Variant report

Variant	rs185122102
Chromosome Location	chr11:9320535-9320536
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:9320121..9324688-chr11:9334835..9338165,5	K562	blood:
2	chr11:9285320..9287424-chr11:9318280..9320535,2	K562	blood:
3	chr11:9316306..9317973-chr11:9319550..9321312,2	K562	blood:
4	chr11:9320121..9322582-chr11:9335462..9337660,2	K562	blood:

Variant related genes	Relation type
ENSG00000184014	Chromatin interaction
ENSG00000166471	Chromatin interaction

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

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	esv32901	chr11:9311131-9328869	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv508617	chr11:9314027-9408562	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	27 gene(s)	inside rSNPs	diseases
10	esv1819846	chr11:9316937-9324496	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	esv1824476	chr11:9316937-9324496	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	esv1838674	chr11:9316937-9324496	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	nsv553456	chr11:9316937-9324496	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
14	esv1001197	chr11:9316963-9326487	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
15	nsv553457	chr11:9320346-9324496	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 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	chr11:9287400-9332600	Weak transcription	HMEC	breast
2	chr11:9287400-9333000	Weak transcription	Gastric	stomach
3	chr11:9287800-9328400	Weak transcription	A549	lung
4	chr11:9287800-9333800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:9288200-9321200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:9288600-9323200	Weak transcription	Pancreas	Pancrea
7	chr11:9291600-9322600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr11:9296600-9332600	Weak transcription	Right Ventricle	heart
9	chr11:9296600-9333000	Weak transcription	Psoas Muscle	Psoas
10	chr11:9296600-9334800	Weak transcription	Aorta	Aorta
11	chr11:9296800-9332800	Weak transcription	Brain Angular Gyrus	brain
12	chr11:9296800-9333200	Weak transcription	Colon Smooth Muscle	Colon
13	chr11:9296800-9333200	Weak transcription	Ovary	ovary
14	chr11:9297000-9321400	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr11:9297000-9322800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr11:9297200-9321000	Weak transcription	Left Ventricle	heart
17	chr11:9298200-9323800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:9301600-9321200	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr11:9301600-9321600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:9302200-9324800	Weak transcription	Fetal Brain Male	brain
21	chr11:9302600-9320600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:9302600-9321600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr11:9302600-9325200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr11:9302600-9332600	Weak transcription	Esophagus	oesophagus
25	chr11:9302600-9333200	Weak transcription	Spleen	Spleen
26	chr11:9302600-9333400	Weak transcription	Fetal Brain Female	brain
27	chr11:9302600-9333600	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr11:9302600-9334600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr11:9302600-9334800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr11:9302800-9320600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr11:9302800-9321600	Weak transcription	Brain Anterior Caudate	brain
32	chr11:9302800-9334600	Weak transcription	NH-A	brain
33	chr11:9303200-9332000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr11:9303200-9333000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr11:9303400-9320600	Weak transcription	Osteobl	bone
36	chr11:9303400-9334000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr11:9305800-9332800	Weak transcription	NHDF-Ad	bronchial
38	chr11:9306000-9332600	Weak transcription	Brain Germinal Matrix	brain
39	chr11:9306400-9321600	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr11:9306400-9322200	Weak transcription	Rectal Smooth Muscle	rectum
41	chr11:9307600-9322000	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr11:9308000-9325000	Weak transcription	Brain Cingulate Gyrus	brain
43	chr11:9308200-9323000	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr11:9308200-9329200	Weak transcription	Brain Hippocampus Middle	brain
45	chr11:9308200-9332600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr11:9308200-9334800	Weak transcription	Primary B cells from cord blood	blood
47	chr11:9308400-9324000	Weak transcription	Stomach Smooth Muscle	stomach
48	chr11:9309400-9333800	Weak transcription	Adipose Nuclei	Adipose
49	chr11:9310000-9328400	Weak transcription	Fetal Heart	heart
50	chr11:9310600-9321200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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