Variant report

Variant	rs10808583
Chromosome Location	chr8:130718020-130718021
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:130717351..130718895-chr8:130719468..130721279,2	K562	blood:
2	chr8:130709158..130713272-chr8:130716107..130718644,3	K562	blood:
3	chr8:130715407..130717008-chr8:130717100..130719495,2	MCF-7	breast:
4	chr8:130699308..130701478-chr8:130717660..130720655,2	K562	blood:
5	chr8:130717459..130720769-chr8:130721541..130726036,4	MCF-7	breast:
6	chr8:130711772..130714340-chr8:130717144..130719006,2	K562	blood:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10104593	0.85[ASN][1000 genomes]
rs1074286	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10956487	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10956488	0.84[AMR][1000 genomes]
rs10956490	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11984666	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2062078	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3886937	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3886938	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4130415	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4144736	0.81[ASN][1000 genomes]
rs4144738	0.83[ASN][1000 genomes]
rs4335095	0.85[ASN][1000 genomes]
rs4345520	0.85[ASN][1000 genomes]
rs4425724	0.87[ASN][1000 genomes]
rs4571702	0.85[ASN][1000 genomes]
rs4733724	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4733725	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4733726	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4733727	0.87[ASN][1000 genomes]
rs4733728	0.87[ASN][1000 genomes]
rs60228607	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6470763	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6470764	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6470765	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6651255	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6985118	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6986256	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7004355	0.85[ASN][1000 genomes]
rs7341636	0.87[ASN][1000 genomes]
rs7388479	0.83[ASN][1000 genomes]
rs7814941	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7815955	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7816131	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7816342	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7816625	0.84[ASN][1000 genomes]
rs7826493	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7828785	0.84[ASN][1000 genomes]
rs7833174	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7841981	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7846627	0.87[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8387	chr8:130711059-130756654	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130708200-130720200	Weak transcription	Esophagus	oesophagus
2	chr8:130710600-130719800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:130710800-130719200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:130710800-130719200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr8:130710800-130719400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr8:130710800-130719800	Weak transcription	NHLF	lung
7	chr8:130710800-130720000	Weak transcription	HSMMtube	muscle
8	chr8:130714600-130719800	Weak transcription	K562	blood
9	chr8:130714600-130720000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr8:130714600-130720000	Weak transcription	Fetal Stomach	stomach
11	chr8:130714600-130720000	Weak transcription	HSMM	muscle
12	chr8:130716600-130719800	Weak transcription	Fetal Muscle Leg	muscle
13	chr8:130716800-130720000	Weak transcription	Fetal Lung	lung
14	chr8:130716800-130720200	Weak transcription	Fetal Kidney	kidney
15	chr8:130717000-130719200	ZNF genes & repeats	A549	lung
16	chr8:130717000-130720000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr8:130717000-130720000	Weak transcription	Fetal Intestine Large	intestine
18	chr8:130717000-130720200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:130717000-130720200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:130718000-130719200	Enhancers	HUVEC	blood vessel

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