Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9696 |
| ensemblid | ENSG00000058453.17 |
| hgncid | 21299 |
| symbol | CROCC |
| name | ciliary rootlet coiled-coil, rootletin |
| refseq_nuc | NM_014675.5 |
| refseq_prot | NP_055490.4 |
| ensembl_nuc | ENST00000375541.10 |
| ensembl_prot | ENSP00000364691.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 16921931 |
| end | 16972964 |
| strand | + |
| ver | v1.2 |
| region | chr1:16921931-16972964 |
| region5000 | chr1:16916931-16977964 |
| regionname0 | CROCC_chr1_16921931_16972964 |
| regionname5000 | CROCC_chr1_16916931_16977964 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2017 | 156 | 14 | 48 | 67 | 9 | 16 | 47 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0002 | 0/0 | 2017 | 12 | 8 | 4 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0003 | 0/0 | 2017 | 12 | 4 | 1 | 4 | 0 | 3 | 4 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0004 | 0/0 | 2017 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0005 | 0/0 | 2017 | 6 | 4 | 0 | 0 | 1 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0006 | 0/0 | 2017 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0007 | 0/0 | 2017 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0008 | 0/0 | 2017 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0009 | 0/0 | 2017 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0010 | 0/0 | 2017 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0011 | 0/0 | 2017 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0012 | 0/0 | 2017 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0013 | 0/0 | 2017 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0014 | 0/0 | 2017 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0015 | 0/0 | 2017 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0016 | 0/0 | 2017 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0017 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0018 | 0/0 | 2017 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0019 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0020 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0021 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0022 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0023 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0024 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0025 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0026 | 0/0 | 2017 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0027 | 0/0 | 2017 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0028 | 0/0 | 2017 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0029 | 0/0 | 2017 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0030 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0031 | 0/0 | 2017 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0032 | 0/0 | 2017 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| a0033 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | MSLGL others(2012): Show |
chr1 | 16916931 | 16977964 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 6051 | 51 | 1 | 19 | 28 | 2 | 1 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0002 | 0/0 | 6051 | 44 | 3 | 12 | 21 | 2 | 6 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0003 | 0/1 | 6051 | 42 | 6 | 11 | 15 | 3 | 6 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0007 | 0/0 | 6051 | 6 | 0 | 3 | 0 | 2 | 1 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0013 | 0/0 | 6051 | 3 | 1 | 0 | 2 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0019 | 0/0 | 6051 | 2 | 2 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0022 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0031 | 0/0 | 6051 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0033 | 0/0 | 6051 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0036 | 0/0 | 6051 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0037 | 0/0 | 6051 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0039 | 1/0 | 6051 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0042 | 0/0 | 6051 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0001c0049 | 0/0 | 6051 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0002c0006 | 0/0 | 6051 | 6 | 3 | 3 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0002c0012 | 0/0 | 6051 | 3 | 3 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0002c0018 | 0/0 | 6051 | 2 | 1 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0002c0025 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0003c0004 | 0/0 | 6051 | 7 | 0 | 1 | 3 | 0 | 3 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0003c0009 | 0/0 | 6051 | 4 | 4 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0003c0026 | 0/0 | 6051 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0004c0008 | 0/0 | 6051 | 6 | 0 | 0 | 6 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0005c0005 | 0/0 | 6051 | 6 | 4 | 0 | 0 | 1 | 1 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0006c0010 | 0/0 | 6051 | 4 | 4 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0007c0014 | 0/0 | 6051 | 3 | 2 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0008c0011 | 0/0 | 6051 | 3 | 3 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0009c0017 | 0/0 | 6051 | 2 | 1 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0010c0040 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0010c0050 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0011c0016 | 0/0 | 6051 | 2 | 2 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0012c0015 | 0/0 | 6051 | 2 | 0 | 0 | 0 | 0 | 2 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0013c0020 | 0/0 | 6051 | 2 | 2 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0014c0052 | 0/0 | 6051 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0015c0047 | 0/0 | 6051 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0016c0045 | 0/0 | 6051 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0017c0034 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0018c0023 | 0/0 | 6051 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0019c0021 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0020c0029 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0021c0043 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0022c0044 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0023c0024 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0024c0035 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0025c0027 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0026c0030 | 0/0 | 6051 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0027c0041 | 0/0 | 6051 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0028c0038 | 0/0 | 6051 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0029c0051 | 0/0 | 6051 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0030c0046 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0031c0028 | 0/0 | 6051 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0032c0032 | 0/0 | 6051 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 | ||
| a0033c0048 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ATGAG others(6046): Show |
chr1 | 16916931 | 16977964 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6660 | 43 | 1 | 19 | 21 | 1 | 1 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0001t0005 | 0/0 | 6661 | 4 | 0 | 0 | 4 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0001c0001t0008 | 0/0 | 6660 | 3 | 0 | 0 | 3 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0001t0017 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0002t0001 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0002t0002 | 0/0 | 6660 | 33 | 3 | 7 | 18 | 2 | 3 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0002t0003 | 0/0 | 6661 | 9 | 0 | 3 | 3 | 0 | 3 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0001c0002t0011 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0003t0001 | 0/0 | 6660 | 37 | 5 | 11 | 12 | 3 | 6 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0003t0005 | 0/0 | 6661 | 4 | 1 | 0 | 3 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0001c0003t0018 | 0/1 | 6660 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0007t0001 | 0/0 | 6660 | 6 | 0 | 3 | 0 | 2 | 1 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0013t0001 | 0/0 | 6660 | 3 | 1 | 0 | 2 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0019t0003 | 0/0 | 6661 | 2 | 2 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0001c0022t0001 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0031t0001 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0033t0001 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0036t0002 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0037t0002 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0039t0002 | 1/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0042t0001 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0001c0049t0001 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0002c0006t0004 | 0/0 | 6660 | 6 | 3 | 3 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0002c0012t0006 | 0/0 | 6660 | 3 | 3 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0002c0018t0001 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0002c0018t0006 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0002c0025t0006 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0003c0004t0001 | 0/0 | 6660 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0003c0004t0002 | 0/0 | 6660 | 6 | 0 | 1 | 3 | 0 | 2 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0003c0009t0002 | 0/0 | 6660 | 4 | 4 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0003c0026t0016 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0004c0008t0001 | 0/0 | 6660 | 3 | 0 | 0 | 3 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0004c0008t0005 | 0/0 | 6661 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0004c0008t0009 | 0/0 | 6660 | 2 | 0 | 0 | 2 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0005c0005t0002 | 0/0 | 6660 | 5 | 4 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0005c0005t0003 | 0/0 | 6661 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0006c0010t0007 | 0/0 | 6662 | 2 | 2 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6657): Show |
chr1 | 16916931 | 16977964 |
| a0006c0010t0010 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0006c0010t0014 | 0/0 | 6662 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6657): Show |
chr1 | 16916931 | 16977964 |
| a0007c0014t0001 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0007c0014t0002 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0007c0014t0005 | 0/0 | 6661 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0008c0011t0004 | 0/0 | 6660 | 3 | 3 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0009c0017t0001 | 0/0 | 6660 | 2 | 1 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0010c0040t0010 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0010c0050t0007 | 0/0 | 6662 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6657): Show |
chr1 | 16916931 | 16977964 |
| a0011c0016t0002 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0011c0016t0004 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0012c0015t0005 | 0/0 | 6661 | 2 | 0 | 0 | 0 | 0 | 2 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0013c0020t0004 | 0/0 | 6660 | 2 | 2 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0014c0052t0005 | 0/0 | 6661 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0015c0047t0002 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0016c0045t0001 | 0/0 | 6660 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0017c0034t0002 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0018c0023t0003 | 0/0 | 6661 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0019c0021t0004 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0020c0029t0002 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0021c0043t0006 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0022c0044t0003 | 0/0 | 6661 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0023c0024t0001 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0024c0035t0015 | 0/0 | 6661 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0025c0027t0002 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0026c0030t0008 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0027c0041t0002 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0028c0038t0009 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0029c0051t0012 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0030c0046t0013 | 0/0 | 6660 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0031c0028t0003 | 0/0 | 6661 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6656): Show |
chr1 | 16916931 | 16977964 |
| a0032c0032t0001 | 0/0 | 6660 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6655): Show |
chr1 | 16916931 | 16977964 |
| a0033c0048t0007 | 0/0 | 6662 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | ACAGC others(6657): Show |
chr1 | 16916931 | 16977964 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0008g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0008g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0001t0017g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0002t0011g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0003t0018g0064 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0007t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0007t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0007t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0007t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0007t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0013t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0013t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0013t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0019t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0022t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0031t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0033t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0036t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0037t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0039t0002g0197 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0042t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0001c0049t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0002c0006t0004g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0002c0006t0004g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0002c0006t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0002c0006t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0002c0012t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0002c0012t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0002c0012t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0002c0018t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0002c0018t0006g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0002c0025t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0004t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0004t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0004t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0004t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0004t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0004t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0009t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0009t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0009t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0009t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0003c0026t0016g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0004c0008t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0004c0008t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0004c0008t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0004c0008t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0004c0008t0009g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0005c0005t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0005c0005t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0005c0005t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0005c0005t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0005c0005t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0005c0005t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0006c0010t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0006c0010t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0006c0010t0010g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0006c0010t0014g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0007c0014t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0007c0014t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0007c0014t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0008c0011t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0008c0011t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0009c0017t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0010c0040t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0010c0050t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0011c0016t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0011c0016t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0012c0015t0005g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0012c0015t0005g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0013c0020t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0013c0020t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0014c0052t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0015c0047t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0016c0045t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0017c0034t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0018c0023t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0019c0021t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0020c0029t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0021c0043t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0022c0044t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0023c0024t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0024c0035t0015g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0025c0027t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0026c0030t0008g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0027c0041t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0028c0038t0009g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0029c0051t0012g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0030c0046t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0031c0028t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0032c0032t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| a0033c0048t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | GBR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0066 | EUR | GBR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | CHS | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0085 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00639 | hp2 | a0001 | c0007 | t0001 | g0069 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00642 | hp1 | a0007 | c0014 | t0005 | g0088 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00738 | hp1 | a0014 | c0052 | t0005 | g0035 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00738 | hp2 | a0001 | c0007 | t0001 | g0001 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG00741 | hp2 | a0001 | c0007 | t0001 | g0003 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01069 | hp2 | a0002 | c0006 | t0004 | g0012 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01071 | hp1 | a0002 | c0018 | t0006 | g0031 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01071 | hp2 | a0002 | c0006 | t0004 | g0012 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01074 | hp1 | a0001 | c0002 | t0011 | g0180 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01106 | hp1 | a0015 | c0047 | t0002 | g0159 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01106 | hp2 | a0016 | c0045 | t0001 | g0118 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01109 | hp1 | a0002 | c0006 | t0004 | g0011 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0183 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0134 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01175 | hp1 | a0003 | c0004 | t0002 | g0137 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01175 | hp2 | a0009 | c0017 | t0001 | g0010 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0168 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | PUR | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0058 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0054 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01358 | hp1 | a0001 | c0042 | t0001 | g0075 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0165 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0169 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0161 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01496 | hp1 | a0001 | c0049 | t0001 | g0030 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01515 | hp1 | a0001 | c0007 | t0001 | g0023 | EUR | IBS | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0176 | EUR | IBS | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01517 | hp1 | a0001 | c0007 | t0001 | g0079 | EUR | IBS | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0175 | EUR | IBS | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0084 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01975 | hp1 | a0001 | c0033 | t0001 | g0126 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0166 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0056 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0095 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02055 | hp1 | a0001 | c0019 | t0003 | g0013 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02055 | hp2 | a0017 | c0034 | t0002 | g0155 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02056 | hp2 | a0001 | c0003 | t0005 | g0145 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02129 | hp1 | a0001 | c0003 | t0005 | g0078 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02135 | hp2 | a0004 | c0008 | t0001 | g0007 | EAS | KHV | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02145 | hp1 | a0010 | c0040 | t0010 | g0201 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02145 | hp2 | a0002 | c0012 | t0006 | g0048 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02155 | hp2 | a0018 | c0023 | t0003 | g0186 | EAS | CDX | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02165 | hp2 | a0001 | c0013 | t0001 | g0146 | EAS | CDX | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02257 | hp1 | a0007 | c0014 | t0002 | g0087 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02257 | hp2 | a0011 | c0016 | t0004 | g0043 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0003 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02280 | hp1 | a0006 | c0010 | t0007 | g0151 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0141 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0167 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0177 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02451 | hp2 | a0005 | c0005 | t0002 | g0158 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02622 | hp1 | a0005 | c0005 | t0002 | g0156 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02622 | hp2 | a0019 | c0021 | t0004 | g0002 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02630 | hp1 | a0010 | c0050 | t0007 | g0153 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02630 | hp2 | a0003 | c0009 | t0002 | g0044 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02723 | hp1 | a0008 | c0011 | t0004 | g0002 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02723 | hp2 | a0001 | c0022 | t0001 | g0034 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0059 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0132 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02738 | hp1 | a0012 | c0015 | t0005 | g0077 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0196 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02809 | hp1 | a0002 | c0012 | t0006 | g0050 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02809 | hp2 | a0003 | c0009 | t0002 | g0038 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02818 | hp1 | a0006 | c0010 | t0010 | g0150 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02818 | hp2 | a0008 | c0011 | t0004 | g0042 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02886 | hp1 | a0020 | c0029 | t0002 | g0019 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02886 | hp2 | a0002 | c0025 | t0006 | g0047 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0164 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02896 | hp2 | a0002 | c0006 | t0004 | g0160 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02965 | hp1 | a0006 | c0010 | t0007 | g0149 | AFR | ESN | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02965 | hp2 | a0002 | c0018 | t0001 | g0037 | AFR | ESN | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02970 | hp1 | a0013 | c0020 | t0004 | g0212 | AFR | ESN | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0090 | AFR | ESN | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03098 | hp1 | a0001 | c0003 | t0005 | g0070 | AFR | MSL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03098 | hp2 | a0013 | c0020 | t0004 | g0211 | AFR | MSL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03139 | hp1 | a0003 | c0009 | t0002 | g0129 | AFR | ESN | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03139 | hp2 | a0001 | c0013 | t0001 | g0004 | AFR | ESN | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03225 | hp1 | a0021 | c0043 | t0006 | g0063 | AFR | MSL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03225 | hp2 | a0005 | c0005 | t0002 | g0157 | AFR | MSL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03239 | hp2 | a0001 | c0037 | t0002 | g0195 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03453 | hp1 | a0022 | c0044 | t0003 | g0210 | AFR | MSL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03453 | hp2 | a0006 | c0010 | t0014 | g0152 | AFR | MSL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0055 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0081 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0163 | AFR | ESN | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03516 | hp2 | a0023 | c0024 | t0001 | g0004 | AFR | ESN | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03540 | hp1 | a0024 | c0035 | t0015 | g0200 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03540 | hp2 | a0025 | c0027 | t0002 | g0040 | AFR | GWD | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03579 | hp1 | a0001 | c0019 | t0003 | g0013 | AFR | MSL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0089 | AFR | MSL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0178 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03669 | hp2 | a0001 | c0007 | t0001 | g0001 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0174 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0143 | SAS | PJL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03831 | hp1 | a0003 | c0004 | t0002 | g0041 | SAS | BEB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0192 | SAS | BEB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG04115 | hp1 | a0003 | c0004 | t0001 | g0051 | SAS | STU | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0193 | SAS | STU | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG04184 | hp1 | a0005 | c0005 | t0003 | g0017 | SAS | BEB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG04184 | hp2 | a0001 | c0036 | t0002 | g0206 | SAS | BEB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | STU | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0188 | SAS | STU | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18944 | hp2 | a0001 | c0003 | t0005 | g0053 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18946 | hp2 | a0026 | c0030 | t0008 | g0029 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18947 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18947 | hp2 | a0004 | c0008 | t0001 | g0007 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18952 | hp1 | a0001 | c0031 | t0001 | g0094 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18963 | hp2 | a0027 | c0041 | t0002 | g0162 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18964 | hp2 | a0004 | c0008 | t0009 | g0072 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18967 | hp1 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18967 | hp2 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18972 | hp1 | a0003 | c0004 | t0002 | g0148 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18972 | hp2 | a0004 | c0008 | t0005 | g0062 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18977 | hp1 | a0004 | c0008 | t0001 | g0061 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18980 | hp2 | a0003 | c0004 | t0002 | g0154 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18981 | hp1 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18981 | hp2 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18990 | hp1 | a0001 | c0003 | t0001 | g0082 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18993 | hp1 | a0003 | c0004 | t0002 | g0135 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18997 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18998 | hp1 | a0004 | c0008 | t0009 | g0001 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19009 | hp1 | a0028 | c0038 | t0009 | g0071 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19009 | hp2 | a0003 | c0026 | t0016 | g0046 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19011 | hp1 | a0029 | c0051 | t0012 | g0015 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19011 | hp2 | a0001 | c0003 | t0001 | g0083 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19043 | hp1 | a0030 | c0046 | t0013 | g0198 | AFR | LWK | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0133 | AFR | LWK | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19054 | hp1 | a0031 | c0028 | t0003 | g0138 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19057 | hp2 | a0032 | c0032 | t0001 | g0140 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0209 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19064 | hp2 | a0001 | c0013 | t0001 | g0106 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19240 | hp1 | a0003 | c0009 | t0002 | g0045 | AFR | YRI | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA19240 | hp2 | a0007 | c0014 | t0001 | g0086 | AFR | YRI | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0068 | AFR | ASW | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA20129 | hp2 | a0033 | c0048 | t0007 | g0020 | AFR | ASW | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA20752 | hp1 | a0005 | c0005 | t0002 | g0018 | EUR | TSI | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0033 | EUR | TSI | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA20805 | hp1 | a0001 | c0001 | t0017 | g0121 | EUR | TSI | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0067 | EUR | TSI | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA20905 | hp1 | a0012 | c0015 | t0005 | g0074 | SAS | GIH | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA20905 | hp2 | a0003 | c0004 | t0002 | g0136 | SAS | GIH | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02559 | hp1 | a0009 | c0017 | t0001 | g0010 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG02559 | hp2 | a0005 | c0005 | t0002 | g0016 | AFR | ACB | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03471 | hp1 | a0008 | c0011 | t0004 | g0002 | AFR | MSL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| HG03471 | hp2 | a0002 | c0006 | t0004 | g0011 | AFR | MSL | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18955 | hp1 | a0001 | c0001 | t0008 | g0028 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA20300 | hp1 | a0011 | c0016 | t0002 | g0039 | AFR | USA | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA21309 | hp1 | a0002 | c0006 | t0004 | g0179 | AFR | LWK | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| NA21309 | hp2 | a0002 | c0012 | t0006 | g0049 | AFR | LWK | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0018 | g0064 | REF | REF | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| homoSapiens | grch38p0 | a0001 | c0039 | t0002 | g0197 | REF | REF | CROCC_chr1_16916931_16977964 | CROCC | chr1 | 16916931 | 16977964 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16922705 | G | A | 1 | a0019 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.103G>A | p.Ala35Thr | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/37 | 191/6660 | 103/6054 | 35/2017 | chr1 | 16922705 | |||
| chr1:16922724 | A | G | 1 | a0014 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.122A>G | p.Asp41Gly | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/37 | 210/6660 | 122/6054 | 41/2017 | chr1 | 16922724 | |||
| chr1:16924361 | C | T | 1 | a0029 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.233C>T | p.Ser78Leu | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/37 | 321/6660 | 233/6054 | 78/2017 | chr1 | 16924361 | |||
| chr1:16924380 | G | C | 1 | a0018 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.252G>C | p.Gln84His | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/37 | 340/6660 | 252/6054 | 84/2017 | chr1 | 16924380 | |||
| chr1:16930289 | A | G | 1 | a0030 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.625A>G | p.Thr209Ala | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 6/37 | 713/6660 | 625/6054 | 209/2017 | chr1 | 16930289 | |||
| chr1:16936678 | G | A | 1 | a0012 | 2 | HG02738.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.998G>A | p.Arg333Gln | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/37 | 1086/6660 | 998/6054 | 333/2017 | chr1 | 16936678 | |||
| chr1:16936708 | G | A | 1 | a0023 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1028G>A | p.Ser343Asn | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/37 | 1116/6660 | 1028/6054 | 343/2017 | chr1 | 16936708 | |||
| chr1:16936719 | C | T | 1 | a0016 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1039C>T | p.Arg347Trp | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/37 | 1127/6660 | 1039/6054 | 347/2017 | chr1 | 16936719 | |||
| chr1:16936735 | G | A | 2 | a0008 a0019 |
4 | HG02622.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
missense_variant | MODERATE | c.1055G>A | p.Arg352Gln | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/37 | 1143/6660 | 1055/6054 | 352/2017 | chr1 | 16936735 | |||
| chr1:16936795 | G | A | 4 | a0003 a0011 a0025 others(1): Show |
16 | HG01175.hp1 HG02257.hp2 HG02630.hp2 others(13): Show |
missense_variant | MODERATE | c.1115G>A | p.Arg372Gln | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/37 | 1203/6660 | 1115/6054 | 372/2017 | chr1 | 16936795 | |||
| chr1:16938425 | C | T | 3 | a0013 a0022 a0029 |
4 | HG02970.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.1316C>T | p.Ala439Val | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 11/37 | 1404/6660 | 1316/6054 | 439/2017 | chr1 | 16938425 | |||
| chr1:16939065 | C | T | 1 | a0029 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.1531C>T | p.Pro511Ser | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 12/37 | 1619/6660 | 1531/6054 | 511/2017 | chr1 | 16939065 | |||
| chr1:16939969 | G | C | 2 | a0013 a0022 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1684G>C | p.Glu562Gln | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/37 | 1772/6660 | 1684/6054 | 562/2017 | chr1 | 16939969 | |||
| chr1:16940041 | G | C | 2 | a0020 a0029 |
2 | HG02886.hp1 NA19011.hp1 |
missense_variant | MODERATE | c.1756G>C | p.Asp586His | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/37 | 1844/6660 | 1756/6054 | 586/2017 | chr1 | 16940041 | |||
| chr1:16944201 | G | A | 1 | a0026 | 1 | NA18946.hp2 | missense_variant | MODERATE | c.1910G>A | p.Arg637Gln | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/37 | 1998/6660 | 1910/6054 | 637/2017 | chr1 | 16944201 | |||
| chr1:16945556 | C | T | 1 | a0022 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.2086C>T | p.Arg696Trp | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 15/37 | 2174/6660 | 2086/6054 | 696/2017 | chr1 | 16945556 | |||
| chr1:16946948 | C | T | 2 | a0007 a0021 |
4 | HG00642.hp1 HG02257.hp1 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.2471C>T | p.Thr824Met | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/37 | 2559/6660 | 2471/6054 | 824/2017 | chr1 | 16946948 | |||
| chr1:16948518 | G | A | 1 | a0025 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.2702G>A | p.Arg901His | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 18/37 | 2790/6660 | 2702/6054 | 901/2017 | chr1 | 16948518 | |||
| chr1:16954740 | G | A | 3 | a0005 a0017 a0020 |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
missense_variant | MODERATE | c.3328G>A | p.Val1110Met | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 23/37 | 3416/6660 | 3328/6054 | 1110/2017 | chr1 | 16954740 | |||
| chr1:16954806 | G | A | 1 | a0024 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.3394G>A | p.Ala1132Thr | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 23/37 | 3482/6660 | 3394/6054 | 1132/2017 | chr1 | 16954806 | |||
| chr1:16954873 | G | A | 1 | a0018 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.3461G>A | p.Arg1154His | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 23/37 | 3549/6660 | 3461/6054 | 1154/2017 | chr1 | 16954873 | |||
| chr1:16955417 | C | T | 1 | a0027 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.3571C>T | p.Arg1191Trp | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 24/37 | 3659/6660 | 3571/6054 | 1191/2017 | chr1 | 16955417 | |||
| chr1:16955531 | G | A | 1 | a0031 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.3685G>A | p.Ala1229Thr | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 24/37 | 3773/6660 | 3685/6054 | 1229/2017 | chr1 | 16955531 | |||
| chr1:16960806 | A | G | 9 | a0005 a0006 a0010 others(6): Show |
19 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(16): Show |
missense_variant | MODERATE | c.4081A>G | p.Thr1361Ala | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/37 | 4169/6660 | 4081/6054 | 1361/2017 | chr1 | 16960806 | |||
| chr1:16965728 | G | A | 2 | a0005 a0020 |
7 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
missense_variant | MODERATE | c.4411G>A | p.Gly1471Arg | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 28/37 | 4499/6660 | 4411/6054 | 1471/2017 | chr1 | 16965728 | |||
| chr1:16965879 | C | G | 1 | a0032 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.4562C>G | p.Ala1521Gly | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 28/37 | 4650/6660 | 4562/6054 | 1521/2017 | chr1 | 16965879 | |||
| chr1:16966411 | G | T | 1 | a0033 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.4700G>T | p.Arg1567Leu | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/37 | 4788/6660 | 4700/6054 | 1567/2017 | chr1 | 16966411 | |||
| chr1:16969269 | A | G | 10 | a0002 a0005 a0008 others(7): Show |
30 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(27): Show |
missense_variant | MODERATE | c.5230A>G | p.Ser1744Gly | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 32/37 | 5318/6660 | 5230/6054 | 1744/2017 | chr1 | 16969269 | |||
| chr1:16969866 | C | G | 2 | a0004 a0028 |
7 | HG02135.hp2 NA18947.hp2 NA18964.hp2 others(4): Show |
missense_variant | MODERATE | c.5383C>G | p.Arg1795Gly | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 33/37 | 5471/6660 | 5383/6054 | 1795/2017 | chr1 | 16969866 | |||
| chr1:16969911 | G | A | 1 | a0006 | 4 | HG02280.hp1 HG02818.hp1 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.5428G>A | p.Gly1810Ser | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 33/37 | 5516/6660 | 5428/6054 | 1810/2017 | chr1 | 16969911 | |||
| chr1:16970298 | G | A | 1 | a0013 | 2 | HG02970.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.5497G>A | p.Val1833Ile | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 34/37 | 5585/6660 | 5497/6054 | 1833/2017 | chr1 | 16970298 | |||
| chr1:16970356 | G | A | 1 | a0028 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.5555G>A | p.Arg1852His | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 34/37 | 5643/6660 | 5555/6054 | 1852/2017 | chr1 | 16970356 | |||
| chr1:16970637 | T | C | 1 | a0009 | 2 | HG01175.hp2 HG02559.hp1 |
missense_variant&splice_region_variant | MODERATE | c.5654T>C | p.Val1885Ala | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/37 | 5742/6660 | 5654/6054 | 1885/2017 | chr1 | 16970637 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16924341 | A | G | 4 | a0001c0049 a0006c0010 a0010c0050 others(1): Show |
7 | HG01496.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
synonymous_variant | LOW | c.213A>G | p.Thr71Thr | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/37 | 301/6660 | 213/6054 | 71/2017 | chr1 | 16924341 | |||
| chr1:16924353 | G | A | 1 | a0001c0022 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.225G>A | p.Ser75Ser | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/37 | 313/6660 | 225/6054 | 75/2017 | chr1 | 16924353 | |||
| chr1:16930150 | G | T | 2 | a0015c0047 a0033c0048 |
2 | HG01106.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.564G>T | p.Ser188Ser | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 5/37 | 652/6660 | 564/6054 | 188/2017 | chr1 | 16930150 | |||
| chr1:16936749 | C | T | 1 | a0022c0044 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1069C>T | p.Leu357Leu | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/37 | 1157/6660 | 1069/6054 | 357/2017 | chr1 | 16936749 | |||
| chr1:16936760 | G | A | 2 | a0002c0012 a0002c0025 |
4 | HG02145.hp2 HG02809.hp1 HG02886.hp2 others(1): Show |
synonymous_variant | LOW | c.1080G>A | p.Gln360Gln | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/37 | 1168/6660 | 1080/6054 | 360/2017 | chr1 | 16936760 | |||
| chr1:16938444 | T | C | 1 | a0029c0051 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.1335T>C | p.Asp445Asp | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 11/37 | 1423/6660 | 1335/6054 | 445/2017 | chr1 | 16938444 | |||
| chr1:16944256 | G | A | 6 | a0001c0001 a0001c0031 a0001c0033 others(3): Show |
56 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(53): Show |
