Variant report

Variant	rs7312621
Chromosome Location	chr12:32943529-32943530
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1046150	1.00[CEU][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10743802	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10771994	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10771995	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10772000	0.94[ASN][1000 genomes]
rs10844349	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11052246	0.94[ASN][1000 genomes]
rs12612	0.93[CEU][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35960561	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6488084	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6488086	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6488088	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6488089	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6488091	0.93[CEU][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6488092	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6488093	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7298089	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7304383	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7308383	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7308500	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7312241	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7956824	0.93[CEU][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7957460	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7968908	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9394	0.81[AMR][1000 genomes];0.93[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	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	esv1851844	chr12:32929596-32953032	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32933200-32944800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr12:32934000-32944000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:32934200-32945200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr12:32936200-32948800	Weak transcription	Fetal Stomach	stomach
5	chr12:32936400-32947000	Weak transcription	Fetal Heart	heart
6	chr12:32937400-32945400	Weak transcription	NHEK	skin
7	chr12:32938600-32948600	Weak transcription	Gastric	stomach
8	chr12:32938600-32952200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:32938800-32945000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr12:32938800-32950600	Weak transcription	Brain Hippocampus Middle	brain
11	chr12:32939000-32944800	Weak transcription	Stomach Smooth Muscle	stomach
12	chr12:32939200-32955200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:32939400-32945200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:32939600-32944800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr12:32939600-32945000	Weak transcription	Fetal Intestine Large	intestine
16	chr12:32940600-32946600	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr12:32940800-32961800	Weak transcription	Colonic Mucosa	Colon
18	chr12:32941000-32944400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr12:32941200-32944400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:32941200-32949200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:32941800-32944800	Weak transcription	Placenta	Placenta
22	chr12:32941800-32945000	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr12:32941800-32948800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr12:32941800-33033400	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr12:32942000-32949400	Strong transcription	Liver	Liver
26	chr12:32942000-32957400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr12:32942200-32943600	Strong transcription	Left Ventricle	heart
28	chr12:32942200-32950600	Weak transcription	Ovary	ovary
29	chr12:32942400-32944200	Weak transcription	Fetal Intestine Small	intestine
30	chr12:32942400-32950600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:32942600-32944200	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr12:32942600-32944800	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr12:32942600-32945000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr12:32942800-32944400	Weak transcription	HepG2	liver
35	chr12:32943000-32945000	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr12:32943200-32944400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr12:32943200-32946000	Strong transcription	HMEC	breast
38	chr12:32943200-32948200	Weak transcription	Right Ventricle	heart
39	chr12:32943400-32944400	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr12:32943400-32945000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr12:32943400-32945000	Weak transcription	Placenta Amnion	Placenta Amnion

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