Variant report

Variant	rs6906645
Chromosome Location	chr6:57130574-57130575
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:57125429..57127143-chr6:57128713..57131182,2	K562	blood:
2	chr6:57128467..57134592-chr6:57180122..57183939,9	MCF-7	breast:

Variant related genes	Relation type
ENSG00000146143	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10080526	0.81[ASN][1000 genomes]
rs10949013	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10949014	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13210430	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16888410	0.86[CHB][hapmap];0.81[CHD][hapmap]
rs16888420	0.81[ASN][1000 genomes]
rs16888435	0.85[ASN][1000 genomes]
rs16888439	0.93[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs183418	0.81[ASN][1000 genomes]
rs223289	1.00[CEU][hapmap];0.83[CHB][hapmap];0.92[JPT][hapmap];0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs34331825	0.95[ASN][1000 genomes]
rs62415955	0.83[ASN][1000 genomes]
rs62418081	0.82[ASN][1000 genomes]
rs6900622	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6905517	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6905598	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9464431	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9475804	0.85[ASN][1000 genomes]
rs9475805	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9475808	0.85[ASN][1000 genomes]
rs984684	0.93[CHB][hapmap];0.91[CHD][hapmap];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491933	chr6:56177722-57171010	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv934026	chr6:56382056-57184218	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv533050	chr6:56504480-57297586	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1034095	chr6:57102042-57162808	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv528165	chr6:57104266-57130574	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57123800-57130600	Enhancers	Colon Smooth Muscle	Colon
2	chr6:57125200-57133200	Enhancers	Rectal Smooth Muscle	rectum
3	chr6:57126400-57130800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:57127800-57130600	Enhancers	NHDF-Ad	bronchial
5	chr6:57127800-57130800	Weak transcription	Ovary	ovary
6	chr6:57127800-57132200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr6:57128200-57130600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:57128400-57132600	Weak transcription	Adipose Nuclei	Adipose
9	chr6:57128800-57130600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:57128800-57130600	Enhancers	Osteobl	bone
11	chr6:57128800-57132200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:57128800-57132600	Weak transcription	Fetal Muscle Leg	muscle
13	chr6:57129600-57130800	Enhancers	Fetal Lung	lung
14	chr6:57129800-57131400	Enhancers	HSMM	muscle
15	chr6:57129800-57132800	Enhancers	HSMMtube	muscle
16	chr6:57130000-57130600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:57130000-57131400	Enhancers	HUVEC	blood vessel
18	chr6:57130200-57130600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:57130200-57131000	Active TSS	Fetal Brain Male	brain
20	chr6:57130200-57131200	Flanking Active TSS	NHLF	lung
21	chr6:57130200-57131400	Enhancers	Fetal Stomach	stomach
22	chr6:57130200-57132400	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr6:57130400-57130600	Enhancers	NH-A	brain
24	chr6:57130400-57130800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:57130400-57131000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:57130400-57131000	Enhancers	NHEK	skin
27	chr6:57130400-57131200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr6:57130400-57132000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:57130400-57132200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr6:57130400-57133000	Enhancers	Stomach Smooth Muscle	stomach

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