Variant report

Variant	rs9373011
Chromosome Location	chr6:132389048-132389049
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	6:132269655-132282174..6:132386945-132395246	GM12878	blood:
2	6:132182612-132191683..6:132386945-132395246	Hela-S3	cervix:

Variant related genes	Relation type
ENSG00000118523	Chromatin interaction
ENSG00000227220	Chromatin interaction
ENSG00000197594	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10457579	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11154656	0.87[JPT][hapmap]
rs1206738	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1206739	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12193041	0.93[CEU][hapmap];0.87[CHB][hapmap];0.88[JPT][hapmap];0.93[EUR][1000 genomes]
rs12197826	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.95[ASN][1000 genomes]
rs12202729	0.81[TSI][hapmap]
rs12212906	0.92[EUR][1000 genomes]
rs12214663	0.92[EUR][1000 genomes]
rs12214716	0.87[EUR][1000 genomes]
rs2022391	0.84[CHB][hapmap];0.90[JPT][hapmap]
rs2223258	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2327195	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2327196	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs233928	0.90[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap]
rs233929	0.90[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap]
rs233930	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs233931	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs233932	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs4349833	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6900348	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6903186	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7356961	0.94[CEU][hapmap];0.90[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap];0.92[EUR][1000 genomes]
rs7357002	0.94[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes]
rs737454	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7742135	0.92[EUR][1000 genomes]
rs9321318	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9373007	0.93[EUR][1000 genomes]
rs9373010	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.84[MKK][hapmap];0.97[TSI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9385593	0.92[EUR][1000 genomes]
rs9388965	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9399007	0.94[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes]
rs9402383	0.88[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.83[TSI][hapmap];0.88[EUR][1000 genomes]
rs9483372	0.94[CEU][hapmap];0.89[CHB][hapmap];0.82[CHD][hapmap];0.89[JPT][hapmap];0.86[TSI][hapmap];0.92[EUR][1000 genomes]
rs9483376	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs9483377	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.96[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	nsv427768	chr6:132300468-132398477	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132384400-132389200	Enhancers	HUVEC	blood vessel
2	chr6:132385200-132390600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:132385200-132391400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:132385400-132391600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr6:132385400-132391600	Weak transcription	HSMMtube	muscle
6	chr6:132385800-132390400	Weak transcription	Osteobl	bone
7	chr6:132386200-132390400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr6:132386200-132391600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:132386200-132394200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:132387000-132391200	Weak transcription	HSMM	muscle
11	chr6:132387400-132391600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:132387600-132391400	Weak transcription	HMEC	breast
13	chr6:132387600-132391400	Weak transcription	NHEK	skin
14	chr6:132388200-132389400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:132388400-132389200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:132388800-132389200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:132388800-132389200	Enhancers	NHDF-Ad	bronchial
18	chr6:132389000-132389400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:132389000-132390000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:132389000-132391600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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