Variant report

Variant	rs62026958
Chromosome Location	chr16:12639025-12639026
allele	C/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	chr16:12636690-12639643	GM12878	blood:	n/a	n/a
2	POLR2A	chr16:12636727-12640562	GM12891	blood:	n/a	n/a
3	ELK1	chr16:12638858-12639218	GM12878	blood:	n/a	n/a
4	PML	chr16:12638936-12640499	GM12878	blood:	n/a	n/a
5	SRF	chr16:12638882-12639130	HepG2	liver:	n/a	chr16:12639030-12639047 chr16:12639064-12639074
6	TBP	chr16:12638964-12639252	GM12878	blood:	n/a	n/a
7	FOXA2	chr16:12638910-12639370	HepG2	liver:	n/a	n/a
8	RCOR1	chr16:12638468-12639046	HepG2	liver:	n/a	n/a
9	POLR2A	chr16:12636855-12640530	GM12891	blood:	n/a	n/a
10	SRF	chr16:12638929-12639123	GM12878	blood:	n/a	chr16:12639030-12639047 chr16:12639064-12639074
11	CEBPB	chr16:12638349-12639295	HepG2	liver:	n/a	n/a
12	EP300	chr16:12638846-12639399	HepG2	liver:	n/a	n/a
13	POLR2A	chr16:12637143-12640374	GM12878	blood:	n/a	n/a
14	MTA3	chr16:12636806-12639043	GM12878	blood:	n/a	n/a
15	MAZ	chr16:12638948-12639355	HepG2	liver:	n/a	n/a
16	POLR2A	chr16:12636967-12640529	GM12878	blood:	n/a	n/a
17	POLR2A	chr16:12638866-12639353	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
ENSG00000260601	TF binding region

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

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10492793	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10492794	0.89[AFR][1000 genomes]
rs12926189	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12928698	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1641880	0.85[EUR][1000 genomes]
rs3830063	0.90[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs8048146	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043096	chr16:12013915-12840769	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv571463	chr16:12367791-12783535	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1051242	chr16:12482972-12897243	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv542749	chr16:12482972-12897243	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1035581	chr16:12516946-12863700	ZNF genes & repeats Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv1051607	chr16:12522130-13347676	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv542750	chr16:12522130-13347676	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
8	nsv571465	chr16:12625395-12639800	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1054084	chr16:12625727-12650247	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv431433	chr16:12628409-12654408	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	esv1842867	chr16:12632286-12678721	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1039338	chr16:12632918-12642955	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv1040887	chr16:12632918-12650247	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	esv2751546	chr16:12635498-12674704	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv1040358	chr16:12636982-12650247	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr16:12613000-12670800	Weak transcription	Pancreas	Pancrea
2	chr16:12625800-12643400	Weak transcription	Gastric	stomach
3	chr16:12627000-12642200	Weak transcription	Right Ventricle	heart
4	chr16:12632800-12640200	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr16:12632800-12641000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr16:12632800-12646600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr16:12632800-12663800	Weak transcription	Aorta	Aorta
8	chr16:12633000-12646600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr16:12633200-12640600	Weak transcription	Stomach Mucosa	stomach
10	chr16:12633200-12640800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr16:12633400-12654400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr16:12633600-12640000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr16:12633800-12640000	Weak transcription	NHEK	skin
14	chr16:12634200-12640600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr16:12635000-12644200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr16:12635400-12640600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr16:12635600-12639200	Weak transcription	Esophagus	oesophagus
18	chr16:12635600-12641000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr16:12636000-12642600	Flanking Active TSS	GM12878-XiMat	blood
20	chr16:12636400-12640600	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr16:12637200-12639200	Flanking Active TSS	HepG2	liver
22	chr16:12637200-12642200	Enhancers	Spleen	Spleen
23	chr16:12637600-12641800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr16:12637600-12642400	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr16:12637600-12642800	Enhancers	Primary B cells from cord blood	blood
26	chr16:12638000-12639400	Enhancers	HSMMtube	muscle
27	chr16:12638200-12639200	Enhancers	HSMM	muscle
28	chr16:12638200-12639200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr16:12638200-12641000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr16:12638400-12639400	Enhancers	Brain Angular Gyrus	brain
31	chr16:12638400-12639800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr16:12638400-12639800	Enhancers	Brain Hippocampus Middle	brain
33	chr16:12638400-12641200	Enhancers	Brain Substantia Nigra	brain
34	chr16:12638600-12639200	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr16:12638600-12639600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr16:12638600-12639800	Enhancers	Primary T cells fromperipheralblood	blood
37	chr16:12638600-12641600	Weak transcription	Fetal Muscle Leg	muscle
38	chr16:12638600-12643000	Enhancers	Primary B cells from peripheral blood	blood
39	chr16:12638600-12644000	Weak transcription	Primary T cells from cord blood	blood
40	chr16:12638800-12639200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr16:12638800-12639200	Weak transcription	Lung	lung
42	chr16:12638800-12641000	Weak transcription	Fetal Muscle Trunk	muscle
43	chr16:12638800-12645400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr16:12639000-12639400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr16:12639000-12639400	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr16:12639000-12639600	Weak transcription	Fetal Thymus	thymus

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