synonymous_variant | LOW | c.1965G>A | p.Ala655Ala | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/37 | 2053/6660 | 1965/6054 | 655/2017 | chr1 | 16944256 | |||
| chr1:16945582 | C | T | 2 | a0001c0019 a0001c0033 |
3 | HG01975.hp1 HG02055.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.2112C>T | p.Ala704Ala | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 15/37 | 2200/6660 | 2112/6054 | 704/2017 | chr1 | 16945582 | |||
| chr1:16946282 | C | T | 2 | a0015c0047 a0033c0048 |
2 | HG01106.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.2160C>T | p.Leu720Leu | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 16/37 | 2248/6660 | 2160/6054 | 720/2017 | chr1 | 16946282 | |||
| chr1:16946964 | C | T | 1 | a0001c0042 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.2487C>T | p.Arg829Arg | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/37 | 2575/6660 | 2487/6054 | 829/2017 | chr1 | 16946964 | |||
| chr1:16946988 | G | A | 1 | a0001c0031 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.2511G>A | p.Ala837Ala | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/37 | 2599/6660 | 2511/6054 | 837/2017 | chr1 | 16946988 | |||
| chr1:16955464 | C | T | 1 | a0006c0010 | 4 | HG02280.hp1 HG02818.hp1 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.3618C>T | p.Gly1206Gly | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 24/37 | 3706/6660 | 3618/6054 | 1206/2017 | chr1 | 16955464 | |||
| chr1:16956078 | G | A | 9 | a0001c0002 a0001c0019 a0001c0036 others(6): Show |
58 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(55): Show |
synonymous_variant | LOW | c.3786G>A | p.Gly1262Gly | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/37 | 3874/6660 | 3786/6054 | 1262/2017 | chr1 | 16956078 | |||
| chr1:16960919 | T | C | 12 | a0001c0003 a0001c0007 a0001c0022 others(9): Show |
65 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(62): Show |
synonymous_variant | LOW | c.4194T>C | p.Ala1398Ala | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/37 | 4282/6660 | 4194/6054 | 1398/2017 | chr1 | 16960919 | |||
| chr1:16961021 | G | A | 1 | a0001c0019 | 2 | HG02055.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.4296G>A | p.Gln1432Gln | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/37 | 4384/6660 | 4296/6054 | 1432/2017 | chr1 | 16961021 | |||
| chr1:16961123 | C | G | 1 | a0002c0025 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.4398C>G | p.Pro1466Pro | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/37 | 4486/6660 | 4398/6054 | 1466/2017 | chr1 | 16961123 | |||
| chr1:16966073 | C | T | 2 | a0006c0010 a0010c0050 |
5 | HG02280.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
synonymous_variant | LOW | c.4650C>T | p.Thr1550Thr | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 29/37 | 4738/6660 | 4650/6054 | 1550/2017 | chr1 | 16966073 | |||
| chr1:16966448 | G | A | 1 | a0001c0036 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.4737G>A | p.Ala1579Ala | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/37 | 4825/6660 | 4737/6054 | 1579/2017 | chr1 | 16966448 | |||
| chr1:16969184 | T | C | 48 | a0001c0001 a0001c0002 a0001c0003 others(45): Show |
221 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(218): Show |
synonymous_variant | LOW | c.5145T>C | p.Ala1715Ala | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 32/37 | 5233/6660 | 5145/6054 | 1715/2017 | chr1 | 16969184 | |||
| chr1:16970387 | G | A | 1 | a0001c0007 | 6 | HG00639.hp2 HG00738.hp2 HG00741.hp2 others(3): Show |
synonymous_variant | LOW | c.5586G>A | p.Arg1862Arg | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 34/37 | 5674/6660 | 5586/6054 | 1862/2017 | chr1 | 16970387 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16922005 | A | G | 33 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(30): Show |
133 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(130): Show |
5_prime_UTR_variant | MODIFIER | c.-14A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 1/37 | 14 | chr1 | 16922005 | ||||||
| chr1:16922016 | C | A | 2 | a0001c0002t0011 a0029c0051t0012 |
2 | HG01074.hp1 NA19011.hp1 |
5_prime_UTR_variant | MODIFIER | c.-3C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 1/37 | 3 | chr1 | 16922016 | ||||||
| chr1:16972489 | G | C | 1 | a0001c0001t0017 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 43 | chr1 | 16972489 | ||||||
| chr1:16972511 | G | GC | 13 | a0001c0001t0005 a0001c0002t0003 a0001c0003t0005 others(10): Show |
29 | HG00642.hp1 HG00738.hp1 HG01243.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*72dupC | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 73 | INFO_REALIGN_3_PRIME | chr1 | 16972511 | |||||
| chr1:16972514 | C | G | 4 | a0001c0001t0008 a0003c0026t0016 a0026c0030t0008 others(1): Show |
6 | NA18946.hp2 NA18955.hp1 NA18967.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*68C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 68 | chr1 | 16972514 | ||||||
| chr1:16972519 | A | C | 67 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(64): Show |
228 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*73A>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 73 | chr1 | 16972519 | ||||||
| chr1:16972519 | A | G | 1 | a0001c0002t0002 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*73A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 73 | chr1 | 16972519 | ||||||
| chr1:16972520 | C | CCG | 4 | a0006c0010t0007 a0006c0010t0014 a0010c0050t0007 others(1): Show |
5 | HG02280.hp1 HG02630.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*75_*76insGC | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 76 | INFO_REALIGN_3_PRIME | chr1 | 16972520 | |||||
| chr1:16972632 | C | T | 9 | a0002c0006t0004 a0002c0012t0006 a0002c0018t0006 others(6): Show |
19 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*186C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 186 | chr1 | 16972632 | ||||||
| chr1:16972633 | A | G | 15 | a0002c0006t0004 a0002c0012t0006 a0002c0018t0006 others(12): Show |
26 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*187A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 187 | chr1 | 16972633 | ||||||
| chr1:16972760 | C | T | 1 | a0006c0010t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*314C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 314 | chr1 | 16972760 | ||||||
| chr1:16972777 | G | A | 2 | a0004c0008t0009 a0028c0038t0009 |
3 | NA18964.hp2 NA18998.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*331G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 331 | chr1 | 16972777 | ||||||
| chr1:16972840 | C | G | 1 | a0024c0035t0015 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*394C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 394 | chr1 | 16972840 | ||||||
| chr1:16972947 | A | G | 16 | a0002c0006t0004 a0002c0012t0006 a0002c0018t0006 others(13): Show |
27 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*501A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 37/37 | 501 | chr1 | 16972947 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16922232 | A | T | 1 | a0001c0002t0002g0213 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.60+154A>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 1/36 | chr1 | 16922232 | |||||||
| chr1:16922302 | G | A | 2 | a0001c0002t0002g0213 a0029c0051t0012g0015 |
2 | NA19011.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.60+224G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 1/36 | chr1 | 16922302 | |||||||
| chr1:16922390 | G | A | 160 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(157): Show |
170 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.61-273G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 1/36 | chr1 | 16922390 | |||||||
| chr1:16922434 | C | T | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.61-229C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 1/36 | chr1 | 16922434 | |||||||
| chr1:16922568 | C | T | 1 | a0015c0047t0002g0159 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.61-95C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 1/36 | chr1 | 16922568 | |||||||
| chr1:16922900 | A | G | 161 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(158): Show |
171 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.196+102A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16922900 | |||||||
| chr1:16922965 | G | T | 4 | a0005c0005t0002g0156 a0005c0005t0002g0157 a0005c0005t0002g0158 others(1): Show |
4 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+167G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16922965 | |||||||
| chr1:16922990 | C | T | 1 | a0003c0004t0002g0154 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.196+192C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16922990 | |||||||
| chr1:16923034 | T | C | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.196+236T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16923034 | |||||||
| chr1:16923040 | C | T | 1 | a0015c0047t0002g0159 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.196+242C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16923040 | |||||||
| chr1:16923089 | G | A | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.196+291G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16923089 | |||||||
| chr1:16923397 | C | T | 5 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(2): Show |
5 | HG02280.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+599C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16923397 | |||||||
| chr1:16923646 | T | C | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-679T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16923646 | |||||||
| chr1:16923663 | T | C | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.197-662T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16923663 | |||||||
| chr1:16923666 | T | G | 5 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(2): Show |
5 | HG02280.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-659T>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16923666 | |||||||
| chr1:16923674 | C | CT | 10 | a0001c0002t0002g0202 a0001c0002t0002g0203 a0001c0002t0002g0204 others(7): Show |
10 | HG00544.hp1 HG04184.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.197-627dupT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | INFO_REALIGN_3_PRIME | chr1 | 16923674 | ||||||
| chr1:16923674 | C | CTTTTTTT others(3): Show |
5 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(2): Show |
5 | HG02280.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-636_197-627dup others(10): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | INFO_REALIGN_3_PRIME | chr1 | 16923674 | ||||||
| chr1:16923674 | CT | C | 16 | a0001c0001t0001g0142 a0001c0001t0001g0147 a0001c0003t0001g0141 others(13): Show |
16 | HG01106.hp1 HG02055.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.197-627delT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | INFO_REALIGN_3_PRIME | chr1 | 16923674 | ||||||
| chr1:16923674 | CTT | C | 130 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0052 others(127): Show |
140 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.197-628_197-627del others(2): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | INFO_REALIGN_3_PRIME | chr1 | 16923674 | ||||||
| chr1:16923674 | CTTT | C | 9 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(6): Show |
9 | HG01074.hp2 HG01168.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-629_197-627del others(3): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | INFO_REALIGN_3_PRIME | chr1 | 16923674 | ||||||
| chr1:16923702 | A | G | 1 | a0032c0032t0001g0140 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.197-623A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16923702 | |||||||
| chr1:16923742 | G | A | 1 | a0022c0044t0003g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.197-583G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16923742 | |||||||
| chr1:16923878 | G | A | 5 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(2): Show |
5 | HG02280.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-447G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16923878 | |||||||
| chr1:16923927 | T | C | 3 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 |
5 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-398T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16923927 | |||||||
| chr1:16924001 | T | C | 5 | a0003c0004t0002g0148 a0013c0020t0004g0211 a0013c0020t0004g0212 others(2): Show |
5 | HG02970.hp1 HG03098.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-324T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16924001 | |||||||
| chr1:16924078 | T | C | 162 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(159): Show |
172 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.197-247T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16924078 | |||||||
| chr1:16924114 | C | G | 1 | a0010c0040t0010g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.197-211C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16924114 | |||||||
| chr1:16924155 | C | T | 2 | a0003c0004t0002g0148 a0029c0051t0012g0015 |
2 | NA18972.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.197-170C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16924155 | |||||||
| chr1:16924237 | G | A | 4 | a0001c0001t0008g0026 a0001c0001t0008g0027 a0001c0001t0008g0028 others(1): Show |
4 | NA18946.hp2 NA18955.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-88G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16924237 | |||||||
| chr1:16924267 | G | C | 7 | a0001c0049t0001g0030 a0006c0010t0007g0149 a0006c0010t0007g0151 others(4): Show |
7 | HG01496.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-58G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 2/36 | chr1 | 16924267 | |||||||
| chr1:16924492 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.351+13C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16924492 | |||||||
| chr1:16924496 | T | C | 6 | a0001c0049t0001g0030 a0006c0010t0007g0149 a0006c0010t0007g0151 others(3): Show |
6 | HG01496.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+17T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16924496 | |||||||
| chr1:16924560 | C | T | 142 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(139): Show |
152 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.351+81C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16924560 | |||||||
| chr1:16924630 | G | A | 1 | a0001c0002t0002g0161 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.351+151G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16924630 | |||||||
| chr1:16924709 | G | T | 5 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(2): Show |
5 | HG02280.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+230G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16924709 | |||||||
| chr1:16924727 | G | A | 1 | a0027c0041t0002g0162 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.351+248G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16924727 | |||||||
| chr1:16924787 | G | A | 1 | a0002c0018t0006g0031 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.351+308G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16924787 | |||||||
| chr1:16924914 | C | T | 2 | a0002c0018t0006g0031 a0029c0051t0012g0015 |
2 | HG01071.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.351+435C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16924914 | |||||||
| chr1:16924955 | A | G | 1 | a0024c0035t0015g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.351+476A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16924955 | |||||||
| chr1:16925897 | G | T | 6 | a0003c0004t0002g0135 a0003c0004t0002g0136 a0003c0004t0002g0137 others(3): Show |
6 | HG01175.hp1 NA18972.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+1418G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16925897 | |||||||
| chr1:16925967 | C | T | 3 | a0001c0003t0001g0132 a0001c0003t0001g0133 a0001c0003t0001g0134 |
3 | HG01168.hp1 HG02735.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.351+1488C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16925967 | |||||||
| chr1:16926158 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.351+1679C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16926158 | |||||||
| chr1:16926170 | C | T | 1 | a0024c0035t0015g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.351+1691C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16926170 | |||||||
| chr1:16926225 | G | A | 1 | a0002c0018t0006g0031 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.351+1746G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16926225 | |||||||
| chr1:16926633 | C | T | 144 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(141): Show |
154 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.351+2154C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16926633 | |||||||
| chr1:16926634 | G | A | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2155G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16926634 | |||||||
| chr1:16926775 | C | T | 5 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(2): Show |
5 | HG02280.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2296C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16926775 | |||||||
| chr1:16926779 | T | A | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.351+2300T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16926779 | |||||||
| chr1:16926821 | G | A | 2 | a0001c0013t0001g0004 a0023c0024t0001g0004 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.351+2342G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16926821 | |||||||
| chr1:16926888 | T | C | 1 | a0001c0001t0005g0036 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.351+2409T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16926888 | |||||||
| chr1:16927108 | C | CAG | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.351+2631_351+2632d others(4): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | INFO_REALIGN_3_PRIME | chr1 | 16927108 | ||||||
| chr1:16927216 | C | T | 1 | a0010c0050t0007g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.352-2630C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16927216 | |||||||
| chr1:16927307 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.352-2539G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16927307 | |||||||
| chr1:16927333 | C | T | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-2513C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16927333 | |||||||
| chr1:16927449 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.352-2397C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16927449 | |||||||
| chr1:16927572 | G | A | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-2274G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16927572 | |||||||
| chr1:16927642 | G | A | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-2204G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16927642 | |||||||
| chr1:16927651 | A | G | 13 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(10): Show |
13 | HG00738.hp1 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.352-2195A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16927651 | |||||||
| chr1:16927731 | G | A | 3 | a0001c0002t0002g0163 a0001c0002t0002g0164 a0001c0019t0003g0013 |
4 | HG02055.hp1 HG02896.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-2115G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16927731 | |||||||
| chr1:16927789 | C | T | 2 | a0001c0001t0001g0025 a0003c0009t0002g0129 |
2 | HG01168.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.352-2057C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16927789 | |||||||
| chr1:16927937 | G | C | 143 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(140): Show |
153 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.352-1909G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16927937 | |||||||
| chr1:16928135 | G | A | 3 | a0001c0013t0001g0004 a0002c0018t0001g0037 a0023c0024t0001g0004 |
3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.352-1711G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928135 | |||||||
| chr1:16928165 | G | A | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-1681G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928165 | |||||||
| chr1:16928370 | G | C | 6 | a0001c0002t0002g0014 a0001c0002t0002g0165 a0001c0002t0002g0169 others(3): Show |
7 | HG01243.hp1 HG01358.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.352-1476G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928370 | |||||||
| chr1:16928419 | T | C | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-1427T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928419 | |||||||
| chr1:16928421 | C | G | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-1425C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928421 | |||||||
| chr1:16928444 | G | A | 143 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(140): Show |
153 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.352-1402G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928444 | |||||||
| chr1:16928736 | T | G | 2 | a0001c0002t0002g0202 a0029c0051t0012g0015 |
