Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:81105972..81108126-chr14:81297370..81299564,2	K562	blood:

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

rs_ID	r²[population]
rs10498546	0.82[ASN][1000 genomes]
rs12432896	0.88[EUR][1000 genomes]
rs12434405	0.90[EUR][1000 genomes]
rs12435900	0.84[AFR][1000 genomes]
rs17110799	0.84[AFR][1000 genomes]
rs17110803	0.84[AFR][1000 genomes]
rs17110880	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1871457	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2122429	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2596115	0.81[ASN][1000 genomes]
rs2619671	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs56341421	0.84[AFR][1000 genomes]
rs58877537	0.83[EUR][1000 genomes]
rs7153490	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7160951	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72689058	0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs72689070	0.87[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs72689071	0.89[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs72689095	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8017017	0.89[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs8017133	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8017609	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8017722	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8022733	0.85[EUR][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	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv565290	chr14:81085129-81230117	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81083400-81109400	Weak transcription	Dnd41	blood
2	chr14:81099000-81109600	Weak transcription	Thymus	Thymus
3	chr14:81105400-81112800	Weak transcription	HSMM	muscle
4	chr14:81105800-81112000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr14:81106200-81112400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr14:81106200-81135400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr14:81107000-81112200	Weak transcription	A549	lung
8	chr14:81107200-81110400	Weak transcription	HUVEC	blood vessel

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