Variant report

Variant	rs4359785
Chromosome Location	chr3:113555292-113555293
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:113548993..113551007-chr3:113552942..113555704,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10804511	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2566981	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2566983	0.84[AFR][1000 genomes]
rs2566984	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2566985	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59292926	1.00[AMR][1000 genomes]
rs60238096	1.00[AMR][1000 genomes]
rs6781200	1.00[AMR][1000 genomes]
rs6799923	1.00[AMR][1000 genomes]
rs6800121	1.00[AMR][1000 genomes]
rs72952678	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72952679	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72952680	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72952687	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72954664	1.00[AMR][1000 genomes]
rs72954670	1.00[AMR][1000 genomes]
rs72954674	1.00[AMR][1000 genomes]
rs72954676	1.00[AMR][1000 genomes]
rs72954680	1.00[AMR][1000 genomes]
rs72954688	1.00[AMR][1000 genomes]
rs7628645	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7646432	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7650388	1.00[AMR][1000 genomes]
rs7650416	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013506	chr3:112890608-113680951	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv482804	chr3:113432431-113581672	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv829678	chr3:113446177-113633053	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv877351	chr3:113450495-113637424	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv1013746	chr3:113460162-113646657	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv432478	chr3:113492402-113614489	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
7	nsv460822	chr3:113543081-113600970	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv591302	chr3:113543081-113600970	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113549400-113557600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:113549600-113557000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr3:113549800-113557600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr3:113549800-113557600	Weak transcription	NHDF-Ad	bronchial
5	chr3:113550000-113557200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr3:113550000-113557400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr3:113550000-113557600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr3:113550000-113557600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr3:113551800-113557400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr3:113552200-113557000	Weak transcription	Primary B cells from peripheral blood	blood
11	chr3:113552600-113557000	Weak transcription	GM12878-XiMat	blood
12	chr3:113552800-113557800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:113553200-113557200	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr3:113553200-113557200	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr3:113553600-113557000	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr3:113554400-113557200	Weak transcription	Fetal Intestine Large	intestine
17	chr3:113554400-113557400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:113554400-113557400	Weak transcription	Fetal Kidney	kidney
19	chr3:113554400-113557400	Weak transcription	HUVEC	blood vessel
20	chr3:113554600-113556800	Weak transcription	HepG2	liver
21	chr3:113554600-113557400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr3:113554600-113557400	Weak transcription	HMEC	breast
23	chr3:113554600-113557400	Weak transcription	NHEK	skin
24	chr3:113554600-113557600	Weak transcription	Liver	Liver
25	chr3:113554600-113557600	Weak transcription	Duodenum Mucosa	Duodenum
26	chr3:113554800-113557400	Weak transcription	Hela-S3	cervix
27	chr3:113554800-113557600	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr3:113554800-113557600	Weak transcription	Stomach Mucosa	stomach

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