Variant report

Variant	rs12284020
Chromosome Location	chr11:36432697-36432698
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:36432501..36434246-chr11:36442338..36444522,2	K562	blood:
2	chr11:36432655..36434682-chr11:36437304..36439623,2	K562	blood:
3	chr11:36432298..36434335-chr11:36439830..36441750,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12224636	0.93[CEU][hapmap];0.97[EUR][1000 genomes]
rs12270583	0.82[CEU][hapmap]
rs34066413	0.97[EUR][1000 genomes]
rs34096374	0.97[EUR][1000 genomes]
rs34636059	0.97[EUR][1000 genomes]
rs34852721	0.97[EUR][1000 genomes]
rs34941068	0.97[EUR][1000 genomes]
rs35825266	0.96[EUR][1000 genomes]
rs60892952	0.96[EUR][1000 genomes]
rs71481977	0.96[EUR][1000 genomes]
rs71481978	0.96[EUR][1000 genomes]
rs765539	0.80[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv467791	chr11:36108497-36999385	Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv554003	chr11:36108497-36999385	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	esv2761662	chr11:36429857-36434542	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:36400200-36475400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:36400800-36443600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr11:36403000-36438200	Weak transcription	Ovary	ovary
4	chr11:36407200-36441800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr11:36408400-36433000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:36413000-36471000	Weak transcription	Aorta	Aorta
7	chr11:36413200-36441600	Weak transcription	HSMMtube	muscle
8	chr11:36414800-36475600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr11:36418200-36436800	Weak transcription	Pancreas	Pancrea
10	chr11:36420200-36434800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:36420200-36434800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:36420400-36453200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:36420600-36435200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:36420600-36435200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr11:36421400-36435000	Strong transcription	Cortex derived primary cultured neurospheres	brain
16	chr11:36423400-36441800	Weak transcription	HMEC	breast
17	chr11:36425800-36439000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr11:36425800-36441400	Weak transcription	Fetal Kidney	kidney
19	chr11:36426200-36435200	Strong transcription	Fetal Intestine Small	intestine
20	chr11:36426400-36434400	Weak transcription	HSMM	muscle
21	chr11:36426400-36435200	Strong transcription	Fetal Intestine Large	intestine
22	chr11:36427400-36434200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr11:36427800-36434200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr11:36428000-36435000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr11:36428200-36432800	Enhancers	Primary B cells from peripheral blood	blood
26	chr11:36428200-36435000	Enhancers	Primary hematopoietic stem cells	blood
27	chr11:36428800-36435000	Enhancers	Fetal Thymus	thymus
28	chr11:36429200-36434800	Weak transcription	Stomach Mucosa	stomach
29	chr11:36429600-36433600	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr11:36429600-36436600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:36429800-36433400	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr11:36429800-36433600	Enhancers	Placenta	Placenta
33	chr11:36429800-36434600	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr11:36430000-36433000	Enhancers	Spleen	Spleen
35	chr11:36430000-36433600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:36430000-36433600	Enhancers	Adipose Nuclei	Adipose
37	chr11:36430000-36433600	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr11:36430000-36433800	Enhancers	HUVEC	blood vessel
39	chr11:36430000-36434000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr11:36430000-36434400	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr11:36430000-36434800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr11:36430200-36433600	Genic enhancers	Rectal Mucosa Donor 29	rectum
43	chr11:36430200-36433600	Genic enhancers	Rectal Mucosa Donor 31	rectum
44	chr11:36430400-36432800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr11:36430400-36433400	Enhancers	GM12878-XiMat	blood
46	chr11:36430400-36435000	Enhancers	Brain Substantia Nigra	brain
47	chr11:36430600-36432800	Weak transcription	Brain Angular Gyrus	brain
48	chr11:36430600-36433000	Enhancers	Lung	lung
49	chr11:36430600-36433400	Enhancers	Left Ventricle	heart
50	chr11:36430600-36433600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood

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