Variant report

Variant	rs183670982
Chromosome Location	chr11:120224742-120224743
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:120223412..120225236-chr11:120267280..120269601,2	K562	blood:
2	chr11:120206632..120208724-chr11:120224150..120227495,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000196914	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv529003	chr11:120209386-120355230	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1050935	chr11:120224544-120276373	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120215400-120225600	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr11:120216000-120224800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:120216000-120239000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:120216400-120244800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:120217200-120228600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:120217200-120232000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:120217400-120225600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr11:120217400-120234000	Weak transcription	Aorta	Aorta
9	chr11:120217600-120257000	Weak transcription	HSMM	muscle
10	chr11:120218000-120228400	Enhancers	Liver	Liver
11	chr11:120218200-120224800	Weak transcription	NH-A	brain
12	chr11:120218200-120225600	Weak transcription	Psoas Muscle	Psoas
13	chr11:120218200-120229600	Weak transcription	GM12878-XiMat	blood
14	chr11:120218600-120224800	Weak transcription	Fetal Kidney	kidney
15	chr11:120218600-120231800	Weak transcription	Rectal Smooth Muscle	rectum
16	chr11:120218600-120232000	Weak transcription	Fetal Stomach	stomach
17	chr11:120218600-120232400	Weak transcription	HUVEC	blood vessel
18	chr11:120218800-120224800	Weak transcription	Osteobl	bone
19	chr11:120218800-120230600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:120220400-120232800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr11:120220600-120225000	Weak transcription	HSMMtube	muscle
22	chr11:120220600-120232000	Weak transcription	Colon Smooth Muscle	Colon
23	chr11:120220800-120225200	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr11:120222600-120225000	Enhancers	K562	blood
25	chr11:120222800-120226000	Enhancers	HepG2	liver
26	chr11:120223200-120225600	Enhancers	Duodenum Mucosa	Duodenum
27	chr11:120223200-120225800	Enhancers	Fetal Intestine Small	intestine
28	chr11:120223200-120225800	Enhancers	Fetal Lung	lung
29	chr11:120223200-120225800	Enhancers	Left Ventricle	heart
30	chr11:120223400-120224800	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr11:120223400-120225200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr11:120223400-120225200	Enhancers	Gastric	stomach
33	chr11:120223400-120225200	Enhancers	Pancreas	Pancrea
34	chr11:120223400-120225200	Enhancers	Right Atrium	heart
35	chr11:120223400-120225200	Enhancers	Stomach Mucosa	stomach
36	chr11:120223400-120226400	Enhancers	Fetal Intestine Large	intestine
37	chr11:120223400-120226400	Enhancers	Ovary	ovary
38	chr11:120223400-120226400	Enhancers	Right Ventricle	heart
39	chr11:120223600-120226400	Enhancers	Small Intestine	intestine
40	chr11:120223800-120225800	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr11:120224000-120224800	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr11:120224000-120224800	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr11:120224200-120224800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr11:120224200-120224800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr11:120224200-120225000	Enhancers	Esophagus	oesophagus
46	chr11:120224200-120225200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr11:120224200-120225200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr11:120224400-120224800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr11:120224400-120225000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr11:120224400-120225000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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