Variant report

Variant	rs6955517
Chromosome Location	chr7:150180018-150180019
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:150172387..150174291-chr7:150178480..150181498,3	K562	blood:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11971105	1.00[AMR][1000 genomes]
rs11977854	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11978881	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11978890	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6947074	1.00[AMR][1000 genomes]
rs7783564	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7784631	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1015582	chr7:149967986-150285104	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
5	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
6	nsv1025129	chr7:150146593-150266217	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1031309	chr7:150171651-150222230	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv970606	chr7:150179372-150181886	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150175200-150180400	Enhancers	Adipose Nuclei	Adipose
2	chr7:150176600-150180400	Enhancers	Fetal Thymus	thymus
3	chr7:150176800-150180200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:150176800-150180400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr7:150177000-150180200	Weak transcription	Liver	Liver
6	chr7:150177200-150180400	Enhancers	Primary hematopoietic stem cells	blood
7	chr7:150177200-150180800	Enhancers	Primary B cells from cord blood	blood
8	chr7:150177400-150181400	Weak transcription	NHEK	skin
9	chr7:150177400-150181800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr7:150177600-150180400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
11	chr7:150177600-150181000	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr7:150177800-150180400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr7:150178000-150182400	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr7:150178200-150180200	Enhancers	Thymus	Thymus
15	chr7:150178400-150180200	Enhancers	HUVEC	blood vessel
16	chr7:150178400-150181200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
17	chr7:150178800-150180200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr7:150178800-150180200	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr7:150178800-150180800	Enhancers	Primary T cells fromperipheralblood	blood
20	chr7:150179000-150180800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr7:150179000-150181000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr7:150179000-150181400	Weak transcription	Primary B cells from peripheral blood	blood
23	chr7:150179200-150180200	Enhancers	Fetal Muscle Leg	muscle
24	chr7:150179200-150180800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr7:150179400-150180200	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr7:150179400-150180200	Weak transcription	Right Atrium	heart
27	chr7:150179400-150180200	Weak transcription	GM12878-XiMat	blood
28	chr7:150179400-150180600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr7:150179400-150181000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr7:150179600-150180200	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr7:150179600-150181000	Weak transcription	Duodenum Mucosa	Duodenum
32	chr7:150180000-150180200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
33	chr7:150180000-150180400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
34	chr7:150180000-150180400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr7:150180000-150181000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
36	chr7:150180000-150181600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:150180000-150181600	Flanking Active TSS	Dnd41	blood
38	chr7:150180000-150181800	Flanking Active TSS	Primary T cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links