Variant report

Variant	rs2470726
Chromosome Location	chr8:95273784-95273785
allele	A/G
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	POLR2A	chr8:95264764-95275103	IMR90	lung:	n/a	n/a
2	IRF4	chr8:95273750-95274509	GM12878	blood:	n/a	n/a
3	POLR2A	chr8:95270042-95274844	HCT-116	colon:	n/a	n/a
4	POLR2A	chr8:95272370-95274824	PBDE	blood:	n/a	n/a
5	POU2F2	chr8:95273764-95274743	GM12878	blood:	n/a	n/a
6	POLR2A	chr8:95270203-95274737	U87	brain:	n/a	n/a
7	POLR2A	chr8:95273713-95274771	GM12892	blood:	n/a	n/a
8	POLR2A	chr8:95273771-95274683	GM12891	blood:	n/a	n/a
9	MTA3	chr8:95273757-95275191	GM12878	blood:	n/a	n/a
10	MAZ	chr8:95273576-95275360	IMR90	lung:	n/a	chr8:95274691-95274700
11	SPI1	chr8:95273763-95274080	GM12891	blood:	n/a	n/a
12	CHD1	chr8:95269601-95275342	IMR90	lung:	n/a	n/a
13	MXI1	chr8:95271947-95275039	IMR90	lung:	n/a	n/a
14	POLR2A	chr8:95273440-95274786	GM12878	blood:	n/a	n/a
15	TCF12	chr8:95273702-95274972	A549	lung:	n/a	n/a
16	POLR2A	chr8:95273769-95274700	GM12892	blood:	n/a	n/a
17	POLR2A	chr8:95273656-95274835	GM12892	blood:	n/a	n/a
18	POLR2A	chr8:95273723-95274855	GM12892	blood:	n/a	n/a
19	BHLHE40	chr8:95273763-95274889	GM12878	blood:	n/a	chr8:95274546-95274562 chr8:95274538-95274554 chr8:95274552-95274568 chr8:95274549-95274565
20	POLR2A	chr8:95264619-95274882	U87	brain:	n/a	n/a
21	POLR2A	chr8:95273675-95274669	GM12891	blood:	n/a	n/a
22	IRF4	chr8:95273712-95274515	GM12878	blood:	n/a	n/a
23	YY1	chr8:95273738-95274069	GM12892	blood:	n/a	n/a
24	RELA	chr8:95273498-95274933	GM12891	blood:	n/a	n/a
25	POLR2A	chr8:95269480-95274882	U87	brain:	n/a	n/a
26	YY1	chr8:95273668-95274774	GM12878	blood:	n/a	chr8:95274551-95274565 chr8:95274537-95274546 chr8:95274548-95274562 chr8:95274553-95274562 chr8:95274618-95274627
27	RUNX3	chr8:95273738-95274819	GM12878	blood:	n/a	n/a
28	NFIC	chr8:95273686-95274932	GM12878	blood:	n/a	n/a
29	SPI1	chr8:95273733-95274039	GM12878	blood:	n/a	n/a
30	SPI1	chr8:95273607-95274137	GM12891	blood:	n/a	n/a
31	YY1	chr8:95273736-95274278	GM12891	blood:	n/a	n/a
32	POLR2A	chr8:95273454-95274757	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
GEM	TF binding region

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs2250208	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2445715	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2445716	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2470722	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2470723	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2470724	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2470725	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2514791	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2515147	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs923313	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[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	nsv1024907	chr8:95188944-95296378	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv539677	chr8:95188944-95296378	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1024893	chr8:95189085-95293557	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1035036	chr8:95213244-95283014	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv831401	chr8:95218297-95393968	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1022382	chr8:95261955-95283587	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1023617	chr8:95261955-95284414	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
9	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95259600-95274000	Weak transcription	Primary T cells from cord blood	blood
2	chr8:95263000-95273800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:95263000-95273800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:95267800-95274000	Weak transcription	Gastric	stomach
5	chr8:95269800-95274000	Transcr. at gene 5' and 3'	Pancreatic Islets	Pancreatic Islet
6	chr8:95270200-95273800	Enhancers	HSMM	muscle
7	chr8:95270200-95274800	Active TSS	Rectal Mucosa Donor 29	rectum
8	chr8:95270200-95275000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
9	chr8:95270600-95273800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr8:95270600-95274800	Active TSS	Brain Anterior Caudate	brain
11	chr8:95271000-95274800	Active TSS	Brain Cingulate Gyrus	brain
12	chr8:95271200-95274800	Active TSS	Brain Inferior Temporal Lobe	brain
13	chr8:95271200-95274800	Active TSS	Brain Substantia Nigra	brain
14	chr8:95271600-95273800	Flanking Active TSS	HMEC	breast
15	chr8:95271600-95273800	Flanking Active TSS	Osteobl	bone
16	chr8:95271600-95274800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
17	chr8:95271800-95273800	Enhancers	NHEK	skin
18	chr8:95271800-95275000	Active TSS	Colonic Mucosa	Colon
19	chr8:95272000-95274000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr8:95272400-95273800	Enhancers	Brain Germinal Matrix	brain
21	chr8:95272400-95273800	Weak transcription	HUVEC	blood vessel
22	chr8:95272400-95274000	Active TSS	Lung	lung
23	chr8:95272600-95273800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:95272600-95274000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
25	chr8:95272600-95274000	Enhancers	Placenta	Placenta
26	chr8:95272600-95274000	Active TSS	Rectal Mucosa Donor 31	rectum
27	chr8:95272600-95274600	Active TSS	Sigmoid Colon	Sigmoid Colon
28	chr8:95272600-95274800	Active TSS	Brain Angular Gyrus	brain
29	chr8:95272600-95275000	Active TSS	Esophagus	oesophagus
30	chr8:95272800-95274000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr8:95272800-95274000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
32	chr8:95272800-95274000	Weak transcription	Spleen	Spleen
33	chr8:95272800-95274200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
34	chr8:95272800-95274800	Active TSS	Fetal Brain Female	brain
35	chr8:95272800-95275000	Active TSS	Ovary	ovary
36	chr8:95273000-95273800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr8:95273000-95273800	Flanking Active TSS	GM12878-XiMat	blood
38	chr8:95273000-95274200	Active TSS	Stomach Smooth Muscle	stomach
39	chr8:95273000-95274400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:95273000-95274800	Active TSS	Duodenum Smooth Muscle	Duodenum
41	chr8:95273000-95274800	Active TSS	Rectal Smooth Muscle	rectum
42	chr8:95273200-95273800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:95273200-95273800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr8:95273200-95273800	Weak transcription	Fetal Brain Male	brain
45	chr8:95273200-95273800	Flanking Active TSS	Fetal Intestine Small	intestine
46	chr8:95273200-95274200	Bivalent/Poised TSS	Thymus	Thymus
47	chr8:95273200-95274400	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:95273200-95274600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
49	chr8:95273200-95274600	Active TSS	Placenta Amnion	Placenta Amnion
50	chr8:95273200-95274800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

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