Variant report

Variant	rs17085164
Chromosome Location	chr5:95168219-95168220
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:95165646..95168602-chr5:95177618..95179620,3	MCF-7	breast:
2	chr5:95167615..95170613-chr5:95172553..95174092,2	MCF-7	breast:
3	chr5:95156501..95159437-chr5:95167856..95170336,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000173221	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11135439	1.00[ASN][1000 genomes]
rs17463444	1.00[ASN][1000 genomes]
rs17463911	1.00[ASN][1000 genomes]
rs17464446	1.00[ASN][1000 genomes]
rs257683	1.00[ASN][1000 genomes]
rs28926194	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35129919	1.00[ASN][1000 genomes]
rs60575087	1.00[ASN][1000 genomes]
rs6556889	1.00[ASN][1000 genomes]
rs6888777	1.00[ASN][1000 genomes]
rs6891719	1.00[ASN][1000 genomes]

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	nsv830409	chr5:95006686-95204496	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1015180	chr5:95134357-95286446	Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv882389	chr5:95144952-95173887	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95159800-95169800	Weak transcription	Fetal Kidney	kidney
2	chr5:95160200-95169800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr5:95160600-95168800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:95160600-95170000	Weak transcription	Right Atrium	heart
5	chr5:95160600-95170400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr5:95160800-95168800	Weak transcription	Placenta	Placenta
7	chr5:95160800-95169000	Weak transcription	Psoas Muscle	Psoas
8	chr5:95160800-95169800	Weak transcription	Fetal Heart	heart
9	chr5:95160800-95169800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr5:95161400-95168400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr5:95161600-95171400	Weak transcription	Small Intestine	intestine
12	chr5:95161800-95168800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr5:95161800-95169800	Weak transcription	Thymus	Thymus
14	chr5:95161800-95170000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr5:95162400-95169600	Weak transcription	Hela-S3	cervix
16	chr5:95164200-95168400	Weak transcription	A549	lung
17	chr5:95164200-95168600	Weak transcription	Stomach Mucosa	stomach
18	chr5:95164200-95171400	Weak transcription	Spleen	Spleen
19	chr5:95164400-95168400	Weak transcription	Primary B cells from cord blood	blood
20	chr5:95164400-95168400	Weak transcription	Liver	Liver
21	chr5:95164400-95169000	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr5:95164400-95169800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr5:95164600-95168800	Weak transcription	Fetal Thymus	thymus
24	chr5:95164600-95169000	Weak transcription	Duodenum Mucosa	Duodenum
25	chr5:95164600-95169800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr5:95164800-95168800	Weak transcription	HepG2	liver
27	chr5:95164800-95169000	Weak transcription	Fetal Intestine Large	intestine
28	chr5:95164800-95169600	Weak transcription	Fetal Intestine Small	intestine
29	chr5:95164800-95170200	Weak transcription	Colonic Mucosa	Colon
30	chr5:95164800-95170400	Weak transcription	Lung	lung
31	chr5:95167400-95168800	Weak transcription	Pancreas	Pancrea
32	chr5:95167400-95169600	Enhancers	Primary T cells from cord blood	blood
33	chr5:95167400-95169600	Enhancers	Dnd41	blood
34	chr5:95167600-95169800	Weak transcription	Colon Smooth Muscle	Colon
35	chr5:95167800-95168800	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr5:95167800-95169800	Weak transcription	Aorta	Aorta
37	chr5:95167800-95170000	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr5:95167800-95170400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr5:95168000-95169000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr5:95168000-95169000	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr5:95168000-95169200	Enhancers	K562	blood
42	chr5:95168000-95169400	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr5:95168000-95169600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr5:95168000-95169800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr5:95168000-95169800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr5:95168000-95169800	Enhancers	GM12878-XiMat	blood
47	chr5:95168000-95170400	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr5:95168200-95168600	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr5:95168200-95168600	Weak transcription	Gastric	stomach
50	chr5:95168200-95169000	Weak transcription	Primary T helper naive cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links