Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1325466	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1821127	0.89[ASN][1000 genomes]
rs2104418	0.83[EUR][1000 genomes]
rs2328940	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3825441	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4885286	0.85[EUR][1000 genomes]
rs5021641	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6562886	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6562887	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7321494	0.82[CHB][hapmap]
rs7330729	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7983831	0.86[EUR][1000 genomes]
rs7991823	0.89[ASN][1000 genomes]
rs7992747	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7998651	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9565154	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9565157	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9573529	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9573531	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9573532	0.87[ASN][1000 genomes]
rs9573533	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498067	chr13:75178898-76012362	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	esv2761803	chr13:75943309-76161774	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh 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:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:75948000-75958400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr13:75948400-75957400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr13:75949200-75958400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr13:75949200-75959200	Weak transcription	Left Ventricle	heart
5	chr13:75949400-75959200	Weak transcription	Psoas Muscle	Psoas
6	chr13:75950200-75959200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr13:75951800-75959200	Weak transcription	Fetal Thymus	thymus
8	chr13:75953200-75959200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr13:75953400-75957400	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr13:75953800-75957200	Weak transcription	Liver	Liver
11	chr13:75954000-75957400	Weak transcription	HepG2	liver
12	chr13:75954000-75959000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr13:75954400-75956800	Enhancers	Fetal Heart	heart
14	chr13:75956000-75957600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr13:75956200-75961800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr13:75956400-75957200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr13:75956400-75964600	Weak transcription	Right Ventricle	heart

Quick Search: