Variant report

Variant	rs13424871
Chromosome Location	chr2:212531352-212531353
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	KAP1	chr2:212531266-212531475	K562	blood:	n/a	n/a

Variant related genes	Relation type
ERBB4	TF binding region

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10179476	0.88[ASN][1000 genomes]
rs10181864	0.82[ASN][1000 genomes]
rs10183757	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs10190554	0.88[ASN][1000 genomes]
rs10191972	0.85[ASN][1000 genomes]
rs10207288	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10932392	0.85[ASN][1000 genomes]
rs11893380	0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12328907	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12470629	0.88[ASN][1000 genomes]
rs12476100	1.00[JPT][hapmap]
rs12694250	0.85[ASN][1000 genomes]
rs13001867	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs13003212	0.90[ASN][1000 genomes]
rs13016387	0.82[ASN][1000 genomes]
rs13019022	0.88[ASN][1000 genomes]
rs13019783	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs13026360	0.85[ASN][1000 genomes]
rs13420886	0.85[ASN][1000 genomes]
rs16846710	1.00[JPT][hapmap]
rs17413784	0.82[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1829615	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1851168	1.00[JPT][hapmap]
rs1851191	0.88[ASN][1000 genomes]
rs2272024	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs34579531	0.88[ASN][1000 genomes]
rs34658976	0.85[ASN][1000 genomes]
rs34678713	0.88[ASN][1000 genomes]
rs34807898	0.86[ASN][1000 genomes]
rs35762488	0.85[ASN][1000 genomes]
rs35882647	0.86[ASN][1000 genomes]
rs3817429	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs4315465	0.85[ASN][1000 genomes]
rs4423543	1.00[JPT][hapmap]
rs4493186	0.82[ASN][1000 genomes]
rs58225230	0.92[ASN][1000 genomes]
rs59853762	0.85[ASN][1000 genomes]
rs60655490	0.90[ASN][1000 genomes]
rs61257038	0.85[ASN][1000 genomes]
rs6435654	0.80[ASN][1000 genomes]
rs6705698	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs6705988	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs6710649	0.86[ASN][1000 genomes]
rs6714941	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6722300	0.90[ASN][1000 genomes]
rs6725181	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6732128	0.91[EUR][1000 genomes]
rs6759039	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs6759054	0.92[ASN][1000 genomes]
rs71422749	0.82[EUR][1000 genomes]
rs71422750	0.85[ASN][1000 genomes]
rs7425341	0.88[ASN][1000 genomes]
rs7588697	0.88[ASN][1000 genomes]
rs9798120	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754366	chr2:212470494-212541494	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
2	nsv460070	chr2:212492764-212541377	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
3	nsv584322	chr2:212492764-212541377	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
4	nsv875783	chr2:212530466-212564895	Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212467400-212546800	Weak transcription	Aorta	Aorta
2	chr2:212521200-212540400	Weak transcription	Fetal Heart	heart
3	chr2:212521400-212540800	Weak transcription	Fetal Kidney	kidney
4	chr2:212522800-212537800	Weak transcription	Pancreas	Pancrea
5	chr2:212528800-212545200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr2:212529600-212533800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:212530200-212546800	Weak transcription	Left Ventricle	heart
8	chr2:212530600-212531600	Enhancers	Dnd41	blood

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