Variant report

Variant	rs567564483
Chromosome Location	chr11:66885384-66885385
allele	C/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	PAX5	chr11:66885146-66885885	GM12892	blood:	n/a	n/a
2	POLR2A	chr11:66885108-66886634	GM12892	blood:	n/a	n/a
3	MAZ	chr11:66885004-66887904	IMR90	lung:	n/a	chr11:66886120-66886129 chr11:66886002-66886011 chr11:66887263-66887273
4	POLR2A	chr11:66884978-66886367	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr11:66885239-66886986	GM18526	blood:	n/a	n/a
6	POLR2A	chr11:66885381-66886231	HUVEC	blood vessel:	n/a	n/a
7	MTA3	chr11:66884877-66885461	GM12878	blood:	n/a	n/a
8	POLR2A	chr11:66885185-66885537	GM12878	blood:	n/a	n/a
9	POLR2A	chr11:66885236-66887001	GM12892	blood:	n/a	n/a
10	POLR2A	chr11:66885165-66887278	GM18505	blood:	n/a	n/a
11	MAZ	chr11:66885269-66887072	GM12878	blood:	n/a	chr11:66886120-66886129 chr11:66886002-66886011
12	EBF1	chr11:66885081-66885470	GM12878	blood:	n/a	n/a
13	POLR2A	chr11:66885163-66887241	GM19099	blood:	n/a	n/a
14	BACH1	chr11:66885141-66886766	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr11:66885377-66886246	GM12891	blood:	n/a	n/a
16	POLR2A	chr11:66885289-66885540	HUVEC	blood vessel:	n/a	n/a
17	POLR2A	chr11:66885063-66886246	HUVEC	blood vessel:	n/a	n/a
18	POLR2A	chr11:66885089-66887088	PANC-1	pancreas:	n/a	n/a
19	MAX	chr11:66885080-66885506	H1-hESC	embryonic stem cell:	n/a	n/a
20	SIN3AK20	chr11:66884940-66885505	PANC-1	pancreas:	n/a	n/a
21	POLR2A	chr11:66885251-66887004	GM15510	blood:	n/a	n/a
22	POLR2A	chr11:66885193-66886962	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:66885191-66886967	GM12878	blood:	n/a	n/a
24	POLR2A	chr11:66885108-66886178	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr11:66885235-66887051	GM18951	blood:	n/a	n/a
26	POLR2A	chr11:66885064-66885429	H1-hESC	embryonic stem cell:	n/a	n/a
27	ELF1	chr11:66885088-66886214	GM12878	blood:	n/a	chr11:66886042-66886054 chr11:66886063-66886075 chr11:66885889-66885901
28	TAF1	chr11:66885030-66885509	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr11:66885187-66887042	GM19193	blood:	n/a	n/a
30	TAF1	chr11:66885091-66885529	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr11:66885341-66886953	GM10847	blood:	n/a	n/a
32	MAX	chr11:66885168-66885439	GM12878	blood:	n/a	n/a
33	POLR2A	chr11:66884975-66886963	H1-hESC	embryonic stem cell:	n/a	n/a
34	YY1	chr11:66885116-66886224	GM12892	blood:	n/a	chr11:66886062-66886076 chr11:66885282-66885293

No.	Distal block	Cell Line	Cell type
1	chr11:66884866..66886450-chr11:67007040..67008886,2	MCF-7	breast:
2	chr11:66884756..66886465-chr11:66946415..66948664,2	MCF-7	breast:
3	chr11:66885158..66886682-chr11:67030764..67032501,2	K562	blood:
4	chr11:66885002..66889173-chr11:67005085..67009324,11	K562	blood:
5	chr11:66884916..66890908-chr11:67005112..67010354,8	MCF-7	breast:
6	chr11:66821404..66826403-chr11:66884710..66889541,16	MCF-7	breast:
7	chr11:66883623..66889678-chr11:67005085..67009894,16	K562	blood:
8	chr11:66847793..66850553-chr11:66883657..66886437,2	MCF-7	breast:

Variant related genes	Relation type
KDM2A	TF binding region
ENSG00000173156	Chromatin interaction
ENSG00000173120	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv532287	chr11:66784014-67023899	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	esv3412807	chr11:66884326-66888124	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv3397435	chr11:66884601-66887149	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
5	esv3400268	chr11:66884676-66888099	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	esv3328460	chr11:66884901-66888249	Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr11:66881000-66886800	Weak transcription	K562	blood
2	chr11:66883600-66886000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr11:66884200-66885400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:66884400-66885400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:66884800-66885400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr11:66884800-66885400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr11:66884800-66885400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
8	chr11:66884800-66885400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
9	chr11:66884800-66885400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
10	chr11:66884800-66885400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr11:66884800-66886200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr11:66884800-66888800	Active TSS	Rectal Mucosa Donor 29	rectum
13	chr11:66884800-66889200	Active TSS	Duodenum Smooth Muscle	Duodenum
14	chr11:66885000-66885400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
15	chr11:66885000-66885400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:66885000-66885400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
17	chr11:66885000-66885400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr11:66885000-66885400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr11:66885000-66885400	Flanking Active TSS	Primary B cells from cord blood	blood
20	chr11:66885000-66885400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
21	chr11:66885000-66885400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
22	chr11:66885000-66885400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
23	chr11:66885000-66885400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
24	chr11:66885000-66885400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
25	chr11:66885000-66885400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
26	chr11:66885000-66885400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:66885000-66885400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr11:66885000-66885400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:66885000-66885400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:66885000-66885400	Flanking Active TSS	Adipose Nuclei	Adipose
31	chr11:66885000-66885400	Flanking Active TSS	Liver	Liver
32	chr11:66885000-66885400	Flanking Active TSS	Brain Anterior Caudate	brain
33	chr11:66885000-66885400	Flanking Active TSS	Colonic Mucosa	Colon
34	chr11:66885000-66885400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
35	chr11:66885000-66885400	Flanking Active TSS	Fetal Intestine Large	intestine
36	chr11:66885000-66885400	Flanking Active TSS	Fetal Intestine Small	intestine
37	chr11:66885000-66885400	Flanking Active TSS	Fetal Muscle Trunk	muscle
38	chr11:66885000-66885400	Flanking Active TSS	Fetal Muscle Leg	muscle
39	chr11:66885000-66885400	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
40	chr11:66885000-66885400	Flanking Active TSS	Right Atrium	heart
41	chr11:66885000-66885400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr11:66885000-66885400	Flanking Active TSS	Stomach Mucosa	stomach
43	chr11:66885000-66885400	Flanking Active TSS	Stomach Smooth Muscle	stomach
44	chr11:66885000-66885400	Flanking Active TSS	GM12878-XiMat	blood
45	chr11:66885000-66885400	Enhancers	HepG2	liver
46	chr11:66885000-66885600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr11:66885000-66885600	Enhancers	NHDF-Ad	bronchial
48	chr11:66885000-66885800	Active TSS	Muscle Satellite Cultured Cells	--
49	chr11:66885000-66885800	Enhancers	NHLF	lung
50	chr11:66885000-66886000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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