Variant report

Variant	rs3794674
Chromosome Location	chr16:31721083-31721084
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr16:31720936-31721480	HepG2	liver:	n/a	n/a
2	POLR2A	chr16:31718748-31725396	HepG2	liver:	n/a	n/a
3	POLR2A	chr16:31721040-31725468	GM12892	blood:	n/a	n/a
4	POLR2A	chr16:31718943-31727784	HepG2	liver:	n/a	n/a
5	POLR2A	chr16:31715130-31726933	HepG2	liver:	n/a	n/a
6	POLR2A	chr16:31718974-31728173	GM12878	blood:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:31469625..31472736-chr16:31718738..31721377,3	K562	blood:
2	chr16:31518291..31520186-chr16:31719579..31721600,2	MCF-7	breast:
3	chr16:31467317..31473648-chr16:31720179..31727010,13	MCF-7	breast:
4	chr16:31469625..31472005-chr16:31718738..31721377,2	K562	blood:

No data

Variant related genes	Relation type
ZNF720	TF binding region
ENSG00000140688	Chromatin interaction
ENSG00000260267	Chromatin interaction
ENSG00000140691	Chromatin interaction
ENSG00000260625	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1034614	0.92[ASN][1000 genomes]
rs11859426	0.98[ASN][1000 genomes]
rs11861974	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11862133	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11862739	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11864739	0.92[ASN][1000 genomes]
rs11864893	0.88[ASN][1000 genomes]
rs11864895	0.87[ASN][1000 genomes]
rs11865512	0.94[ASN][1000 genomes]
rs11866346	1.00[ASN][1000 genomes]
rs11866699	1.00[ASN][1000 genomes]
rs11866828	0.98[ASN][1000 genomes]
rs17535906	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs17839515	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17839518	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs17839519	1.00[CHB][hapmap];0.89[ASN][1000 genomes]
rs17839521	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17839522	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17839526	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2239969	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2359234	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2884666	0.98[ASN][1000 genomes]
rs34146726	0.98[ASN][1000 genomes]
rs3751741	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4417563	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs56935657	0.98[ASN][1000 genomes]
rs56946315	0.89[ASN][1000 genomes]
rs57283435	0.98[ASN][1000 genomes]
rs57475804	0.97[ASN][1000 genomes]
rs59413238	0.88[ASN][1000 genomes]
rs59741846	0.81[ASN][1000 genomes]
rs60195538	0.91[ASN][1000 genomes]
rs60286885	0.94[ASN][1000 genomes]
rs60382362	0.98[ASN][1000 genomes]
rs61548031	0.90[ASN][1000 genomes]
rs7187594	0.89[CHB][hapmap];0.86[JPT][hapmap];0.98[ASN][1000 genomes]
rs7192946	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7193169	0.82[ASN][1000 genomes]
rs7194865	0.90[ASN][1000 genomes]
rs7195523	0.88[ASN][1000 genomes]
rs7200637	0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs72483446	0.89[ASN][1000 genomes]
rs8046495	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs8054672	0.93[ASN][1000 genomes]
rs8056595	0.90[ASN][1000 genomes]
rs8057733	0.98[ASN][1000 genomes]
rs8062014	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv905747	chr16:31394179-31888684	Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	123 gene(s)	inside rSNPs	diseases
2	esv3344221	chr16:31526786-31821640	Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
3	esv3323903	chr16:31526802-31821640	Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
4	esv3504445	chr16:31526873-31821580	Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
5	esv3504446	chr16:31526873-31821580	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
6	esv3366795	chr16:31534951-31827424	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
7	nsv833195	chr16:31576112-31763222	ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
8	nsv1057598	chr16:31608831-31726446	Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
9	nsv1067321	chr16:31652036-31959992	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
10	nsv918074	chr16:31669781-31935033	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
11	nsv1063037	chr16:31669981-31934894	Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
12	nsv542903	chr16:31669981-31934894	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31712600-31724200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr16:31712600-31724200	Weak transcription	Psoas Muscle	Psoas
3	chr16:31712600-31724200	Weak transcription	HSMM	muscle
4	chr16:31712800-31724200	Weak transcription	HSMMtube	muscle
5	chr16:31712800-31724200	Weak transcription	NHDF-Ad	bronchial
6	chr16:31712800-31724400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr16:31712800-31724600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr16:31713000-31724400	Weak transcription	Right Atrium	heart
9	chr16:31713200-31724000	Weak transcription	Fetal Heart	heart
10	chr16:31713200-31724200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr16:31713400-31722400	Strong transcription	Fetal Intestine Small	intestine
12	chr16:31713400-31724000	Weak transcription	K562	blood
13	chr16:31713400-31724200	Weak transcription	Fetal Brain Male	brain
14	chr16:31713600-31722200	Strong transcription	Stomach Smooth Muscle	stomach
15	chr16:31713800-31721400	Strong transcription	HUES6 Cell Line	embryonic stem cell
16	chr16:31713800-31721400	Strong transcription	Fetal Muscle Trunk	muscle
17	chr16:31713800-31721600	Strong transcription	Primary B cells from peripheral blood	blood
18	chr16:31713800-31721800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr16:31713800-31722200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr16:31713800-31722600	Strong transcription	Fetal Stomach	stomach
21	chr16:31714000-31721400	Strong transcription	Fetal Muscle Leg	muscle
22	chr16:31714000-31721800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr16:31714000-31722800	Strong transcription	Fetal Brain Female	brain
24	chr16:31714200-31721400	Strong transcription	Gastric	stomach
25	chr16:31714200-31721600	Strong transcription	Duodenum Mucosa	Duodenum
26	chr16:31714200-31721600	Strong transcription	Fetal Intestine Large	intestine
27	chr16:31714200-31721800	Strong transcription	Liver	Liver
28	chr16:31714200-31721800	Strong transcription	GM12878-XiMat	blood
29	chr16:31714200-31722200	Strong transcription	Right Ventricle	heart
30	chr16:31714200-31722400	Strong transcription	Brain Germinal Matrix	brain
31	chr16:31714400-31721200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr16:31714400-31721400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr16:31714400-31721400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr16:31714400-31721400	Strong transcription	Lung	lung
35	chr16:31714600-31721600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr16:31714600-31724200	Weak transcription	Fetal Kidney	kidney
37	chr16:31714800-31721200	Strong transcription	HepG2	liver
38	chr16:31715000-31721400	Strong transcription	Aorta	Aorta
39	chr16:31715800-31724200	Weak transcription	NHLF	lung
40	chr16:31716200-31724200	Weak transcription	Hela-S3	cervix
41	chr16:31717200-31723400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr16:31718000-31721400	Strong transcription	Esophagus	oesophagus
43	chr16:31718000-31724200	Weak transcription	Stomach Mucosa	stomach
44	chr16:31718200-31724200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr16:31718200-31724200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr16:31718600-31724000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr16:31718600-31724200	Weak transcription	Colon Smooth Muscle	Colon
48	chr16:31719000-31724400	Weak transcription	Osteobl	bone
49	chr16:31719200-31724600	Weak transcription	Small Intestine	intestine
50	chr16:31719400-31724000	Weak transcription	Primary hematopoietic stem cells	blood

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