Variant report

Variant	rs6659316
Chromosome Location	chr1:211826467-211826468
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:211750915..211755112-chr1:211826013..211829699,5	K562	blood:
2	chr1:211750437..211753125-chr1:211823737..211827672,4	MCF-7	breast:
3	chr1:211750060..211753695-chr1:211824093..211827463,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000170385	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11119794	1.00[CHB][hapmap]
rs11578614	1.00[CHB][hapmap]
rs12074002	1.00[CHB][hapmap];0.88[CHD][hapmap]
rs12561861	1.00[CHB][hapmap]
rs12724388	1.00[JPT][hapmap]
rs12736496	1.00[JPT][hapmap]
rs12751701	1.00[JPT][hapmap]
rs1530400	0.81[CEU][hapmap];0.83[GIH][hapmap]
rs17017716	1.00[CHB][hapmap]
rs2184844	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2794731	1.00[CHB][hapmap];0.88[CHD][hapmap]
rs55661489	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56094815	1.00[ASN][1000 genomes]
rs6540695	1.00[JPT][hapmap]
rs6661565	1.00[CHB][hapmap]
rs6666442	1.00[JPT][hapmap]
rs6673372	1.00[JPT][hapmap]
rs701926	1.00[CHB][hapmap]
rs7511687	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7516189	0.96[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.80[TSI][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7526473	0.92[ASN][1000 genomes]
rs7526891	1.00[CHB][hapmap]
rs7527002	1.00[CHB][hapmap]
rs7539988	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7551341	0.84[CEU][hapmap];0.95[MEX][hapmap]
rs7553718	0.84[CEU][hapmap];0.95[MEX][hapmap]
rs7554315	0.81[CEU][hapmap];0.86[GIH][hapmap];0.83[MEX][hapmap]
rs7554588	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211811400-211829600	Enhancers	Fetal Intestine Small	intestine
2	chr1:211811600-211828200	Enhancers	Fetal Intestine Large	intestine
3	chr1:211817400-211827000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr1:211817400-211827400	Weak transcription	Fetal Heart	heart
5	chr1:211817600-211826800	Weak transcription	Gastric	stomach
6	chr1:211817600-211827000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr1:211817600-211830600	Weak transcription	Right Atrium	heart
8	chr1:211818400-211828400	Weak transcription	Adipose Nuclei	Adipose
9	chr1:211820400-211826800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:211821800-211828400	Weak transcription	Colonic Mucosa	Colon
11	chr1:211822000-211826800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:211822000-211826800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:211822200-211827000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:211822200-211827000	Weak transcription	NHEK	skin
15	chr1:211822200-211828400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr1:211822400-211827000	Weak transcription	K562	blood
17	chr1:211822600-211826800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:211822800-211827600	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr1:211822800-211828200	Weak transcription	Liver	Liver
20	chr1:211822800-211828200	Weak transcription	Pancreas	Pancrea
21	chr1:211823200-211827000	Weak transcription	A549	lung
22	chr1:211823400-211826800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr1:211824000-211826600	Weak transcription	HUVEC	blood vessel
24	chr1:211824000-211826800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:211824000-211828200	Weak transcription	Stomach Mucosa	stomach
26	chr1:211824400-211828000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr1:211825800-211828800	Enhancers	Placenta	Placenta
28	chr1:211826400-211827200	Enhancers	HepG2	liver
29	chr1:211826400-211827400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:211826400-211828400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr1:211826400-211828600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr1:211826400-211828600	Flanking Active TSS	Hela-S3	cervix

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