Variant report

Variant	rs1706765
Chromosome Location	chr15:45432055-45432056
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	chr15:45431968..45434188-chr15:45440208..45442818,2	K562	blood:

Variant related genes	Relation type
ENSG00000137857	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12438970	1.00[CEU][hapmap]
rs1617207	0.92[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs1625404	0.81[ASN][1000 genomes]
rs1625779	0.84[ASN][1000 genomes]
rs1632144	0.84[ASN][1000 genomes]
rs1648280	0.94[JPT][hapmap]
rs1648290	0.90[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs1648291	0.94[JPT][hapmap]
rs1648292	0.94[JPT][hapmap]
rs1648298	0.94[JPT][hapmap]
rs1648300	0.94[JPT][hapmap]
rs1648301	0.94[JPT][hapmap]
rs1648314	0.90[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs1648315	0.83[ASN][1000 genomes]
rs1706779	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1706819	0.90[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs1706823	0.94[JPT][hapmap]
rs1706828	0.94[JPT][hapmap]
rs2458240	0.94[JPT][hapmap]
rs2458241	0.94[JPT][hapmap]
rs2668750	0.94[JPT][hapmap]
rs2899376	0.94[JPT][hapmap]
rs2899377	0.94[JPT][hapmap]
rs938129	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs938130	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916374	chr15:45058112-45769052	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv932147	chr15:45319178-45872076	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv427961	chr15:45338381-45491634	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
4	nsv457124	chr15:45381998-45460422	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	nsv569312	chr15:45381998-45460422	Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
6	esv1823029	chr15:45387102-45482245	Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
7	nsv904186	chr15:45394406-45434493	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv869616	chr15:45401411-45736209	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
9	nsv569313	chr15:45413541-45457458	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	nsv457125	chr15:45420718-45450323	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv569314	chr15:45420718-45450323	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv518213	chr15:45421758-45464768	Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 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	chr15:45426400-45435200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr15:45426600-45438400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr15:45426600-45440200	Weak transcription	HMEC	breast
4	chr15:45426800-45438200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr15:45427400-45437200	Strong transcription	Esophagus	oesophagus
6	chr15:45427600-45458600	Weak transcription	Right Atrium	heart
7	chr15:45428600-45433400	Weak transcription	Brain Hippocampus Middle	brain
8	chr15:45428600-45438200	Weak transcription	Brain Substantia Nigra	brain
9	chr15:45428600-45444400	Weak transcription	Pancreas	Pancrea
10	chr15:45428600-45449000	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr15:45429200-45438200	Weak transcription	Placenta	Placenta
12	chr15:45429400-45443800	Weak transcription	Ovary	ovary
13	chr15:45430000-45441200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr15:45430200-45446200	Weak transcription	Brain Anterior Caudate	brain
15	chr15:45430600-45433000	Weak transcription	Lung	lung
16	chr15:45431400-45432200	Enhancers	Liver	Liver
17	chr15:45431400-45432600	Enhancers	Stomach Mucosa	stomach
18	chr15:45431400-45449000	Weak transcription	Brain Cingulate Gyrus	brain
19	chr15:45431800-45433200	Weak transcription	Gastric	stomach
20	chr15:45431800-45435200	Weak transcription	NHEK	skin
21	chr15:45431800-45442600	Weak transcription	Fetal Intestine Small	intestine

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