Variant report

Variant	rs4889381
Chromosome Location	chr16:81815223-81815224
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	WRNIP1	chr16:81815092-81815333	GM12878	blood:	n/a	n/a
2	MTA3	chr16:81814836-81815391	GM12878	blood:	n/a	n/a
3	POLR2A	chr16:81814915-81815484	GM12878	blood:	n/a	n/a
4	CTCF	chr16:81815140-81815290	GM06990	blood:	n/a	n/a
5	POLR2A	chr16:81814978-81815559	GM12892	blood:	n/a	n/a
6	CTCF	chr16:81815142-81815469	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
PLCG2	TF binding region

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12925961	0.87[EUR][1000 genomes]
rs12926919	0.88[EUR][1000 genomes]
rs4273032	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4888175	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55768769	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56350744	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs60780862	0.84[AMR][1000 genomes]
rs72834726	0.87[ASN][1000 genomes]
rs72834729	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72834730	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948448	chr16:81198147-81906766	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
2	nsv573365	chr16:81804972-81975892	Strong transcription Bivalent/Poised TSS Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81813800-81816400	Weak transcription	Lung	lung
2	chr16:81813800-81817200	Weak transcription	Left Ventricle	heart
3	chr16:81813800-81817800	Weak transcription	Right Atrium	heart
4	chr16:81814000-81816400	Weak transcription	Small Intestine	intestine
5	chr16:81814000-81817200	Weak transcription	Liver	Liver
6	chr16:81814000-81817600	Weak transcription	Gastric	stomach
7	chr16:81814200-81815600	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr16:81814200-81816200	Weak transcription	Duodenum Mucosa	Duodenum
9	chr16:81814200-81816400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr16:81814200-81816400	Weak transcription	Pancreas	Pancrea
11	chr16:81814200-81816400	Weak transcription	Spleen	Spleen
12	chr16:81814200-81818200	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr16:81814200-81818200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr16:81814200-81818400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr16:81814400-81816400	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr16:81814400-81816800	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr16:81814400-81817200	Genic enhancers	Primary B cells from peripheral blood	blood
18	chr16:81814400-81831800	Weak transcription	Adipose Nuclei	Adipose
19	chr16:81814600-81818000	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr16:81814800-81815400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
21	chr16:81814800-81817800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr16:81814800-81818200	Enhancers	Primary hematopoietic stem cells	blood
23	chr16:81815000-81815400	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr16:81815000-81815600	Flanking Active TSS	GM12878-XiMat	blood
25	chr16:81815200-81815400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
26	chr16:81815200-81815600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr16:81815200-81815600	Bivalent Enhancer	Placenta	Placenta
28	chr16:81815200-81818600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr16:81815200-81830000	Weak transcription	Esophagus	oesophagus

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