Variant report

Variant	rs2605381
Chromosome Location	chr12:74929925-74929926
allele	C/G
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	JUND	chr12:74929877-74929929	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:74687125..74689371-chr12:74929648..74931476,2	K562	blood:

Variant related genes	Relation type
ATXN7L3B	TF binding region

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10506693	0.90[ASN][1000 genomes]
rs12809241	0.90[ASN][1000 genomes]
rs12825946	0.94[ASN][1000 genomes]
rs1493796	0.98[ASN][1000 genomes]
rs1493801	0.90[ASN][1000 genomes]
rs1493810	0.92[ASN][1000 genomes]
rs17113674	0.94[ASN][1000 genomes]
rs17113675	0.94[ASN][1000 genomes]
rs17113679	0.94[ASN][1000 genomes]
rs17113748	0.90[ASN][1000 genomes]
rs17113750	0.86[ASN][1000 genomes]
rs1824539	0.90[ASN][1000 genomes]
rs2061579	0.90[ASN][1000 genomes]
rs2126136	0.94[ASN][1000 genomes]
rs2365919	0.94[ASN][1000 genomes]
rs2605375	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2613902	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2641470	0.82[ASN][1000 genomes]
rs2641471	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs34706013	0.90[ASN][1000 genomes]
rs35454023	0.94[ASN][1000 genomes]
rs35957931	0.90[ASN][1000 genomes]
rs36030036	0.87[ASN][1000 genomes]
rs4547177	0.94[ASN][1000 genomes]
rs4882643	0.86[ASN][1000 genomes]
rs58783285	0.94[ASN][1000 genomes]
rs590352	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60905363	0.94[ASN][1000 genomes]
rs67506065	0.86[ASN][1000 genomes]
rs7132047	0.90[ASN][1000 genomes]
rs725181	0.90[ASN][1000 genomes]
rs7295970	0.90[ASN][1000 genomes]
rs7300059	0.90[ASN][1000 genomes]
rs7304361	0.90[ASN][1000 genomes]
rs7962722	0.94[ASN][1000 genomes]
rs9668146	0.90[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	nsv1039468	chr12:74080586-75000246	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv899292	chr12:74835107-74934162	Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv899293	chr12:74835107-74995760	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv559414	chr12:74850206-74931349	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
5	nsv899295	chr12:74854750-74984992	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv559417	chr12:74857957-74931349	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
7	nsv470303	chr12:74880668-74945356	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	n/a
8	nsv899296	chr12:74880668-74974630	Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74929400-74930000	ZNF genes & repeats	GM12878-XiMat	blood
2	chr12:74929800-74930600	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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