Variant report

Variant	rs188813301
Chromosome Location	chr2:142396218-142396219
allele	A/T
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	nsv834393	chr2:142256714-142431564	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
2	nsv583214	chr2:142299923-142458316	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv1011019	chr2:142314999-142430460	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	nsv875244	chr2:142336104-142421500	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	nsv875245	chr2:142336104-142421500	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	nsv583234	chr2:142376540-142404955	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
7	nsv511815	chr2:142394301-142397766	Weak transcription	TF binding region	1 gene(s)	inside rSNPs	n/a
8	esv3441379	chr2:142395007-142397855	Weak transcription	TF binding region	1 gene(s)	inside rSNPs	n/a
9	esv3494711	chr2:142395182-142397805	Weak transcription	TF binding region	1 gene(s)	inside rSNPs	n/a
10	esv2511578	chr2:142395547-142397356	Weak transcription	n/a	n/a	inside rSNPs	n/a
11	esv2151280	chr2:142395817-142396667	Weak transcription	n/a	n/a	inside rSNPs	n/a
12	esv3347193	chr2:142395867-142396694	Weak transcription	n/a	n/a	inside rSNPs	n/a
13	esv3376257	chr2:142395889-142396701	Weak transcription	n/a	n/a	inside rSNPs	n/a
14	esv3404801	chr2:142396016-142396684	Weak transcription	n/a	n/a	inside rSNPs	n/a
15	esv3494710	chr2:142396083-142396629	Weak transcription	n/a	n/a	inside rSNPs	n/a
16	esv3494713	chr2:142396083-142396629	Weak transcription	n/a	n/a	inside rSNPs	n/a
17	esv3494712	chr2:142396138-142396703	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142393000-142399800	Weak transcription	ES-WA7 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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