Variant report

Variant	rs9321274
Chromosome Location	chr6:131424799-131424800
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs28664083	1.00[AMR][1000 genomes]
rs58336107	1.00[AMR][1000 genomes]
rs9483198	1.00[AMR][1000 genomes]
rs9483202	1.00[AMR][1000 genomes]
rs9483204	1.00[AMR][1000 genomes]
rs9483211	1.00[AMR][1000 genomes]
rs9492751	1.00[AMR][1000 genomes]
rs9492752	1.00[AMR][1000 genomes]
rs9492754	1.00[AMR][1000 genomes]
rs9492765	1.00[AMR][1000 genomes]
rs9492778	1.00[AMR][1000 genomes]
rs9492789	1.00[AMR][1000 genomes]
rs9492798	1.00[AMR][1000 genomes]
rs9492823	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032955	chr6:131298803-131818502	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538443	chr6:131298803-131818502	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv830807	chr6:131390952-131581931	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1019112	chr6:131409284-131452300	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2761029	chr6:131413789-131452312	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1016925	chr6:131418532-131452300	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 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	chr6:131422400-131428000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:131423000-131425400	Enhancers	Duodenum Mucosa	Duodenum
3	chr6:131423000-131425400	Enhancers	Osteobl	bone
4	chr6:131423000-131426000	Enhancers	Fetal Intestine Large	intestine
5	chr6:131423600-131428000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr6:131423600-131428000	Weak transcription	NHEK	skin
7	chr6:131423800-131428000	Weak transcription	HSMM	muscle
8	chr6:131424000-131425600	Enhancers	HepG2	liver
9	chr6:131424000-131428400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr6:131424200-131425200	Enhancers	NH-A	brain
11	chr6:131424200-131428000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr6:131424400-131425000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr6:131424400-131425400	Enhancers	Fetal Intestine Small	intestine
14	chr6:131424400-131425400	Enhancers	A549	lung
15	chr6:131424600-131427400	Weak transcription	HUVEC	blood vessel

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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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