Variant report

Variant	rs28743032
Chromosome Location	chr4:53980308-53980309
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:53978972..53981461-chr4:53984171..53987382,3	K562	blood:
2	chr4:53979124..53981859-chr4:53991405..53994171,2	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12331589	0.98[AFR][1000 genomes]
rs17082303	0.88[AFR][1000 genomes]
rs17082339	0.98[AFR][1000 genomes]
rs28367019	1.00[AFR][1000 genomes]
rs28448601	1.00[AFR][1000 genomes]
rs28458908	1.00[AFR][1000 genomes]
rs28568831	1.00[AFR][1000 genomes]
rs28570026	0.98[AFR][1000 genomes]
rs28658311	1.00[AFR][1000 genomes]
rs28692639	1.00[AFR][1000 genomes]
rs28799619	0.96[AFR][1000 genomes]
rs28861447	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004889	chr4:53436500-54106281	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv537094	chr4:53436500-54106281	Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 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	chr4:53965800-53986000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr4:53968400-53983200	Weak transcription	NHEK	skin
3	chr4:53968400-53984600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:53969200-53983200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr4:53978800-54008000	Weak transcription	Primary T cells from cord blood	blood
6	chr4:53979200-53980400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr4:53979200-53980600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr4:53979400-53980600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:53979400-53980600	Enhancers	Osteobl	bone
10	chr4:53979600-53982600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr4:53979600-53983200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr4:53979800-53980400	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr4:53979800-53980600	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr4:53980000-53980800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:53980000-53982800	Weak transcription	HMEC	breast
16	chr4:53980000-53983000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:53980000-53983400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr4:53980000-53985400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr4:53980000-53985800	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr4:53980000-53985800	Weak transcription	NHLF	lung
21	chr4:53980000-53986800	Weak transcription	Aorta	Aorta
22	chr4:53980200-53980600	Flanking Active TSS	NHDF-Ad	bronchial
23	chr4:53980200-53981000	Weak transcription	GM12878-XiMat	blood

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