Variant report

Variant	rs535899785
Chromosome Location	chr7:136831830-136831831
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	esv2753059	chr7:136633745-136893745	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1028902	chr7:136727136-136858804	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv608462	chr7:136746607-136839390	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv464730	chr7:136825522-136882925	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv608463	chr7:136825522-136882925	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv831149	chr7:136831665-137006468	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136830000-136832000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr7:136830200-136834000	Enhancers	Colon Smooth Muscle	Colon
3	chr7:136830200-136834400	Enhancers	Fetal Heart	heart
4	chr7:136830400-136832400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:136830400-136832400	Enhancers	HSMM	muscle
6	chr7:136830600-136832400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:136830600-136833800	Enhancers	Fetal Stomach	stomach
8	chr7:136830800-136833000	Enhancers	HSMMtube	muscle
9	chr7:136830800-136834000	Enhancers	Placenta Amnion	Placenta Amnion
10	chr7:136831000-136832000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:136831000-136833000	Enhancers	Rectal Smooth Muscle	rectum
12	chr7:136831200-136832000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:136831200-136832000	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr7:136831200-136832000	Flanking Active TSS	Osteobl	bone
15	chr7:136831400-136832200	Enhancers	Brain Germinal Matrix	brain
16	chr7:136831400-136832200	Enhancers	Fetal Kidney	kidney
17	chr7:136831400-136833200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr7:136831600-136832000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:136831600-136832600	Enhancers	NHLF	lung
20	chr7:136831800-136832000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:136831800-136832000	Weak transcription	NHDF-Ad	bronchial
22	chr7:136831800-136832400	Enhancers	HMEC	breast
23	chr7:136831800-136833000	Enhancers	NH-A	brain

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