Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:50399505..50401481-chr10:50433007..50435119,2	K562	blood:

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10745252	1.00[ASN][1000 genomes]
rs10776546	1.00[ASN][1000 genomes]
rs10857443	1.00[ASN][1000 genomes]
rs10857445	1.00[ASN][1000 genomes]
rs11593489	1.00[ASN][1000 genomes]
rs2002392	1.00[ASN][1000 genomes]
rs2377950	1.00[ASN][1000 genomes]
rs2377951	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2377952	0.85[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2377985	1.00[ASN][1000 genomes]
rs2377987	1.00[ASN][1000 genomes]
rs2377991	1.00[ASN][1000 genomes]
rs2377992	1.00[ASN][1000 genomes]
rs2889807	1.00[ASN][1000 genomes]
rs4514329	1.00[ASN][1000 genomes]
rs4838465	0.85[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61748312	0.83[EUR][1000 genomes]
rs6537509	1.00[ASN][1000 genomes]
rs6537510	1.00[ASN][1000 genomes]
rs7094605	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7394346	1.00[ASN][1000 genomes]
rs7893648	1.00[ASN][1000 genomes]
rs7906560	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7912808	1.00[ASN][1000 genomes]
rs7922135	1.00[ASN][1000 genomes]
rs7923767	1.00[ASN][1000 genomes]
rs9645532	1.00[ASN][1000 genomes]
rs9645533	1.00[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	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 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	chr10:50397000-50401600	Weak transcription	HUVEC	blood vessel
2	chr10:50398600-50402600	Weak transcription	Right Atrium	heart
3	chr10:50398600-50403400	Weak transcription	Spleen	Spleen
4	chr10:50399200-50402400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr10:50399200-50402400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:50399200-50404600	Weak transcription	K562	blood
7	chr10:50399400-50401800	Weak transcription	Primary B cells from peripheral blood	blood
8	chr10:50399400-50402400	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr10:50399600-50401800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr10:50399600-50402600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr10:50399800-50400600	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr10:50399800-50402200	Weak transcription	Primary B cells from cord blood	blood
13	chr10:50400000-50401400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr10:50400000-50401800	Weak transcription	GM12878-XiMat	blood

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