Variant report

Variant	rs11789689
Chromosome Location	chr9:101818796-101818797
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	chr9:101797638..101801423-chr9:101817658..101821818,3	K562	blood:

Variant related genes	Relation type
ENSG00000204291	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10988660	0.91[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs2075666	0.91[CHB][hapmap];0.90[JPT][hapmap];0.87[MEX][hapmap];0.85[ASN][1000 genomes]
rs3780621	0.91[CHB][hapmap];0.91[JPT][hapmap];0.87[MEX][hapmap];0.85[ASN][1000 genomes]
rs3824511	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4742755	0.81[MEX][hapmap]
rs4742756	0.85[YRI][hapmap]
rs4742758	0.81[YRI][hapmap]
rs60891605	0.85[ASN][1000 genomes]
rs949802	0.91[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs976240	0.87[MEX][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893618	chr9:101800106-101886071	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101782000-101819800	Weak transcription	Colonic Mucosa	Colon
2	chr9:101793800-101837600	Weak transcription	Psoas Muscle	Psoas
3	chr9:101798400-101819800	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr9:101804000-101820000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr9:101805800-101819400	Strong transcription	Adipose Nuclei	Adipose
6	chr9:101805800-101820600	Weak transcription	Right Ventricle	heart
7	chr9:101807000-101831800	Strong transcription	Fetal Muscle Trunk	muscle
8	chr9:101807400-101819000	Strong transcription	Fetal Stomach	stomach
9	chr9:101807600-101831800	Strong transcription	Fetal Muscle Leg	muscle
10	chr9:101807800-101819800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr9:101809200-101821600	Weak transcription	Brain Anterior Caudate	brain
12	chr9:101810600-101819800	Enhancers	Primary T cells fromperipheralblood	blood
13	chr9:101811200-101820000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:101813000-101819400	Weak transcription	NHLF	lung
15	chr9:101813200-101833000	Weak transcription	Lung	lung
16	chr9:101813600-101825600	Weak transcription	Aorta	Aorta
17	chr9:101814000-101819200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr9:101814200-101819200	Weak transcription	NHDF-Ad	bronchial
19	chr9:101814200-101819400	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr9:101814200-101820200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr9:101814200-101826600	Weak transcription	Fetal Intestine Large	intestine
22	chr9:101814200-101829400	Weak transcription	Fetal Intestine Small	intestine
23	chr9:101814400-101819000	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr9:101814400-101820200	Enhancers	Thymus	Thymus
25	chr9:101814600-101819600	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr9:101814800-101819200	Enhancers	Primary T cells from cord blood	blood
27	chr9:101814800-101820000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr9:101814800-101820200	Weak transcription	Right Atrium	heart
29	chr9:101815600-101819800	Enhancers	HSMM	muscle
30	chr9:101815600-101820600	Strong transcription	Stomach Smooth Muscle	stomach
31	chr9:101815600-101821400	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr9:101816000-101819000	Strong transcription	Colon Smooth Muscle	Colon
33	chr9:101816000-101819200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr9:101816000-101819400	Weak transcription	Spleen	Spleen
35	chr9:101816000-101819800	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr9:101816200-101844200	Weak transcription	Gastric	stomach
37	chr9:101816400-101819000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr9:101816400-101819200	Weak transcription	Dnd41	blood
39	chr9:101816600-101818800	Strong transcription	Rectal Smooth Muscle	rectum
40	chr9:101816600-101819800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr9:101816600-101820000	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr9:101816800-101819800	Enhancers	NH-A	brain
43	chr9:101816800-101821200	Enhancers	HMEC	breast
44	chr9:101816800-101822400	Enhancers	Osteobl	bone
45	chr9:101817000-101818800	Strong transcription	Left Ventricle	heart
46	chr9:101817000-101820200	Strong transcription	Duodenum Smooth Muscle	Duodenum
47	chr9:101817000-101821600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr9:101817200-101819000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr9:101817400-101818800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr9:101817400-101818800	Enhancers	Hela-S3	cervix

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