Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:14960895..14963438-chr6:14965726..14968229,3	K562	blood:
2	chr6:14959260..14962811-chr6:14965257..14968674,4	K562	blood:

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

rs_ID	r²[population]
rs11752683	0.84[EUR][1000 genomes]
rs12193983	0.93[EUR][1000 genomes]
rs12196558	0.91[EUR][1000 genomes]
rs1555642	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2661089	0.87[EUR][1000 genomes]
rs2762329	0.93[EUR][1000 genomes]
rs28520668	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs379905	0.97[ASN][1000 genomes]
rs396228	0.97[ASN][1000 genomes]
rs404305	0.97[ASN][1000 genomes]
rs407140	0.97[ASN][1000 genomes]
rs432319	0.97[ASN][1000 genomes]
rs432442	0.95[EUR][1000 genomes]
rs447977	0.86[ASN][1000 genomes]
rs57581425	0.91[EUR][1000 genomes]
rs58479121	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs672419	0.95[EUR][1000 genomes]
rs6908722	0.91[EUR][1000 genomes]
rs7750689	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7755150	0.91[EUR][1000 genomes]
rs7766473	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7768948	0.96[EUR][1000 genomes]
rs7771215	0.92[EUR][1000 genomes]
rs837170	0.94[EUR][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	nsv1031668	chr6:14774036-15044308	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv538138	chr6:14774036-15044308	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv883453	chr6:14926320-15001506	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:14933600-14964800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:14933800-14969600	Weak transcription	Right Atrium	heart
3	chr6:14946600-14965000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr6:14957600-14964800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr6:14961200-14964800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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