2 | NA19011.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.352-1110T>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928736 | |||||||
| chr1:16928764 | T | C | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-1082T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928764 | |||||||
| chr1:16928770 | T | C | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-1076T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928770 | |||||||
| chr1:16928784 | C | T | 1 | a0002c0018t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.352-1062C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928784 | |||||||
| chr1:16928887 | C | T | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.352-959C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928887 | |||||||
| chr1:16928890 | G | A | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.352-956G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928890 | |||||||
| chr1:16928893 | C | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG00558.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.352-953C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928893 | |||||||
| chr1:16928913 | G | A | 18 | a0003c0004t0002g0041 a0003c0004t0002g0135 a0003c0004t0002g0136 others(15): Show |
19 | HG01175.hp1 HG02257.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.352-933G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928913 | |||||||
| chr1:16928940 | C | T | 1 | a0001c0002t0002g0199 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.352-906C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928940 | |||||||
| chr1:16928941 | G | C | 152 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(149): Show |
162 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.352-905G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928941 | |||||||
| chr1:16928983 | C | T | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-863C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16928983 | |||||||
| chr1:16929028 | C | T | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.352-818C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929028 | |||||||
| chr1:16929071 | C | T | 18 | a0003c0004t0002g0041 a0003c0004t0002g0135 a0003c0004t0002g0136 others(15): Show |
19 | HG01175.hp1 HG02257.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.352-775C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929071 | |||||||
| chr1:16929167 | C | T | 157 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(154): Show |
167 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.352-679C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929167 | |||||||
| chr1:16929229 | G | A | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.352-617G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929229 | |||||||
| chr1:16929294 | A | G | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-552A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929294 | |||||||
| chr1:16929296 | A | G | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-550A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929296 | |||||||
| chr1:16929314 | T | C | 4 | a0002c0012t0006g0048 a0002c0012t0006g0049 a0002c0012t0006g0050 others(1): Show |
4 | HG02145.hp2 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-532T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929314 | |||||||
| chr1:16929407 | T | C | 4 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 others(1): Show |
4 | HG02970.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-439T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929407 | |||||||
| chr1:16929443 | TC | T | 152 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(149): Show |
162 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.352-401delC | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | INFO_REALIGN_3_PRIME | chr1 | 16929443 | ||||||
| chr1:16929456 | T | C | 11 | a0003c0009t0002g0038 a0005c0005t0002g0016 a0005c0005t0002g0018 others(8): Show |
11 | HG01106.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.352-390T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929456 | |||||||
| chr1:16929463 | C | G | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG01928.hp1 HG01975.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-383C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929463 | |||||||
| chr1:16929541 | A | G | 6 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0015c0047t0002g0159 others(3): Show |
6 | HG01106.hp1 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.352-305A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929541 | |||||||
| chr1:16929596 | G | C | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.352-250G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929596 | |||||||
| chr1:16929635 | G | A | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-211G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929635 | |||||||
| chr1:16929741 | C | T | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.352-105C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929741 | |||||||
| chr1:16929818 | G | A | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.352-28G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 3/36 | chr1 | 16929818 | |||||||
| chr1:16930097 | G | A | 3 | a0003c0009t0002g0129 a0011c0016t0002g0039 a0025c0027t0002g0040 |
3 | HG03139.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.538-27G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 4/36 | chr1 | 16930097 | |||||||
| chr1:16930113 | C | T | 1 | a0030c0046t0013g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.538-11C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 4/36 | chr1 | 16930113 | |||||||
| chr1:16930355 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0122 a0001c0001t0017g0121 |
3 | HG01074.hp2 HG01081.hp2 NA20805.hp1 |
splice_region_variant&intron_variant | LOW | c.683+8C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 6/36 | chr1 | 16930355 | |||||||
| chr1:16930692 | G | GTCCGAGG others(8): Show |
13 | a0001c0001t0001g0120 a0003c0009t0002g0129 a0005c0005t0002g0016 others(10): Show |
13 | HG02055.hp2 HG02129.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.849+101_849+102ins others(15): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 7/36 | INFO_REALIGN_3_PRIME | chr1 | 16930692 | ||||||
| chr1:16930698 | G | A | 2 | a0003c0004t0001g0051 a0003c0004t0002g0041 |
2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.849+104G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 7/36 | chr1 | 16930698 | |||||||
| chr1:16930726 | G | A | 1 | a0001c0002t0002g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.849+132G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 7/36 | chr1 | 16930726 | |||||||
| chr1:16930807 | C | T | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.849+213C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 7/36 | chr1 | 16930807 | |||||||
| chr1:16930859 | G | C | 141 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(138): Show |
151 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.849+265G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 7/36 | chr1 | 16930859 | |||||||
| chr1:16930875 | G | A | 1 | a0001c0003t0001g0141 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.849+281G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 7/36 | chr1 | 16930875 | |||||||
| chr1:16931622 | T | C | 1 | a0003c0004t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.956+225T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16931622 | |||||||
| chr1:16931687 | G | A | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.956+290G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16931687 | |||||||
| chr1:16931761 | AT | A | 15 | a0001c0001t0001g0052 a0001c0001t0001g0123 a0001c0001t0001g0124 others(12): Show |
15 | HG01928.hp1 HG01975.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.956+376delT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | INFO_REALIGN_3_PRIME | chr1 | 16931761 | ||||||
| chr1:16931812 | G | A | 1 | a0011c0016t0002g0039 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.956+415G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16931812 | |||||||
| chr1:16931820 | G | A | 65 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(62): Show |
69 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.956+423G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16931820 | |||||||
| chr1:16931832 | C | A | 63 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(60): Show |
67 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.956+435C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16931832 | |||||||
| chr1:16931923 | AT | A | 66 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(63): Show |
70 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.956+542delT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | INFO_REALIGN_3_PRIME | chr1 | 16931923 | ||||||
| chr1:16931958 | G | C | 3 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 |
3 | HG01258.hp2 HG02004.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.956+561G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16931958 | |||||||
| chr1:16931981 | G | T | 7 | a0005c0005t0002g0018 a0005c0005t0002g0156 a0005c0005t0002g0157 others(4): Show |
7 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.956+584G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16931981 | |||||||
| chr1:16932062 | A | T | 1 | a0001c0001t0005g0036 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.956+665A>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932062 | |||||||
| chr1:16932066 | C | T | 2 | a0005c0005t0002g0016 a0029c0051t0012g0015 |
2 | HG02559.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.956+669C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932066 | |||||||
| chr1:16932089 | T | G | 3 | a0008c0011t0004g0002 a0008c0011t0004g0042 a0019c0021t0004g0002 |
4 | HG02622.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.956+692T>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932089 | |||||||
| chr1:16932307 | G | C | 1 | a0001c0001t0001g0005 | 2 | HG00558.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.956+910G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932307 | |||||||
| chr1:16932332 | C | T | 1 | a0031c0028t0003g0138 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.956+935C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932332 | |||||||
| chr1:16932409 | C | T | 2 | a0005c0005t0002g0016 a0029c0051t0012g0015 |
2 | HG02559.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.956+1012C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932409 | |||||||
| chr1:16932470 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.956+1073G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932470 | |||||||
| chr1:16932494 | C | T | 1 | a0001c0037t0002g0195 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.956+1097C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932494 | |||||||
| chr1:16932676 | G | A | 1 | a0001c0001t0005g0057 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.956+1279G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932676 | |||||||
| chr1:16932783 | T | C | 2 | a0005c0005t0002g0016 a0029c0051t0012g0015 |
2 | HG02559.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.956+1386T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932783 | |||||||
| chr1:16932797 | C | T | 1 | a0001c0003t0005g0053 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.956+1400C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932797 | |||||||
| chr1:16932821 | C | T | 1 | a0033c0048t0007g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.956+1424C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932821 | |||||||
| chr1:16932864 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0122 |
2 | HG01074.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.956+1467A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16932864 | |||||||
| chr1:16933241 | G | A | 65 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(62): Show |
69 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.956+1844G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16933241 | |||||||
| chr1:16933428 | T | C | 2 | a0005c0005t0002g0016 a0029c0051t0012g0015 |
2 | HG02559.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.956+2031T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16933428 | |||||||
| chr1:16933448 | C | G | 7 | a0005c0005t0002g0018 a0005c0005t0002g0156 a0005c0005t0002g0157 others(4): Show |
7 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.956+2051C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16933448 | |||||||
| chr1:16933527 | G | A | 1 | a0001c0003t0001g0058 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.956+2130G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16933527 | |||||||
| chr1:16933626 | G | A | 2 | a0005c0005t0002g0016 a0029c0051t0012g0015 |
2 | HG02559.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.956+2229G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16933626 | |||||||
| chr1:16933628 | A | G | 74 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(71): Show |
78 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.956+2231A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16933628 | |||||||
| chr1:16933715 | G | A | 65 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(62): Show |
69 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.956+2318G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16933715 | |||||||
| chr1:16933803 | C | G | 65 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(62): Show |
69 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.956+2406C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16933803 | |||||||
| chr1:16933839 | C | T | 3 | a0005c0005t0002g0156 a0005c0005t0002g0157 a0005c0005t0002g0158 |
3 | HG02451.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.956+2442C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16933839 | |||||||
| chr1:16933854 | C | T | 3 | a0005c0005t0002g0156 a0005c0005t0002g0157 a0005c0005t0002g0158 |
3 | HG02451.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.956+2457C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16933854 | |||||||
| chr1:16934019 | C | G | 1 | a0009c0017t0001g0010 | 2 | HG01175.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.957-2618C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16934019 | |||||||
| chr1:16934197 | A | G | 2 | a0005c0005t0002g0016 a0029c0051t0012g0015 |
2 | HG02559.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.957-2440A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16934197 | |||||||
| chr1:16934308 | A | ATTT | 3 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 |
5 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.957-2320_957-2318d others(5): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | INFO_REALIGN_3_PRIME | chr1 | 16934308 | ||||||
| chr1:16934362 | C | T | 2 | a0005c0005t0002g0016 a0029c0051t0012g0015 |
2 | HG02559.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.957-2275C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16934362 | |||||||
| chr1:16934634 | G | A | 1 | a0001c0002t0002g0165 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.957-2003G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16934634 | |||||||
| chr1:16934704 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.957-1933G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16934704 | |||||||
| chr1:16934860 | C | G | 1 | a0022c0044t0003g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.957-1777C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16934860 | |||||||
| chr1:16934892 | C | CT | 5 | a0001c0001t0001g0147 a0001c0002t0002g0194 a0001c0002t0003g0209 others(2): Show |
5 | HG01106.hp2 HG01168.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.957-1727dupT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | INFO_REALIGN_3_PRIME | chr1 | 16934892 | ||||||
| chr1:16934892 | CT | C | 13 | a0001c0002t0002g0163 a0001c0002t0002g0171 a0001c0002t0002g0172 others(10): Show |
13 | HG02055.hp2 HG02622.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.957-1727delT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | INFO_REALIGN_3_PRIME | chr1 | 16934892 | ||||||
| chr1:16934981 | C | T | 7 | a0005c0005t0002g0018 a0005c0005t0002g0156 a0005c0005t0002g0157 others(4): Show |
7 | HG02055.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.957-1656C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16934981 | |||||||
| chr1:16934986 | A | G | 2 | a0005c0005t0002g0016 a0029c0051t0012g0015 |
2 | HG02559.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.957-1651A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16934986 | |||||||
| chr1:16935018 | G | A | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.957-1619G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16935018 | |||||||
| chr1:16935268 | C | G | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.957-1369C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16935268 | |||||||
| chr1:16935495 | T | A | 74 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(71): Show |
78 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.957-1142T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16935495 | |||||||
| chr1:16935513 | T | C | 93 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(90): Show |
98 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(95): Show |
intron_variant | MODIFIER | c.957-1124T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16935513 | |||||||
| chr1:16935517 | T | G | 1 | a0001c0003t0001g0060 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.957-1120T>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16935517 | |||||||
| chr1:16935522 | GCCATTCT others(13): Show |
G | 1 | a0001c0003t0001g0060 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.957-1112_957-1093d others(22): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | INFO_REALIGN_3_PRIME | chr1 | 16935522 | ||||||
| chr1:16935582 | G | A | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.957-1055G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16935582 | |||||||
| chr1:16935719 | T | C | 161 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(158): Show |
173 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(170): Show |
intron_variant | MODIFIER | c.957-918T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16935719 | |||||||
| chr1:16935919 | G | C | 1 | a0001c0002t0003g0174 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.957-718G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16935919 | |||||||
| chr1:16935920 | A | C | 1 | a0001c0002t0003g0174 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.957-717A>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16935920 | |||||||
| chr1:16936027 | AC | A | 94 | a0001c0001t0001g0091 a0001c0002t0001g0119 a0001c0002t0002g0014 others(91): Show |
99 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(96): Show |
intron_variant | MODIFIER | c.957-605delC | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | INFO_REALIGN_3_PRIME | chr1 | 16936027 | ||||||
| chr1:16936084 | G | A | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.957-553G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16936084 | |||||||
| chr1:16936447 | G | T | 5 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.957-190G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16936447 | |||||||
| chr1:16936449 | A | G | 5 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.957-188A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16936449 | |||||||
| chr1:16936458 | A | G | 5 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.957-179A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16936458 | |||||||
| chr1:16936544 | T | C | 5 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(2): Show |
5 | HG02280.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.957-93T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 8/36 | chr1 | 16936544 | |||||||
| chr1:16936897 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1193+24C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/36 | chr1 | 16936897 | |||||||
| chr1:16937021 | C | G | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1193+148C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/36 | chr1 | 16937021 | |||||||
| chr1:16937062 | G | A | 152 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(149): Show |
162 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(159): Show |
intron_variant | MODIFIER | c.1193+189G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/36 | chr1 | 16937062 | |||||||
| chr1:16937088 | C | T | 2 | a0001c0003t0001g0089 a0001c0003t0001g0090 |
2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1193+215C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/36 | chr1 | 16937088 | |||||||
| chr1:16937109 | C | A | 2 | a0001c0002t0002g0175 a0001c0002t0002g0176 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1193+236C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/36 | chr1 | 16937109 | |||||||
