Variant report

Variant	rs11568778
Chromosome Location	chr9:101900410-101900411
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:101894017..101896453-chr9:101898927..101901266,2	K562	blood:
2	chr9:101895206..101897891-chr9:101899277..101901035,2	MCF-7	breast:
3	chr9:101764789..101766455-chr9:101899453..101902305,3	K562	blood:
4	chr9:101864389..101869659-chr9:101898096..101900514,5	MCF-7	breast:
5	chr9:101899920..101901969-chr9:101905038..101907406,2	K562	blood:
6	chr9:101747587..101749233-chr9:101899420..101901955,2	K562	blood:
7	chr9:101869195..101872022-chr9:101900402..101902081,2	K562	blood:
8	chr9:101898800..101901227-chr9:101901633..101903156,2	K562	blood:
9	chr9:101898521..101900717-chr9:101901631..101904454,3	K562	blood:
10	chr9:101875608..101878128-chr9:101899514..101901966,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000106799	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10733709	1.00[CHB][hapmap];0.82[JPT][hapmap];0.95[ASN][1000 genomes]
rs10760668	0.88[ASN][1000 genomes]
rs10760669	0.90[ASN][1000 genomes]
rs10760671	0.91[CHB][hapmap];0.90[ASN][1000 genomes]
rs10760672	0.91[CHB][hapmap];0.90[ASN][1000 genomes]
rs10760673	0.91[CHB][hapmap];0.97[CHD][hapmap];0.90[ASN][1000 genomes]
rs10760674	0.96[ASN][1000 genomes]
rs10819636	0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10819638	0.91[CHB][hapmap];0.90[ASN][1000 genomes]
rs10819640	0.91[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10988706	0.90[CHB][hapmap];0.90[ASN][1000 genomes]
rs10988709	0.91[CHB][hapmap];0.82[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10988713	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10988715	0.94[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10988716	0.95[CHB][hapmap];0.90[ASN][1000 genomes]
rs10988717	0.91[CHB][hapmap];0.82[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10988723	0.96[ASN][1000 genomes]
rs11568752	0.91[CHB][hapmap];0.80[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11568753	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11568770	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12346650	0.87[CHB][hapmap];0.87[CHD][hapmap]
rs12685571	0.91[CHB][hapmap];0.82[JPT][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12686782	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1699413	0.87[ASN][1000 genomes]
rs1888225	0.91[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1973518	0.86[ASN][1000 genomes]
rs334351	0.91[ASN][1000 genomes]
rs334353	0.91[CHB][hapmap];0.97[CHD][hapmap];0.91[ASN][1000 genomes]
rs334354	0.91[CHB][hapmap];0.97[CHD][hapmap];0.90[ASN][1000 genomes]
rs334362	0.85[ASN][1000 genomes]
rs334363	0.87[ASN][1000 genomes]
rs334364	0.87[ASN][1000 genomes]
rs334366	0.87[ASN][1000 genomes]
rs334367	0.87[ASN][1000 genomes]
rs334370	0.85[ASN][1000 genomes]
rs3739798	0.91[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3780619	1.00[LWK][hapmap]
rs44466	0.84[ASN][1000 genomes]
rs597457	0.91[CHB][hapmap];0.91[ASN][1000 genomes]
rs6478973	0.90[ASN][1000 genomes]
rs7041311	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7042852	1.00[CHB][hapmap];0.88[CHD][hapmap];0.82[JPT][hapmap];0.96[ASN][1000 genomes]
rs7874221	0.91[CHB][hapmap];0.97[CHD][hapmap];0.90[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	nsv893619	chr9:101835165-101936231	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv831666	chr9:101874985-102018690	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv1792736	chr9:101891126-101909372	Flanking Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101870000-101908600	Weak transcription	Brain Germinal Matrix	brain
2	chr9:101876600-101904200	Weak transcription	Liver	Liver
3	chr9:101878800-101903200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr9:101882200-101901400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr9:101882200-101903000	Weak transcription	Fetal Muscle Leg	muscle
6	chr9:101885200-101901600	Weak transcription	A549	lung
7	chr9:101888200-101907000	Weak transcription	HepG2	liver
8	chr9:101889400-101904000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr9:101889600-101901000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr9:101889800-101904400	Weak transcription	Lung	lung
11	chr9:101890000-101900800	Weak transcription	Fetal Intestine Small	intestine
12	chr9:101890000-101914200	Weak transcription	Pancreas	Pancrea
13	chr9:101890200-101904800	Weak transcription	Fetal Intestine Large	intestine
14	chr9:101890200-101907600	Weak transcription	Gastric	stomach
15	chr9:101890400-101908400	Weak transcription	Hela-S3	cervix
16	chr9:101890600-101900800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr9:101890600-101901600	Weak transcription	Fetal Lung	lung
18	chr9:101890600-101907000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr9:101890600-101908800	Weak transcription	Right Ventricle	heart
20	chr9:101890800-101903600	Weak transcription	Right Atrium	heart
21	chr9:101891400-101903600	Weak transcription	Dnd41	blood
22	chr9:101891600-101900800	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr9:101892400-101902600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:101892600-101902800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr9:101892600-101914200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr9:101892800-101901000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr9:101892800-101905800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr9:101892800-101921000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr9:101893000-101902800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr9:101893000-101904200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr9:101893200-101901400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr9:101893800-101902600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr9:101894200-101906800	Weak transcription	Fetal Kidney	kidney
34	chr9:101894200-101907600	Weak transcription	HUVEC	blood vessel
35	chr9:101894800-101900800	Weak transcription	Left Ventricle	heart
36	chr9:101895000-101900800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr9:101895000-101900800	Weak transcription	Fetal Stomach	stomach
38	chr9:101895000-101907200	Weak transcription	Spleen	Spleen
39	chr9:101895000-101914200	Weak transcription	Esophagus	oesophagus
40	chr9:101895200-101903800	Weak transcription	Fetal Muscle Trunk	muscle
41	chr9:101895400-101904200	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr9:101895800-101902800	Weak transcription	Fetal Heart	heart
43	chr9:101896800-101900800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr9:101897000-101900800	Weak transcription	Psoas Muscle	Psoas
45	chr9:101897000-101902600	Weak transcription	HSMMtube	muscle
46	chr9:101897200-101901000	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr9:101897600-101900800	Weak transcription	Aorta	Aorta
48	chr9:101897600-101901000	Enhancers	Primary hematopoietic stem cells	blood
49	chr9:101897600-101907400	Weak transcription	HMEC	breast
50	chr9:101897600-101913400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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