Variant report

Variant	rs7857850
Chromosome Location	chr9:15442328-15442329
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr9:15442286-15442475	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
SNAPC3	TF binding region

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10115540	0.87[ASN][1000 genomes]
rs10733292	0.87[ASN][1000 genomes]
rs10756664	0.87[ASN][1000 genomes]
rs10756665	0.87[ASN][1000 genomes]
rs10756666	0.82[ASN][1000 genomes]
rs10756667	0.93[ASN][1000 genomes]
rs10756668	0.88[ASN][1000 genomes]
rs10756669	0.93[ASN][1000 genomes]
rs1123038	0.90[ASN][1000 genomes]
rs4510952	0.82[ASN][1000 genomes]
rs4741501	0.82[ASN][1000 genomes]
rs4741502	0.81[ASN][1000 genomes]
rs4741503	0.93[ASN][1000 genomes]
rs4741504	0.92[ASN][1000 genomes]
rs4741506	0.92[ASN][1000 genomes]
rs6474923	0.93[ASN][1000 genomes]
rs7023290	0.91[ASN][1000 genomes]
rs7026910	0.82[ASN][1000 genomes]
rs7026970	0.95[ASN][1000 genomes]
rs7040353	0.90[ASN][1000 genomes]
rs7046713	0.93[ASN][1000 genomes]
rs7470309	0.95[ASN][1000 genomes]
rs7470323	0.95[ASN][1000 genomes]
rs907076	0.82[ASN][1000 genomes]
rs9650683	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517975	chr9:15286446-15534070	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1030287	chr9:15332709-15458001	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv892626	chr9:15389610-15694690	Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	nsv831520	chr9:15404866-15444447	Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
7	nsv892628	chr9:15420805-15528290	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15424000-15443400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr9:15424000-15443600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr9:15426400-15442800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr9:15426400-15443600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:15426400-15443600	Weak transcription	Gastric	stomach
6	chr9:15426400-15468200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr9:15426600-15442400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr9:15426600-15443400	Weak transcription	Fetal Heart	heart
9	chr9:15427000-15443400	Weak transcription	NHEK	skin
10	chr9:15431400-15442400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr9:15431400-15442800	Weak transcription	Brain Angular Gyrus	brain
12	chr9:15431400-15443400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr9:15431400-15443400	Weak transcription	Pancreas	Pancrea
14	chr9:15431400-15443600	Weak transcription	Aorta	Aorta
15	chr9:15431400-15443600	Weak transcription	Brain Cingulate Gyrus	brain
16	chr9:15431400-15443600	Weak transcription	Esophagus	oesophagus
17	chr9:15431400-15445800	Weak transcription	Right Ventricle	heart
18	chr9:15431400-15446000	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr9:15431400-15447800	Weak transcription	Psoas Muscle	Psoas
20	chr9:15431600-15443400	Weak transcription	Stomach Mucosa	stomach
21	chr9:15432200-15443600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr9:15433400-15492400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr9:15434000-15464000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr9:15434400-15443400	Weak transcription	Colon Smooth Muscle	Colon
25	chr9:15434400-15443600	Weak transcription	Brain Hippocampus Middle	brain
26	chr9:15434400-15443600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr9:15434400-15443600	Weak transcription	K562	blood
28	chr9:15434400-15443800	Weak transcription	HSMMtube	muscle
29	chr9:15434800-15442600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr9:15434800-15443600	Weak transcription	Rectal Smooth Muscle	rectum
31	chr9:15434800-15443600	Weak transcription	Stomach Smooth Muscle	stomach
32	chr9:15435000-15443200	Weak transcription	Brain Anterior Caudate	brain
33	chr9:15435000-15443400	Weak transcription	Fetal Brain Male	brain
34	chr9:15435000-15443400	Weak transcription	Ovary	ovary
35	chr9:15435000-15443600	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr9:15435000-15443600	Weak transcription	Left Ventricle	heart
37	chr9:15435000-15444400	Weak transcription	Brain Substantia Nigra	brain
38	chr9:15435200-15443200	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr9:15435200-15443200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr9:15435200-15443200	Weak transcription	Colonic Mucosa	Colon
41	chr9:15435200-15443200	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr9:15435200-15443400	Weak transcription	NHLF	lung
43	chr9:15435200-15443600	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr9:15435200-15443600	Weak transcription	HMEC	breast
45	chr9:15435200-15443600	Weak transcription	NHDF-Ad	bronchial
46	chr9:15435400-15443200	Weak transcription	NH-A	brain
47	chr9:15435400-15443600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr9:15435400-15443800	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr9:15436400-15443400	Weak transcription	HUVEC	blood vessel
50	chr9:15436600-15443200	Weak transcription	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links