Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9595 |
| ensemblid | ENSG00000115165.10 |
| hgncid | 9506 |
| symbol | CYTIP |
| name | cytohesin 1 interacting protein |
| refseq_nuc | NM_004288.5 |
| refseq_prot | NP_004279.3 |
| ensembl_nuc | ENST00000264192.8 |
| ensembl_prot | ENSP00000264192.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 157414619 |
| end | 157444089 |
| strand | - |
| ver | v1.2 |
| region | chr2:157414619-157444089 |
| region5000 | chr2:157409619-157449089 |
| regionname0 | CYTIP_chr2_157414619_157444089 |
| regionname5000 | CYTIP_chr2_157409619_157449089 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 359 | 307 | 88 | 70 | 92 | 14 | 41 | 62 | CYTIP_chr2_157409619_157449089 | CYTIP | MSLQR others(354): Show |
chr2 | 157409619 | 157449089 |
| a0002 | 0/0 | 359 | 7 | 0 | 0 | 6 | 0 | 1 | 5 | CYTIP_chr2_157409619_157449089 | CYTIP | MSLQR others(354): Show |
chr2 | 157409619 | 157449089 |
| a0003 | 0/0 | 359 | 3 | 0 | 0 | 2 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | MSLQR others(354): Show |
chr2 | 157409619 | 157449089 |
| a0004 | 0/0 | 359 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | MSLQR others(354): Show |
chr2 | 157409619 | 157449089 |
| a0005 | 0/0 | 359 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | MSLQR others(354): Show |
chr2 | 157409619 | 157449089 |
| a0006 | 0/0 | 359 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | MSLQR others(354): Show |
chr2 | 157409619 | 157449089 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1077 | 305 | 86 | 70 | 92 | 14 | 41 | CYTIP_chr2_157409619_157449089 | CYTIP | ATGTC others(1072): Show |
chr2 | 157409619 | 157449089 | ||
| a0001c0004 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | ATGTC others(1072): Show |
chr2 | 157409619 | 157449089 | ||
| a0001c0005 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | ATGTC others(1072): Show |
chr2 | 157409619 | 157449089 | ||
| a0002c0002 | 0/0 | 1077 | 7 | 0 | 0 | 6 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | ATGTC others(1072): Show |
chr2 | 157409619 | 157449089 | ||
| a0003c0003 | 0/0 | 1077 | 3 | 0 | 0 | 2 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | ATGTC others(1072): Show |
chr2 | 157409619 | 157449089 | ||
| a0004c0006 | 0/0 | 1077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | ATGTC others(1072): Show |
chr2 | 157409619 | 157449089 | ||
| a0005c0007 | 0/0 | 1077 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | ATGTC others(1072): Show |
chr2 | 157409619 | 157449089 | ||
| a0006c0008 | 0/0 | 1077 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | ATGTC others(1072): Show |
chr2 | 157409619 | 157449089 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2207 | 205 | 30 | 53 | 78 | 13 | 31 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0001c0001t0002 | 1/0 | 2207 | 50 | 42 | 5 | 0 | 0 | 2 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0001c0001t0003 | 0/0 | 2207 | 19 | 0 | 10 | 6 | 0 | 3 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0001c0001t0004 | 0/0 | 2196 | 11 | 8 | 0 | 2 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2191): Show |
chr2 | 157409619 | 157449089 |
| a0001c0001t0005 | 0/0 | 2207 | 6 | 0 | 0 | 6 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0001c0001t0006 | 0/0 | 2207 | 6 | 6 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0001c0001t0007 | 0/1 | 2207 | 3 | 0 | 1 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0001c0001t0008 | 0/0 | 2196 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2191): Show |
chr2 | 157409619 | 157449089 |
| a0001c0001t0010 | 0/0 | 2207 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0001c0001t0011 | 0/0 | 2207 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0001c0001t0012 | 0/0 | 2207 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0001c0001t0013 | 0/0 | 2207 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | GTGCT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0001c0004t0001 | 0/0 | 2207 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0001c0005t0009 | 0/0 | 2207 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0002c0002t0001 | 0/0 | 2207 | 3 | 0 | 0 | 3 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0002c0002t0003 | 0/0 | 2207 | 3 | 0 | 0 | 2 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0002c0002t0005 | 0/0 | 2207 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0003c0003t0001 | 0/0 | 2207 | 3 | 0 | 0 | 2 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0004c0006t0001 | 0/0 | 2207 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0005c0007t0001 | 0/0 | 2207 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| a0006c0008t0001 | 0/0 | 2207 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | GTACT others(2202): Show |
chr2 | 157409619 | 157449089 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0004 | 0/0 | 5 | 1 | 2 | 1 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0231 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0004g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0006g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0007g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0007g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0010g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0011g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0012g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0001t0013g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0001c0005t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0002c0002t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0003c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0003c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0004c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0005c0007t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| a0006c0008t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00099 | hp2 | a0001 | c0001 | t0007 | g0033 | EUR | GBR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | GBR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | FIN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0212 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00544 | hp2 | a0004 | c0006 | t0001 | g0157 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00609 | hp1 | a0002 | c0002 | t0005 | g0205 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00738 | hp1 | a0001 | c0001 | t0013 | g0259 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02071 | hp1 | a0003 | c0003 | t0001 | g0256 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0255 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02145 | hp1 | a0001 | c0004 | t0001 | g0131 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CDX | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02451 | hp1 | a0001 | c0005 | t0009 | g0057 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | KHV | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0254 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0197 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02698 | hp1 | a0001 | c0001 | t0012 | g0258 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0248 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0233 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | BEB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03927 | hp2 | a0001 | c0001 | t0008 | g0134 | SAS | BEB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG04184 | hp2 | a0002 | c0002 | t0003 | g0206 | SAS | BEB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0043 | SAS | STU | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | STU | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG04204 | hp2 | a0001 | c0001 | t0010 | g0153 | SAS | STU | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | YRI | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | CHB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | YRI | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | YRI | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | LWK | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19057 | hp1 | a0002 | c0002 | t0003 | g0203 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19068 | hp1 | a0005 | c0007 | t0001 | g0213 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | TSI | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA20905 | hp2 | a0006 | c0008 | t0001 | g0137 | SAS | GIH | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | USA | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | USA | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | USA | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | USA | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | LWK | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0257 | REF | REF | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0231 | REF | REF | CYTIP_chr2_157409619_157449089 | CYTIP | chr2 | 157409619 | 157449089 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:157415708 | C | T | 1 | a0004 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.1049G>A | p.Arg350His | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 1118/2207 | 1049/1080 | 350/359 | chr2 | 157415708 | |||
| chr2:157415820 | T | C | 1 | a0005 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.937A>G | p.Met313Val | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 1006/2207 | 937/1080 | 313/359 | chr2 | 157415820 | |||
| chr2:157427401 | T | C | 1 | a0006 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.496A>G | p.Thr166Ala | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/8 | 565/2207 | 496/1080 | 166/359 | chr2 | 157427401 | |||
| chr2:157434402 | G | C | 2 | a0002 a0006 |
8 | HG00609.hp1 HG04184.hp2 NA18963.hp2 others(5): Show |
missense_variant | MODERATE | c.247C>G | p.Gln83Glu | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/8 | 316/2207 | 247/1080 | 83/359 | chr2 | 157434402 | |||
| chr2:157443957 | G | C | 1 | a0003 | 3 | HG02071.hp1 HG02132.hp1 HG02602.hp2 |
missense_variant | MODERATE | c.64C>G | p.Pro22Ala | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/8 | 133/2207 | 64/1080 | 22/359 | chr2 | 157443957 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:157415956 | C | T | 1 | a0001c0004 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.801G>A | p.Glu267Glu | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 870/2207 | 801/1080 | 267/359 | chr2 | 157415956 | |||
| chr2:157415995 | C | T | 2 | a0001c0004 a0001c0005 |
2 | HG02145.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.762G>A | p.Thr254Thr | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 831/2207 | 762/1080 | 254/359 | chr2 | 157415995 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:157414727 | T | G | 2 | a0001c0001t0003 a0002c0002t0003 |
22 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*950A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 950 | chr2 | 157414727 | ||||||
| chr2:157415000 | C | T | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(15): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*677G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 677 | chr2 | 157415000 | ||||||
