Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54677 |
| ensemblid | ENSG00000005469.12 |
| hgncid | 2366 |
| symbol | CROT |
| name | carnitine O-octanoyltransferase |
| refseq_nuc | NM_021151.4 |
| refseq_prot | NP_066974.2 |
| ensembl_nuc | ENST00000331536.8 |
| ensembl_prot | ENSP00000331981.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 87345664 |
| end | 87399794 |
| strand | + |
| ver | v1.2 |
| region | chr7:87345664-87399794 |
| region5000 | chr7:87340664-87404794 |
| regionname0 | CROT_chr7_87345664_87399794 |
| regionname5000 | CROT_chr7_87340664_87404794 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 612 | 251 | 77 | 41 | 106 | 9 | 16 | 77 | CROT_chr7_87340664_87404794 | CROT | MENQL others(607): Show |
chr7 | 87340664 | 87404794 |
| a0002 | 0/0 | 612 | 22 | 10 | 2 | 0 | 2 | 8 | 0 | CROT_chr7_87340664_87404794 | CROT | MENQL others(607): Show |
chr7 | 87340664 | 87404794 |
| a0003 | 0/0 | 612 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | MENQL others(607): Show |
chr7 | 87340664 | 87404794 |
| a0004 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | MENQL others(607): Show |
chr7 | 87340664 | 87404794 |
| a0005 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | MENQL others(607): Show |
chr7 | 87340664 | 87404794 |
| a0006 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | MENQL others(607): Show |
chr7 | 87340664 | 87404794 |
| a0007 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | MENQL others(607): Show |
chr7 | 87340664 | 87404794 |
| a0008 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | MENQL others(607): Show |
chr7 | 87340664 | 87404794 |
| a0009 | 0/0 | 612 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | MENQL others(607): Show |
chr7 | 87340664 | 87404794 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1836 | 251 | 77 | 41 | 106 | 9 | 16 | CROT_chr7_87340664_87404794 | CROT | ATGGA others(1831): Show |
chr7 | 87340664 | 87404794 | ||
| a0002c0002 | 0/0 | 1836 | 22 | 10 | 2 | 0 | 2 | 8 | CROT_chr7_87340664_87404794 | CROT | ATGGA others(1831): Show |
chr7 | 87340664 | 87404794 | ||
| a0003c0003 | 0/0 | 1836 | 3 | 0 | 3 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | ATGGA others(1831): Show |
chr7 | 87340664 | 87404794 | ||
| a0004c0005 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | ATGGA others(1831): Show |
chr7 | 87340664 | 87404794 | ||
| a0005c0008 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | ATGGA others(1831): Show |
chr7 | 87340664 | 87404794 | ||
| a0006c0004 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | ATGGA others(1831): Show |
chr7 | 87340664 | 87404794 | ||
| a0007c0007 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | ATGGA others(1831): Show |
chr7 | 87340664 | 87404794 | ||
| a0008c0009 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | ATGGA others(1831): Show |
chr7 | 87340664 | 87404794 | ||
| a0009c0006 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | ATGGA others(1831): Show |
chr7 | 87340664 | 87404794 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3205 | 220 | 58 | 40 | 95 | 9 | 16 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0001c0001t0003 | 0/0 | 3214 | 16 | 15 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3209): Show |
chr7 | 87340664 | 87404794 |
| a0001c0001t0004 | 0/0 | 3205 | 5 | 0 | 0 | 5 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0001c0001t0005 | 0/0 | 3205 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0001c0001t0006 | 0/0 | 3205 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0001c0001t0007 | 0/0 | 3205 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0001c0001t0008 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0001c0001t0009 | 0/0 | 3205 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0001c0001t0010 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3209): Show |
chr7 | 87340664 | 87404794 |
| a0002c0002t0001 | 0/0 | 3205 | 7 | 7 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0002c0002t0002 | 0/0 | 3205 | 15 | 3 | 2 | 0 | 2 | 8 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0003c0003t0002 | 0/0 | 3205 | 3 | 0 | 3 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0004c0005t0001 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0005c0008t0001 | 0/0 | 3205 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0006c0004t0001 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0007c0007t0001 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0008c0009t0001 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| a0009c0006t0001 | 0/0 | 3205 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | AGTCC others(3200): Show |
chr7 | 87340664 | 87404794 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 2 | 9 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0009 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0003g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0004g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0006g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0007g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0008g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0001c0001t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0002g0003 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0003c0003t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0004c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0005c0008t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0006c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0007c0007t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0008c0009t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| a0009c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0022 | EUR | GBR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0073 | EUR | FIN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00423 | hp1 | a0001 | c0001 | t0008 | g0024 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00544 | hp2 | a0004 | c0005 | t0001 | g0002 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0070 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01943 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02004 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0200 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02148 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CDX | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0210 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0208 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0166 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0201 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02818 | hp2 | a0005 | c0008 | t0001 | g0156 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0069 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0181 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0036 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0071 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0022 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0072 | SAS | STU | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0167 | SAS | STU | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18969 | hp1 | a0006 | c0004 | t0001 | g0161 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18984 | hp1 | a0007 | c0007 | t0001 | g0002 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19005 | hp1 | a0008 | c0009 | t0001 | g0211 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0198 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ASW | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA20752 | hp2 | a0009 | c0006 | t0001 | g0084 | EUR | TSI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | USA | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | USA | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | USA | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0078 | REF | REF | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0009 | REF | REF | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87349142 | T | C | 1 | a0003 | 3 | HG01943.hp1 HG02004.hp1 HG02148.hp1 |
missense_variant | MODERATE | c.74T>C | p.Val25Ala | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/18 | 290/3205 | 74/1839 | 25/612 | chr7 | 87349142 | |||
| chr7:87361430 | G | A | 1 | a0006 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.281G>A | p.Arg94His | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 5/18 | 497/3205 | 281/1839 | 94/612 | chr7 | 87361430 | |||
| chr7:87361507 | A | G | 1 | a0008 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.358A>G | p.Thr120Ala | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 5/18 | 574/3205 | 358/1839 | 120/612 | chr7 | 87361507 | |||
| chr7:87391707 | G | C | 2 | a0002 a0003 |
25 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(22): Show |
missense_variant | MODERATE | c.1420G>C | p.Val474Leu | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/18 | 1636/3205 | 1420/1839 | 474/612 | chr7 | 87391707 | |||
| chr7:87392810 | C | G | 1 | a0005 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1585C>G | p.Leu529Val | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 16/18 | 1801/3205 | 1585/1839 | 529/612 | chr7 | 87392810 | |||
| chr7:87392948 | C | A | 1 | a0004 | 1 | HG00544.hp2 | missense_variant&splice_region_variant | MODERATE | c.1599C>A | p.Ser533Arg | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/18 | 1815/3205 | 1599/1839 | 533/612 | chr7 | 87392948 | |||
| chr7:87392992 | A | G | 1 | a0007 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.1643A>G | p.Tyr548Cys | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/18 | 1859/3205 | 1643/1839 | 548/612 | chr7 | 87392992 | |||
| chr7:87393031 | A | G | 1 | a0009 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1682A>G | p.Asn561Ser | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/18 | 1898/3205 | 1682/1839 | 561/612 | chr7 | 87393031 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87345679 | C | T | 1 | a0001c0001t0004 | 5 | HG02080.hp2 NA18942.hp2 NA18966.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-201C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/18 | 3390 | chr7 | 87345679 | ||||||
| chr7:87345694 | G | C | 1 | a0001c0001t0005 | 3 | HG02040.hp1 NA19011.hp1 NA19065.hp2 |
5_prime_UTR_variant | MODIFIER | c.-186G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/18 | 3375 | chr7 | 87345694 | ||||||
| chr7:87345709 | G | T | 2 | a0001c0001t0003 a0001c0001t0010 |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-171G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/18 | 3360 | chr7 | 87345709 | ||||||
| chr7:87345714 | T | C | 1 | a0001c0001t0006 | 2 | HG00423.hp2 NA18990.hp2 |
5_prime_UTR_variant | MODIFIER | c.-166T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/18 | 3355 | chr7 | 87345714 | ||||||
| chr7:87345727 | T | TGCGGCAG others(2): Show |
2 | a0001c0001t0003 a0001c0001t0010 |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-147_-139dupAGAGGC others(3): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/18 | 3327 | INFO_REALIGN_3_PRIME | chr7 | 87345727 | |||||
| chr7:87398843 | C | T | 2 | a0002c0002t0002 a0003c0003t0002 |
18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*199C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 18/18 | 199 | chr7 | 87398843 | ||||||
| chr7:87399104 | C | A | 1 | a0001c0001t0008 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*460C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 18/18 | 460 | chr7 | 87399104 | ||||||
| chr7:87399342 | G | A | 1 | a0001c0001t0007 | 2 | HG02109.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*698G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 18/18 | 698 | chr7 | 87399342 | ||||||
| chr7:87399521 | A | T | 1 | a0001c0001t0010 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*877A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 18/18 | 877 | chr7 | 87399521 | ||||||
| chr7:87399710 | T | A | 1 | a0001c0001t0009 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1066T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 18/18 | 1066 | chr7 | 87399710 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:87345827 | T | TTAAGTCG others(13): Show |
12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113+75_-113+76ins others(20): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 87345827 | ||||||
| chr7:87345916 | T | C | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113+149T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87345916 | |||||||
| chr7:87345920 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
7 | HG02109.hp1 HG02145.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+153G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87345920 | |||||||
| chr7:87345950 | G | A | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113+183G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87345950 | |||||||
| chr7:87346030 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-113+263G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346030 | |||||||
| chr7:87346031 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-113+264C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346031 | |||||||
| chr7:87346107 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-112-233C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346107 | |||||||
| chr7:87346120 | T | C | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-112-220T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346120 | |||||||
| chr7:87346198 | CGT | C | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-112-137_-112-136d others(4): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 87346198 | ||||||
