Variant report

Variant	rs10838529
Chromosome Location	chr11:45931502-45931503
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	chr11:45927639-45933214	K562	blood:	n/a	n/a
2	POLR2A	chr11:45928064-45933219	GM12878	blood:	n/a	n/a
3	POLR2A	chr11:45927693-45931524	GM19193	blood:	n/a	n/a
4	POLR2A	chr11:45931437-45931852	HL-60	blood:	n/a	n/a
5	POLR2A	chr11:45931273-45931777	K562	blood:	n/a	n/a
6	POLR2A	chr11:45927753-45932920	GM18505	blood:	n/a	n/a
7	POLR2A	chr11:45931474-45931718	GM12878	blood:	n/a	n/a
8	POLR2A	chr11:45928206-45931597	GM12891	blood:	n/a	n/a
9	POLR2A	chr11:45927292-45932078	GM12892	blood:	n/a	n/a
10	POLR2A	chr11:45929605-45931574	K562	blood:	n/a	n/a
11	POLR2A	chr11:45928253-45931814	GM12892	blood:	n/a	n/a
12	POLR2A	chr11:45931374-45932110	H1-neurons	neurons:	n/a	n/a
13	POLR2A	chr11:45928582-45931752	GM12891	blood:	n/a	n/a
14	POLR2A	chr11:45931222-45931751	GM12878	blood:	n/a	n/a
15	POLR2A	chr11:45923263-45931805	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:45890873..45893526-chr11:45930539..45932384,2	K562	blood:

Variant related genes	Relation type
C11orf94	TF binding region
ENSG00000255498	TF binding region
ENSG00000121671	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11038709	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2271845	1.00[ASW][hapmap];0.91[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];0.91[GIH][hapmap];0.89[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.89[YRI][hapmap];1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2280329	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3789023	0.94[CHB][hapmap];0.80[CHD][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.80[TSI][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4505038	0.86[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];0.86[GIH][hapmap];0.88[JPT][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55884539	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56148819	0.84[ASN][1000 genomes]
rs7114162	0.94[CHB][hapmap];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897314	chr11:45816020-45965129	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv1047462	chr11:45898630-45953696	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv516442	chr11:45899962-45983385	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	esv1794798	chr11:45903280-45953636	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	esv1805505	chr11:45912324-45956109	Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	esv1807609	chr11:45915859-45940195	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	esv1798496	chr11:45925495-45948304	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr11:45921400-45933000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr11:45922200-45931800	Weak transcription	Primary B cells from cord blood	blood
3	chr11:45922400-45934800	Weak transcription	A549	lung
4	chr11:45922600-45932400	Weak transcription	Hela-S3	cervix
5	chr11:45922600-45932400	Weak transcription	Osteobl	bone
6	chr11:45922600-45934400	Weak transcription	HMEC	breast
7	chr11:45922600-45938400	Weak transcription	Fetal Kidney	kidney
8	chr11:45923000-45938000	Weak transcription	NHDF-Ad	bronchial
9	chr11:45923000-45938400	Weak transcription	Right Atrium	heart
10	chr11:45923200-45932200	Weak transcription	HSMM	muscle
11	chr11:45923200-45935600	Weak transcription	NH-A	brain
12	chr11:45923400-45931600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr11:45923400-45932000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:45923400-45932400	Weak transcription	HepG2	liver
15	chr11:45923400-45934800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:45923600-45936600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr11:45924600-45936400	Strong transcription	Fetal Brain Female	brain
18	chr11:45926600-45935400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr11:45927000-45932200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr11:45927000-45936200	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr11:45927000-45936600	Weak transcription	K562	blood
22	chr11:45927200-45937600	Weak transcription	Stomach Mucosa	stomach
23	chr11:45927400-45932200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr11:45927400-45935000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr11:45928000-45932400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr11:45928000-45937800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr11:45928400-45934400	Weak transcription	GM12878-XiMat	blood
28	chr11:45928800-45933200	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr11:45929800-45931800	Genic enhancers	Brain Anterior Caudate	brain
30	chr11:45929800-45938000	Strong transcription	Fetal Intestine Small	intestine
31	chr11:45930000-45935000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr11:45930000-45937400	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr11:45930200-45935800	Weak transcription	Primary hematopoietic stem cells	blood
34	chr11:45930200-45936200	Strong transcription	Primary T cells fromperipheralblood	blood
35	chr11:45930200-45936200	Weak transcription	HSMMtube	muscle
36	chr11:45930200-45937000	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr11:45930200-45937200	Strong transcription	Thymus	Thymus
38	chr11:45930400-45932000	Weak transcription	Fetal Lung	lung
39	chr11:45930400-45932400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr11:45930400-45933400	Strong transcription	Liver	Liver
41	chr11:45930400-45934800	Weak transcription	Colon Smooth Muscle	Colon
42	chr11:45930400-45937600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr11:45930400-45937600	Strong transcription	Fetal Stomach	stomach
44	chr11:45930400-45937800	Strong transcription	Fetal Intestine Large	intestine
45	chr11:45930400-45938000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr11:45930400-45938000	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr11:45930400-45938000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr11:45930400-45938000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr11:45930400-45938000	Strong transcription	Rectal Mucosa Donor 29	rectum
50	chr11:45930600-45933200	Strong transcription	Ovary	ovary

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