Variant report

Variant	rs6918402
Chromosome Location	chr6:54732919-54732920
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:54704497..54716767-chr6:54728797..54750947,71	MCF-7	breast:
2	chr6:54721521..54725055-chr6:54731692..54735464,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000168143	Chromatin interaction
ENSG00000224984	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10456176	0.96[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10948866	0.96[CEU][hapmap];0.94[CHB][hapmap];0.91[GIH][hapmap];0.91[JPT][hapmap];0.93[TSI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10948867	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10948870	0.94[ASN][1000 genomes]
rs1155749	0.88[CHB][hapmap];0.92[JPT][hapmap];0.95[ASN][1000 genomes]
rs12192659	0.85[CEU][hapmap];1.00[CHB][hapmap];0.82[EUR][1000 genomes]
rs12208341	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12208348	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12211168	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1393776	0.81[CHB][hapmap]
rs1472679	0.96[CEU][hapmap];0.94[CHB][hapmap];0.91[GIH][hapmap];0.91[JPT][hapmap];0.93[TSI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs171224	0.81[CEU][hapmap];0.88[CHB][hapmap]
rs181155	0.81[CEU][hapmap];0.88[CHB][hapmap]
rs1963697	0.81[CHB][hapmap]
rs2143798	0.83[ASN][1000 genomes]
rs2179786	0.87[CHB][hapmap];0.83[ASN][1000 genomes]
rs2207025	0.81[CEU][hapmap];0.81[CHB][hapmap]
rs2207026	0.82[CEU][hapmap];0.83[CHB][hapmap]
rs239781	0.81[CEU][hapmap];0.87[CHB][hapmap]
rs239783	0.81[CEU][hapmap];0.87[CHB][hapmap]
rs239790	0.81[CEU][hapmap];0.87[CHB][hapmap]
rs239796	0.81[CEU][hapmap];0.87[CHB][hapmap]
rs239801	0.88[CHB][hapmap]
rs239837	0.81[CEU][hapmap];0.87[CHB][hapmap]
rs2816812	0.81[CEU][hapmap];0.87[CHB][hapmap]
rs4715489	0.94[ASN][1000 genomes]
rs6459034	0.81[CEU][hapmap];0.87[CHB][hapmap]
rs6910384	0.94[ASN][1000 genomes]
rs6926997	0.81[CHB][hapmap]
rs6937970	0.96[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7741915	0.87[CHB][hapmap]
rs7752349	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7761336	0.88[CHB][hapmap];0.91[JPT][hapmap];0.95[ASN][1000 genomes]
rs7765721	0.96[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs924712	0.81[CEU][hapmap];0.88[CHB][hapmap];0.84[JPT][hapmap];0.95[ASN][1000 genomes]
rs931766	0.96[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs931767	0.95[ASN][1000 genomes]
rs9349740	0.81[CHB][hapmap]
rs9370345	0.80[CHB][hapmap]
rs9382403	0.81[CHB][hapmap]
rs9396003	0.94[ASN][1000 genomes]
rs971526	0.96[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs973205	0.93[ASW][hapmap];0.96[CEU][hapmap];0.94[CHB][hapmap];0.91[GIH][hapmap];0.83[JPT][hapmap];0.95[TSI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs988913	0.81[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885900	chr6:54517968-54852462	Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv2763553	chr6:54687979-54820487	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	esv3334773	chr6:54732770-54733058	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54725600-54737400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr6:54725600-54737600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr6:54726600-54739600	Weak transcription	Small Intestine	intestine
4	chr6:54727200-54748800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:54727400-54740400	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr6:54727400-54743800	Weak transcription	Pancreas	Pancrea
7	chr6:54729200-54733400	Weak transcription	HMEC	breast
8	chr6:54730400-54733600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr6:54730400-54735800	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr6:54730400-54743800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr6:54731000-54733400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr6:54731600-54737200	Weak transcription	Hela-S3	cervix
13	chr6:54731600-54739400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr6:54731800-54733400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr6:54731800-54738800	Weak transcription	Fetal Intestine Large	intestine
16	chr6:54731800-54738800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr6:54732200-54739200	Weak transcription	Fetal Intestine Small	intestine
18	chr6:54732600-54734600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:54732800-54733000	Weak transcription	Stomach Mucosa	stomach
20	chr6:54732800-54733400	Enhancers	NHEK	skin
21	chr6:54732800-54734200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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