| chr1:16937167 | G | A | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1193+294G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/36 | chr1 | 16937167 | |||||||
| chr1:16937224 | G | A | 51 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(48): Show |
53 | HG00544.hp1 HG01074.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.1193+351G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/36 | chr1 | 16937224 | |||||||
| chr1:16937275 | C | A | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1194-366C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/36 | chr1 | 16937275 | |||||||
| chr1:16937347 | C | T | 1 | a0001c0002t0002g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1194-294C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/36 | chr1 | 16937347 | |||||||
| chr1:16937352 | C | CA | 66 | a0001c0001t0008g0026 a0001c0002t0001g0119 a0001c0002t0002g0014 others(63): Show |
71 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.1194-276dupA | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/36 | INFO_REALIGN_3_PRIME | chr1 | 16937352 | ||||||
| chr1:16937595 | A | G | 4 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(1): Show |
6 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1194-46A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 9/36 | chr1 | 16937595 | |||||||
| chr1:16937747 | A | C | 1 | a0001c0003t0001g0132 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1290+10A>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 10/36 | chr1 | 16937747 | |||||||
| chr1:16937801 | G | A | 55 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0006 others(52): Show |
62 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1290+64G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 10/36 | chr1 | 16937801 | |||||||
| chr1:16937980 | T | A | 74 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(71): Show |
78 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.1290+243T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 10/36 | chr1 | 16937980 | |||||||
| chr1:16938040 | C | T | 16 | a0003c0004t0001g0051 a0003c0004t0002g0041 a0003c0004t0002g0135 others(13): Show |
16 | HG01175.hp1 HG02257.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1290+303C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 10/36 | chr1 | 16938040 | |||||||
| chr1:16938108 | C | T | 1 | a0022c0044t0003g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1291-292C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 10/36 | chr1 | 16938108 | |||||||
| chr1:16938141 | TCTGTGTG others(4): Show |
T | 63 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(60): Show |
67 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.1291-255_1291-245d others(13): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 10/36 | INFO_REALIGN_3_PRIME | chr1 | 16938141 | ||||||
| chr1:16938368 | A | G | 74 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(71): Show |
78 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.1291-32A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 10/36 | chr1 | 16938368 | |||||||
| chr1:16938395 | T | G | 2 | a0001c0002t0002g0161 a0001c0002t0002g0177 |
2 | HG01361.hp2 HG02451.hp1 |
splice_region_variant&intron_variant | LOW | c.1291-5T>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 10/36 | chr1 | 16938395 | |||||||
| chr1:16938546 | G | A | 1 | a0002c0018t0006g0031 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1374+63G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 11/36 | chr1 | 16938546 | |||||||
| chr1:16938676 | A | G | 74 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(71): Show |
78 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.1374+193A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 11/36 | chr1 | 16938676 | |||||||
| chr1:16938832 | A | G | 70 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(67): Show |
74 | HG00544.hp1 HG00642.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.1375-77A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 11/36 | chr1 | 16938832 | |||||||
| chr1:16938871 | C | G | 4 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 others(1): Show |
4 | HG02970.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375-38C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 11/36 | chr1 | 16938871 | |||||||
| chr1:16939209 | T | TGGGGGC | 54 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(51): Show |
58 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.1608+80_1608+85dup others(6): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 12/36 | INFO_REALIGN_3_PRIME | chr1 | 16939209 | ||||||
| chr1:16939283 | G | T | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1608+141G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 12/36 | chr1 | 16939283 | |||||||
| chr1:16939551 | C | G | 6 | a0001c0002t0002g0173 a0001c0002t0002g0190 a0001c0002t0002g0208 others(3): Show |
6 | HG00639.hp1 NA18946.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1609-343C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 12/36 | chr1 | 16939551 | |||||||
| chr1:16939622 | G | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0116 a0029c0051t0012g0015 |
3 | NA19011.hp1 NA19054.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1609-272G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 12/36 | chr1 | 16939622 | |||||||
| chr1:16939635 | G | A | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1609-259G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 12/36 | chr1 | 16939635 | |||||||
| chr1:16939637 | T | C | 2 | a0001c0003t0001g0022 a0001c0003t0001g0065 |
2 | NA19056.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1609-257T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 12/36 | chr1 | 16939637 | |||||||
| chr1:16939692 | A | G | 1 | a0003c0026t0016g0046 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1609-202A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 12/36 | chr1 | 16939692 | |||||||
| chr1:16939729 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1609-165C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 12/36 | chr1 | 16939729 | |||||||
| chr1:16939862 | C | A | 3 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 |
3 | HG00099.hp2 NA20129.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1609-32C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 12/36 | chr1 | 16939862 | |||||||
| chr1:16939888 | C | A | 3 | a0008c0011t0004g0002 a0008c0011t0004g0042 a0019c0021t0004g0002 |
4 | HG02622.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1609-6C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 12/36 | chr1 | 16939888 | |||||||
| chr1:16940153 | C | T | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.1808+60C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16940153 | |||||||
| chr1:16940342 | G | A | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1808+249G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16940342 | |||||||
| chr1:16940383 | C | T | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1808+290C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16940383 | |||||||
| chr1:16940390 | A | AT | 13 | a0001c0001t0001g0052 a0001c0001t0001g0091 a0001c0001t0001g0113 others(10): Show |
13 | HG01975.hp1 HG01993.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.1808+313dupT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr1 | 16940390 | ||||||
| chr1:16940390 | A | ATT | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1808+312_1808+313d others(4): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr1 | 16940390 | ||||||
| chr1:16940390 | AT | A | 6 | a0001c0001t0001g0122 a0001c0003t0001g0134 a0001c0007t0001g0069 others(3): Show |
6 | HG00639.hp2 HG01081.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1808+313delT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr1 | 16940390 | ||||||
| chr1:16940447 | G | A | 1 | a0006c0010t0007g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1808+354G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16940447 | |||||||
| chr1:16940543 | C | G | 9 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1808+450C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16940543 | |||||||
| chr1:16940547 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1808+454C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16940547 | |||||||
| chr1:16940708 | C | CAGTTTTG others(3): Show |
5 | a0001c0002t0002g0173 a0001c0002t0002g0190 a0001c0002t0002g0208 others(2): Show |
5 | NA18946.hp1 NA18981.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1808+616_1808+625d others(12): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr1 | 16940708 | ||||||
| chr1:16940807 | A | G | 55 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(52): Show |
59 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.1808+714A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16940807 | |||||||
| chr1:16940867 | G | T | 1 | a0002c0018t0006g0031 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1808+774G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16940867 | |||||||
| chr1:16941001 | C | T | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1808+908C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941001 | |||||||
| chr1:16941180 | A | G | 6 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1808+1087A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941180 | |||||||
| chr1:16941237 | C | T | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1808+1144C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941237 | |||||||
| chr1:16941369 | G | A | 1 | a0031c0028t0003g0138 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1808+1276G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941369 | |||||||
| chr1:16941390 | A | G | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1808+1297A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941390 | |||||||
| chr1:16941432 | A | T | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1808+1339A>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941432 | |||||||
| chr1:16941435 | T | A | 1 | a0008c0011t0004g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1808+1342T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941435 | |||||||
| chr1:16941499 | C | T | 5 | a0001c0001t0008g0026 a0001c0001t0008g0027 a0001c0001t0008g0028 others(2): Show |
5 | NA18946.hp2 NA18955.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1808+1406C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941499 | |||||||
| chr1:16941521 | G | T | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1808+1428G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941521 | |||||||
| chr1:16941675 | C | T | 1 | a0001c0001t0008g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1808+1582C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941675 | |||||||
| chr1:16941679 | C | T | 1 | a0001c0001t0008g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1808+1586C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941679 | |||||||
| chr1:16941680 | C | G | 1 | a0001c0001t0008g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1808+1587C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941680 | |||||||
| chr1:16941686 | G | T | 1 | a0001c0001t0008g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1808+1593G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941686 | |||||||
| chr1:16941687 | G | T | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1808+1594G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941687 | |||||||
| chr1:16941708 | A | G | 1 | a0001c0001t0008g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1808+1615A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941708 | |||||||
| chr1:16941710 | C | G | 1 | a0001c0001t0008g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1808+1617C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941710 | |||||||
| chr1:16941731 | CA | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(61): Show |
66 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1808+1654delA | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr1 | 16941731 | ||||||
| chr1:16941834 | C | A | 74 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(71): Show |
78 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.1808+1741C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16941834 | |||||||
| chr1:16942249 | C | T | 51 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(48): Show |
53 | HG00544.hp1 HG01074.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.1809-1851C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16942249 | |||||||
| chr1:16942280 | G | A | 1 | a0001c0002t0003g0178 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1809-1820G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16942280 | |||||||
| chr1:16942338 | C | G | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1809-1762C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16942338 | |||||||
| chr1:16942370 | G | T | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1809-1730G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16942370 | |||||||
| chr1:16942981 | T | G | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1809-1119T>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16942981 | |||||||
| chr1:16943077 | T | C | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1809-1023T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943077 | |||||||
| chr1:16943110 | C | T | 3 | a0001c0013t0001g0004 a0002c0018t0001g0037 a0023c0024t0001g0004 |
3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1809-990C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943110 | |||||||
| chr1:16943126 | C | T | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1809-974C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943126 | |||||||
| chr1:16943157 | G | A | 1 | a0002c0006t0004g0179 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1809-943G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943157 | |||||||
| chr1:16943228 | G | A | 1 | a0010c0050t0007g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1809-872G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943228 | |||||||
| chr1:16943232 | T | C | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.1809-868T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943232 | |||||||
| chr1:16943240 | A | G | 1 | a0031c0028t0003g0138 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1809-860A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943240 | |||||||
| chr1:16943309 | G | A | 4 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 others(1): Show |
4 | HG02970.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809-791G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943309 | |||||||
| chr1:16943454 | C | T | 1 | a0001c0002t0002g0189 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1809-646C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943454 | |||||||
| chr1:16943497 | T | C | 201 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(198): Show |
215 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.1809-603T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943497 | |||||||
| chr1:16943550 | T | A | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1809-550T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943550 | |||||||
| chr1:16943613 | T | C | 75 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(72): Show |
79 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.1809-487T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943613 | |||||||
| chr1:16943678 | T | G | 1 | a0024c0035t0015g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1809-422T>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943678 | |||||||
| chr1:16943752 | A | C | 1 | a0001c0003t0001g0084 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1809-348A>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943752 | |||||||
| chr1:16943794 | G | A | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1809-306G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943794 | |||||||
| chr1:16943826 | C | T | 6 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1809-274C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943826 | |||||||
| chr1:16943891 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1809-209G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16943891 | |||||||
| chr1:16944003 | T | G | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1809-97T>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 13/36 | chr1 | 16944003 | |||||||
| chr1:16944285 | G | T | 2 | a0001c0003t0001g0089 a0001c0003t0001g0090 |
2 | HG02970.hp2 HG03579.hp2 |
splice_region_variant&intron_variant | LOW | c.1991+3G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944285 | |||||||
| chr1:16944297 | G | A | 3 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 |
5 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1991+15G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944297 | |||||||
| chr1:16944300 | A | T | 3 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 |
5 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1991+18A>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944300 | |||||||
| chr1:16944311 | A | G | 3 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 |
5 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1991+29A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944311 | |||||||
| chr1:16944350 | C | CG | 2 | a0029c0051t0012g0015 a0030c0046t0013g0198 |
2 | NA19011.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1991+68_1991+69ins others(1): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944350 | |||||||
| chr1:16944516 | C | T | 2 | a0001c0002t0002g0194 a0001c0003t0001g0132 |
2 | HG01243.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1991+234C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944516 | |||||||
| chr1:16944549 | C | T | 6 | a0001c0002t0002g0194 a0001c0003t0001g0132 a0002c0012t0006g0048 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1991+267C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944549 | |||||||
| chr1:16944676 | G | T | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.1991+394G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944676 | |||||||
| chr1:16944811 | G | A | 1 | a0002c0012t0006g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1991+529G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944811 | |||||||
| chr1:16944838 | A | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
15 | HG01106.hp1 HG01175.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1991+556A>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944838 | |||||||
| chr1:16944954 | C | T | 1 | a0005c0005t0002g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1992-508C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944954 | |||||||
| chr1:16944959 | G | A | 1 | a0005c0005t0002g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1992-503G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944959 | |||||||
| chr1:16944961 | A | G | 1 | a0005c0005t0002g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1992-501A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944961 | |||||||
| chr1:16944986 | A | G | 1 | a0001c0002t0002g0161 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1992-476A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16944986 | |||||||
| chr1:16945048 | C | T | 1 | a0029c0051t0012g0015 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1992-414C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16945048 | |||||||
| chr1:16945257 | T | C | 1 | a0001c0031t0001g0094 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1992-205T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16945257 | |||||||
| chr1:16945397 | G | A | 1 | a0010c0050t0007g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1992-65G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 14/36 | chr1 | 16945397 | |||||||
| chr1:16945823 | G | A | 3 | a0008c0011t0004g0002 a0008c0011t0004g0042 a0019c0021t0004g0002 |
4 | HG02622.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2136+217G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 15/36 | chr1 | 16945823 | |||||||
| chr1:16945888 | G | C | 9 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(6): Show |
9 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2136+282G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 15/36 | chr1 | 16945888 | |||||||
| chr1:16945941 | A | G | 77 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(74): Show |
82 | HG00544.hp1 HG00639.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.2137-318A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 15/36 | chr1 | 16945941 | |||||||
| chr1:16946008 | G | T | 54 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(51): Show |
58 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.2137-251G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 15/36 | chr1 | 16946008 | |||||||
| chr1:16946157 | A | C | 7 | a0001c0003t0001g0008 a0001c0003t0001g0022 a0001c0003t0001g0060 others(4): Show |
8 | HG01123.hp2 HG02056.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.2137-102A>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 15/36 | chr1 | 16946157 | |||||||
