Variant report

Variant	rs1417610
Chromosome Location	chr1:119977761-119977762
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	MYC	chr1:119977668-119978042	MCF10A-Er-Src	breast:	n/a	n/a
2	MYC	chr1:119977718-119978049	MCF10A-Er-Src	breast:	n/a	n/a
3	FOS	chr1:119977689-119978091	MCF10A-Er-Src	breast:	n/a	chr1:119977869-119977877 chr1:119977869-119977876 chr1:119977869-119977877
4	FOS	chr1:119977713-119978081	MCF10A-Er-Src	breast:	n/a	chr1:119977869-119977877 chr1:119977869-119977876 chr1:119977869-119977877
5	FOS	chr1:119977713-119978079	MCF10A-Er-Src	breast:	n/a	chr1:119977869-119977877 chr1:119977869-119977876 chr1:119977869-119977877
6	FOS	chr1:119977705-119978084	MCF10A-Er-Src	breast:	n/a	chr1:119977869-119977877 chr1:119977869-119977876 chr1:119977869-119977877
7	E2F4	chr1:119977620-119977980	MCF10A-Er-Src	breast:	n/a	n/a
8	STAT3	chr1:119977747-119977996	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
ENSG00000232780	TF binding region
HSD3BP2	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]
rs10489812	0.85[CEU][hapmap]
rs10754396	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10923824	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11580104	0.84[CEU][hapmap]
rs12022215	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12024495	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12035458	0.87[CHB][hapmap]
rs12217015	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12402935	0.87[CHB][hapmap]
rs12405488	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12411080	0.94[CHB][hapmap]
rs12411115	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1341015	0.85[CEU][hapmap]
rs1361530	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1417607	0.85[CEU][hapmap]
rs1417608	0.85[CEU][hapmap]
rs1417609	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1538988	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1538990	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17023641	0.87[CHB][hapmap]
rs1891030	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2050892	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2050893	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2185556	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2854961	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs35311226	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3753258	0.81[ASN][1000 genomes]
rs3765948	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3765952	0.87[CHB][hapmap];0.88[CHD][hapmap]
rs3765956	0.87[CHB][hapmap]
rs3795660	0.87[CHB][hapmap]
rs4659003	0.93[CHB][hapmap]
rs4659174	0.85[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs5003333	0.85[CEU][hapmap]
rs57770425	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59522974	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[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	nsv932014	chr1:119476480-120471049	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
2	nsv917091	chr1:119688975-120023222	Enhancers Flanking Active TSS Weak transcription Strong transcription 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	18 gene(s)	inside rSNPs	diseases
3	esv34089	chr1:119752112-120072961	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1000391	chr1:119837978-120287056	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv535077	chr1:119837978-120287056	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv1004662	chr1:119847447-120154798	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
7	esv2763647	chr1:119929442-120154798	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
8	nsv946176	chr1:119960027-119989077	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 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	chr1:119974600-119980800	Weak transcription	Fetal Intestine Small	intestine
2	chr1:119975200-119980600	Weak transcription	Fetal Intestine Large	intestine
3	chr1:119977400-119977800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:119977400-119978200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:119977400-119978200	Enhancers	HMEC	breast
6	chr1:119977600-119978000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:119977600-119978000	Enhancers	NHDF-Ad	bronchial
8	chr1:119977600-119978200	Enhancers	NHEK	skin

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