Variant report

Variant	rs57452205
Chromosome Location	chr15:59285184-59285185
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:59283452..59286029-chr15:59288574..59290145,2	K562	blood:
2	chr15:59283452..59285421-chr15:59287409..59290074,2	K562	blood:
3	chr15:59281637..59284410-chr15:59285057..59286558,2	K562	blood:
4	chr15:59279694..59282503-chr15:59284876..59287172,2	MCF-7	breast:
5	chr15:59279815..59281388-chr15:59284282..59285956,2	K562	blood:

Variant related genes	Relation type
ENSG00000157450	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs12438949	0.90[EUR][1000 genomes]
rs12443442	0.82[EUR][1000 genomes]
rs16941051	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16941055	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17236439	0.82[EUR][1000 genomes]
rs28383512	0.90[EUR][1000 genomes]
rs28383514	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28383519	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28383520	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28383523	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28383536	0.90[EUR][1000 genomes]
rs28383549	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28383553	0.90[EUR][1000 genomes]
rs28383561	0.90[EUR][1000 genomes]
rs3751538	1.00[AMR][1000 genomes]
rs55646764	0.81[AFR][1000 genomes]
rs57057009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57750394	0.82[EUR][1000 genomes]
rs57803886	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs58014933	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs58207484	0.90[EUR][1000 genomes]
rs58321899	0.90[EUR][1000 genomes]
rs58827061	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs59037515	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs60533405	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60628647	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs60899149	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60964484	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61369543	0.90[EUR][1000 genomes]
rs61690344	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6494066	0.94[ASN][1000 genomes]
rs73418826	0.82[EUR][1000 genomes]
rs74017339	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs74017345	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74017356	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs74017357	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34110	chr15:58949991-59381634	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv527307	chr15:59103328-60018487	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
3	esv1850946	chr15:59174539-59429160	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
4	nsv904271	chr15:59249584-59393011	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv520679	chr15:59268410-59376531	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv520872	chr15:59268410-59395184	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59280800-59295200	Weak transcription	Gastric	stomach
2	chr15:59280800-59308800	Weak transcription	Esophagus	oesophagus
3	chr15:59280800-59327800	Weak transcription	Small Intestine	intestine
4	chr15:59281000-59292400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr15:59281200-59352600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr15:59281400-59294800	Weak transcription	Psoas Muscle	Psoas
7	chr15:59281400-59305800	Weak transcription	Brain Substantia Nigra	brain
8	chr15:59281400-59323200	Weak transcription	Ovary	ovary
9	chr15:59281400-59347800	Weak transcription	Colonic Mucosa	Colon
10	chr15:59281600-59311000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr15:59281800-59285800	Weak transcription	Colon Smooth Muscle	Colon
12	chr15:59281800-59287200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr15:59281800-59297800	Weak transcription	Duodenum Mucosa	Duodenum
14	chr15:59281800-59352200	Weak transcription	Aorta	Aorta
15	chr15:59281800-59353400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr15:59282000-59287200	Weak transcription	Adipose Nuclei	Adipose
17	chr15:59282000-59287200	Weak transcription	Brain Hippocampus Middle	brain
18	chr15:59282000-59305800	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr15:59282000-59323000	Weak transcription	Fetal Lung	lung
20	chr15:59282000-59323200	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr15:59282000-59323200	Weak transcription	Fetal Kidney	kidney
22	chr15:59282200-59287200	Weak transcription	Brain Anterior Caudate	brain
23	chr15:59282400-59286800	Weak transcription	HUVEC	blood vessel
24	chr15:59282400-59288800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr15:59282400-59290600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr15:59282400-59291000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr15:59282400-59296800	Weak transcription	NH-A	brain
28	chr15:59282400-59297400	Weak transcription	HMEC	breast
29	chr15:59282400-59305400	Weak transcription	Fetal Heart	heart
30	chr15:59282400-59308600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr15:59282400-59323200	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr15:59282400-59323400	Weak transcription	NHLF	lung
33	chr15:59282600-59286400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr15:59282600-59287000	Weak transcription	Brain Germinal Matrix	brain
35	chr15:59282600-59287000	Strong transcription	Fetal Stomach	stomach
36	chr15:59282600-59288800	Strong transcription	Fetal Intestine Small	intestine
37	chr15:59282600-59297600	Weak transcription	NHDF-Ad	bronchial
38	chr15:59282600-59306400	Weak transcription	Brain Angular Gyrus	brain
39	chr15:59282800-59287200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr15:59282800-59287400	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr15:59282800-59292600	Weak transcription	Left Ventricle	heart
42	chr15:59282800-59297200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr15:59283000-59285200	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr15:59283000-59286000	Strong transcription	Osteobl	bone
45	chr15:59283000-59287000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr15:59283000-59287200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:59283000-59287400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr15:59283200-59285200	Strong transcription	Fetal Muscle Leg	muscle
49	chr15:59283200-59287000	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr15:59283200-59287400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links