Variant report

Variant	rs72794135
Chromosome Location	chr16:83032676-83032677
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1025054	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16959005	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16959008	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17745108	0.89[EUR][1000 genomes]
rs56184188	0.80[EUR][1000 genomes]
rs56387206	0.87[EUR][1000 genomes]
rs56907994	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58556368	0.80[EUR][1000 genomes]
rs6565098	0.97[ASN][1000 genomes]
rs7185868	0.80[EUR][1000 genomes]
rs7203552	0.81[ASN][1000 genomes]
rs72792118	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72792121	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72792126	0.80[EUR][1000 genomes]
rs72792134	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72792137	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72792140	0.84[EUR][1000 genomes]
rs72792141	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72792142	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72792143	0.84[EUR][1000 genomes]
rs72792145	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72792147	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72792148	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72792149	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72792150	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72792154	0.93[EUR][1000 genomes]
rs72792155	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72792158	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72792160	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72792161	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72792163	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72792164	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72792167	0.86[ASN][1000 genomes]
rs72792168	0.94[ASN][1000 genomes]
rs72792170	0.94[ASN][1000 genomes]
rs72792172	0.94[ASN][1000 genomes]
rs72792173	0.94[ASN][1000 genomes]
rs72794129	0.97[ASN][1000 genomes]
rs72794130	0.97[ASN][1000 genomes]
rs72794131	0.97[ASN][1000 genomes]
rs72794133	0.97[ASN][1000 genomes]
rs72794134	0.97[ASN][1000 genomes]
rs72794137	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72794139	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72794141	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72794143	0.97[ASN][1000 genomes]
rs72794145	0.97[ASN][1000 genomes]
rs72794146	0.97[ASN][1000 genomes]
rs72794147	0.97[ASN][1000 genomes]
rs72794152	0.92[ASN][1000 genomes]
rs72794153	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72794155	0.84[ASN][1000 genomes]
rs72794156	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72794158	0.92[ASN][1000 genomes]
rs7499717	0.97[ASN][1000 genomes]
rs7499882	0.97[ASN][1000 genomes]
rs7500702	0.87[EUR][1000 genomes]
rs8054750	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	nsv907029	chr16:82951179-83044665	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv907030	chr16:82959437-83044665	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1056005	chr16:82987872-83055420	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1055246	chr16:82988025-83056132	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1064172	chr16:82988932-83046695	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv522570	chr16:82988977-83044665	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv573383	chr16:82988977-83044665	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv573384	chr16:82994130-83044665	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	esv3324286	chr16:83028451-83032749	Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:83021600-83035200	Weak transcription	Psoas Muscle	Psoas
2	chr16:83021800-83035000	Weak transcription	Aorta	Aorta
3	chr16:83029800-83035800	Weak transcription	Right Atrium	heart
4	chr16:83029800-83038200	Weak transcription	Right Ventricle	heart
5	chr16:83030200-83035800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr16:83030200-83037000	Weak transcription	NHEK	skin
7	chr16:83030200-83047200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr16:83030200-83053200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr16:83030400-83036000	Weak transcription	HSMM	muscle
10	chr16:83030600-83047000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr16:83030800-83033400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr16:83030800-83036200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr16:83030800-83036200	Weak transcription	Left Ventricle	heart
14	chr16:83030800-83036200	Weak transcription	Pancreas	Pancrea
15	chr16:83030800-83036200	Weak transcription	Osteobl	bone
16	chr16:83030800-83039000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr16:83031000-83035800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr16:83032200-83033600	Enhancers	Fetal Intestine Large	intestine
19	chr16:83032200-83033600	Enhancers	Fetal Intestine Small	intestine
20	chr16:83032400-83034800	Weak transcription	HUVEC	blood vessel
21	chr16:83032600-83032800	Enhancers	Duodenum Mucosa	Duodenum
22	chr16:83032600-83032800	Enhancers	Duodenum Smooth Muscle	Duodenum

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