Variant report

Variant	rs1950103
Chromosome Location	chr12:76215500-76215501
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs1275555	0.84[EUR][1000 genomes]
rs1290030	0.90[ASN][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	nsv1040583	chr12:75742802-76360276	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv948653	chr12:75773464-76220618	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv832463	chr12:76136551-76316703	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv899315	chr12:76163309-76385096	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1041730	chr12:76198863-76331900	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv521900	chr12:76212383-76215754	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:76208800-76221200	Enhancers	NHLF	lung
2	chr12:76209800-76216400	Weak transcription	Fetal Heart	heart
3	chr12:76211800-76217200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:76212400-76216000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:76212400-76216400	Enhancers	HMEC	breast
6	chr12:76212800-76216600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr12:76213400-76218200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr12:76213400-76218400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr12:76213400-76218600	Weak transcription	Esophagus	oesophagus
10	chr12:76213600-76217400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:76213600-76217600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr12:76213600-76219200	Weak transcription	Fetal Kidney	kidney
13	chr12:76214000-76215600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr12:76214400-76216600	Enhancers	Fetal Lung	lung
15	chr12:76214600-76216200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:76215000-76215600	Enhancers	Muscle Satellite Cultured Cells	--
17	chr12:76215000-76215800	Enhancers	NHEK	skin
18	chr12:76215000-76216400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr12:76215000-76216400	Enhancers	Stomach Smooth Muscle	stomach
20	chr12:76215000-76218000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr12:76215000-76219000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr12:76215000-76219800	Weak transcription	Aorta	Aorta
23	chr12:76215000-76220600	Enhancers	NHDF-Ad	bronchial
24	chr12:76215000-76223800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr12:76215200-76216000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:76215200-76216600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr12:76215200-76217200	Enhancers	Fetal Stomach	stomach
28	chr12:76215200-76217400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr12:76215200-76219000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr12:76215400-76217200	Weak transcription	NH-A	brain
31	chr12:76215400-76217200	Weak transcription	Osteobl	bone
32	chr12:76215400-76217400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr12:76215400-76218600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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