Variant report
Variant | rs73060168 |
---|---|
Chromosome Location | chr1:192611312-192611313 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:61)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:192611292-192611342 | GM06990 | blood: | n/a |
2 | chr1:192611292-192611342 | AG09319 | gingival: | n/a |
3 | chr1:192611292-192611342 | GM19239 | blood: | n/a |
4 | chr1:192611292-192611342 | ovcar-3 | ovarian: | n/a |
5 | chr1:192611292-192611342 | AG10803 | skin: | n/a |
6 | chr1:192611292-192611342 | HAEpiC | amniotic membrane: | n/a |
7 | chr1:192611292-192611342 | HPAEpiC | pulmonary alveolar: | n/a |
8 | chr1:192611292-192611342 | AG09309 | skin: | n/a |
9 | chr1:192611292-192611342 | HepG2 | liver: | n/a |
10 | chr1:192611292-192611342 | MCF-7 | breast: | n/a |
11 | chr1:192611292-192611342 | LNCaP | prostate: | n/a |
12 | chr1:192611292-192611342 | NHDF-neo | bronchial: | n/a |
13 | chr1:192611292-192611342 | NT2-D1 | testis: | n/a |
14 | chr1:192611292-192611342 | BJ | skin: | n/a |
15 | chr1:192611292-192611342 | HEEpiC | esophagus: | n/a |
16 | chr1:192611292-192611342 | HCT-116 | colon: | n/a |
17 | chr1:192611292-192611342 | SK-N-SH_RA | brain: | n/a |
18 | chr1:192611292-192611342 | HCPEpiC | choroid plexus: | n/a |
19 | chr1:192611292-192611342 | HL-60 | blood: | n/a |
20 | chr1:192611292-192611342 | CMK | blood: | n/a |
21 | chr1:192611292-192611342 | RPTEC | kidney: | n/a |
22 | chr1:192611292-192611342 | PFSK-1 | brain: | n/a |
23 | chr1:192611292-192611342 | NHBE | bronchial: | n/a |
24 | chr1:192611292-192611342 | BE2_C | brain: | n/a |
25 | chr1:192611292-192611342 | A549 | lung: | n/a |
26 | chr1:192611292-192611342 | HEK293 | kidney: | embryo |
27 | chr1:192611292-192611342 | NB4 | blood: | n/a |
28 | chr1:192611292-192611342 | Hepatocyte | liver: | n/a |
29 | chr1:192611292-192611342 | GM12878 | blood: | n/a |
30 | chr1:192611292-192611342 | Jurkat | blood: | n/a |
31 | chr1:192611292-192611342 | H1-hESC | embryonic stem cell: | embryo |
32 | chr1:192611292-192611342 | PANC-1 | pancreas: | n/a |
33 | chr1:192611292-192611342 | T-47D | breast: | n/a |
34 | chr1:192611292-192611342 | SK-N-MC | brain: | n/a |
35 | chr1:192611292-192611342 | HIPEpiC | eye: | n/a |
36 | chr1:192611292-192611342 | HUVEC | blood vessel: | n/a |
37 | chr1:192611292-192611342 | AG04450 | lung: | fetal |
38 | chr1:192611292-192611342 | AoSMC | blood vessel: | n/a |
39 | chr1:192611292-192611342 | HMEC | breast: | n/a |
40 | chr1:192611292-192611342 | AG04449 | skin: | fetal |
41 | chr1:192611292-192611342 | GM12891 | blood: | n/a |
42 | chr1:192611292-192611342 | ECC-1 | luminal epithelium: | n/a |
43 | chr1:192611292-192611342 | ProgFib | skin: | n/a |
44 | chr1:192611292-192611342 | HCM | heart: | n/a |
45 | chr1:192611292-192611342 | PrEC | prostate: | n/a |
46 | chr1:192611292-192611342 | K562 | blood: | n/a |
47 | chr1:192611292-192611342 | HRCEpiC | kidney: | n/a |
48 | chr1:192611292-192611342 | IMR90 | lung: | fetal |
49 | chr1:192611292-192611342 | SAEC | small airway: | n/a |
50 | chr1:192611292-192611342 | NH-A | brain: | n/a |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
RGS13 | CpG island |
rs_ID | r2[population] |
---|---|
rs10157757 | 1.00[EUR][1000 genomes] |
rs10489515 | 1.00[EUR][1000 genomes] |
rs10489517 | 1.00[EUR][1000 genomes] |
rs10921269 | 1.00[EUR][1000 genomes] |
rs1342808 | 1.00[EUR][1000 genomes] |
rs1418719 | 1.00[EUR][1000 genomes] |
rs16834594 | 1.00[EUR][1000 genomes] |
rs16834597 | 1.00[EUR][1000 genomes] |
rs16834625 | 1.00[EUR][1000 genomes] |
rs16834852 | 1.00[EUR][1000 genomes] |
rs16834867 | 1.00[EUR][1000 genomes] |
rs16834872 | 1.00[EUR][1000 genomes] |
rs16834876 | 1.00[EUR][1000 genomes] |
rs41512544 | 1.00[EUR][1000 genomes] |
rs55747130 | 1.00[EUR][1000 genomes] |
rs56031935 | 1.00[EUR][1000 genomes] |
rs57189481 | 1.00[EUR][1000 genomes] |
rs57630083 | 1.00[EUR][1000 genomes] |
rs57963116 | 1.00[EUR][1000 genomes] |
rs60569899 | 1.00[AFR][1000 genomes] |
rs6680350 | 1.00[EUR][1000 genomes] |
rs6683145 | 1.00[EUR][1000 genomes] |
rs6689962 | 1.00[EUR][1000 genomes] |
rs6702235 | 1.00[EUR][1000 genomes] |
rs6702236 | 1.00[EUR][1000 genomes] |
rs73060161 | 1.00[AFR][1000 genomes] |
rs73060162 | 1.00[AFR][1000 genomes] |
rs73060166 | 1.00[AFR][1000 genomes] |
rs73060190 | 1.00[EUR][1000 genomes] |
rs73062239 | 1.00[EUR][1000 genomes] |
rs73062264 | 1.00[EUR][1000 genomes] |
rs73062267 | 1.00[EUR][1000 genomes] |
rs73062271 | 1.00[EUR][1000 genomes] |
rs73062273 | 1.00[EUR][1000 genomes] |
rs73062285 | 1.00[EUR][1000 genomes] |
rs73062286 | 1.00[EUR][1000 genomes] |
rs73062290 | 1.00[EUR][1000 genomes] |
rs73064112 | 1.00[EUR][1000 genomes] |
rs74130451 | 1.00[EUR][1000 genomes] |
rs74130466 | 1.00[EUR][1000 genomes] |
rs7538953 | 1.00[EUR][1000 genomes] |
rs7552270 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532618 | chr1:192537006-193149179 | Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 70 gene(s) | inside rSNPs | diseases |
2 | nsv467005 | chr1:192549912-192625360 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv548659 | chr1:192549912-192625360 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv548660 | chr1:192609268-192945348 | Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 22 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:192600200-192620400 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr1:192609600-192614000 | Weak transcription | Ovary | ovary |
3 | chr1:192609800-192613000 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
4 | chr1:192609800-192613400 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |