002g0144 |
2 | HG01069.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.220+13972T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10885894 | |||||||
| chr19:10886040 | T | C | 4 | a0001c0001t0004g0133 a0001c0001t0005g0134 a0001c0001t0005g0188 others(1): Show |
4 | NA18946.hp1 NA18995.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+14118T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10886040 | |||||||
| chr19:10886056 | C | CT | 9 | a0001c0001t0001g0258 a0001c0001t0001g0289 a0001c0001t0002g0029 others(6): Show |
9 | HG01175.hp2 HG01515.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+14151dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10886056 | ||||||
| chr19:10886056 | CT | C | 9 | a0001c0001t0001g0206 a0001c0001t0001g0247 a0001c0001t0002g0038 others(6): Show |
9 | HG00099.hp2 HG02896.hp2 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+14151delT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10886056 | ||||||
| chr19:10886144 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.220+14222C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10886144 | |||||||
| chr19:10886217 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.220+14295C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10886217 | |||||||
| chr19:10886318 | C | T | 2 | a0001c0001t0002g0251 a0001c0001t0002g0254 |
2 | NA18981.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.220+14396C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10886318 | |||||||
| chr19:10886348 | C | T | 4 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+14426C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10886348 | |||||||
| chr19:10886513 | C | A | 1 | a0001c0001t0002g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.220+14591C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10886513 | |||||||
| chr19:10886543 | G | C | 1 | a0001c0001t0002g0097 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.220+14621G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10886543 | |||||||
| chr19:10887042 | G | A | 2 | a0001c0001t0002g0089 a0001c0005t0002g0090 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.220+15120G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10887042 | |||||||
| chr19:10887131 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.220+15209G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10887131 | |||||||
| chr19:10887250 | T | C | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220+15328T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10887250 | |||||||
| chr19:10887264 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.220+15342T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10887264 | |||||||
| chr19:10887319 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.220+15397G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10887319 | |||||||
| chr19:10887343 | C | T | 189 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(186): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.220+15421C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10887343 | |||||||
| chr19:10887417 | A | AGCCTGCA others(8): Show |
1 | a0001c0001t0002g0029 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.220+15497_220+1551 others(19): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10887417 | ||||||
| chr19:10887608 | A | T | 1 | a0002c0003t0001g0094 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.220+15686A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10887608 | |||||||
| chr19:10887996 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.220+16074C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10887996 | |||||||
| chr19:10888083 | G | A | 1 | a0001c0001t0002g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.220+16161G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888083 | |||||||
| chr19:10888126 | T | G | 2 | a0001c0001t0006g0168 a0001c0001t0006g0169 |
2 | HG02071.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.220+16204T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888126 | |||||||
| chr19:10888169 | A | G | 154 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(151): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.220+16247A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888169 | |||||||
| chr19:10888179 | TAGCACCA others(6): Show |
T | 1 | a0001c0001t0001g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.220+16260_220+1627 others(17): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10888179 | ||||||
| chr19:10888210 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.220+16288T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888210 | |||||||
| chr19:10888294 | C | T | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220+16372C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888294 | |||||||
| chr19:10888400 | C | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0304 |
2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.220+16478C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888400 | |||||||
| chr19:10888461 | G | C | 72 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(69): Show |
75 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.221-16490G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888461 | |||||||
| chr19:10888471 | C | T | 1 | a0001c0001t0002g0030 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.221-16480C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888471 | |||||||
| chr19:10888530 | C | G | 1 | a0001c0001t0012g0083 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.221-16421C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888530 | |||||||
| chr19:10888656 | A | G | 1 | a0001c0001t0002g0104 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.221-16295A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888656 | |||||||
| chr19:10888669 | T | C | 4 | a0001c0001t0001g0243 a0001c0001t0002g0033 a0001c0001t0002g0059 others(1): Show |
4 | HG00621.hp2 NA18957.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-16282T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888669 | |||||||
| chr19:10888672 | T | C | 1 | a0001c0002t0015g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.221-16279T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888672 | |||||||
| chr19:10888703 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.221-16248G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888703 | |||||||
| chr19:10888729 | C | T | 1 | a0002c0003t0001g0094 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.221-16222C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888729 | |||||||
| chr19:10888903 | A | G | 1 | a0001c0005t0013g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221-16048A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10888903 | |||||||
| chr19:10889025 | A | C | 3 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 |
3 | HG02451.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.221-15926A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10889025 | |||||||
| chr19:10889071 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.221-15880G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10889071 | |||||||
| chr19:10889104 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.221-15847C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10889104 | |||||||
| chr19:10889315 | A | AT | 12 | a0001c0001t0001g0232 a0001c0001t0001g0238 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01952.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-15619dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10889315 | ||||||
| chr19:10889401 | G | A | 4 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-15550G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10889401 | |||||||
| chr19:10889441 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.221-15510A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10889441 | |||||||
| chr19:10889481 | A | AT | 8 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0203 others(5): Show |
8 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.221-15451dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10889481 | ||||||
| chr19:10889481 | AT | A | 145 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(142): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.221-15451delT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10889481 | ||||||
| chr19:10889644 | C | A | 3 | a0001c0001t0002g0242 a0001c0004t0002g0069 a0001c0004t0019g0020 |
3 | HG02257.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.221-15307C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10889644 | |||||||
| chr19:10889645 | C | A | 3 | a0001c0001t0002g0242 a0001c0004t0002g0069 a0001c0004t0019g0020 |
3 | HG02257.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.221-15306C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10889645 | |||||||
| chr19:10889655 | C | T | 1 | a0001c0005t0013g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221-15296C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10889655 | |||||||
| chr19:10889973 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.221-14978A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10889973 | |||||||
| chr19:10890062 | A | C | 1 | a0001c0001t0001g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.221-14889A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890062 | |||||||
| chr19:10890079 | C | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0288 |
2 | HG02258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.221-14872C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890079 | |||||||
| chr19:10890183 | T | C | 1 | a0002c0003t0001g0095 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.221-14768T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890183 | |||||||
| chr19:10890260 | G | GTT | 7 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0052 others(4): Show |
7 | HG00738.hp1 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-14688_221-1468 others(6): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10890260 | ||||||
| chr19:10890265 | G | T | 81 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(78): Show |
