Variant report

Variant	rs9215
Chromosome Location	chr11:9302261-9302262
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	chr11:9301124..9302676-chr11:9383482..9385931,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10734643	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10743101	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11042260	0.96[EUR][1000 genomes]
rs1136330	0.96[EUR][1000 genomes]
rs11600994	0.86[EUR][1000 genomes]
rs11601190	0.87[EUR][1000 genomes]
rs11601229	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11601340	0.96[EUR][1000 genomes]
rs11601383	0.96[EUR][1000 genomes]
rs11604198	0.86[EUR][1000 genomes]
rs11604607	0.86[EUR][1000 genomes]
rs11606740	0.86[EUR][1000 genomes]
rs11606969	0.87[EUR][1000 genomes]
rs4351820	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4622264	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4910036	0.89[EUR][1000 genomes]
rs4910038	0.89[EUR][1000 genomes]
rs4910039	0.82[EUR][1000 genomes]
rs55980718	0.86[EUR][1000 genomes]
rs55989000	0.89[EUR][1000 genomes]
rs7394938	0.86[EUR][1000 genomes]
rs7395754	0.89[EUR][1000 genomes]
rs7396336	0.83[EUR][1000 genomes]
rs956516	0.82[EUR][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	esv33264	chr11:9007612-9311131	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer 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 miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1040049	chr11:9152536-9363488	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv916534	chr11:9188436-9516241	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
4	nsv1053045	chr11:9208881-9363488	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats 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	21 gene(s)	inside rSNPs	diseases
5	nsv540947	chr11:9208881-9363488	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	nsv1055078	chr11:9252857-9538877	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
7	nsv515891	chr11:9275898-9334961	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv7669	chr11:9290376-9335028	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9287400-9319600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:9287400-9332600	Weak transcription	HMEC	breast
3	chr11:9287400-9333000	Weak transcription	Gastric	stomach
4	chr11:9287600-9304800	Weak transcription	NHEK	skin
5	chr11:9287600-9319200	Weak transcription	NHLF	lung
6	chr11:9287800-9302400	Weak transcription	Brain Germinal Matrix	brain
7	chr11:9287800-9305200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr11:9287800-9312200	Weak transcription	K562	blood
9	chr11:9287800-9328400	Weak transcription	A549	lung
10	chr11:9287800-9333800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr11:9288000-9320400	Weak transcription	Fetal Kidney	kidney
12	chr11:9288200-9321200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:9288600-9323200	Weak transcription	Pancreas	Pancrea
14	chr11:9289600-9311600	Weak transcription	HepG2	liver
15	chr11:9289600-9314400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr11:9290000-9318000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr11:9291600-9322600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr11:9293800-9311000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr11:9296000-9307600	Weak transcription	Primary B cells from cord blood	blood
20	chr11:9296200-9303000	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr11:9296600-9307400	Weak transcription	Lung	lung
22	chr11:9296600-9320000	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr11:9296600-9332600	Weak transcription	Right Ventricle	heart
24	chr11:9296600-9333000	Weak transcription	Psoas Muscle	Psoas
25	chr11:9296600-9334800	Weak transcription	Aorta	Aorta
26	chr11:9296800-9307800	Weak transcription	Brain Hippocampus Middle	brain
27	chr11:9296800-9319800	Weak transcription	Brain Substantia Nigra	brain
28	chr11:9296800-9332800	Weak transcription	Brain Angular Gyrus	brain
29	chr11:9296800-9333200	Weak transcription	Colon Smooth Muscle	Colon
30	chr11:9296800-9333200	Weak transcription	Ovary	ovary
31	chr11:9297000-9302400	Weak transcription	NHDF-Ad	bronchial
32	chr11:9297000-9307800	Weak transcription	HUVEC	blood vessel
33	chr11:9297000-9321400	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr11:9297000-9322800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr11:9297200-9321000	Weak transcription	Left Ventricle	heart
36	chr11:9298200-9323800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr11:9299200-9303600	Weak transcription	Fetal Lung	lung
38	chr11:9299200-9320000	Weak transcription	HSMMtube	muscle
39	chr11:9299400-9305600	Weak transcription	Fetal Muscle Leg	muscle
40	chr11:9299600-9312400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr11:9300400-9302400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr11:9300600-9302600	Enhancers	Primary T cells fromperipheralblood	blood
43	chr11:9301000-9302800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr11:9301200-9302600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr11:9301200-9303800	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr11:9301400-9302600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr11:9301400-9302600	Strong transcription	Fetal Muscle Trunk	muscle
48	chr11:9301400-9302600	Enhancers	Fetal Thymus	thymus
49	chr11:9301400-9302800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:9301400-9303200	Enhancers	Primary T killer naive cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links