Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79800 |
| ensemblid | ENSG00000138380.18 |
| hgncid | 14435 |
| symbol | CARF |
| name | calcium responsive transcription factor |
| refseq_nuc | NM_024744.17 |
| refseq_prot | NP_079020.13 |
| ensembl_nuc | ENST00000438828.4 |
| ensembl_prot | ENSP00000414644.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 202912275 |
| end | 202988263 |
| strand | + |
| ver | v1.2 |
| region | chr2:202912275-202988263 |
| region5000 | chr2:202907275-202993263 |
| regionname0 | CARF_chr2_202912275_202988263 |
| regionname5000 | CARF_chr2_202907275_202993263 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 725 | 285 | 62 | 51 | 134 | 6 | 30 | 99 | CARF_chr2_202907275_202993263 | CARF | MEQSN others(720): Show |
chr2 | 202907275 | 202993263 |
| a0002 | 0/0 | 725 | 23 | 19 | 4 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | MEQSN others(720): Show |
chr2 | 202907275 | 202993263 |
| a0003 | 0/0 | 725 | 14 | 1 | 5 | 4 | 4 | 0 | 3 | CARF_chr2_202907275_202993263 | CARF | MEQSN others(720): Show |
chr2 | 202907275 | 202993263 |
| a0004 | 0/0 | 725 | 8 | 0 | 0 | 8 | 0 | 0 | 6 | CARF_chr2_202907275_202993263 | CARF | MEQSN others(720): Show |
chr2 | 202907275 | 202993263 |
| a0005 | 0/0 | 725 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | MEQSN others(720): Show |
chr2 | 202907275 | 202993263 |
| a0006 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | MEQSN others(720): Show |
chr2 | 202907275 | 202993263 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2175 | 277 | 55 | 51 | 133 | 6 | 30 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0001c0005 | 0/0 | 2175 | 5 | 5 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0001c0008 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0001c0011 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0002c0002 | 0/0 | 2175 | 22 | 19 | 3 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0002c0012 | 0/0 | 2175 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0003c0003 | 0/0 | 2175 | 9 | 0 | 5 | 0 | 4 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0003c0007 | 0/0 | 2175 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0003c0009 | 0/0 | 2175 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0003c0013 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0004c0004 | 0/0 | 2175 | 8 | 0 | 0 | 8 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0005c0006 | 0/0 | 2175 | 3 | 3 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 | ||
| a0006c0010 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | ATGGA others(2170): Show |
chr2 | 202907275 | 202993263 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7975 | 17 | 5 | 2 | 9 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0002 | 1/0 | 7974 | 24 | 16 | 5 | 1 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7969): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0003 | 0/0 | 7969 | 24 | 2 | 5 | 13 | 0 | 4 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7964): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0004 | 0/0 | 8027 | 22 | 1 | 2 | 17 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8022): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0005 | 0/0 | 7971 | 18 | 3 | 2 | 9 | 0 | 4 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7966): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0006 | 0/0 | 7977 | 17 | 0 | 3 | 11 | 1 | 2 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7972): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0007 | 0/0 | 8029 | 14 | 0 | 5 | 5 | 1 | 3 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8024): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0008 | 0/0 | 7973 | 11 | 4 | 2 | 5 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7968): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0009 | 0/0 | 7974 | 5 | 0 | 2 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7969): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0010 | 0/1 | 8033 | 9 | 1 | 4 | 1 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8028): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0011 | 0/0 | 7967 | 9 | 0 | 4 | 3 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7962): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0012 | 0/0 | 7979 | 6 | 0 | 1 | 4 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7974): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0013 | 0/0 | 8027 | 5 | 0 | 0 | 4 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8022): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0015 | 0/0 | 7974 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7969): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0016 | 0/0 | 8031 | 4 | 0 | 3 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8026): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0017 | 0/0 | 8039 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8034): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0018 | 0/0 | 8027 | 3 | 1 | 0 | 1 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8022): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0019 | 0/0 | 8025 | 3 | 0 | 0 | 2 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8020): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0020 | 0/0 | 8033 | 3 | 3 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8028): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0021 | 0/0 | 8029 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8024): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0022 | 0/0 | 7957 | 3 | 2 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7952): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0023 | 0/0 | 7975 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0025 | 0/0 | 7975 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0026 | 0/0 | 8031 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8026): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0027 | 0/0 | 8055 | 2 | 0 | 2 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8050): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0028 | 0/0 | 8031 | 2 | 0 | 1 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8026): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0029 | 0/0 | 8033 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8028): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0031 | 0/0 | 7951 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7946): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0032 | 0/0 | 7969 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7964): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0033 | 0/0 | 7971 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7966): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0034 | 0/0 | 7981 | 2 | 1 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7976): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0035 | 0/0 | 8001 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7996): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0038 | 0/0 | 7970 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7965): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0039 | 0/0 | 7970 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7965): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0040 | 0/0 | 7972 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7967): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0041 | 0/0 | 7974 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7969): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0042 | 0/0 | 7974 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7969): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0045 | 0/0 | 8027 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8022): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0046 | 0/0 | 8025 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8020): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0047 | 0/0 | 8051 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8046): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0048 | 0/0 | 8023 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8018): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0049 | 0/0 | 8027 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8022): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0050 | 0/0 | 8029 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8024): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0051 | 0/0 | 8053 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8048): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0052 | 0/0 | 8055 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8050): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0053 | 0/0 | 8025 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8020): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0054 | 0/0 | 8029 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8024): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0055 | 0/0 | 8053 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8048): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0056 | 0/0 | 8027 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8022): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0057 | 0/0 | 8045 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8040): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0058 | 0/0 | 8025 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8020): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0059 | 0/0 | 8029 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8024): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0060 | 0/0 | 8029 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8024): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0061 | 0/0 | 8029 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8024): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0062 | 0/0 | 8061 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8056): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0063 | 0/0 | 8027 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8022): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0064 | 0/0 | 8029 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8024): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0065 | 0/0 | 8031 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8026): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0066 | 0/0 | 8031 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8026): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0067 | 0/0 | 8033 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8028): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0068 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8030): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0069 | 0/0 | 8059 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8054): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0070 | 0/0 | 8033 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8028): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0071 | 0/0 | 8035 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8030): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0072 | 0/0 | 8023 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8018): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0073 | 0/0 | 8031 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8026): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0074 | 0/0 | 8033 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8028): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0077 | 0/0 | 7965 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7960): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0078 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7968): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0079 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7968): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0080 | 0/0 | 7979 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7974): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0081 | 0/0 | 7981 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7976): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0082 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0083 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7968): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0085 | 0/0 | 7971 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7966): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0087 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7968): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0088 | 0/0 | 7965 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7960): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0089 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7968): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0090 | 0/0 | 7979 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7974): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0091 | 0/0 | 7975 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0092 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7968): Show |
chr2 | 202907275 | 202993263 |
| a0001c0001t0093 | 0/0 | 8033 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8028): Show |
chr2 | 202907275 | 202993263 |
| a0001c0005t0030 | 0/0 | 7985 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7980): Show |
chr2 | 202907275 | 202993263 |
| a0001c0005t0044 | 0/0 | 7985 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7980): Show |
chr2 | 202907275 | 202993263 |
| a0001c0005t0075 | 0/0 | 8027 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8022): Show |
chr2 | 202907275 | 202993263 |
| a0001c0005t0076 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0001c0008t0001 | 0/0 | 7975 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0001c0011t0006 | 0/0 | 7977 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7972): Show |
chr2 | 202907275 | 202993263 |
| a0002c0002t0001 | 0/0 | 7975 | 20 | 17 | 3 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0002c0002t0043 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0002c0002t0084 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0002c0012t0001 | 0/0 | 7975 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0003c0003t0014 | 0/0 | 7970 | 4 | 0 | 2 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7965): Show |
chr2 | 202907275 | 202993263 |
| a0003c0003t0036 | 0/0 | 7966 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7961): Show |
chr2 | 202907275 | 202993263 |
| a0003c0003t0037 | 0/0 | 7974 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7969): Show |
chr2 | 202907275 | 202993263 |
| a0003c0003t0094 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7955): Show |
chr2 | 202907275 | 202993263 |
| a0003c0003t0095 | 0/0 | 7966 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7961): Show |
chr2 | 202907275 | 202993263 |
| a0003c0007t0037 | 0/0 | 7974 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7969): Show |
chr2 | 202907275 | 202993263 |
| a0003c0007t0097 | 0/0 | 7972 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7967): Show |
chr2 | 202907275 | 202993263 |
| a0003c0009t0014 | 0/0 | 7970 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7965): Show |
chr2 | 202907275 | 202993263 |
| a0003c0009t0096 | 0/0 | 7968 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7963): Show |
chr2 | 202907275 | 202993263 |
| a0003c0013t0098 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7970): Show |
chr2 | 202907275 | 202993263 |
| a0004c0004t0009 | 0/0 | 7974 | 5 | 0 | 0 | 5 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7969): Show |
chr2 | 202907275 | 202993263 |
| a0004c0004t0015 | 0/0 | 7974 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7969): Show |
chr2 | 202907275 | 202993263 |
| a0005c0006t0002 | 0/0 | 7974 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7969): Show |
chr2 | 202907275 | 202993263 |
| a0005c0006t0024 | 0/0 | 7974 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(7969): Show |
chr2 | 202907275 | 202993263 |
| a0006c0010t0086 | 0/0 | 8027 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | GCCTG others(8022): Show |
chr2 | 202907275 | 202993263 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0072 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0007g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0008g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0008g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0008g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0008g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0008g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0009g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0009g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0009g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0010g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0010g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0010g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0010g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0010g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0010g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0010g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0010g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0011g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0011g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0011g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0011g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0011g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0011g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0011g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0011g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0011g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0012g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0012g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0012g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0012g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0012g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0013g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0013g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0013g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0013g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0013g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0015g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0016g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0016g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0016g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0017g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0017g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0017g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0018g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0018g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0018g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0019g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0019g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0019g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0020g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0020g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0021g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0021g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0021g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0022g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0022g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0022g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0023g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0023g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0025g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0025g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0026g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0026g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0027g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0027g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0028g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0028g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0029g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0031g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0031g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0032g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0032g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0033g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0033g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0034g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0034g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0035g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0035g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0038g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0039g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0040g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0041g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0042g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0045g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0046g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0047g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0048g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0049g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0050g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0051g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0052g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0053g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0054g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0055g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0056g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0057g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0058g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0059g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0060g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0061g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0062g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0063g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0064g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0065g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0066g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0067g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0068g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0069g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0070g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0071g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0072g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0073g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0074g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0077g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0078g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0079g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0080g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0081g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0082g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0083g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0085g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0087g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0088g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0089g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0090g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0091g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0092g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0001t0093g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0005t0030g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0005t0030g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0005t0044g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0005t0075g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0005t0076g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0008t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0008t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0001c0011t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0043g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0002t0084g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0002c0012t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0003t0014g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0003t0014g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0003t0014g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0003t0014g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0003t0036g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0003t0037g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0003t0094g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0003t0095g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0007t0037g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0007t0097g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0009t0014g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0009t0096g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0003c0013t0098g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0004c0004t0009g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0004c0004t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0004c0004t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0004c0004t0009g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0004c0004t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0004c0004t0015g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0004c0004t0015g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0004c0004t0015g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0005c0006t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0005c0006t0024g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0005c0006t0024g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| a0006c0010t0086g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0283 | EUR | FIN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00323 | hp2 | a0001 | c0001 | t0012 | g0216 | EUR | FIN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00408 | hp2 | a0001 | c0001 | t0049 | g0035 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00423 | hp2 | a0001 | c0001 | t0019 | g0170 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00438 | hp1 | a0001 | c0001 | t0058 | g0121 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00438 | hp2 | a0003 | c0009 | t0096 | g0021 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00544 | hp1 | a0001 | c0001 | t0071 | g0164 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0227 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00597 | hp2 | a0001 | c0001 | t0013 | g0242 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0208 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00642 | hp2 | a0001 | c0001 | t0073 | g0237 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00673 | hp1 | a0001 | c0001 | t0063 | g0155 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00673 | hp2 | a0001 | c0001 | t0080 | g0006 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00733 | hp1 | a0001 | c0001 | t0093 | g0255 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00735 | hp1 | a0003 | c0003 | t0095 | g0002 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0162 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00738 | hp1 | a0001 | c0001 | t0009 | g0100 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00738 | hp2 | a0003 | c0003 | t0094 | g0020 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00741 | hp1 | a0001 | c0001 | t0010 | g0161 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0139 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01081 | hp1 | a0001 | c0001 | t0069 | g0022 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01081 | hp2 | a0001 | c0001 | t0012 | g0225 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0282 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01099 | hp2 | a0003 | c0003 | t0014 | g0016 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01106 | hp1 | a0001 | c0001 | t0010 | g0254 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0284 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0119 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01109 | hp2 | a0002 | c0012 | t0001 | g0308 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01167 | hp1 | a0003 | c0003 | t0037 | g0013 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0287 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0219 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0304 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0305 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0289 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0142 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0152 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01192 | hp2 | a0001 | c0001 | t0074 | g0148 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0250 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01256 | hp1 | a0001 | c0001 | t0016 | g0003 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01258 | hp2 | a0001 | c0001 | t0016 | g0003 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01346 | hp1 | a0001 | c0001 | t0010 | g0160 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01346 | hp2 | a0001 | c0001 | t0060 | g0039 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0132 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01358 | hp2 | a0001 | c0001 | t0054 | g0151 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0129 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01361 | hp2 | a0001 | c0001 | t0055 | g0042 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01496 | hp1 | a0001 | c0001 | t0028 | g0159 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01496 | hp2 | a0003 | c0003 | t0014 | g0015 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01515 | hp1 | a0003 | c0003 | t0014 | g0019 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01515 | hp2 | a0001 | c0001 | t0029 | g0009 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01516 | hp1 | a0003 | c0003 | t0036 | g0001 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0207 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01517 | hp1 | a0001 | c0001 | t0029 | g0009 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01517 | hp2 | a0003 | c0003 | t0036 | g0001 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0315 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01884 | hp2 | a0003 | c0013 | t0098 | g0012 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01943 | hp1 | a0001 | c0001 | t0009 | g0101 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01943 | hp2 | a0001 | c0001 | t0008 | g0215 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01952 | hp2 | a0001 | c0001 | t0011 | g0141 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01975 | hp1 | a0001 | c0001 | t0091 | g0217 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01981 | hp1 | a0001 | c0001 | t0016 | g0023 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG01981 | hp2 | a0001 | c0001 | t0011 | g0211 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0110 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02055 | hp1 | a0006 | c0010 | t0086 | g0028 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02056 | hp1 | a0001 | c0001 | t0010 | g0038 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02056 | hp2 | a0001 | c0001 | t0012 | g0118 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02071 | hp1 | a0001 | c0001 | t0050 | g0049 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02071 | hp2 | a0001 | c0001 | t0021 | g0043 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02080 | hp1 | a0001 | c0001 | t0077 | g0056 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02080 | hp2 | a0001 | c0001 | t0061 | g0045 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02083 | hp1 | a0001 | c0001 | t0008 | g0281 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02083 | hp2 | a0001 | c0001 | t0021 | g0269 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0224 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02129 | hp2 | a0004 | c0004 | t0009 | g0093 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02132 | hp1 | a0004 | c0004 | t0009 | g0090 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02132 | hp2 | a0001 | c0001 | t0059 | g0275 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0197 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02145 | hp1 | a0001 | c0005 | t0044 | g0290 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02148 | hp2 | a0001 | c0001 | t0011 | g0131 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0247 | EAS | CDX | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CDX | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02257 | hp2 | a0005 | c0006 | t0024 | g0060 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0312 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02258 | hp2 | a0001 | c0001 | t0032 | g0296 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02273 | hp2 | a0001 | c0001 | t0027 | g0168 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02280 | hp2 | a0001 | c0001 | t0068 | g0051 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02293 | hp2 | a0001 | c0001 | t0008 | g0114 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02300 | hp1 | a0001 | c0001 | t0027 | g0273 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0111 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02451 | hp1 | a0001 | c0005 | t0030 | g0323 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0034 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0126 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0314 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02602 | hp1 | a0001 | c0001 | t0013 | g0252 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0115 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02622 | hp1 | a0005 | c0006 | t0002 | g0048 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02630 | hp1 | a0001 | c0001 | t0020 | g0053 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0310 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02717 | hp2 | a0001 | c0005 | t0030 | g0292 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02809 | hp2 | a0001 | c0001 | t0039 | g0096 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0309 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02818 | hp2 | a0001 | c0001 | t0020 | g0050 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0205 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0300 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02895 | hp2 | a0001 | c0005 | t0075 | g0291 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02896 | hp1 | a0001 | c0001 | t0022 | g0298 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02896 | hp2 | a0002 | c0002 | t0084 | g0319 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02897 | hp1 | a0001 | c0001 | t0022 | g0299 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02970 | hp1 | a0001 | c0008 | t0001 | g0286 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02976 | hp1 | a0001 | c0001 | t0034 | g0204 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0302 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03041 | hp2 | a0001 | c0001 | t0020 | g0054 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03098 | hp1 | a0001 | c0001 | t0040 | g0058 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0320 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0316 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03139 | hp2 | a0005 | c0006 | t0024 | g0071 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0318 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03209 | hp1 | a0001 | c0001 | t0067 | g0055 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0317 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03225 | hp2 | a0001 | c0001 | t0035 | g0235 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03239 | hp1 | a0001 | c0001 | t0016 | g0024 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03239 | hp2 | a0001 | c0001 | t0042 | g0088 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0163 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03453 | hp2 | a0001 | c0001 | t0035 | g0147 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03490 | hp1 | a0001 | c0001 | t0019 | g0246 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0005 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03491 | hp1 | a0001 | c0001 | t0010 | g0294 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0176 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03492 | hp2 | a0001 | c0001 | t0010 | g0295 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0183 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0321 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0307 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0057 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03579 | hp2 | a0001 | c0005 | t0076 | g0047 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0127 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03688 | hp1 | a0001 | c0001 | t0007 | g0153 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0251 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03704 | hp2 | a0001 | c0001 | t0056 | g0257 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03710 | hp1 | a0001 | c0001 | t0015 | g0293 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03710 | hp2 | a0001 | c0001 | t0011 | g0185 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0193 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03831 | hp2 | a0001 | c0001 | t0018 | g0158 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03834 | hp1 | a0001 | c0001 | t0022 | g0214 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0249 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0194 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0245 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0146 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0122 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0206 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG04228 | hp1 | a0001 | c0001 | t0072 | g0149 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0258 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0103 | EAS | CHB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18747 | hp2 | a0001 | c0001 | t0051 | g0262 | EAS | CHB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18906 | hp1 | a0001 | c0001 | t0026 | g0036 | AFR | YRI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | YRI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18940 | hp1 | a0001 | c0001 | t0017 | g0041 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18945 | hp1 | a0001 | c0001 | t0012 | g0029 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18946 | hp1 | a0001 | c0001 | t0079 | g0006 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18948 | hp1 | a0001 | c0011 | t0006 | g0231 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18948 | hp2 | a0001 | c0001 | t0009 | g0074 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18951 | hp1 | a0001 | c0001 | t0023 | g0187 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18951 | hp2 | a0001 | c0001 | t0021 | g0177 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18952 | hp1 | a0003 | c0007 | t0097 | g0018 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18954 | hp2 | a0001 | c0001 | t0007 | g0238 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18959 | hp1 | a0001 | c0001 | t0034 | g0213 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18959 | hp2 | a0001 | c0001 | t0007 | g0244 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18962 | hp1 | a0001 | c0001 | t0031 | g0179 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18962 | hp2 | a0001 | c0001 | t0008 | g0198 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18965 | hp2 | a0001 | c0001 | t0065 | g0044 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18966 | hp1 | a0004 | c0004 | t0009 | g0089 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18966 | hp2 | a0003 | c0007 | t0037 | g0014 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18968 | hp1 | a0001 | c0001 | t0023 | g0004 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18968 | hp2 | a0004 | c0004 | t0015 | g0091 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18969 | hp1 | a0001 | c0001 | t0006 | g0279 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18969 | hp2 | a0004 | c0004 | t0015 | g0094 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0228 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18972 | hp1 | a0001 | c0001 | t0081 | g0137 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18972 | hp2 | a0004 | c0004 | t0009 | g0059 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18974 | hp2 | a0001 | c0001 | t0008 | g0236 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18977 | hp1 | a0001 | c0001 | t0064 | g0105 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18978 | hp1 | a0001 | c0001 | t0025 | g0239 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18981 | hp1 | a0001 | c0001 | t0019 | g0173 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18981 | hp2 | a0001 | c0001 | t0006 | g0109 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18982 | hp2 | a0001 | c0001 | t0025 | g0243 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18984 | hp1 | a0001 | c0001 | t0011 | g0232 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18986 | hp2 | a0001 | c0001 | t0031 | g0181 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18988 | hp1 | a0001 | c0001 | t0083 | g0136 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18988 | hp2 | a0001 | c0001 | t0009 | g0099 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18991 | hp2 | a0001 | c0001 | t0017 | g0264 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18993 | hp1 | a0001 | c0001 | t0007 | g0154 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18993 | hp2 | a0001 | c0001 | t0089 | g0123 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0134 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18995 | hp1 | a0001 | c0001 | t0018 | g0175 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18995 | hp2 | a0001 | c0001 | t0008 | g0143 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18998 | hp1 | a0001 | c0001 | t0013 | g0240 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA18999 | hp2 | a0001 | c0001 | t0033 | g0025 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19001 | hp1 | a0001 | c0001 | t0062 | g0156 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19003 | hp2 | a0001 | c0001 | t0012 | g0199 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19004 | hp1 | a0001 | c0001 | t0006 | g0218 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0140 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19009 | hp2 | a0001 | c0001 | t0057 | g0167 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19010 | hp1 | a0001 | c0001 | t0090 | g0186 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19010 | hp2 | a0001 | c0001 | t0053 | g0266 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0306 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19057 | hp1 | a0001 | c0001 | t0013 | g0241 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19057 | hp2 | a0001 | c0001 | t0078 | g0026 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19062 | hp1 | a0001 | c0001 | t0088 | g0188 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19062 | hp2 | a0001 | c0001 | t0017 | g0272 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19064 | hp1 | a0001 | c0001 | t0012 | g0223 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19064 | hp2 | a0004 | c0004 | t0009 | g0070 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0248 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19065 | hp2 | a0001 | c0001 | t0011 | g0113 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19066 | hp1 | a0001 | c0001 | t0066 | g0253 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19066 | hp2 | a0001 | c0001 | t0087 | g0184 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19070 | hp1 | a0001 | c0001 | t0052 | g0261 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19070 | hp2 | a0001 | c0001 | t0006 | g0226 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19077 | hp2 | a0001 | c0001 | t0013 | g0157 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19078 | hp2 | a0001 | c0001 | t0092 | g0180 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19081 | hp2 | a0001 | c0001 | t0023 | g0004 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19083 | hp1 | a0001 | c0001 | t0085 | g0201 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19084 | hp2 | a0004 | c0004 | t0015 | g0092 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19085 | hp2 | a0003 | c0009 | t0014 | g0017 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19086 | hp1 | a0001 | c0001 | t0046 | g0260 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19086 | hp2 | a0001 | c0001 | t0033 | g0027 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19087 | hp1 | a0001 | c0001 | t0011 | g0178 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19088 | hp1 | a0001 | c0001 | t0009 | g0073 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19088 | hp2 | a0001 | c0001 | t0048 | g0166 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | YRI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA19240 | hp2 | a0001 | c0001 | t0032 | g0297 | AFR | YRI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ASW | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0313 | AFR | ASW | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA20752 | hp1 | a0001 | c0001 | t0028 | g0120 | EUR | TSI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA20752 | hp2 | a0003 | c0003 | t0014 | g0002 | EUR | TSI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02109 | hp1 | a0001 | c0001 | t0082 | g0046 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02109 | hp2 | a0001 | c0001 | t0038 | g0097 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02486 | hp1 | a0001 | c0001 | t0018 | g0052 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02486 | hp2 | a0001 | c0008 | t0001 | g0285 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02559 | hp1 | a0002 | c0002 | t0043 | g0322 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG02559 | hp2 | a0001 | c0001 | t0047 | g0037 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG06807 | hp1 | a0001 | c0001 | t0026 | g0150 | AFR | USA | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0311 | AFR | USA | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA20300 | hp2 | a0001 | c0001 | t0045 | g0221 | AFR | USA | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA21309 | hp1 | a0001 | c0001 | t0070 | g0256 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| NA21309 | hp2 | a0001 | c0001 | t0041 | g0081 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0033 | REF | REF | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0072 | REF | REF | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:202942892 | A | T | 1 | a0002 | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
missense_variant | MODERATE | c.231A>T | p.Gln77His | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/17 | 1388/7974 | 231/2178 | 77/725 | chr2 | 202942892 | |||
| chr2:202954047 | T | C | 1 | a0006 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.470T>C | p.Val157Ala | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/17 | 1627/7974 | 470/2178 | 157/725 | chr2 | 202954047 | |||
| chr2:202982094 | A | T | 1 | a0003 | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
missense_variant | MODERATE | c.1712A>T | p.Tyr571Phe | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/17 | 2869/7974 | 1712/2178 | 571/725 | chr2 | 202982094 | |||
| chr2:202982142 | C | T | 1 | a0004 | 8 | HG02129.hp2 HG02132.hp1 NA18966.hp1 others(5): Show |
missense_variant | MODERATE | c.1760C>T | p.Pro587Leu | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/17 | 2917/7974 | 1760/2178 | 587/725 | chr2 | 202982142 | |||
| chr2:202983619 | A | G | 1 | a0005 | 3 | HG02257.hp2 HG02622.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.2173A>G | p.Thr725Ala | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3330/7974 | 2173/2178 | 725/725 | chr2 | 202983619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:202942805 | C | G | 1 | a0003c0013 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.144C>G | p.Pro48Pro | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/17 | 1301/7974 | 144/2178 | 48/725 | chr2 | 202942805 | |||
| chr2:202952621 | A | G | 1 | a0001c0011 | 1 | NA18948.hp1 | synonymous_variant | LOW | c.369A>G | p.Thr123Thr | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/17 | 1526/7974 | 369/2178 | 123/725 | chr2 | 202952621 | |||
| chr2:202954132 | C | T | 1 | a0003c0009 | 2 | HG00438.hp2 NA19085.hp2 |
splice_region_variant&synonymous_variant | LOW | c.555C>T | p.Thr185Thr | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/17 | 1712/7974 | 555/2178 | 185/725 | chr2 | 202954132 | |||
| chr2:202955716 | T | C | 1 | a0003c0007 | 2 | NA18952.hp1 NA18966.hp2 |
synonymous_variant | LOW | c.600T>C | p.Ser200Ser | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/17 | 1757/7974 | 600/2178 | 200/725 | chr2 | 202955716 | |||
| chr2:202971577 | A | C | 1 | a0002c0012 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1170A>C | p.Ser390Ser | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/17 | 2327/7974 | 1170/2178 | 390/725 | chr2 | 202971577 | |||
| chr2:202974364 | C | T | 1 | a0001c0005 | 5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
synonymous_variant | LOW | c.1362C>T | p.Pro454Pro | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/17 | 2519/7974 | 1362/2178 | 454/725 | chr2 | 202974364 | |||
| chr2:202977292 | G | A | 1 | a0001c0008 | 2 | HG02486.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.1518G>A | p.Gly506Gly | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/17 | 2675/7974 | 1518/2178 | 506/725 | chr2 | 202977292 | |||
| chr2:202982401 | G | A | 2 | a0002c0002 a0002c0012 |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
synonymous_variant | LOW | c.2019G>A | p.Gln673Gln | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/17 | 3176/7974 | 2019/2178 | 673/725 | chr2 | 202982401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:202912476 | C | CT | 95 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(92): Show |
287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
5_prime_UTR_variant | MODIFIER | c.-956_-955insT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/17 | 29426 | chr2 | 202912476 | ||||||
| chr2:202912503 | C | T | 10 | a0003c0003t0014 a0003c0003t0036 a0003c0003t0037 others(7): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-929C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/17 | chr2 | 202912503 | |||||||
| chr2:202912527 | T | G | 1 | a0002c0002t0043 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-905T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/17 | 29376 | chr2 | 202912527 | ||||||
| chr2:202913019 | A | G | 1 | a0003c0013t0098 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-413A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/17 | 28884 | chr2 | 202913019 | ||||||