84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.221-14686G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890265 | |||||||
| chr19:10890269 | G | GT | 15 | a0001c0001t0001g0067 a0001c0001t0001g0170 a0001c0001t0001g0232 others(12): Show |
15 | HG00323.hp2 HG00741.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.221-14667dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10890269 | ||||||
| chr19:10890269 | G | T | 77 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(74): Show |
80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.221-14682G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890269 | |||||||
| chr19:10890270 | T | G | 1 | a0001c0001t0002g0030 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.221-14681T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890270 | |||||||
| chr19:10890270 | T | TG | 70 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(67): Show |
73 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.221-14681_221-1468 others(5): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890270 | |||||||
| chr19:10890274 | T | G | 1 | a0002c0003t0001g0095 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.221-14677T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890274 | |||||||
| chr19:10890318 | A | G | 2 | a0002c0003t0001g0094 a0002c0003t0001g0095 |
2 | HG00140.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.221-14633A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890318 | |||||||
| chr19:10890353 | C | T | 22 | a0001c0001t0001g0181 a0001c0001t0002g0021 a0001c0001t0002g0025 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.221-14598C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890353 | |||||||
| chr19:10890467 | C | A | 2 | a0002c0003t0001g0094 a0002c0003t0001g0095 |
2 | HG00140.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.221-14484C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890467 | |||||||
| chr19:10890531 | G | A | 1 | a0001c0001t0002g0139 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.221-14420G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890531 | |||||||
| chr19:10890569 | A | G | 154 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(151): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.221-14382A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890569 | |||||||
| chr19:10890740 | C | T | 10 | a0001c0001t0002g0013 a0001c0001t0002g0027 a0001c0001t0002g0123 others(7): Show |
10 | HG01255.hp2 HG01516.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.221-14211C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890740 | |||||||
| chr19:10890764 | T | C | 1 | a0001c0001t0012g0083 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.221-14187T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890764 | |||||||
| chr19:10890764 | T | TAC | 21 | a0001c0001t0001g0148 a0001c0001t0001g0161 a0001c0001t0001g0229 others(18): Show |
22 | HG00733.hp2 HG01109.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.221-14177_221-1417 others(6): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10890764 | ||||||
| chr19:10890774 | C | CACAT | 35 | a0001c0001t0001g0075 a0001c0001t0002g0001 a0001c0001t0002g0028 others(32): Show |
37 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.221-14176_221-1417 others(8): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10890774 | ||||||
| chr19:10890774 | C | CACATAT | 3 | a0001c0001t0001g0243 a0001c0001t0002g0066 a0001c0002t0001g0114 |
3 | HG02280.hp1 HG02738.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.221-14176_221-1417 others(10): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10890774 | ||||||
| chr19:10890774 | CAT | C | 5 | a0001c0001t0001g0192 a0001c0001t0001g0197 a0001c0001t0001g0206 others(2): Show |
5 | HG00099.hp2 HG01358.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-14156_221-1415 others(6): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10890774 | ||||||
| chr19:10890776 | T | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
282 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.221-14175T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890776 | |||||||
| chr19:10890778 | T | C | 6 | a0001c0001t0001g0192 a0001c0001t0001g0197 a0001c0001t0001g0206 others(3): Show |
6 | HG00099.hp2 HG01358.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-14173T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890778 | |||||||
| chr19:10890790 | TA | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0237 a0001c0001t0001g0324 |
3 | HG02040.hp2 HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.221-14160delA | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890790 | |||||||
| chr19:10890791 | A | AT | 7 | a0001c0001t0001g0010 a0001c0001t0001g0233 a0001c0001t0001g0311 others(4): Show |
8 | HG01109.hp1 HG02145.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.221-14159dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10890791 | ||||||
| chr19:10890791 | A | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0314 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.221-14160A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890791 | |||||||
| chr19:10890792 | TA | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0220 a0001c0001t0001g0280 others(6): Show |
9 | HG00642.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-14158delA | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890792 | |||||||
| chr19:10890793 | A | AT | 16 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0201 others(13): Show |
16 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.221-14157dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10890793 | ||||||
| chr19:10890793 | A | T | 52 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0019 others(49): Show |
53 | HG00140.hp1 HG00323.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.221-14158A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890793 | |||||||
| chr19:10890794 | TA | T | 6 | a0001c0001t0001g0158 a0001c0001t0001g0286 a0001c0001t0001g0287 others(3): Show |
6 | HG00597.hp2 HG01928.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-14156delA | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890794 | |||||||
| chr19:10890795 | A | AT | 14 | a0001c0001t0001g0165 a0001c0001t0001g0170 a0001c0001t0001g0216 others(11): Show |
14 | HG00733.hp1 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-14131dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10890795 | ||||||
| chr19:10890795 | A | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.221-14156A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890795 | |||||||
| chr19:10890795 | AT | A | 9 | a0001c0001t0001g0263 a0001c0001t0001g0317 a0001c0001t0002g0016 others(6): Show |
9 | HG03688.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-14131delT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10890795 | ||||||
| chr19:10890796 | T | TA | 55 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0181 others(52): Show |
55 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.221-14155_221-1415 others(5): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890796 | |||||||
| chr19:10890796 | T | TATA | 15 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0033 others(12): Show |
16 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.221-14155_221-1415 others(7): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890796 | |||||||
| chr19:10890796 | T | TATATA | 7 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0127 others(4): Show |
7 | HG01168.hp2 HG01358.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-14155_221-1415 others(9): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890796 | |||||||
| chr19:10890797 | T | A | 24 | a0001c0001t0001g0176 a0001c0001t0002g0013 a0001c0001t0002g0027 others(21): Show |
24 | HG00423.hp1 HG00738.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.221-14154T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890797 | |||||||
| chr19:10890798 | T | A | 21 | a0001c0001t0001g0241 a0001c0001t0002g0011 a0001c0001t0002g0017 others(18): Show |
21 | HG01168.hp2 HG01934.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-14153T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890798 | |||||||
| chr19:10890799 | T | A | 4 | a0001c0001t0001g0176 a0001c0001t0002g0098 a0001c0001t0002g0099 others(1): Show |
4 | HG02015.hp2 HG02451.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-14152T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890799 | |||||||
| chr19:10890800 | T | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0152 |
2 | NA19086.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.221-14151T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890800 | |||||||
| chr19:10890828 | T | C | 69 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(66): Show |
69 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.221-14123T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890828 | |||||||
| chr19:10890842 | C | T | 2 | a0001c0001t0002g0086 a0001c0001t0002g0088 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.221-14109C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890842 | |||||||
| chr19:10890867 | G | A | 1 | a0001c0002t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.221-14084G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10890867 | |||||||
| chr19:10891400 | G | C | 7 | a0001c0001t0002g0100 a0001c0001t0002g0117 a0001c0001t0002g0120 others(4): Show |
7 | HG00323.hp2 HG00733.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-13551G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10891400 | |||||||
| chr19:10891473 | G | A | 2 | a0001c0001t0003g0035 a0001c0001t0003g0063 |
2 | HG01243.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.221-13478G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10891473 | |||||||
| chr19:10891589 | C | A | 73 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(70): Show |
76 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.221-13362C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10891589 | |||||||
| chr19:10891625 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.221-13326T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10891625 | |||||||