| chr2:157415025 | A | T | 1 | a0001c0005t0009 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*652T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 652 | chr2 | 157415025 | ||||||
| chr2:157415034 | A | T | 1 | a0001c0001t0006 | 6 | HG02615.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*643T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 643 | chr2 | 157415034 | ||||||
| chr2:157415035 | A | G | 2 | a0001c0001t0003 a0002c0002t0003 |
22 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*642T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 642 | chr2 | 157415035 | ||||||
| chr2:157415056 | T | C | 1 | a0001c0001t0010 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*621A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 621 | chr2 | 157415056 | ||||||
| chr2:157415246 | C | G | 2 | a0001c0001t0005 a0002c0002t0005 |
7 | HG00423.hp1 HG00609.hp1 HG02015.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*431G>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 431 | chr2 | 157415246 | ||||||
| chr2:157415314 | T | C | 1 | a0001c0001t0011 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*363A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 363 | chr2 | 157415314 | ||||||
| chr2:157415513 | TTAAGAAG others(4): Show |
T | 2 | a0001c0001t0004 a0001c0001t0008 |
12 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*153_*163delTATGCT others(5): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 8/8 | 153 | chr2 | 157415513 | ||||||
| chr2:157444069 | G | C | 2 | a0001c0001t0007 a0001c0001t0012 |
3 | HG00099.hp2 HG01346.hp1 HG02698.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-49C>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/8 | chr2 | 157444069 | |||||||
| chr2:157444087 | T | C | 1 | a0001c0001t0013 | 1 | HG00738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-67A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/8 | 67 | chr2 | 157444087 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:157416236 | A | C | 1 | a0001c0004t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.614-93T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157416236 | |||||||
| chr2:157416337 | C | G | 3 | a0001c0001t0003g0028 a0001c0001t0003g0225 a0001c0001t0003g0233 |
4 | HG01167.hp1 HG01169.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-194G>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157416337 | |||||||
| chr2:157416413 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.614-270C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157416413 | |||||||
| chr2:157416438 | T | G | 6 | a0001c0001t0001g0036 a0001c0001t0006g0031 a0001c0001t0006g0048 others(3): Show |
7 | HG02145.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.614-295A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157416438 | |||||||
| chr2:157416971 | G | A | 5 | a0001c0001t0006g0031 a0001c0001t0006g0048 a0001c0001t0006g0064 others(2): Show |
6 | HG02615.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.614-828C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157416971 | |||||||
| chr2:157416977 | G | T | 1 | a0001c0005t0009g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-834C>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157416977 | |||||||
| chr2:157416980 | T | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0152 a0001c0001t0001g0170 others(1): Show |
4 | HG01261.hp1 HG02683.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-837A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157416980 | |||||||
| chr2:157416980 | T | TGA | 4 | a0001c0001t0001g0090 a0001c0001t0002g0012 a0001c0001t0002g0220 others(1): Show |
5 | HG01192.hp1 HG02698.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.614-839_614-838dup others(2): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157416980 | |||||||
| chr2:157416982 | A | T | 21 | a0001c0001t0002g0069 a0001c0001t0003g0008 a0001c0001t0003g0028 others(18): Show |
25 | HG00544.hp2 HG01106.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.614-839T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157416982 | |||||||
| chr2:157417189 | G | A | 1 | a0001c0005t0009g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-1046C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157417189 | |||||||
| chr2:157417238 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.614-1095A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157417238 | |||||||
| chr2:157417330 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0200 |
2 | NA18956.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.614-1187G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157417330 | |||||||
| chr2:157417533 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0056 |
3 | HG02572.hp1 HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.613+990C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157417533 | |||||||
| chr2:157417630 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.613+893A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157417630 | |||||||
| chr2:157417631 | A | C | 7 | a0001c0001t0002g0020 a0001c0001t0002g0044 a0001c0001t0002g0045 others(4): Show |
8 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.613+892T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157417631 | |||||||
| chr2:157417696 | T | A | 1 | a0001c0005t0009g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.613+827A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157417696 | |||||||
| chr2:157417696 | T | TAA | 4 | a0001c0001t0004g0003 a0001c0001t0004g0105 a0001c0001t0004g0106 others(1): Show |
8 | HG02258.hp2 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.613+825_613+826dup others(2): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157417696 | |||||||
| chr2:157417697 | A | T | 7 | a0001c0001t0002g0020 a0001c0001t0002g0044 a0001c0001t0002g0045 others(4): Show |
8 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.613+826T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157417697 | |||||||
| chr2:157417810 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.613+713A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157417810 | |||||||
| chr2:157418109 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.613+414C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157418109 | |||||||
| chr2:157418280 | C | T | 1 | a0001c0005t0009g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.613+243G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157418280 | |||||||
| chr2:157418322 | C | T | 1 | a0001c0005t0009g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.613+201G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157418322 | |||||||
| chr2:157418341 | T | C | 3 | a0001c0001t0002g0156 a0001c0001t0002g0240 a0001c0001t0012g0258 |
3 | HG01099.hp1 HG01123.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.613+182A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157418341 | |||||||
| chr2:157418381 | T | C | 1 | a0001c0005t0009g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.613+142A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 7/7 | chr2 | 157418381 | |||||||
| chr2:157418599 | T | TA | 228 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.547-11dupT | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157418599 | |||||||
| chr2:157418866 | T | A | 24 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0053 others(21): Show |
29 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.547-277A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157418866 | |||||||
| chr2:157418881 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.547-292A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157418881 | |||||||
| chr2:157418952 | A | G | 18 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0053 others(15): Show |
22 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.547-363T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157418952 | |||||||
| chr2:157419204 | T | C | 18 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0053 others(15): Show |
22 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.547-615A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157419204 | |||||||
| chr2:157419286 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.547-697G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157419286 | |||||||
| chr2:157419355 | C | T | 19 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0053 others(16): Show |
23 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.547-766G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157419355 | |||||||
| chr2:157419466 | A | G | 1 | a0001c0001t0003g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.547-877T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157419466 | |||||||
| chr2:157419614 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0167 |
3 | NA18967.hp2 NA19002.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.547-1025G>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157419614 | |||||||
| chr2:157419706 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.547-1117A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157419706 | |||||||
| chr2:157419952 | A | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0177 |
3 | HG01069.hp1 HG01071.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.547-1363T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157419952 | |||||||
| chr2:157420117 | C | A | 1 | a0001c0004t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.547-1528G>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420117 | |||||||
| chr2:157420211 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.547-1622T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420211 | |||||||
| chr2:157420231 | G | A | 1 | a0001c0005t0009g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.547-1642C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420231 | |||||||
| chr2:157420289 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0228 |
2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.547-1700C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420289 | |||||||
| chr2:157420336 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.547-1747G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420336 | |||||||
| chr2:157420588 | T | C | 2 | a0001c0004t0001g0131 a0001c0005t0009g0057 |
2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.547-1999A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420588 | |||||||
| chr2:157420650 | C | CA | 5 | a0001c0001t0001g0159 a0001c0001t0002g0002 a0001c0001t0002g0104 others(2): Show |
9 | HG02897.hp1 HG02922.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.547-2062dupT | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420650 | |||||||
| chr2:157420650 | C | CAA | 9 | a0001c0001t0003g0008 a0001c0001t0003g0075 a0001c0001t0003g0087 others(6): Show |
12 | HG01346.hp2 HG01361.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.547-2063_547-2062d others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420650 | |||||||