| chr7:87346245 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-112-95C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346245 | |||||||
| chr7:87346248 | C | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-112-92C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346248 | |||||||
| chr7:87346252 | T | A | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-112-88T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346252 | |||||||
| chr7:87346730 | A | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+300A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87346730 | |||||||
| chr7:87346900 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
7 | HG02109.hp1 HG02145.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+470C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87346900 | |||||||
| chr7:87347145 | G | A | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+715G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87347145 | |||||||
| chr7:87347276 | A | G | 7 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0037 others(4): Show |
12 | HG01243.hp1 HG02257.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-22+846A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87347276 | |||||||
| chr7:87347281 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22+851G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87347281 | |||||||
| chr7:87347494 | C | T | 1 | a0008c0009t0001g0211 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-22+1064C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87347494 | |||||||
| chr7:87347615 | A | G | 1 | a0002c0002t0002g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-22+1185A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87347615 | |||||||
| chr7:87347697 | G | GT | 11 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
15 | HG01496.hp1 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-22+1278dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 87347697 | ||||||
| chr7:87348065 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-21-983T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348065 | |||||||
| chr7:87348067 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-21-981T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348067 | |||||||
| chr7:87348109 | A | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-939A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348109 | |||||||
| chr7:87348149 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-21-899C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348149 | |||||||
| chr7:87348179 | C | T | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-869C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348179 | |||||||
| chr7:87348222 | T | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0046 others(4): Show |
18 | HG01358.hp1 HG01496.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.-21-826T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348222 | |||||||
| chr7:87348252 | C | T | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-796C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348252 | |||||||
| chr7:87348270 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-21-778A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348270 | |||||||
| chr7:87348332 | A | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-716A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348332 | |||||||
| chr7:87348386 | G | C | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-662G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348386 | |||||||
| chr7:87348393 | G | A | 13 | a0001c0001t0001g0044 a0001c0001t0003g0006 a0001c0001t0003g0010 others(10): Show |
18 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21-655G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348393 | |||||||
| chr7:87348435 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-21-613A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348435 | |||||||
| chr7:87348526 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-21-522T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348526 | |||||||
| chr7:87348531 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-21-517T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348531 | |||||||
| chr7:87348571 | G | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-21-477G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348571 | |||||||
| chr7:87348578 | T | C | 25 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0041 others(22): Show |
33 | HG00323.hp2 HG00639.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.-21-470T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348578 | |||||||
| chr7:87348602 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-21-446T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348602 | |||||||
| chr7:87348698 | T | A | 1 | a0001c0001t0001g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-21-350T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348698 | |||||||
| chr7:87348928 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-21-120A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348928 | |||||||
| chr7:87348931 | A | G | 1 | a0001c0001t0009g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-21-117A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348931 | |||||||
| chr7:87348945 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-21-103C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348945 | |||||||
| chr7:87349031 | C | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-21-17C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87349031 | |||||||
| chr7:87349238 | T | C | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+55T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349238 | |||||||
| chr7:87349319 | C | T | 1 | a0001c0001t0009g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.115+136C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349319 | |||||||
| chr7:87349413 | T | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+230T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349413 | |||||||
| chr7:87349462 | C | T | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+279C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349462 | |||||||
| chr7:87349523 | A | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+340A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349523 | |||||||
| chr7:87349526 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115+343C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349526 | |||||||
| chr7:87349545 | G | GAATACAT others(2): Show |
3 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 |
3 | HG02040.hp1 NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.115+365_115+373dup others(9): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87349545 | ||||||
| chr7:87349613 | C | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0062 others(5): Show |
10 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.115+430C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349613 | |||||||
| chr7:87349618 | T | C | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+435T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349618 | |||||||
| chr7:87349639 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.115+456T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349639 | |||||||
| chr7:87349773 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0068 |
3 | NA18948.hp2 NA18974.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.115+590T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349773 | |||||||
| chr7:87349796 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
7 | HG02109.hp1 HG02145.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+613T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349796 | |||||||
| chr7:87350007 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115+824A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350007 | |||||||
| chr7:87350026 | A | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(9): Show |
17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+843A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350026 | |||||||
| chr7:87350146 | G | C | 1 | a0001c0001t0001g0018 | 2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.115+963G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350146 | |||||||
| chr7:87350148 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115+965T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350148 | |||||||
| chr7:87350203 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
150 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.115+1020A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350203 | |||||||
| chr7:87350388 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.115+1205G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350388 | |||||||
| chr7:87350544 | G | A | 11 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0031 others(8): Show |
16 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.115+1361G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350544 | |||||||
| chr7:87350736 | G | C | 1 | a0001c0001t0009g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.115+1553G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350736 | |||||||
| chr7:87350881 | C | T | 4 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0034 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+1698C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350881 | |||||||
| chr7:87350935 | T | A | 2 | a0001c0001t0004g0012 a0001c0001t0004g0076 |
4 | HG02080.hp2 NA18942.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+1752T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350935 | |||||||
| chr7:87350992 | T | C | 1 | a0001c0001t0001g0013 | 3 | NA18963.hp1 NA18974.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.115+1809T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350992 | |||||||
| chr7:87351022 | A | AG | 17 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0042 others(14): Show |
24 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.115+1839_115+1840i others(3): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351022 | |||||||
| chr7:87351034 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+1851T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351034 | |||||||
| chr7:87351080 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+1897A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351080 | |||||||
| chr7:87351113 | C | A | 1 | a0001c0001t0001g0152 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.115+1930C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351113 | |||||||
| chr7:87351136 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115+1953G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351136 | |||||||
| chr7:87351183 | C | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2000C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351183 | |||||||
| chr7:87351186 | G | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2003G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351186 | |||||||
| chr7:87351308 | CA | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
148 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.115+2149delA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87351308 | ||||||
| chr7:87351308 | CAA | C | 25 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
36 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.115+2148_115+2149d others(4): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87351308 | ||||||
| chr7:87351324 | A | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG00741.hp1 HG01109.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.115+2141A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351324 | |||||||
| chr7:87351327 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA18962.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.115+2144A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351327 | |||||||
| chr7:87351339 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2156G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351339 | |||||||
| chr7:87351513 | A | ATTAGCTC others(336): Show |
1 | a0001c0001t0001g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.115+2344_115+2345i others(345): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87351513 | ||||||
| chr7:87351513 | A | ATTAGCTC others(337): Show |
1 | a0001c0001t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115+2344_115+2345i others(346): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87351513 | ||||||
| chr7:87351513 | A | ATTAGCTC others(341): Show |
1 | a0001c0001t0007g0016 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.115+2344_115+2345i others(350): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87351513 | ||||||
| chr7:87351699 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2516G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351699 | |||||||
| chr7:87351940 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2757A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351940 | |||||||
| chr7:87352092 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.115+2909T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352092 | |||||||
| chr7:87352207 | T | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
150 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.115+3024T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352207 | |||||||
| chr7:87352485 | G | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.115+3302G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352485 | |||||||
| chr7:87352487 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3304C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352487 | |||||||
