Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:62854491..62857008-chr1:62859970..62862634,2	K562	blood:

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10789110	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10889326	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10889328	0.91[EUR][1000 genomes]
rs10889329	0.90[EUR][1000 genomes]
rs1413821	0.88[ASN][1000 genomes]
rs1473754	1.00[ASN][1000 genomes]
rs17123603	1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1886829	1.00[ASN][1000 genomes]
rs2065701	0.91[EUR][1000 genomes]
rs2095403	1.00[ASN][1000 genomes]
rs2104448	0.89[ASN][1000 genomes]
rs3861942	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4514267	1.00[ASN][1000 genomes]
rs4915615	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4915617	0.88[EUR][1000 genomes]
rs4915833	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4915834	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4915837	1.00[ASN][1000 genomes]
rs60459828	0.88[ASN][1000 genomes]
rs6587974	0.89[MEX][hapmap];0.87[AMR][1000 genomes]
rs6587975	0.89[MEX][hapmap];0.85[AMR][1000 genomes]
rs6687215	0.83[MEX][hapmap];0.82[AMR][1000 genomes]
rs6693540	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6699962	0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs72929746	0.88[ASN][1000 genomes]
rs7512888	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7543765	1.00[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];1.00[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	nsv1013582	chr1:62723703-62910632	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62848000-62871800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:62853600-62856800	Weak transcription	HepG2	liver
3	chr1:62855000-62860200	Weak transcription	Brain Hippocampus Middle	brain
4	chr1:62856200-62862400	Weak transcription	NHEK	skin
5	chr1:62856400-62856800	Enhancers	Fetal Stomach	stomach
6	chr1:62856400-62861000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr1:62856600-62857400	Enhancers	Fetal Muscle Leg	muscle
8	chr1:62856600-62857400	Enhancers	Hela-S3	cervix
9	chr1:62856600-62857800	Weak transcription	Placenta	Placenta

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