| chr2:202913085 | A | C | 1 | a0001c0001t0093 | 1 | HG00733.hp1 | 5_prime_UTR_variant | MODIFIER | c.-347A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/17 | 28818 | chr2 | 202913085 | ||||||
| chr2:202917993 | G | T | 1 | a0005c0006t0024 | 2 | HG02257.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-213G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/17 | 23910 | chr2 | 202917993 | ||||||
| chr2:202924409 | G | A | 1 | a0001c0005t0044 | 1 | HG02145.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-50G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/17 | chr2 | 202924409 | |||||||
| chr2:202983679 | G | A | 10 | a0003c0003t0014 a0003c0003t0036 a0003c0003t0037 others(7): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*55G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 55 | chr2 | 202983679 | ||||||
| chr2:202983711 | G | A | 1 | a0001c0001t0045 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 87 | chr2 | 202983711 | ||||||
| chr2:202983945 | A | C | 1 | a0001c0001t0092 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 321 | chr2 | 202983945 | ||||||
| chr2:202984001 | G | A | 45 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(42): Show |
108 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*377G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 377 | chr2 | 202984001 | ||||||
| chr2:202984605 | T | C | 2 | a0001c0001t0038 a0001c0001t0039 |
2 | HG02109.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*981T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 981 | chr2 | 202984605 | ||||||
| chr2:202984690 | A | C | 1 | a0001c0001t0091 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1066A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1066 | chr2 | 202984690 | ||||||
| chr2:202984800 | A | T | 4 | a0001c0001t0023 a0001c0001t0088 a0001c0001t0089 others(1): Show |
6 | NA18951.hp1 NA18968.hp1 NA18993.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1176A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1176 | chr2 | 202984800 | ||||||
| chr2:202984813 | T | C | 4 | a0001c0005t0030 a0001c0005t0044 a0001c0005t0075 others(1): Show |
5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1189T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1189 | chr2 | 202984813 | ||||||
| chr2:202984857 | A | C | 1 | a0001c0001t0087 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1233A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1233 | chr2 | 202984857 | ||||||
| chr2:202984930 | C | T | 1 | a0006c0010t0086 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1306C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1306 | chr2 | 202984930 | ||||||
| chr2:202985005 | G | A | 1 | a0003c0003t0036 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1381G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1381 | chr2 | 202985005 | ||||||
| chr2:202985025 | C | T | 1 | a0001c0001t0085 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1401C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1401 | chr2 | 202985025 | ||||||
| chr2:202985059 | A | C | 1 | a0002c0002t0084 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1435A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1435 | chr2 | 202985059 | ||||||
| chr2:202985116 | C | T | 1 | a0001c0001t0083 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1492C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1492 | chr2 | 202985116 | ||||||
| chr2:202985190 | A | G | 1 | a0001c0001t0039 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1566A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1566 | chr2 | 202985190 | ||||||
| chr2:202985288 | C | G | 10 | a0003c0003t0014 a0003c0003t0036 a0003c0003t0037 others(7): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1664C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1664 | chr2 | 202985288 | ||||||
| chr2:202985744 | G | C | 96 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(93): Show |
288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*2120G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2120 | chr2 | 202985744 | ||||||
| chr2:202985785 | G | A | 96 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(93): Show |
288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*2161G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2161 | chr2 | 202985785 | ||||||
| chr2:202986013 | A | T | 2 | a0001c0001t0073 a0001c0001t0074 |
2 | HG00642.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2389A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2389 | chr2 | 202986013 | ||||||
| chr2:202986419 | G | T | 1 | a0001c0001t0081 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2795G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2795 | chr2 | 202986419 | ||||||
| chr2:202986568 | A | G | 5 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0042 others(2): Show |
15 | HG00738.hp1 HG01943.hp1 HG02129.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2944A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2944 | chr2 | 202986568 | ||||||
| chr2:202986615 | CAGTT | C | 9 | a0003c0003t0014 a0003c0003t0036 a0003c0003t0037 others(6): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2995_*2998delTAGT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2995 | INFO_REALIGN_3_PRIME | chr2 | 202986615 | |||||
| chr2:202986621 | G | A | 1 | a0001c0001t0083 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2997G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2997 | chr2 | 202986621 | ||||||
| chr2:202986867 | C | CAT | 4 | a0001c0001t0006 a0001c0011t0006 a0003c0003t0037 others(1): Show |
20 | HG00597.hp1 HG01167.hp1 HG01168.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3243_*3244insAT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | ||||||
| chr2:202986867 | C | CATAT | 3 | a0001c0001t0012 a0001c0001t0080 a0001c0001t0090 |
8 | HG00323.hp2 HG00673.hp2 HG01081.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3243_*3244insATAT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | ||||||
| chr2:202986867 | C | CATATAT | 2 | a0001c0001t0034 a0001c0001t0081 |
3 | HG02976.hp1 NA18959.hp1 NA18972.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3243_*3244insATAT others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | ||||||
| chr2:202986867 | CGT | C | 10 | a0001c0001t0008 a0001c0001t0040 a0001c0001t0078 others(7): Show |
23 | HG01099.hp2 HG01496.hp2 HG01515.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3244_*3245delGT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | ||||||
| chr2:202986867 | CGTAT | C | 6 | a0001c0001t0005 a0001c0001t0033 a0001c0001t0038 others(3): Show |
24 | HG00438.hp2 HG00609.hp1 HG00741.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3244_*3247delGTAT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | ||||||
| chr2:202986867 | CGTATAT | C | 4 | a0001c0001t0003 a0001c0001t0032 a0003c0003t0036 others(1): Show |
29 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3244_*3249delGTAT others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | ||||||
| chr2:202986867 | CGTATATA others(1): Show |
C | 1 | a0001c0001t0011 | 9 | HG00642.hp1 HG01952.hp2 HG01981.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3244_*3251delGTAT others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | ||||||
| chr2:202986867 | CGTATATA others(3): Show |
C | 2 | a0001c0001t0077 a0001c0001t0088 |
2 | HG02080.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3244_*3253delGTAT others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | ||||||
| chr2:202986867 | CGTATATA others(5): Show |
C | 1 | a0003c0003t0094 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3244_*3255delGTAT others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | ||||||
| chr2:202986867 | CGTATATA others(11): Show |
C | 1 | a0001c0001t0022 | 3 | HG02896.hp1 HG02897.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3244_*3261delGTAT others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | ||||||
| chr2:202986867 | CGTATATA others(17): Show |
C | 1 | a0001c0001t0031 | 2 | NA18962.hp1 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3244_*3267delGTAT others(20): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | ||||||
| chr2:202986868 | G | A | 14 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0012 others(11): Show |
51 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3244G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986868 | ||||||
| chr2:202986868 | G | GTA | 11 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0015 others(8): Show |
21 | HG01109.hp2 HG01169.hp1 HG01257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3283_*3284dupTA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3285 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | G | GTATA | 3 | a0001c0001t0009 a0002c0002t0001 a0004c0004t0009 |
8 | HG00738.hp1 HG01168.hp2 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3281_*3284dupTATA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3285 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | G | GTATATA | 3 | a0001c0001t0009 a0002c0002t0001 a0002c0002t0043 |
3 | HG02559.hp1 HG03195.hp2 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3279_*3284dupTATA others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3285 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | G | GTATATAT others(3): Show |
1 | a0001c0001t0025 | 2 | NA18978.hp1 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3252_*3253insCATA others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3253 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | G | GTATATAT others(5): Show |
2 | a0001c0001t0002 a0002c0002t0001 |
2 | HG02148.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3273_*3284dupTATA others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3285 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | G | GTATATAT others(9): Show |
1 | a0002c0002t0001 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3269_*3284dupTATA others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3285 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | G | GTATGTAT others(7): Show |
1 | a0001c0001t0001 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3247_*3248insGTAT others(10): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3248 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | G | GTATGTAT others(11): Show |
1 | a0001c0001t0001 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3247_*3248insGTAT others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3248 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | GTA | G | 2 | a0001c0001t0002 a0002c0002t0001 |
4 | HG00733.hp2 HG02257.hp1 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3283_*3284delTA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3283 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | GTATA | G | 3 | a0001c0001t0002 a0001c0008t0001 a0002c0002t0001 |
8 | HG02486.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3281_*3284delTATA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3281 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | GTATATA | G | 2 | a0001c0001t0002 a0005c0006t0002 |
4 | HG02622.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3279_*3284delTATA others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3279 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | GTATATAT others(3): Show |
G | 1 | a0003c0013t0098 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3275_*3284delTATA others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3275 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986868 | GTATATAT others(19): Show |
G | 1 | a0001c0001t0002 | 2 | HG03130.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3259_*3284delTATA others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3259 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | |||||
| chr2:202986871 | T | TATATATA others(9): Show |
1 | a0001c0005t0076 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3262_*3263insCATA others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3263 | INFO_REALIGN_3_PRIME | chr2 | 202986871 | |||||
| chr2:202986877 | T | TATATATA others(3): Show |
2 | a0001c0005t0030 a0001c0005t0044 |
3 | HG02145.hp1 HG02451.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3262_*3263insCATA others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3263 | INFO_REALIGN_3_PRIME | chr2 | 202986877 | |||||
| chr2:202986881 | T | TATATATA others(49): Show |
1 | a0001c0001t0026 | 2 | HG06807.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(52): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986881 | |||||
| chr2:202986881 | T | TATATATA others(51): Show |
1 | a0001c0001t0020 | 3 | HG02630.hp1 HG02818.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986881 | |||||
| chr2:202986881 | T | TATATATA others(53): Show |
1 | a0001c0001t0068 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(56): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986881 | |||||
| chr2:202986883 | T | TATACATA others(19): Show |
1 | a0001c0001t0035 | 2 | HG03225.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3262_*3263insCATA others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3263 | INFO_REALIGN_3_PRIME | chr2 | 202986883 | |||||
| chr2:202986883 | T | TATACGTA others(45): Show |
1 | a0006c0010t0086 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3262_*3263insCGTA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3263 | INFO_REALIGN_3_PRIME | chr2 | 202986883 | |||||
| chr2:202986883 | T | TATATATA others(47): Show |
1 | a0001c0001t0054 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986883 | |||||
| chr2:202986883 | T | TATATATA others(49): Show |
1 | a0001c0001t0065 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(52): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986883 | |||||
| chr2:202986883 | T | TATATATA others(51): Show |
1 | a0001c0001t0067 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986883 | |||||
| chr2:202986884 | A | ATATATAT others(51): Show |
1 | a0001c0001t0074 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3270_*3271insCATA others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3271 | INFO_REALIGN_3_PRIME | chr2 | 202986884 | |||||
| chr2:202986885 | T | C | 1 | a0001c0001t0025 | 2 | NA18978.hp1 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3261T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3261 | chr2 | 202986885 | ||||||
| chr2:202986885 | T | TATATACA others(41): Show |
1 | a0001c0001t0048 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(44): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | |||||
| chr2:202986885 | T | TATATACA others(47): Show |
1 | a0001c0001t0050 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | |||||
| chr2:202986885 | T | TATATACA others(45): Show |
1 | a0001c0001t0018 | 3 | HG02486.hp1 HG03831.hp2 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | |||||
| chr2:202986885 | T | TATATACA others(45): Show |
2 | a0001c0001t0013 a0001c0001t0056 |
6 | HG00597.hp2 HG02602.hp1 HG03704.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | |||||
| chr2:202986885 | T | TATATACA others(47): Show |
1 | a0001c0001t0007 | 14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | |||||
| chr2:202986885 | T | TATATACA others(47): Show |
1 | a0001c0001t0060 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | |||||
| chr2:202986885 | T | TATATATA others(79): Show |
1 | a0001c0001t0062 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(82): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | |||||
| chr2:202986885 | T | TATATATA others(47): Show |
1 | a0001c0001t0064 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | |||||
| chr2:202986885 | T | TATATATA others(49): Show |
1 | a0001c0001t0066 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(52): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | |||||
| chr2:202986885 | T | TATATATA others(41): Show |
1 | a0001c0001t0072 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3274_*3275insCATA others(44): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3275 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | |||||
| chr2:202986885 | T | TGTATATA others(51): Show |
1 | a0001c0001t0029 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3261_*3262insGTAT others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3262 | chr2 | 202986885 | ||||||
| chr2:202986886 | A | ATATATAT others(77): Show |
1 | a0001c0001t0069 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3270_*3271insCATA others(80): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3271 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | |||||
| chr2:202986886 | A | ATATATAT others(49): Show |
2 | a0001c0001t0016 a0001c0001t0073 |
5 | HG00642.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3270_*3271insCATA others(52): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3271 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | |||||
| chr2:202986886 | A | ATATATAT others(51): Show |
1 | a0001c0001t0010 | 8 | HG00735.hp2 HG00741.hp1 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3270_*3271insCATA others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3271 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | |||||
| chr2:202986886 | A | ATATATAT others(49): Show |
1 | a0001c0001t0028 | 2 | HG01496.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3270_*3271insCGTA others(52): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3271 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | |||||
| chr2:202986886 | A | ATATATAT others(51): Show |
2 | a0001c0001t0070 a0001c0001t0093 |
2 | HG00733.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3272_*3273insCATA others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3273 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | |||||
| chr2:202986886 | A | ATATATAT others(53): Show |
1 | a0001c0001t0071 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3272_*3273insCATA others(56): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3273 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | |||||
| chr2:202986886 | A | G | 1 | a0001c0001t0029 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3262A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3262 | chr2 | 202986886 | ||||||
| chr2:202986887 | T | TACATATA others(43): Show |
1 | a0001c0001t0046 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3264_*3265insCATA others(46): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3265 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(57): Show |
1 | a0001c0001t0017 | 3 | NA18940.hp1 NA18991.hp2 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(60): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(69): Show |
1 | a0001c0001t0047 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(72): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(45): Show |
1 | a0001c0001t0049 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(71): Show |
1 | a0001c0001t0051 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(74): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(73): Show |
1 | a0001c0001t0052 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(76): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(43): Show |
1 | a0001c0001t0053 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(46): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(73): Show |
1 | a0001c0001t0027 | 2 | HG02273.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(76): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(43): Show |
1 | a0001c0001t0019 | 3 | HG00423.hp2 HG03490.hp1 NA18981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(46): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(45): Show |
3 | a0001c0001t0004 a0001c0001t0045 a0001c0005t0075 |
24 | HG00609.hp2 HG01099.hp1 HG01255.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(63): Show |
1 | a0001c0001t0057 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(66): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(47): Show |
1 | a0001c0001t0059 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATACATA others(47): Show |
1 | a0001c0001t0061 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATATACA others(45): Show |
1 | a0001c0001t0063 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986887 | T | TATATACA others(47): Show |
1 | a0001c0001t0021 | 3 | HG02071.hp2 HG02083.hp2 NA18951.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | |||||
| chr2:202986889 | T | TACATATA others(71): Show |
1 | a0001c0001t0055 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(74): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986889 | |||||
| chr2:202986889 | T | TACATATA others(43): Show |
1 | a0001c0001t0058 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(46): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986889 | |||||
| chr2:202986964 | C | CT | 9 | a0003c0003t0014 a0003c0003t0036 a0003c0003t0037 others(6): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3349dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3350 | INFO_REALIGN_3_PRIME | chr2 | 202986964 | |||||
| chr2:202987706 | G | A | 1 | a0001c0001t0092 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4082G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 4082 | chr2 | 202987706 | ||||||
| chr2:202987864 | A | C | 98 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(95): Show |
290 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*4240A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 4240 | chr2 | 202987864 | ||||||
| chr2:202987905 | G | C | 97 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(94): Show |
291 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*4281G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 4281 | chr2 | 202987905 | ||||||
| chr2:202988007 | A | C | 3 | a0001c0001t0033 a0001c0001t0078 a0001c0001t0081 |
4 | NA18972.hp1 NA18999.hp2 NA19057.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4383A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 4383 | chr2 | 202988007 | ||||||
| chr2:202988089 | C | T | 1 | a0001c0001t0032 | 2 | HG02258.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4465C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 4465 | chr2 | 202988089 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:202913175 | C | T | 1 | a0001c0005t0030g0323 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-330+73C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913175 | |||||||
| chr2:202913180 | G | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-330+78G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913180 | |||||||
| chr2:202913264 | A | G | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-330+162A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913264 | |||||||
| chr2:202913477 | A | T | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-330+375A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913477 | |||||||
| chr2:202913522 | T | C | 4 | a0001c0001t0016g0003 a0001c0001t0016g0023 a0001c0001t0016g0024 others(1): Show |
5 | HG01081.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-330+420T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913522 | |||||||
| chr2:202913772 | C | T | 2 | a0001c0001t0022g0298 a0001c0001t0022g0299 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-330+670C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913772 | |||||||
| chr2:202913882 | A | G | 2 | a0001c0001t0032g0296 a0001c0001t0032g0297 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-330+780A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913882 | |||||||
| chr2:202913956 | A | T | 2 | a0001c0001t0022g0298 a0001c0001t0022g0299 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-330+854A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913956 | |||||||
| chr2:202913957 | CT | C | 3 | a0001c0001t0033g0025 a0001c0001t0033g0027 a0001c0001t0078g0026 |
3 | NA18999.hp2 NA19057.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-330+859delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202913957 | ||||||
| chr2:202914099 | G | A | 1 | a0006c0010t0086g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-330+997G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914099 | |||||||
| chr2:202914283 | A | G | 2 | a0001c0001t0010g0294 a0001c0001t0010g0295 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-330+1181A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914283 | |||||||
| chr2:202914553 | T | C | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-330+1451T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914553 | |||||||
| chr2:202914736 | G | A | 4 | a0001c0001t0003g0032 a0001c0001t0006g0031 a0001c0001t0008g0030 others(1): Show |
4 | NA18945.hp1 NA18954.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+1634G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914736 | |||||||
| chr2:202914779 | C | CA | 44 | a0001c0001t0004g0040 a0001c0001t0008g0034 a0001c0001t0010g0038 others(41): Show |
45 | HG00408.hp2 HG00438.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-330+1689dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202914779 | ||||||
| chr2:202914788 | A | C | 1 | a0001c0001t0015g0293 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-330+1686A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914788 | |||||||
| chr2:202914791 | AC | A | 117 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(114): Show |
121 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-330+1690delC | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914791 | |||||||
| chr2:202914792 | C | A | 202 | a0001c0001t0001g0128 a0001c0001t0002g0061 a0001c0001t0002g0062 others(199): Show |
205 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.-330+1690C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914792 | |||||||
