Variant report

Variant	rs200086436
Chromosome Location	chr14:97413506-97413507
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044202	chr14:97155291-97683983	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542179	chr14:97155291-97683983	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948620	chr14:97334444-98133191	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv832867	chr14:97365919-97541763	Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv902212	chr14:97413032-97474908	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97408600-97428600	Weak transcription	Thymus	Thymus
2	chr14:97409600-97419000	Strong transcription	Dnd41	blood
3	chr14:97411200-97415400	Weak transcription	Primary B cells from cord blood	blood
4	chr14:97412200-97415800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr14:97412200-97415800	Weak transcription	GM12878-XiMat	blood
6	chr14:97412400-97415600	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr14:97412400-97415600	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr14:97412400-97415600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr14:97412400-97415800	Weak transcription	Primary T cells from cord blood	blood
10	chr14:97412400-97415800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr14:97412400-97415800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr14:97412600-97415800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr14:97412600-97415800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr14:97412600-97415800	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr14:97412600-97415800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr14:97412800-97415400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr14:97412800-97415800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr14:97413200-97413800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr14:97413400-97415600	Enhancers	Primary neutrophils fromperipheralblood	blood

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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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