Variant report

Variant	rs200662252
Chromosome Location	chr3:111243561-111243562
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv997756	chr3:111226058-111376585	Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv3946	chr3:111236035-111283038	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	esv3323258	chr3:111241762-111246760	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
6	esv3394909	chr3:111242287-111250120	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
7	esv3495322	chr3:111242429-111249881	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
8	esv3495321	chr3:111242562-111250210	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
9	esv2466211	chr3:111243007-111249538	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
10	esv3495319	chr3:111243012-111250160	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	n/a
11	nsv513066	chr3:111243020-111249059	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
12	nsv436392	chr3:111243479-111249604	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	n/a
13	esv2113452	chr3:111243500-111249092	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
14	nsv435756	chr3:111243500-111249426	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
15	esv3463474	chr3:111243512-111249092	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
16	esv3463476	chr3:111243512-111249092	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111236400-111249600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:111242400-111243600	Enhancers	Primary B cells from peripheral blood	blood
3	chr3:111243400-111244200	Weak transcription	Placenta	Placenta

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

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