Variant report

Variant	rs56338436
Chromosome Location	chr15:32977750-32977751
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10519737	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634570	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12148394	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17816224	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68050511	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422296	chr15:32798938-33221215	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv469587	chr15:32821940-32986579	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv482780	chr15:32821940-32986579	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv456785	chr15:32926076-33352989	Genic enhancers Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv568913	chr15:32926076-33352989	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv482680	chr15:32958401-33154005	Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv568915	chr15:32965357-32994056	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv456787	chr15:32968923-33023951	Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv568916	chr15:32968923-33023951	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:32961200-32980200	Weak transcription	Thymus	Thymus
2	chr15:32964600-32990800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr15:32964800-32993800	Weak transcription	Fetal Brain Male	brain
4	chr15:32965000-32983600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr15:32970000-32977800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr15:32970000-32982600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr15:32970200-32977800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr15:32970200-32979400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr15:32970200-32979600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr15:32972000-32979400	Weak transcription	HepG2	liver
11	chr15:32973200-32986000	Weak transcription	Brain Germinal Matrix	brain
12	chr15:32974000-32978400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr15:32974000-32981000	Enhancers	HMEC	breast
14	chr15:32974200-32978000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr15:32974800-32978400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr15:32974800-32978600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr15:32975000-32978600	Strong transcription	Liver	Liver
18	chr15:32975000-32983200	Weak transcription	Brain Substantia Nigra	brain
19	chr15:32975000-32983400	Weak transcription	Brain Angular Gyrus	brain
20	chr15:32975200-32977800	Weak transcription	Fetal Muscle Leg	muscle
21	chr15:32975200-32980200	Weak transcription	Placenta	Placenta
22	chr15:32975200-32983400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr15:32975200-32983800	Weak transcription	Brain Anterior Caudate	brain
24	chr15:32975200-32986000	Weak transcription	Brain Hippocampus Middle	brain
25	chr15:32975400-32978200	Enhancers	NH-A	brain
26	chr15:32976200-32978400	Flanking Active TSS	NHEK	skin
27	chr15:32976400-32980800	Enhancers	NHDF-Ad	bronchial
28	chr15:32976600-32977800	Weak transcription	Adipose Nuclei	Adipose
29	chr15:32976600-32977800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr15:32976600-32978000	Weak transcription	HUVEC	blood vessel
31	chr15:32976600-32978200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr15:32976600-32978200	Active TSS	HSMMtube	muscle
33	chr15:32976600-32979400	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr15:32976600-32980200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr15:32976600-32980200	Weak transcription	Fetal Brain Female	brain
36	chr15:32976800-32977800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr15:32976800-32978000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr15:32976800-32978000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr15:32977000-32980400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr15:32977000-32983800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr15:32977200-32978000	Enhancers	Osteobl	bone
42	chr15:32977400-32978200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:32977600-32977800	Enhancers	Brain Cingulate Gyrus	brain
44	chr15:32977600-32977800	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr15:32977600-32977800	Enhancers	HSMM	muscle
46	chr15:32977600-32978200	Enhancers	A549	lung
47	chr15:32977600-32979800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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