| chr2:157420650 | C | CAAA | 7 | a0001c0001t0003g0080 a0001c0001t0003g0086 a0001c0001t0003g0252 others(4): Show |
8 | HG01106.hp1 HG01433.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.547-2064_547-2062d others(5): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420650 | |||||||
| chr2:157420650 | CA | C | 60 | a0001c0001t0001g0022 a0001c0001t0001g0058 a0001c0001t0001g0065 others(57): Show |
67 | HG00140.hp2 HG00609.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.547-2062delT | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420650 | |||||||
| chr2:157420650 | CAA | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.547-2063_547-2062d others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420650 | |||||||
| chr2:157420654 | A | C | 1 | a0001c0001t0001g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.547-2065T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420654 | |||||||
| chr2:157420998 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.547-2409A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157420998 | |||||||
| chr2:157421035 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.547-2446G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421035 | |||||||
| chr2:157421165 | T | C | 3 | a0001c0001t0003g0075 a0001c0001t0003g0141 a0001c0001t0003g0162 |
3 | HG02523.hp2 NA18951.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.547-2576A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421165 | |||||||
| chr2:157421178 | A | C | 1 | a0001c0001t0002g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.547-2589T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421178 | |||||||
| chr2:157421182 | C | A | 18 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0053 others(15): Show |
22 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.547-2593G>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421182 | |||||||
| chr2:157421195 | G | A | 26 | a0001c0001t0001g0036 a0001c0001t0003g0008 a0001c0001t0003g0028 others(23): Show |
31 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.547-2606C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421195 | |||||||
| chr2:157421283 | A | G | 26 | a0001c0001t0001g0036 a0001c0001t0003g0008 a0001c0001t0003g0028 others(23): Show |
31 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.547-2694T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421283 | |||||||
| chr2:157421356 | T | G | 26 | a0001c0001t0001g0036 a0001c0001t0003g0008 a0001c0001t0003g0028 others(23): Show |
31 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.547-2767A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421356 | |||||||
| chr2:157421514 | G | A | 1 | a0001c0005t0009g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.547-2925C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421514 | |||||||
| chr2:157421693 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.547-3104C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421693 | |||||||
| chr2:157421701 | T | C | 26 | a0001c0001t0001g0036 a0001c0001t0003g0008 a0001c0001t0003g0028 others(23): Show |
31 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.547-3112A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421701 | |||||||
| chr2:157421733 | G | C | 26 | a0001c0001t0001g0036 a0001c0001t0003g0008 a0001c0001t0003g0028 others(23): Show |
31 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.547-3144C>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421733 | |||||||
| chr2:157421988 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.547-3399C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157421988 | |||||||
| chr2:157422077 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.547-3488C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157422077 | |||||||
| chr2:157422122 | G | A | 47 | a0001c0001t0001g0036 a0001c0001t0002g0012 a0001c0001t0002g0020 others(44): Show |
58 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(55): Show |
intron_variant | MODIFIER | c.547-3533C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157422122 | |||||||
| chr2:157422137 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.547-3548G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157422137 | |||||||
| chr2:157422164 | C | T | 18 | a0001c0001t0003g0008 a0001c0001t0003g0028 a0001c0001t0003g0053 others(15): Show |
22 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.547-3575G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157422164 | |||||||
| chr2:157422228 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.547-3639C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157422228 | |||||||
| chr2:157422543 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.547-3954C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157422543 | |||||||
| chr2:157422618 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.547-4029G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157422618 | |||||||
| chr2:157422670 | C | CA | 5 | a0001c0001t0001g0115 a0001c0001t0002g0012 a0001c0001t0002g0220 others(2): Show |
6 | HG02145.hp1 HG02738.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-4082dupT | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157422670 | |||||||
| chr2:157422670 | C | CAA | 22 | a0001c0001t0001g0036 a0001c0001t0003g0008 a0001c0001t0003g0028 others(19): Show |
27 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.547-4083_547-4082d others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157422670 | |||||||
| chr2:157422684 | A | G | 1 | a0001c0005t0009g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.547-4095T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157422684 | |||||||
| chr2:157422985 | A | G | 2 | a0001c0001t0002g0045 a0001c0001t0002g0047 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.546+4366T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157422985 | |||||||
| chr2:157423090 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.546+4261T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423090 | |||||||
| chr2:157423466 | T | TAAAAAAA others(299): Show |
1 | a0001c0001t0001g0040 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.546+3884_546+3885i others(308): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(298): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0024 others(2): Show |
11 | NA18612.hp1 NA18948.hp1 NA18963.hp1 others(8): Show |
intron_variant | MODIFIER | c.546+3884_546+3885i others(307): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(299): Show |
7 | a0001c0001t0001g0016 a0001c0001t0001g0150 a0001c0001t0001g0169 others(4): Show |
8 | HG00597.hp1 HG00597.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+3884_546+3885i others(308): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(300): Show |
1 | a0001c0001t0011g0043 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.546+3884_546+3885i others(309): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(301): Show |
2 | a0001c0001t0001g0017 a0001c0001t0005g0151 |
3 | HG02165.hp1 NA18967.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.546+3884_546+3885i others(310): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(307): Show |
1 | a0001c0001t0005g0202 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.546+3884_546+3885i others(316): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(309): Show |
5 | a0001c0001t0001g0098 a0001c0001t0001g0102 a0001c0001t0001g0143 others(2): Show |
5 | HG00558.hp2 HG00609.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+3884_546+3885i others(318): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(310): Show |
3 | a0001c0001t0001g0152 a0001c0001t0001g0174 a0001c0001t0007g0033 |
4 | HG00099.hp2 HG01261.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+3884_546+3885i others(319): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(311): Show |
1 | a0001c0001t0001g0089 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.546+3884_546+3885i others(320): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(312): Show |
1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.546+3884_546+3885i others(321): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(314): Show |
4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG02015.hp1 HG02015.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+3884_546+3885i others(323): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(315): Show |
2 | a0001c0001t0001g0094 a0001c0001t0005g0120 |
2 | HG03831.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.546+3884_546+3885i others(324): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(316): Show |
1 | a0001c0001t0005g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.546+3884_546+3885i others(325): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(317): Show |
1 | a0001c0001t0010g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.546+3884_546+3885i others(326): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(320): Show |
1 | a0001c0001t0001g0160 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.546+3884_546+3885i others(329): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(322): Show |
1 | a0001c0001t0001g0154 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+3884_546+3885i others(331): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(325): Show |
1 | a0002c0002t0005g0205 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.546+3884_546+3885i others(334): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(326): Show |
1 | a0001c0001t0005g0161 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.546+3884_546+3885i others(335): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(327): Show |
1 | a0001c0001t0001g0177 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.546+3884_546+3885i others(336): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(332): Show |
4 | a0001c0001t0001g0178 a0001c0001t0001g0199 a0001c0001t0001g0215 others(1): Show |
4 | HG02523.hp1 HG02602.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+3884_546+3885i others(341): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(333): Show |
2 | a0001c0001t0001g0084 a0003c0003t0001g0255 |
2 | HG02132.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.546+3884_546+3885i others(342): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(334): Show |
1 | a0001c0001t0001g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.546+3884_546+3885i others(343): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(335): Show |
1 | a0001c0001t0001g0021 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.546+3884_546+3885i others(344): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423466 | T | TAAAAAAA others(344): Show |
1 | a0001c0001t0001g0155 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.546+3884_546+3885i others(353): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423466 | |||||||
| chr2:157423474 | A | C | 26 | a0001c0001t0001g0036 a0001c0001t0002g0013 a0001c0001t0003g0008 others(23): Show |
32 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.546+3877T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423474 | |||||||
