Variant report

Variant	rs4413678
Chromosome Location	chr7:19017705-19017706
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10282136	0.91[YRI][hapmap]
rs9886098	0.82[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531020	chr7:18971153-19261019	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1032870	chr7:18982862-19021763	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv538765	chr7:18982862-19021763	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18991400-19025000	Weak transcription	Primary B cells from cord blood	blood
2	chr7:19011600-19018600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr7:19011600-19018800	Enhancers	HMEC	breast
4	chr7:19011600-19018800	Enhancers	NHEK	skin
5	chr7:19012000-19018600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:19012200-19018600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr7:19013800-19040800	Weak transcription	Aorta	Aorta
8	chr7:19015600-19020600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr7:19015800-19042400	Weak transcription	Left Ventricle	heart
10	chr7:19016400-19018200	Enhancers	Fetal Stomach	stomach
11	chr7:19016400-19018600	Enhancers	HSMM	muscle
12	chr7:19016400-19018600	Enhancers	HUVEC	blood vessel
13	chr7:19016800-19017800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:19016800-19018600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:19017000-19017800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:19017000-19017800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:19017000-19017800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr7:19017000-19017800	Enhancers	Fetal Heart	heart
19	chr7:19017200-19017800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr7:19017200-19017800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr7:19017200-19017800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr7:19017200-19017800	Enhancers	Hela-S3	cervix
23	chr7:19017200-19017800	Flanking Active TSS	Osteobl	bone
24	chr7:19017200-19018000	Flanking Active TSS	NH-A	brain
25	chr7:19017200-19018000	Flanking Active TSS	NHDF-Ad	bronchial
26	chr7:19017200-19018600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:19017200-19018600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:19017200-19019600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr7:19017400-19018200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:19017400-19019400	Enhancers	NHLF	lung
31	chr7:19017400-19026000	Weak transcription	HSMMtube	muscle
32	chr7:19017600-19018200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr7:19017600-19018200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr7:19017600-19018200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr7:19017600-19022600	Weak transcription	Stomach Smooth Muscle	stomach
36	chr7:19017600-19029800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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