Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:45173246..45175048-chr10:45176578..45179846,3	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10736830	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10751358	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10793552	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11239222	0.83[ASN][1000 genomes]
rs12220526	0.84[ASN][1000 genomes]
rs12245478	0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12254934	0.96[ASN][1000 genomes]
rs12266496	0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1480603	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1600614	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6593436	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7069781	0.85[ASN][1000 genomes]
rs7084823	0.84[ASN][1000 genomes]
rs7085278	0.98[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7088688	0.98[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7097094	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7098668	0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7897547	0.97[ASN][1000 genomes]
rs7903994	0.97[ASN][1000 genomes]
rs7907854	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7919204	0.97[ASN][1000 genomes]
rs899888	0.96[ASN][1000 genomes]
rs999473	0.83[AFR][1000 genomes];0.83[AMR][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	esv2422287	chr10:45044161-45257684	Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv831843	chr10:45084703-45280032	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv525947	chr10:45163568-45182316	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45176200-45185800	Weak transcription	Aorta	Aorta
2	chr10:45178400-45180600	Weak transcription	Fetal Stomach	stomach
3	chr10:45178800-45180000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr10:45178800-45180000	Weak transcription	Fetal Muscle Trunk	muscle
5	chr10:45178800-45180000	Weak transcription	Fetal Muscle Leg	muscle
6	chr10:45178800-45180400	Weak transcription	Right Atrium	heart
7	chr10:45179000-45179400	Weak transcription	Ovary	ovary

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