Variant report

Variant	rs567762093
Chromosome Location	chr2:206128018-206128019
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998485	chr2:205407813-206184006	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv536122	chr2:205407813-206184006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1012780	chr2:206124954-206546271	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv1833855	chr2:206125313-206129806	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv1840166	chr2:206127438-206129806	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
6	esv3459020	chr2:206127621-206130132	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
7	esv3459021	chr2:206127897-206129976	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
8	nsv819159	chr2:206127941-206129943	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
9	esv3459018	chr2:206127951-206129941	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
10	esv3459017	chr2:206127954-206129938	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
11	esv3459022	chr2:206127970-206129885	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
12	esv3459023	chr2:206127970-206129885	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
13	nsv821879	chr2:206128007-206129697	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
14	nsv821880	chr2:206128007-206129731	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
15	nsv821881	chr2:206128007-206129792	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
16	nsv821882	chr2:206128007-206129860	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
17	nsv820342	chr2:206128007-206129947	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:206097200-206170600	Weak transcription	HSMMtube	muscle
2	chr2:206108400-206145200	Weak transcription	HSMM	muscle
3	chr2:206113400-206139800	Weak transcription	Pancreas	Pancrea
4	chr2:206118200-206156600	Weak transcription	Aorta	Aorta
5	chr2:206127800-206128200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr2:206128000-206128200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:206128000-206128200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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