Variant report

Variant	rs886675
Chromosome Location	chr7:6199635-6199636
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:6198597..6201773-chr7:6386005..6390187,3	MCF-7	breast:
2	chr7:6199039..6200525-chr7:6362284..6363316,17	MCF-7	breast:
3	chr7:6142710..6146060-chr7:6197801..6200881,4	MCF-7	breast:
4	chr7:6199558..6200447-chr7:6362313..6363284,3	MCF-7	breast:
5	chr7:6198247..6199856-chr7:6202022..6204046,2	MCF-7	breast:
6	chr7:6199470..6202116-chr7:6204941..6208439,5	K562	blood:

Variant related genes	Relation type
ENSG00000106346	Chromatin interaction
ENSG00000178397	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10085518	0.85[YRI][hapmap]
rs10254043	0.96[CEU][hapmap];0.81[GIH][hapmap];0.95[MEX][hapmap];0.93[AMR][1000 genomes]
rs10257461	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10265503	0.88[AMR][1000 genomes]
rs10272684	0.86[MEX][hapmap]
rs11762792	0.96[CEU][hapmap];0.88[GIH][hapmap];1.00[MEX][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12667826	0.92[CEU][hapmap];0.87[AMR][1000 genomes]
rs3793207	0.82[GIH][hapmap]
rs4035512	0.96[CEU][hapmap];0.88[GIH][hapmap];1.00[MEX][hapmap];0.87[AMR][1000 genomes]
rs61729726	0.93[AMR][1000 genomes]
rs6463528	0.88[AMR][1000 genomes]
rs6463540	0.90[YRI][hapmap]
rs6961833	0.88[AMR][1000 genomes]
rs6962767	0.90[YRI][hapmap]
rs6979025	0.86[AMR][1000 genomes]
rs7777433	0.90[YRI][hapmap]
rs7780867	0.92[AMR][1000 genomes]
rs7788049	0.83[AMR][1000 genomes]
rs7791225	0.90[YRI][hapmap]
rs7807841	0.84[YRI][hapmap]
rs9886265	0.80[CEU][hapmap];0.85[GIH][hapmap];0.95[MEX][hapmap];0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533108	chr7:5488018-6316581	Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	390 gene(s)	inside rSNPs	diseases
2	nsv948912	chr7:5803903-6623553	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
3	nsv1034060	chr7:5814823-6745710	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
4	nsv538711	chr7:5814823-6745710	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
5	nsv1028242	chr7:5819084-6645024	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
6	nsv538712	chr7:5819084-6645024	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
7	nsv949531	chr7:5949371-6753694	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	129 gene(s)	inside rSNPs	diseases
8	nsv1021037	chr7:6070792-6426966	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
9	nsv538713	chr7:6070792-6426966	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
10	esv1795897	chr7:6170251-6212118	Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
11	nsv522155	chr7:6172654-6212656	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
12	nsv530989	chr7:6176729-6438197	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
13	nsv527386	chr7:6187783-6208369	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
14	nsv818475	chr7:6187783-6212656	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
15	nsv522217	chr7:6189780-6212656	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
16	nsv887426	chr7:6190126-6212656	Strong transcription Genic enhancers Weak transcription Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
17	nsv887427	chr7:6190126-6213396	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6146800-6218200	Weak transcription	Stomach Mucosa	stomach
2	chr7:6160600-6201800	Strong transcription	Fetal Thymus	thymus
3	chr7:6161400-6202200	Strong transcription	Primary T cells fromperipheralblood	blood
4	chr7:6167400-6205600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr7:6172800-6202600	Strong transcription	Dnd41	blood
6	chr7:6173200-6204800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:6173800-6205000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:6174200-6204800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr7:6174400-6200600	Strong transcription	Primary T helper cells PMA-I stimulated	--
10	chr7:6174600-6202200	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr7:6174800-6200000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:6175400-6204200	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr7:6177600-6202400	Strong transcription	Primary B cells from peripheral blood	blood
14	chr7:6178200-6201800	Strong transcription	Liver	Liver
15	chr7:6178200-6204600	Strong transcription	Thymus	Thymus
16	chr7:6178600-6199800	Strong transcription	H1 Cell Line	embryonic stem cell
17	chr7:6180200-6204800	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr7:6181200-6205400	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr7:6181200-6211800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr7:6181400-6202400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr7:6182200-6201000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr7:6182200-6202400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr7:6182400-6200200	Strong transcription	Sigmoid Colon	Sigmoid Colon
24	chr7:6182400-6201600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr7:6182600-6201600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr7:6183800-6205400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:6184000-6199800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr7:6184000-6200800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr7:6184000-6205200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:6184000-6218600	Strong transcription	Fetal Intestine Small	intestine
31	chr7:6184200-6205400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:6186600-6202000	Strong transcription	Duodenum Mucosa	Duodenum
33	chr7:6190000-6211200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr7:6190200-6200800	Weak transcription	Hela-S3	cervix
35	chr7:6190800-6201800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr7:6191800-6200400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr7:6192000-6201800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr7:6192400-6204000	Weak transcription	HMEC	breast
39	chr7:6192600-6200000	Weak transcription	HSMM	muscle
40	chr7:6193000-6203600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr7:6193600-6202000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr7:6194000-6201800	Weak transcription	Small Intestine	intestine
43	chr7:6194600-6202200	Weak transcription	Psoas Muscle	Psoas
44	chr7:6194600-6203000	Strong transcription	NHEK	skin
45	chr7:6194600-6211400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:6196400-6200200	Strong transcription	Pancreas	Pancrea
47	chr7:6196400-6201000	Strong transcription	Primary B cells from cord blood	blood
48	chr7:6196600-6205200	Strong transcription	A549	lung
49	chr7:6197200-6199800	Weak transcription	NHDF-Ad	bronchial
50	chr7:6197200-6200400	Weak transcription	Fetal Kidney	kidney

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