Variant report

Variant	rs35937061
Chromosome Location	chr18:12776785-12776786
allele	C/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	YY1	chr18:12776664-12777108	H1-hESC	embryonic stem cell:	n/a	n/a
2	YY1	chr18:12776780-12777045	H1-hESC	embryonic stem cell:	n/a	n/a
3	NFYB	chr18:12776001-12776814	K562	blood:	n/a	n/a
4	SP1	chr18:12776103-12776788	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr18:12776768-12777022	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr18:12776401-12776800	H1-hESC	embryonic stem cell:	n/a	n/a

Variant related genes	Relation type
ENSG00000260302	TF binding region

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12608033	0.84[EUR][1000 genomes]
rs12955574	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1941075	0.83[EUR][1000 genomes]
rs2542153	0.98[ASN][1000 genomes]
rs2542170	0.87[ASN][1000 genomes]
rs2847289	0.90[ASN][1000 genomes]
rs2847303	0.89[ASN][1000 genomes]
rs2847304	0.87[ASN][1000 genomes]
rs34695860	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3786155	0.82[EUR][1000 genomes]
rs4325641	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6505764	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9965888	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063125	chr18:12046892-12918251	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
2	esv3528039	chr18:12396582-12851293	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
3	esv3528041	chr18:12396641-12851245	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv1062014	chr18:12687210-13183383	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
5	nsv543655	chr18:12687210-13183383	Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
6	nsv1064273	chr18:12697601-12828251	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv1062149	chr18:12728115-12783898	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv1064844	chr18:12748045-12953235	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	68 gene(s)	inside rSNPs	diseases
9	nsv543656	chr18:12748045-12953235	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	68 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12767400-12815800	Weak transcription	Gastric	stomach
2	chr18:12774200-12776800	Active TSS	Dnd41	blood
3	chr18:12774800-12777600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
4	chr18:12775000-12778000	ZNF genes & repeats	Fetal Thymus	thymus
5	chr18:12776000-12777200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr18:12776000-12793600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr18:12776200-12777000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr18:12776200-12777200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr18:12776200-12777200	Weak transcription	Thymus	Thymus
10	chr18:12776200-12785800	Weak transcription	Primary T cells from cord blood	blood
11	chr18:12776200-12791600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr18:12776200-12792600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr18:12776200-12793800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr18:12776200-12793800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr18:12776200-12794000	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr18:12776200-12800800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr18:12776400-12776800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
18	chr18:12776400-12777200	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr18:12776400-12800000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr18:12776600-12776800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr18:12776600-12776800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr18:12776600-12777800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr18:12776600-12778200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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