Variant report

Variant	rs10492612
Chromosome Location	chr13:92297692-92297693
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:92293314..92295446-chr13:92296832..92298493,2	K562	blood:
2	chr13:91998514..92002509-chr13:92292790..92300343,7	K562	blood:
3	chr13:92291806..92294892-chr13:92297523..92300021,4	K562	blood:
4	chr13:92272945..92275845-chr13:92297688..92299571,2	K562	blood:
5	chr13:92297130..92298943-chr13:92307852..92310452,2	K562	blood:
6	chr13:92296687..92299526-chr13:92415724..92417645,2	K562	blood:
7	chr13:92070589..92072533-chr13:92296462..92299293,2	K562	blood:
8	chr13:92297056..92300246-chr13:92301325..92305110,3	K562	blood:
9	chr13:92262226..92264214-chr13:92297323..92300140,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000215417	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10492613	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16946339	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16946341	0.85[AMR][1000 genomes]
rs16946352	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16946357	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16946360	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16946362	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16946371	1.00[AMR][1000 genomes]
rs16946374	1.00[AMR][1000 genomes]
rs16946377	1.00[AMR][1000 genomes]
rs16946381	1.00[AMR][1000 genomes]
rs16946386	1.00[AMR][1000 genomes]
rs16946389	1.00[AMR][1000 genomes]
rs16946392	1.00[AMR][1000 genomes]
rs16946394	1.00[AMR][1000 genomes]
rs16946396	1.00[AMR][1000 genomes]
rs16946397	1.00[AMR][1000 genomes]
rs16946400	1.00[AMR][1000 genomes]
rs16946404	1.00[AMR][1000 genomes]
rs16946405	0.87[AMR][1000 genomes]
rs16946406	0.87[AMR][1000 genomes]
rs16946407	1.00[AMR][1000 genomes]
rs16946415	1.00[AMR][1000 genomes]
rs17388158	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55965175	1.00[AMR][1000 genomes]
rs57140832	1.00[AMR][1000 genomes]
rs57792448	1.00[AMR][1000 genomes]
rs57927413	1.00[AMR][1000 genomes]
rs57977827	1.00[AMR][1000 genomes]
rs58927659	1.00[AMR][1000 genomes]
rs59048158	0.87[AMR][1000 genomes]
rs59240177	1.00[AMR][1000 genomes]
rs59356035	1.00[AMR][1000 genomes]
rs59594682	1.00[AMR][1000 genomes]
rs60874154	1.00[AMR][1000 genomes]
rs60875456	1.00[AMR][1000 genomes]
rs61249711	1.00[AMR][1000 genomes]
rs73607976	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73607979	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73609965	1.00[AMR][1000 genomes]
rs73609967	1.00[AMR][1000 genomes]
rs73609971	1.00[AMR][1000 genomes]
rs73609975	1.00[AMR][1000 genomes]
rs73609976	1.00[AMR][1000 genomes]
rs73609977	1.00[AMR][1000 genomes]
rs73609983	1.00[AMR][1000 genomes]
rs73609984	1.00[AMR][1000 genomes]
rs73609985	1.00[AMR][1000 genomes]
rs73609986	1.00[AMR][1000 genomes]
rs73609987	1.00[AMR][1000 genomes]
rs73609989	1.00[AMR][1000 genomes]
rs73612008	1.00[AMR][1000 genomes]
rs74104924	0.87[AMR][1000 genomes]
rs74104930	1.00[AMR][1000 genomes]
rs9589321	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042947	chr13:91571040-92416897	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
2	nsv541871	chr13:91571040-92416897	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
3	nsv1049382	chr13:92024240-92521180	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv541873	chr13:92024240-92521180	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv562714	chr13:92056911-92304974	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv562715	chr13:92061878-92299609	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1041168	chr13:92062057-92301861	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv949582	chr13:92062331-92301861	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1040707	chr13:92072034-92302281	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1040709	chr13:92173603-92318362	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	esv2753383	chr13:92226599-92462699	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	nsv900882	chr13:92228446-92304974	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv529268	chr13:92267310-92531263	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr13:92296400-92297800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr13:92296600-92298200	Enhancers	Hela-S3	cervix
3	chr13:92297200-92298200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr13:92297400-92297800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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