Variant report

Variant	rs10205381
Chromosome Location	chr2:113753124-113753125
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs12616801	0.81[YRI][hapmap]
rs13382878	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs13413331	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs17042601	1.00[MEX][hapmap]
rs6542114	1.00[MEX][hapmap]

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	nsv532471	chr2:113682449-113862981	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv997348	chr2:113688093-113986508	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1007254	chr2:113726982-113887782	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv535894	chr2:113726982-113887782	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv874878	chr2:113742734-113776076	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113750600-113754400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
2	chr2:113751200-113753200	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr2:113751200-113755600	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr2:113751400-113755600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr2:113751600-113753200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr2:113751800-113755600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr2:113752000-113753200	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr2:113752000-113754400	Enhancers	Primary T cells from cord blood	blood
9	chr2:113752000-113755600	Enhancers	Primary T cells fromperipheralblood	blood
10	chr2:113753000-113753200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
11	chr2:113753000-113753200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr2:113753000-113753200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr2:113753000-113753400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
14	chr2:113753000-113753800	Enhancers	K562	blood
15	chr2:113753000-113754400	Enhancers	Fetal Thymus	thymus
16	chr2:113753000-113755200	Enhancers	Dnd41	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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