Variant report

Variant	rs1823924
Chromosome Location	chr12:32976221-32976222
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs2022140	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2389107	0.82[AMR][1000 genomes]
rs4931044	0.84[AMR][1000 genomes]
rs4931045	0.82[AMR][1000 genomes]
rs6488095	0.84[AMR][1000 genomes]
rs7303077	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7308045	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7962334	0.82[AMR][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	nsv530421	chr12:32825335-33465991	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1054440	chr12:32872999-33150460	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv532334	chr12:32884789-33034791	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv531961	chr12:32966192-32997952	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32941800-33033400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr12:32943800-33026800	Weak transcription	Fetal Kidney	kidney
3	chr12:32944200-32989400	Weak transcription	Hela-S3	cervix
4	chr12:32949200-32987000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr12:32949200-33007800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:32961000-32989800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr12:32963000-32986800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr12:32965000-32977800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:32965000-32996200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:32966600-32977800	Strong transcription	Duodenum Mucosa	Duodenum
11	chr12:32967000-32977800	Strong transcription	Rectal Mucosa Donor 31	rectum
12	chr12:32967000-32979000	Strong transcription	Rectal Mucosa Donor 29	rectum
13	chr12:32968400-32977400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr12:32970400-32977600	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr12:32970800-32978600	Weak transcription	Small Intestine	intestine
16	chr12:32971200-32981400	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr12:32971400-32976600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr12:32972000-33029000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr12:32972400-32977600	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr12:32972600-32977600	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr12:32972600-32977600	Strong transcription	Fetal Intestine Large	intestine
22	chr12:32972600-32978600	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr12:32972800-32977600	Strong transcription	HepG2	liver
24	chr12:32973000-32976400	Strong transcription	Liver	Liver
25	chr12:32973000-32989600	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr12:32974000-32980800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr12:32974000-32987000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr12:32974200-33030400	Weak transcription	Right Ventricle	heart
29	chr12:32974400-32992600	Weak transcription	Pancreas	Pancrea
30	chr12:32974600-32977800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:32974600-32978400	Weak transcription	Fetal Intestine Small	intestine
32	chr12:32974600-32981600	Weak transcription	Gastric	stomach
33	chr12:32974600-32987000	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr12:32974600-32987000	Weak transcription	Colonic Mucosa	Colon
35	chr12:32974600-32991000	Weak transcription	Fetal Stomach	stomach
36	chr12:32974600-33004400	Weak transcription	Ovary	ovary
37	chr12:32975000-32977200	Weak transcription	Adipose Nuclei	Adipose
38	chr12:32975400-32977000	Genic enhancers	Fetal Heart	heart
39	chr12:32975800-32977600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr12:32975800-32979000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr12:32975800-33020000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:32976000-32976400	Weak transcription	NHEK	skin
43	chr12:32976000-32976600	Weak transcription	Left Ventricle	heart
44	chr12:32976000-32977400	Strong transcription	HMEC	breast
45	chr12:32976000-32977600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr12:32976000-32981000	Weak transcription	Stomach Smooth Muscle	stomach
47	chr12:32976000-32983000	Weak transcription	Placenta	Placenta
48	chr12:32976000-32986600	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr12:32976000-32986800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr12:32976200-32978600	Weak transcription	Placenta Amnion	Placenta Amnion

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