| chr2:202914796 | C | A | 279 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(276): Show |
286 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.-330+1694C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914796 | |||||||
| chr2:202914826 | T | C | 1 | a0001c0001t0082g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-330+1724T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914826 | |||||||
| chr2:202914952 | T | A | 1 | a0001c0005t0076g0047 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-330+1850T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914952 | |||||||
| chr2:202914957 | T | A | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-330+1855T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914957 | |||||||
| chr2:202915103 | G | A | 1 | a0005c0006t0002g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-330+2001G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915103 | |||||||
| chr2:202915120 | G | A | 2 | a0001c0001t0049g0035 a0001c0001t0050g0049 |
2 | HG00408.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-330+2018G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915120 | |||||||
| chr2:202915236 | C | T | 1 | a0002c0002t0084g0319 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-330+2134C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915236 | |||||||
| chr2:202915241 | C | G | 1 | a0001c0001t0082g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-330+2139C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915241 | |||||||
| chr2:202915381 | T | G | 7 | a0001c0001t0018g0052 a0001c0001t0020g0050 a0001c0001t0020g0053 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-330+2279T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915381 | |||||||
| chr2:202915390 | G | C | 1 | a0001c0001t0077g0056 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-330+2288G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915390 | |||||||
| chr2:202915496 | A | G | 5 | a0001c0005t0030g0292 a0001c0005t0030g0323 a0001c0005t0044g0290 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-329-2381A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915496 | |||||||
| chr2:202915756 | T | C | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-329-2121T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915756 | |||||||
| chr2:202915792 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-329-2085A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915792 | |||||||
| chr2:202915873 | G | A | 1 | a0001c0001t0008g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-329-2004G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915873 | |||||||
| chr2:202916095 | G | T | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-329-1782G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916095 | |||||||
| chr2:202916112 | C | A | 1 | a0001c0001t0082g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-329-1765C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916112 | |||||||
| chr2:202916162 | T | TTTTA | 4 | a0001c0001t0040g0058 a0002c0002t0001g0317 a0002c0002t0001g0318 others(1): Show |
4 | HG02559.hp1 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-329-1683_-329-168 others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916162 | ||||||
| chr2:202916162 | T | TTTTATTT others(1): Show |
13 | a0002c0002t0001g0307 a0002c0002t0001g0309 a0002c0002t0001g0310 others(10): Show |
13 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-329-1687_-329-168 others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916162 | ||||||
| chr2:202916162 | T | TTTTATTT others(5): Show |
7 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(4): Show |
7 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-329-1691_-329-168 others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916162 | ||||||
| chr2:202916162 | TTTTA | T | 241 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(238): Show |
247 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-329-1683_-329-168 others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916162 | ||||||
| chr2:202916162 | TTTTATTT others(1): Show |
T | 3 | a0001c0001t0001g0288 a0001c0001t0007g0287 a0001c0001t0007g0289 |
3 | HG01167.hp2 HG01169.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-329-1687_-329-168 others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916162 | ||||||
| chr2:202916288 | C | T | 7 | a0001c0001t0018g0052 a0001c0001t0020g0050 a0001c0001t0020g0053 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-329-1589C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916288 | |||||||
| chr2:202916348 | C | T | 276 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0106 others(273): Show |
283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.-329-1529C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916348 | |||||||
| chr2:202916397 | G | T | 2 | a0001c0008t0001g0285 a0001c0008t0001g0286 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-329-1480G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916397 | |||||||
| chr2:202916449 | G | A | 1 | a0001c0001t0064g0105 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-329-1428G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916449 | |||||||
| chr2:202916482 | G | A | 1 | a0001c0001t0040g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-329-1395G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916482 | |||||||
| chr2:202916517 | C | T | 1 | a0001c0001t0007g0284 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-329-1360C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916517 | |||||||
| chr2:202916549 | C | T | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG00738.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-329-1328C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916549 | |||||||
| chr2:202916699 | A | T | 2 | a0001c0008t0001g0285 a0001c0008t0001g0286 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-329-1178A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916699 | |||||||
| chr2:202916806 | GGCCCAAG others(16): Show |
G | 9 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0112 others(6): Show |
9 | HG01257.hp2 HG01258.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-329-1069_-329-104 others(27): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916806 | ||||||
| chr2:202916833 | A | C | 9 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0112 others(6): Show |
9 | HG01257.hp2 HG01258.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-329-1044A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916833 | |||||||
| chr2:202917017 | C | T | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-329-860C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917017 | |||||||
| chr2:202917018 | G | A | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-329-859G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917018 | |||||||
| chr2:202917026 | C | T | 1 | a0001c0001t0009g0099 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-329-851C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917026 | |||||||
| chr2:202917103 | T | C | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-329-774T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917103 | |||||||
| chr2:202917210 | C | CA | 173 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(170): Show |
179 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.-329-641dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202917210 | ||||||
| chr2:202917210 | C | CAA | 82 | a0001c0001t0001g0107 a0001c0001t0001g0128 a0001c0001t0001g0130 others(79): Show |
82 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-329-642_-329-641d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202917210 | ||||||
| chr2:202917210 | C | CAAA | 15 | a0001c0001t0001g0106 a0001c0001t0003g0116 a0001c0001t0003g0117 others(12): Show |
15 | HG00438.hp1 HG00621.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-329-643_-329-641d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202917210 | ||||||
| chr2:202917210 | C | CAAAAAAA others(3): Show |
1 | a0003c0003t0036g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-329-650_-329-641d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202917210 | ||||||
| chr2:202917237 | G | T | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-329-640G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917237 | |||||||
| chr2:202917238 | C | T | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-329-639C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917238 | |||||||
| chr2:202917247 | G | T | 2 | a0001c0008t0001g0285 a0001c0008t0001g0286 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-329-630G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917247 | |||||||
| chr2:202917652 | T | A | 1 | a0001c0001t0005g0176 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-329-225T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917652 | |||||||
| chr2:202917657 | A | G | 1 | a0001c0001t0005g0176 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-329-220A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917657 | |||||||
| chr2:202918286 | C | T | 312 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(309): Show |
318 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(315): Show |
intron_variant | MODIFIER | c.-163+243C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918286 | |||||||
| chr2:202918336 | C | T | 1 | a0001c0001t0018g0175 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-163+293C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918336 | |||||||
| chr2:202918337 | G | C | 1 | a0001c0001t0021g0177 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-163+294G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918337 | |||||||
| chr2:202918347 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0280 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-163+304C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918347 | |||||||
| chr2:202918373 | T | C | 1 | a0001c0001t0010g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-163+330T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918373 | |||||||
| chr2:202918486 | T | C | 279 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(276): Show |
286 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.-163+443T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918486 | |||||||
| chr2:202918525 | C | T | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-163+482C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918525 | |||||||
| chr2:202918545 | C | CA | 8 | a0001c0001t0003g0182 a0001c0001t0005g0183 a0001c0001t0007g0122 others(5): Show |
8 | HG03516.hp1 HG04115.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.-163+510dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 202918545 | ||||||
| chr2:202918591 | T | G | 1 | a0001c0001t0005g0115 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-163+548T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918591 | |||||||
| chr2:202918622 | A | G | 2 | a0001c0001t0001g0278 a0001c0001t0006g0279 |
2 | NA18969.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-163+579A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918622 | |||||||
| chr2:202918761 | G | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-163+718G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918761 | |||||||
| chr2:202918843 | G | C | 3 | a0001c0001t0009g0073 a0001c0001t0009g0074 a0001c0001t0009g0099 |
3 | NA18948.hp2 NA18988.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-163+800G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918843 | |||||||
| chr2:202919404 | G | C | 1 | a0001c0001t0001g0011 | 2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-163+1361G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919404 | |||||||
| chr2:202919479 | A | G | 106 | a0001c0001t0003g0258 a0001c0001t0004g0010 a0001c0001t0004g0040 others(103): Show |
109 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-163+1436A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919479 | |||||||
| chr2:202919577 | T | G | 1 | a0001c0001t0011g0185 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-163+1534T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919577 | |||||||
| chr2:202919638 | G | T | 1 | a0001c0001t0008g0236 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-163+1595G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919638 | |||||||
| chr2:202919676 | C | A | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-163+1633C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919676 | |||||||
| chr2:202919721 | G | A | 2 | a0001c0001t0022g0298 a0001c0001t0022g0299 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-163+1678G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919721 | |||||||
| chr2:202919855 | T | G | 5 | a0001c0001t0023g0004 a0001c0001t0023g0187 a0001c0001t0088g0188 others(2): Show |
6 | NA18951.hp1 NA18968.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-163+1812T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919855 | |||||||
| chr2:202919870 | A | G | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-163+1827A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919870 | |||||||
| chr2:202919910 | AAAAGGGT others(1): Show |
A | 36 | a0001c0001t0004g0010 a0001c0001t0004g0165 a0001c0001t0004g0169 others(33): Show |
37 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.-163+1871_-163+187 others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 202919910 | ||||||
| chr2:202920149 | T | C | 2 | a0001c0001t0003g0116 a0001c0001t0003g0124 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-163+2106T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920149 | |||||||
| chr2:202920177 | C | T | 7 | a0001c0001t0004g0174 a0001c0001t0004g0276 a0001c0001t0004g0277 others(4): Show |
7 | HG00438.hp1 HG00609.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-163+2134C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920177 | |||||||
| chr2:202920311 | C | G | 1 | a0001c0001t0004g0274 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-163+2268C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920311 | |||||||
| chr2:202920353 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0280 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-163+2310C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920353 | |||||||
| chr2:202920851 | G | A | 1 | a0002c0002t0001g0317 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-163+2808G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920851 | |||||||
| chr2:202920852 | C | A | 1 | a0002c0002t0001g0317 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-163+2809C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920852 | |||||||
| chr2:202921071 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-163+3028G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921071 | |||||||
| chr2:202921168 | A | T | 1 | a0001c0001t0027g0273 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-163+3125A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921168 | |||||||
| chr2:202921244 | G | T | 2 | a0001c0001t0035g0147 a0001c0001t0035g0235 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-162-3053G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921244 | |||||||
| chr2:202921551 | A | G | 101 | a0001c0001t0001g0007 a0001c0001t0001g0128 a0001c0001t0001g0130 others(98): Show |
103 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.-162-2746A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921551 | |||||||
| chr2:202921710 | G | A | 1 | a0001c0001t0012g0199 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-162-2587G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921710 | |||||||
| chr2:202921879 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-162-2418G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921879 | |||||||
| chr2:202922076 | A | G | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162-2221A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922076 | |||||||
| chr2:202922088 | C | A | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-162-2209C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922088 | |||||||
| chr2:202922089 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-162-2208A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922089 | |||||||
| chr2:202922397 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-162-1900A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922397 | |||||||
| chr2:202922538 | C | A | 1 | a0001c0001t0058g0121 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-162-1759C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922538 | |||||||
| chr2:202922682 | A | G | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-162-1615A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922682 | |||||||
| chr2:202922802 | C | T | 3 | a0001c0001t0038g0097 a0001c0001t0039g0096 a0001c0001t0040g0058 |
3 | HG02109.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-162-1495C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922802 | |||||||
| chr2:202923048 | C | T | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-162-1249C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923048 | |||||||
| chr2:202923082 | A | C | 1 | a0001c0001t0088g0188 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-162-1215A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923082 | |||||||
| chr2:202923190 | G | A | 2 | a0001c0001t0073g0237 a0001c0001t0074g0148 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-162-1107G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923190 | |||||||
| chr2:202923197 | C | T | 1 | a0002c0002t0001g0318 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-162-1100C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923197 | |||||||
| chr2:202923244 | A | G | 1 | a0001c0001t0011g0146 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-162-1053A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923244 | |||||||
| chr2:202923685 | G | A | 1 | a0001c0001t0004g0282 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-162-612G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923685 | |||||||
| chr2:202923726 | A | G | 1 | a0001c0001t0082g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-162-571A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923726 | |||||||
| chr2:202923918 | G | A | 1 | a0001c0001t0006g0200 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-162-379G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923918 | |||||||
| chr2:202924205 | T | G | 4 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0075 others(1): Show |
4 | HG02615.hp2 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162-92T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202924205 | |||||||
| chr2:202924227 | T | C | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-162-70T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202924227 | |||||||
| chr2:202924956 | C | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+541C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202924956 | |||||||
| chr2:202924969 | C | G | 2 | a0001c0001t0038g0097 a0001c0001t0039g0096 |
2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+554C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202924969 | |||||||
| chr2:202925003 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-44+588A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925003 | |||||||
| chr2:202925080 | A | G | 1 | a0001c0001t0056g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-44+665A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925080 | |||||||
| chr2:202925379 | T | C | 1 | a0001c0001t0040g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+964T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925379 | |||||||
| chr2:202925558 | A | G | 1 | a0005c0006t0002g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-44+1143A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925558 | |||||||
| chr2:202925588 | C | T | 1 | a0002c0002t0001g0306 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+1173C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925588 | |||||||
| chr2:202925975 | C | A | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44+1560C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925975 | |||||||
| chr2:202926166 | T | C | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+1751T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926166 | |||||||
| chr2:202926240 | T | C | 1 | a0001c0001t0072g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-44+1825T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926240 | |||||||
| chr2:202926482 | A | G | 1 | a0001c0001t0087g0184 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-44+2067A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926482 | |||||||
| chr2:202926596 | C | T | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44+2181C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926596 | |||||||
| chr2:202926610 | G | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+2195G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926610 | |||||||
| chr2:202926846 | A | G | 2 | a0001c0001t0001g0234 a0001c0001t0005g0183 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-44+2431A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926846 | |||||||
| chr2:202927024 | G | T | 1 | a0001c0001t0040g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+2609G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927024 | |||||||
| chr2:202927189 | G | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+2774G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927189 | |||||||
| chr2:202927323 | CTTTT | C | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-44+2915_-44+2918d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202927323 | ||||||
| chr2:202927326 | T | C | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44+2911T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927326 | |||||||
| chr2:202927370 | C | A | 2 | a0001c0001t0022g0298 a0001c0001t0022g0299 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-44+2955C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927370 | |||||||
| chr2:202927408 | T | G | 20 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(17): Show |
20 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+2993T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927408 | |||||||
| chr2:202927521 | A | G | 1 | a0001c0001t0005g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-44+3106A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927521 | |||||||
| chr2:202927905 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+3490A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927905 | |||||||
| chr2:202928053 | G | C | 1 | a0001c0001t0082g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-44+3638G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928053 | |||||||
| chr2:202928084 | T | C | 2 | a0001c0001t0003g0116 a0001c0001t0003g0124 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-44+3669T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928084 | |||||||
| chr2:202928093 | C | T | 278 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(275): Show |
285 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.-44+3678C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928093 | |||||||
| chr2:202928364 | G | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0280 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-44+3949G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928364 | |||||||
| chr2:202928377 | C | T | 1 | a0003c0009t0096g0021 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-44+3962C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928377 | |||||||
| chr2:202928378 | G | A | 1 | a0001c0001t0003g0032 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-44+3963G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928378 | |||||||
| chr2:202928478 | G | A | 3 | a0001c0001t0005g0125 a0001c0001t0008g0236 a0001c0001t0085g0201 |
3 | NA18974.hp2 NA18977.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-44+4063G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928478 | |||||||
| chr2:202928582 | C | T | 1 | a0001c0001t0055g0042 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-44+4167C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928582 | |||||||
| chr2:202928591 | A | G | 2 | a0001c0001t0001g0233 a0001c0001t0011g0232 |
2 | HG02040.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-44+4176A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928591 | |||||||
| chr2:202928653 | C | A | 129 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(126): Show |
132 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-44+4238C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928653 | |||||||
| chr2:202928664 | G | A | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44+4249G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928664 | |||||||
| chr2:202928753 | G | A | 2 | a0001c0001t0035g0147 a0001c0001t0035g0235 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-44+4338G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928753 | |||||||
| chr2:202928786 | A | G | 2 | a0001c0001t0038g0097 a0001c0001t0039g0096 |
2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+4371A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928786 | |||||||
| chr2:202928899 | T | G | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-44+4484T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928899 | |||||||
| chr2:202928992 | A | G | 1 | a0001c0001t0009g0099 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-44+4577A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928992 | |||||||
