Variant report

Variant	rs16882537
Chromosome Location	chr5:53555533-53555534
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:53555281..53557666-chr5:53578051..53579974,2	K562	blood:
2	chr5:53546187..53547942-chr5:53555155..53557445,2	K562	blood:
3	chr5:53549466..53553439-chr5:53553747..53557926,5	K562	blood:
4	chr5:53546187..53549034-chr5:53553826..53556655,3	K562	blood:
5	chr5:53555302..53559015-chr5:53605132..53608618,4	K562	blood:
6	chr5:53554867..53556640-chr5:53605133..53607533,2	MCF-7	breast:
7	chr5:53553559..53556155-chr5:53606428..53609248,4	K562	blood:

Variant related genes	Relation type
ENSG00000185305	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10038691	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10056778	1.00[EUR][1000 genomes]
rs10056892	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10062081	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10071081	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10072882	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12332105	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12332445	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13360423	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16882550	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28366402	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28553319	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28712367	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6889727	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72754233	1.00[EUR][1000 genomes]
rs72754234	1.00[EUR][1000 genomes]
rs72754235	1.00[EUR][1000 genomes]
rs72754240	1.00[EUR][1000 genomes]
rs72754242	1.00[EUR][1000 genomes]
rs72754250	1.00[EUR][1000 genomes]
rs72754252	1.00[EUR][1000 genomes]
rs72754254	1.00[EUR][1000 genomes]
rs72754268	1.00[EUR][1000 genomes]
rs72754270	1.00[EUR][1000 genomes]
rs72754271	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72754272	1.00[EUR][1000 genomes]
rs72754274	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72754275	1.00[EUR][1000 genomes]
rs72754280	1.00[EUR][1000 genomes]
rs72756244	1.00[EUR][1000 genomes]
rs72756250	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72756257	1.00[EUR][1000 genomes]
rs72756268	1.00[EUR][1000 genomes]
rs72756270	1.00[EUR][1000 genomes]
rs72756274	1.00[EUR][1000 genomes]
rs72756281	1.00[EUR][1000 genomes]
rs72756283	0.85[EUR][1000 genomes]
rs72756286	0.85[EUR][1000 genomes]
rs72756289	0.85[EUR][1000 genomes]
rs7715184	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7720558	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9292045	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9885300	1.00[EUR][1000 genomes]
rs9885301	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9885454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032632	chr5:52667145-53655624	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv880713	chr5:53198059-53906103	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv881616	chr5:53305742-53639975	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
4	nsv881018	chr5:53305742-53744849	Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
5	nsv880734	chr5:53305742-53770217	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	12 gene(s)	inside rSNPs	diseases
6	nsv881161	chr5:53305742-53815495	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
7	nsv881600	chr5:53305742-53823285	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
8	nsv598176	chr5:53311502-53739530	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
9	nsv880773	chr5:53311918-53815495	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
10	nsv1024303	chr5:53317896-53788276	Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
11	nsv1029224	chr5:53317896-53812899	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
12	nsv949098	chr5:53317990-53816782	Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
13	nsv1020517	chr5:53324930-53759046	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
14	nsv1017768	chr5:53326385-53752165	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
15	nsv1032352	chr5:53327170-53762973	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
16	nsv598177	chr5:53333477-53755208	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
17	nsv881056	chr5:53368869-53744849	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
18	nsv881408	chr5:53386267-53815495	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
19	nsv1031072	chr5:53490130-53698866	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
20	nsv880304	chr5:53524508-53727092	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:53537400-53575200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr5:53543200-53556600	Weak transcription	Fetal Lung	lung
3	chr5:53548400-53555800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:53549400-53569800	Weak transcription	Fetal Intestine Small	intestine
5	chr5:53550800-53559400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr5:53551000-53555800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr5:53551200-53556400	Weak transcription	Fetal Heart	heart
8	chr5:53553000-53555600	Enhancers	NHEK	skin
9	chr5:53553200-53555600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr5:53553400-53555800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr5:53553600-53568600	Weak transcription	Primary T cells from cord blood	blood
12	chr5:53554000-53555800	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr5:53554400-53557800	Enhancers	K562	blood
14	chr5:53554800-53555800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr5:53554800-53556200	Enhancers	NHLF	lung
16	chr5:53554800-53560400	Weak transcription	Left Ventricle	heart
17	chr5:53555000-53572400	Weak transcription	Right Ventricle	heart
18	chr5:53555200-53555600	Enhancers	NHDF-Ad	bronchial
19	chr5:53555200-53557000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:53555400-53555600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
21	chr5:53555400-53555800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:53555400-53556000	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr5:53555400-53566200	Weak transcription	HMEC	breast

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