| chr7:87352488 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.115+3305G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352488 | |||||||
| chr7:87352684 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3501A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352684 | |||||||
| chr7:87352708 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3525A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352708 | |||||||
| chr7:87352753 | C | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3570C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352753 | |||||||
| chr7:87352799 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3616C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352799 | |||||||
| chr7:87352875 | A | G | 15 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0051 others(12): Show |
23 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.115+3692A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352875 | |||||||
| chr7:87353007 | A | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.115+3824A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353007 | |||||||
| chr7:87353117 | G | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0051 others(12): Show |
23 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.115+3934G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353117 | |||||||
| chr7:87353133 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+3950G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353133 | |||||||
| chr7:87353149 | A | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG01167.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.115+3966A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353149 | |||||||
| chr7:87353155 | C | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.115+3972C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353155 | |||||||
| chr7:87353172 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.115+3989T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353172 | |||||||
| chr7:87353173 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.115+3990G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353173 | |||||||
| chr7:87353348 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.115+4165C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353348 | |||||||
| chr7:87353391 | C | T | 1 | a0009c0006t0001g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.115+4208C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353391 | |||||||
| chr7:87353406 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+4223C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353406 | |||||||
| chr7:87353541 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.115+4358G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353541 | |||||||
| chr7:87353549 | A | G | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
8 | HG01496.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+4366A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353549 | |||||||
| chr7:87353621 | G | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.115+4438G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353621 | |||||||
| chr7:87353768 | G | GA | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+4587dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87353768 | ||||||
| chr7:87353790 | G | A | 1 | a0001c0001t0009g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.115+4607G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353790 | |||||||
| chr7:87353800 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+4617G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353800 | |||||||
| chr7:87353949 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+4766G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353949 | |||||||
| chr7:87354012 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0060 |
4 | HG00323.hp2 HG01175.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+4829C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354012 | |||||||
| chr7:87354232 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.116-4974G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354232 | |||||||
| chr7:87354250 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4956T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354250 | |||||||
| chr7:87354258 | G | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4948G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354258 | |||||||
| chr7:87354336 | G | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4870G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354336 | |||||||
| chr7:87354399 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.116-4807A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354399 | |||||||
| chr7:87354434 | T | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4772T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354434 | |||||||
| chr7:87354703 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4503C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354703 | |||||||
| chr7:87354767 | A | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0194 |
2 | NA18942.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.116-4439A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354767 | |||||||
| chr7:87354769 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.116-4437T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354769 | |||||||
| chr7:87354951 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4255T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354951 | |||||||
| chr7:87354952 | C | G | 10 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(7): Show |
11 | HG00423.hp2 HG02040.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.116-4254C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354952 | |||||||
| chr7:87355103 | A | AT | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0152 others(2): Show |
5 | HG02615.hp1 HG02976.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-4089dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87355103 | ||||||
| chr7:87355103 | AT | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.116-4089delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87355103 | ||||||
| chr7:87355130 | C | T | 1 | a0002c0002t0002g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.116-4076C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355130 | |||||||
| chr7:87355214 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3992C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355214 | |||||||
| chr7:87355349 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(105): Show |
142 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.116-3857C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355349 | |||||||
| chr7:87355559 | T | C | 1 | a0001c0001t0010g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.116-3647T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355559 | |||||||
| chr7:87355576 | C | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.116-3630C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355576 | |||||||
| chr7:87355723 | GA | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3482delA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355723 | |||||||
| chr7:87355806 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3400C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355806 | |||||||
| chr7:87355816 | G | GAGTATAT others(5): Show |
1 | a0002c0002t0002g0070 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.116-3378_116-3367d others(14): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87355816 | ||||||
| chr7:87355827 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3379A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355827 | |||||||
| chr7:87355850 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3356G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355850 | |||||||
| chr7:87355866 | T | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3340T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355866 | |||||||
| chr7:87355912 | T | G | 1 | a0001c0001t0007g0016 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.116-3294T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355912 | |||||||
| chr7:87355977 | AATTTT | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3213_116-3209d others(7): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87355977 | ||||||
| chr7:87356115 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3091A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356115 | |||||||
| chr7:87356121 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0180 |
3 | HG00099.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.116-3085C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356121 | |||||||
| chr7:87356252 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.116-2954T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356252 | |||||||
| chr7:87356257 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-2949T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356257 | |||||||
| chr7:87356403 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0058 others(2): Show |
6 | HG00323.hp2 HG00639.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-2803C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356403 | |||||||
| chr7:87356828 | C | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0135 others(1): Show |
4 | HG01978.hp2 HG02148.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-2378C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356828 | |||||||
| chr7:87357000 | T | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0041 others(30): Show |
48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.116-2206T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357000 | |||||||
| chr7:87357060 | G | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | NA18990.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.116-2146G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357060 | |||||||
| chr7:87357105 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-2101G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357105 | |||||||
| chr7:87357182 | T | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(1): Show |
5 | HG02055.hp1 HG02451.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.116-2024T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357182 | |||||||
| chr7:87357207 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1999G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357207 | |||||||
| chr7:87357316 | C | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0058 others(4): Show |
8 | HG00323.hp2 HG00639.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-1890C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357316 | |||||||
| chr7:87357380 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.116-1826C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357380 | |||||||
| chr7:87357547 | T | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0003g0040 others(1): Show |
5 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-1659T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357547 | |||||||
| chr7:87357655 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0157 |
3 | HG02615.hp1 HG02976.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.116-1551G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357655 | |||||||
| chr7:87357680 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.116-1526G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357680 | |||||||
| chr7:87357746 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1460C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357746 | |||||||
| chr7:87357828 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.116-1378T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357828 | |||||||
| chr7:87357881 | G | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1325G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357881 | |||||||
| chr7:87357936 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1270G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357936 | |||||||
| chr7:87357939 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.116-1267G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357939 | |||||||
| chr7:87357940 | G | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0135 others(1): Show |
4 | HG01978.hp2 HG02148.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1266G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357940 | |||||||
| chr7:87358072 | C | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1134C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358072 | |||||||
| chr7:87358203 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.116-1003C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358203 | |||||||
| chr7:87358242 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(1): Show |
5 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-964C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358242 | |||||||
| chr7:87358252 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 |
4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-954T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358252 | |||||||
| chr7:87358339 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.116-867A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358339 | |||||||
| chr7:87358438 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-768C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358438 | |||||||
| chr7:87358446 | C | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-760C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358446 | |||||||