| chr2:202929020 | AC | A | 113 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(110): Show |
116 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-44+4606delC | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929020 | |||||||
| chr2:202929539 | T | C | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-44+5124T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929539 | |||||||
| chr2:202929595 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-44+5180T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929595 | |||||||
| chr2:202929716 | G | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+5301G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929716 | |||||||
| chr2:202929757 | T | C | 4 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+5342T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929757 | |||||||
| chr2:202929910 | G | A | 1 | a0001c0001t0007g0238 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-44+5495G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929910 | |||||||
| chr2:202930061 | G | C | 2 | a0001c0001t0038g0097 a0001c0001t0039g0096 |
2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+5646G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930061 | |||||||
| chr2:202930349 | G | A | 2 | a0001c0001t0038g0097 a0001c0001t0039g0096 |
2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+5934G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930349 | |||||||
| chr2:202930906 | G | A | 1 | a0002c0002t0001g0317 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-44+6491G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930906 | |||||||
| chr2:202930962 | T | C | 1 | a0001c0001t0035g0235 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-44+6547T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930962 | |||||||
| chr2:202930968 | C | CT | 22 | a0001c0001t0003g0194 a0001c0001t0004g0172 a0001c0001t0004g0277 others(19): Show |
22 | HG00609.hp2 HG00733.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-44+6575dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202930968 | ||||||
| chr2:202930968 | CT | C | 6 | a0001c0001t0003g0202 a0001c0001t0004g0259 a0001c0001t0007g0287 others(3): Show |
6 | HG01167.hp2 HG01256.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+6575delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202930968 | ||||||
| chr2:202930994 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+6579A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930994 | |||||||
| chr2:202930998 | G | A | 1 | a0001c0001t0082g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-44+6583G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930998 | |||||||
| chr2:202931039 | G | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+6624G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931039 | |||||||
| chr2:202931215 | G | A | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-44+6800G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931215 | |||||||
| chr2:202931264 | T | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+6849T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931264 | |||||||
| chr2:202931267 | C | T | 18 | a0001c0001t0010g0038 a0001c0001t0010g0160 a0001c0001t0010g0161 others(15): Show |
20 | HG00544.hp1 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+6852C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931267 | |||||||
| chr2:202931520 | C | T | 1 | a0001c0001t0082g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-44+7105C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931520 | |||||||
| chr2:202931655 | G | A | 1 | a0001c0001t0055g0042 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-44+7240G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931655 | |||||||
| chr2:202931727 | GCAATAAC others(35): Show |
G | 5 | a0001c0005t0030g0292 a0001c0005t0030g0323 a0001c0005t0044g0290 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+7340_-44+7381d others(44): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202931727 | ||||||
| chr2:202932091 | C | G | 15 | a0001c0001t0001g0011 a0001c0001t0001g0280 a0003c0003t0014g0002 others(12): Show |
17 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.-44+7676C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932091 | |||||||
| chr2:202932131 | T | C | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44+7716T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932131 | |||||||
| chr2:202932265 | C | T | 21 | a0001c0001t0002g0095 a0001c0001t0003g0190 a0001c0001t0003g0191 others(18): Show |
21 | HG00544.hp2 HG00738.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.-44+7850C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932265 | |||||||
| chr2:202932288 | TCA | T | 3 | a0001c0001t0002g0063 a0001c0001t0002g0068 a0001c0001t0002g0079 |
3 | HG01257.hp1 HG01952.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-44+7876_-44+7877d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202932288 | ||||||
| chr2:202932318 | G | T | 1 | a0001c0001t0018g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-44+7903G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932318 | |||||||
| chr2:202932472 | G | A | 1 | a0001c0001t0056g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-44+8057G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932472 | |||||||
| chr2:202932612 | G | A | 1 | a0001c0001t0040g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+8197G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932612 | |||||||
| chr2:202932735 | T | C | 1 | a0001c0001t0004g0277 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-44+8320T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932735 | |||||||
| chr2:202932824 | A | G | 1 | a0006c0010t0086g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-44+8409A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932824 | |||||||
| chr2:202932831 | T | G | 1 | a0005c0006t0002g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-44+8416T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932831 | |||||||
| chr2:202932842 | G | A | 1 | a0003c0003t0037g0013 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-44+8427G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932842 | |||||||
| chr2:202933451 | G | A | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-43-8409G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933451 | |||||||
| chr2:202933484 | T | G | 2 | a0001c0008t0001g0285 a0001c0008t0001g0286 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-43-8376T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933484 | |||||||
| chr2:202933531 | C | G | 1 | a0005c0006t0024g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-43-8329C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933531 | |||||||
| chr2:202933595 | C | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-8265C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933595 | |||||||
| chr2:202933642 | TC | T | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43-8217delC | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933642 | |||||||
| chr2:202933862 | C | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-7998C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933862 | |||||||
| chr2:202933862 | CTTTCTTT others(3): Show |
C | 105 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(102): Show |
108 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-43-7984_-43-7975d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202933862 | ||||||
| chr2:202933924 | CTTTCTTT others(13): Show |
C | 1 | a0001c0001t0046g0260 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-43-7932_-43-7913d others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202933924 | ||||||
| chr2:202934057 | T | A | 1 | a0001c0001t0006g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-43-7803T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934057 | |||||||
| chr2:202934179 | A | T | 1 | a0001c0001t0066g0253 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-43-7681A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934179 | |||||||
| chr2:202934256 | A | G | 1 | a0001c0001t0019g0173 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-43-7604A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934256 | |||||||
| chr2:202934290 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-43-7570C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934290 | |||||||
| chr2:202934632 | G | A | 6 | a0001c0001t0016g0003 a0001c0001t0016g0023 a0001c0001t0016g0024 others(3): Show |
7 | HG01081.hp1 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-7228G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934632 | |||||||
| chr2:202934665 | G | A | 8 | a0001c0001t0018g0052 a0001c0001t0020g0050 a0001c0001t0020g0053 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-7195G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934665 | |||||||
| chr2:202934670 | G | A | 1 | a0001c0001t0007g0119 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-43-7190G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934670 | |||||||
| chr2:202934905 | A | G | 1 | a0001c0001t0002g0076 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-43-6955A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934905 | |||||||
| chr2:202935023 | G | A | 1 | a0003c0007t0037g0014 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-43-6837G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935023 | |||||||
| chr2:202935024 | T | C | 1 | a0001c0001t0007g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-43-6836T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935024 | |||||||
| chr2:202935101 | A | AATATATA others(3): Show |
1 | a0001c0001t0005g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-43-6746_-43-6737d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202935101 | ||||||
| chr2:202935101 | A | AATATATA others(13): Show |
127 | a0001c0001t0001g0007 a0001c0001t0001g0102 a0001c0001t0001g0106 others(124): Show |
129 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-43-6756_-43-6737d others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202935101 | ||||||
| chr2:202935324 | TTATA | T | 270 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(267): Show |
277 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.-43-6520_-43-6517d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202935324 | ||||||
| chr2:202935324 | TTATATA | T | 8 | a0001c0001t0018g0052 a0001c0001t0020g0050 a0001c0001t0020g0053 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-6522_-43-6517d others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202935324 | ||||||
| chr2:202935367 | G | A | 1 | a0002c0002t0001g0309 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-43-6493G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935367 | |||||||
| chr2:202935660 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-43-6200G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935660 | |||||||
| chr2:202935666 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-43-6194C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935666 | |||||||
| chr2:202935708 | A | G | 3 | a0001c0001t0001g0229 a0001c0001t0005g0228 a0001c0001t0006g0140 |
3 | NA18970.hp1 NA18991.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-43-6152A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935708 | |||||||
| chr2:202935730 | T | C | 24 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0107 others(21): Show |
24 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.-43-6130T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935730 | |||||||
| chr2:202935800 | TC | T | 5 | a0001c0001t0001g0203 a0001c0001t0005g0145 a0001c0001t0008g0126 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-6059delC | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935800 | |||||||
| chr2:202936212 | T | G | 1 | a0001c0001t0003g0195 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-43-5648T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202936212 | |||||||
| chr2:202936276 | T | G | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-43-5584T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202936276 | |||||||
| chr2:202936503 | T | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-5357T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202936503 | |||||||
| chr2:202936538 | G | C | 2 | a0001c0001t0049g0035 a0001c0001t0050g0049 |
2 | HG00408.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-43-5322G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202936538 | |||||||
| chr2:202936980 | A | G | 1 | a0001c0001t0006g0031 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-43-4880A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202936980 | |||||||
| chr2:202937108 | G | A | 1 | a0006c0010t0086g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43-4752G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937108 | |||||||
| chr2:202937172 | G | A | 1 | a0001c0001t0007g0238 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-4688G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937172 | |||||||
| chr2:202937356 | CAG | C | 9 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0112 others(6): Show |
9 | HG01257.hp2 HG01258.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-4501_-43-4500d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202937356 | ||||||
| chr2:202937458 | TA | T | 23 | a0001c0001t0008g0034 a0002c0002t0001g0300 a0002c0002t0001g0301 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-43-4401delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937458 | |||||||
| chr2:202937459 | A | T | 1 | a0002c0002t0001g0318 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-43-4401A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937459 | |||||||
| chr2:202937465 | T | G | 1 | a0001c0001t0003g0195 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-43-4395T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937465 | |||||||
| chr2:202937636 | T | G | 1 | a0001c0001t0042g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-43-4224T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937636 | |||||||
| chr2:202937796 | T | C | 1 | a0001c0001t0003g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-43-4064T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937796 | |||||||
| chr2:202937815 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-43-4045G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937815 | |||||||
| chr2:202937903 | G | A | 3 | a0001c0001t0005g0127 a0001c0001t0005g0176 a0001c0001t0005g0206 |
3 | HG03491.hp2 HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-43-3957G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937903 | |||||||
| chr2:202937930 | T | TA | 10 | a0001c0001t0006g0207 a0001c0001t0011g0146 a0001c0001t0011g0178 others(7): Show |
11 | HG00438.hp2 HG00735.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-3914dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202937930 | ||||||
| chr2:202937930 | TA | T | 107 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(104): Show |
109 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-43-3914delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202937930 | ||||||
| chr2:202937946 | AT | A | 5 | a0001c0001t0001g0203 a0001c0001t0005g0145 a0001c0001t0008g0126 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-3913delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937946 | |||||||
| chr2:202937964 | T | G | 1 | a0001c0001t0003g0195 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-43-3896T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937964 | |||||||
| chr2:202938057 | G | A | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-43-3803G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938057 | |||||||
| chr2:202938060 | T | G | 1 | a0001c0001t0003g0195 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-43-3800T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938060 | |||||||
| chr2:202938144 | T | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0280 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-43-3716T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938144 | |||||||
| chr2:202938209 | A | G | 1 | a0001c0001t0009g0074 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-43-3651A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938209 | |||||||
| chr2:202938315 | C | T | 1 | a0001c0001t0004g0172 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-43-3545C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938315 | |||||||
| chr2:202938353 | A | G | 1 | a0002c0002t0043g0322 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-43-3507A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938353 | |||||||
| chr2:202938432 | T | A | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-43-3428T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938432 | |||||||
| chr2:202938515 | C | T | 1 | a0001c0001t0006g0104 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-43-3345C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938515 | |||||||
| chr2:202938612 | T | C | 1 | a0001c0001t0009g0099 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-43-3248T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938612 | |||||||
| chr2:202938651 | T | G | 128 | a0001c0001t0001g0007 a0001c0001t0001g0102 a0001c0001t0001g0106 others(125): Show |
131 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-43-3209T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938651 | |||||||
| chr2:202938652 | T | G | 2 | a0001c0001t0001g0128 a0001c0008t0001g0285 |
2 | HG00621.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-43-3208T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938652 | |||||||
| chr2:202938659 | GT | G | 123 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(120): Show |
126 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-43-3191delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202938659 | ||||||
| chr2:202938778 | G | A | 3 | a0001c0001t0003g0190 a0001c0001t0003g0191 a0001c0001t0003g0192 |
3 | HG00544.hp2 NA18998.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-43-3082G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938778 | |||||||
| chr2:202938906 | C | T | 1 | a0001c0001t0010g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-43-2954C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938906 | |||||||
| chr2:202939198 | T | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0280 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-43-2662T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939198 | |||||||
| chr2:202939566 | C | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-2294C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939566 | |||||||
| chr2:202939682 | TTTC | T | 11 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(8): Show |
12 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-2175_-43-2173d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202939682 | ||||||
| chr2:202939685 | C | CT | 21 | a0001c0001t0001g0011 a0001c0001t0001g0112 a0001c0001t0001g0280 others(18): Show |
22 | HG00621.hp2 HG01257.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.-43-2154dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202939685 | ||||||
| chr2:202939685 | CT | C | 6 | a0001c0001t0003g0192 a0001c0001t0003g0220 a0001c0001t0022g0298 others(3): Show |
6 | HG01496.hp1 HG02896.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-2154delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202939685 | ||||||
| chr2:202939685 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0010g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-43-2164_-43-2154d others(13): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202939685 | ||||||
| chr2:202939689 | T | C | 3 | a0001c0001t0005g0129 a0001c0001t0038g0097 a0001c0001t0039g0096 |
3 | HG01361.hp1 HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-43-2171T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939689 | |||||||
| chr2:202939690 | T | C | 1 | a0002c0002t0001g0315 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-43-2170T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939690 | |||||||
| chr2:202939691 | T | C | 1 | a0001c0001t0005g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-43-2169T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939691 | |||||||
| chr2:202939970 | A | G | 1 | a0001c0001t0017g0272 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-43-1890A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939970 | |||||||
| chr2:202940023 | C | G | 11 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0112 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-1837C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940023 | |||||||
| chr2:202940115 | C | G | 1 | a0001c0001t0003g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-43-1745C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940115 | |||||||
| chr2:202940180 | T | A | 1 | a0001c0001t0082g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-43-1680T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940180 | |||||||
| chr2:202940195 | A | C | 1 | a0001c0001t0005g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-43-1665A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940195 | |||||||
| chr2:202940311 | A | G | 287 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(284): Show |
294 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.-43-1549A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940311 | |||||||
| chr2:202940485 | ATGG | A | 4 | a0001c0001t0013g0157 a0001c0001t0013g0240 a0001c0001t0013g0241 others(1): Show |
4 | HG00597.hp2 NA18998.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-1371_-43-1369d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202940485 | ||||||
| chr2:202940722 | T | C | 1 | a0006c0010t0086g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43-1138T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940722 | |||||||
| chr2:202940741 | T | C | 24 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0107 others(21): Show |
24 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.-43-1119T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940741 | |||||||
| chr2:202940817 | G | C | 1 | a0001c0005t0075g0291 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-43-1043G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940817 | |||||||
| chr2:202940829 | G | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-1031G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940829 | |||||||
| chr2:202941085 | A | T | 1 | a0001c0001t0066g0253 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-43-775A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941085 | |||||||
| chr2:202941206 | C | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-654C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941206 | |||||||
| chr2:202941206 | C | T | 1 | a0001c0001t0035g0235 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-43-654C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941206 | |||||||
| chr2:202941216 | T | C | 131 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(128): Show |
134 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-43-644T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941216 | |||||||
| chr2:202941328 | T | A | 1 | a0001c0001t0018g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-43-532T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941328 | |||||||
| chr2:202941351 | A | T | 279 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(276): Show |
286 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.-43-509A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941351 | |||||||
| chr2:202941626 | T | C | 1 | a0001c0001t0025g0243 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-43-234T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941626 | |||||||
| chr2:202941639 | G | A | 1 | a0001c0001t0047g0037 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-43-221G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941639 | |||||||
| chr2:202941714 | GTTAATTT others(1): Show |
G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-140_-43-133del others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202941714 | ||||||
| chr2:202942001 | C | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.78+21C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942001 | |||||||
| chr2:202942082 | A | C | 2 | a0001c0001t0010g0294 a0001c0001t0010g0295 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.78+102A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942082 | |||||||
| chr2:202942105 | G | A | 2 | a0001c0001t0051g0262 a0001c0001t0052g0261 |
2 | NA18747.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.78+125G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942105 | |||||||
| chr2:202942144 | C | T | 2 | a0001c0001t0013g0252 a0001c0001t0072g0149 |
2 | HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.78+164C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942144 | |||||||
| chr2:202942235 | G | A | 1 | a0005c0006t0002g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78+255G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942235 | |||||||
| chr2:202942291 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0280 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.78+311G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942291 | |||||||
| chr2:202942360 | A | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.78+380A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942360 | |||||||
| chr2:202942710 | C | T | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79-30C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942710 | |||||||
