Variant report

Variant	rs191769778
Chromosome Location	chr15:31741336-31741337
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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	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
10	nsv1046271	chr15:31741255-31795961	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription 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:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31733800-31741800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr15:31734400-31750000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:31740000-31741400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr15:31740000-31741400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr15:31740000-31742000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr15:31740200-31741400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr15:31740200-31741400	Enhancers	GM12878-XiMat	blood
8	chr15:31740200-31742000	Enhancers	Primary hematopoietic stem cells	blood
9	chr15:31740200-31742000	Enhancers	HUVEC	blood vessel
10	chr15:31740600-31741400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr15:31740600-31741400	Enhancers	NHEK	skin
12	chr15:31740600-31741600	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr15:31740600-31741800	Enhancers	K562	blood
14	chr15:31740800-31741400	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr15:31740800-31741400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr15:31740800-31741400	Enhancers	Esophagus	oesophagus
17	chr15:31740800-31741400	Enhancers	Fetal Thymus	thymus
18	chr15:31740800-31741400	Enhancers	Stomach Mucosa	stomach
19	chr15:31740800-31741800	Enhancers	Placenta	Placenta
20	chr15:31741000-31741400	Enhancers	Primary T cells fromperipheralblood	blood
21	chr15:31741000-31741400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr15:31741000-31741400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr15:31741000-31741400	Enhancers	Fetal Muscle Leg	muscle
24	chr15:31741000-31741600	Enhancers	HSMMtube	muscle
25	chr15:31741000-31742000	Enhancers	Spleen	Spleen
26	chr15:31741200-31741400	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr15:31741200-31741800	Enhancers	Gastric	stomach
28	chr15:31741200-31743600	Weak transcription	Primary T killer memory cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links