Variant report

Variant	rs561661526
Chromosome Location	chr11:16917703-16917704
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	chr11:16915696..16917926-chr11:16944462..16946191,2	MCF-7	breast:
2	chr11:16910866..16914588-chr11:16915188..16918653,3	MCF-7	breast:

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	nsv832077	chr11:16834545-17059176	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv7688	chr11:16912759-16939804	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv2757425	chr11:16915291-16934130	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2759805	chr11:16915291-16934130	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1038987	chr11:16916438-16927022	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2754709	chr11:16917219-16927022	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16910000-16917800	Weak transcription	Lung	lung
2	chr11:16912200-16923600	Weak transcription	A549	lung
3	chr11:16912400-16919400	Weak transcription	Liver	Liver
4	chr11:16913000-16918400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr11:16913800-16921800	Enhancers	Fetal Heart	heart
6	chr11:16914000-16927400	Weak transcription	HSMMtube	muscle
7	chr11:16914400-16919200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:16914600-16921200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr11:16915400-16918200	Weak transcription	Fetal Intestine Large	intestine
10	chr11:16915400-16918400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr11:16915800-16917800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr11:16915800-16918000	Weak transcription	Right Ventricle	heart
13	chr11:16915800-16919000	Weak transcription	Right Atrium	heart
14	chr11:16915800-16921400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr11:16915800-16921400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:16915800-16922800	Weak transcription	HMEC	breast
17	chr11:16916000-16917800	Weak transcription	Stomach Mucosa	stomach
18	chr11:16916000-16918400	Weak transcription	Pancreas	Pancrea
19	chr11:16916000-16918800	Weak transcription	Adipose Nuclei	Adipose
20	chr11:16916000-16919000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr11:16916000-16923000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr11:16916000-16924400	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr11:16916000-16931000	Weak transcription	Spleen	Spleen
24	chr11:16916600-16918200	Weak transcription	Fetal Intestine Small	intestine
25	chr11:16916800-16917800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
26	chr11:16916800-16918000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr11:16916800-16919000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr11:16916800-16920200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr11:16917000-16918400	Weak transcription	Fetal Kidney	kidney
30	chr11:16917200-16918400	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr11:16917200-16918600	Weak transcription	Duodenum Mucosa	Duodenum
32	chr11:16917200-16919400	Enhancers	Gastric	stomach
33	chr11:16917400-16918000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr11:16917400-16918200	Enhancers	Left Ventricle	heart
35	chr11:16917600-16918000	Weak transcription	Colonic Mucosa	Colon
36	chr11:16917600-16918200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:16917600-16918600	Weak transcription	Brain Anterior Caudate	brain
38	chr11:16917600-16919200	Weak transcription	NHDF-Ad	bronchial
39	chr11:16917600-16920200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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