| chr1:16946997 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01943.hp2 HG02293.hp1 |
splice_region_variant&intron_variant | LOW | c.2514+6C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16946997 | |||||||
| chr1:16946998 | A | C | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
splice_region_variant&intron_variant | LOW | c.2514+7A>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16946998 | |||||||
| chr1:16947172 | T | A | 1 | a0001c0002t0011g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2514+181T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947172 | |||||||
| chr1:16947184 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2514+193A>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947184 | |||||||
| chr1:16947199 | A | G | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.2514+208A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947199 | |||||||
| chr1:16947335 | G | A | 1 | a0002c0012t0006g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2514+344G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947335 | |||||||
| chr1:16947384 | G | A | 6 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2514+393G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947384 | |||||||
| chr1:16947437 | C | G | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2514+446C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947437 | |||||||
| chr1:16947468 | C | CAAT | 17 | a0001c0001t0001g0009 a0001c0001t0001g0096 a0001c0001t0001g0117 others(14): Show |
18 | HG00741.hp1 HG01168.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.2514+508_2514+510d others(5): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr1 | 16947468 | ||||||
| chr1:16947468 | C | CAATAAT | 9 | a0001c0002t0002g0173 a0001c0002t0002g0213 a0001c0002t0003g0191 others(6): Show |
9 | HG02257.hp2 HG02280.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2514+505_2514+510d others(8): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr1 | 16947468 | ||||||
| chr1:16947468 | C | CAATAATA others(2): Show |
19 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0202 others(16): Show |
22 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2514+502_2514+510d others(11): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr1 | 16947468 | ||||||
| chr1:16947468 | C | CAATAATA others(5): Show |
23 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(20): Show |
24 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.2514+499_2514+510d others(14): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr1 | 16947468 | ||||||
| chr1:16947468 | C | CAATAATA others(8): Show |
5 | a0001c0002t0002g0171 a0001c0002t0002g0181 a0001c0002t0002g0182 others(2): Show |
5 | HG03669.hp1 NA18982.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.2514+496_2514+510d others(17): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr1 | 16947468 | ||||||
| chr1:16947468 | CAAT | C | 9 | a0002c0018t0001g0037 a0005c0005t0002g0016 a0005c0005t0002g0018 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2514+508_2514+510d others(5): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr1 | 16947468 | ||||||
| chr1:16947482 | A | ATAATAAT others(11): Show |
6 | a0001c0002t0002g0170 a0001c0002t0002g0172 a0001c0002t0002g0187 others(3): Show |
6 | HG02074.hp1 HG02155.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.2514+508_2514+509i others(20): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr1 | 16947482 | ||||||
| chr1:16947487 | A | AATAATAA others(11): Show |
1 | a0024c0035t0015g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2514+510_2514+511i others(20): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr1 | 16947487 | ||||||
| chr1:16947496 | A | G | 1 | a0020c0029t0002g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2514+505A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947496 | |||||||
| chr1:16947633 | A | G | 198 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(195): Show |
211 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.2514+642A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947633 | |||||||
| chr1:16947634 | G | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0091 others(12): Show |
16 | HG00544.hp2 HG00558.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.2514+643G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947634 | |||||||
| chr1:16947738 | T | C | 1 | a0001c0003t0005g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2515-593T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947738 | |||||||
| chr1:16947823 | C | T | 6 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2515-508C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947823 | |||||||
| chr1:16947824 | A | G | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.2515-507A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947824 | |||||||
| chr1:16947843 | G | T | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.2515-488G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947843 | |||||||
| chr1:16947999 | C | T | 1 | a0001c0003t0001g0081 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2515-332C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16947999 | |||||||
| chr1:16948041 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2515-290G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 17/36 | chr1 | 16948041 | |||||||
| chr1:16948551 | G | A | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2708+27G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 18/36 | chr1 | 16948551 | |||||||
| chr1:16948607 | C | G | 65 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(62): Show |
69 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.2708+83C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 18/36 | chr1 | 16948607 | |||||||
| chr1:16948765 | A | C | 1 | a0001c0002t0002g0185 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2709-34A>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 18/36 | chr1 | 16948765 | |||||||
| chr1:16949042 | G | A | 1 | a0001c0002t0002g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2836+116G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16949042 | |||||||
| chr1:16949062 | A | ACTTAGAT | 3 | a0001c0003t0001g0132 a0001c0003t0001g0133 a0001c0003t0001g0134 |
3 | HG01168.hp1 HG02735.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2836+139_2836+145d others(9): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | INFO_REALIGN_3_PRIME | chr1 | 16949062 | ||||||
| chr1:16949127 | G | T | 70 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(67): Show |
74 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(71): Show |
intron_variant | MODIFIER | c.2836+201G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16949127 | |||||||
| chr1:16949174 | G | A | 1 | a0022c0044t0003g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2836+248G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16949174 | |||||||
| chr1:16949400 | A | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(60): Show |
65 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.2836+474A>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16949400 | |||||||
| chr1:16949590 | T | C | 3 | a0001c0013t0001g0004 a0002c0018t0001g0037 a0023c0024t0001g0004 |
3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2836+664T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16949590 | |||||||
| chr1:16949728 | C | T | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.2836+802C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16949728 | |||||||
| chr1:16949862 | T | C | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.2836+936T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16949862 | |||||||
| chr1:16949961 | G | T | 3 | a0001c0003t0001g0132 a0001c0003t0001g0133 a0001c0003t0001g0134 |
3 | HG01168.hp1 HG02735.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2837-992G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16949961 | |||||||
| chr1:16949966 | G | A | 3 | a0008c0011t0004g0002 a0008c0011t0004g0042 a0019c0021t0004g0002 |
4 | HG02622.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2837-987G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16949966 | |||||||
| chr1:16950132 | C | T | 53 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0006 others(50): Show |
60 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.2837-821C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16950132 | |||||||
| chr1:16950173 | C | T | 1 | a0001c0019t0003g0013 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2837-780C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16950173 | |||||||
| chr1:16950354 | C | T | 3 | a0001c0003t0001g0132 a0001c0003t0001g0133 a0001c0003t0001g0134 |
3 | HG01168.hp1 HG02735.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2837-599C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16950354 | |||||||
| chr1:16950393 | T | C | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2837-560T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16950393 | |||||||
| chr1:16950483 | CT | C | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.2837-469delT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16950483 | |||||||
| chr1:16950487 | G | GTA | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.2837-466_2837-465i others(4): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16950487 | |||||||
| chr1:16950648 | G | T | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2837-305G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16950648 | |||||||
| chr1:16950837 | C | A | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2837-116C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 19/36 | chr1 | 16950837 | |||||||
| chr1:16951309 | C | G | 3 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0014g0152 |
3 | HG02280.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3006+187C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16951309 | |||||||
| chr1:16951457 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3006+335A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16951457 | |||||||
| chr1:16951670 | C | G | 6 | a0001c0001t0008g0026 a0001c0001t0008g0027 a0001c0001t0008g0028 others(3): Show |
6 | NA18946.hp2 NA18955.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.3006+548C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16951670 | |||||||
| chr1:16951882 | C | CT | 9 | a0003c0009t0002g0045 a0005c0005t0002g0016 a0005c0005t0002g0018 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3006+772dupT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | INFO_REALIGN_3_PRIME | chr1 | 16951882 | ||||||
| chr1:16951882 | CT | C | 182 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(179): Show |
195 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(192): Show |
intron_variant | MODIFIER | c.3006+772delT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | INFO_REALIGN_3_PRIME | chr1 | 16951882 | ||||||
| chr1:16952037 | G | A | 3 | a0001c0013t0001g0004 a0002c0018t0001g0037 a0023c0024t0001g0004 |
3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3006+915G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952037 | |||||||
| chr1:16952039 | G | A | 1 | a0001c0002t0003g0191 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3006+917G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952039 | |||||||
| chr1:16952134 | A | G | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3006+1012A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952134 | |||||||
| chr1:16952184 | T | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0096 a0001c0001t0001g0117 others(1): Show |
5 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.3006+1062T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952184 | |||||||
| chr1:16952198 | C | T | 3 | a0001c0003t0001g0080 a0001c0003t0001g0144 a0001c0003t0005g0053 |
3 | NA18944.hp2 NA18963.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.3006+1076C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952198 | |||||||
| chr1:16952201 | T | C | 3 | a0001c0003t0001g0080 a0001c0003t0001g0144 a0001c0003t0005g0053 |
3 | NA18944.hp2 NA18963.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.3006+1079T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952201 | |||||||
| chr1:16952210 | T | G | 3 | a0001c0003t0001g0080 a0001c0003t0001g0144 a0001c0003t0005g0053 |
3 | NA18944.hp2 NA18963.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.3006+1088T>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952210 | |||||||
| chr1:16952212 | G | A | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3006+1090G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952212 | |||||||
| chr1:16952292 | G | A | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3007-1010G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952292 | |||||||
| chr1:16952302 | G | A | 1 | a0001c0002t0003g0174 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3007-1000G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952302 | |||||||
| chr1:16952356 | G | A | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3007-946G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952356 | |||||||
| chr1:16952527 | G | A | 1 | a0001c0049t0001g0030 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3007-775G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952527 | |||||||
| chr1:16952554 | G | A | 3 | a0001c0013t0001g0004 a0002c0018t0001g0037 a0023c0024t0001g0004 |
3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3007-748G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952554 | |||||||
| chr1:16952558 | C | T | 1 | a0001c0003t0001g0060 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3007-744C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952558 | |||||||
| chr1:16952619 | C | T | 2 | a0003c0004t0001g0051 a0003c0004t0002g0041 |
2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3007-683C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952619 | |||||||
| chr1:16952773 | C | A | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3007-529C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952773 | |||||||
| chr1:16952794 | A | T | 1 | a0010c0050t0007g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3007-508A>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952794 | |||||||
| chr1:16952821 | C | A | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3007-481C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952821 | |||||||
| chr1:16952900 | C | A | 1 | a0001c0013t0001g0106 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3007-402C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952900 | |||||||
| chr1:16952914 | C | G | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3007-388C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952914 | |||||||
| chr1:16952990 | C | T | 1 | a0030c0046t0013g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3007-312C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16952990 | |||||||
| chr1:16953076 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3007-226G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16953076 | |||||||
| chr1:16953110 | A | G | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3007-192A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16953110 | |||||||
| chr1:16953133 | C | T | 1 | a0003c0009t0002g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3007-169C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16953133 | |||||||
| chr1:16953143 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3007-159G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 20/36 | chr1 | 16953143 | |||||||
| chr1:16953498 | A | G | 9 | a0001c0001t0001g0103 a0005c0005t0002g0016 a0005c0005t0002g0018 others(6): Show |
9 | HG01346.hp1 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3186+17A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953498 | |||||||
| chr1:16953527 | A | T | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+46A>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953527 | |||||||
| chr1:16953530 | T | C | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+49T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953530 | |||||||
| chr1:16953550 | T | C | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+69T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953550 | |||||||
| chr1:16953556 | T | C | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+75T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953556 | |||||||
| chr1:16953562 | G | A | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+81G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953562 | |||||||
| chr1:16953566 | G | T | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+85G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953566 | |||||||
| chr1:16953580 | GGCC | G | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+100_3186+102d others(5): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953580 | |||||||
| chr1:16953584 | A | C | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+103A>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953584 | |||||||
| chr1:16953590 | C | T | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+109C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953590 | |||||||
| chr1:16953612 | T | C | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+131T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953612 | |||||||
| chr1:16953623 | G | T | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+142G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953623 | |||||||
| chr1:16953625 | G | T | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+144G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953625 | |||||||
| chr1:16953644 | C | T | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+163C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953644 | |||||||
| chr1:16953657 | T | C | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3186+176T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953657 | |||||||
| chr1:16953701 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3186+220T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953701 | |||||||
| chr1:16953744 | C | T | 65 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(62): Show |
69 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.3186+263C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953744 | |||||||
| chr1:16953759 | C | G | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+278C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953759 | |||||||
| chr1:16953826 | G | C | 73 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(70): Show |
77 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(74): Show |
intron_variant | MODIFIER | c.3186+345G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953826 | |||||||
| chr1:16953827 | T | C | 70 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(67): Show |
74 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(71): Show |
intron_variant | MODIFIER | c.3186+346T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953827 | |||||||
| chr1:16953852 | A | T | 16 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(13): Show |
16 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3186+371A>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953852 | |||||||
| chr1:16953865 | G | A | 10 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(7): Show |
10 | HG01106.hp1 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.3187-358G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953865 | |||||||
| chr1:16953887 | T | C | 13 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(10): Show |
13 | HG01106.hp1 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3187-336T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953887 | |||||||
| chr1:16953888 | G | A | 13 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(10): Show |
13 | HG01106.hp1 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3187-335G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953888 | |||||||
| chr1:16953924 | G | T | 8 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(5): Show |
8 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3187-299G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953924 | |||||||
| chr1:16953943 | A | G | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3187-280A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16953943 | |||||||
| chr1:16954010 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3187-213T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954010 | |||||||
| chr1:16954041 | G | A | 16 | a0003c0009t0002g0038 a0004c0008t0009g0072 a0005c0005t0002g0016 others(13): Show |
16 | HG01106.hp1 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3187-182G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954041 | |||||||
| chr1:16954056 | G | A | 1 | a0003c0004t0002g0041 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3187-167G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954056 | |||||||
| chr1:16954083 | T | A | 6 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3187-140T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954083 | |||||||
