Variant report

Variant	rs4506910
Chromosome Location	chr16:79764739-79764740
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	chr16:79762471..79764929-chr16:79784561..79786086,2	K562	blood:
2	chr16:79763806..79766331-chr16:79796283..79799098,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10871377	0.81[ASN][1000 genomes]
rs11150194	0.81[ASN][1000 genomes]
rs11150195	0.81[ASN][1000 genomes]
rs11150196	0.80[ASN][1000 genomes]
rs11150197	0.80[ASN][1000 genomes]
rs11640485	0.82[ASN][1000 genomes]
rs11640827	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11646174	0.80[ASN][1000 genomes]
rs11648369	0.83[ASN][1000 genomes]
rs11649433	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11649483	0.84[ASN][1000 genomes]
rs11864576	0.81[ASN][1000 genomes]
rs11864742	0.81[ASN][1000 genomes]
rs12373096	0.81[ASN][1000 genomes]
rs12598937	0.81[ASN][1000 genomes]
rs12600028	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12716880	0.82[ASN][1000 genomes]
rs12921991	0.82[ASN][1000 genomes]
rs12932883	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12935201	0.81[ASN][1000 genomes]
rs3813578	0.81[ASN][1000 genomes]
rs4243178	0.83[ASN][1000 genomes]
rs4243179	0.82[ASN][1000 genomes]
rs4274450	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4325577	0.80[ASN][1000 genomes]
rs4360949	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4387616	0.95[ASN][1000 genomes]
rs4395087	0.80[ASN][1000 genomes]
rs4420544	0.84[ASN][1000 genomes]
rs4426362	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4450408	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4556800	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4609863	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4632143	0.81[ASN][1000 genomes]
rs4889017	0.82[ASN][1000 genomes]
rs4889018	0.81[ASN][1000 genomes]
rs4889019	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4889020	0.81[ASN][1000 genomes]
rs4889021	0.80[ASN][1000 genomes]
rs6564694	0.81[ASN][1000 genomes]
rs7186075	0.81[ASN][1000 genomes]
rs7190488	0.81[ASN][1000 genomes]
rs7192691	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7196084	0.81[ASN][1000 genomes]
rs8049118	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8049124	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8054169	0.82[ASN][1000 genomes]
rs8055670	0.82[AMR][1000 genomes]
rs8056945	0.80[ASN][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	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv906992	chr16:79649394-79769790	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv530714	chr16:79661581-79925435	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv833296	chr16:79692236-79889727	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv833297	chr16:79732501-79920419	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:79756800-79774200	Weak transcription	Ovary	ovary
2	chr16:79761600-79765600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr16:79762600-79765800	Weak transcription	Left Ventricle	heart
4	chr16:79763400-79765600	Enhancers	Fetal Intestine Large	intestine
5	chr16:79763600-79765600	Enhancers	Fetal Intestine Small	intestine
6	chr16:79764200-79765400	Enhancers	Duodenum Mucosa	Duodenum

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