| chr7:87358481 | C | CA | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.116-706dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87358481 | ||||||
| chr7:87358481 | C | CAA | 6 | a0001c0001t0001g0090 a0001c0001t0001g0195 a0001c0001t0003g0006 others(3): Show |
9 | HG01243.hp1 HG01934.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-707_116-706dup others(2): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87358481 | ||||||
| chr7:87358481 | CAAA | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-708_116-706del others(3): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87358481 | ||||||
| chr7:87358551 | A | C | 1 | a0001c0001t0001g0183 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.116-655A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358551 | |||||||
| chr7:87358552 | A | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-654A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358552 | |||||||
| chr7:87358630 | GA | G | 7 | a0001c0001t0001g0053 a0001c0001t0001g0205 a0001c0001t0001g0206 others(4): Show |
9 | HG01496.hp1 HG02109.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.116-571delA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87358630 | ||||||
| chr7:87358702 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0003g0040 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.116-504T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358702 | |||||||
| chr7:87358848 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0002c0002t0001g0056 others(1): Show |
4 | HG02615.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-358G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358848 | |||||||
| chr7:87358887 | T | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-319T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358887 | |||||||
| chr7:87358928 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-278G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358928 | |||||||
| chr7:87359040 | C | T | 14 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
16 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.116-166C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87359040 | |||||||
| chr7:87359051 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-155T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87359051 | |||||||
| chr7:87359177 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.116-29A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87359177 | |||||||
| chr7:87359347 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.240+17T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87359347 | |||||||
| chr7:87359354 | A | AT | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+25dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 87359354 | ||||||
| chr7:87359723 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0044 others(30): Show |
44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.240+393G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87359723 | |||||||
| chr7:87359731 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0128 |
2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.240+401A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87359731 | |||||||
| chr7:87359847 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0093 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+517C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87359847 | |||||||
| chr7:87360039 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.240+709A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360039 | |||||||
| chr7:87360159 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.240+829G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360159 | |||||||
| chr7:87360334 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0017 others(7): Show |
24 | HG00408.hp2 HG01358.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.240+1004A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360334 | |||||||
| chr7:87360378 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-1012T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360378 | |||||||
| chr7:87360616 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.241-774C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360616 | |||||||
| chr7:87360720 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.241-670T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360720 | |||||||
| chr7:87360894 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-496T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360894 | |||||||
| chr7:87361073 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-317G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87361073 | |||||||
| chr7:87361146 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG02155.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.241-244A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87361146 | |||||||
| chr7:87361179 | C | A | 5 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
5 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-211C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87361179 | |||||||
| chr7:87361201 | G | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-189G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87361201 | |||||||
| chr7:87361718 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.423-10T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 5/17 | chr7 | 87361718 | |||||||
| chr7:87362026 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+174G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362026 | |||||||
| chr7:87362209 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.547+357A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362209 | |||||||
| chr7:87362280 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+428G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362280 | |||||||
| chr7:87362304 | C | CT | 6 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0125 others(3): Show |
7 | HG01175.hp2 HG02109.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.547+471dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362304 | ||||||
| chr7:87362304 | CT | C | 25 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0043 others(22): Show |
33 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.547+471delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362304 | ||||||
| chr7:87362304 | CTT | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0158 |
6 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+470_547+471del others(2): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362304 | ||||||
| chr7:87362304 | CTTTT | C | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
8 | HG01496.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.547+468_547+471del others(4): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362304 | ||||||
| chr7:87362324 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.547+472G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362324 | |||||||
| chr7:87362359 | C | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0018 others(33): Show |
48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.547+507C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362359 | |||||||
| chr7:87362362 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+510C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362362 | |||||||
| chr7:87362404 | T | C | 41 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0018 others(38): Show |
54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.547+552T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362404 | |||||||
| chr7:87362408 | T | C | 4 | a0001c0001t0001g0137 a0001c0001t0004g0012 a0001c0001t0004g0076 others(1): Show |
6 | HG02080.hp2 NA18942.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+556T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362408 | |||||||
| chr7:87362429 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0192 |
2 | HG00140.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.547+577T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362429 | |||||||
| chr7:87362542 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+690C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362542 | |||||||
| chr7:87362579 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.547+727G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362579 | |||||||
| chr7:87362631 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.547+779T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362631 | |||||||
| chr7:87362642 | AT | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0003g0031 others(3): Show |
7 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.547+801delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362642 | ||||||
| chr7:87362729 | GT | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0083 a0001c0001t0001g0103 others(1): Show |
4 | HG02735.hp2 HG03491.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+884delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362729 | ||||||
| chr7:87363009 | C | A | 1 | a0001c0001t0004g0100 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.547+1157C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363009 | |||||||
| chr7:87363131 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.547+1279C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363131 | |||||||
| chr7:87363369 | A | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+1517A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363369 | |||||||
| chr7:87363489 | T | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+1637T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363489 | |||||||
| chr7:87363654 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+1802G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363654 | |||||||
| chr7:87363855 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547+2003T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363855 | |||||||
| chr7:87364127 | A | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+2275A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364127 | |||||||
| chr7:87364221 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+2369C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364221 | |||||||
| chr7:87364235 | C | G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0018 others(38): Show |
54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.547+2383C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364235 | |||||||
| chr7:87364487 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.547+2635C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364487 | |||||||
| chr7:87364578 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.547+2726G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364578 | |||||||
| chr7:87364599 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.547+2747G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364599 | |||||||
| chr7:87365070 | A | G | 1 | a0001c0001t0001g0018 | 2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.547+3218A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365070 | |||||||
| chr7:87365147 | T | G | 2 | a0002c0002t0001g0056 a0002c0002t0001g0057 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.547+3295T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365147 | |||||||
| chr7:87365191 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+3339T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365191 | |||||||
| chr7:87365214 | C | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+3362C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365214 | |||||||
| chr7:87365232 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.547+3380T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365232 | |||||||
| chr7:87365243 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.547+3391C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365243 | |||||||
| chr7:87365292 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+3440C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365292 | |||||||
| chr7:87365381 | G | A | 1 | a0001c0001t0009g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.547+3529G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365381 | |||||||
| chr7:87365444 | C | T | 1 | a0001c0001t0010g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.547+3592C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365444 | |||||||
| chr7:87365459 | C | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0018 others(31): Show |
48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.547+3607C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365459 | |||||||
| chr7:87365489 | C | CA | 35 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0041 others(32): Show |
47 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.547+3650dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87365489 | ||||||
| chr7:87365612 | TTTTG | T | 22 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(19): Show |
30 | HG01243.hp1 HG01496.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.548-3758_548-3755d others(6): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87365612 | ||||||
| chr7:87365618 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.548-3758T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365618 | |||||||
| chr7:87365622 | C | CT | 6 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0064 others(3): Show |
6 | HG01934.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.548-3738dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87365622 | ||||||
| chr7:87365622 | C | CTT | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-3739_548-3738d others(4): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87365622 | ||||||
