Variant report

Variant	rs6955350
Chromosome Location	chr7:2990594-2990595
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:2977581..2980387-chr7:2990593..2992867,3	K562	blood:
2	chr7:2989552..2992141-chr7:2994341..2996900,2	MCF-7	breast:
3	chr7:2990535..2992301-chr7:2993612..2996277,2	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10246445	1.00[CEU][hapmap]
rs1078230	1.00[ASN][1000 genomes]
rs12530632	1.00[ASN][1000 genomes]
rs12535598	1.00[ASN][1000 genomes]
rs12536249	1.00[ASN][1000 genomes]
rs12536265	1.00[ASN][1000 genomes]
rs17132867	1.00[EUR][1000 genomes]
rs17736807	1.00[ASN][1000 genomes]
rs17737044	1.00[ASN][1000 genomes]
rs41373352	1.00[ASN][1000 genomes]
rs41386651	1.00[ASN][1000 genomes]
rs41466946	1.00[ASN][1000 genomes]
rs41467947	1.00[ASN][1000 genomes]
rs4428569	1.00[ASN][1000 genomes]
rs61731201	1.00[ASN][1000 genomes]
rs9648301	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022612	chr7:2789555-3019200	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1022938	chr7:2899514-3131881	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv605873	chr7:2920067-3204177	Bivalent Enhancer Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv1025727	chr7:2938301-3064008	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS 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	4 gene(s)	inside rSNPs	diseases
5	nsv1026476	chr7:2965034-3311344	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv538656	chr7:2965034-3311344	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv464260	chr7:2966138-3315572	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv605874	chr7:2966138-3315572	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
9	nsv1018287	chr7:2967524-3298539	Genic enhancers Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
10	nsv538657	chr7:2967524-3298539	Bivalent/Poised TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:2968600-2999400	Weak transcription	Right Atrium	heart
2	chr7:2968800-2992000	Weak transcription	Esophagus	oesophagus
3	chr7:2974200-2996000	Weak transcription	HUVEC	blood vessel
4	chr7:2975800-2996800	Weak transcription	Duodenum Mucosa	Duodenum
5	chr7:2980000-2999800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:2981200-2992400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:2984200-2992000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr7:2984200-2993800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:2984400-2994000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:2985200-2993600	Weak transcription	Fetal Intestine Small	intestine
11	chr7:2985400-2992600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr7:2985400-2996200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:2985800-2991800	Weak transcription	Thymus	Thymus
14	chr7:2986000-2993200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:2986400-2992000	Weak transcription	Fetal Thymus	thymus
16	chr7:2986400-2995000	Weak transcription	Spleen	Spleen
17	chr7:2987000-2993200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr7:2987400-2991800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr7:2987400-2991800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr7:2987600-2991600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr7:2987600-2991600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr7:2987600-2992000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr7:2988000-2990600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
24	chr7:2988200-2991800	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr7:2988400-2991200	Enhancers	Primary B cells from peripheral blood	blood
26	chr7:2988600-2992400	Weak transcription	NHEK	skin
27	chr7:2988800-2991400	Genic enhancers	Primary B cells from cord blood	blood
28	chr7:2989200-2992000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr7:2989200-2992400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr7:2989400-2991000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr7:2989600-2991400	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr7:2989800-2991000	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
33	chr7:2989800-2991000	ZNF genes & repeats	GM12878-XiMat	blood
34	chr7:2989800-2992000	Strong transcription	Primary T cells fromperipheralblood	blood
35	chr7:2989800-2992200	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr7:2989800-2997800	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr7:2990000-2991200	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr7:2990000-2991200	Enhancers	Primary hematopoietic stem cells	blood
39	chr7:2990000-2991200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr7:2990000-2992200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr7:2990000-2993000	Strong transcription	Primary T cells from cord blood	blood
42	chr7:2990400-2990800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:2990400-2991200	Genic enhancers	Primary T helper naive cells from peripheral blood	blood

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