| chr19:10891626 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.221-13325C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10891626 | |||||||
| chr19:10891903 | A | G | 327 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(324): Show |
336 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.221-13048A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10891903 | |||||||
| chr19:10891954 | A | T | 1 | a0001c0001t0001g0022 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.221-12997A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10891954 | |||||||
| chr19:10891971 | T | C | 7 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0001t0002g0136 others(4): Show |
7 | HG00639.hp1 HG02293.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-12980T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10891971 | |||||||
| chr19:10892005 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.221-12946C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10892005 | |||||||
| chr19:10892080 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.221-12871G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10892080 | |||||||
| chr19:10892186 | A | C | 153 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(150): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.221-12765A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10892186 | |||||||
| chr19:10892232 | G | A | 1 | a0001c0001t0008g0014 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.221-12719G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10892232 | |||||||
| chr19:10892246 | A | G | 3 | a0001c0001t0002g0046 a0001c0001t0002g0051 a0001c0001t0002g0068 |
3 | HG02040.hp1 NA18944.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.221-12705A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10892246 | |||||||
| chr19:10892547 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.221-12404G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10892547 | |||||||
| chr19:10892666 | CCTCCATT others(18): Show |
C | 2 | a0001c0001t0002g0031 a0001c0001t0002g0064 |
2 | HG00140.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.221-12283_221-1225 others(29): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10892666 | ||||||
| chr19:10892685 | C | T | 70 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(67): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.221-12266C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10892685 | |||||||
| chr19:10892853 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.221-12098C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10892853 | |||||||
| chr19:10892882 | G | A | 2 | a0002c0003t0001g0094 a0002c0003t0001g0095 |
2 | HG00140.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.221-12069G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10892882 | |||||||
| chr19:10893367 | C | A | 1 | a0001c0006t0017g0342 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.221-11584C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10893367 | |||||||
| chr19:10893402 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.221-11549G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10893402 | |||||||
| chr19:10893554 | G | A | 79 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(76): Show |
82 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.221-11397G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10893554 | |||||||
| chr19:10893697 | G | C | 2 | a0001c0001t0002g0251 a0001c0001t0002g0254 |
2 | NA18981.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.221-11254G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10893697 | |||||||
| chr19:10893702 | A | G | 2 | a0001c0001t0002g0041 a0001c0001t0002g0073 |
2 | NA18947.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.221-11249A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10893702 | |||||||
| chr19:10894025 | G | C | 2 | a0001c0001t0002g0031 a0001c0001t0002g0064 |
2 | HG00140.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.221-10926G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10894025 | |||||||
| chr19:10894099 | G | A | 4 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-10852G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10894099 | |||||||
| chr19:10894143 | C | T | 1 | a0001c0005t0013g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221-10808C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10894143 | |||||||
| chr19:10894157 | C | T | 19 | a0001c0001t0002g0004 a0001c0001t0002g0013 a0001c0001t0002g0027 others(16): Show |
20 | HG01069.hp2 HG01071.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.221-10794C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10894157 | |||||||
| chr19:10894315 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.221-10636C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10894315 | |||||||
| chr19:10894377 | T | C | 1 | a0001c0001t0003g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.221-10574T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10894377 | |||||||
| chr19:10894454 | C | G | 3 | a0001c0001t0002g0242 a0001c0004t0002g0069 a0001c0004t0019g0020 |
3 | HG02257.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.221-10497C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10894454 | |||||||
| chr19:10894716 | G | GT | 9 | a0001c0001t0001g0007 a0001c0001t0001g0170 a0001c0001t0001g0309 others(6): Show |
10 | HG00597.hp2 HG01074.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.221-10221dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10894716 | ||||||
| chr19:10894716 | GT | G | 60 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(57): Show |
63 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.221-10221delT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10894716 | ||||||
| chr19:10894904 | C | T | 1 | a0001c0001t0006g0169 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.221-10047C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10894904 | |||||||
| chr19:10894945 | G | A | 78 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(75): Show |
81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.221-10006G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10894945 | |||||||
| chr19:10895043 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.221-9908C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10895043 | |||||||
| chr19:10895061 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.221-9890A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10895061 | |||||||
| chr19:10895120 | T | C | 1 | a0001c0001t0011g0015 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.221-9831T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10895120 | |||||||
| chr19:10895219 | C | T | 5 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0331 others(2): Show |
5 | HG02258.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-9732C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10895219 | |||||||
| chr19:10895483 | C | T | 2 | a0002c0003t0001g0094 a0002c0003t0001g0095 |
2 | HG00140.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.221-9468C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10895483 | |||||||
| chr19:10895632 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.221-9319C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10895632 | |||||||
| chr19:10895690 | G | T | 1 | a0001c0001t0002g0147 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.221-9261G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10895690 | |||||||
| chr19:10895822 | A | C | 2 | a0001c0001t0002g0051 a0001c0001t0002g0068 |
2 | NA18944.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.221-9129A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10895822 | |||||||
| chr19:10896032 | A | G | 182 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(179): Show |
186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.221-8919A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10896032 | |||||||
| chr19:10896073 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.221-8878C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10896073 | |||||||
| chr19:10896115 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0202 a0001c0001t0002g0179 |
3 | HG02683.hp1 HG02735.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.221-8836C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10896115 | |||||||
| chr19:10896445 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.221-8506A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10896445 | |||||||
| chr19:10896478 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.221-8473C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10896478 | |||||||
| chr19:10896506 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.221-8445T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10896506 | |||||||
| chr19:10896762 | G | A | 5 | a0001c0001t0002g0065 a0001c0001t0002g0091 a0001c0001t0002g0092 others(2): Show |
5 | NA18946.hp2 NA18985.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-8189G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10896762 | |||||||
| chr19:10896917 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.221-8034G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10896917 | |||||||
| chr19:10896997 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.221-7954G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10896997 | |||||||
| chr19:10897173 | C | A | 1 | a0001c0001t0001g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.221-7778C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10897173 | |||||||
| chr19:10897343 | T | G | 1 | a0001c0001t0002g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.221-7608T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10897343 | |||||||
| chr19:10897546 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.221-7405G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10897546 | |||||||
| chr19:10897881 | G | A | 6 | a0001c0001t0002g0037 a0001c0001t0002g0066 a0001c0001t0002g0072 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-7070G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10897881 | |||||||