| chr7:87365664 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.548-3712G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365664 | |||||||
| chr7:87365709 | A | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0007g0016 others(2): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-3667A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365709 | |||||||
| chr7:87365710 | C | T | 36 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0027 others(33): Show |
43 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.548-3666C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365710 | |||||||
| chr7:87365797 | A | G | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0190 others(4): Show |
8 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.548-3579A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365797 | |||||||
| chr7:87365812 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.548-3564C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365812 | |||||||
| chr7:87365854 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.548-3522C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365854 | |||||||
| chr7:87365883 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.548-3493G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365883 | |||||||
| chr7:87366097 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.548-3279C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366097 | |||||||
| chr7:87366242 | A | AT | 14 | a0001c0001t0001g0026 a0001c0001t0001g0058 a0001c0001t0001g0059 others(11): Show |
19 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.548-3124dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87366242 | ||||||
| chr7:87366331 | G | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0043 others(18): Show |
27 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.548-3045G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366331 | |||||||
| chr7:87366606 | T | C | 32 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0043 others(29): Show |
45 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.548-2770T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366606 | |||||||
| chr7:87366635 | C | G | 32 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0043 others(29): Show |
45 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.548-2741C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366635 | |||||||
| chr7:87366643 | A | G | 1 | a0001c0001t0007g0016 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.548-2733A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366643 | |||||||
| chr7:87366665 | G | A | 1 | a0001c0001t0007g0016 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.548-2711G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366665 | |||||||
| chr7:87366683 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(126): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.548-2693T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366683 | |||||||
| chr7:87366766 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0085 others(8): Show |
15 | HG02258.hp1 HG02559.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.548-2610C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366766 | |||||||
| chr7:87366783 | G | A | 4 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0003g0040 others(1): Show |
4 | HG02572.hp2 HG02723.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-2593G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366783 | |||||||
| chr7:87366895 | G | A | 29 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0043 others(26): Show |
42 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.548-2481G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366895 | |||||||
| chr7:87367033 | A | G | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.548-2343A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367033 | |||||||
| chr7:87367091 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.548-2285G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367091 | |||||||
| chr7:87367107 | T | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.548-2269T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367107 | |||||||
| chr7:87367173 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(180): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.548-2203A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367173 | |||||||
| chr7:87367760 | C | G | 1 | a0001c0001t0007g0016 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.548-1616C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367760 | |||||||
| chr7:87367847 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(179): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.548-1529T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367847 | |||||||
| chr7:87367895 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.548-1481C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367895 | |||||||
| chr7:87368092 | G | A | 2 | a0001c0001t0003g0010 a0001c0001t0003g0039 |
4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-1284G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368092 | |||||||
| chr7:87368187 | C | T | 1 | a0001c0001t0003g0039 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.548-1189C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368187 | |||||||
| chr7:87368193 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0149 |
2 | HG00597.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.548-1183T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368193 | |||||||
| chr7:87368202 | C | T | 1 | a0001c0001t0003g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.548-1174C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368202 | |||||||
| chr7:87368378 | C | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.548-998C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368378 | |||||||
| chr7:87368400 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0085 others(9): Show |
16 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.548-976G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368400 | |||||||
| chr7:87368490 | C | T | 1 | a0009c0006t0001g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.548-886C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368490 | |||||||
| chr7:87368927 | T | A | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0010g0036 |
3 | HG02572.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.548-449T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368927 | |||||||
| chr7:87369007 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.548-369C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87369007 | |||||||
| chr7:87369019 | C | T | 132 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.548-357C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87369019 | |||||||
| chr7:87369526 | G | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.656+42G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369526 | |||||||
| chr7:87369547 | A | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0085 others(9): Show |
16 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.656+63A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369547 | |||||||
| chr7:87369593 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.656+109A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369593 | |||||||
| chr7:87369612 | A | T | 1 | a0001c0001t0001g0020 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.656+128A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369612 | |||||||
| chr7:87369620 | AT | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.656+137delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369620 | |||||||
| chr7:87369621 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.656+137T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369621 | |||||||
| chr7:87369828 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.656+344T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369828 | |||||||
| chr7:87369874 | C | T | 168 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(165): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.656+390C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369874 | |||||||
| chr7:87370222 | G | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0083 a0001c0001t0001g0103 |
3 | HG02735.hp2 HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.656+738G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370222 | |||||||
| chr7:87370395 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.656+911C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370395 | |||||||
| chr7:87370398 | G | A | 12 | a0002c0002t0002g0003 a0002c0002t0002g0022 a0002c0002t0002g0069 others(9): Show |
18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.656+914G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370398 | |||||||
| chr7:87370528 | A | C | 12 | a0002c0002t0002g0003 a0002c0002t0002g0022 a0002c0002t0002g0069 others(9): Show |
18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.656+1044A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370528 | |||||||
| chr7:87370549 | T | C | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0051 others(17): Show |
28 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.656+1065T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370549 | |||||||
| chr7:87370711 | C | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.656+1227C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370711 | |||||||
| chr7:87371007 | A | G | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0010g0036 |
3 | HG02572.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.656+1523A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87371007 | |||||||
| chr7:87371022 | T | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0010g0036 |
3 | HG02572.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.656+1538T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87371022 | |||||||
| chr7:87371040 | A | G | 12 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(9): Show |
16 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.656+1556A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87371040 | |||||||
| chr7:87371509 | T | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(163): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.656+2025T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87371509 | |||||||
| chr7:87371957 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.656+2473G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87371957 | |||||||
| chr7:87372006 | A | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0039 |
4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+2522A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372006 | |||||||
| chr7:87372007 | C | A | 10 | a0001c0001t0001g0064 a0001c0001t0001g0097 a0001c0001t0001g0098 others(7): Show |
10 | HG01109.hp1 HG01123.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.656+2523C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372007 | |||||||
| chr7:87372007 | C | CA | 6 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0185 others(3): Show |
8 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.656+2536dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 87372007 | ||||||
| chr7:87372007 | CA | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(89): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.656+2536delA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 87372007 | ||||||
| chr7:87372008 | A | C | 9 | a0001c0001t0001g0064 a0001c0001t0001g0098 a0001c0001t0001g0099 others(6): Show |
9 | HG01123.hp2 HG01167.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.656+2524A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372008 | |||||||
| chr7:87372019 | A | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.656+2535A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372019 | |||||||
| chr7:87372235 | A | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0047 others(4): Show |
11 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.656+2751A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372235 | |||||||
| chr7:87372360 | T | C | 1 | a0001c0001t0009g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.656+2876T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372360 | |||||||
| chr7:87372440 | A | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0066 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.656+2956A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372440 | |||||||
| chr7:87372763 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.657-2869G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372763 | |||||||
| chr7:87372816 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.657-2816A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372816 | |||||||
| chr7:87372825 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0003g0038 |
2 | HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.657-2807A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372825 | |||||||
| chr7:87372933 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.657-2699G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372933 | |||||||
| chr7:87373047 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.657-2585T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373047 | |||||||
| chr7:87373074 | G | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.657-2558G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373074 | |||||||
| chr7:87373086 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.657-2546T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373086 | |||||||
