Variant report

Variant	rs74011972
Chromosome Location	chr15:33077986-33077987
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs28660998	1.00[ASN][1000 genomes]
rs55736222	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422296	chr15:32798938-33221215	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv456785	chr15:32926076-33352989	Genic enhancers Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv568913	chr15:32926076-33352989	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv482680	chr15:32958401-33154005	Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv832961	chr15:33021177-33134988	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv903977	chr15:33040782-33117302	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33060600-33097600	Weak transcription	Thymus	Thymus
2	chr15:33061200-33141000	Weak transcription	Placenta	Placenta
3	chr15:33062600-33111200	Weak transcription	Gastric	stomach
4	chr15:33063200-33082400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:33063800-33094400	Weak transcription	Fetal Stomach	stomach
6	chr15:33065800-33098600	Weak transcription	Colonic Mucosa	Colon
7	chr15:33067200-33089000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr15:33067400-33078800	Weak transcription	HSMMtube	muscle
9	chr15:33070600-33078600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr15:33071400-33081000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr15:33071400-33082600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr15:33072400-33078800	Weak transcription	HSMM	muscle
13	chr15:33072600-33090200	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr15:33072800-33087200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr15:33074200-33078600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr15:33074400-33082200	Weak transcription	NH-A	brain
17	chr15:33074600-33079200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr15:33074800-33084200	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr15:33075000-33080400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr15:33075000-33082200	Weak transcription	A549	lung
21	chr15:33075000-33096400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr15:33075600-33079200	Weak transcription	HepG2	liver
23	chr15:33077000-33078400	Weak transcription	Osteobl	bone
24	chr15:33077000-33079000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr15:33077000-33079400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr15:33077000-33079600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr15:33077000-33082000	Weak transcription	NHDF-Ad	bronchial
28	chr15:33077200-33079200	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr15:33077800-33079400	Strong transcription	NHLF	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links