Variant report

Variant	rs1151508
Chromosome Location	chr11:65743779-65743780
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:19)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:19 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:65743416-65743787	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr11:65743157-65744094	U87	brain:	n/a	n/a
3	POLR2A	chr11:65743159-65744862	K562	blood:	n/a	n/a
4	POLR2A	chr11:65743394-65744368	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:65743134-65743961	GM12892	blood:	n/a	n/a
6	POLR2A	chr11:65742873-65743865	SK-N-MC	brain:	n/a	n/a
7	POLR2A	chr11:65742671-65743876	PANC-1	pancreas:	n/a	n/a
8	POLR2A	chr11:65743527-65744800	HL-60	blood:	n/a	n/a
9	POLR2A	chr11:65742864-65745188	GM12891	blood:	n/a	n/a
10	POLR2A	chr11:65743675-65744736	K562	blood:	n/a	n/a
11	POLR2A	chr11:65743401-65743806	GM12878	blood:	n/a	n/a
12	POLR2A	chr11:65743234-65744303	GM12878	blood:	n/a	n/a
13	POLR2A	chr11:65743539-65743869	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr11:65742494-65745636	GM12878	blood:	n/a	n/a
15	POLR2A	chr11:65743049-65745415	GM12892	blood:	n/a	n/a
16	POLR2A	chr11:65743511-65744080	GM12891	blood:	n/a	n/a
17	POLR2A	chr11:65743195-65744088	U87	brain:	n/a	n/a
18	POLR2A	chr11:65743069-65745339	GM12892	blood:	n/a	n/a
19	POLR2A	chr11:65743172-65744008	Hela-S3	cervix:	n/a	n/a

No data

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:65742158..65748813-chr11:65749011..65756801,11	MCF-7	breast:
2	chr11:65729174..65730832-chr11:65742979..65745166,3	MCF-7	breast:

No data

Variant related genes	Relation type
SART1	TF binding region
ENSG00000175467	Chromatin interaction
ENSG00000254867	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1143916	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1144796	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1191715	1.00[AMR][1000 genomes]
rs1201503	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1203799	1.00[AMR][1000 genomes]
rs1630638	1.00[AMR][1000 genomes]
rs1783562	1.00[AMR][1000 genomes]
rs4930332	1.00[AMR][1000 genomes]
rs590381	1.00[AFR][1000 genomes]
rs6591196	1.00[AMR][1000 genomes]
rs73498471	1.00[AMR][1000 genomes]
rs7947668	1.00[AMR][1000 genomes]
rs948477	1.00[AMR][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	nsv430401	chr11:65419324-65788024	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
2	nsv897762	chr11:65613218-65758854	Active TSS Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	185 gene(s)	inside rSNPs	diseases
3	nsv897765	chr11:65623708-65758854	Strong transcription Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
4	nsv832191	chr11:65632329-65806120	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
5	nsv948711	chr11:65692760-65949674	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
6	nsv897768	chr11:65715210-65842064	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
7	nsv897769	chr11:65727799-65828625	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases
8	esv3335923	chr11:65741698-66175759	Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 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	chr11:65729800-65746200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:65730600-65767800	Weak transcription	Right Atrium	heart
3	chr11:65731000-65744600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr11:65731200-65747400	Strong transcription	HUES6 Cell Line	embryonic stem cell
5	chr11:65731200-65747800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:65731200-65748600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr11:65731200-65749600	Strong transcription	Fetal Intestine Small	intestine
8	chr11:65731400-65747600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:65731400-65747600	Strong transcription	Fetal Thymus	thymus
10	chr11:65731400-65748000	Strong transcription	Thymus	Thymus
11	chr11:65731600-65747400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr11:65731600-65747800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr11:65731800-65749000	Strong transcription	Fetal Stomach	stomach
14	chr11:65732000-65747200	Strong transcription	Lung	lung
15	chr11:65732400-65748800	Strong transcription	Stomach Smooth Muscle	stomach
16	chr11:65732800-65748200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr11:65735200-65750600	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr11:65735800-65756600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr11:65736200-65744000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr11:65736400-65767400	Weak transcription	Psoas Muscle	Psoas
21	chr11:65736800-65744400	Weak transcription	HepG2	liver
22	chr11:65736800-65745000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr11:65736800-65747800	Strong transcription	Fetal Muscle Trunk	muscle
24	chr11:65737000-65748000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr11:65737200-65744000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr11:65737200-65747800	Strong transcription	Placenta	Placenta
27	chr11:65737200-65747800	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr11:65737600-65744800	Weak transcription	Small Intestine	intestine
29	chr11:65737600-65748000	Strong transcription	Fetal Muscle Leg	muscle
30	chr11:65737800-65744200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr11:65737800-65744600	Weak transcription	HUVEC	blood vessel
32	chr11:65737800-65756600	Weak transcription	Stomach Mucosa	stomach
33	chr11:65738000-65743800	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr11:65738200-65744600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr11:65738200-65744800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr11:65739000-65747800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:65739200-65749600	Strong transcription	Fetal Brain Female	brain
38	chr11:65739400-65747200	Strong transcription	Brain Hippocampus Middle	brain
39	chr11:65739400-65747400	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr11:65739600-65748000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr11:65739600-65748800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:65739600-65756400	Weak transcription	Fetal Kidney	kidney
43	chr11:65739800-65747600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr11:65739800-65756400	Weak transcription	Hela-S3	cervix
45	chr11:65740000-65747200	Strong transcription	Spleen	Spleen
46	chr11:65740600-65748000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr11:65740800-65745400	Strong transcription	Rectal Smooth Muscle	rectum
48	chr11:65740800-65745600	Strong transcription	Fetal Lung	lung
49	chr11:65740800-65748000	Strong transcription	Skeletal Muscle Male	skeletal muscle
50	chr11:65741000-65746800	Strong transcription	Brain Substantia Nigra	brain

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