Variant report

Variant	rs5744306
Chromosome Location	chr1:86936310-86936311
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1407142	0.85[ASN][1000 genomes]
rs4647848	0.83[LWK][hapmap]
rs5744303	0.92[ASN][1000 genomes]
rs5744314	0.82[AFR][1000 genomes]
rs5744321	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5744349	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs926065	0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003838	chr1:86591841-87212231	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86933000-86937800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr1:86933000-86938000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr1:86933000-86942800	Weak transcription	K562	blood
4	chr1:86933200-86936800	Weak transcription	Osteobl	bone
5	chr1:86934200-86938000	Active TSS	Rectal Mucosa Donor 31	rectum
6	chr1:86934600-86936400	Active TSS	Fetal Intestine Small	intestine
7	chr1:86934600-86938200	Active TSS	Fetal Intestine Large	intestine
8	chr1:86934600-86938800	Active TSS	Rectal Mucosa Donor 29	rectum
9	chr1:86935400-86942800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr1:86935800-86936600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:86936000-86938000	Enhancers	NHDF-Ad	bronchial
12	chr1:86936200-86937000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
13	chr1:86936200-86937200	Enhancers	Fetal Heart	heart
14	chr1:86936200-86939400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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