Variant report

Variant	rs11894313
Chromosome Location	chr2:114117210-114117211
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs2004323	0.80[EUR][1000 genomes]
rs4088308	0.84[EUR][1000 genomes]
rs55637730	0.80[EUR][1000 genomes]
rs55769337	0.80[EUR][1000 genomes]
rs56082174	0.80[EUR][1000 genomes]
rs56111627	0.80[EUR][1000 genomes]
rs56215109	0.80[EUR][1000 genomes]
rs59766856	0.80[EUR][1000 genomes]
rs60409272	0.80[EUR][1000 genomes]
rs60600282	0.80[EUR][1000 genomes]
rs6710412	0.80[EUR][1000 genomes]
rs72611922	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757826	chr2:114074949-114253780	Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv2759085	chr2:114074949-114428678	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114106800-114129800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:114110600-114124600	Weak transcription	A549	lung
3	chr2:114114400-114122600	Weak transcription	Fetal Intestine Small	intestine
4	chr2:114114800-114117400	Enhancers	NHEK	skin
5	chr2:114115000-114117600	Enhancers	HMEC	breast
6	chr2:114115400-114117400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:114115800-114120000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:114116200-114117400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:114116800-114118200	Weak transcription	HSMM	muscle
10	chr2:114116800-114118600	Weak transcription	Lung	lung
11	chr2:114116800-114119200	Weak transcription	Fetal Muscle Leg	muscle
12	chr2:114116800-114121000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr2:114116800-114126200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr2:114117000-114118000	Weak transcription	HSMMtube	muscle
15	chr2:114117000-114126600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

Quick Search:

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

what's new

Quick links