Variant report

Variant	rs35520914
Chromosome Location	chr11:108382528-108382529
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:108368444..108370288-chr11:108381123..108383752,3	K562	blood:
2	chr11:108380083..108382717-chr11:108385975..108388358,2	K562	blood:
3	chr11:108366425..108370806-chr11:108379844..108383752,5	K562	blood:
4	chr11:108366379..108367925-chr11:108380828..108383134,2	K562	blood:
5	chr11:108377166..108379267-chr11:108381672..108383561,2	K562	blood:

Variant related genes	Relation type
ENSG00000178202	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs12099333	1.00[AMR][1000 genomes]
rs7948491	1.00[AMR][1000 genomes]
rs990252	1.00[AMR][1000 genomes]

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	nsv1052254	chr11:108122683-108845008	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv541164	chr11:108122683-108845008	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv832263	chr11:108183372-108384391	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108369600-108384000	Weak transcription	Fetal Kidney	kidney
2	chr11:108370400-108408800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:108371800-108406400	Weak transcription	Gastric	stomach
4	chr11:108372000-108401200	Weak transcription	Esophagus	oesophagus
5	chr11:108377600-108384400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr11:108379800-108389200	Strong transcription	Placenta	Placenta
7	chr11:108380000-108382800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr11:108380000-108383000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr11:108380000-108384200	Genic enhancers	NHEK	skin
10	chr11:108380200-108382600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr11:108380200-108382600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:108380200-108382600	Weak transcription	K562	blood
13	chr11:108380200-108384800	Weak transcription	Brain Anterior Caudate	brain
14	chr11:108380400-108384400	Weak transcription	Stomach Mucosa	stomach
15	chr11:108380800-108384000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:108380800-108384000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:108380800-108384000	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr11:108381000-108385600	Strong transcription	Liver	Liver
19	chr11:108381000-108408800	Weak transcription	Duodenum Mucosa	Duodenum
20	chr11:108381200-108383000	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr11:108381400-108382800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr11:108381600-108383800	Enhancers	HMEC	breast
23	chr11:108381600-108385400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr11:108381800-108383400	Weak transcription	Lung	lung
25	chr11:108381800-108383400	Enhancers	NHDF-Ad	bronchial
26	chr11:108381800-108383600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr11:108381800-108384200	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr11:108382000-108382800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr11:108382000-108382800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:108382000-108384000	Weak transcription	GM12878-XiMat	blood
31	chr11:108382000-108384200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr11:108382000-108384200	Weak transcription	Primary T cells from cord blood	blood
33	chr11:108382000-108384400	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr11:108382000-108384400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr11:108382000-108396000	Weak transcription	Pancreas	Pancrea
36	chr11:108382200-108383400	Enhancers	HSMM	muscle
37	chr11:108382200-108383600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr11:108382200-108384000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr11:108382200-108384400	Weak transcription	Rectal Smooth Muscle	rectum
40	chr11:108382200-108385000	Weak transcription	Primary hematopoietic stem cells	blood
41	chr11:108382200-108385600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:108382200-108385600	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr11:108382400-108383200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr11:108382400-108383200	Enhancers	Muscle Satellite Cultured Cells	--
45	chr11:108382400-108383600	Weak transcription	HSMMtube	muscle

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