Variant report

Variant	rs10844349
Chromosome Location	chr12:32938452-32938453
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1046150	0.81[CEU][hapmap];0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10743802	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10743804	0.82[CHB][hapmap];0.80[JPT][hapmap]
rs10771994	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10771995	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10772000	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10772004	0.87[CHB][hapmap];0.89[JPT][hapmap];0.81[ASN][1000 genomes]
rs11052232	0.84[ASN][1000 genomes]
rs11052243	0.85[ASN][1000 genomes]
rs11052246	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12612	0.87[CEU][hapmap];0.94[CHB][hapmap];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35960561	0.82[ASN][1000 genomes]
rs6488084	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6488086	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6488088	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6488089	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6488091	0.86[CEU][hapmap];0.94[CHB][hapmap];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6488092	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6488093	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7296809	0.87[ASN][1000 genomes]
rs7298089	0.82[ASN][1000 genomes]
rs7304383	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7308383	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7308500	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7312241	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7312621	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7956824	0.86[CEU][hapmap];0.94[CHB][hapmap];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7957460	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7968908	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9394	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[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:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32925000-32938600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr12:32929400-32942200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr12:32929600-32941600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:32929800-32941200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:32929800-32941600	Weak transcription	Fetal Intestine Small	intestine
6	chr12:32931400-32942200	Weak transcription	Left Ventricle	heart
7	chr12:32933200-32944800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr12:32934000-32944000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr12:32934200-32945200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr12:32936200-32948800	Weak transcription	Fetal Stomach	stomach
11	chr12:32936400-32947000	Weak transcription	Fetal Heart	heart
12	chr12:32937400-32938800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr12:32937400-32945400	Weak transcription	NHEK	skin
14	chr12:32938000-32942000	Weak transcription	Liver	Liver
15	chr12:32938200-32939200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr12:32938200-32942000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr12:32938400-32938600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:32938400-32938600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr12:32938400-32938600	Active TSS	Gastric	stomach
20	chr12:32938400-32938800	Enhancers	Brain Hippocampus Middle	brain
21	chr12:32938400-32939200	Enhancers	Brain Cingulate Gyrus	brain

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