Variant report

Variant	rs2265628
Chromosome Location	chr1:119868598-119868599
allele	G/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	STAT3	chr1:119868546-119868643	MCF10A-Er-Src	breast:	n/a	n/a
2	STAT3	chr1:119868528-119868733	MCF10A-Er-Src	breast:	n/a	n/a
3	STAT1	chr1:119867837-119869334	Hela-S3	cervix:	n/a	n/a

Variant related genes	Relation type
ENSG00000232650	TF binding region

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10754394	0.93[EUR][1000 genomes]
rs10802089	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10923796	0.93[EUR][1000 genomes]
rs1409056	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1418024	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1418025	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1891224	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2153738	0.82[EUR][1000 genomes]
rs2226102	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2243981	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2253988	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2254528	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2254664	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2257016	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2265629	0.82[ASN][1000 genomes]
rs2265630	0.82[EUR][1000 genomes]
rs2477889	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2477890	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2885445	0.93[EUR][1000 genomes]
rs6428814	0.93[EUR][1000 genomes]
rs6672571	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs699771	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838512	0.82[EUR][1000 genomes]
rs838513	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs838514	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs838515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs838516	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs838517	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs838519	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs838520	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs838523	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs838524	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs838525	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs838526	0.82[EUR][1000 genomes]
rs838527	0.82[EUR][1000 genomes]
rs866788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs947422	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs947423	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs947424	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs947425	1.00[EUR][1000 genomes];1.00[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	nsv547615	chr1:119828542-119875730	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	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
6	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
7	esv2761649	chr1:119840645-119925936	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	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

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:119859400-119869800	Weak transcription	Right Atrium	heart
2	chr1:119865000-119869000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr1:119865800-119869400	Enhancers	GM12878-XiMat	blood
4	chr1:119866600-119869000	Weak transcription	Fetal Thymus	thymus
5	chr1:119867000-119869000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:119867000-119869000	Weak transcription	Dnd41	blood
7	chr1:119867400-119869000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:119867600-119868800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr1:119867800-119869000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr1:119867800-119870200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:119868000-119868600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:119868000-119868800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr1:119868000-119868800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
14	chr1:119868000-119868800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
15	chr1:119868000-119869200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
16	chr1:119868000-119869200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
17	chr1:119868000-119869600	Enhancers	HepG2	liver
18	chr1:119868000-119871600	Flanking Active TSS	Liver	Liver
19	chr1:119868200-119869200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr1:119868200-119869200	Enhancers	Colon Smooth Muscle	Colon
21	chr1:119868400-119869000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
22	chr1:119868400-119869000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr1:119868400-119869400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:119868400-119869600	Enhancers	H9 Cell Line	embryonic stem cell
25	chr1:119868400-119869600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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