| chr2:202943417 | T | C | 3 | a0001c0001t0023g0004 a0001c0001t0023g0187 a0001c0001t0090g0186 |
4 | NA18951.hp1 NA18968.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+450T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943417 | |||||||
| chr2:202943587 | T | TAC | 71 | a0001c0001t0001g0278 a0001c0001t0001g0280 a0001c0001t0002g0061 others(68): Show |
73 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.306+662_306+663dup others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | ||||||
| chr2:202943587 | T | TACAC | 39 | a0001c0001t0001g0011 a0001c0001t0001g0288 a0001c0001t0002g0064 others(36): Show |
40 | HG00642.hp2 HG01496.hp1 HG02071.hp2 others(37): Show |
intron_variant | MODIFIER | c.306+660_306+663dup others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | ||||||
| chr2:202943587 | T | TACACAC | 41 | a0001c0001t0003g0108 a0001c0001t0003g0132 a0001c0001t0003g0191 others(38): Show |
42 | HG00642.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.306+658_306+663dup others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | ||||||
| chr2:202943587 | T | TACACACA others(1): Show |
38 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0107 others(35): Show |
38 | HG00408.hp1 HG00408.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.306+656_306+663dup others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | ||||||
| chr2:202943587 | T | TACACACA others(3): Show |
25 | a0001c0001t0001g0112 a0001c0001t0003g0117 a0001c0001t0003g0190 others(22): Show |
26 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.306+654_306+663dup others(10): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | ||||||
| chr2:202943587 | T | TACACACA others(5): Show |
13 | a0001c0001t0001g0203 a0001c0001t0002g0087 a0001c0001t0004g0165 others(10): Show |
13 | HG01109.hp1 HG01358.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.306+652_306+663dup others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | ||||||
| chr2:202943587 | T | TACACACA others(7): Show |
6 | a0001c0001t0001g0234 a0001c0001t0007g0289 a0001c0001t0008g0057 others(3): Show |
6 | HG01169.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+650_306+663dup others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | ||||||
| chr2:202943587 | T | TACACACA others(9): Show |
3 | a0001c0001t0005g0110 a0001c0001t0005g0145 a0001c0001t0007g0287 |
3 | HG01167.hp2 HG02040.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.306+648_306+663dup others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | ||||||
| chr2:202943587 | T | TCACACAC others(12): Show |
1 | a0001c0001t0003g0192 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.306+620_306+621ins others(19): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943587 | |||||||
| chr2:202943587 | TAC | T | 22 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0003g0202 others(19): Show |
22 | HG00597.hp1 HG00733.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.306+662_306+663del others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | ||||||
| chr2:202943587 | TACAC | T | 3 | a0001c0001t0038g0097 a0001c0001t0039g0096 a0002c0002t0043g0322 |
3 | HG02109.hp2 HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.306+660_306+663del others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | ||||||
| chr2:202943587 | TACACACA others(5): Show |
T | 2 | a0001c0001t0003g0116 a0001c0001t0003g0124 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.306+652_306+663del others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | ||||||
| chr2:202943617 | CACACACA others(7): Show |
C | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.306+652_306+665del others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943617 | ||||||
| chr2:202943619 | CACACACA others(5): Show |
C | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.306+654_306+665del others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943619 | ||||||
| chr2:202943631 | T | C | 107 | a0001c0001t0003g0108 a0001c0001t0004g0010 a0001c0001t0004g0040 others(104): Show |
110 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.306+664T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943631 | |||||||
| chr2:202943633 | T | C | 1 | a0001c0001t0004g0270 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.306+666T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943633 | |||||||
| chr2:202943652 | G | GT | 106 | a0001c0001t0001g0229 a0001c0001t0004g0010 a0001c0001t0004g0040 others(103): Show |
109 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.306+696dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943652 | ||||||
| chr2:202943686 | C | T | 1 | a0006c0010t0086g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+719C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943686 | |||||||
| chr2:202943809 | G | A | 29 | a0001c0001t0002g0061 a0001c0001t0009g0073 a0001c0001t0009g0074 others(26): Show |
30 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.306+842G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943809 | |||||||
| chr2:202944032 | A | T | 1 | a0001c0001t0040g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.306+1065A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944032 | |||||||
| chr2:202944064 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0003g0220 |
2 | HG00621.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.306+1097G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944064 | |||||||
| chr2:202944112 | G | A | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.306+1145G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944112 | |||||||
| chr2:202944151 | T | C | 1 | a0001c0001t0071g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.306+1184T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944151 | |||||||
| chr2:202944332 | C | T | 2 | a0001c0008t0001g0285 a0001c0008t0001g0286 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.306+1365C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944332 | |||||||
| chr2:202944394 | T | G | 1 | a0001c0001t0060g0039 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.306+1427T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944394 | |||||||
| chr2:202944555 | A | G | 1 | a0001c0001t0008g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.306+1588A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944555 | |||||||
| chr2:202944650 | C | T | 5 | a0001c0005t0030g0292 a0001c0005t0030g0323 a0001c0005t0044g0290 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+1683C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944650 | |||||||
| chr2:202944661 | A | G | 1 | a0001c0001t0008g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.306+1694A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944661 | |||||||
| chr2:202944807 | A | AC | 280 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(277): Show |
287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.306+1840_306+1841i others(3): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944807 | |||||||
| chr2:202945116 | C | G | 1 | a0001c0001t0003g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.306+2149C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945116 | |||||||
| chr2:202945307 | A | T | 1 | a0001c0001t0023g0187 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.306+2340A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945307 | |||||||
| chr2:202945410 | C | G | 1 | a0001c0001t0003g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.306+2443C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945410 | |||||||
| chr2:202945411 | C | T | 4 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0075 others(1): Show |
4 | HG02615.hp2 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+2444C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945411 | |||||||
| chr2:202945644 | G | T | 1 | a0001c0001t0035g0235 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.306+2677G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945644 | |||||||
| chr2:202945672 | G | A | 2 | a0003c0007t0037g0014 a0003c0007t0097g0018 |
2 | NA18952.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.306+2705G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945672 | |||||||
| chr2:202945915 | T | C | 2 | a0001c0008t0001g0285 a0001c0008t0001g0286 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.306+2948T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945915 | |||||||
| chr2:202946590 | G | A | 2 | a0001c0001t0035g0147 a0001c0001t0035g0235 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.306+3623G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202946590 | |||||||
| chr2:202946692 | A | G | 1 | a0001c0001t0006g0219 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.306+3725A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202946692 | |||||||
| chr2:202946866 | C | A | 1 | a0001c0001t0062g0156 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.306+3899C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202946866 | |||||||
| chr2:202946905 | G | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+3938G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202946905 | |||||||
| chr2:202946920 | G | A | 3 | a0001c0001t0004g0040 a0001c0001t0007g0248 a0001c0001t0047g0037 |
3 | HG02559.hp2 NA19030.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.306+3953G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202946920 | |||||||
| chr2:202947124 | T | C | 280 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(277): Show |
287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.306+4157T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202947124 | |||||||
| chr2:202947179 | A | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+4212A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202947179 | |||||||
| chr2:202947189 | A | C | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+4222A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202947189 | |||||||
| chr2:202947325 | A | C | 3 | a0001c0001t0004g0010 a0001c0001t0004g0171 a0001c0001t0004g0259 |
4 | NA18974.hp1 NA18984.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+4358A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202947325 | |||||||
| chr2:202948200 | C | A | 130 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(127): Show |
133 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.307-4359C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202948200 | |||||||
| chr2:202948344 | T | G | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.307-4215T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202948344 | |||||||
| chr2:202948783 | C | T | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.307-3776C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202948783 | |||||||
| chr2:202948784 | G | A | 1 | a0005c0006t0024g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.307-3775G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202948784 | |||||||
| chr2:202948808 | T | A | 1 | a0001c0001t0005g0125 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.307-3751T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202948808 | |||||||
| chr2:202948912 | CT | C | 7 | a0001c0001t0018g0052 a0001c0001t0020g0050 a0001c0001t0020g0053 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-3643delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202948912 | ||||||
| chr2:202949132 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.307-3427G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949132 | |||||||
| chr2:202949342 | C | CA | 23 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0107 others(20): Show |
23 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.307-3202dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949342 | ||||||
| chr2:202949342 | CA | C | 14 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(11): Show |
15 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.307-3202delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949342 | ||||||
| chr2:202949486 | C | CT | 14 | a0001c0001t0082g0046 a0003c0003t0014g0002 a0003c0003t0014g0015 others(11): Show |
15 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.307-3066dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949486 | ||||||
| chr2:202949515 | A | ATTT | 36 | a0001c0001t0001g0112 a0001c0001t0001g0130 a0001c0001t0003g0191 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.307-3043_307-3041d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949515 | ||||||
| chr2:202949516 | T | TTTTTTA | 7 | a0001c0001t0007g0122 a0001c0001t0010g0294 a0001c0001t0010g0295 others(4): Show |
7 | HG02630.hp1 HG02818.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-3041_307-3040i others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949516 | ||||||
| chr2:202949516 | TTTA | T | 103 | a0001c0001t0001g0007 a0001c0001t0001g0128 a0001c0001t0001g0189 others(100): Show |
106 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.307-2995_307-2993d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949516 | ||||||
| chr2:202949516 | TTTATTA | T | 43 | a0001c0001t0001g0011 a0001c0001t0001g0280 a0001c0001t0002g0061 others(40): Show |
44 | HG00642.hp1 HG00733.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.307-2998_307-2993d others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949516 | ||||||
| chr2:202949516 | TTTATTAT others(2): Show |
T | 15 | a0001c0001t0002g0077 a0001c0001t0003g0132 a0001c0001t0003g0209 others(12): Show |
15 | HG01255.hp1 HG01358.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.307-3001_307-2993d others(11): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949516 | ||||||
| chr2:202949516 | TTTATTAT others(5): Show |
T | 3 | a0001c0001t0004g0263 a0001c0001t0008g0034 a0001c0001t0011g0141 |
3 | HG01952.hp2 HG02451.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.307-3004_307-2993d others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949516 | ||||||
| chr2:202949519 | A | T | 85 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0107 others(82): Show |
87 | HG00544.hp2 HG00597.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.307-3040A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949519 | |||||||
| chr2:202949522 | A | T | 67 | a0001c0001t0001g0007 a0001c0001t0001g0128 a0001c0001t0001g0203 others(64): Show |
69 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.307-3037A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949522 | |||||||
| chr2:202949525 | A | T | 18 | a0001c0001t0003g0108 a0001c0001t0003g0192 a0001c0001t0003g0193 others(15): Show |
18 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.307-3034A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949525 | |||||||
| chr2:202949528 | A | T | 2 | a0001c0001t0032g0296 a0001c0008t0001g0285 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.307-3031A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949528 | |||||||
| chr2:202949531 | A | T | 2 | a0001c0001t0004g0263 a0001c0001t0008g0034 |
2 | HG02451.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.307-3028A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949531 | |||||||
| chr2:202949608 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.307-2951T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949608 | |||||||
| chr2:202949619 | C | G | 20 | a0002c0002t0001g0300 a0002c0002t0001g0302 a0002c0002t0001g0303 others(17): Show |
20 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.307-2940C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949619 | |||||||
| chr2:202949684 | G | A | 1 | a0001c0001t0082g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.307-2875G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949684 | |||||||
| chr2:202949971 | A | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-2588A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949971 | |||||||
| chr2:202950092 | A | C | 1 | a0005c0006t0024g0060 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.307-2467A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202950092 | |||||||
| chr2:202950324 | T | G | 1 | a0001c0001t0015g0293 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.307-2235T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202950324 | |||||||
| chr2:202950745 | A | G | 8 | a0001c0001t0018g0052 a0001c0001t0020g0050 a0001c0001t0020g0053 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-1814A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202950745 | |||||||
| chr2:202951011 | A | T | 4 | a0001c0001t0001g0229 a0001c0001t0005g0228 a0001c0001t0006g0140 others(1): Show |
4 | HG03834.hp1 NA18970.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-1548A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951011 | |||||||
| chr2:202951017 | T | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-1542T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951017 | |||||||
| chr2:202951073 | G | A | 1 | a0001c0001t0082g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.307-1486G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951073 | |||||||
| chr2:202951131 | T | C | 279 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(276): Show |
286 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.307-1428T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951131 | |||||||
| chr2:202951252 | A | G | 1 | a0001c0001t0021g0177 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.307-1307A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951252 | |||||||
| chr2:202951259 | T | C | 1 | a0001c0001t0011g0208 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.307-1300T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951259 | |||||||
| chr2:202951686 | T | G | 1 | a0001c0001t0060g0039 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.307-873T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951686 | |||||||
| chr2:202951771 | G | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-788G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951771 | |||||||
| chr2:202951836 | C | CT | 14 | a0001c0001t0019g0173 a0003c0003t0014g0002 a0003c0003t0014g0015 others(11): Show |
15 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.307-709dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202951836 | ||||||
| chr2:202951872 | G | A | 1 | a0001c0001t0006g0224 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.307-687G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951872 | |||||||
| chr2:202951979 | C | T | 1 | a0001c0001t0007g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.307-580C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951979 | |||||||
| chr2:202952035 | G | A | 2 | a0003c0007t0037g0014 a0003c0007t0097g0018 |
2 | NA18952.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.307-524G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202952035 | |||||||
| chr2:202952534 | A | AT | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-13dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202952534 | ||||||
| chr2:202952699 | A | C | 2 | a0001c0001t0010g0162 a0001c0001t0010g0254 |
2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.427+20A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202952699 | |||||||
| chr2:202952758 | C | A | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.427+79C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202952758 | |||||||
| chr2:202952816 | C | T | 1 | a0001c0001t0042g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.427+137C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202952816 | |||||||
| chr2:202953498 | G | GT | 135 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(132): Show |
138 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.428-488dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 202953498 | ||||||
| chr2:202953498 | G | GTT | 57 | a0001c0001t0001g0128 a0001c0001t0001g0288 a0001c0001t0002g0065 others(54): Show |
57 | HG00621.hp1 HG00642.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.428-489_428-488dup others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 202953498 | ||||||
| chr2:202953498 | G | GTTT | 101 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(98): Show |
104 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.428-490_428-488dup others(3): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 202953498 | ||||||
| chr2:202953498 | G | GTTTT | 22 | a0001c0001t0004g0270 a0001c0001t0007g0119 a0001c0001t0007g0122 others(19): Show |
23 | HG00438.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.428-491_428-488dup others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 202953498 | ||||||
| chr2:202953498 | G | T | 1 | a0001c0001t0040g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.428-507G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202953498 | |||||||
| chr2:202953576 | A | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.428-429A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202953576 | |||||||
| chr2:202953577 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0280 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.428-428T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202953577 | |||||||
| chr2:202953852 | A | G | 280 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(277): Show |
287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.428-153A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202953852 | |||||||
| chr2:202953971 | T | C | 2 | a0001c0008t0001g0285 a0001c0008t0001g0286 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.428-34T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202953971 | |||||||
| chr2:202954431 | A | G | 1 | a0001c0001t0021g0269 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.557+297A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954431 | |||||||
| chr2:202954689 | G | T | 1 | a0001c0001t0002g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.557+555G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954689 | |||||||
| chr2:202954710 | TA | T | 18 | a0001c0001t0003g0132 a0001c0001t0003g0195 a0001c0001t0003g0209 others(15): Show |
18 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.557+593delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 202954710 | ||||||
| chr2:202954748 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.557+614A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954748 | |||||||
| chr2:202954764 | C | T | 1 | a0001c0001t0020g0054 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.557+630C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954764 | |||||||
| chr2:202954800 | G | A | 1 | a0001c0001t0003g0209 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.557+666G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954800 | |||||||
| chr2:202954826 | G | A | 1 | a0002c0002t0084g0319 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.557+692G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954826 | |||||||
| chr2:202954963 | G | A | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.558-711G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954963 | |||||||
| chr2:202955052 | A | T | 279 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(276): Show |
286 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.558-622A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202955052 | |||||||
| chr2:202955054 | ATTTGT | A | 7 | a0004c0004t0009g0059 a0004c0004t0009g0070 a0004c0004t0009g0090 others(4): Show |
7 | HG02129.hp2 HG02132.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.558-616_558-612del others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 202955054 | ||||||
| chr2:202955296 | A | G | 3 | a0001c0001t0031g0179 a0001c0001t0031g0181 a0001c0001t0087g0184 |
3 | NA18962.hp1 NA18986.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.558-378A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202955296 | |||||||
| chr2:202955476 | T | C | 24 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0107 others(21): Show |
24 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.558-198T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202955476 | |||||||
| chr2:202955552 | T | C | 113 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(110): Show |
116 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.558-122T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202955552 | |||||||
| chr2:202955574 | A | T | 1 | a0001c0001t0007g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.558-100A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202955574 | |||||||
| chr2:202955825 | C | G | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0006g0111 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+67C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202955825 | |||||||
| chr2:202955863 | T | C | 1 | a0001c0001t0005g0228 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.642+105T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202955863 | |||||||
| chr2:202955901 | T | C | 1 | a0001c0005t0075g0291 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.642+143T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202955901 | |||||||
| chr2:202956200 | T | C | 4 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(1): Show |
4 | HG00735.hp1 HG01099.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+442T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202956200 | |||||||
| chr2:202956261 | T | G | 5 | a0001c0001t0023g0004 a0001c0001t0023g0187 a0001c0001t0088g0188 others(2): Show |
6 | NA18951.hp1 NA18968.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+503T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202956261 | |||||||
| chr2:202956539 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0003g0220 |
2 | HG00621.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.642+781C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202956539 | |||||||