| chr2:157423842 | A | T | 1 | a0001c0005t0009g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.546+3509T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157423842 | |||||||
| chr2:157424010 | C | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0245 |
5 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+3341G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157424010 | |||||||
| chr2:157424308 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02055.hp1 HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.546+3043C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157424308 | |||||||
| chr2:157424326 | T | C | 1 | a0001c0001t0002g0013 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.546+3025A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157424326 | |||||||
| chr2:157424516 | G | GAT | 18 | a0001c0001t0001g0163 a0001c0001t0003g0008 a0001c0001t0003g0028 others(15): Show |
22 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.546+2833_546+2834d others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157424516 | |||||||
| chr2:157424518 | T | G | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.546+2833A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157424518 | |||||||
| chr2:157424646 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.546+2705G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157424646 | |||||||
| chr2:157424704 | T | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(70): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.546+2647A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157424704 | |||||||
| chr2:157424963 | T | C | 5 | a0001c0001t0002g0009 a0001c0001t0002g0245 a0001c0001t0004g0106 others(2): Show |
7 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+2388A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157424963 | |||||||
| chr2:157425147 | G | A | 11 | a0001c0001t0001g0035 a0001c0001t0001g0181 a0001c0001t0002g0009 others(8): Show |
13 | HG00609.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.546+2204C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157425147 | |||||||
| chr2:157425317 | T | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.546+2034A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157425317 | |||||||
| chr2:157425341 | A | G | 7 | a0001c0001t0001g0035 a0001c0001t0002g0009 a0001c0001t0002g0034 others(4): Show |
9 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+2010T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157425341 | |||||||
| chr2:157425471 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0002g0020 |
4 | HG02572.hp1 HG02895.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+1880T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157425471 | |||||||
| chr2:157425527 | T | C | 1 | a0001c0001t0002g0122 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.546+1824A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157425527 | |||||||
| chr2:157425570 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.546+1781T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157425570 | |||||||
| chr2:157425828 | CT | C | 17 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0039 others(14): Show |
21 | HG00544.hp1 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.546+1522delA | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157425828 | |||||||
| chr2:157426368 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.546+983G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426368 | |||||||
| chr2:157426375 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0130 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.546+976A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426375 | |||||||
| chr2:157426466 | T | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(9): Show |
18 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.546+885A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426466 | |||||||
| chr2:157426500 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.546+851G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426500 | |||||||
| chr2:157426529 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.546+822T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426529 | |||||||
| chr2:157426690 | T | C | 11 | a0001c0001t0001g0023 a0001c0001t0001g0163 a0001c0001t0001g0164 others(8): Show |
12 | HG01928.hp2 HG02132.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.546+661A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426690 | |||||||
| chr2:157426755 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.546+596G>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426755 | |||||||
| chr2:157426756 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.546+595G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426756 | |||||||
| chr2:157426787 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.546+564T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426787 | |||||||
| chr2:157426830 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.546+521A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426830 | |||||||
| chr2:157426841 | C | T | 1 | a0001c0001t0004g0003 | 5 | HG02258.hp2 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+510G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426841 | |||||||
| chr2:157426907 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.546+444T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426907 | |||||||
| chr2:157426918 | C | T | 16 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(13): Show |
26 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.546+433G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426918 | |||||||
| chr2:157426958 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.546+393C>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426958 | |||||||
| chr2:157426975 | C | T | 1 | a0002c0002t0003g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.546+376G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426975 | |||||||
| chr2:157426976 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
11 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.546+375C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157426976 | |||||||
| chr2:157427061 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.546+290T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157427061 | |||||||
| chr2:157427062 | T | C | 1 | a0002c0002t0003g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.546+289A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157427062 | |||||||
| chr2:157427198 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(204): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.546+153T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157427198 | |||||||
| chr2:157427245 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.546+106C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 6/7 | chr2 | 157427245 | |||||||
| chr2:157427424 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG03041.hp2 | splice_region_variant&intron_variant | LOW | c.477-4A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157427424 | |||||||
| chr2:157427432 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0097 |
2 | NA18968.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.477-12T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157427432 | |||||||
| chr2:157427513 | T | A | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.477-93A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157427513 | |||||||
| chr2:157427544 | C | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.477-124G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157427544 | |||||||
| chr2:157427986 | A | C | 1 | a0001c0001t0002g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.477-566T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157427986 | |||||||
| chr2:157428036 | A | G | 19 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(16): Show |
29 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.477-616T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428036 | |||||||
| chr2:157428197 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.477-777G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428197 | |||||||
| chr2:157428336 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.477-916T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428336 | |||||||
| chr2:157428377 | G | T | 3 | a0001c0001t0001g0143 a0001c0001t0001g0170 a0001c0001t0001g0174 |
3 | HG02683.hp2 HG03017.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.477-957C>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428377 | |||||||
| chr2:157428378 | C | A | 12 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0039 others(9): Show |
15 | HG00544.hp1 HG00733.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.477-958G>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428378 | |||||||
| chr2:157428486 | T | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
11 | HG00639.hp1 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.477-1066A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428486 | |||||||
| chr2:157428625 | C | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0039 others(9): Show |
15 | HG00544.hp1 HG00733.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.477-1205G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428625 | |||||||
| chr2:157428748 | A | G | 1 | a0001c0001t0002g0013 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.477-1328T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428748 | |||||||
| chr2:157428751 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.477-1331G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428751 | |||||||
| chr2:157428752 | A | T | 1 | a0001c0001t0002g0049 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.477-1332T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428752 | |||||||
| chr2:157428767 | C | T | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.477-1347G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428767 | |||||||
| chr2:157428854 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.477-1434A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428854 | |||||||
| chr2:157428865 | C | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(10): Show |
23 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.477-1445G>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428865 | |||||||
| chr2:157428947 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.477-1527C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428947 | |||||||
| chr2:157428961 | G | A | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.477-1541C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157428961 | |||||||
| chr2:157429447 | T | C | 1 | a0001c0001t0013g0259 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.476+1112A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157429447 | |||||||
| chr2:157429533 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.476+1026G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157429533 | |||||||