| chr19:10897901 | C | G | 1 | a0001c0001t0002g0149 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.221-7050C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10897901 | |||||||
| chr19:10897902 | G | A | 2 | a0002c0003t0001g0094 a0002c0003t0001g0095 |
2 | HG00140.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.221-7049G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10897902 | |||||||
| chr19:10897951 | A | G | 4 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-7000A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10897951 | |||||||
| chr19:10897963 | C | T | 3 | a0001c0001t0002g0242 a0001c0004t0002g0069 a0001c0004t0019g0020 |
3 | HG02257.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.221-6988C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10897963 | |||||||
| chr19:10898049 | A | G | 2 | a0001c0001t0002g0089 a0001c0005t0002g0090 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.221-6902A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10898049 | |||||||
| chr19:10898061 | T | G | 71 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(68): Show |
74 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.221-6890T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10898061 | |||||||
| chr19:10898092 | C | T | 1 | a0001c0001t0020g0277 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.221-6859C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10898092 | |||||||
| chr19:10898476 | C | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.221-6475C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10898476 | |||||||
| chr19:10898551 | C | G | 8 | a0001c0001t0001g0181 a0001c0001t0002g0025 a0001c0001t0002g0140 others(5): Show |
8 | HG00408.hp2 HG00597.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-6400C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10898551 | |||||||
| chr19:10898589 | G | C | 9 | a0001c0001t0002g0100 a0001c0001t0002g0117 a0001c0001t0002g0120 others(6): Show |
9 | HG00323.hp2 HG00733.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-6362G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10898589 | |||||||
| chr19:10898678 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.221-6273G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10898678 | |||||||
| chr19:10899033 | G | GT | 100 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0163 others(97): Show |
104 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-5898dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10899033 | ||||||
| chr19:10899033 | G | GTT | 17 | a0001c0001t0001g0243 a0001c0001t0001g0333 a0001c0001t0002g0049 others(14): Show |
17 | HG01952.hp2 HG02015.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.221-5899_221-5898d others(4): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10899033 | ||||||
| chr19:10899161 | G | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | HG02486.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-5790G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10899161 | |||||||
| chr19:10899228 | G | A | 3 | a0001c0001t0002g0242 a0001c0004t0002g0069 a0001c0004t0019g0020 |
3 | HG02257.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.221-5723G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10899228 | |||||||
| chr19:10899278 | C | T | 80 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(77): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.221-5673C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10899278 | |||||||
| chr19:10899541 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0275 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.221-5410C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10899541 | |||||||
| chr19:10899723 | C | CT | 6 | a0001c0001t0001g0165 a0001c0001t0002g0054 a0001c0001t0002g0125 others(3): Show |
6 | HG01516.hp1 NA18967.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-5213dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10899723 | ||||||
| chr19:10899964 | G | A | 1 | a0001c0001t0002g0189 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.221-4987G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10899964 | |||||||
| chr19:10899990 | C | T | 2 | a0001c0001t0002g0028 a0001c0001t0002g0082 |
2 | HG02080.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.221-4961C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10899990 | |||||||
| chr19:10900006 | C | T | 1 | a0001c0001t0004g0080 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.221-4945C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10900006 | |||||||
| chr19:10900146 | C | CA | 70 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(67): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.221-4798dupA | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10900146 | ||||||
| chr19:10900205 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0284 a0001c0005t0013g0096 |
3 | HG01943.hp2 HG04115.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.221-4746G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10900205 | |||||||
| chr19:10900363 | G | T | 1 | a0001c0001t0002g0315 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.221-4588G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10900363 | |||||||
| chr19:10900422 | C | G | 1 | a0001c0002t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.221-4529C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10900422 | |||||||
| chr19:10900561 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.221-4390T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10900561 | |||||||
| chr19:10900596 | T | C | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.221-4355T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10900596 | |||||||
| chr19:10900963 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.221-3988G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10900963 | |||||||
| chr19:10901004 | C | T | 69 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(66): Show |
69 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.221-3947C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901004 | |||||||
| chr19:10901086 | A | G | 2 | a0001c0001t0002g0175 a0001c0001t0002g0180 |
2 | NA18985.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.221-3865A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901086 | |||||||
| chr19:10901202 | T | G | 1 | a0001c0006t0017g0342 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.221-3749T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901202 | |||||||
| chr19:10901373 | C | T | 2 | a0001c0001t0006g0168 a0001c0001t0006g0169 |
2 | HG02071.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.221-3578C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901373 | |||||||
| chr19:10901708 | G | A | 2 | a0001c0001t0002g0025 a0001c0001t0007g0026 |
2 | NA19062.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.221-3243G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901708 | |||||||
| chr19:10901723 | C | G | 1 | a0001c0001t0001g0302 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.221-3228C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901723 | |||||||
| chr19:10901903 | A | C | 7 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0232 others(4): Show |
7 | HG00621.hp1 NA18956.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-3048A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901903 | |||||||
| chr19:10901904 | G | C | 7 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0232 others(4): Show |
7 | HG00621.hp1 NA18956.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-3047G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901904 | |||||||
| chr19:10901905 | T | C | 7 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0232 others(4): Show |
7 | HG00621.hp1 NA18956.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-3046T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901905 | |||||||
| chr19:10901908 | T | C | 7 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0232 others(4): Show |
7 | HG00621.hp1 NA18956.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-3043T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901908 | |||||||
| chr19:10901928 | A | G | 7 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0232 others(4): Show |
7 | HG00621.hp1 NA18956.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-3023A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901928 | |||||||
| chr19:10901934 | T | G | 7 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0232 others(4): Show |
7 | HG00621.hp1 NA18956.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-3017T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901934 | |||||||
| chr19:10901936 | A | G | 7 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0232 others(4): Show |
7 | HG00621.hp1 NA18956.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-3015A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901936 | |||||||
| chr19:10901940 | A | C | 7 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0232 others(4): Show |
7 | HG00621.hp1 NA18956.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-3011A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901940 | |||||||
| chr19:10901943 | T | C | 7 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0232 others(4): Show |
7 | HG00621.hp1 NA18956.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-3008T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10901943 | |||||||
| chr19:10901948 | C | CAAAAAAA others(28): Show |
2 | a0001c0001t0001g0232 a0001c0001t0001g0327 |
2 | NA18994.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.221-3001_221-3000i others(37): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10901948 | ||||||
| chr19:10901948 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0318 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.221-3001_221-3000i others(38): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10901948 | ||||||
| chr19:10901948 | C | CAAAAAAA others(30): Show |
2 | a0001c0001t0001g0226 a0001c0001t0001g0301 |
