Variant report

Variant	rs4734130
Chromosome Location	chr8:107096458-107096459
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	chr8:107065574..107067380-chr8:107096296..107097895,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10955412	0.83[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs10955413	0.91[ASN][1000 genomes]
rs11781331	0.81[ASN][1000 genomes]
rs11997513	0.91[ASN][1000 genomes]
rs12155858	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12155859	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12155862	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12155864	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12541635	0.91[ASN][1000 genomes]
rs13274603	0.87[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs1366969	0.85[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs1429675	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1835266	1.00[ASN][1000 genomes]
rs1896916	1.00[ASN][1000 genomes]
rs1896918	0.91[ASN][1000 genomes]
rs1896919	0.91[ASN][1000 genomes]
rs2099150	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28709304	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2881036	0.90[ASN][1000 genomes]
rs2881037	0.91[ASN][1000 genomes]
rs4099936	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4734131	1.00[ASN][1000 genomes]
rs4734893	0.82[CEU][hapmap]
rs4734896	0.90[ASN][1000 genomes]
rs4734897	0.90[ASN][1000 genomes]
rs6469038	0.86[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs7016835	0.99[ASN][1000 genomes]
rs727419	0.86[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs736627	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7459459	0.90[ASN][1000 genomes]
rs7464413	0.90[ASN][1000 genomes]
rs9642802	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs993177	0.87[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][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	nsv1021369	chr8:106493317-107243322	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv611840	chr8:106913294-107265915	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv611842	chr8:107076421-107115482	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv891262	chr8:107076421-107209378	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv611843	chr8:107088426-107104545	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv2830191	chr8:107088426-107115482	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107090600-107099000	Weak transcription	Esophagus	oesophagus
2	chr8:107093400-107096600	Enhancers	Colon Smooth Muscle	Colon
3	chr8:107093400-107096600	Enhancers	HUVEC	blood vessel
4	chr8:107093800-107099000	Weak transcription	Gastric	stomach
5	chr8:107094200-107096600	Enhancers	Rectal Smooth Muscle	rectum
6	chr8:107094600-107099000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr8:107095000-107097600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr8:107095600-107098800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:107095600-107099000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr8:107095600-107099200	Weak transcription	Fetal Lung	lung
11	chr8:107095800-107096800	Enhancers	Dnd41	blood
12	chr8:107095800-107097200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr8:107095800-107098000	Weak transcription	Stomach Mucosa	stomach
14	chr8:107095800-107098800	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr8:107095800-107098800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr8:107095800-107099000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:107095800-107099000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr8:107095800-107099200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr8:107096000-107097200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr8:107096000-107097200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr8:107096000-107097400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:107096000-107097800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr8:107096000-107098600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:107096000-107098800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr8:107096000-107098800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:107096000-107098800	Weak transcription	Brain Substantia Nigra	brain
27	chr8:107096000-107098800	Weak transcription	NHEK	skin
28	chr8:107096000-107099000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:107096000-107099000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr8:107096200-107096600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr8:107096200-107097200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr8:107096200-107098000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr8:107096200-107098600	Weak transcription	HMEC	breast
34	chr8:107096200-107098800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr8:107096200-107098800	Weak transcription	Brain Hippocampus Middle	brain
36	chr8:107096200-107099000	Weak transcription	Fetal Kidney	kidney
37	chr8:107096400-107097200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr8:107096400-107098600	Weak transcription	NHDF-Ad	bronchial
39	chr8:107096400-107098800	Weak transcription	Adipose Nuclei	Adipose

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