Variant report

Variant	rs8061423
Chromosome Location	chr16:70670806-70670807
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:70663629..70665540-chr16:70670216..70672264,2	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11075774	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12102388	1.00[EUR][1000 genomes]
rs12102523	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12102525	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13335470	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13336968	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13338169	0.83[AMR][1000 genomes]
rs1902563	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28434516	1.00[EUR][1000 genomes]
rs28780486	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28814369	1.00[EUR][1000 genomes]
rs59710171	0.83[AMR][1000 genomes]
rs60020150	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60337219	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60611474	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60774382	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7186416	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73575026	0.83[AMR][1000 genomes]
rs8056766	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8063038	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8064109	0.92[AMR][1000 genomes]
rs8064220	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9938385	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517391	chr16:70666410-70840490	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv457517	chr16:70666722-70840490	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv572945	chr16:70666722-70840490	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70666000-70679000	Weak transcription	Spleen	Spleen
2	chr16:70669400-70672800	Weak transcription	Esophagus	oesophagus
3	chr16:70669400-70673000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr16:70669400-70673200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr16:70669400-70673200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr16:70669400-70673200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr16:70669400-70673200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr16:70669400-70679000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr16:70669600-70671000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr16:70669600-70672600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr16:70669600-70672600	Weak transcription	Fetal Stomach	stomach
12	chr16:70669600-70672600	Weak transcription	NHEK	skin
13	chr16:70669600-70672800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr16:70669600-70672800	Weak transcription	Colon Smooth Muscle	Colon
15	chr16:70669600-70672800	Weak transcription	HSMMtube	muscle
16	chr16:70669600-70672800	Weak transcription	NH-A	brain
17	chr16:70669600-70673000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr16:70669600-70673000	Weak transcription	Ovary	ovary
19	chr16:70669600-70673200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr16:70669600-70674600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr16:70669600-70679000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr16:70669600-70679400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr16:70669600-70687800	Weak transcription	Right Atrium	heart
24	chr16:70670000-70672800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr16:70670200-70673000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr16:70670400-70672800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr16:70670400-70672800	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr16:70670400-70672800	Weak transcription	NHDF-Ad	bronchial
29	chr16:70670400-70672800	Weak transcription	Osteobl	bone
30	chr16:70670600-70672800	Weak transcription	Aorta	Aorta
31	chr16:70670600-70673000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr16:70670600-70675200	Weak transcription	HUVEC	blood vessel
33	chr16:70670600-70680000	Weak transcription	Fetal Intestine Small	intestine
34	chr16:70670800-70672400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr16:70670800-70673000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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