Variant report

Variant	rs3119823
Chromosome Location	chr13:30577128-30577129
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1122694	0.93[ASN][1000 genomes]
rs11616638	0.88[ASN][1000 genomes]
rs11617050	0.87[ASN][1000 genomes]
rs11620285	0.88[ASN][1000 genomes]
rs11620467	0.87[ASN][1000 genomes]
rs17588454	0.88[ASN][1000 genomes]
rs28366394	0.87[ASN][1000 genomes]
rs3119824	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs35831078	0.88[ASN][1000 genomes]
rs4534683	0.88[ASN][1000 genomes]
rs4583075	0.88[ASN][1000 genomes]
rs4583076	0.88[ASN][1000 genomes]
rs4769796	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4769797	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4769798	0.94[ASN][1000 genomes]
rs4991495	0.88[ASN][1000 genomes]
rs536937	0.84[ASN][1000 genomes]
rs59372413	0.87[ASN][1000 genomes]
rs60452760	0.87[ASN][1000 genomes]
rs60621210	0.87[ASN][1000 genomes]
rs637375	0.87[ASN][1000 genomes]
rs638330	0.80[ASN][1000 genomes]
rs647790	0.82[ASN][1000 genomes]
rs73159367	0.86[ASN][1000 genomes]
rs73159377	0.88[ASN][1000 genomes]
rs73159380	0.88[ASN][1000 genomes]
rs73159381	0.88[ASN][1000 genomes]
rs73159382	0.88[ASN][1000 genomes]
rs73159383	0.87[ASN][1000 genomes]
rs73159384	0.87[ASN][1000 genomes]
rs7317000	0.85[ASN][1000 genomes]
rs7329842	0.88[ASN][1000 genomes]
rs7333713	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs860181	0.87[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	esv3520592	chr13:30243601-30648554	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	esv3520593	chr13:30243601-30648554	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30569200-30578400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr13:30569200-30580000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr13:30573400-30577400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr13:30574000-30578000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr13:30574400-30579400	Weak transcription	Spleen	Spleen
6	chr13:30574800-30577400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr13:30576000-30577400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr13:30576000-30577400	Enhancers	NHDF-Ad	bronchial
9	chr13:30576200-30577200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr13:30576200-30577200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr13:30576200-30577200	Enhancers	NHLF	lung
12	chr13:30576200-30577200	Enhancers	Osteobl	bone
13	chr13:30576200-30577400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr13:30576200-30577400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr13:30576200-30577400	Enhancers	NHEK	skin
16	chr13:30576400-30577200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr13:30576400-30577200	Enhancers	Placenta	Placenta
18	chr13:30576400-30577400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr13:30576400-30577400	Enhancers	HMEC	breast
20	chr13:30576400-30577600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr13:30576600-30577200	Enhancers	HSMM	muscle
22	chr13:30576600-30578000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr13:30576800-30578400	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr13:30577000-30578400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr13:30577000-30578400	Weak transcription	NH-A	brain
26	chr13:30577000-30580600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links