| chr2:157429541 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.476+1018C>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157429541 | |||||||
| chr2:157429584 | G | T | 1 | a0001c0001t0001g0135 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.476+975C>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157429584 | |||||||
| chr2:157429752 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.476+807C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157429752 | |||||||
| chr2:157429789 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.476+770C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157429789 | |||||||
| chr2:157429995 | C | T | 1 | a0001c0001t0003g0141 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.476+564G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157429995 | |||||||
| chr2:157430022 | C | CA | 17 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(14): Show |
23 | HG00621.hp2 HG01106.hp1 HG02004.hp2 others(20): Show |
intron_variant | MODIFIER | c.476+536dupT | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157430022 | |||||||
| chr2:157430022 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.476+527_476+536del others(10): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157430022 | |||||||
| chr2:157430143 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.476+416T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157430143 | |||||||
| chr2:157430250 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.476+309T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157430250 | |||||||
| chr2:157430298 | A | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(10): Show |
23 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.476+261T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157430298 | |||||||
| chr2:157430300 | A | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(10): Show |
23 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.476+259T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157430300 | |||||||
| chr2:157430424 | AC | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0079 others(4): Show |
12 | HG00741.hp2 HG01106.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.476+134delG | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157430424 | |||||||
| chr2:157430442 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.476+117C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 5/7 | chr2 | 157430442 | |||||||
| chr2:157430984 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.280-22T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157430984 | |||||||
| chr2:157431031 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.280-69A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157431031 | |||||||
| chr2:157431206 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.280-244T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157431206 | |||||||
| chr2:157431251 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.280-289A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157431251 | |||||||
| chr2:157431422 | G | A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0176 a0001c0001t0001g0188 others(1): Show |
4 | HG00323.hp2 HG02735.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-460C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157431422 | |||||||
| chr2:157431582 | TTAGGCAC others(3): Show |
T | 1 | a0001c0001t0002g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.280-630_280-621del others(10): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157431582 | |||||||
| chr2:157431757 | A | T | 3 | a0001c0001t0001g0066 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02280.hp2 HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.280-795T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157431757 | |||||||
| chr2:157431950 | A | G | 11 | a0001c0001t0001g0247 a0001c0001t0003g0053 a0001c0001t0013g0259 others(8): Show |
11 | HG00609.hp1 HG00738.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.280-988T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157431950 | |||||||
| chr2:157432146 | T | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(9): Show |
18 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.280-1184A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157432146 | |||||||
| chr2:157432388 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0216 a0001c0001t0001g0217 |
5 | HG00423.hp2 HG00621.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-1426C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157432388 | |||||||
| chr2:157432393 | A | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(9): Show |
18 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.280-1431T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157432393 | |||||||
| chr2:157432468 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.280-1506A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157432468 | |||||||
| chr2:157432735 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.279+1635G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157432735 | |||||||
| chr2:157432789 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0189 |
2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.279+1581C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157432789 | |||||||
| chr2:157432987 | T | G | 8 | a0002c0002t0001g0052 a0002c0002t0001g0204 a0002c0002t0001g0207 others(5): Show |
8 | HG00609.hp1 HG04184.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+1383A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157432987 | |||||||
| chr2:157433009 | C | A | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.279+1361G>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433009 | |||||||
| chr2:157433013 | T | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0239 |
2 | NA18951.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.279+1357A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433013 | |||||||
| chr2:157433026 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.279+1344T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433026 | |||||||
| chr2:157433246 | C | T | 2 | a0001c0001t0002g0069 a0001c0001t0002g0076 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.279+1124G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433246 | |||||||
| chr2:157433305 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
5 | HG00639.hp1 HG02258.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+1065G>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433305 | |||||||
| chr2:157433346 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.279+1024A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433346 | |||||||
| chr2:157433407 | A | ATAAAACA others(22): Show |
1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.279+934_279+962dup others(29): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433407 | |||||||
| chr2:157433605 | A | C | 13 | a0001c0001t0001g0110 a0001c0001t0002g0002 a0001c0001t0002g0018 others(10): Show |
18 | HG02004.hp2 HG02486.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.279+765T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433605 | |||||||
| chr2:157433645 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.279+725A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433645 | |||||||
| chr2:157433777 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0002g0020 |
4 | HG02572.hp1 HG02895.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+593G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433777 | |||||||
| chr2:157433797 | A | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(9): Show |
18 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.279+573T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433797 | |||||||
| chr2:157433957 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.279+413A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157433957 | |||||||
| chr2:157434018 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.279+352T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157434018 | |||||||
| chr2:157434089 | G | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(10): Show |
23 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.279+281C>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157434089 | |||||||
| chr2:157434183 | T | G | 1 | a0001c0001t0003g0095 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.279+187A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157434183 | |||||||
| chr2:157434293 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.279+77A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157434293 | |||||||
| chr2:157434320 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+50G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 3/7 | chr2 | 157434320 | |||||||
| chr2:157434541 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(24): Show |
43 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.225-117C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 2/7 | chr2 | 157434541 | |||||||
| chr2:157434595 | T | TAG | 199 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.224+101_224+102dup others(2): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 2/7 | chr2 | 157434595 | |||||||
| chr2:157434595 | T | TAGAG | 3 | a0001c0001t0001g0021 a0001c0001t0002g0012 a0001c0001t0002g0180 |
5 | HG01069.hp1 HG01071.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+99_224+102dupC others(3): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 2/7 | chr2 | 157434595 | |||||||
| chr2:157434676 | A | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(202): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.224+22T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 2/7 | chr2 | 157434676 | |||||||
| chr2:157434812 | A | ATC | 9 | a0001c0001t0001g0027 a0001c0001t0001g0067 a0001c0001t0001g0078 others(6): Show |
10 | HG00544.hp1 HG00639.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.175-67_175-66dupGA | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434812 | |||||||
| chr2:157434812 | A | ATCTCTCT others(3): Show |
1 | a0001c0001t0001g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.175-75_175-66dupGA others(8): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434812 | |||||||
| chr2:157434812 | ATC | A | 30 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(27): Show |
34 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.175-67_175-66delGA | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434812 | |||||||
| chr2:157434812 | ATCTC | A | 20 | a0001c0001t0001g0025 a0001c0001t0001g0055 a0001c0001t0001g0060 others(17): Show |
21 | HG00323.hp1 HG00558.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.175-69_175-66delGA others(2): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434812 | |||||||
| chr2:157434812 | ATCTCTC | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0117 a0001c0001t0001g0129 others(5): Show |
10 | HG00140.hp2 HG00738.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.175-71_175-66delGA others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434812 | |||||||