| chr2:202956542 | C | T | 4 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+784C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202956542 | |||||||
| chr2:202957017 | G | A | 1 | a0001c0001t0011g0146 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.642+1259G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957017 | |||||||
| chr2:202957070 | T | C | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.642+1312T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957070 | |||||||
| chr2:202957166 | T | G | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.642+1408T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957166 | |||||||
| chr2:202957289 | G | T | 1 | a0001c0001t0005g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.642+1531G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957289 | |||||||
| chr2:202957472 | G | A | 3 | a0001c0001t0003g0190 a0001c0001t0003g0191 a0001c0001t0003g0192 |
3 | HG00544.hp2 NA18998.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.642+1714G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957472 | |||||||
| chr2:202957775 | C | T | 3 | a0001c0001t0038g0097 a0001c0001t0039g0096 a0001c0001t0040g0058 |
3 | HG02109.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.642+2017C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957775 | |||||||
| chr2:202957984 | G | T | 2 | a0001c0001t0035g0147 a0001c0001t0035g0235 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.642+2226G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957984 | |||||||
| chr2:202958168 | C | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.642+2410C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958168 | |||||||
| chr2:202958247 | A | ATGTG | 5 | a0001c0005t0030g0292 a0001c0005t0030g0323 a0001c0005t0044g0290 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.642+2490_642+2491i others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958247 | ||||||
| chr2:202958247 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0025g0243 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.642+2490_642+2491i others(18): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958247 | ||||||
| chr2:202958249 | A | ATGTG | 3 | a0001c0001t0001g0011 a0001c0001t0001g0280 a0003c0013t0098g0012 |
4 | HG01884.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+2519_642+2522d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | ||||||
| chr2:202958249 | A | ATGTGTG | 21 | a0001c0001t0003g0108 a0001c0001t0003g0116 a0001c0001t0003g0117 others(18): Show |
22 | HG00621.hp2 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.642+2517_642+2522d others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | ||||||
| chr2:202958249 | A | ATGTGTGT others(3): Show |
46 | a0001c0001t0001g0130 a0001c0001t0001g0233 a0001c0001t0002g0061 others(43): Show |
46 | HG00323.hp2 HG00733.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.642+2513_642+2522d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | ||||||
| chr2:202958249 | A | ATGTGTGT others(5): Show |
21 | a0001c0001t0002g0078 a0001c0001t0003g0008 a0001c0001t0003g0222 others(18): Show |
21 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.642+2511_642+2522d others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | ||||||
| chr2:202958249 | A | ATGTGTGT others(7): Show |
11 | a0001c0001t0002g0068 a0001c0001t0004g0040 a0001c0001t0004g0249 others(8): Show |
11 | HG00323.hp1 HG01081.hp1 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+2509_642+2522d others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | ||||||
| chr2:202958249 | A | ATGTGTGT others(9): Show |
81 | a0001c0001t0002g0077 a0001c0001t0004g0010 a0001c0001t0004g0165 others(78): Show |
84 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.642+2507_642+2522d others(18): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | ||||||
| chr2:202958249 | A | ATGTGTGT others(11): Show |
11 | a0001c0001t0007g0119 a0001c0001t0007g0153 a0001c0001t0007g0154 others(8): Show |
11 | HG01109.hp1 HG01346.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+2505_642+2522d others(20): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | ||||||
| chr2:202958249 | A | ATGTGTGT others(13): Show |
4 | a0001c0001t0004g0250 a0001c0001t0004g0270 a0001c0001t0010g0161 others(1): Show |
4 | HG00741.hp1 HG01255.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+2503_642+2522d others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | ||||||
| chr2:202958249 | A | G | 6 | a0001c0001t0025g0243 a0001c0005t0030g0292 a0001c0005t0030g0323 others(3): Show |
6 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+2491A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958249 | |||||||
| chr2:202958249 | ATGTG | A | 3 | a0001c0001t0008g0215 a0001c0001t0091g0217 a0005c0006t0002g0048 |
3 | HG01943.hp2 HG01975.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.642+2519_642+2522d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | ||||||
| chr2:202958350 | G | A | 2 | a0001c0001t0003g0116 a0001c0001t0003g0124 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.642+2592G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958350 | |||||||
| chr2:202958387 | A | G | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.642+2629A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958387 | |||||||
| chr2:202958677 | C | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.643-2560C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958677 | |||||||
| chr2:202958723 | GGTAAAAC others(3): Show |
G | 2 | a0001c0001t0001g0234 a0001c0001t0005g0183 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.643-2511_643-2502d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958723 | ||||||
| chr2:202958819 | C | T | 1 | a0001c0001t0011g0178 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.643-2418C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958819 | |||||||
| chr2:202958903 | C | CA | 101 | a0001c0001t0001g0007 a0001c0001t0001g0128 a0001c0001t0001g0203 others(98): Show |
103 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.643-2313dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958903 | ||||||
| chr2:202958903 | C | CAA | 6 | a0001c0001t0001g0130 a0001c0001t0001g0288 a0001c0001t0005g0129 others(3): Show |
6 | HG01361.hp1 HG02055.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.643-2314_643-2313d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958903 | ||||||
| chr2:202958903 | CA | C | 19 | a0001c0001t0003g0191 a0001c0001t0007g0287 a0001c0005t0030g0292 others(16): Show |
20 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.643-2313delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958903 | ||||||
| chr2:202958984 | CTT | C | 114 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(111): Show |
117 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.643-2250_643-2249d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958984 | ||||||
| chr2:202958994 | T | C | 4 | a0001c0001t0001g0189 a0001c0001t0005g0197 a0001c0001t0008g0198 others(1): Show |
4 | HG00408.hp1 HG02083.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-2243T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958994 | |||||||
| chr2:202959191 | G | A | 2 | a0001c0001t0073g0237 a0001c0001t0074g0148 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.643-2046G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202959191 | |||||||
| chr2:202959236 | T | TAA | 156 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(153): Show |
160 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.643-2000_643-1999i others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202959236 | ||||||
| chr2:202959533 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.643-1704C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202959533 | |||||||
| chr2:202959608 | C | G | 1 | a0001c0005t0044g0290 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.643-1629C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202959608 | |||||||
| chr2:202959815 | CA | C | 269 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(266): Show |
275 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.643-1408delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202959815 | ||||||
| chr2:202959815 | CAA | C | 14 | a0002c0002t0001g0302 a0003c0003t0014g0002 a0003c0003t0014g0015 others(11): Show |
15 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.643-1409_643-1408d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202959815 | ||||||
| chr2:202960051 | A | C | 3 | a0001c0001t0023g0004 a0001c0001t0023g0187 a0001c0001t0090g0186 |
4 | NA18951.hp1 NA18968.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-1186A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960051 | |||||||
| chr2:202960075 | T | C | 2 | a0001c0001t0004g0282 a0001c0001t0007g0283 |
2 | HG00323.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.643-1162T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960075 | |||||||
| chr2:202960320 | A | G | 1 | a0005c0006t0002g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.643-917A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960320 | |||||||
| chr2:202960335 | C | T | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.643-902C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960335 | |||||||
| chr2:202960383 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.643-854A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960383 | |||||||
| chr2:202960704 | ACCTTCCC others(1): Show |
A | 15 | a0001c0001t0038g0097 a0001c0001t0039g0096 a0003c0003t0014g0002 others(12): Show |
16 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.643-517_643-510del others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202960704 | ||||||
| chr2:202960728 | A | G | 2 | a0001c0001t0007g0284 a0001c0001t0054g0151 |
2 | HG01106.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.643-509A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960728 | |||||||
| chr2:202960779 | T | TTCCCTCC others(1): Show |
13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.643-450_643-443dup others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202960779 | ||||||
| chr2:202961510 | T | G | 1 | a0001c0001t0088g0188 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.832+84T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202961510 | |||||||
| chr2:202961673 | G | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+247G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202961673 | |||||||
| chr2:202961691 | A | G | 1 | a0001c0001t0034g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832+265A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202961691 | |||||||
| chr2:202961730 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0280 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.832+304T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202961730 | |||||||
| chr2:202961825 | T | G | 1 | a0001c0001t0002g0075 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.832+399T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202961825 | |||||||
| chr2:202962267 | G | A | 1 | a0001c0001t0002g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.832+841G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962267 | |||||||
| chr2:202962357 | G | A | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.832+931G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962357 | |||||||
| chr2:202962709 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+1283A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962709 | |||||||
| chr2:202962711 | G | A | 1 | a0001c0001t0011g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.832+1285G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962711 | |||||||
| chr2:202962712 | T | TTTACTTT others(48): Show |
1 | a0001c0001t0011g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.832+1286_832+1287i others(57): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962712 | |||||||
| chr2:202962714 | G | A | 1 | a0001c0001t0011g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.832+1288G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962714 | |||||||
| chr2:202962757 | T | C | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+1331T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962757 | |||||||
| chr2:202962926 | T | C | 283 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(280): Show |
290 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.832+1500T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962926 | |||||||
| chr2:202962952 | C | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+1526C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962952 | |||||||
| chr2:202962967 | T | TA | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+1544dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202962967 | ||||||
| chr2:202963280 | T | C | 1 | a0006c0010t0086g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832+1854T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202963280 | |||||||
| chr2:202963315 | CA | C | 248 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(245): Show |
255 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.832+1907delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202963315 | ||||||
| chr2:202963416 | G | T | 1 | a0002c0002t0043g0322 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+1990G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202963416 | |||||||
| chr2:202963469 | G | A | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.832+2043G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202963469 | |||||||
| chr2:202963905 | C | T | 1 | a0001c0001t0005g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.832+2479C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202963905 | |||||||
| chr2:202964074 | T | TATAA | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+2649_832+2652d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964074 | ||||||
| chr2:202964138 | A | C | 1 | a0001c0001t0004g0263 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.832+2712A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964138 | |||||||
| chr2:202964175 | T | C | 1 | a0001c0001t0063g0155 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.832+2749T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964175 | |||||||
| chr2:202964183 | A | G | 5 | a0001c0001t0011g0178 a0001c0001t0031g0179 a0001c0001t0031g0181 others(2): Show |
5 | NA18962.hp1 NA18986.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+2757A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964183 | |||||||
| chr2:202964210 | G | A | 5 | a0001c0005t0030g0292 a0001c0005t0030g0323 a0001c0005t0044g0290 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-2768G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964210 | |||||||
| chr2:202964270 | C | CTTTG | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.833-2688_833-2685d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964270 | ||||||
| chr2:202964294 | T | G | 2 | a0001c0008t0001g0285 a0001c0008t0001g0286 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.833-2684T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964294 | |||||||
| chr2:202964301 | T | A | 282 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(279): Show |
289 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.833-2677T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964301 | |||||||
| chr2:202964303 | G | A | 1 | a0001c0001t0025g0239 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.833-2675G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964303 | |||||||
| chr2:202964502 | A | C | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-2476A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964502 | |||||||
| chr2:202964561 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-2417A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964561 | |||||||
| chr2:202964601 | C | A | 2 | a0001c0001t0035g0147 a0001c0001t0035g0235 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.833-2377C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964601 | |||||||
| chr2:202964859 | T | TTA | 17 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(14): Show |
18 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.833-2106_833-2105d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964859 | ||||||
| chr2:202964883 | G | GTA | 29 | a0001c0001t0001g0229 a0001c0001t0003g0032 a0001c0001t0003g0182 others(26): Show |
31 | HG00323.hp1 HG00438.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.833-2078_833-2077d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964883 | ||||||
| chr2:202964883 | G | GTATA | 93 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(90): Show |
95 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.833-2080_833-2077d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964883 | ||||||
| chr2:202964883 | G | GTATATA | 3 | a0001c0001t0004g0265 a0001c0001t0061g0045 a0001c0001t0069g0022 |
3 | HG01081.hp1 HG02080.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.833-2082_833-2077d others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964883 | ||||||
| chr2:202964883 | GTA | G | 24 | a0001c0001t0035g0235 a0002c0002t0001g0300 a0002c0002t0001g0301 others(21): Show |
24 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.833-2078_833-2077d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964883 | ||||||
| chr2:202964885 | A | G | 1 | a0001c0001t0012g0199 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.833-2093A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964885 | |||||||
| chr2:202964900 | T | C | 3 | a0005c0006t0002g0048 a0005c0006t0024g0060 a0005c0006t0024g0071 |
3 | HG02257.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.833-2078T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964900 | |||||||
| chr2:202964900 | T | TATAC | 6 | a0001c0001t0027g0168 a0001c0001t0027g0273 a0001c0001t0051g0262 others(3): Show |
6 | HG01361.hp2 HG02055.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.833-2077_833-2076i others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964900 | ||||||
| chr2:202964902 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0003g0220 a0003c0013t0098g0012 |
3 | HG00621.hp1 HG01884.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.833-2076C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964902 | |||||||
| chr2:202964950 | A | G | 1 | a0001c0001t0007g0119 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.833-2028A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964950 | |||||||
| chr2:202965505 | T | C | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-1473T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202965505 | |||||||
| chr2:202965666 | G | A | 1 | a0001c0001t0060g0039 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.833-1312G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202965666 | |||||||
| chr2:202965921 | A | G | 1 | a0006c0010t0086g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.833-1057A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202965921 | |||||||
| chr2:202966073 | A | C | 286 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(283): Show |
293 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.833-905A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966073 | |||||||
| chr2:202966104 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.833-874A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966104 | |||||||
| chr2:202966128 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-850A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966128 | |||||||
| chr2:202966253 | T | C | 3 | a0003c0003t0014g0002 a0003c0003t0014g0016 a0003c0003t0095g0002 |
3 | HG00735.hp1 HG01099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.833-725T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966253 | |||||||
| chr2:202966299 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.833-679G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966299 | |||||||
| chr2:202966442 | G | T | 1 | a0001c0001t0056g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.833-536G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966442 | |||||||
| chr2:202966489 | T | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-489T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966489 | |||||||
| chr2:202966529 | A | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-449A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966529 | |||||||
| chr2:202966629 | G | A | 124 | a0001c0001t0001g0007 a0001c0001t0001g0102 a0001c0001t0001g0106 others(121): Show |
126 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.833-349G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966629 | |||||||
| chr2:202966692 | A | T | 1 | a0002c0002t0001g0317 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.833-286A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966692 | |||||||
| chr2:202966723 | T | A | 2 | a0001c0001t0038g0097 a0001c0001t0039g0096 |
2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.833-255T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966723 | |||||||
| chr2:202966918 | T | C | 5 | a0001c0005t0030g0292 a0001c0005t0030g0323 a0001c0005t0044g0290 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-60T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966918 | |||||||
| chr2:202967397 | A | G | 8 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(5): Show |
9 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.953+299A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202967397 | |||||||
| chr2:202967563 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0280 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.953+465A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202967563 | |||||||
| chr2:202967850 | T | C | 283 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(280): Show |
290 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.953+752T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202967850 | |||||||
| chr2:202967851 | G | A | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.953+753G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202967851 | |||||||
| chr2:202968102 | A | G | 1 | a0001c0005t0075g0291 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.953+1004A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968102 | |||||||
| chr2:202968144 | C | T | 4 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(1): Show |
4 | HG00735.hp1 HG01099.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.953+1046C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968144 | |||||||
| chr2:202968158 | C | G | 1 | a0001c0001t0061g0045 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.953+1060C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968158 | |||||||
| chr2:202968160 | T | C | 1 | a0001c0001t0040g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.953+1062T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968160 | |||||||
| chr2:202968178 | C | T | 1 | a0001c0001t0064g0105 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.953+1080C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968178 | |||||||
| chr2:202968179 | G | A | 1 | a0001c0001t0005g0125 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.953+1081G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968179 | |||||||
| chr2:202968246 | C | T | 1 | a0004c0004t0015g0091 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.953+1148C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968246 | |||||||
| chr2:202968295 | G | A | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.953+1197G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968295 | |||||||
| chr2:202968767 | C | T | 2 | a0005c0006t0024g0060 a0005c0006t0024g0071 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.954-1152C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968767 | |||||||
| chr2:202969110 | T | G | 2 | a0001c0001t0022g0298 a0001c0001t0022g0299 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.954-809T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969110 | |||||||
| chr2:202969116 | C | G | 1 | a0001c0001t0083g0136 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.954-803C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969116 | |||||||
| chr2:202969154 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.954-765A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969154 | |||||||
| chr2:202969250 | G | T | 1 | a0001c0001t0002g0082 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.954-669G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969250 | |||||||
| chr2:202969578 | A | AAAAT | 3 | a0002c0002t0001g0306 a0002c0002t0001g0318 a0002c0002t0043g0322 |
3 | HG02559.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.954-302_954-299dup others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 202969578 | ||||||
| chr2:202969578 | AAAAT | A | 269 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(266): Show |
275 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.954-302_954-299del others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 202969578 | ||||||
| chr2:202969578 | AAAATAAA others(9): Show |
A | 19 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(16): Show |
19 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.954-314_954-299del others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 202969578 | ||||||
| chr2:202969578 | AAAATAAA others(13): Show |
A | 9 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0112 others(6): Show |
9 | HG01257.hp2 HG01258.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.954-318_954-299del others(20): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 202969578 | ||||||
