Variant report

Variant	rs16934037
Chromosome Location	chr12:29378456-29378457
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:29376867..29378651-chr12:29381952..29383534,2	K562	blood:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11050133	0.89[EUR][1000 genomes]
rs11050134	1.00[EUR][1000 genomes]
rs11050137	0.89[EUR][1000 genomes]
rs11050138	1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12299091	1.00[CHB][hapmap];0.89[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12299148	1.00[CHB][hapmap];0.89[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12299228	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12307346	0.89[EUR][1000 genomes]
rs12309283	1.00[CHB][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]
rs12309340	1.00[CHB][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]
rs12319661	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12320498	1.00[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs766764	1.00[EUR][1000 genomes]
rs7960832	0.90[EUR][1000 genomes]
rs7960834	0.89[EUR][1000 genomes]
rs9804966	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9804995	1.00[CHB][hapmap];0.83[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9804996	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532233	chr12:29009388-29496179	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv995123	chr12:29095272-29571558	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1053641	chr12:29268813-29854413	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29360400-29381000	Weak transcription	HUVEC	blood vessel
2	chr12:29365600-29378600	Weak transcription	Small Intestine	intestine
3	chr12:29366200-29393200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr12:29374400-29378600	Weak transcription	Fetal Intestine Large	intestine
5	chr12:29374400-29380200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr12:29374800-29382800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr12:29375200-29381000	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr12:29376400-29379000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr12:29376600-29378800	Enhancers	Placenta	Placenta
10	chr12:29376800-29378600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr12:29376800-29380200	Enhancers	Osteobl	bone
12	chr12:29377000-29381600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr12:29377000-29385200	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr12:29377200-29379200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr12:29377400-29378600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr12:29377400-29378800	Weak transcription	NHDF-Ad	bronchial
17	chr12:29377600-29379000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr12:29377800-29378600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr12:29377800-29379400	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr12:29378000-29379000	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr12:29378200-29381400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr12:29378400-29379000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr12:29378400-29379000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr12:29378400-29379000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:29378400-29379000	Enhancers	Fetal Intestine Small	intestine
26	chr12:29378400-29379200	Enhancers	Adipose Nuclei	Adipose
27	chr12:29378400-29381000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr12:29378400-29381600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr12:29378400-29383200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr12:29378400-29383200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr12:29378400-29383400	Enhancers	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links