| chr1:16954083 | T | C | 184 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(181): Show |
197 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.3187-140T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954083 | |||||||
| chr1:16954094 | G | A | 8 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(5): Show |
8 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3187-129G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954094 | |||||||
| chr1:16954105 | A | G | 16 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(13): Show |
16 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3187-118A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954105 | |||||||
| chr1:16954114 | C | T | 6 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3187-109C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954114 | |||||||
| chr1:16954120 | C | T | 1 | a0017c0034t0002g0155 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3187-103C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954120 | |||||||
| chr1:16954132 | C | T | 1 | a0006c0010t0014g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3187-91C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954132 | |||||||
| chr1:16954137 | G | A | 6 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3187-86G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954137 | |||||||
| chr1:16954148 | T | C | 15 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(12): Show |
15 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.3187-75T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954148 | |||||||
| chr1:16954155 | C | G | 15 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(12): Show |
15 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.3187-68C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 21/36 | chr1 | 16954155 | |||||||
| chr1:16954508 | T | C | 131 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(128): Show |
140 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.3321+151T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 22/36 | chr1 | 16954508 | |||||||
| chr1:16954532 | C | T | 1 | a0001c0002t0003g0178 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3321+175C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 22/36 | chr1 | 16954532 | |||||||
| chr1:16954550 | G | A | 3 | a0005c0005t0002g0156 a0005c0005t0002g0157 a0005c0005t0002g0158 |
3 | HG02451.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3322-184G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 22/36 | chr1 | 16954550 | |||||||
| chr1:16955163 | G | A | 1 | a0001c0003t0005g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3466-149G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 23/36 | chr1 | 16955163 | |||||||
| chr1:16955264 | C | CG | 60 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(57): Show |
64 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.3466-41dupG | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 23/36 | INFO_REALIGN_3_PRIME | chr1 | 16955264 | ||||||
| chr1:16955619 | C | G | 1 | a0001c0002t0002g0169 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3704+69C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 24/36 | chr1 | 16955619 | |||||||
| chr1:16955910 | C | T | 1 | a0001c0002t0002g0185 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3705-87C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 24/36 | chr1 | 16955910 | |||||||
| chr1:16955930 | G | A | 54 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(51): Show |
58 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.3705-67G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 24/36 | chr1 | 16955930 | |||||||
| chr1:16955975 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3705-22C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 24/36 | chr1 | 16955975 | |||||||
| chr1:16956223 | T | C | 1 | a0001c0001t0008g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3864+67T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16956223 | |||||||
| chr1:16956580 | C | T | 3 | a0002c0012t0006g0048 a0002c0012t0006g0049 a0002c0012t0006g0050 |
3 | HG02145.hp2 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3864+424C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16956580 | |||||||
| chr1:16956712 | C | T | 1 | a0016c0045t0001g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3864+556C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16956712 | |||||||
| chr1:16956728 | T | TA | 9 | a0003c0004t0002g0041 a0003c0009t0002g0038 a0006c0010t0007g0149 others(6): Show |
9 | HG01106.hp1 HG02280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3864+587dupA | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | INFO_REALIGN_3_PRIME | chr1 | 16956728 | ||||||
| chr1:16956950 | C | G | 3 | a0001c0013t0001g0004 a0002c0018t0001g0037 a0023c0024t0001g0004 |
3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3864+794C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16956950 | |||||||
| chr1:16956998 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3864+842G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16956998 | |||||||
| chr1:16957061 | C | T | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3864+905C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957061 | |||||||
| chr1:16957363 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3864+1207C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957363 | |||||||
| chr1:16957385 | C | T | 3 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0014g0152 |
3 | HG02280.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3865-1198C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957385 | |||||||
| chr1:16957535 | C | T | 1 | a0001c0003t0001g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3865-1048C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957535 | |||||||
| chr1:16957678 | C | T | 1 | a0006c0010t0010g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3865-905C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957678 | |||||||
| chr1:16957733 | C | T | 1 | a0006c0010t0007g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3865-850C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957733 | |||||||
| chr1:16957752 | A | T | 1 | a0003c0004t0002g0136 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3865-831A>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957752 | |||||||
| chr1:16957761 | A | G | 3 | a0001c0013t0001g0004 a0002c0018t0001g0037 a0023c0024t0001g0004 |
3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3865-822A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957761 | |||||||
| chr1:16957846 | C | G | 1 | a0010c0050t0007g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3865-737C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957846 | |||||||
| chr1:16957866 | C | A | 1 | a0001c0002t0003g0191 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3865-717C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957866 | |||||||
| chr1:16957939 | C | T | 54 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(51): Show |
58 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.3865-644C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957939 | |||||||
| chr1:16957956 | T | A | 1 | a0001c0002t0003g0191 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3865-627T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957956 | |||||||
| chr1:16957997 | C | CG | 8 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(5): Show |
8 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3865-586_3865-585i others(3): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957997 | |||||||
| chr1:16957998 | CT | C | 109 | a0001c0001t0001g0024 a0001c0002t0001g0119 a0001c0002t0002g0014 others(106): Show |
120 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.3865-584delT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957998 | |||||||
| chr1:16957999 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(90): Show |
96 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.3865-584T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16957999 | |||||||
| chr1:16958001 | C | G | 2 | a0007c0014t0001g0086 a0007c0014t0005g0088 |
2 | HG00642.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3865-582C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16958001 | |||||||
| chr1:16958003 | T | C | 118 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(115): Show |
129 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.3865-580T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16958003 | |||||||
| chr1:16958443 | G | C | 11 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(8): Show |
11 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3865-140G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16958443 | |||||||
| chr1:16958527 | A | G | 65 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(62): Show |
69 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.3865-56A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 25/36 | chr1 | 16958527 | |||||||
| chr1:16958765 | G | A | 1 | a0001c0002t0002g0165 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.4032+15G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16958765 | |||||||
| chr1:16958803 | C | T | 54 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(51): Show |
58 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.4032+53C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16958803 | |||||||
| chr1:16958944 | G | A | 1 | a0012c0015t0005g0074 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4032+194G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16958944 | |||||||
| chr1:16958969 | A | G | 65 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(62): Show |
69 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.4032+219A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16958969 | |||||||
| chr1:16959091 | C | T | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4032+341C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16959091 | |||||||
| chr1:16959183 | C | T | 1 | a0001c0013t0001g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4032+433C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16959183 | |||||||
| chr1:16959275 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4032+525C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16959275 | |||||||
| chr1:16959514 | T | C | 1 | a0016c0045t0001g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4032+764T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16959514 | |||||||
| chr1:16959536 | G | A | 11 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(8): Show |
11 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.4032+786G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16959536 | |||||||
| chr1:16959673 | C | T | 4 | a0007c0014t0001g0086 a0007c0014t0002g0087 a0007c0014t0005g0088 others(1): Show |
4 | HG00642.hp1 HG02257.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.4032+923C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16959673 | |||||||
| chr1:16959715 | A | G | 65 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(62): Show |
69 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.4032+965A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16959715 | |||||||
| chr1:16959964 | A | G | 8 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(5): Show |
8 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4033-794A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16959964 | |||||||
| chr1:16960008 | T | C | 65 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(62): Show |
69 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.4033-750T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16960008 | |||||||
| chr1:16960009 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0096 a0001c0001t0001g0117 others(1): Show |
5 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.4033-749G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16960009 | |||||||
| chr1:16960032 | C | T | 1 | a0030c0046t0013g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4033-726C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16960032 | |||||||
| chr1:16960265 | C | T | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4033-493C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16960265 | |||||||
| chr1:16960341 | C | T | 65 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(62): Show |
69 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.4033-417C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16960341 | |||||||
| chr1:16960673 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4033-85A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16960673 | |||||||
| chr1:16960741 | T | A | 1 | a0005c0005t0002g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4033-17T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 26/36 | chr1 | 16960741 | |||||||
| chr1:16961143 | C | T | 1 | a0001c0002t0003g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4405+13C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16961143 | |||||||
| chr1:16961144 | C | G | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4405+14C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16961144 | |||||||
| chr1:16961144 | C | T | 55 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(52): Show |
59 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.4405+14C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16961144 | |||||||
| chr1:16961295 | C | A | 1 | a0001c0042t0001g0075 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4405+165C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16961295 | |||||||
| chr1:16961444 | G | T | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4405+314G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16961444 | |||||||
| chr1:16961521 | C | T | 3 | a0004c0008t0001g0007 a0004c0008t0001g0061 a0004c0008t0005g0062 |
4 | HG02135.hp2 NA18947.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.4405+391C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16961521 | |||||||
| chr1:16961595 | TG | T | 3 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 |
3 | HG00099.hp2 NA20129.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4405+469delG | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16961595 | ||||||
| chr1:16961644 | C | T | 2 | a0001c0002t0002g0172 a0001c0002t0002g0187 |
2 | NA18952.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.4405+514C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16961644 | |||||||
| chr1:16961704 | T | C | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4405+574T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16961704 | |||||||
| chr1:16961812 | A | G | 8 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(5): Show |
8 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4405+682A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16961812 | |||||||
| chr1:16961894 | T | C | 8 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(5): Show |
8 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4405+764T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16961894 | |||||||
| chr1:16962069 | TTG | T | 15 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(12): Show |
15 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.4405+941_4405+942d others(4): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16962069 | ||||||
| chr1:16962070 | TG | T | 3 | a0001c0002t0002g0177 a0001c0002t0003g0209 a0020c0029t0002g0019 |
3 | HG02451.hp1 HG02886.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.4405+941delG | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962070 | |||||||
| chr1:16962071 | G | T | 55 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(52): Show |
59 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.4405+941G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962071 | |||||||
| chr1:16962126 | G | C | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4405+996G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962126 | |||||||
| chr1:16962221 | C | T | 1 | a0001c0002t0003g0192 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4405+1091C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962221 | |||||||
| chr1:16962309 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4405+1179G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962309 | |||||||
| chr1:16962346 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4405+1216C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962346 | |||||||
| chr1:16962534 | CA | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0093 a0001c0001t0001g0117 others(3): Show |
6 | HG00099.hp1 HG01943.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.4405+1431delA | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16962534 | ||||||
| chr1:16962551 | A | AAC | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4405+1422_4405+142 others(6): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16962551 | ||||||
| chr1:16962556 | A | AAC | 9 | a0001c0002t0002g0170 a0001c0002t0002g0175 a0001c0002t0002g0190 others(6): Show |
9 | HG00544.hp1 HG01517.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.4405+1427_4405+142 others(6): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16962556 | ||||||
| chr1:16962556 | A | AC | 62 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0111 others(59): Show |
66 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.4405+1426_4405+142 others(5): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962556 | |||||||
| chr1:16962556 | A | C | 138 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(135): Show |
148 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.4405+1426A>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962556 | |||||||
| chr1:16962558 | A | G | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4405+1428A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962558 | |||||||
| chr1:16962560 | A | G | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4405+1430A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962560 | |||||||
| chr1:16962627 | G | C | 1 | a0005c0005t0002g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4405+1497G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962627 | |||||||
| chr1:16962706 | G | A | 1 | a0032c0032t0001g0140 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4405+1576G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962706 | |||||||
| chr1:16962708 | A | G | 2 | a0015c0047t0002g0159 a0033c0048t0007g0020 |
2 | HG01106.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4405+1578A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962708 | |||||||
| chr1:16962954 | G | T | 1 | a0001c0002t0003g0191 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4405+1824G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16962954 | |||||||
| chr1:16963037 | G | A | 4 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0014g0152 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4405+1907G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963037 | |||||||
| chr1:16963112 | G | A | 1 | a0004c0008t0005g0062 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.4405+1982G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963112 | |||||||
| chr1:16963185 | G | GA | 10 | a0001c0001t0001g0091 a0001c0001t0001g0107 a0001c0001t0008g0026 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.4405+2075dupA | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16963185 | ||||||
| chr1:16963185 | GA | G | 61 | a0001c0001t0001g0120 a0001c0002t0001g0119 a0001c0002t0002g0014 others(58): Show |
64 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.4405+2075delA | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16963185 | ||||||
| chr1:16963208 | G | T | 1 | a0001c0002t0003g0191 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4405+2078G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963208 | |||||||
| chr1:16963263 | C | A | 2 | a0005c0005t0002g0156 a0005c0005t0002g0158 |
2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.4405+2133C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963263 | |||||||
| chr1:16963416 | C | T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(55): Show |
60 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.4405+2286C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963416 | |||||||
| chr1:16963417 | G | A | 12 | a0001c0002t0002g0170 a0001c0002t0002g0171 a0001c0002t0002g0172 others(9): Show |
12 | HG02074.hp1 HG02155.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.4405+2287G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963417 | |||||||
| chr1:16963563 | A | G | 205 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(202): Show |
218 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(215): Show |
intron_variant | MODIFIER | c.4406-2160A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963563 | |||||||
| chr1:16963570 | C | T | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4406-2153C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963570 | |||||||
| chr1:16963595 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4406-2128G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963595 | |||||||
