Variant report

Variant	rs2789963
Chromosome Location	chr1:223097331-223097332
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	chr1:223097266-223097333	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:223093236..223095130-chr1:223096668..223099706,3	K562	blood:
2	chr1:223092526..223094736-chr1:223096745..223098289,2	K562	blood:

Variant related genes	Relation type
DISP1	TF binding region

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1890615	0.80[ASN][1000 genomes]
rs1970382	0.81[ASN][1000 genomes]
rs2254329	0.80[ASN][1000 genomes]
rs2609343	0.80[ASN][1000 genomes]
rs2609384	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2609387	0.94[ASN][1000 genomes]
rs2609391	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2609392	0.81[ASN][1000 genomes]
rs2609393	0.81[ASN][1000 genomes]
rs2609394	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2609395	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2609396	0.81[ASN][1000 genomes]
rs2609397	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2609398	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2609401	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2609402	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2609404	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2609408	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2789960	0.81[ASN][1000 genomes]
rs2789962	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2789964	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2789965	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2789968	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2789969	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2789970	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2789971	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2789973	0.82[ASN][1000 genomes]
rs2789974	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3101114	0.86[AMR][1000 genomes];0.94[ASN][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	nsv999185	chr1:222500725-223278032	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv535304	chr1:222500725-223278032	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv1012537	chr1:222755091-223512243	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	nsv873206	chr1:222985197-223124916	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1014896	chr1:223070446-223327185	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv873207	chr1:223078802-223292632	Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223083200-223101400	Weak transcription	Fetal Heart	heart
2	chr1:223083600-223101600	Weak transcription	Fetal Stomach	stomach
3	chr1:223090800-223101600	Weak transcription	Pancreas	Pancrea
4	chr1:223092400-223098600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:223092400-223101400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr1:223092400-223116200	Weak transcription	Primary B cells from cord blood	blood
7	chr1:223093000-223097400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:223093000-223101200	Weak transcription	Adipose Nuclei	Adipose
9	chr1:223094000-223099800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:223094000-223099800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:223094000-223101400	Weak transcription	HSMM	muscle
12	chr1:223094600-223099800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr1:223094800-223097400	Enhancers	Stomach Mucosa	stomach
14	chr1:223095000-223098000	Enhancers	Fetal Lung	lung
15	chr1:223095400-223098000	Enhancers	Ovary	ovary
16	chr1:223095600-223099000	Weak transcription	Right Atrium	heart
17	chr1:223095600-223100000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr1:223095600-223101400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:223095800-223097600	Weak transcription	Osteobl	bone
20	chr1:223096000-223101400	Weak transcription	Fetal Kidney	kidney
21	chr1:223096400-223098200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr1:223096600-223097400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:223096600-223098200	Enhancers	Colon Smooth Muscle	Colon
24	chr1:223096800-223098200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:223096800-223099600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr1:223097000-223097600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:223097000-223097800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:223097000-223097800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr1:223097000-223097800	Enhancers	NHLF	lung
30	chr1:223097000-223098400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr1:223097200-223097400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr1:223097200-223097400	Enhancers	Rectal Smooth Muscle	rectum
33	chr1:223097200-223098000	Enhancers	Fetal Muscle Leg	muscle
34	chr1:223097200-223098000	Enhancers	HepG2	liver
35	chr1:223097200-223098800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr1:223097200-223100200	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr1:223097200-223101600	Weak transcription	Psoas Muscle	Psoas

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