Variant report

Variant	rs59610272
Chromosome Location	chr15:31739844-31739845
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs72724946	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054147	chr15:31014507-31972706	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv542306	chr15:31014507-31972706	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats 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	esv34100	chr15:31496514-31792591	Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv903840	chr15:31589970-31800149	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv1051589	chr15:31728004-31972706	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv542320	chr15:31728004-31972706	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv469633	chr15:31731003-31904613	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv482330	chr15:31731003-31904613	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv903844	chr15:31736091-31781988	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31733400-31741000	Weak transcription	Spleen	Spleen
2	chr15:31733800-31741800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr15:31734200-31740400	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr15:31734200-31740800	Weak transcription	Placenta	Placenta
5	chr15:31734200-31740800	Weak transcription	Stomach Mucosa	stomach
6	chr15:31734400-31740200	Weak transcription	Esophagus	oesophagus
7	chr15:31734400-31740600	Weak transcription	Adipose Nuclei	Adipose
8	chr15:31734400-31740800	Weak transcription	Fetal Thymus	thymus
9	chr15:31734400-31750000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:31734600-31740600	Weak transcription	Primary T cells from cord blood	blood
11	chr15:31734600-31741200	Weak transcription	Gastric	stomach
12	chr15:31735400-31740600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr15:31735400-31741000	Weak transcription	HSMMtube	muscle
14	chr15:31736400-31740200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr15:31736400-31740200	Weak transcription	Primary B cells from peripheral blood	blood
16	chr15:31736400-31740200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr15:31736400-31740200	Weak transcription	HUVEC	blood vessel
18	chr15:31736600-31740000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr15:31736600-31740400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr15:31736600-31740600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr15:31736600-31741000	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr15:31736800-31740000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr15:31736800-31740200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr15:31737000-31740000	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr15:31737000-31740200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr15:31738000-31740200	Weak transcription	GM12878-XiMat	blood
27	chr15:31739400-31740600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr15:31739400-31741000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr15:31739600-31740600	Weak transcription	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links