Variant report

Variant	rs570727875
Chromosome Location	chr4:74759939-74759940
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:74759338..74760983-chr4:74763696..74765672,2	K562	blood:
2	chr4:74758611..74762453-chr4:74763527..74766152,5	K562	blood:

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	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv530126	chr4:74376622-74843892	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv432612	chr4:74723372-74774372	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv525980	chr4:74731526-75382209	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	esv3348061	chr4:74759910-74760131	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74752000-74760600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:74757000-74760000	Enhancers	Fetal Intestine Large	intestine
3	chr4:74757200-74760000	Weak transcription	Fetal Kidney	kidney
4	chr4:74757200-74770400	Enhancers	NHDF-Ad	bronchial
5	chr4:74757400-74761000	Weak transcription	Stomach Mucosa	stomach
6	chr4:74757600-74760200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr4:74757600-74760600	Weak transcription	Pancreas	Pancrea
8	chr4:74757600-74761200	Weak transcription	Spleen	Spleen
9	chr4:74758200-74760200	Weak transcription	Adipose Nuclei	Adipose
10	chr4:74758200-74760800	Weak transcription	Osteobl	bone
11	chr4:74758600-74760000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:74758600-74760000	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr4:74758800-74761200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr4:74759000-74760000	Weak transcription	Fetal Intestine Small	intestine
15	chr4:74759000-74760200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr4:74759000-74761000	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr4:74759200-74760200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:74759200-74760600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr4:74759200-74764600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr4:74759800-74760400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr4:74759800-74761200	Enhancers	Fetal Stomach	stomach
22	chr4:74759800-74770400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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