| chr1:16963619 | G | A | 1 | a0005c0005t0002g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4406-2104G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963619 | |||||||
| chr1:16963798 | G | GT | 6 | a0001c0002t0002g0182 a0001c0002t0003g0166 a0001c0002t0003g0207 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.4406-1920dupT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16963798 | ||||||
| chr1:16963803 | TG | T | 12 | a0001c0002t0003g0209 a0005c0005t0002g0016 a0005c0005t0002g0018 others(9): Show |
12 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.4406-1919delG | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963803 | |||||||
| chr1:16963804 | G | T | 59 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(56): Show |
62 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.4406-1919G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963804 | |||||||
| chr1:16963857 | G | A | 1 | a0001c0003t0001g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4406-1866G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963857 | |||||||
| chr1:16963858 | C | T | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4406-1865C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963858 | |||||||
| chr1:16963865 | G | A | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4406-1858G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963865 | |||||||
| chr1:16963899 | G | T | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4406-1824G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963899 | |||||||
| chr1:16963998 | ATGTT | A | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4406-1724_4406-172 others(8): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16963998 | |||||||
| chr1:16964058 | A | G | 1 | a0001c0003t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4406-1665A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964058 | |||||||
| chr1:16964111 | TTTTTC | T | 55 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0006 others(52): Show |
62 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.4406-1597_4406-159 others(9): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16964111 | ||||||
| chr1:16964137 | A | ATT | 44 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0163 others(41): Show |
47 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.4406-1572_4406-157 others(6): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16964137 | ||||||
| chr1:16964137 | AT | A | 7 | a0001c0001t0001g0117 a0001c0001t0001g0124 a0001c0001t0008g0026 others(4): Show |
7 | HG01943.hp1 HG02145.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.4406-1571delT | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16964137 | ||||||
| chr1:16964139 | T | TA | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4406-1584_4406-158 others(5): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964139 | |||||||
| chr1:16964140 | T | TA | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4406-1583_4406-158 others(5): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964140 | |||||||
| chr1:16964141 | T | A | 1 | a0001c0013t0001g0106 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4406-1582T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964141 | |||||||
| chr1:16964282 | AC | A | 2 | a0003c0009t0002g0044 a0003c0009t0002g0045 |
2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4406-1440delC | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964282 | |||||||
| chr1:16964284 | T | A | 2 | a0003c0009t0002g0044 a0003c0009t0002g0045 |
2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4406-1439T>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964284 | |||||||
| chr1:16964318 | CTCTTT | C | 53 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(50): Show |
56 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.4406-1387_4406-138 others(9): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | INFO_REALIGN_3_PRIME | chr1 | 16964318 | ||||||
| chr1:16964519 | G | C | 8 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4406-1204G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964519 | |||||||
| chr1:16964573 | C | T | 1 | a0017c0034t0002g0155 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4406-1150C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964573 | |||||||
| chr1:16964604 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4406-1119C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964604 | |||||||
| chr1:16964605 | G | A | 3 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 |
3 | HG01258.hp2 HG02004.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4406-1118G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964605 | |||||||
| chr1:16964634 | C | G | 53 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(50): Show |
56 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.4406-1089C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964634 | |||||||
| chr1:16964706 | C | T | 5 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG01943.hp2 HG02132.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.4406-1017C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964706 | |||||||
| chr1:16964741 | C | T | 5 | a0001c0002t0002g0184 a0001c0002t0002g0202 a0001c0002t0002g0203 others(2): Show |
5 | HG00544.hp1 HG02015.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.4406-982C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964741 | |||||||
| chr1:16964808 | G | A | 1 | a0003c0004t0002g0135 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4406-915G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964808 | |||||||
| chr1:16964875 | G | A | 6 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.4406-848G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964875 | |||||||
| chr1:16964970 | C | T | 1 | a0002c0018t0006g0031 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.4406-753C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16964970 | |||||||
| chr1:16965108 | C | T | 10 | a0001c0001t0001g0052 a0001c0001t0001g0114 a0001c0001t0001g0123 others(7): Show |
10 | HG00558.hp1 HG01928.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.4406-615C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16965108 | |||||||
| chr1:16965259 | A | G | 7 | a0005c0005t0002g0016 a0005c0005t0002g0018 a0005c0005t0002g0156 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.4406-464A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16965259 | |||||||
| chr1:16965366 | G | C | 208 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(205): Show |
222 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(219): Show |
intron_variant | MODIFIER | c.4406-357G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16965366 | |||||||
| chr1:16965702 | C | T | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4406-21C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 27/36 | chr1 | 16965702 | |||||||
| chr1:16965909 | A | G | 19 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(16): Show |
21 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.4575+17A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 28/36 | chr1 | 16965909 | |||||||
| chr1:16966182 | C | T | 1 | a0020c0029t0002g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4696+63C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 29/36 | chr1 | 16966182 | |||||||
| chr1:16966228 | G | A | 5 | a0005c0005t0002g0157 a0008c0011t0004g0002 a0008c0011t0004g0042 others(2): Show |
6 | HG02257.hp2 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.4696+109G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 29/36 | chr1 | 16966228 | |||||||
| chr1:16966290 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0098 |
2 | NA19056.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.4697-118G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 29/36 | chr1 | 16966290 | |||||||
| chr1:16966375 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0001t0001g0103 |
3 | HG00642.hp2 HG01168.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4697-33G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 29/36 | chr1 | 16966375 | |||||||
| chr1:16966599 | C | T | 3 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 |
3 | HG02970.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4860+28C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16966599 | |||||||
| chr1:16966889 | G | A | 2 | a0001c0003t0001g0032 a0001c0003t0001g0033 |
2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.4860+318G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16966889 | |||||||
| chr1:16967059 | GA | G | 124 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(121): Show |
133 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.4860+498delA | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr1 | 16967059 | ||||||
| chr1:16967165 | G | C | 155 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(152): Show |
167 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.4860+594G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16967165 | |||||||
| chr1:16967188 | T | C | 4 | a0013c0020t0004g0211 a0013c0020t0004g0212 a0022c0044t0003g0210 others(1): Show |
4 | HG02970.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4860+617T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16967188 | |||||||
| chr1:16967321 | TG | T | 4 | a0006c0010t0007g0149 a0006c0010t0007g0151 a0006c0010t0010g0150 others(1): Show |
4 | HG02280.hp1 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4860+752delG | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr1 | 16967321 | ||||||
| chr1:16967358 | C | T | 12 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(9): Show |
15 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.4860+787C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16967358 | |||||||
| chr1:16967394 | C | T | 1 | a0024c0035t0015g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4861-809C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16967394 | |||||||
| chr1:16967397 | G | A | 44 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(41): Show |
46 | HG00544.hp1 HG01074.hp1 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.4861-806G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16967397 | |||||||
| chr1:16967527 | G | C | 11 | a0001c0013t0001g0004 a0006c0010t0007g0149 a0006c0010t0007g0151 others(8): Show |
11 | HG01106.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.4861-676G>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16967527 | |||||||
| chr1:16967669 | T | C | 1 | a0030c0046t0013g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4861-534T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16967669 | |||||||
| chr1:16967763 | C | G | 1 | a0001c0002t0003g0166 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4861-440C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16967763 | |||||||
| chr1:16967970 | A | G | 6 | a0001c0003t0001g0080 a0001c0003t0001g0144 a0001c0003t0005g0053 others(3): Show |
6 | HG02129.hp1 HG02738.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.4861-233A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16967970 | |||||||
| chr1:16968004 | G | A | 1 | a0001c0003t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4861-199G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16968004 | |||||||
| chr1:16968040 | G | A | 1 | a0033c0048t0007g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4861-163G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16968040 | |||||||
| chr1:16968159 | G | A | 4 | a0002c0012t0006g0048 a0002c0012t0006g0049 a0002c0012t0006g0050 others(1): Show |
4 | HG01071.hp1 HG02145.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4861-44G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16968159 | |||||||
| chr1:16968190 | A | G | 31 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(28): Show |
34 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.4861-13A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 30/36 | chr1 | 16968190 | |||||||
| chr1:16968651 | T | C | 1 | a0024c0035t0015g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5076+233T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 31/36 | chr1 | 16968651 | |||||||
| chr1:16968752 | G | A | 1 | a0005c0005t0002g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5076+334G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 31/36 | chr1 | 16968752 | |||||||
| chr1:16968912 | T | C | 2 | a0003c0004t0001g0051 a0003c0004t0002g0041 |
2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.5077-204T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 31/36 | chr1 | 16968912 | |||||||
| chr1:16969453 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.5301+113C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 32/36 | chr1 | 16969453 | |||||||
| chr1:16969700 | C | T | 1 | a0001c0003t0005g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.5302-85C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 32/36 | chr1 | 16969700 | |||||||
| chr1:16970227 | C | T | 14 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(11): Show |
17 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.5452-26C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 33/36 | chr1 | 16970227 | |||||||
| chr1:16970501 | G | A | 1 | a0001c0002t0002g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5652+48G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 34/36 | chr1 | 16970501 | |||||||
| chr1:16970522 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5652+69C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 34/36 | chr1 | 16970522 | |||||||
| chr1:16970567 | G | T | 2 | a0001c0013t0001g0004 a0023c0024t0001g0004 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5653-69G>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 34/36 | chr1 | 16970567 | |||||||
| chr1:16970623 | C | G | 7 | a0002c0006t0004g0179 a0002c0012t0006g0048 a0002c0012t0006g0049 others(4): Show |
7 | HG01071.hp1 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.5653-13C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 34/36 | chr1 | 16970623 | |||||||
| chr1:16970794 | C | T | 119 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(116): Show |
128 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.5784+27C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | chr1 | 16970794 | |||||||
| chr1:16971088 | T | C | 33 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(30): Show |
36 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.5784+321T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | chr1 | 16971088 | |||||||
| chr1:16971092 | T | C | 41 | a0001c0002t0001g0119 a0001c0002t0002g0014 a0001c0002t0002g0161 others(38): Show |
42 | HG00544.hp1 HG01243.hp1 HG01358.hp2 others(39): Show |
intron_variant | MODIFIER | c.5784+325T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | chr1 | 16971092 | |||||||
| chr1:16971210 | A | AGT | 39 | a0001c0002t0002g0014 a0001c0002t0002g0161 a0001c0002t0002g0164 others(36): Show |
41 | HG00544.hp1 HG01074.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.5785-214_5785-213d others(4): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | INFO_REALIGN_3_PRIME | chr1 | 16971210 | ||||||
| chr1:16971210 | A | AGTGT | 6 | a0001c0002t0002g0163 a0001c0002t0002g0175 a0001c0002t0002g0193 others(3): Show |
6 | HG01517.hp2 HG02155.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.5785-216_5785-213d others(6): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | INFO_REALIGN_3_PRIME | chr1 | 16971210 | ||||||
| chr1:16971210 | A | AGTGTGT | 4 | a0001c0002t0002g0172 a0001c0002t0002g0176 a0001c0002t0002g0187 others(1): Show |
4 | HG01515.hp2 NA18952.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.5785-218_5785-213d others(8): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | INFO_REALIGN_3_PRIME | chr1 | 16971210 | ||||||
| chr1:16971210 | AGT | A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0096 a0001c0001t0001g0101 others(9): Show |
12 | HG00642.hp2 HG01069.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.5785-214_5785-213d others(4): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | INFO_REALIGN_3_PRIME | chr1 | 16971210 | ||||||
| chr1:16971210 | AGTGT | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(46): Show |
51 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.5785-216_5785-213d others(6): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | INFO_REALIGN_3_PRIME | chr1 | 16971210 | ||||||
| chr1:16971210 | AGTGTGT | A | 30 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0100 others(27): Show |
33 | HG00558.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.5785-218_5785-213d others(8): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | INFO_REALIGN_3_PRIME | chr1 | 16971210 | ||||||
| chr1:16971210 | AGTGTGTG others(1): Show |
A | 64 | a0001c0001t0017g0121 a0001c0003t0001g0001 a0001c0003t0001g0003 others(61): Show |
71 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.5785-220_5785-213d others(10): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | INFO_REALIGN_3_PRIME | chr1 | 16971210 | ||||||
| chr1:16971210 | AGTGTGTG others(3): Show |
A | 3 | a0005c0005t0003g0017 a0011c0016t0002g0039 a0020c0029t0002g0019 |
3 | HG02886.hp1 HG04184.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5785-222_5785-213d others(12): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | INFO_REALIGN_3_PRIME | chr1 | 16971210 | ||||||
| chr1:16971210 | AGTGTGTG others(5): Show |
A | 1 | a0030c0046t0013g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5785-224_5785-213d others(14): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | INFO_REALIGN_3_PRIME | chr1 | 16971210 | ||||||
| chr1:16971210 | AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0001g0142 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5785-228_5785-213d others(18): Show |
CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | INFO_REALIGN_3_PRIME | chr1 | 16971210 | ||||||
| chr1:16971359 | C | A | 1 | a0001c0002t0003g0167 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5785-106C>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | chr1 | 16971359 | |||||||
| chr1:16971440 | C | T | 1 | a0010c0040t0010g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5785-25C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 35/36 | chr1 | 16971440 | |||||||
| chr1:16971726 | T | C | 1 | a0022c0044t0003g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5967+79T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16971726 | |||||||
| chr1:16971752 | C | T | 4 | a0002c0012t0006g0048 a0002c0012t0006g0049 a0002c0012t0006g0050 others(1): Show |
4 | HG01071.hp1 HG02145.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.5967+105C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16971752 | |||||||
| chr1:16971759 | G | A | 24 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(21): Show |
27 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.5967+112G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16971759 | |||||||
| chr1:16971859 | C | G | 1 | a0007c0014t0002g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5967+212C>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16971859 | |||||||
| chr1:16971887 | C | T | 1 | a0003c0004t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5967+240C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16971887 | |||||||
| chr1:16971891 | G | A | 1 | a0001c0003t0001g0134 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.5967+244G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16971891 | |||||||
| chr1:16972001 | A | G | 81 | a0001c0001t0017g0121 a0001c0003t0001g0001 a0001c0003t0001g0003 others(78): Show |
91 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.5967+354A>G | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16972001 | |||||||
| chr1:16972075 | G | A | 26 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(23): Show |
29 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.5968-285G>A | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16972075 | |||||||
| chr1:16972115 | C | T | 2 | a0001c0037t0002g0195 a0003c0004t0002g0136 |
2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.5968-245C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16972115 | |||||||
| chr1:16972185 | C | T | 17 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(14): Show |
20 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.5968-175C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16972185 | |||||||
| chr1:16972231 | C | T | 16 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(13): Show |
19 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.5968-129C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16972231 | |||||||
| chr1:16972256 | T | C | 24 | a0002c0006t0004g0011 a0002c0006t0004g0012 a0002c0006t0004g0160 others(21): Show |
27 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.5968-104T>C | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16972256 | |||||||
| chr1:16972284 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5968-76C>T | CROCC | ENSG00000058453.17 | transcript | ENST00000375541.10 | protein_coding | 36/36 | chr1 | 16972284 |