Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:137418322..137420614-chr7:137421011..137423413,2	K562	blood:
2	chr7:137400906..137403879-chr7:137418023..137420463,3	K562	blood:

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10215033	0.86[ASN][1000 genomes]
rs10240406	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10257746	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10262883	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10263086	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10269716	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1559489	0.86[ASN][1000 genomes]
rs17169427	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2059320	0.95[ASN][1000 genomes]
rs2113425	0.86[ASN][1000 genomes]
rs3778802	0.84[EUR][1000 genomes]
rs3778804	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs3800638	0.84[EUR][1000 genomes]
rs3800639	0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs3800640	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs3800642	1.00[ASN][1000 genomes]
rs3800643	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3800652	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55953418	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57538683	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57957290	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6467715	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73460689	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7779850	1.00[ASN][1000 genomes]
rs7803175	0.83[AMR][1000 genomes];0.99[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	nsv1022793	chr7:137187383-137619359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137411000-137424800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr7:137413400-137432200	Weak transcription	Aorta	Aorta
3	chr7:137414200-137419600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr7:137416600-137424400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:137416600-137438000	Weak transcription	NH-A	brain
6	chr7:137418600-137419600	Enhancers	Placenta	Placenta
7	chr7:137418800-137419600	Enhancers	HSMMtube	muscle
8	chr7:137418800-137419800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr7:137419200-137419600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr7:137419200-137431000	Weak transcription	Osteobl	bone
11	chr7:137419400-137424800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:137419400-137438200	Weak transcription	HSMM	muscle

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