Variant report

Variant	rs1211783
Chromosome Location	chr11:63748991-63748992
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:63746729-63750197	K562	blood:	n/a	n/a
2	POLR2A	chr11:63748823-63749113	HepG2	liver:	n/a	n/a
3	POLR2A	chr11:63748169-63749243	PFSK-1	brain:	n/a	n/a

Variant related genes	Relation type
OTUB1	TF binding region

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1187867	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs161053	1.00[YRI][hapmap]
rs224174	1.00[YRI][hapmap]
rs2875719	0.82[AFR][1000 genomes]
rs3019784	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3132752	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320119	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320120	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320123	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320147	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320148	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320149	0.91[AFR][1000 genomes]
rs320153	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34036129	1.00[AMR][1000 genomes]
rs35352499	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs368421	1.00[YRI][hapmap]
rs4472946	1.00[YRI][hapmap]
rs497037	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4980510	1.00[AMR][1000 genomes]
rs4980513	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs565004	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs576548	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60969355	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6591828	0.85[AFR][1000 genomes]
rs6591829	0.87[AFR][1000 genomes]
rs7116315	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7126106	1.00[AMR][1000 genomes]
rs7126239	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7130472	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7130979	0.85[AFR][1000 genomes]
rs901492	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051171	chr11:62987064-63835715	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
2	nsv468590	chr11:63639881-63783352	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv555181	chr11:63639881-63783352	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv897629	chr11:63664882-63866959	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv897630	chr11:63664882-63924446	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
6	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
7	nsv897639	chr11:63691049-63844683	Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	esv1849906	chr11:63719273-63880383	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv1042075	chr11:63732454-63813164	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	esv29993	chr11:63738642-63864211	Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
11	nsv897640	chr11:63744152-63835611	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
12	nsv897641	chr11:63744152-63844683	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
13	nsv897642	chr11:63744152-63866959	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
14	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63743000-63753000	Weak transcription	Aorta	Aorta
2	chr11:63744000-63753000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr11:63744000-63753000	Weak transcription	Fetal Kidney	kidney
4	chr11:63744000-63753000	Weak transcription	Small Intestine	intestine
5	chr11:63744200-63749000	Weak transcription	Primary B cells from cord blood	blood
6	chr11:63744200-63749600	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr11:63744200-63749800	Weak transcription	Primary T cells from cord blood	blood
8	chr11:63744200-63749800	Weak transcription	NHDF-Ad	bronchial
9	chr11:63744200-63753000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr11:63744200-63753000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr11:63744400-63749000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr11:63744400-63749800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:63744400-63749800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr11:63744400-63750400	Strong transcription	Fetal Intestine Small	intestine
15	chr11:63744400-63752000	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr11:63744400-63753000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr11:63744400-63753000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr11:63744400-63753000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr11:63744400-63753000	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr11:63744400-63753000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr11:63744400-63753000	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr11:63744400-63753000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr11:63744400-63753000	Weak transcription	Brain Substantia Nigra	brain
24	chr11:63744400-63753000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr11:63744400-63753000	Weak transcription	Fetal Brain Male	brain
26	chr11:63744400-63753000	Weak transcription	Fetal Intestine Large	intestine
27	chr11:63744400-63753000	Weak transcription	Fetal Lung	lung
28	chr11:63744400-63753000	Weak transcription	Psoas Muscle	Psoas
29	chr11:63744400-63753000	Weak transcription	HSMMtube	muscle
30	chr11:63744400-63753000	Weak transcription	HUVEC	blood vessel
31	chr11:63744400-63753000	Weak transcription	Osteobl	bone
32	chr11:63744400-63753400	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr11:63744600-63749000	Weak transcription	NH-A	brain
34	chr11:63744600-63753000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr11:63744800-63749800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr11:63745000-63753000	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr11:63745200-63749000	Strong transcription	Fetal Muscle Leg	muscle
38	chr11:63745200-63753000	Weak transcription	K562	blood
39	chr11:63746200-63753200	Weak transcription	Ovary	ovary
40	chr11:63746400-63753000	Weak transcription	Brain Germinal Matrix	brain
41	chr11:63746600-63749800	Weak transcription	Brain Hippocampus Middle	brain
42	chr11:63746600-63753000	Weak transcription	Colonic Mucosa	Colon
43	chr11:63746800-63749200	Weak transcription	Fetal Thymus	thymus
44	chr11:63746800-63752800	Weak transcription	HMEC	breast
45	chr11:63746800-63753000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:63746800-63753000	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr11:63746800-63753000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr11:63746800-63753000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:63746800-63753000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:63746800-63753000	Weak transcription	Liver	Liver

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