2 | HG00621.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.221-3001_221-3000i others(39): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10901948 | ||||||
| chr19:10901948 | C | CAAAAAAA others(31): Show |
1 | a0001c0001t0001g0219 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.221-3001_221-3000i others(40): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10901948 | ||||||
| chr19:10901948 | C | CAAAAAAA others(32): Show |
1 | a0001c0001t0001g0330 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.221-3001_221-3000i others(41): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10901948 | ||||||
| chr19:10902009 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.221-2942C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902009 | |||||||
| chr19:10902024 | G | A | 64 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(61): Show |
64 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.221-2927G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902024 | |||||||
| chr19:10902033 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221-2918C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902033 | |||||||
| chr19:10902070 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-2881T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902070 | |||||||
| chr19:10902104 | C | T | 2 | a0001c0001t0002g0089 a0001c0005t0002g0090 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.221-2847C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902104 | |||||||
| chr19:10902126 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.221-2825C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902126 | |||||||
| chr19:10902273 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.221-2678C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902273 | |||||||
| chr19:10902290 | C | CT | 81 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0148 others(78): Show |
82 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.221-2640dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10902290 | ||||||
| chr19:10902290 | CT | C | 14 | a0001c0001t0001g0194 a0001c0001t0001g0225 a0001c0001t0001g0227 others(11): Show |
14 | HG00140.hp1 HG00323.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-2640delT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10902290 | ||||||
| chr19:10902290 | CTT | C | 8 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0065 others(5): Show |
8 | HG00140.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-2641_221-2640d others(4): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10902290 | ||||||
| chr19:10902290 | CTTT | C | 61 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(58): Show |
64 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.221-2642_221-2640d others(5): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10902290 | ||||||
| chr19:10902294 | T | C | 7 | a0001c0001t0002g0117 a0001c0001t0002g0120 a0001c0001t0002g0121 others(4): Show |
7 | HG00733.hp2 HG01109.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-2657T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902294 | |||||||
| chr19:10902295 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.221-2656T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902295 | |||||||
| chr19:10902352 | G | A | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.221-2599G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902352 | |||||||
| chr19:10902357 | G | C | 7 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0232 others(4): Show |
7 | HG00621.hp1 NA18956.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-2594G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902357 | |||||||
| chr19:10902589 | G | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.221-2362G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902589 | |||||||
| chr19:10902608 | CT | C | 150 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(147): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.221-2326delT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10902608 | ||||||
| chr19:10902712 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.221-2239G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902712 | |||||||
| chr19:10902775 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.221-2176T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902775 | |||||||
| chr19:10902801 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.221-2150G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902801 | |||||||
| chr19:10902861 | C | G | 1 | a0002c0003t0001g0094 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.221-2090C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10902861 | |||||||
| chr19:10903238 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.221-1713G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10903238 | |||||||
| chr19:10903271 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.221-1680G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10903271 | |||||||
| chr19:10903564 | CT | C | 28 | a0001c0001t0001g0019 a0001c0001t0001g0195 a0001c0001t0001g0247 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.221-1372delT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 10903564 | ||||||
| chr19:10903578 | T | A | 3 | a0001c0001t0002g0242 a0001c0004t0002g0069 a0001c0004t0019g0020 |
3 | HG02257.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.221-1373T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10903578 | |||||||
| chr19:10903579 | T | A | 81 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(78): Show |
84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.221-1372T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10903579 | |||||||
| chr19:10903581 | A | T | 81 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(78): Show |
84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.221-1370A>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10903581 | |||||||
| chr19:10903775 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0002g0097 a0001c0001t0002g0098 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-1176C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10903775 | |||||||
| chr19:10904033 | C | T | 4 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-918C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10904033 | |||||||
| chr19:10904261 | C | T | 78 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(75): Show |
81 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.221-690C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10904261 | |||||||
| chr19:10904526 | G | A | 4 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-425G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10904526 | |||||||
| chr19:10904688 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.221-263C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10904688 | |||||||
| chr19:10904765 | C | T | 1 | a0001c0001t0016g0274 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221-186C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10904765 | |||||||
| chr19:10904846 | C | G | 1 | a0001c0001t0002g0115 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.221-105C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10904846 | |||||||
| chr19:10904891 | G | A | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.221-60G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 1/15 | chr19 | 10904891 | |||||||
| chr19:10905182 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.346+106A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905182 | |||||||
| chr19:10905287 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.346+211C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905287 | |||||||
| chr19:10905394 | GGCC | G | 128 | a0001c0001t0001g0075 a0001c0001t0001g0146 a0001c0001t0001g0148 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.346+319_346+321del others(3): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905394 | |||||||
| chr19:10905400 | C | T | 128 | a0001c0001t0001g0075 a0001c0001t0001g0146 a0001c0001t0001g0148 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.346+324C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905400 | |||||||
| chr19:10905401 | T | TTA | 128 | a0001c0001t0001g0075 a0001c0001t0001g0146 a0001c0001t0001g0148 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.346+325_346+326ins others(2): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905401 | |||||||
| chr19:10905403 | T | G | 128 | a0001c0001t0001g0075 a0001c0001t0001g0146 a0001c0001t0001g0148 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.346+327T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905403 | |||||||
| chr19:10905578 | G | T | 1 | a0001c0001t0012g0083 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.346+502G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905578 | |||||||
| chr19:10905610 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.346+534C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905610 | |||||||
| chr19:10905669 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.346+593G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905669 | |||||||
| chr19:10905784 | G | C | 2 | a0001c0001t0002g0042 a0001c0001t0002g0048 |
2 | NA18939.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.346+708G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905784 | |||||||
| chr19:10905942 | C | CT | 78 | a0001c0001t0001g0067 a0001c0001t0001g0148 a0001c0001t0001g0165 others(75): Show |
78 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.346+890dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 10905942 | ||||||
| chr19:10905942 | C | CTT | 10 | a0001c0001t0001g0146 a0001c0001t0001g0170 a0001c0001t0001g0264 others(7): Show |
10 | HG02809.hp1 HG03041.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.346+889_346+890dup others(2): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 10905942 | ||||||
| chr19:10905942 | C | CTTTTTTT others(6): Show |
1 | a0001c0006t0017g0342 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.346+878_346+890dup others(13): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 10905942 | ||||||
| chr19:10905942 | CT | C | 16 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0193 others(13): Show |
