Variant report

Variant	rs529620114
Chromosome Location	chr11:9952567-9952568
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933855	chr11:9645441-10130519	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	esv2762895	chr11:9849511-9954549	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv896988	chr11:9912052-10012511	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1041148	chr11:9927980-9954537	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv896989	chr11:9951968-10059623	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9894400-9978600	Weak transcription	Left Ventricle	heart
2	chr11:9910000-9954600	Weak transcription	Pancreas	Pancrea
3	chr11:9917800-9952600	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr11:9929200-9966800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:9929600-9953000	Weak transcription	HSMMtube	muscle
6	chr11:9943400-9980600	Weak transcription	Primary T cells from cord blood	blood
7	chr11:9944600-9952800	Weak transcription	Liver	Liver
8	chr11:9944800-9961000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:9944800-9969000	Weak transcription	Ovary	ovary
10	chr11:9945000-9954000	Weak transcription	HMEC	breast
11	chr11:9945000-9967600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr11:9945400-9964800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr11:9945600-9955200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr11:9945600-9958400	Weak transcription	NHDF-Ad	bronchial
15	chr11:9950200-9980400	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr11:9951000-9953000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr11:9951200-9952800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:9951200-9952800	Strong transcription	Adipose Nuclei	Adipose
19	chr11:9951200-9955000	Weak transcription	Right Ventricle	heart
20	chr11:9951600-9953000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr11:9951600-9954400	Weak transcription	Brain Angular Gyrus	brain
22	chr11:9951800-9952600	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr11:9951800-9952800	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr11:9951800-9953000	Strong transcription	Stomach Smooth Muscle	stomach
25	chr11:9952000-9952600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
26	chr11:9952000-9952600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:9952000-9952800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr11:9952000-9953000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr11:9952000-9953000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr11:9952000-9953000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr11:9952000-9953000	Strong transcription	Fetal Muscle Leg	muscle
32	chr11:9952200-9952600	ZNF genes & repeats	Lung	lung
33	chr11:9952200-9952600	Flanking Active TSS	K562	blood
34	chr11:9952200-9952800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
35	chr11:9952200-9952800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr11:9952200-9952800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr11:9952200-9952800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr11:9952200-9952800	Strong transcription	Aorta	Aorta
39	chr11:9952200-9952800	Strong transcription	Fetal Intestine Large	intestine
40	chr11:9952200-9953000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr11:9952200-9953000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:9952200-9953000	ZNF genes & repeats	Esophagus	oesophagus
43	chr11:9952200-9953000	ZNF genes & repeats	Fetal Intestine Small	intestine
44	chr11:9952200-9953000	Strong transcription	Fetal Stomach	stomach
45	chr11:9952200-9953200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr11:9952400-9952600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
47	chr11:9952400-9952600	Genic enhancers	Placenta	Placenta
48	chr11:9952400-9952600	ZNF genes & repeats	Thymus	Thymus
49	chr11:9952400-9952800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr11:9952400-9952800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood

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