| chr7:87373218 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.657-2414T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373218 | |||||||
| chr7:87373418 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.657-2214G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373418 | |||||||
| chr7:87373458 | C | G | 8 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0104 others(5): Show |
8 | HG00423.hp1 HG01978.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-2174C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373458 | |||||||
| chr7:87373499 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.657-2133C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373499 | |||||||
| chr7:87373547 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.657-2085A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373547 | |||||||
| chr7:87373750 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.657-1882C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373750 | |||||||
| chr7:87373896 | C | A | 5 | a0002c0002t0001g0014 a0002c0002t0001g0056 a0002c0002t0001g0057 others(2): Show |
7 | HG02109.hp2 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-1736C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373896 | |||||||
| chr7:87374114 | A | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.657-1518A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87374114 | |||||||
| chr7:87374608 | C | G | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.657-1024C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87374608 | |||||||
| chr7:87374965 | T | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.657-667T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87374965 | |||||||
| chr7:87375063 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.657-569G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375063 | |||||||
| chr7:87375166 | T | A | 1 | a0001c0001t0007g0016 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.657-466T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375166 | |||||||
| chr7:87375285 | A | G | 5 | a0002c0002t0001g0014 a0002c0002t0001g0056 a0002c0002t0001g0057 others(2): Show |
7 | HG02109.hp2 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-347A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375285 | |||||||
| chr7:87375311 | G | T | 1 | a0001c0001t0003g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.657-321G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375311 | |||||||
| chr7:87375480 | T | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0170 a0001c0001t0004g0012 others(2): Show |
8 | HG02040.hp2 HG02080.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-152T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375480 | |||||||
| chr7:87375594 | C | G | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.657-38C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375594 | |||||||
| chr7:87375749 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.750+24C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 8/17 | chr7 | 87375749 | |||||||
| chr7:87375775 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG01109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.750+50T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 8/17 | chr7 | 87375775 | |||||||
| chr7:87375971 | C | CT | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.876+29dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 87375971 | ||||||
| chr7:87376157 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.876+204G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376157 | |||||||
| chr7:87376368 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.876+415C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376368 | |||||||
| chr7:87376633 | A | AT | 18 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0121 others(15): Show |
22 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.876+695dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 87376633 | ||||||
| chr7:87376718 | C | G | 17 | a0002c0002t0001g0014 a0002c0002t0001g0056 a0002c0002t0001g0057 others(14): Show |
25 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.877-631C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376718 | |||||||
| chr7:87376777 | A | G | 1 | a0001c0001t0009g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.877-572A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376777 | |||||||
| chr7:87376815 | C | A | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.877-534C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376815 | |||||||
| chr7:87376970 | G | A | 1 | a0001c0001t0007g0016 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.877-379G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376970 | |||||||
| chr7:87376971 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0055 others(4): Show |
8 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.877-378A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376971 | |||||||
| chr7:87377198 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.877-151A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87377198 | |||||||
| chr7:87377251 | G | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.877-98G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87377251 | |||||||
| chr7:87377292 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.877-57A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87377292 | |||||||
| chr7:87377536 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0158 |
6 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.978+86G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87377536 | |||||||
| chr7:87377576 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.978+126A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87377576 | |||||||
| chr7:87377829 | G | C | 1 | a0001c0001t0001g0023 | 2 | HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.978+379G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87377829 | |||||||
| chr7:87377863 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.978+413A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87377863 | |||||||
| chr7:87378287 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.978+837A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378287 | |||||||
| chr7:87378293 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0194 |
2 | NA18942.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.978+843C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378293 | |||||||
| chr7:87378294 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.978+844A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378294 | |||||||
| chr7:87378306 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.978+856A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378306 | |||||||
| chr7:87378340 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.978+890C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378340 | |||||||
| chr7:87378341 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.978+891G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378341 | |||||||
| chr7:87378346 | C | CA | 31 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0048 others(28): Show |
43 | HG00621.hp2 HG00735.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.978+912dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87378346 | ||||||
| chr7:87378346 | C | CAA | 113 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.978+911_978+912dup others(2): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87378346 | ||||||
| chr7:87378346 | C | CAAA | 10 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0063 others(7): Show |
10 | HG00423.hp1 HG01978.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.978+910_978+912dup others(3): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87378346 | ||||||
| chr7:87378428 | T | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0055 others(2): Show |
6 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.978+978T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378428 | |||||||
| chr7:87378487 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.978+1037A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378487 | |||||||
| chr7:87378492 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.978+1042C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378492 | |||||||
| chr7:87378573 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.978+1123A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378573 | |||||||
| chr7:87378639 | T | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(176): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.978+1189T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378639 | |||||||
| chr7:87378907 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0055 others(3): Show |
7 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+1457C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378907 | |||||||
| chr7:87378962 | T | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0194 |
2 | NA18942.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.978+1512T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378962 | |||||||
| chr7:87379045 | C | G | 4 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0034 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+1595C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379045 | |||||||
| chr7:87379092 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.978+1642T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379092 | |||||||
| chr7:87379134 | C | T | 1 | a0008c0009t0001g0211 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.978+1684C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379134 | |||||||
| chr7:87379420 | T | A | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.978+1970T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379420 | |||||||
| chr7:87379478 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.978+2028C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379478 | |||||||
| chr7:87379697 | C | A | 1 | a0002c0002t0002g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.979-2213C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379697 | |||||||
| chr7:87379879 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0006c0004t0001g0161 |
3 | NA18969.hp1 NA18998.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.979-2031G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379879 | |||||||
| chr7:87380122 | T | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0107 a0001c0001t0001g0129 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-1788T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380122 | |||||||
| chr7:87380141 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.979-1769A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380141 | |||||||
| chr7:87380245 | T | TCCTATTT others(143): Show |
1 | a0001c0001t0001g0116 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.979-1652_979-1651i others(152): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87380245 | ||||||
| chr7:87380245 | T | TCCTATTT others(143): Show |
1 | a0001c0001t0001g0126 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.979-1604_979-1603i others(152): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87380245 | ||||||
| chr7:87380245 | T | TCCTATTT others(143): Show |
121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.979-1664_979-1515d others(152): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87380245 | ||||||
| chr7:87380353 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.979-1557A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380353 | |||||||
| chr7:87380405 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.979-1505T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380405 | |||||||
| chr7:87380888 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.979-1022G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380888 | |||||||
| chr7:87380974 | G | A | 2 | a0001c0001t0003g0010 a0001c0001t0003g0039 |
4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-936G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380974 | |||||||
| chr7:87381370 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.979-540C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381370 | |||||||
| chr7:87381390 | T | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG00741.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.979-520T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381390 | |||||||
| chr7:87381391 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.979-519G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381391 | |||||||
| chr7:87381531 | T | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0080 |
3 | HG00621.hp2 HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.979-379T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381531 | |||||||
| chr7:87381572 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.979-338G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381572 | |||||||
| chr7:87381727 | T | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0108 |
2 | HG00738.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.979-183T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381727 | |||||||
| chr7:87381751 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0085 others(10): Show |
17 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.979-159T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381751 | |||||||
| chr7:87382033 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1062+40G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 11/17 | chr7 | 87382033 | |||||||
