Variant report

Variant	rs7085278
Chromosome Location	chr10:45176021-45176022
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:45169027..45172416-chr10:45173196..45176853,3	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10736830	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10751358	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10793552	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10793555	0.82[ASN][1000 genomes]
rs10900092	0.82[EUR][1000 genomes]
rs10900100	0.81[ASN][1000 genomes]
rs10900103	0.81[ASN][1000 genomes]
rs10900105	0.81[ASN][1000 genomes]
rs11239211	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11239222	0.85[ASN][1000 genomes]
rs11239228	0.81[ASN][1000 genomes]
rs11239229	0.81[ASN][1000 genomes]
rs11239231	0.81[ASN][1000 genomes]
rs12220526	0.86[ASN][1000 genomes]
rs12245478	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12254934	0.98[ASN][1000 genomes]
rs12261103	0.81[ASN][1000 genomes]
rs12266496	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1480603	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1480604	0.82[ASN][1000 genomes]
rs1600614	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17156847	0.81[ASN][1000 genomes]
rs2069046	0.81[ASN][1000 genomes]
rs6593436	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6593437	0.80[ASN][1000 genomes]
rs7068119	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7069781	0.87[ASN][1000 genomes]
rs7070255	0.81[ASN][1000 genomes]
rs7070868	0.81[ASN][1000 genomes]
rs7084823	0.86[ASN][1000 genomes]
rs7088026	0.82[ASN][1000 genomes]
rs7088366	0.98[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7088688	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7091495	0.81[ASN][1000 genomes]
rs7097094	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7098668	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73287673	0.81[ASN][1000 genomes]
rs7893447	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7895327	0.81[ASN][1000 genomes]
rs7897547	0.99[ASN][1000 genomes]
rs7903994	0.99[ASN][1000 genomes]
rs7905942	0.81[ASN][1000 genomes]
rs7907854	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7910031	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7917498	0.81[ASN][1000 genomes]
rs7919204	0.99[ASN][1000 genomes]
rs899888	0.98[ASN][1000 genomes]
rs999473	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[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	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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45171400-45177200	Weak transcription	Fetal Lung	lung
2	chr10:45172800-45177800	Weak transcription	Brain Germinal Matrix	brain
3	chr10:45174400-45176200	Enhancers	Aorta	Aorta
4	chr10:45175200-45177600	Weak transcription	Fetal Muscle Leg	muscle

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