Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:118693119..118695515-chr8:118696203..118698417,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10089009	0.80[EUR][1000 genomes]
rs10093232	0.90[EUR][1000 genomes]
rs10108248	0.90[EUR][1000 genomes]
rs10955822	0.90[EUR][1000 genomes]
rs10955823	0.84[EUR][1000 genomes]
rs1160474	0.80[EUR][1000 genomes]
rs1383176	0.90[EUR][1000 genomes]
rs1396351	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1508566	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1508569	0.83[EUR][1000 genomes]
rs16890041	0.90[EUR][1000 genomes]
rs17753197	0.91[EUR][1000 genomes]
rs218017	0.84[CEU][hapmap];0.83[JPT][hapmap]
rs218018	0.88[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap]
rs34660998	0.88[EUR][1000 genomes]
rs4604472	0.90[EUR][1000 genomes]
rs6469700	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6469701	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7815693	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7838659	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019636	chr8:118598433-118946091	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv539734	chr8:118598433-118946091	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv831438	chr8:118679896-118823600	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv891410	chr8:118684994-118730344	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118689200-118698600	Weak transcription	HMEC	breast
2	chr8:118689200-118718600	Weak transcription	Osteobl	bone
3	chr8:118690800-118701400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr8:118692400-118714400	Weak transcription	HSMM	muscle
5	chr8:118693000-118698400	Weak transcription	NHEK	skin
6	chr8:118694600-118723800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr8:118695000-118703400	Weak transcription	Aorta	Aorta

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