16 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.346+890delT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 10905942 | ||||||
| chr19:10905943 | T | C | 8 | a0001c0001t0002g0117 a0001c0001t0002g0120 a0001c0001t0002g0121 others(5): Show |
8 | HG00733.hp2 HG01109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.346+867T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905943 | |||||||
| chr19:10905944 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.346+868T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10905944 | |||||||
| chr19:10906041 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.346+965C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10906041 | |||||||
| chr19:10906259 | C | T | 1 | a0001c0004t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.346+1183C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10906259 | |||||||
| chr19:10906461 | T | C | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.346+1385T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10906461 | |||||||
| chr19:10906583 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.347-1456G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10906583 | |||||||
| chr19:10906861 | C | CTTTAT | 100 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
107 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.347-1119_347-1115d others(7): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 10906861 | ||||||
| chr19:10906861 | C | CTTTATTT others(3): Show |
22 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0164 others(19): Show |
22 | HG01099.hp1 HG01243.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.347-1124_347-1115d others(12): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 10906861 | ||||||
| chr19:10906861 | C | CTTTATTT others(8): Show |
3 | a0001c0001t0001g0162 a0001c0001t0001g0209 a0001c0001t0012g0083 |
3 | NA18961.hp1 NA19064.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.347-1129_347-1115d others(17): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 10906861 | ||||||
| chr19:10906861 | C | CTTTATTT others(33): Show |
1 | a0001c0001t0001g0324 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.347-1154_347-1115d others(42): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 10906861 | ||||||
| chr19:10906861 | CTTTAT | C | 53 | a0001c0001t0001g0181 a0001c0001t0001g0216 a0001c0001t0001g0217 others(50): Show |
54 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.347-1119_347-1115d others(7): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 10906861 | ||||||
| chr19:10906861 | CTTTATTT others(3): Show |
C | 63 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.347-1124_347-1115d others(12): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 10906861 | ||||||
| chr19:10906861 | CTTTATTT others(8): Show |
C | 6 | a0001c0001t0001g0170 a0001c0001t0002g0097 a0001c0001t0002g0099 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-1129_347-1115d others(17): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr19 | 10906861 | ||||||
| chr19:10907154 | G | A | 3 | a0001c0001t0002g0037 a0001c0001t0002g0110 a0003c0007t0002g0070 |
3 | HG02809.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.347-885G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10907154 | |||||||
| chr19:10907727 | G | A | 149 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(146): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.347-312G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10907727 | |||||||
| chr19:10907903 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.347-136C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10907903 | |||||||
| chr19:10907929 | A | G | 1 | a0001c0005t0013g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347-110A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10907929 | |||||||
| chr19:10907945 | C | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02965.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.347-94C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 2/15 | chr19 | 10907945 | |||||||
| chr19:10908200 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.453+55C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 3/15 | chr19 | 10908200 | |||||||
| chr19:10908693 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.454-410C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 3/15 | chr19 | 10908693 | |||||||
| chr19:10908756 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.454-347C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 3/15 | chr19 | 10908756 | |||||||
| chr19:10908867 | G | A | 70 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(67): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.454-236G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 3/15 | chr19 | 10908867 | |||||||
| chr19:10908905 | C | A | 2 | a0001c0001t0002g0004 a0001c0001t0002g0127 |
3 | HG01069.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.454-198C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 3/15 | chr19 | 10908905 | |||||||
| chr19:10909219 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.558+12G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10909219 | |||||||
| chr19:10909310 | T | C | 4 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(1): Show |
4 | HG02698.hp2 HG02738.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+103T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10909310 | |||||||
| chr19:10909318 | T | C | 280 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(277): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.558+111T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10909318 | |||||||
| chr19:10909405 | T | C | 62 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(59): Show |
65 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.558+198T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10909405 | |||||||
| chr19:10909474 | G | A | 2 | a0001c0001t0002g0041 a0001c0001t0002g0073 |
2 | NA18947.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.558+267G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10909474 | |||||||
| chr19:10909487 | G | A | 2 | a0001c0001t0002g0089 a0001c0005t0002g0090 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.558+280G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10909487 | |||||||
| chr19:10909510 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.558+303C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10909510 | |||||||
| chr19:10909563 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.558+356G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10909563 | |||||||
| chr19:10909739 | A | AAAAC | 147 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(144): Show |
150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.558+548_558+551dup others(4): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 10909739 | ||||||
| chr19:10909759 | A | C | 1 | a0001c0001t0002g0108 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.558+552A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10909759 | |||||||
| chr19:10909814 | G | A | 1 | a0001c0001t0002g0246 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.558+607G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10909814 | |||||||
| chr19:10909990 | G | A | 1 | a0001c0005t0013g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.558+783G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10909990 | |||||||
| chr19:10910039 | G | T | 1 | a0001c0001t0001g0335 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.558+832G>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10910039 | |||||||
| chr19:10910154 | G | A | 2 | a0002c0003t0001g0094 a0002c0003t0001g0095 |
2 | HG00140.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.558+947G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10910154 | |||||||
| chr19:10910279 | C | T | 2 | a0001c0002t0001g0112 a0001c0002t0001g0114 |
2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.558+1072C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10910279 | |||||||
| chr19:10910357 | T | C | 6 | a0001c0001t0002g0037 a0001c0001t0002g0066 a0001c0001t0002g0072 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.558+1150T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10910357 | |||||||
| chr19:10910588 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.558+1381A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10910588 | |||||||
| chr19:10910767 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.559-1417T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10910767 | |||||||
| chr19:10910859 | C | T | 1 | a0001c0001t0004g0133 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.559-1325C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10910859 | |||||||
| chr19:10910983 | T | C | 1 | a0001c0002t0015g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.559-1201T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10910983 | |||||||
| chr19:10911364 | G | C | 1 | a0001c0001t0001g0303 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.559-820G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10911364 | |||||||
| chr19:10911397 | C | T | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.559-787C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10911397 | |||||||
| chr19:10911483 | T | C | 78 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(75): Show |
81 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.559-701T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10911483 | |||||||
| chr19:10912004 | C | T | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.559-180C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10912004 | |||||||
| chr19:10912059 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0237 a0001c0001t0001g0238 others(5): Show |
9 | HG01109.hp1 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.559-125C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10912059 | |||||||
| chr19:10912133 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.559-51C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 4/15 | chr19 | 10912133 | |||||||
