Variant report

Variant	rs201365060
Chromosome Location	chr11:120746884-120746885
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv1053607	chr11:120540795-120802006	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1038264	chr11:120582595-120799335	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv541181	chr11:120582595-120799335	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3417008	chr11:120744342-120748140	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
5	esv3395329	chr11:120744742-120749140	Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv3332666	chr11:120746527-120747270	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120704400-120748800	Weak transcription	Brain Substantia Nigra	brain
2	chr11:120729200-120751200	Weak transcription	Ovary	ovary
3	chr11:120738600-120747400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr11:120738600-120755600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr11:120739000-120749200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr11:120739200-120755600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr11:120740200-120748200	Weak transcription	Brain Germinal Matrix	brain
8	chr11:120740200-120752400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr11:120740400-120752600	Weak transcription	Fetal Brain Male	brain
10	chr11:120743200-120747600	Strong transcription	Brain Anterior Caudate	brain
11	chr11:120745000-120747400	Strong transcription	Brain Cingulate Gyrus	brain
12	chr11:120745000-120752400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:120745000-120754200	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr11:120745200-120747200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr11:120745200-120747200	Strong transcription	Brain Angular Gyrus	brain
16	chr11:120746000-120747600	Strong transcription	Brain Hippocampus Middle	brain
17	chr11:120746200-120754600	Weak transcription	Spleen	Spleen
18	chr11:120746400-120748600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr11:120746600-120747200	Strong transcription	Brain Inferior Temporal Lobe	brain
20	chr11:120746600-120748400	Strong transcription	Fetal Lung	lung
21	chr11:120746800-120747200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr11:120746800-120747200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
23	chr11:120746800-120747200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr11:120746800-120747200	Strong transcription	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links