Variant report

Variant	rs7920279
Chromosome Location	chr10:26967984-26967985
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr10:26967853-26968029	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr10:26967830-26968049	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:26952451..26954548-chr10:26967592..26969154,2	K562	blood:
2	chr10:26958878..26961575-chr10:26966609..26969572,2	K562	blood:
3	chr10:26965108..26970102-chr10:26984839..26987979,6	K562	blood:
4	chr10:26961383..26963009-chr10:26967023..26968974,2	K562	blood:
5	chr10:26965218..26966801-chr10:26966890..26969574,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000227932	TF binding region
ENSG00000148459	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10128125	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10128192	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10829048	0.96[ASN][1000 genomes]
rs11015219	0.94[AFR][1000 genomes]
rs11015220	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11015226	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11015230	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11015233	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11015234	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12242239	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12242414	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12245051	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12246285	0.96[ASN][1000 genomes]
rs12247299	0.96[ASN][1000 genomes]
rs12247597	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12252298	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12252358	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12252368	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12255583	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12255942	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12260035	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12260298	0.96[ASN][1000 genomes]
rs12260466	0.92[ASN][1000 genomes]
rs12262082	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12262401	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12263262	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12263578	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12264509	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12265505	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12265633	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12265746	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12267744	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12268883	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12269520	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17754039	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17754051	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1980754	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2005120	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34314417	0.92[ASN][1000 genomes]
rs34901510	0.96[ASN][1000 genomes]
rs35534478	0.96[ASN][1000 genomes]
rs35687107	0.96[ASN][1000 genomes]
rs35827769	0.96[ASN][1000 genomes]
rs4309054	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7097696	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72485013	0.90[ASN][1000 genomes]
rs72485015	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72485017	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72485018	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72485022	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72485023	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72485026	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs753705	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7899631	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7900674	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7906473	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	esv3436664	chr10:26860755-26969397	Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1041766	chr10:26890945-26969381	Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1046911	chr10:26894348-26969381	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1044057	chr10:26894348-26971879	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv516275	chr10:26896432-26968171	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv3333006	chr10:26908323-26985227	Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	esv3415799	chr10:26929831-27233591	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26963400-26969400	Weak transcription	Thymus	Thymus
2	chr10:26965600-26969400	Weak transcription	Fetal Thymus	thymus
3	chr10:26967000-26973800	Weak transcription	K562	blood
4	chr10:26967800-26968000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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