Variant report

Variant	rs35635659
Chromosome Location	chr8:105603096-105603097
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	CBX3	chr8:105601843-105603096	K562	blood:	n/a	n/a
2	NFYB	chr8:105602640-105603281	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:105599361..105601982-chr8:105602248..105604776,3	MCF-7	breast:

Variant related genes	Relation type
LRP12	TF binding region
ENSG00000147650	Chromatin interaction

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10505062	0.83[EUR][1000 genomes]
rs10955357	0.88[EUR][1000 genomes]
rs11775166	0.91[EUR][1000 genomes]
rs11775331	0.88[EUR][1000 genomes]
rs11776230	0.95[EUR][1000 genomes]
rs11781863	0.81[EUR][1000 genomes]
rs11782169	0.93[EUR][1000 genomes]
rs11782366	0.86[EUR][1000 genomes]
rs11783063	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11783104	0.95[EUR][1000 genomes]
rs11783651	0.83[EUR][1000 genomes]
rs11784193	0.83[EUR][1000 genomes]
rs11785071	0.81[EUR][1000 genomes]
rs11787202	0.81[EUR][1000 genomes]
rs12675273	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12675605	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12676758	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12677524	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12677793	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12678904	0.83[EUR][1000 genomes]
rs12680652	0.83[EUR][1000 genomes]
rs12681898	0.83[EUR][1000 genomes]
rs13250005	0.90[AFR][1000 genomes]
rs13250948	0.83[EUR][1000 genomes]
rs13254058	0.86[EUR][1000 genomes]
rs13254678	0.86[EUR][1000 genomes]
rs13257283	0.88[EUR][1000 genomes]
rs13260018	0.86[EUR][1000 genomes]
rs13262954	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13265309	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13265320	0.86[EUR][1000 genomes]
rs13266739	0.83[EUR][1000 genomes]
rs13268122	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13270263	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13279448	0.83[EUR][1000 genomes]
rs1438355	0.85[EUR][1000 genomes]
rs1837203	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2880074	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs33999897	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34008887	0.91[EUR][1000 genomes]
rs34145689	0.83[EUR][1000 genomes]
rs34155810	0.83[EUR][1000 genomes]
rs34155867	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34299626	0.81[EUR][1000 genomes]
rs34306176	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34340810	0.86[EUR][1000 genomes]
rs34435802	0.81[EUR][1000 genomes]
rs34493777	0.83[EUR][1000 genomes]
rs34556973	0.85[EUR][1000 genomes]
rs34690452	0.86[EUR][1000 genomes]
rs34695252	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs34873943	0.83[EUR][1000 genomes]
rs34881302	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34971735	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35013911	0.83[EUR][1000 genomes]
rs35085883	0.86[EUR][1000 genomes]
rs35140929	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35258168	0.86[EUR][1000 genomes]
rs35263244	0.95[EUR][1000 genomes]
rs35379160	0.91[EUR][1000 genomes]
rs35394104	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35467682	0.91[EUR][1000 genomes]
rs35517423	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35649342	0.83[EUR][1000 genomes]
rs35767747	0.83[EUR][1000 genomes]
rs35795037	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4288345	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4552868	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4593510	0.83[EUR][1000 genomes]
rs66494641	0.88[EUR][1000 genomes]
rs67089516	0.91[EUR][1000 genomes]
rs67555988	0.85[EUR][1000 genomes]
rs6984152	0.80[EUR][1000 genomes]
rs6990243	0.83[EUR][1000 genomes]
rs6994764	0.83[EUR][1000 genomes]
rs6995010	0.93[EUR][1000 genomes]
rs7004507	0.83[EUR][1000 genomes]
rs7009594	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs71520889	0.81[EUR][1000 genomes]
rs71520891	0.83[EUR][1000 genomes]
rs71520893	0.83[EUR][1000 genomes]
rs71520897	0.83[EUR][1000 genomes]
rs71520900	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs71520901	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs731126	0.91[EUR][1000 genomes]
rs7821181	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7824500	0.91[EUR][1000 genomes]
rs7834086	0.83[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	nsv1016087	chr8:105228670-105934368	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1026754	chr8:105382508-106030916	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
3	nsv539709	chr8:105382508-106030916	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
4	nsv831417	chr8:105455814-105625608	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
5	nsv508522	chr8:105532034-105614403	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv2422460	chr8:105573376-105746329	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr8:105602000-105605600	Weak transcription	Small Intestine	intestine
2	chr8:105602400-105606000	Weak transcription	HUVEC	blood vessel
3	chr8:105602400-105607600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:105602600-105603600	Enhancers	K562	blood
5	chr8:105602800-105603600	Enhancers	Dnd41	blood
6	chr8:105602800-105604200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:105602800-105607400	Weak transcription	Thymus	Thymus
8	chr8:105603000-105603400	Weak transcription	Fetal Thymus	thymus

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