| chr2:202969578 | AAAATAAA others(17): Show |
A | 2 | a0001c0001t0062g0156 a0001c0001t0066g0253 |
2 | NA19001.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.954-322_954-299del others(24): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 202969578 | ||||||
| chr2:202969617 | A | G | 7 | a0001c0001t0004g0174 a0001c0001t0004g0276 a0001c0001t0004g0277 others(4): Show |
7 | HG00438.hp1 HG00609.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.954-302A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969617 | |||||||
| chr2:202969673 | A | C | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.954-246A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969673 | |||||||
| chr2:202969678 | C | G | 282 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(279): Show |
289 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.954-241C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969678 | |||||||
| chr2:202969913 | A | T | 2 | a0001c0001t0003g0116 a0001c0001t0003g0124 |
2 | HG02809.hp1 NA19240.hp1 |
splice_region_variant&intron_variant | LOW | c.954-6A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969913 | |||||||
| chr2:202970346 | A | G | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1097+284A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970346 | |||||||
| chr2:202970421 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1097+359C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970421 | |||||||
| chr2:202970454 | A | C | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1097+392A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970454 | |||||||
| chr2:202970624 | G | A | 1 | a0001c0001t0003g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1097+562G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970624 | |||||||
| chr2:202970723 | A | G | 1 | a0001c0001t0056g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1097+661A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970723 | |||||||
| chr2:202970892 | T | A | 24 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0107 others(21): Show |
24 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1098-613T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970892 | |||||||
| chr2:202971067 | C | T | 1 | a0001c0001t0028g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1098-438C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202971067 | |||||||
| chr2:202971187 | T | C | 2 | a0001c0001t0004g0277 a0001c0001t0059g0275 |
2 | HG00609.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1098-318T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202971187 | |||||||
| chr2:202971745 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0280 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
splice_region_variant&intron_variant | LOW | c.1331+7T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202971745 | |||||||
| chr2:202971784 | G | C | 12 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(9): Show |
13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1331+46G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202971784 | |||||||
| chr2:202971914 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0006g0279 |
2 | NA18969.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1331+176C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202971914 | |||||||
| chr2:202972474 | C | G | 1 | a0001c0001t0004g0245 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1331+736C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972474 | |||||||
| chr2:202972475 | G | A | 1 | a0001c0001t0082g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1331+737G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972475 | |||||||
| chr2:202972674 | T | TA | 14 | a0001c0001t0002g0095 a0001c0001t0003g0191 a0001c0001t0003g0195 others(11): Show |
14 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1331+957dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | ||||||
| chr2:202972674 | T | TAA | 97 | a0001c0001t0003g0124 a0001c0001t0003g0135 a0001c0001t0004g0010 others(94): Show |
100 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1331+956_1331+957d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | ||||||
| chr2:202972674 | T | TAAA | 102 | a0001c0001t0001g0007 a0001c0001t0001g0128 a0001c0001t0001g0203 others(99): Show |
104 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1331+955_1331+957d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | ||||||
| chr2:202972674 | T | TAAAA | 6 | a0001c0001t0001g0130 a0001c0001t0003g0222 a0001c0001t0005g0145 others(3): Show |
6 | HG02055.hp2 HG02056.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1331+954_1331+957d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | ||||||
| chr2:202972674 | TA | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1331+957delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | ||||||
| chr2:202972674 | TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0013g0252 a0001c0001t0072g0149 |
2 | HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1331+946_1331+957d others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | ||||||
| chr2:202972850 | G | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1331+1112G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972850 | |||||||
| chr2:202972896 | T | A | 1 | a0006c0010t0086g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1331+1158T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972896 | |||||||
| chr2:202972945 | A | T | 1 | a0004c0004t0009g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1331+1207A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972945 | |||||||
| chr2:202972951 | T | C | 2 | a0001c0001t0035g0147 a0001c0001t0035g0235 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1331+1213T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972951 | |||||||
| chr2:202973022 | C | G | 2 | a0001c0001t0073g0237 a0001c0001t0074g0148 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1331+1284C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973022 | |||||||
| chr2:202973452 | A | G | 4 | a0001c0001t0010g0160 a0001c0001t0010g0161 a0001c0001t0010g0162 others(1): Show |
4 | HG00735.hp2 HG00741.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1332-882A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973452 | |||||||
| chr2:202973579 | T | C | 2 | a0001c0001t0035g0147 a0001c0001t0035g0235 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1332-755T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973579 | |||||||
| chr2:202973669 | A | G | 1 | a0001c0001t0008g0034 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1332-665A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973669 | |||||||
| chr2:202973825 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0280 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1332-509C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973825 | |||||||
| chr2:202973859 | G | A | 19 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(16): Show |
19 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1332-475G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973859 | |||||||
| chr2:202974238 | T | C | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1332-96T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202974238 | |||||||
| chr2:202974685 | G | A | 1 | a0001c0001t0004g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1494+189G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202974685 | |||||||
| chr2:202974886 | G | A | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1494+390G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202974886 | |||||||
| chr2:202974903 | A | AAT | 5 | a0001c0001t0007g0152 a0001c0001t0007g0284 a0001c0001t0007g0287 others(2): Show |
5 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1494+419_1494+420d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 202974903 | ||||||
| chr2:202974905 | T | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1494+409T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202974905 | |||||||
| chr2:202974918 | C | T | 1 | a0001c0001t0003g0138 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1494+422C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202974918 | |||||||
| chr2:202975076 | C | T | 23 | a0002c0002t0001g0300 a0002c0002t0001g0301 a0002c0002t0001g0302 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.1494+580C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202975076 | |||||||
| chr2:202975300 | C | T | 3 | a0002c0002t0001g0301 a0002c0002t0001g0304 a0002c0002t0001g0305 |
3 | HG00733.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1494+804C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202975300 | |||||||
| chr2:202975477 | C | T | 5 | a0002c0002t0001g0301 a0002c0002t0001g0302 a0002c0002t0001g0304 others(2): Show |
5 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1494+981C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202975477 | |||||||
| chr2:202975842 | C | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1494+1346C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202975842 | |||||||
| chr2:202975853 | T | C | 1 | a0001c0001t0003g0192 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1494+1357T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202975853 | |||||||
| chr2:202976028 | G | A | 283 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(280): Show |
290 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.1495-1241G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976028 | |||||||
| chr2:202976087 | A | C | 282 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(279): Show |
289 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1495-1182A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976087 | |||||||
| chr2:202976091 | A | C | 106 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(103): Show |
109 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1495-1178A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976091 | |||||||
| chr2:202976095 | A | C | 106 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(103): Show |
109 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1495-1174A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976095 | |||||||
| chr2:202976099 | A | C | 106 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(103): Show |
109 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1495-1170A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976099 | |||||||
| chr2:202976250 | G | T | 15 | a0001c0008t0001g0285 a0001c0008t0001g0286 a0003c0003t0014g0002 others(12): Show |
16 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1495-1019G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976250 | |||||||
| chr2:202976335 | C | T | 9 | a0001c0001t0002g0063 a0001c0001t0002g0068 a0001c0001t0002g0069 others(6): Show |
9 | HG01257.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495-934C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976335 | |||||||
| chr2:202976388 | G | A | 1 | a0001c0005t0076g0047 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1495-881G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976388 | |||||||
| chr2:202976477 | A | G | 1 | a0001c0001t0041g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1495-792A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976477 | |||||||
| chr2:202976716 | C | CT | 317 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(314): Show |
324 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(321): Show |
intron_variant | MODIFIER | c.1495-538dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 202976716 | ||||||
| chr2:202977006 | T | A | 1 | a0001c0001t0002g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1495-263T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202977006 | |||||||
| chr2:202977805 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1558+473G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202977805 | |||||||
| chr2:202977823 | C | G | 1 | a0001c0001t0089g0123 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1558+491C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202977823 | |||||||
| chr2:202977938 | C | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558+606C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202977938 | |||||||
| chr2:202977990 | C | T | 1 | a0001c0001t0040g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1558+658C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202977990 | |||||||
| chr2:202978410 | G | T | 113 | a0001c0001t0004g0010 a0001c0001t0004g0040 a0001c0001t0004g0165 others(110): Show |
116 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1558+1078G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202978410 | |||||||
| chr2:202978562 | A | G | 3 | a0001c0001t0027g0168 a0001c0001t0027g0273 a0001c0001t0055g0042 |
3 | HG01361.hp2 HG02273.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1558+1230A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202978562 | |||||||
| chr2:202978624 | C | A | 1 | a0001c0001t0002g0095 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1558+1292C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202978624 | |||||||
| chr2:202979449 | G | A | 1 | a0001c0001t0005g0183 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1559-2106G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202979449 | |||||||
| chr2:202979757 | C | T | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1559-1798C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202979757 | |||||||
| chr2:202979758 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1559-1797G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202979758 | |||||||
| chr2:202980164 | C | T | 24 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0107 others(21): Show |
24 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1559-1391C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980164 | |||||||
| chr2:202980250 | G | C | 2 | a0005c0006t0024g0060 a0005c0006t0024g0071 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1559-1305G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980250 | |||||||
| chr2:202980578 | A | C | 99 | a0001c0001t0001g0007 a0001c0001t0001g0128 a0001c0001t0001g0130 others(96): Show |
101 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1559-977A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980578 | |||||||
| chr2:202980616 | G | GTA | 14 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0006g0109 others(11): Show |
14 | HG01109.hp2 HG01361.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1559-894_1559-893d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | G | GTATA | 15 | a0001c0001t0001g0130 a0001c0001t0002g0066 a0001c0001t0003g0193 others(12): Show |
16 | HG00738.hp1 HG01109.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1559-896_1559-893d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | G | GTATATA | 33 | a0001c0001t0001g0203 a0001c0001t0002g0083 a0001c0001t0002g0084 others(30): Show |
33 | HG00423.hp2 HG00733.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.1559-898_1559-893d others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | G | GTATATAT others(1): Show |
41 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0002g0067 others(38): Show |
41 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1559-900_1559-893d others(10): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | G | GTATATAT others(3): Show |
32 | a0001c0001t0002g0076 a0001c0001t0002g0079 a0001c0001t0002g0080 others(29): Show |
32 | HG00544.hp1 HG00609.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1559-902_1559-893d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | G | GTATATAT others(5): Show |
22 | a0001c0001t0001g0102 a0001c0001t0002g0061 a0001c0001t0002g0062 others(19): Show |
22 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.1559-904_1559-893d others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | G | GTATATAT others(7): Show |
11 | a0001c0001t0001g0189 a0001c0001t0004g0172 a0001c0001t0009g0099 others(8): Show |
11 | HG00408.hp1 HG00642.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1559-906_1559-893d others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | G | GTATATAT others(9): Show |
3 | a0001c0001t0003g0190 a0001c0001t0048g0166 a0001c0001t0058g0121 |
3 | HG00438.hp1 HG00544.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1559-908_1559-893d others(18): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | G | GTATATAT others(11): Show |
6 | a0001c0001t0001g0234 a0001c0001t0005g0210 a0001c0001t0007g0152 others(3): Show |
6 | HG01175.hp2 HG02055.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1559-910_1559-893d others(20): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | G | GTATATAT others(13): Show |
4 | a0001c0001t0004g0276 a0001c0001t0005g0183 a0001c0001t0009g0074 others(1): Show |
4 | HG03516.hp1 NA18948.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1559-912_1559-893d others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | G | GTATATAT others(15): Show |
1 | a0001c0001t0011g0146 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1559-914_1559-893d others(24): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | G | GTATATAT others(47): Show |
1 | a0001c0001t0035g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1559-893_1559-892i others(56): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTA | G | 8 | a0001c0001t0003g0116 a0001c0001t0003g0124 a0001c0001t0011g0211 others(5): Show |
8 | HG01981.hp2 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1559-894_1559-893d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATA | G | 10 | a0001c0001t0004g0040 a0001c0001t0022g0298 a0001c0001t0022g0299 others(7): Show |
11 | HG01515.hp2 HG01517.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1559-896_1559-893d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATATAT others(1): Show |
G | 3 | a0001c0001t0004g0271 a0001c0001t0011g0208 a0002c0002t0001g0321 |
3 | HG00642.hp1 HG03516.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.1559-900_1559-893d others(10): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATATAT others(3): Show |
G | 3 | a0001c0001t0003g0132 a0001c0001t0004g0250 a0001c0001t0060g0039 |
3 | HG01255.hp2 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1559-902_1559-893d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATATAT others(5): Show |
G | 7 | a0001c0001t0004g0010 a0001c0001t0004g0171 a0001c0001t0004g0267 others(4): Show |
8 | HG00438.hp2 HG02083.hp2 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.1559-904_1559-893d others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATATAT others(7): Show |
G | 2 | a0001c0001t0002g0095 a0001c0001t0004g0259 |
2 | HG01975.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1559-906_1559-893d others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATATAT others(9): Show |
G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0280 a0002c0002t0001g0307 others(1): Show |
5 | HG02572.hp2 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1559-908_1559-893d others(18): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATATAT others(11): Show |
G | 13 | a0001c0001t0004g0169 a0001c0001t0004g0265 a0003c0003t0014g0002 others(10): Show |
14 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1559-910_1559-893d others(20): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATATAT others(15): Show |
G | 2 | a0001c0001t0032g0296 a0001c0001t0032g0297 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1559-914_1559-893d others(24): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATATAT others(19): Show |
G | 1 | a0001c0001t0004g0282 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1559-918_1559-893d others(28): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATATAT others(21): Show |
G | 73 | a0001c0001t0001g0007 a0001c0001t0001g0128 a0001c0001t0001g0229 others(70): Show |
75 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1559-920_1559-893d others(30): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATATAT others(23): Show |
G | 2 | a0001c0001t0079g0006 a0001c0001t0080g0006 |
2 | HG00673.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1559-922_1559-893d others(32): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980616 | GTATATAT others(29): Show |
G | 1 | a0006c0010t0086g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1559-928_1559-893d others(38): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | ||||||
| chr2:202980623 | T | TATATATA others(4): Show |
1 | a0001c0001t0001g0112 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1559-931_1559-921d others(13): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980623 | ||||||
| chr2:202980629 | T | G | 2 | a0003c0009t0014g0017 a0003c0009t0096g0021 |
2 | HG00438.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1559-926T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980629 | |||||||
| chr2:202980630 | A | T | 2 | a0003c0009t0014g0017 a0003c0009t0096g0021 |
2 | HG00438.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1559-925A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980630 | |||||||
| chr2:202980631 | T | G | 1 | a0001c0001t0002g0095 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1559-924T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980631 | |||||||
| chr2:202980632 | A | T | 1 | a0001c0001t0002g0095 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1559-923A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980632 | |||||||
| chr2:202980635 | T | G | 11 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(8): Show |
12 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1559-920T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980635 | |||||||
| chr2:202980636 | A | T | 11 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(8): Show |
12 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1559-919A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980636 | |||||||
| chr2:202980661 | T | C | 1 | a0005c0006t0024g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1559-894T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980661 | |||||||
| chr2:202980808 | T | G | 2 | a0001c0001t0032g0296 a0001c0001t0032g0297 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1559-747T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980808 | |||||||
| chr2:202980923 | T | C | 281 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0102 others(278): Show |
288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.1559-632T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980923 | |||||||
| chr2:202981105 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1559-450A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981105 | |||||||
| chr2:202981210 | C | A | 1 | a0001c0001t0007g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1559-345C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981210 | |||||||
| chr2:202981213 | C | T | 1 | a0001c0001t0007g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1559-342C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981213 | |||||||
| chr2:202981273 | T | C | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1559-282T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981273 | |||||||
| chr2:202981291 | G | A | 1 | a0001c0001t0017g0041 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1559-264G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981291 | |||||||
| chr2:202981396 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1559-159G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981396 | |||||||
| chr2:202981453 | A | T | 1 | a0001c0001t0012g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1559-102A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981453 | |||||||
| chr2:202981509 | T | C | 5 | a0001c0005t0030g0292 a0001c0005t0030g0323 a0001c0005t0044g0290 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1559-46T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981509 | |||||||
| chr2:202981779 | G | A | 1 | a0001c0001t0005g0176 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1689+94G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 15/16 | chr2 | 202981779 | |||||||
| chr2:202981801 | T | C | 1 | a0003c0013t0098g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1689+116T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 15/16 | chr2 | 202981801 | |||||||
| chr2:202981820 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1689+135C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 15/16 | chr2 | 202981820 | |||||||
| chr2:202982051 | G | A | 1 | a0001c0001t0035g0235 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1690-21G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 15/16 | chr2 | 202982051 | |||||||
| chr2:202982602 | C | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.2059+161C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/16 | chr2 | 202982602 | |||||||
| chr2:202982626 | T | A | 1 | a0001c0001t0006g0226 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2059+185T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/16 | chr2 | 202982626 | |||||||
| chr2:202982659 | G | A | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.2059+218G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/16 | chr2 | 202982659 | |||||||
| chr2:202982694 | A | G | 13 | a0003c0003t0014g0002 a0003c0003t0014g0015 a0003c0003t0014g0016 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.2059+253A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/16 | chr2 | 202982694 | |||||||
| chr2:202983180 | A | G | 1 | a0001c0001t0004g0270 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2060-326A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/16 | chr2 | 202983180 |