| chr7:87382228 | AC | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0085 others(10): Show |
17 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1170+48delC | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 12/17 | chr7 | 87382228 | |||||||
| chr7:87382388 | G | A | 16 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0043 others(13): Show |
21 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1171-25G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 12/17 | chr7 | 87382388 | |||||||
| chr7:87382393 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0085 others(10): Show |
17 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1171-20C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 12/17 | chr7 | 87382393 | |||||||
| chr7:87382591 | A | G | 1 | a0001c0001t0005g0200 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1301+48A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87382591 | |||||||
| chr7:87382668 | A | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0039 |
4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+125A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87382668 | |||||||
| chr7:87382793 | T | C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0062 others(5): Show |
10 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1301+250T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87382793 | |||||||
| chr7:87382817 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+274G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87382817 | |||||||
| chr7:87382911 | C | T | 1 | a0002c0002t0001g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1301+368C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87382911 | |||||||
| chr7:87383003 | A | G | 16 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0043 others(13): Show |
21 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1301+460A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383003 | |||||||
| chr7:87383006 | T | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0080 |
3 | HG00621.hp2 HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1301+463T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383006 | |||||||
| chr7:87383099 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1301+556C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383099 | |||||||
| chr7:87383106 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+563G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383106 | |||||||
| chr7:87383147 | A | G | 12 | a0002c0002t0002g0003 a0002c0002t0002g0022 a0002c0002t0002g0069 others(9): Show |
18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1301+604A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383147 | |||||||
| chr7:87383154 | A | G | 14 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0153 others(11): Show |
18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1301+611A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383154 | |||||||
| chr7:87383267 | C | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0039 |
4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+724C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383267 | |||||||
| chr7:87383315 | C | T | 16 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0043 others(13): Show |
21 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1301+772C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383315 | |||||||
| chr7:87383367 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1301+824T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383367 | |||||||
| chr7:87383382 | A | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1301+839A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383382 | |||||||
| chr7:87383497 | C | CT | 5 | a0001c0001t0003g0031 a0001c0001t0003g0033 a0001c0001t0003g0040 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1301+970dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 87383497 | ||||||
| chr7:87383497 | CT | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1301+970delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 87383497 | ||||||
| chr7:87383742 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1301+1199G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383742 | |||||||
| chr7:87383790 | C | T | 1 | a0001c0001t0007g0016 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1301+1247C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383790 | |||||||
| chr7:87383792 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1301+1249C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383792 | |||||||
| chr7:87384000 | T | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0180 |
3 | HG00099.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1301+1457T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384000 | |||||||
| chr7:87384004 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0085 others(10): Show |
17 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1301+1461C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384004 | |||||||
| chr7:87384005 | G | A | 4 | a0001c0001t0001g0169 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
4 | HG00544.hp1 NA18747.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301+1462G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384005 | |||||||
| chr7:87384164 | C | T | 14 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0153 others(11): Show |
18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1301+1621C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384164 | |||||||
| chr7:87384261 | A | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1301+1718A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384261 | |||||||
| chr7:87384367 | A | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0068 |
3 | NA18948.hp2 NA18974.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1301+1824A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384367 | |||||||
| chr7:87384376 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1301+1833A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384376 | |||||||
| chr7:87384439 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1301+1896C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384439 | |||||||
| chr7:87384472 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1301+1929C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384472 | |||||||
| chr7:87384764 | G | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0085 others(10): Show |
17 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1301+2221G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384764 | |||||||
| chr7:87385039 | C | T | 17 | a0002c0002t0001g0014 a0002c0002t0001g0056 a0002c0002t0001g0057 others(14): Show |
25 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1301+2496C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385039 | |||||||
| chr7:87385117 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(158): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1301+2574T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385117 | |||||||
| chr7:87385149 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+2606T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385149 | |||||||
| chr7:87385613 | G | A | 12 | a0002c0002t0002g0003 a0002c0002t0002g0022 a0002c0002t0002g0069 others(9): Show |
18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1301+3070G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385613 | |||||||
| chr7:87385816 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1301+3273G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385816 | |||||||
| chr7:87385869 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0203 |
4 | HG01934.hp2 HG02083.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301+3326T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385869 | |||||||
| chr7:87385914 | C | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+3371C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385914 | |||||||
| chr7:87386396 | T | C | 1 | a0005c0008t0001g0156 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1301+3853T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386396 | |||||||
| chr7:87386570 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1301+4027T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386570 | |||||||
| chr7:87386617 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+4074T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386617 | |||||||
| chr7:87386670 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1301+4127G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386670 | |||||||
| chr7:87386683 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+4140T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386683 | |||||||
| chr7:87386744 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1301+4201G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386744 | |||||||
| chr7:87386892 | G | C | 12 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(9): Show |
16 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1301+4349G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386892 | |||||||
| chr7:87387148 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1302-4441A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387148 | |||||||
| chr7:87387173 | G | A | 12 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(9): Show |
16 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1302-4416G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387173 | |||||||
| chr7:87387182 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1302-4407T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387182 | |||||||
| chr7:87387311 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1302-4278T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387311 | |||||||
| chr7:87387517 | G | A | 17 | a0002c0002t0001g0014 a0002c0002t0001g0056 a0002c0002t0001g0057 others(14): Show |
25 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1302-4072G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387517 | |||||||
| chr7:87387520 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1302-4069C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387520 | |||||||
| chr7:87387526 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1302-4063G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387526 | |||||||
| chr7:87388218 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0194 |
2 | NA18942.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1302-3371C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388218 | |||||||
| chr7:87388225 | A | C | 14 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0153 others(11): Show |
18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302-3364A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388225 | |||||||
| chr7:87388547 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1302-3042C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388547 | |||||||
| chr7:87388759 | A | G | 7 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(4): Show |
11 | HG01243.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302-2830A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388759 | |||||||
| chr7:87388805 | A | G | 1 | a0002c0002t0002g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1302-2784A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388805 | |||||||
| chr7:87388954 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1302-2635T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388954 | |||||||
| chr7:87388996 | T | C | 1 | a0001c0001t0010g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1302-2593T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388996 | |||||||
| chr7:87389215 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1302-2374C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389215 | |||||||
| chr7:87389263 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1302-2326C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389263 | |||||||
| chr7:87389280 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1302-2309C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389280 | |||||||
| chr7:87389423 | C | A | 1 | a0001c0001t0010g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1302-2166C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389423 | |||||||
| chr7:87389436 | T | C | 5 | a0002c0002t0001g0014 a0002c0002t0001g0056 a0002c0002t0001g0057 others(2): Show |
7 | HG02109.hp2 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302-2153T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389436 | |||||||
| chr7:87389449 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(121): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1302-2140G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389449 | |||||||
| chr7:87389480 | G | T | 14 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0153 others(11): Show |
18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302-2109G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389480 | |||||||
| chr7:87389507 | A | G | 7 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(4): Show |
11 | HG01243.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302-2082A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389507 | |||||||
| chr7:87389827 | GTTGTTCC | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1302-1760_1302-175 others(11): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 87389827 | ||||||
| chr7:87389860 | A | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(158): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1302-1729A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389860 | |||||||
