Variant report

Variant	rs10102032
Chromosome Location	chr8:19787032-19787033
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	chr8:19786191..19787478-chr8:19970989..19972023,3	K562	blood:

Variant related genes	Relation type
ENSG00000242709	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10092137	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10092531	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10092538	0.91[EUR][1000 genomes]
rs10099404	0.91[EUR][1000 genomes]
rs10102021	0.91[EUR][1000 genomes]
rs10102045	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10102876	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10107119	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10111437	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1031045	0.91[EUR][1000 genomes]
rs10503667	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11992664	0.91[EUR][1000 genomes]
rs11997573	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1470186	0.91[EUR][1000 genomes]
rs17091738	0.91[EUR][1000 genomes]
rs17091742	0.91[EUR][1000 genomes]
rs17482338	0.91[EUR][1000 genomes]
rs1800590	0.91[EUR][1000 genomes]
rs1801177	0.91[EUR][1000 genomes]
rs2410615	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28371439	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28445964	0.91[EUR][1000 genomes]
rs28522139	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28568947	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28575919	0.91[EUR][1000 genomes]
rs28582042	0.91[EUR][1000 genomes]
rs28615996	0.91[EUR][1000 genomes]
rs28645722	0.91[EUR][1000 genomes]
rs28689946	0.91[EUR][1000 genomes]
rs28786747	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35469180	0.82[EUR][1000 genomes]
rs3854905	0.91[EUR][1000 genomes]
rs3900537	0.91[EUR][1000 genomes]
rs3951339	0.91[EUR][1000 genomes]
rs4368997	0.91[EUR][1000 genomes]
rs56043715	0.91[EUR][1000 genomes]
rs59811201	0.91[EUR][1000 genomes]
rs60633545	0.91[EUR][1000 genomes]
rs60901125	0.91[EUR][1000 genomes]
rs6586879	0.91[EUR][1000 genomes]
rs6984990	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6995406	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6996383	0.91[EUR][1000 genomes]
rs6997330	0.91[EUR][1000 genomes]
rs6998260	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6999612	0.91[EUR][1000 genomes]
rs7000460	0.91[EUR][1000 genomes]
rs7008626	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7009128	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7011846	0.83[AFR][1000 genomes]
rs7016529	0.91[EUR][1000 genomes]
rs73667455	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73667459	0.91[EUR][1000 genomes]
rs73667461	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73667462	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73667463	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73667465	0.91[EUR][1000 genomes]
rs73667468	0.91[EUR][1000 genomes]
rs73667469	0.91[EUR][1000 genomes]
rs73667470	0.82[EUR][1000 genomes]
rs7818864	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7835874	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7840666	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7840815	0.91[EUR][1000 genomes]
rs7840959	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890625	chr8:19368697-19799641	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv610759	chr8:19561997-20068842	Enhancers Strong transcription Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv498082	chr8:19722435-19873112	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	esv32767	chr8:19740189-19873082	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv1033511	chr8:19751299-20625091	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv824561	chr8:19786264-19787773	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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