Variant report

Variant	rs7814933
Chromosome Location	chr8:66913227-66913228
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	chr8:66752639..66754285-chr8:66912341..66913991,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000205268	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10092687	1.00[CHB][hapmap]
rs10095931	1.00[CHB][hapmap]
rs10101457	1.00[CHB][hapmap]
rs10113208	1.00[CHB][hapmap]
rs1108213	0.97[ASN][1000 genomes]
rs11984602	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11985050	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11988589	0.84[EUR][1000 genomes]
rs11994407	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12334408	1.00[CHB][hapmap]
rs16932426	1.00[CHB][hapmap]
rs16932461	1.00[CHB][hapmap]
rs16932465	1.00[CHB][hapmap]
rs16932468	1.00[CHB][hapmap]
rs16932544	1.00[CHB][hapmap]
rs17306183	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17307227	1.00[CHB][hapmap]
rs2357567	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2357570	1.00[CHB][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2357571	1.00[CHB][hapmap]
rs28364018	1.00[CHB][hapmap]
rs34464051	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35753080	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4366069	1.00[CHB][hapmap]
rs4380923	1.00[CHB][hapmap]
rs4487748	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4495409	1.00[CHB][hapmap]
rs4495411	1.00[CHB][hapmap]
rs4565445	1.00[CHB][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57683289	0.83[EUR][1000 genomes]
rs58489131	0.97[ASN][1000 genomes]
rs58817197	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62506636	0.97[ASN][1000 genomes]
rs62506637	0.97[ASN][1000 genomes]
rs62506650	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62507386	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472245	1.00[CHB][hapmap]
rs6472251	1.00[CHB][hapmap]
rs6985796	1.00[CHB][hapmap]
rs6988195	1.00[CHB][hapmap]
rs7006334	1.00[CHB][hapmap]
rs7006394	1.00[CHB][hapmap]
rs7008359	1.00[CHB][hapmap]
rs7008578	1.00[CHB][hapmap]
rs7011264	0.97[ASN][1000 genomes]
rs7017127	0.97[ASN][1000 genomes]
rs7812439	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7818219	1.00[CHB][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7834423	1.00[CHB][hapmap]
rs7835948	1.00[CHB][hapmap]
rs7836993	1.00[CHB][hapmap]
rs7845334	1.00[CHB][hapmap]
rs950729	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:66909800-66915400	Enhancers	Primary T cells fromperipheralblood	blood
2	chr8:66909800-66915400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
3	chr8:66910000-66914000	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr8:66910000-66915800	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr8:66910000-66916200	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr8:66910200-66914200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr8:66910200-66914600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr8:66910200-66915200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr8:66910200-66915600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr8:66910200-66917800	Enhancers	Primary T cells from cord blood	blood
11	chr8:66910400-66913800	Enhancers	Primary B cells from peripheral blood	blood
12	chr8:66911800-66917200	Weak transcription	Small Intestine	intestine
13	chr8:66912000-66917000	Weak transcription	Fetal Intestine Large	intestine
14	chr8:66912000-66917000	Weak transcription	Fetal Intestine Small	intestine
15	chr8:66912000-66918400	Weak transcription	Primary B cells from cord blood	blood
16	chr8:66912600-66914000	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr8:66912600-66915400	Enhancers	Fetal Thymus	thymus
18	chr8:66912800-66914000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr8:66912800-66914000	Weak transcription	Hela-S3	cervix
20	chr8:66912800-66914600	Enhancers	Thymus	Thymus
21	chr8:66912800-66915600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:66913000-66914600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr8:66913000-66914600	Enhancers	Dnd41	blood
24	chr8:66913200-66913800	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr8:66913200-66914800	Enhancers	Primary hematopoietic stem cells	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links