| chr19:10912318 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.669+24C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10912318 | |||||||
| chr19:10912355 | C | T | 3 | a0001c0001t0002g0242 a0001c0004t0002g0069 a0001c0004t0019g0020 |
3 | HG02257.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.669+61C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10912355 | |||||||
| chr19:10912419 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.669+125T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10912419 | |||||||
| chr19:10912484 | C | G | 1 | a0001c0001t0001g0329 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.669+190C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10912484 | |||||||
| chr19:10912556 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.669+262G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10912556 | |||||||
| chr19:10912558 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.669+264T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10912558 | |||||||
| chr19:10912591 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.669+297G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10912591 | |||||||
| chr19:10912691 | G | A | 2 | a0001c0001t0001g0201 a0002c0003t0001g0095 |
2 | HG00140.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.669+397G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10912691 | |||||||
| chr19:10912718 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0156 a0001c0001t0001g0157 others(7): Show |
12 | HG00323.hp1 HG00741.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.669+424C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10912718 | |||||||
| chr19:10912758 | C | T | 24 | a0001c0001t0001g0192 a0001c0001t0001g0216 a0001c0001t0001g0217 others(21): Show |
25 | HG01069.hp2 HG01071.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.669+464C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10912758 | |||||||
| chr19:10912938 | C | T | 1 | a0001c0006t0017g0342 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.669+644C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10912938 | |||||||
| chr19:10913123 | T | G | 2 | a0001c0001t0002g0124 a0001c0001t0002g0126 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.670-754T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10913123 | |||||||
| chr19:10913357 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.670-520G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10913357 | |||||||
| chr19:10913487 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG00642.hp1 HG00738.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.670-390G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10913487 | |||||||
| chr19:10913641 | C | T | 1 | a0001c0005t0013g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.670-236C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10913641 | |||||||
| chr19:10913662 | G | A | 6 | a0001c0001t0002g0037 a0001c0001t0002g0066 a0001c0001t0002g0072 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-215G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10913662 | |||||||
| chr19:10913731 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0338 |
2 | HG00558.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.670-146G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10913731 | |||||||
| chr19:10913763 | A | G | 1 | a0002c0003t0001g0094 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.670-114A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 5/15 | chr19 | 10913763 | |||||||
| chr19:10914075 | A | G | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.847+21A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10914075 | |||||||
| chr19:10914187 | C | T | 3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 |
3 | HG02559.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.847+133C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10914187 | |||||||
| chr19:10914310 | C | T | 80 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(77): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+256C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10914310 | |||||||
| chr19:10914311 | G | A | 2 | a0001c0001t0002g0251 a0001c0001t0002g0254 |
2 | NA18981.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.847+257G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10914311 | |||||||
| chr19:10914756 | G | A | 75 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(72): Show |
78 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.847+702G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10914756 | |||||||
| chr19:10914803 | G | A | 1 | a0001c0001t0001g0335 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.847+749G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10914803 | |||||||
| chr19:10914824 | G | C | 2 | a0001c0001t0002g0100 a0001c0001t0002g0122 |
2 | HG00323.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.847+770G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10914824 | |||||||
| chr19:10914890 | G | C | 3 | a0001c0001t0001g0211 a0001c0001t0001g0265 a0001c0001t0001g0267 |
3 | HG01884.hp1 HG01952.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.847+836G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10914890 | |||||||
| chr19:10915236 | T | A | 2 | a0001c0001t0002g0251 a0001c0001t0002g0254 |
2 | NA18981.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.848-1171T>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10915236 | |||||||
| chr19:10915369 | C | T | 1 | a0001c0001t0002g0011 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.848-1038C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10915369 | |||||||
| chr19:10915380 | C | G | 2 | a0001c0001t0002g0097 a0001c0001t0002g0099 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.848-1027C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10915380 | |||||||
| chr19:10915398 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.848-1009G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10915398 | |||||||
| chr19:10915647 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.848-760G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10915647 | |||||||
| chr19:10915743 | G | C | 1 | a0001c0001t0001g0209 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.848-664G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10915743 | |||||||
| chr19:10915748 | C | T | 2 | a0001c0001t0002g0089 a0001c0005t0002g0090 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.848-659C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10915748 | |||||||
| chr19:10916056 | C | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | NA18970.hp2 NA18981.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.848-351C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10916056 | |||||||
| chr19:10916092 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.848-315G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10916092 | |||||||
| chr19:10916277 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.848-130G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10916277 | |||||||
| chr19:10916288 | C | T | 4 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(1): Show |
4 | HG02559.hp1 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-119C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 6/15 | chr19 | 10916288 | |||||||
| chr19:10916646 | T | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0202 |
2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.939-50T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 7/15 | chr19 | 10916646 | |||||||
| chr19:10916837 | C | T | 9 | a0001c0001t0002g0100 a0001c0001t0002g0117 a0001c0001t0002g0120 others(6): Show |
9 | HG00323.hp2 HG00733.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020+60C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10916837 | |||||||
| chr19:10916899 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1020+122C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10916899 | |||||||
| chr19:10916950 | C | A | 144 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(141): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1020+173C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10916950 | |||||||
| chr19:10917199 | A | C | 3 | a0001c0001t0002g0054 a0001c0001t0002g0060 a0001c0001t0002g0078 |
3 | HG02135.hp2 NA18967.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1020+422A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10917199 | |||||||
| chr19:10917338 | G | A | 70 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(67): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1020+561G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10917338 | |||||||
| chr19:10917345 | C | T | 1 | a0002c0003t0001g0095 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1020+568C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10917345 | |||||||
| chr19:10917363 | G | C | 2 | a0002c0003t0001g0094 a0002c0003t0001g0095 |
2 | HG00140.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1020+586G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10917363 | |||||||
| chr19:10917367 | C | T | 2 | a0001c0002t0001g0112 a0001c0002t0001g0114 |
2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1020+590C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10917367 | |||||||
| chr19:10917494 | G | C | 1 | a0001c0001t0002g0028 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1020+717G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10917494 | |||||||
| chr19:10917590 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1020+813C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10917590 | |||||||
| chr19:10917595 | G | C | 2 | a0002c0003t0001g0094 a0002c0003t0001g0095 |
2 | HG00140.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1020+818G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10917595 | |||||||
| chr19:10917718 | C | CT | 83 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0148 others(80): Show |
84 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1020+958dupT | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr19 | 10917718 | ||||||
