Variant report

Variant	rs74029263
Chromosome Location	chr16:82892316-82892317
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs56220520	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58804740	1.00[AFR][1000 genomes]
rs61538662	0.95[AFR][1000 genomes]
rs74029073	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74029260	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74032603	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532599	chr16:82074439-82926863	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
2	nsv573367	chr16:82140561-83040846	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1057341	chr16:82363800-83198907	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
4	nsv542997	chr16:82363800-83198907	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1063617	chr16:82786803-83229529	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	esv2830385	chr16:82841335-82950413	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82848200-82898200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr16:82863200-82892800	Weak transcription	HSMMtube	muscle
3	chr16:82876800-82892400	Weak transcription	HSMM	muscle
4	chr16:82879200-82907000	Weak transcription	Left Ventricle	heart
5	chr16:82880800-82893200	Weak transcription	NHEK	skin
6	chr16:82881400-82892400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr16:82881400-82897600	Weak transcription	HMEC	breast
8	chr16:82886200-82917000	Weak transcription	Right Ventricle	heart
9	chr16:82886400-82898000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr16:82886400-82898600	Weak transcription	Aorta	Aorta
11	chr16:82889600-82894000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr16:82889600-82894200	Weak transcription	Osteobl	bone
13	chr16:82889800-82900400	Weak transcription	NHDF-Ad	bronchial
14	chr16:82891000-82907000	Weak transcription	Psoas Muscle	Psoas
15	chr16:82891600-82897200	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr16:82891600-82907800	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr16:82892000-82892800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr16:82892000-82893800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr16:82892000-82898400	Weak transcription	Fetal Muscle Leg	muscle
20	chr16:82892200-82894000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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