Variant report

No.	Distal block	Cell Line	Cell type
1	chr8:130451014..130452708-chr8:130456649..130459238,2	K562	blood:
2	chr8:130450871..130455095-chr8:130457353..130461574,6	MCF-7	breast:
3	chr8:130438946..130441544-chr8:130456592..130459697,3	K562	blood:
4	chr8:130456549..130458693-chr8:130464674..130467504,3	MCF-7	breast:

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

rs_ID	r²[population]
rs10103083	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10105579	0.87[ASN][1000 genomes]
rs1030626	0.82[EUR][1000 genomes]
rs10808579	0.88[ASN][1000 genomes]
rs10808580	0.88[ASN][1000 genomes]
rs1118872	0.85[ASN][1000 genomes]
rs1124682	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11787238	0.88[ASN][1000 genomes]
rs12545968	0.85[ASN][1000 genomes]
rs12681076	0.82[EUR][1000 genomes]
rs13250815	0.88[ASN][1000 genomes]
rs1465680	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1583247	0.87[ASN][1000 genomes]
rs1594596	0.88[ASN][1000 genomes]
rs1963881	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2007003	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4733549	0.88[ASN][1000 genomes]
rs4733707	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56678522	0.87[ASN][1000 genomes]
rs7015941	0.88[ASN][1000 genomes]
rs744652	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7828127	0.88[ASN][1000 genomes]
rs7831732	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9694939	0.88[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	nsv429942	chr8:130397818-130460011	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1015611	chr8:130449321-130502086	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130448600-130458800	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr8:130451400-130462000	Weak transcription	Thymus	Thymus
3	chr8:130452400-130458200	Weak transcription	Fetal Thymus	thymus
4	chr8:130452600-130457800	Weak transcription	Dnd41	blood
5	chr8:130453800-130457400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr8:130454200-130458000	Strong transcription	K562	blood

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