Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:37748769..37750538-chr2:37760905..37763616,2	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10176881	0.92[ASN][1000 genomes]
rs10181174	0.91[ASN][1000 genomes]
rs11124590	0.93[ASN][1000 genomes]
rs11887848	0.83[ASN][1000 genomes]
rs11888402	0.92[ASN][1000 genomes]
rs11895388	0.93[ASN][1000 genomes]
rs12612951	0.84[ASN][1000 genomes]
rs13002383	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13432740	0.92[ASN][1000 genomes]
rs34369565	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34752978	0.93[ASN][1000 genomes]
rs35422160	0.91[ASN][1000 genomes]
rs35574342	0.82[ASN][1000 genomes]
rs35990829	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4233923	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4404250	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4461243	0.80[EUR][1000 genomes]
rs4538180	0.80[EUR][1000 genomes]
rs4670208	0.84[ASN][1000 genomes]
rs4670724	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4670730	0.84[ASN][1000 genomes]
rs6712065	0.93[ASN][1000 genomes]
rs67348553	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72795708	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833814	chr2:37643132-37840247	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv456374	chr2:37669487-37868214	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv470453	chr2:37669487-37868214	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv581473	chr2:37669487-37868214	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr2:37751600-37763000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr2:37752800-37763000	Weak transcription	Psoas Muscle	Psoas
3	chr2:37757600-37762800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr2:37757600-37763000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:37760000-37765000	Weak transcription	Fetal Heart	heart
6	chr2:37760600-37762800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr2:37760800-37762600	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr2:37760800-37762800	Weak transcription	NH-A	brain
9	chr2:37761000-37762600	Weak transcription	A549	lung
10	chr2:37761000-37762600	Weak transcription	GM12878-XiMat	blood
11	chr2:37761000-37762800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr2:37761000-37762800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr2:37761000-37762800	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr2:37761200-37763000	Weak transcription	Osteobl	bone

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