Variant report

Variant	rs531077131
Chromosome Location	chr1:185785057-185785058
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv548398	chr1:185136458-186003094	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
2	esv3424090	chr1:185679718-186270877	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	esv3505065	chr1:185782529-185786377	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3505059	chr1:185782923-185785823	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2563566	chr1:185783040-185786062	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3505058	chr1:185783079-185786327	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3320936	chr1:185783378-185785589	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv2347927	chr1:185783525-185785498	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv13927	chr1:185783571-185785361	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3320935	chr1:185783576-185785401	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3505056	chr1:185783608-185785406	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3505060	chr1:185783621-185785379	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3505061	chr1:185783628-185785334	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3320938	chr1:185783632-185785367	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3320937	chr1:185783655-185785320	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3505055	chr1:185783656-185785349	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3505057	chr1:185783658-185785345	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3320934	chr1:185783699-185785302	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3505064	chr1:185783709-185785302	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3320939	chr1:185783713-185785300	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv3505066	chr1:185783713-185785300	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185781000-185785200	Weak transcription	NHDF-Ad	bronchial
2	chr1:185782800-185787800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:185783600-185785400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:185785000-185787200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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