Variant report

Variant	rs59199298
Chromosome Location	chr2:20774241-20774242
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:20772999..20776929-chr2:20778925..20783592,5	MCF-7	breast:
2	chr2:20771832..20774645-chr2:20774771..20777739,3	K562	blood:
3	chr2:20772318..20774948-chr2:20792924..20794926,2	K562	blood:
4	chr2:20773082..20775032-chr2:20787909..20789864,2	MCF-7	breast:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs13384848	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13412584	0.82[ASN][1000 genomes]
rs13424119	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13431026	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17718362	0.96[EUR][1000 genomes]
rs17718518	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4666428	1.00[ASN][1000 genomes]
rs56220253	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57203893	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57818033	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60856046	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833537	chr2:20630092-20826816	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv833548	chr2:20682073-20864078	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS 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 target site	32 gene(s)	inside rSNPs	diseases
3	nsv1012037	chr2:20770850-20824893	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv535598	chr2:20770850-20824893	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:20764400-20778200	Enhancers	HepG2	liver
2	chr2:20765600-20780800	Enhancers	Adipose Nuclei	Adipose
3	chr2:20765800-20786200	Enhancers	HUVEC	blood vessel
4	chr2:20766400-20776000	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr2:20766800-20780800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr2:20766800-20781000	Enhancers	Left Ventricle	heart
7	chr2:20767000-20781000	Enhancers	Right Atrium	heart
8	chr2:20767200-20776600	Enhancers	Right Ventricle	heart
9	chr2:20767400-20774400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr2:20767400-20774600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr2:20767400-20778200	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr2:20767800-20778600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr2:20767800-20782600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr2:20768400-20774800	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr2:20768600-20777200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr2:20769200-20774600	Enhancers	Fetal Intestine Small	intestine
17	chr2:20769200-20777000	Weak transcription	HMEC	breast
18	chr2:20769400-20780000	Enhancers	Fetal Intestine Large	intestine
19	chr2:20769800-20781000	Enhancers	Fetal Muscle Leg	muscle
20	chr2:20771200-20774600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:20771400-20774400	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr2:20771400-20774800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr2:20771400-20775000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr2:20771600-20777200	Weak transcription	Psoas Muscle	Psoas
25	chr2:20771600-20777400	Weak transcription	Small Intestine	intestine
26	chr2:20771800-20775000	Enhancers	NH-A	brain
27	chr2:20772200-20775200	Weak transcription	GM12878-XiMat	blood
28	chr2:20772600-20781000	Enhancers	Placenta	Placenta
29	chr2:20772600-20785800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr2:20772800-20774800	Enhancers	Brain Anterior Caudate	brain
31	chr2:20772800-20775400	Enhancers	Brain Cingulate Gyrus	brain
32	chr2:20772800-20775400	Enhancers	Brain Hippocampus Middle	brain
33	chr2:20772800-20775400	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr2:20772800-20779400	Weak transcription	Liver	Liver
35	chr2:20772800-20780800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr2:20773000-20774600	Enhancers	Fetal Stomach	stomach
37	chr2:20773000-20775000	Enhancers	Ovary	ovary
38	chr2:20773000-20775200	Enhancers	Brain Substantia Nigra	brain
39	chr2:20773000-20777800	Weak transcription	Pancreas	Pancrea
40	chr2:20773000-20781000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr2:20773200-20774400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr2:20773200-20774400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr2:20773200-20774400	Enhancers	HSMMtube	muscle
44	chr2:20773200-20774600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr2:20773200-20774800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr2:20773200-20774800	Enhancers	Brain Angular Gyrus	brain
47	chr2:20773200-20774800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr2:20773200-20775000	Enhancers	Fetal Brain Male	brain
49	chr2:20773200-20775600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr2:20773400-20774400	Enhancers	Fetal Lung	lung

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