| chr2:157434812 | ATCTCTCT others(1): Show |
A | 7 | a0001c0001t0001g0243 a0001c0001t0002g0044 a0001c0001t0002g0047 others(4): Show |
7 | HG02004.hp2 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-73_175-66delGA others(6): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434812 | |||||||
| chr2:157434812 | ATCTCTCT others(3): Show |
A | 1 | a0001c0001t0008g0134 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.175-75_175-66delGA others(8): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434812 | |||||||
| chr2:157434837 | T | C | 3 | a0001c0001t0001g0066 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02280.hp2 HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.175-90A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434837 | |||||||
| chr2:157434837 | TCTCTCTC others(17): Show |
T | 1 | a0002c0002t0003g0203 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.175-114_175-91delT others(23): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434837 | |||||||
| chr2:157434839 | TCTCTCTC others(5): Show |
T | 8 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0104 others(5): Show |
13 | HG02486.hp2 HG02896.hp1 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.175-104_175-93delT others(11): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434839 | |||||||
| chr2:157434839 | TCTCTCTC others(9): Show |
T | 1 | a0001c0001t0002g0133 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.175-108_175-93delT others(15): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434839 | |||||||
| chr2:157434839 | TCTCTCTC others(13): Show |
T | 1 | a0002c0002t0003g0051 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.175-112_175-93delT others(19): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434839 | |||||||
| chr2:157434841 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.175-94A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434841 | |||||||
| chr2:157434841 | TCTCTCTC others(3): Show |
T | 1 | a0001c0001t0002g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.175-104_175-95delT others(9): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434841 | |||||||
| chr2:157434841 | TCTCTCTC others(7): Show |
T | 2 | a0001c0001t0006g0048 a0001c0001t0006g0197 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.175-108_175-95delT others(13): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434841 | |||||||
| chr2:157434841 | TCTCTCTC others(9): Show |
T | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0002g0009 others(3): Show |
8 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-110_175-95delT others(15): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434841 | |||||||
| chr2:157434841 | TCTCTCTC others(11): Show |
T | 1 | a0002c0002t0001g0204 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.175-112_175-95delT others(17): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434841 | |||||||
| chr2:157434841 | TCTCTCTC others(13): Show |
T | 5 | a0002c0002t0001g0052 a0002c0002t0001g0207 a0002c0002t0003g0206 others(2): Show |
5 | HG00609.hp1 HG04184.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-114_175-95delT others(19): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434841 | |||||||
| chr2:157434843 | T | A | 1 | a0001c0001t0002g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.175-96A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434843 | |||||||
| chr2:157434843 | T | TCA | 3 | a0001c0001t0001g0168 a0001c0001t0002g0156 a0001c0001t0002g0240 |
3 | HG01099.hp1 HG01123.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.175-97_175-96insTG | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434843 | |||||||
| chr2:157434843 | TCTCTCTC others(3): Show |
T | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.175-106_175-97delT others(9): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434843 | |||||||
| chr2:157434843 | TCTCTCTC others(15): Show |
T | 1 | a0001c0004t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.175-118_175-97delT others(21): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434843 | |||||||
| chr2:157434845 | T | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0074 a0001c0001t0001g0116 others(14): Show |
17 | HG01099.hp1 HG01123.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.175-98A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434845 | |||||||
| chr2:157434845 | T | TCA | 16 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0160 others(13): Show |
19 | HG00673.hp2 HG01346.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.175-99_175-98insTG | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434845 | |||||||
| chr2:157434845 | T | TCACA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0091 others(13): Show |
19 | HG00621.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.175-99_175-98insTG others(2): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434845 | |||||||
| chr2:157434845 | T | TCACACA | 4 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0167 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-99_175-98insTG others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434845 | |||||||
| chr2:157434845 | T | TCACACAC others(3): Show |
1 | a0001c0001t0001g0084 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.175-99_175-98insTG others(8): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434845 | |||||||
| chr2:157434845 | TCTCTCA | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0041 others(1): Show |
4 | HG00738.hp2 HG01255.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-104_175-99delT others(5): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434845 | |||||||
| chr2:157434845 | TCTCTCAC others(3): Show |
T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0154 a0001c0001t0002g0020 |
5 | HG02572.hp1 HG02895.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-108_175-99delT others(9): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434845 | |||||||
| chr2:157434845 | TCTCTCAC others(7): Show |
T | 1 | a0001c0001t0002g0013 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.175-112_175-99delT others(13): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434845 | |||||||
| chr2:157434845 | TCTCTCAC others(9): Show |
T | 1 | a0001c0001t0002g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.175-114_175-99delT others(15): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434845 | |||||||
| chr2:157434847 | T | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
97 | HG00621.hp2 HG00639.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.175-100A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434847 | |||||||
| chr2:157434847 | T | TCA | 10 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(7): Show |
12 | HG01256.hp2 HG01496.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.175-101_175-100ins others(2): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434847 | |||||||
| chr2:157434847 | T | TCACA | 8 | a0001c0001t0001g0010 a0001c0001t0001g0082 a0001c0001t0001g0143 others(5): Show |
8 | HG00423.hp1 HG00423.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.175-101_175-100ins others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434847 | |||||||
| chr2:157434847 | T | TCACACA | 6 | a0001c0001t0001g0102 a0001c0001t0002g0175 a0001c0001t0004g0248 others(3): Show |
7 | HG00558.hp2 HG02132.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-101_175-100ins others(6): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434847 | |||||||
| chr2:157434847 | T | TCACACAC others(3): Show |
1 | a0001c0001t0001g0016 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.175-101_175-100ins others(10): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434847 | |||||||
| chr2:157434847 | TCTCA | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0158 others(2): Show |
6 | HG00544.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-104_175-101del others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434847 | |||||||
| chr2:157434847 | TCTCACAC others(3): Show |
T | 1 | a0001c0001t0004g0003 | 5 | HG02258.hp2 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-110_175-101del others(10): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434847 | |||||||
| chr2:157434847 | TCTCACAC others(21): Show |
T | 1 | a0001c0001t0001g0005 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.175-128_175-101del others(28): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434847 | |||||||
| chr2:157434849 | T | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.175-102A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434849 | |||||||
| chr2:157434849 | T | TCA | 6 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG00597.hp2 HG01192.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-104_175-103dup others(2): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434849 | |||||||
| chr2:157434849 | T | TCACA | 5 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0115 others(2): Show |
5 | HG01099.hp2 HG02738.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-106_175-103dup others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434849 | |||||||
| chr2:157434849 | T | TCTCTCAC others(3): Show |
1 | a0001c0001t0001g0169 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.175-103_175-102ins others(10): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434849 | |||||||
| chr2:157434849 | T | TCTCTCAC others(5): Show |
1 | a0001c0001t0002g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.175-103_175-102ins others(12): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434849 | |||||||
| chr2:157434849 | T | TCTCTCTC others(1): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0032 |
6 | HG01255.hp1 HG01256.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-103_175-102ins others(8): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434849 | |||||||
| chr2:157434849 | T | TCTCTCTC others(3): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0250 |
2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.175-103_175-102ins others(10): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434849 | |||||||
| chr2:157434849 | TCA | T | 4 | a0001c0001t0001g0066 a0001c0001t0001g0089 a0001c0001t0001g0199 others(1): Show |
4 | HG00140.hp1 HG02071.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-104_175-103del others(2): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434849 | |||||||
| chr2:157434849 | TCACA | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0142 |
4 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-106_175-103del others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434849 | |||||||
| chr2:157434849 | TCACACAC others(3): Show |
T | 1 | a0001c0001t0006g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.175-112_175-103del others(10): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434849 | |||||||
| chr2:157434851 | A | T | 8 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0100 others(5): Show |
8 | HG02015.hp1 HG02293.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.175-104T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434851 | |||||||
