Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:106753473..106755811-chr8:106757998..106761586,3	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10106386	0.80[ASN][1000 genomes]
rs1025856	0.89[ASN][1000 genomes]
rs12541049	0.85[EUR][1000 genomes]
rs12542643	0.82[ASN][1000 genomes]
rs12545480	0.82[ASN][1000 genomes]
rs12545946	0.89[ASN][1000 genomes]
rs12546300	0.83[ASN][1000 genomes]
rs12547056	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1372621	0.89[ASN][1000 genomes]
rs1442326	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1578995	0.82[ASN][1000 genomes]
rs16873601	0.82[ASN][1000 genomes]
rs2028552	0.93[ASN][1000 genomes]
rs2165644	0.87[ASN][1000 genomes]
rs3779776	0.89[ASN][1000 genomes]
rs4302813	0.90[AFR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58307372	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6469013	0.91[ASN][1000 genomes]
rs7003445	0.82[ASN][1000 genomes]
rs73305060	0.89[ASN][1000 genomes]
rs73305067	0.89[ASN][1000 genomes]
rs73305069	0.89[ASN][1000 genomes]
rs753534	0.89[ASN][1000 genomes]
rs753535	0.89[ASN][1000 genomes]
rs753536	0.89[ASN][1000 genomes]
rs7836133	0.92[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	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	nsv831418	chr8:106648456-106833333	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv891260	chr8:106737459-106808078	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:106742800-106760000	Weak transcription	Left Ventricle	heart
2	chr8:106743600-106768400	Weak transcription	Psoas Muscle	Psoas
3	chr8:106750000-106768200	Weak transcription	K562	blood
4	chr8:106750200-106760000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:106753400-106759600	Weak transcription	Fetal Lung	lung
6	chr8:106753800-106772000	Weak transcription	Aorta	Aorta
7	chr8:106756600-106759600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:106756800-106759600	Weak transcription	Fetal Heart	heart
9	chr8:106756800-106761600	Weak transcription	Colon Smooth Muscle	Colon
10	chr8:106757200-106768200	Weak transcription	Ovary	ovary
11	chr8:106758000-106759000	Weak transcription	Brain Germinal Matrix	brain
12	chr8:106758000-106759600	Weak transcription	Fetal Brain Female	brain
13	chr8:106758200-106759200	Weak transcription	Fetal Brain Male	brain
14	chr8:106758400-106760800	Enhancers	Cortex derived primary cultured neurospheres	brain

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