Variant report

Variant	rs9745126
Chromosome Location	chr15:59668912-59668913
allele	A/G
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	RAD21	chr15:59668910-59669368	ECC-1	luminal epithelium:	n/a	n/a
2	RAD21	chr15:59668883-59669301	MCF-7	breast:	n/a	n/a
3	CTCF	chr15:59668857-59669237	MCF-7	breast:	n/a	n/a
4	RAD21	chr15:59668875-59669406	HCT-116	colon:	n/a	n/a
5	CTCF	chr15:59668869-59669329	A549	lung:	n/a	n/a
6	PBX3	chr15:59668898-59669295	SK-N-SH	brain:	n/a	n/a
7	CTCF	chr15:59668759-59669497	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:59663587..59666015-chr15:59667547..59669051,2	MCF-7	breast:

Variant related genes	Relation type
MYO1E	TF binding region
ENSG00000157470	Chromatin interaction
ENSG00000157483	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1979513	0.87[EUR][1000 genomes]
rs28362126	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28450445	0.87[EUR][1000 genomes]
rs4555093	0.91[EUR][1000 genomes]
rs6494103	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6494104	0.82[AMR][1000 genomes];0.96[EUR][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	nsv527307	chr15:59103328-60018487	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
2	nsv934082	chr15:59608605-59733211	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	nsv457175	chr15:59609753-59681214	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv569603	chr15:59609753-59681214	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv471246	chr15:59610743-59681214	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv904274	chr15:59623576-59689378	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv904275	chr15:59648633-59726610	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	n/a
8	nsv904276	chr15:59648633-59743010	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	n/a
9	nsv904277	chr15:59666992-59705005	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	n/a
10	nsv524569	chr15:59666992-59712427	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59665800-59674000	Weak transcription	Fetal Kidney	kidney
2	chr15:59665800-59675800	Weak transcription	Brain Hippocampus Middle	brain
3	chr15:59665800-59678400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr15:59665800-59680200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr15:59665800-59691800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:59666000-59672600	Weak transcription	Placenta	Placenta
7	chr15:59666000-59674400	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr15:59666000-59674800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr15:59666000-59676400	Weak transcription	Colon Smooth Muscle	Colon
10	chr15:59666000-59677000	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr15:59666000-59678400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr15:59666000-59678400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr15:59666000-59678800	Weak transcription	Fetal Lung	lung
14	chr15:59666000-59680800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr15:59666200-59671200	Weak transcription	Fetal Intestine Small	intestine
16	chr15:59666200-59671800	Weak transcription	Duodenum Mucosa	Duodenum
17	chr15:59666200-59673200	Weak transcription	Stomach Smooth Muscle	stomach
18	chr15:59666200-59674000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr15:59666200-59680400	Weak transcription	Fetal Stomach	stomach
20	chr15:59666200-59680600	Weak transcription	NHEK	skin
21	chr15:59666200-59681800	Weak transcription	Ovary	ovary
22	chr15:59666400-59680600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr15:59666800-59674000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr15:59667000-59671200	Weak transcription	HepG2	liver
25	chr15:59667200-59670000	Weak transcription	Hela-S3	cervix
26	chr15:59667400-59669000	Weak transcription	Primary B cells from cord blood	blood
27	chr15:59667400-59671400	Weak transcription	Fetal Intestine Large	intestine
28	chr15:59667400-59672800	Weak transcription	Stomach Mucosa	stomach
29	chr15:59667400-59674800	Weak transcription	Fetal Heart	heart
30	chr15:59667400-59691800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr15:59667600-59672600	Weak transcription	Aorta	Aorta
32	chr15:59667600-59673000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr15:59667600-59674200	Weak transcription	Liver	Liver
34	chr15:59667800-59671600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr15:59668800-59669400	Enhancers	A549	lung
36	chr15:59668800-59669600	Enhancers	Primary B cells from peripheral blood	blood
37	chr15:59668800-59670400	Enhancers	GM12878-XiMat	blood

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