Variant report

Variant	rs12732891
Chromosome Location	chr1:225978571-225978572
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:225964922..225971483-chr1:225977225..225981439,8	K562	blood:
2	chr1:225976942..225979751-chr1:225984143..225986122,2	K562	blood:

Variant related genes	Relation type
ENSG00000143742	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1011381	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1011382	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10753408	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10915881	0.84[EUR][1000 genomes]
rs12022324	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12029894	0.84[EUR][1000 genomes]
rs12038486	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12081874	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12742123	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12743139	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12746848	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2078341	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3753661	1.00[YRI][hapmap]
rs4653434	0.82[CEU][hapmap];0.82[CHB][hapmap];0.81[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4653677	0.85[CEU][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4653678	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4653682	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs71646748	0.89[AMR][1000 genomes];0.89[EUR][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	esv1795046	chr1:225874059-226091150	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	esv1834932	chr1:225874059-226091150	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	esv1834948	chr1:225874059-226214882	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv524126	chr1:225973777-226210653	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225966800-225978600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:225967800-225980200	Weak transcription	Stomach Mucosa	stomach
3	chr1:225968200-225980000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:225969800-225983000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:225970200-225978600	Strong transcription	Fetal Thymus	thymus
6	chr1:225970200-225979800	Strong transcription	Primary T cells fromperipheralblood	blood
7	chr1:225970200-225983200	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr1:225970600-225980000	Strong transcription	Duodenum Mucosa	Duodenum
9	chr1:225970600-225980600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr1:225970600-225981800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr1:225970800-225982200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:225971000-225979200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:225971000-225979200	Strong transcription	Rectal Mucosa Donor 31	rectum
14	chr1:225971200-225978600	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr1:225971200-225978800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:225971200-225979600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:225971200-225979800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:225971200-225980000	Strong transcription	NH-A	brain
19	chr1:225971200-225980000	Strong transcription	Osteobl	bone
20	chr1:225971400-225978600	Strong transcription	Placenta	Placenta
21	chr1:225971400-225980000	Strong transcription	Duodenum Smooth Muscle	Duodenum
22	chr1:225971600-225982800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr1:225971800-225980200	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr1:225972200-225978600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
25	chr1:225972400-225980000	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr1:225972800-225979800	Strong transcription	Muscle Satellite Cultured Cells	--
27	chr1:225973000-225978600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:225973000-225980000	Strong transcription	Fetal Lung	lung
29	chr1:225973200-225979800	Strong transcription	A549	lung
30	chr1:225973600-225978600	Strong transcription	NHDF-Ad	bronchial
31	chr1:225973600-225979400	Strong transcription	HSMM	muscle
32	chr1:225973600-225980000	Strong transcription	Skeletal Muscle Female	skeletal muscle
33	chr1:225973600-225983400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:225973800-225979000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:225973800-225986000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:225974000-225978600	Weak transcription	Esophagus	oesophagus
37	chr1:225974600-225985600	Weak transcription	Fetal Heart	heart
38	chr1:225974800-225978600	Weak transcription	Brain Angular Gyrus	brain
39	chr1:225975000-225980600	Weak transcription	Psoas Muscle	Psoas
40	chr1:225975000-225997200	Weak transcription	Brain Substantia Nigra	brain
41	chr1:225975000-225997400	Weak transcription	Aorta	Aorta
42	chr1:225975200-225981200	Weak transcription	Fetal Brain Male	brain
43	chr1:225975400-225981800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr1:225975400-225983800	Weak transcription	Pancreas	Pancrea
45	chr1:225975600-225981600	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr1:225975600-225983400	Weak transcription	NHLF	lung
47	chr1:225976000-225984000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr1:225976200-225984400	Weak transcription	HepG2	liver
49	chr1:225976200-225989000	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr1:225976400-225982400	Weak transcription	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links