| chr2:157434853 | A | T | 5 | a0001c0001t0001g0066 a0001c0001t0001g0078 a0001c0001t0001g0100 others(2): Show |
5 | HG02280.hp2 HG02965.hp2 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-106T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434853 | |||||||
| chr2:157434855 | A | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0066 |
3 | HG02258.hp1 HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.175-108T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434855 | |||||||
| chr2:157434857 | A | T | 2 | a0001c0001t0001g0014 a0001c0001t0002g0196 |
3 | HG02258.hp1 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.175-110T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434857 | |||||||
| chr2:157434859 | A | T | 2 | a0001c0001t0002g0112 a0001c0001t0002g0196 |
2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.175-112T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434859 | |||||||
| chr2:157434900 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.175-153T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157434900 | |||||||
| chr2:157435004 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(24): Show |
43 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.175-257C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157435004 | |||||||
| chr2:157435027 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0032 others(24): Show |
43 | HG00639.hp1 HG00741.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.175-280C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157435027 | |||||||
| chr2:157435193 | A | C | 19 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0002g0002 others(16): Show |
25 | HG02004.hp2 HG02280.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-446T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157435193 | |||||||
| chr2:157435546 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.175-799G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157435546 | |||||||
| chr2:157435628 | C | T | 32 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0067 others(29): Show |
43 | HG00609.hp1 HG00639.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.175-881G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157435628 | |||||||
| chr2:157435779 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.175-1032C>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157435779 | |||||||
| chr2:157435791 | G | T | 12 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0104 others(9): Show |
17 | HG02004.hp2 HG02486.hp2 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.175-1044C>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157435791 | |||||||
| chr2:157435806 | GC | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0195 |
3 | HG01069.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.175-1060delG | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157435806 | |||||||
| chr2:157435938 | A | C | 1 | a0001c0001t0001g0099 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.175-1191T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157435938 | |||||||
| chr2:157435963 | A | C | 2 | a0001c0001t0001g0247 a0001c0001t0013g0259 |
2 | HG00738.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.175-1216T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157435963 | |||||||
| chr2:157436441 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02280.hp2 HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.175-1694G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157436441 | |||||||
| chr2:157436583 | C | CTA | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0232 others(1): Show |
4 | HG02809.hp1 HG02886.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-1838_175-1837d others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157436583 | |||||||
| chr2:157436903 | GA | G | 7 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0002g0009 others(4): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.175-2157delT | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157436903 | |||||||
| chr2:157437014 | A | C | 1 | a0001c0001t0003g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.175-2267T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437014 | |||||||
| chr2:157437122 | A | G | 1 | a0001c0001t0002g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.175-2375T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437122 | |||||||
| chr2:157437135 | G | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.175-2388C>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437135 | |||||||
| chr2:157437144 | A | T | 2 | a0001c0001t0002g0196 a0001c0001t0006g0064 |
2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.175-2397T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437144 | |||||||
| chr2:157437150 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.175-2403C>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437150 | |||||||
| chr2:157437163 | T | A | 1 | a0006c0008t0001g0137 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.175-2416A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437163 | |||||||
| chr2:157437220 | T | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0219 |
2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.175-2473A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437220 | |||||||
| chr2:157437238 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.175-2491T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437238 | |||||||
| chr2:157437371 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.175-2624T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437371 | |||||||
| chr2:157437506 | G | T | 14 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0018 others(11): Show |
20 | HG02004.hp2 HG02486.hp2 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.175-2759C>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437506 | |||||||
| chr2:157437625 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG02280.hp2 HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.175-2878C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437625 | |||||||
| chr2:157437677 | C | A | 1 | a0001c0001t0002g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.175-2930G>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437677 | |||||||
| chr2:157437695 | T | C | 1 | a0001c0001t0002g0221 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.175-2948A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437695 | |||||||
| chr2:157437698 | C | CA | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(204): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.175-2952dupT | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437698 | |||||||
| chr2:157437710 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0218 a0001c0001t0011g0043 |
3 | HG03654.hp1 HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.175-2963C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437710 | |||||||
| chr2:157437711 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.175-2964T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437711 | |||||||
| chr2:157437792 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.175-3045A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437792 | |||||||
| chr2:157437919 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3172A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437919 | |||||||
| chr2:157437930 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3183C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437930 | |||||||
| chr2:157437932 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3185T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437932 | |||||||
| chr2:157437941 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3194G>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437941 | |||||||
| chr2:157437944 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3197G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437944 | |||||||
| chr2:157437947 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3200G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437947 | |||||||
| chr2:157437948 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3201A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437948 | |||||||
| chr2:157437951 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3204C>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437951 | |||||||
| chr2:157437952 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3205C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437952 | |||||||
| chr2:157437953 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3206T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437953 | |||||||
| chr2:157437954 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3207C>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437954 | |||||||
| chr2:157437959 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3212C>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437959 | |||||||
| chr2:157437963 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3216C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437963 | |||||||
| chr2:157437964 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3217C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437964 | |||||||
| chr2:157437973 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3226G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437973 | |||||||
| chr2:157437975 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3228T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437975 | |||||||
| chr2:157437984 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3237T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437984 | |||||||
| chr2:157437986 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3239T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437986 | |||||||
| chr2:157437996 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3249G>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437996 | |||||||
| chr2:157437997 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3250T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157437997 | |||||||
| chr2:157438006 | C | T | 2 | a0001c0001t0002g0220 a0002c0002t0003g0051 |
2 | HG03139.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.175-3259G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438006 | |||||||
| chr2:157438013 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3266G>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438013 | |||||||
| chr2:157438014 | CACTACTG others(12): Show |
C | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3286_175-3268d others(21): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438014 | |||||||
| chr2:157438037 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-3290C>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438037 | |||||||
| chr2:157438056 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.175-3309C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438056 | |||||||
