Variant report

Variant	rs9858457
Chromosome Location	chr3:136249577-136249578
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:136247859..136250822-chr3:136470944..136473511,2	K562	blood:

Variant related genes	Relation type
ENSG00000118007	Chromatin interaction
ENSG00000261758	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs16843991	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28396702	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34165586	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34962604	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35375192	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35644083	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3931416	0.85[AFR][1000 genomes]
rs3932048	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4336059	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4402873	0.82[EUR][1000 genomes]
rs55993001	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56040643	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56047785	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56125228	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56251259	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs59931907	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6439642	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66810260	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6766450	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6769934	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6782151	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6789541	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6789761	0.98[EUR][1000 genomes]
rs6799368	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6804194	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6806795	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7612160	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7615706	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7621017	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7621970	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7623824	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7627292	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7644471	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7648591	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9809184	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9812319	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9819496	0.84[EUR][1000 genomes]
rs9831321	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9832572	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9834631	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9850383	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9866535	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9868120	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948461	chr3:135969755-136349636	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv877519	chr3:136035737-136279390	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv877520	chr3:136056861-136310985	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv877521	chr3:136069286-136310985	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv877523	chr3:136088038-136310985	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	nsv520012	chr3:136088038-136314119	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv877524	chr3:136112109-136295283	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv877525	chr3:136112109-136310985	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv877526	chr3:136149139-136310985	ZNF genes & repeats Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	nsv877527	chr3:136182053-136310985	Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	nsv877528	chr3:136209550-136295283	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	nsv591850	chr3:136209550-136300732	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	nsv460861	chr3:136222954-136425600	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
14	nsv591851	chr3:136222954-136425600	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:136176400-136314200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr3:136176600-136260800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:136176800-136266200	Weak transcription	Hela-S3	cervix
4	chr3:136191400-136268000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr3:136192400-136252400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr3:136195400-136250400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr3:136195400-136278800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:136212200-136323400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr3:136212400-136249600	Weak transcription	Lung	lung
10	chr3:136213000-136251000	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr3:136213000-136252200	Weak transcription	Left Ventricle	heart
12	chr3:136213000-136326600	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr3:136220600-136266200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr3:136221200-136251000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:136221400-136251000	Weak transcription	Liver	Liver
16	chr3:136221600-136251000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr3:136222200-136251000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr3:136222200-136251200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr3:136222400-136266200	Weak transcription	HSMM	muscle
20	chr3:136230400-136251000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr3:136232000-136263600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr3:136232400-136251000	Weak transcription	Adipose Nuclei	Adipose
23	chr3:136232400-136255200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr3:136232600-136251000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr3:136232800-136250800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr3:136246200-136250000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr3:136246600-136286200	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr3:136247200-136249600	Weak transcription	Ovary	ovary
29	chr3:136247200-136251200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr3:136247200-136252400	Weak transcription	Thymus	Thymus
31	chr3:136247200-136319800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr3:136247200-136334800	Weak transcription	Aorta	Aorta
33	chr3:136247400-136270600	Weak transcription	Fetal Thymus	thymus
34	chr3:136247800-136255200	Weak transcription	Fetal Stomach	stomach
35	chr3:136247800-136261600	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr3:136248200-136251200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr3:136248200-136349200	Weak transcription	Rectal Smooth Muscle	rectum
38	chr3:136248600-136250200	Strong transcription	Primary B cells from cord blood	blood
39	chr3:136248600-136250800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:136248600-136251000	Weak transcription	Primary B cells from peripheral blood	blood
41	chr3:136248600-136251200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr3:136248800-136251600	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr3:136249000-136251000	Weak transcription	Fetal Lung	lung
44	chr3:136249200-136249800	Weak transcription	Psoas Muscle	Psoas
45	chr3:136249400-136249800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
46	chr3:136249400-136251000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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