Variant report

Variant	rs792867
Chromosome Location	chr12:32475931-32475932
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1239569	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs171885	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs174436	0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs182010	0.87[ASN][1000 genomes]
rs183790	0.95[ASN][1000 genomes]
rs187789	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs261890	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs261891	0.95[ASN][1000 genomes]
rs261896	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs261897	0.91[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs261899	0.86[ASN][1000 genomes]
rs261900	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs261904	0.95[ASN][1000 genomes]
rs2650120	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2728699	0.87[AMR][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	nsv531960	chr12:32257285-32775277	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	esv2751096	chr12:32280340-32702784	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv558171	chr12:32287259-32559693	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv832366	chr12:32328559-32511360	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32443800-32480400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr12:32449200-32480400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:32449600-32490200	Weak transcription	HSMMtube	muscle
4	chr12:32450400-32480200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr12:32455200-32480400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:32456400-32480400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr12:32457200-32494400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr12:32459200-32480200	Weak transcription	Primary B cells from cord blood	blood
9	chr12:32459200-32480800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:32459400-32480600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr12:32460400-32480600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr12:32460400-32514600	Weak transcription	HMEC	breast
13	chr12:32460600-32480600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:32460800-32480400	Weak transcription	Osteobl	bone
15	chr12:32461000-32480800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr12:32461200-32480200	Weak transcription	HSMM	muscle
17	chr12:32461400-32480000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr12:32461400-32480200	Weak transcription	NH-A	brain
19	chr12:32461800-32480400	Weak transcription	Primary T cells from cord blood	blood
20	chr12:32463000-32480200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr12:32463200-32480200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr12:32463800-32478400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr12:32465400-32480200	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr12:32467000-32480200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr12:32467400-32480400	Weak transcription	Ovary	ovary
26	chr12:32472200-32480200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr12:32472600-32489200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr12:32472800-32479800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr12:32472800-32493600	Weak transcription	Adipose Nuclei	Adipose
30	chr12:32473000-32481000	Weak transcription	Brain Hippocampus Middle	brain
31	chr12:32473200-32479600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr12:32474400-32480400	Weak transcription	Fetal Brain Female	brain
33	chr12:32475000-32490200	Weak transcription	Primary hematopoietic stem cells	blood
34	chr12:32475400-32476400	Enhancers	Brain Angular Gyrus	brain
35	chr12:32475400-32500200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr12:32475600-32476200	Enhancers	Stomach Mucosa	stomach
37	chr12:32475600-32476400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:32475600-32479600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr12:32475600-32480400	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr12:32475600-32480400	Weak transcription	Aorta	Aorta
41	chr12:32475600-32480800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr12:32475600-32480800	Weak transcription	Brain Anterior Caudate	brain
43	chr12:32475600-32480800	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr12:32475600-32481600	Weak transcription	Lung	lung
45	chr12:32475600-32483200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr12:32475600-32532400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr12:32475800-32476400	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr12:32475800-32480400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr12:32475800-32480400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr12:32475800-32480600	Weak transcription	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links