Variant report

Variant	rs145348295
Chromosome Location	chr11:75967833-75967834
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	chr11:75945993..75948366-chr11:75966574..75968254,2	MCF-7	breast:

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049039	chr11:75827548-76023665	Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv897926	chr11:75862571-76004202	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv1040118	chr11:75870189-75995089	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	nsv1053129	chr11:75871240-75997663	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv897930	chr11:75960472-76027936	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv12458	chr11:75967239-75969847	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv523869	chr11:75967695-75967841	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv528902	chr11:75967695-75973078	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75962600-75983600	Weak transcription	Spleen	Spleen
2	chr11:75963200-75976000	Weak transcription	Right Atrium	heart
3	chr11:75965000-75968200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:75965200-75974000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr11:75967400-75968000	Weak transcription	Fetal Thymus	thymus
6	chr11:75967400-75968800	Enhancers	Fetal Brain Male	brain
7	chr11:75967600-75968200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:75967600-75968200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
9	chr11:75967600-75968400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr11:75967600-75968600	Enhancers	Placenta	Placenta
11	chr11:75967600-75968800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr11:75967800-75968000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:75967800-75968000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr11:75967800-75968200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr11:75967800-75968200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr11:75967800-75968200	Enhancers	Fetal Lung	lung
17	chr11:75967800-75968200	Flanking Bivalent TSS/Enh	HepG2	liver
18	chr11:75967800-75968400	Enhancers	Placenta Amnion	Placenta Amnion
19	chr11:75967800-75968600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr11:75967800-75968600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:75967800-75968600	Enhancers	Fetal Muscle Leg	muscle
22	chr11:75967800-75968800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr11:75967800-75968800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr11:75967800-75968800	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links