Variant report

Variant	rs11756544
Chromosome Location	chr6:15397441-15397442
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:15397374-15398325	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:15374975..15376583-chr6:15397138..15400134,2	MCF-7	breast:
2	chr6:15395497..15398020-chr6:15401720..15405105,3	MCF-7	breast:
3	chr6:15391483..15393278-chr6:15395848..15398578,2	K562	blood:

Variant related genes	Relation type
JARID2	TF binding region

Extended variants
information (count: 51 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10484355	0.82[JPT][hapmap];0.97[ASN][1000 genomes]
rs10949294	1.00[JPT][hapmap]
rs10949295	1.00[JPT][hapmap]
rs11757415	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11759478	0.88[JPT][hapmap]
rs12211278	1.00[JPT][hapmap]
rs13192347	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs13194410	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs13195950	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13205396	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs13205612	1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs13208486	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs13214720	0.81[ASN][1000 genomes]
rs16876278	1.00[JPT][hapmap]
rs16876354	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17575737	0.86[JPT][hapmap]
rs17576233	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs17576436	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MKK][hapmap];0.95[ASN][1000 genomes]
rs17576710	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs17637773	1.00[JPT][hapmap]
rs17638192	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17638720	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2237146	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[ASN][1000 genomes]
rs2299051	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2299057	0.95[ASN][1000 genomes]
rs34002211	0.95[ASN][1000 genomes]
rs34764533	0.92[ASN][1000 genomes]
rs35047303	0.95[ASN][1000 genomes]
rs35139070	0.95[ASN][1000 genomes]
rs35364784	0.95[ASN][1000 genomes]
rs35629999	0.95[ASN][1000 genomes]
rs35734069	0.95[ASN][1000 genomes]
rs35918625	0.95[ASN][1000 genomes]
rs56123857	0.95[ASN][1000 genomes]
rs61296041	0.95[ASN][1000 genomes]
rs66478504	0.95[ASN][1000 genomes]
rs6941859	0.95[ASN][1000 genomes]
rs72836327	0.95[ASN][1000 genomes]
rs742102	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7747437	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7767966	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027010	chr6:15201803-15425629	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv538140	chr6:15217899-15547127	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv1030558	chr6:15234675-15449137	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv538141	chr6:15234675-15509163	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv538142	chr6:15243960-15404893	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS 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	27 gene(s)	inside rSNPs	diseases
6	nsv949448	chr6:15279490-15449441	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv1025512	chr6:15291551-15452395	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv538143	chr6:15291551-15452395	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1019927	chr6:15351240-15419257	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv538145	chr6:15351240-15419257	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11756544	TBC1D7	cis	parietal	SCAN
rs11756544	RBM24	cis	parietal	SCAN

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15365000-15402800	Weak transcription	Dnd41	blood
2	chr6:15385200-15398400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr6:15387800-15399200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:15388000-15399200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr6:15389800-15397600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr6:15390600-15397600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr6:15390600-15399800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr6:15390800-15398000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr6:15390800-15399000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:15390800-15399200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr6:15390800-15399200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr6:15390800-15399200	Weak transcription	A549	lung
13	chr6:15390800-15399400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr6:15390800-15400000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:15390800-15400200	Weak transcription	Aorta	Aorta
16	chr6:15391000-15399000	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr6:15391000-15399000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr6:15391000-15399200	Weak transcription	HepG2	liver
19	chr6:15391000-15400000	Weak transcription	Thymus	Thymus
20	chr6:15391600-15400200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr6:15391800-15397600	Weak transcription	K562	blood
22	chr6:15391800-15398400	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr6:15391800-15398800	Weak transcription	Colon Smooth Muscle	Colon
24	chr6:15391800-15399200	Weak transcription	Stomach Mucosa	stomach
25	chr6:15391800-15400200	Weak transcription	Fetal Muscle Trunk	muscle
26	chr6:15392000-15400200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr6:15392200-15398000	Weak transcription	Brain Angular Gyrus	brain
28	chr6:15392200-15398400	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr6:15392200-15398800	Weak transcription	Adipose Nuclei	Adipose
30	chr6:15392200-15399000	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr6:15392200-15399200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:15392200-15399200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:15392200-15400000	Weak transcription	NHLF	lung
34	chr6:15392400-15399000	Weak transcription	NHEK	skin
35	chr6:15392400-15399200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:15392400-15400000	Weak transcription	HMEC	breast
37	chr6:15392600-15397600	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr6:15392800-15397600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr6:15392800-15397600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr6:15392800-15398000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr6:15392800-15398800	Weak transcription	Psoas Muscle	Psoas
42	chr6:15392800-15399000	Weak transcription	Left Ventricle	heart
43	chr6:15392800-15399000	Weak transcription	Right Atrium	heart
44	chr6:15392800-15399200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr6:15392800-15399200	Weak transcription	Pancreas	Pancrea
46	chr6:15392800-15399200	Weak transcription	Spleen	Spleen
47	chr6:15392800-15399800	Weak transcription	Rectal Smooth Muscle	rectum
48	chr6:15393000-15397800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:15393000-15398200	Weak transcription	Brain Hippocampus Middle	brain
50	chr6:15393000-15398400	Weak transcription	Primary B cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links