Variant report

Variant	rs1364713
Chromosome Location	chr8:120262258-120262259
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10505354	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11990379	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.81[ASN][1000 genomes]
rs11994152	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[ASN][1000 genomes]
rs11997485	0.81[ASN][1000 genomes]
rs1364704	0.85[CHD][hapmap]
rs1425068	1.00[CHD][hapmap]
rs16892237	0.85[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs16892267	0.93[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs16892297	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs16892306	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2303398	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.81[ASN][1000 genomes]
rs3739419	0.91[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3812491	1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs41319147	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.81[ASN][1000 genomes]
rs55636028	0.89[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs55714432	0.81[ASN][1000 genomes]
rs56354938	0.81[ASN][1000 genomes]
rs56398539	0.84[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs56840596	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs58857566	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs59656505	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs59699923	0.85[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs60738905	0.81[ASN][1000 genomes]
rs60879825	0.87[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs73709667	0.81[ASN][1000 genomes]
rs73709668	0.81[ASN][1000 genomes]
rs73709669	0.81[ASN][1000 genomes]
rs73709670	0.81[ASN][1000 genomes]
rs73709671	0.81[ASN][1000 genomes]
rs73709673	0.81[ASN][1000 genomes]
rs73709674	0.81[ASN][1000 genomes]
rs73709675	0.81[ASN][1000 genomes]
rs73709676	0.81[ASN][1000 genomes]
rs73709677	0.81[ASN][1000 genomes]
rs73709680	0.81[ASN][1000 genomes]
rs73709681	0.81[ASN][1000 genomes]
rs73709684	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73709685	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73709688	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs73709690	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[ASN][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	nsv868916	chr8:119911943-120762250	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv2758169	chr8:119943309-120275750	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	esv2759639	chr8:119943309-120275750	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120223800-120262400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:120240600-120266800	Weak transcription	Stomach Mucosa	stomach
3	chr8:120241000-120262400	Weak transcription	Fetal Stomach	stomach
4	chr8:120252800-120262400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr8:120253200-120262800	Weak transcription	Adipose Nuclei	Adipose
6	chr8:120255400-120262400	Weak transcription	HepG2	liver
7	chr8:120256400-120262400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr8:120257200-120262800	Weak transcription	Fetal Intestine Large	intestine
9	chr8:120259400-120262600	Weak transcription	HMEC	breast
10	chr8:120261200-120262400	Weak transcription	Fetal Intestine Small	intestine
11	chr8:120261400-120263000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr8:120261400-120263600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:120261600-120263200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr8:120261800-120263600	Weak transcription	NHEK	skin
15	chr8:120261800-120263800	Weak transcription	Hela-S3	cervix
16	chr8:120262000-120263400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:120262000-120263600	Weak transcription	Esophagus	oesophagus
18	chr8:120262000-120263800	Weak transcription	Gastric	stomach
19	chr8:120262000-120264000	Weak transcription	Duodenum Mucosa	Duodenum
20	chr8:120262000-120265000	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr8:120262000-120265000	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr8:120262200-120264000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:120262200-120264000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr8:120262200-120267600	Weak transcription	Liver	Liver

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