Variant report

Variant	rs73136507
Chromosome Location	chr5:95463650-95463651
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:95455996..95458938-chr5:95461251..95464518,3	K562	blood:
2	chr5:95462184..95464791-chr5:95469222..95471712,2	K562	blood:

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs57708299	1.00[EUR][1000 genomes]
rs58041456	1.00[EUR][1000 genomes]
rs59577118	1.00[EUR][1000 genomes]
rs59929901	1.00[EUR][1000 genomes]
rs60867883	1.00[EUR][1000 genomes]
rs73134494	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73134495	1.00[EUR][1000 genomes]
rs73134499	1.00[EUR][1000 genomes]
rs73134502	1.00[EUR][1000 genomes]
rs73136510	0.85[AFR][1000 genomes]
rs73773913	1.00[EUR][1000 genomes]
rs73773915	1.00[EUR][1000 genomes]
rs73773916	1.00[EUR][1000 genomes]
rs73773917	1.00[EUR][1000 genomes]
rs7709310	1.00[AMR][1000 genomes]

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	esv2758003	chr5:95231706-95540433	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	esv2759355	chr5:95231706-95540433	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	esv2757121	chr5:95304236-95539536	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1030444	chr5:95353620-95995619	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
5	nsv537810	chr5:95353620-95995619	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 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	chr5:95458800-95465800	Enhancers	NHEK	skin
2	chr5:95459800-95465200	Enhancers	HMEC	breast
3	chr5:95461600-95464000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr5:95461600-95464000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr5:95461600-95482000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:95461800-95464200	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr5:95461800-95464200	Weak transcription	Stomach Mucosa	stomach
8	chr5:95461800-95465400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr5:95461800-95468600	Weak transcription	HSMM	muscle
10	chr5:95462000-95464000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr5:95462000-95464000	Enhancers	Liver	Liver
12	chr5:95462000-95464000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr5:95462000-95465400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr5:95462200-95465200	Enhancers	HepG2	liver
15	chr5:95462200-95466600	Weak transcription	Fetal Heart	heart
16	chr5:95462800-95465200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr5:95463000-95463800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr5:95463000-95465200	Enhancers	Colon Smooth Muscle	Colon
19	chr5:95463200-95464200	Enhancers	Muscle Satellite Cultured Cells	--
20	chr5:95463400-95464400	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr5:95463600-95464800	Active TSS	Aorta	Aorta
22	chr5:95463600-95465800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:95463600-95468600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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