Variant report

Variant	rs34164761
Chromosome Location	chr16:82898333-82898334
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs12596959	0.90[EUR][1000 genomes]
rs12597819	0.84[EUR][1000 genomes]
rs2216738	0.97[AFR][1000 genomes];0.85[EUR][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:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82879200-82907000	Weak transcription	Left Ventricle	heart
2	chr16:82886200-82917000	Weak transcription	Right Ventricle	heart
3	chr16:82886400-82898600	Weak transcription	Aorta	Aorta
4	chr16:82889800-82900400	Weak transcription	NHDF-Ad	bronchial
5	chr16:82891000-82907000	Weak transcription	Psoas Muscle	Psoas
6	chr16:82891600-82907800	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr16:82892000-82898400	Weak transcription	Fetal Muscle Leg	muscle
8	chr16:82892400-82898800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr16:82897000-82899000	Weak transcription	HSMMtube	muscle
10	chr16:82897600-82898400	ZNF genes & repeats	HMEC	breast
11	chr16:82897800-82898400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr16:82897800-82898800	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr16:82897800-82899800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr16:82897800-82905200	Weak transcription	HSMM	muscle
15	chr16:82898000-82898800	Enhancers	Small Intestine	intestine
16	chr16:82898200-82898400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr16:82898200-82898600	ZNF genes & repeats	NHEK	skin
18	chr16:82898200-82899000	Enhancers	Duodenum Mucosa	Duodenum

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dbSNP/dbVar ID: rs12345 /nsv7879
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