| chr19:10917961 | C | T | 1 | a0001c0004t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1020+1184C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10917961 | |||||||
| chr19:10917963 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1020+1186C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10917963 | |||||||
| chr19:10917973 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1020+1196A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10917973 | |||||||
| chr19:10918391 | A | G | 1 | a0001c0001t0002g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1021-1204A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918391 | |||||||
| chr19:10918404 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1021-1191G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918404 | |||||||
| chr19:10918540 | G | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
12 | HG01099.hp1 HG02486.hp1 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.1021-1055G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918540 | |||||||
| chr19:10918551 | T | C | 2 | a0001c0001t0002g0004 a0001c0001t0002g0127 |
3 | HG01069.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1021-1044T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918551 | |||||||
| chr19:10918625 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1021-970G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918625 | |||||||
| chr19:10918629 | C | A | 1 | a0001c0001t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1021-966C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918629 | |||||||
| chr19:10918630 | G | C | 1 | a0001c0001t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1021-965G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918630 | |||||||
| chr19:10918631 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1021-964C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918631 | |||||||
| chr19:10918633 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1021-962C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918633 | |||||||
| chr19:10918635 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1021-960C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918635 | |||||||
| chr19:10918638 | T | C | 80 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(77): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.1021-957T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918638 | |||||||
| chr19:10918698 | T | G | 1 | a0001c0001t0002g0037 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1021-897T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918698 | |||||||
| chr19:10918733 | C | T | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1021-862C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918733 | |||||||
| chr19:10918992 | C | T | 2 | a0001c0001t0002g0105 a0001c0001t0002g0132 |
2 | NA18962.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1021-603C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918992 | |||||||
| chr19:10918993 | T | C | 80 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(77): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.1021-602T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10918993 | |||||||
| chr19:10919060 | G | A | 75 | a0001c0001t0001g0075 a0001c0001t0001g0243 a0001c0001t0002g0001 others(72): Show |
78 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1021-535G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10919060 | |||||||
| chr19:10919078 | CCTCAGCC others(6): Show |
C | 1 | a0001c0001t0001g0262 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1021-516_1021-504d others(15): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10919078 | |||||||
| chr19:10919168 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1021-427C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10919168 | |||||||
| chr19:10919376 | C | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0238 a0001c0001t0001g0311 others(2): Show |
6 | HG01109.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021-219C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10919376 | |||||||
| chr19:10919590 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18978.hp1 | splice_region_variant&intron_variant | LOW | c.1021-5C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 8/15 | chr19 | 10919590 | |||||||
| chr19:10919689 | A | ACCCACAC others(6): Show |
1 | a0001c0001t0011g0015 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1106+11_1106+23dup others(13): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | 10919689 | ||||||
| chr19:10919703 | C | T | 1 | a0001c0001t0002g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1106+23C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 9/15 | chr19 | 10919703 | |||||||
| chr19:10919860 | T | TTGCTGGG others(7): Show |
1 | a0003c0007t0002g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1107-17_1107-16ins others(14): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 9/15 | chr19 | 10919860 | |||||||
| chr19:10919862 | C | A | 1 | a0003c0007t0002g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1107-15C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 9/15 | chr19 | 10919862 | |||||||
| chr19:10919864 | C | A | 1 | a0003c0007t0002g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1107-13C>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 9/15 | chr19 | 10919864 | |||||||
| chr19:10919865 | T | G | 1 | a0003c0007t0002g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1107-12T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 9/15 | chr19 | 10919865 | |||||||
| chr19:10919866 | T | G | 1 | a0003c0007t0002g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1107-11T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 9/15 | chr19 | 10919866 | |||||||
| chr19:10919867 | T | C | 1 | a0003c0007t0002g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1107-10T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 9/15 | chr19 | 10919867 | |||||||
| chr19:10919873 | C | G | 1 | a0003c0007t0002g0070 | 1 | HG02896.hp2 | splice_region_variant&intron_variant | LOW | c.1107-4C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 9/15 | chr19 | 10919873 | |||||||
| chr19:10919875 | A | C | 1 | a0003c0007t0002g0070 | 1 | HG02896.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1107-2A>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 9/15 | chr19 | 10919875 | |||||||
| chr19:10919876 | G | C | 1 | a0003c0007t0002g0070 | 1 | HG02896.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1107-1G>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 9/15 | chr19 | 10919876 | |||||||
| chr19:10919988 | A | G | 21 | a0001c0001t0001g0220 a0001c0001t0001g0304 a0001c0001t0002g0004 others(18): Show |
22 | HG01069.hp2 HG01071.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1196+22A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/15 | chr19 | 10919988 | |||||||
| chr19:10920098 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1196+132C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/15 | chr19 | 10920098 | |||||||
| chr19:10920123 | GGT | G | 317 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(314): Show |
325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.1196+176_1196+177d others(4): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 10920123 | ||||||
| chr19:10920123 | GGTGT | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0193 a0001c0001t0001g0194 others(6): Show |
10 | HG00408.hp1 HG02080.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.1196+174_1196+177d others(6): Show |
CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 10920123 | ||||||
| chr19:10920127 | T | G | 1 | a0001c0001t0003g0062 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1196+161T>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/15 | chr19 | 10920127 | |||||||
| chr19:10920208 | C | G | 2 | a0001c0001t0002g0089 a0001c0005t0002g0090 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1197-228C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/15 | chr19 | 10920208 | |||||||
| chr19:10920258 | T | C | 2 | a0001c0001t0002g0097 a0001c0001t0002g0099 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1197-178T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 10/15 | chr19 | 10920258 | |||||||
| chr19:10920598 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1334+25G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 11/15 | chr19 | 10920598 | |||||||
| chr19:10920654 | C | T | 1 | a0001c0001t0010g0043 | 1 | HG00423.hp2 | splice_region_variant&intron_variant | LOW | c.1335-5C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 11/15 | chr19 | 10920654 | |||||||
| chr19:10920788 | C | G | 138 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0146 others(135): Show |
141 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1424+40C>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 12/15 | chr19 | 10920788 | |||||||
| chr19:10920998 | G | A | 32 | a0001c0001t0002g0001 a0001c0001t0002g0016 a0001c0001t0002g0029 others(29): Show |
34 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1537+52G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 13/15 | chr19 | 10920998 | |||||||
| chr19:10921036 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1538-14C>T | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 13/15 | chr19 | 10921036 | |||||||
| chr19:10921164 | A | G | 8 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0242 others(5): Show |
8 | HG02257.hp2 HG02965.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615+37A>G | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 14/15 | chr19 | 10921164 | |||||||
| chr19:10921171 | G | A | 1 | a0001c0004t0019g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1615+44G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 14/15 | chr19 | 10921171 | |||||||
| chr19:10921336 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1616-39G>A | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 14/15 | chr19 | 10921336 | |||||||
| chr19:10921472 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1684+29T>C | CARM1 | ENSG00000142453.13 | transcript | ENST00000327064.9 | protein_coding | 15/15 | chr19 | 10921472 |