Variant report
Variant | rs56122790 |
---|---|
Chromosome Location | chr9:103176747-103176748 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:5)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:5 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr9:103168940..103170957-chr9:103175150..103176898,2 | K562 | blood: | |
2 | chr9:103171653..103179256-chr9:103186952..103193020,13 | MCF-7 | breast: | |
3 | chr9:103174960..103177942-chr9:103180157..103183043,3 | K562 | blood: | |
4 | chr9:103174411..103177226-chr9:103182335..103184349,2 | K562 | blood: | |
5 | chr9:103115166..103116974-chr9:103176601..103179072,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000136891 | Chromatin interaction |
ENSG00000066697 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1041565 | 0.88[ASN][1000 genomes] |
rs10465118 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10465119 | 0.95[EUR][1000 genomes] |
rs10465145 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10512270 | 0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10512271 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10819774 | 1.00[ASN][1000 genomes] |
rs10819775 | 0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10819776 | 0.91[ASN][1000 genomes] |
rs10819779 | 0.86[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10819781 | 0.95[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10819782 | 0.89[ASN][1000 genomes] |
rs10819785 | 0.88[ASN][1000 genomes] |
rs10819786 | 0.88[ASN][1000 genomes] |
rs10819787 | 0.88[ASN][1000 genomes] |
rs10819788 | 0.88[ASN][1000 genomes] |
rs10989085 | 0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10989090 | 0.88[ASN][1000 genomes] |
rs10989091 | 0.86[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10989092 | 0.91[ASN][1000 genomes] |
rs10989093 | 0.88[ASN][1000 genomes] |
rs10989094 | 0.91[ASN][1000 genomes] |
rs10989095 | 0.86[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10989097 | 0.89[ASN][1000 genomes] |
rs10989099 | 0.86[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10989103 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10989105 | 0.88[ASN][1000 genomes] |
rs10989107 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10989108 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10989111 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10989112 | 0.88[ASN][1000 genomes] |
rs10989113 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10989114 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10989115 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10989120 | 0.88[ASN][1000 genomes] |
rs10989123 | 0.88[ASN][1000 genomes] |
rs10989124 | 0.95[EUR][1000 genomes] |
rs10989131 | 0.95[EUR][1000 genomes] |
rs10989134 | 0.82[EUR][1000 genomes] |
rs10989140 | 0.95[EUR][1000 genomes] |
rs10989144 | 0.95[EUR][1000 genomes] |
rs10989145 | 0.95[EUR][1000 genomes] |
rs10989147 | 0.95[EUR][1000 genomes] |
rs10989150 | 0.95[EUR][1000 genomes] |
rs10989151 | 0.95[EUR][1000 genomes] |
rs10989154 | 0.95[EUR][1000 genomes] |
rs11793014 | 0.88[ASN][1000 genomes] |
rs12004257 | 0.90[ASN][1000 genomes] |
rs12005378 | 0.80[ASN][1000 genomes] |
rs12056981 | 0.95[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12057047 | 0.88[ASN][1000 genomes] |
rs12236071 | 0.95[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12236952 | 0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12237166 | 0.89[ASN][1000 genomes] |
rs12237481 | 0.95[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12238560 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12682741 | 0.95[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12683122 | 0.95[EUR][1000 genomes] |
rs12683548 | 0.86[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12684454 | 0.89[ASN][1000 genomes] |
rs13286805 | 0.88[ASN][1000 genomes] |
rs13292589 | 0.88[ASN][1000 genomes] |
rs16919136 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs16919174 | 0.95[EUR][1000 genomes] |
rs1930245 | 0.89[ASN][1000 genomes] |
rs1930246 | 0.89[ASN][1000 genomes] |
rs2183990 | 1.00[ASN][1000 genomes] |
rs2183991 | 1.00[ASN][1000 genomes] |
rs2274881 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs34471402 | 0.88[ASN][1000 genomes] |
rs55827987 | 0.95[EUR][1000 genomes] |
rs56012200 | 0.86[EUR][1000 genomes] |
rs56020062 | 0.86[EUR][1000 genomes] |
rs56050588 | 0.86[EUR][1000 genomes] |
rs56163523 | 0.95[EUR][1000 genomes] |
rs56170030 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs59611728 | 0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs7024666 | 0.86[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs7034154 | 0.89[ASN][1000 genomes] |
rs7041933 | 0.89[ASN][1000 genomes] |
rs7042669 | 0.88[ASN][1000 genomes] |
rs7046659 | 0.89[ASN][1000 genomes] |
rs7049241 | 0.88[ASN][1000 genomes] |
rs72735107 | 0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72735110 | 1.00[ASN][1000 genomes] |
rs72735119 | 0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs72735122 | 0.82[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs72735140 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs72735148 | 0.95[EUR][1000 genomes] |
rs72735154 | 0.95[EUR][1000 genomes] |
rs7869933 | 0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv893623 | chr9:102648036-103405197 | Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 51 gene(s) | inside rSNPs | diseases |
2 | nsv825012 | chr9:103152205-103256281 | Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:103174600-103176800 | Weak transcription | Placenta | Placenta |
2 | chr9:103174600-103177000 | Weak transcription | Right Atrium | heart |
3 | chr9:103174600-103188800 | Weak transcription | Esophagus | oesophagus |
4 | chr9:103174800-103177600 | Weak transcription | Rectal Smooth Muscle | rectum |
5 | chr9:103175600-103176800 | Enhancers | K562 | blood |