Variant report

Variant	rs2555932
Chromosome Location	chr2:169673979-169673980
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:169673408..169675097-chr2:169675121..169676627,2	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs472233	0.80[EUR][1000 genomes]
rs490278	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs498231	0.97[ASN][1000 genomes]
rs522893	0.80[EUR][1000 genomes]
rs548367	0.96[ASN][1000 genomes]
rs552445	0.80[EUR][1000 genomes]
rs830027	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs830028	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs830029	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs830030	0.99[ASN][1000 genomes]
rs853666	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs862638	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv915920	chr2:168851960-169696591	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv583599	chr2:169664227-169903096	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:169660000-169676000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr2:169660000-169688200	Weak transcription	Placenta	Placenta
3	chr2:169661400-169676800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr2:169662600-169675600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr2:169668400-169674000	Strong transcription	K562	blood
6	chr2:169670000-169698000	Weak transcription	Stomach Mucosa	stomach
7	chr2:169670200-169690200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr2:169670600-169690800	Weak transcription	Fetal Stomach	stomach
9	chr2:169671000-169676000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr2:169671600-169674000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr2:169672200-169675600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:169672200-169675600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr2:169672400-169674000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:169672400-169675600	Weak transcription	Brain Anterior Caudate	brain
15	chr2:169672600-169675800	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr2:169672600-169676800	Strong transcription	Fetal Intestine Small	intestine
17	chr2:169672800-169674000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:169673000-169674000	Enhancers	Left Ventricle	heart
19	chr2:169673000-169678400	Strong transcription	Fetal Intestine Large	intestine
20	chr2:169673200-169675800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:169673200-169675800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr2:169673200-169675800	Weak transcription	Right Atrium	heart
23	chr2:169673400-169675600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr2:169673400-169675800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr2:169673400-169676000	Weak transcription	Lung	lung
26	chr2:169673400-169679000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr2:169673400-169683200	Weak transcription	Pancreas	Pancrea
28	chr2:169673400-169687600	Weak transcription	Right Ventricle	heart
29	chr2:169673400-169691600	Weak transcription	Colonic Mucosa	Colon
30	chr2:169673400-169692200	Weak transcription	Gastric	stomach
31	chr2:169673600-169674600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr2:169673600-169675400	Weak transcription	Fetal Heart	heart
33	chr2:169673800-169675000	Enhancers	Fetal Thymus	thymus
34	chr2:169673800-169675600	Weak transcription	Adipose Nuclei	Adipose
35	chr2:169673800-169675600	Weak transcription	NHDF-Ad	bronchial
36	chr2:169673800-169675600	Weak transcription	Osteobl	bone
37	chr2:169673800-169675800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:169673800-169675800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr2:169673800-169675800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:169673800-169675800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr2:169673800-169676600	Weak transcription	HMEC	breast

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