Variant report

Variant	rs7097664
Chromosome Location	chr10:21974979-21974980
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	chr10:21815978..21818479-chr10:21973475..21976355,2	K562	blood:
2	chr10:21970179..21972315-chr10:21973680..21976595,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11012810	1.00[ASN][1000 genomes]
rs11498370	1.00[ASN][1000 genomes]
rs12248701	1.00[CEU][hapmap]
rs12354471	0.81[AFR][1000 genomes]
rs60142116	0.82[AFR][1000 genomes]
rs7069907	1.00[MEX][hapmap]
rs7071519	1.00[ASW][hapmap];0.93[LWK][hapmap];0.81[MKK][hapmap]
rs7072340	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap]
rs7076216	1.00[ASN][1000 genomes]
rs7083501	1.00[ASN][1000 genomes]
rs7093279	1.00[ASW][hapmap];0.93[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap]
rs7893818	1.00[ASN][1000 genomes]
rs7895753	0.87[LWK][hapmap];1.00[YRI][hapmap]
rs7899191	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs7901657	1.00[ASN][1000 genomes]
rs7903144	1.00[ASW][hapmap];0.93[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs7909582	0.81[AFR][1000 genomes]
rs7919823	1.00[ASN][1000 genomes]
rs7924175	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs7924290	0.93[LWK][hapmap];0.81[MKK][hapmap]
rs9665499	1.00[ASN][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	nsv1036585	chr10:21833717-21998042	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv550202	chr10:21856475-22027644	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1052464	chr10:21856531-22220087	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	esv1802317	chr10:21866085-22288132	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv894947	chr10:21869609-22117913	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	esv1792771	chr10:21874152-22013644	Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS 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
7	esv1803077	chr10:21878144-22013644	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats 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
8	nsv550203	chr10:21916468-22062729	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21915200-21983800	Weak transcription	Rectal Smooth Muscle	rectum
2	chr10:21923800-21983200	Weak transcription	NHLF	lung
3	chr10:21928600-21988200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr10:21929800-21988000	Weak transcription	HUVEC	blood vessel
5	chr10:21938600-21975600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr10:21938600-21993800	Weak transcription	Lung	lung
7	chr10:21942400-21976200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr10:21942400-21977400	Weak transcription	Adipose Nuclei	Adipose
9	chr10:21942400-21987200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr10:21942600-22004000	Weak transcription	NH-A	brain
11	chr10:21942800-21988400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr10:21943800-22002000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr10:21945200-21976400	Weak transcription	Right Ventricle	heart
14	chr10:21951200-21989000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr10:21951800-21976800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr10:21951800-21978000	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr10:21951800-21989200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr10:21952000-21975400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr10:21952000-21984800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr10:21952000-21988000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr10:21952600-21983600	Weak transcription	Psoas Muscle	Psoas
22	chr10:21952800-21975800	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr10:21955000-21981600	Weak transcription	Placenta	Placenta
24	chr10:21955000-21983800	Weak transcription	Stomach Smooth Muscle	stomach
25	chr10:21955000-21988000	Weak transcription	Fetal Muscle Trunk	muscle
26	chr10:21956800-21988000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr10:21959600-21984600	Weak transcription	Colon Smooth Muscle	Colon
28	chr10:21960400-21983800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr10:21961400-21981000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr10:21961400-21993800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr10:21961600-21980800	Weak transcription	Fetal Intestine Small	intestine
32	chr10:21961600-21983400	Weak transcription	Fetal Stomach	stomach
33	chr10:21962600-21986600	Weak transcription	Fetal Kidney	kidney
34	chr10:21962800-21976000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr10:21962800-21981000	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr10:21962800-21984000	Weak transcription	Thymus	Thymus
37	chr10:21962800-21986800	Weak transcription	Fetal Lung	lung
38	chr10:21962800-21988200	Weak transcription	Duodenum Mucosa	Duodenum
39	chr10:21963000-21975600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr10:21963000-21975600	Weak transcription	Fetal Thymus	thymus
41	chr10:21963000-21976000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr10:21963000-21976000	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr10:21963000-21976000	Weak transcription	HSMMtube	muscle
44	chr10:21963000-21976400	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr10:21963000-21976600	Weak transcription	Fetal Intestine Large	intestine
46	chr10:21963000-21983600	Weak transcription	Aorta	Aorta
47	chr10:21963000-21986800	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr10:21963000-21988000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr10:21963000-21988200	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr10:21963000-21993600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links