Variant report

Variant	rs11691195
Chromosome Location	chr2:31342883-31342884
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs11693385	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948552	chr2:31118599-31595424	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	esv3457466	chr2:31342604-31343147	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3567	chr2:31342647-31343096	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3457465	chr2:31342656-31343126	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3457464	chr2:31342660-31343113	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3457461	chr2:31342675-31343068	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3346199	chr2:31342691-31343065	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3414648	chr2:31342699-31343072	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3457462	chr2:31342711-31343046	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3457467	chr2:31342726-31343057	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv1683223	chr2:31342741-31343056	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31310600-31346800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr2:31329200-31348200	Weak transcription	A549	lung
3	chr2:31332400-31347400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:31332600-31348600	Weak transcription	NHEK	skin
5	chr2:31332600-31348800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:31332600-31349000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr2:31332600-31349000	Weak transcription	HMEC	breast
8	chr2:31332800-31346600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr2:31335200-31344600	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr2:31336400-31343800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr2:31336600-31345000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:31337000-31345800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr2:31337200-31347800	Weak transcription	Brain Germinal Matrix	brain

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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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