| chr7:87389896 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1302-1693G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389896 | |||||||
| chr7:87390081 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1302-1508C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390081 | |||||||
| chr7:87390237 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1302-1352C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390237 | |||||||
| chr7:87390323 | C | T | 1 | a0001c0001t0010g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1302-1266C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390323 | |||||||
| chr7:87390699 | A | G | 1 | a0001c0001t0010g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1302-890A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390699 | |||||||
| chr7:87390812 | T | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1302-777T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390812 | |||||||
| chr7:87390858 | C | T | 2 | a0001c0001t0003g0010 a0001c0001t0003g0039 |
4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302-731C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390858 | |||||||
| chr7:87390986 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1302-603G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390986 | |||||||
| chr7:87390988 | T | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0039 |
4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302-601T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390988 | |||||||
| chr7:87391471 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0192 |
2 | HG00140.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1302-118C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87391471 | |||||||
| chr7:87392016 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1425+304G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392016 | |||||||
| chr7:87392129 | T | C | 14 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0153 others(11): Show |
18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1425+417T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392129 | |||||||
| chr7:87392208 | G | A | 12 | a0002c0002t0002g0003 a0002c0002t0002g0022 a0002c0002t0002g0069 others(9): Show |
18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1426-358G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392208 | |||||||
| chr7:87392397 | T | C | 12 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(9): Show |
16 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1426-169T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392397 | |||||||
| chr7:87392401 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1426-165C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392401 | |||||||
| chr7:87392423 | A | T | 5 | a0001c0001t0001g0149 a0001c0001t0001g0164 a0001c0001t0004g0012 others(2): Show |
7 | HG02071.hp1 HG02080.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1426-143A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392423 | |||||||
| chr7:87392489 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1426-77T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392489 | |||||||
| chr7:87392708 | G | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1505-22G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 15/17 | chr7 | 87392708 | |||||||
| chr7:87393280 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1718+213T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393280 | |||||||
| chr7:87393307 | C | T | 12 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0155 others(9): Show |
16 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1718+240C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393307 | |||||||
| chr7:87393518 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1718+451G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393518 | |||||||
| chr7:87393665 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(173): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1718+598T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393665 | |||||||
| chr7:87393788 | G | A | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | NA18948.hp1 NA18985.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.1718+721G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393788 | |||||||
| chr7:87393879 | A | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1718+812A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393879 | |||||||
| chr7:87393949 | A | C | 1 | a0001c0001t0010g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1718+882A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393949 | |||||||
| chr7:87394003 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1718+936C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394003 | |||||||
| chr7:87394220 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1718+1153G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394220 | |||||||
| chr7:87394321 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1718+1254G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394321 | |||||||
| chr7:87394553 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1718+1486T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394553 | |||||||
| chr7:87394555 | T | TA | 141 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(138): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1718+1499dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87394555 | ||||||
| chr7:87394555 | T | TAA | 31 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0085 others(28): Show |
43 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1718+1498_1718+149 others(6): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87394555 | ||||||
| chr7:87394556 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1718+1489A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394556 | |||||||
| chr7:87394650 | A | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0179 |
2 | NA19003.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1718+1583A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394650 | |||||||
| chr7:87394676 | A | G | 5 | a0002c0002t0001g0014 a0002c0002t0001g0056 a0002c0002t0001g0057 others(2): Show |
7 | HG02109.hp2 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1718+1609A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394676 | |||||||
| chr7:87394713 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1718+1646A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394713 | |||||||
| chr7:87394803 | G | A | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1718+1736G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394803 | |||||||
| chr7:87394987 | G | GA | 19 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0058 others(16): Show |
23 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1718+1930dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87394987 | ||||||
| chr7:87395038 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1718+1971T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395038 | |||||||
| chr7:87395203 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1718+2136G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395203 | |||||||
| chr7:87395270 | G | GT | 121 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1718+2208dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87395270 | ||||||
| chr7:87395270 | G | GTT | 3 | a0001c0001t0001g0061 a0001c0001t0001g0191 a0001c0001t0005g0198 |
3 | HG02572.hp2 HG03225.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1718+2207_1718+220 others(6): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87395270 | ||||||
| chr7:87395294 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1718+2227G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395294 | |||||||
| chr7:87395336 | C | G | 14 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0153 others(11): Show |
18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1718+2269C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395336 | |||||||
| chr7:87395369 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1718+2302A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395369 | |||||||
| chr7:87395402 | C | T | 1 | a0001c0001t0007g0016 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1718+2335C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395402 | |||||||
| chr7:87395517 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1718+2450T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395517 | |||||||
| chr7:87395636 | C | A | 1 | a0001c0001t0001g0017 | 2 | HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1718+2569C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395636 | |||||||
| chr7:87395789 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1718+2722A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395789 | |||||||
| chr7:87395811 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1719-2713A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395811 | |||||||
| chr7:87396030 | T | A | 1 | a0001c0001t0007g0016 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1719-2494T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396030 | |||||||
| chr7:87396031 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG00621.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1719-2493C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396031 | |||||||
| chr7:87396134 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1719-2390G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396134 | |||||||
| chr7:87396451 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1719-2073G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396451 | |||||||
| chr7:87396501 | C | T | 1 | a0001c0001t0007g0016 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1719-2023C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396501 | |||||||
| chr7:87396626 | CTT | C | 12 | a0002c0002t0002g0003 a0002c0002t0002g0022 a0002c0002t0002g0069 others(9): Show |
18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1719-1897_1719-189 others(6): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396626 | |||||||
| chr7:87396690 | T | TA | 142 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1719-1822dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87396690 | ||||||
| chr7:87396690 | T | TAA | 16 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0088 others(13): Show |
23 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1719-1823_1719-182 others(6): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87396690 | ||||||
| chr7:87396741 | T | C | 1 | a0001c0001t0010g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1719-1783T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396741 | |||||||
| chr7:87396858 | G | A | 14 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0153 others(11): Show |
18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1719-1666G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396858 | |||||||
| chr7:87396952 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1719-1572T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396952 | |||||||
| chr7:87397133 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1719-1391C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397133 | |||||||
| chr7:87397217 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(173): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1719-1307A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397217 | |||||||
| chr7:87397257 | A | G | 19 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0002c0002t0001g0014 others(16): Show |
28 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1719-1267A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397257 | |||||||
| chr7:87397349 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1719-1175T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397349 | |||||||
| chr7:87397350 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1719-1174C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397350 | |||||||
| chr7:87397350 | C | CA | 170 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(167): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1719-1161dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87397350 | ||||||
| chr7:87397478 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1719-1046T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397478 | |||||||
| chr7:87397519 | A | T | 1 | a0002c0002t0002g0167 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1719-1005A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397519 | |||||||
| chr7:87398000 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1719-524T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87398000 | |||||||
| chr7:87398103 | C | CT | 115 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1719-408dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87398103 | ||||||
| chr7:87398103 | CT | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0010g0036 others(12): Show |
22 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.1719-408delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87398103 | ||||||
| chr7:87398103 | CTTT | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0208 a0002c0002t0001g0209 |
5 | HG02109.hp2 HG02615.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1719-410_1719-408d others(5): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87398103 | ||||||
| chr7:87398126 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1719-398T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87398126 | |||||||
| chr7:87398520 | A | G | 1 | a0002c0002t0001g0056 | 1 | HG03516.hp2 | splice_region_variant&intron_variant | LOW | c.1719-4A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87398520 |