| chr2:157438308 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG00673.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.175-3561C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438308 | |||||||
| chr2:157438676 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.175-3929C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438676 | |||||||
| chr2:157438677 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.175-3930A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438677 | |||||||
| chr2:157438730 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.175-3983T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438730 | |||||||
| chr2:157438887 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.175-4140A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438887 | |||||||
| chr2:157438892 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.175-4145T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438892 | |||||||
| chr2:157438996 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.175-4249G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157438996 | |||||||
| chr2:157439057 | A | G | 1 | a0001c0005t0009g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.175-4310T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439057 | |||||||
| chr2:157439115 | T | G | 1 | a0001c0001t0002g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.175-4368A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439115 | |||||||
| chr2:157439140 | T | A | 1 | a0001c0001t0001g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.175-4393A>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439140 | |||||||
| chr2:157439180 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.175-4433T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439180 | |||||||
| chr2:157439278 | T | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0193 |
2 | HG01109.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.175-4531A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439278 | |||||||
| chr2:157439287 | C | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0078 others(6): Show |
14 | HG00741.hp2 HG01106.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.175-4540G>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439287 | |||||||
| chr2:157439384 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0002g0020 |
4 | HG02572.hp1 HG02895.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+4463A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439384 | |||||||
| chr2:157439393 | C | T | 15 | a0001c0001t0001g0077 a0001c0001t0002g0002 a0001c0001t0002g0013 others(12): Show |
21 | HG02004.hp2 HG02486.hp2 HG02647.hp2 others(18): Show |
intron_variant | MODIFIER | c.174+4454G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439393 | |||||||
| chr2:157439570 | T | G | 1 | a0001c0001t0001g0066 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.174+4277A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439570 | |||||||
| chr2:157439616 | G | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
11 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+4231C>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439616 | |||||||
| chr2:157439746 | G | A | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | HG00140.hp2 HG00738.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+4101C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439746 | |||||||
| chr2:157439798 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(253): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.174+4049A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439798 | |||||||
| chr2:157439812 | T | C | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0002g0009 others(7): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.174+4035A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157439812 | |||||||
| chr2:157440091 | C | A | 1 | a0001c0001t0004g0109 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.174+3756G>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157440091 | |||||||
| chr2:157440255 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.174+3592G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157440255 | |||||||
| chr2:157440268 | A | G | 23 | a0001c0001t0001g0019 a0001c0001t0001g0065 a0001c0001t0001g0066 others(20): Show |
31 | HG02004.hp2 HG02109.hp1 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.174+3579T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157440268 | |||||||
| chr2:157440288 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.174+3559T>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157440288 | |||||||
| chr2:157440380 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.174+3467G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157440380 | |||||||
| chr2:157440421 | C | A | 1 | a0001c0001t0002g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.174+3426G>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157440421 | |||||||
| chr2:157440764 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.174+3083C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157440764 | |||||||
| chr2:157441090 | CTAA | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.174+2754_174+2756d others(5): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441090 | |||||||
| chr2:157441379 | C | T | 1 | a0001c0001t0006g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.174+2468G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441379 | |||||||
| chr2:157441426 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.174+2421T>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441426 | |||||||
| chr2:157441593 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.174+2254A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441593 | |||||||
| chr2:157441603 | TAC | T | 21 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0123 others(18): Show |
24 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.174+2242_174+2243d others(4): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441603 | |||||||
| chr2:157441603 | TACAC | T | 28 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0001g0041 others(25): Show |
39 | HG00733.hp2 HG02004.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.174+2240_174+2243d others(6): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441603 | |||||||
| chr2:157441603 | TACACACA others(1): Show |
T | 39 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(36): Show |
48 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.174+2236_174+2243d others(10): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441603 | |||||||
| chr2:157441603 | TACACACA others(3): Show |
T | 24 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(21): Show |
25 | HG00639.hp1 HG00738.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.174+2234_174+2243d others(12): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441603 | |||||||
| chr2:157441603 | TACACACA others(5): Show |
T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0209 others(2): Show |
5 | HG01070.hp2 HG01074.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+2232_174+2243d others(14): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441603 | |||||||
| chr2:157441603 | TACACACA others(7): Show |
T | 10 | a0001c0001t0001g0208 a0001c0001t0003g0053 a0001c0001t0005g0202 others(7): Show |
10 | HG00609.hp1 HG04184.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.174+2230_174+2243d others(16): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441603 | |||||||
| chr2:157441633 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.174+2214G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441633 | |||||||
| chr2:157441639 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.174+2208G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441639 | |||||||
| chr2:157441763 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.174+2084A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441763 | |||||||
| chr2:157441891 | A | G | 5 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+1956T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157441891 | |||||||
| chr2:157442033 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0011g0043 |
3 | HG01175.hp1 HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.174+1814G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157442033 | |||||||
| chr2:157442118 | T | C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(2): Show |
7 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+1729A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157442118 | |||||||
| chr2:157442395 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0249 others(3): Show |
11 | HG00741.hp2 HG01192.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+1452C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157442395 | |||||||
| chr2:157442472 | CA | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(205): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.174+1374delT | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157442472 | |||||||
| chr2:157442554 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.174+1293C>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157442554 | |||||||
| chr2:157442735 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(224): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.174+1112G>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157442735 | |||||||
| chr2:157442776 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.174+1071T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157442776 | |||||||
| chr2:157442838 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0002g0038 |
2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.174+1009T>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157442838 | |||||||
| chr2:157442868 | G | A | 2 | a0001c0001t0006g0031 a0001c0001t0006g0246 |
3 | HG02615.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.174+979C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157442868 | |||||||
| chr2:157442903 | T | G | 2 | a0001c0001t0001g0247 a0001c0001t0004g0248 |
2 | HG01361.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.174+944A>C | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157442903 | |||||||
| chr2:157442953 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.174+894C>T | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157442953 | |||||||
| chr2:157443180 | G | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(2): Show |
7 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+667C>A | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157443180 | |||||||
| chr2:157443338 | C | CAA | 6 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0249 others(3): Show |
11 | HG00741.hp2 HG01192.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+507_174+508dup others(2): Show |
CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157443338 | |||||||
| chr2:157443572 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.174+275A>G | CYTIP | ENSG00000115165.10 | transcript | ENST00000264192.8 | protein_coding | 1/7 | chr2 | 157443572 |