Variant report

Variant	rs10444871
Chromosome Location	chr15:92479785-92479786
allele	A/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	SPI1	chr15:92479304-92479949	GM12878	blood:	n/a	n/a
2	SPI1	chr15:92479289-92479811	HL-60	blood:	n/a	n/a
3	SPI1	chr15:92479474-92479797	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:92461295..92463798-chr15:92477370..92479994,2	K562	blood:
2	chr15:92467181..92469484-chr15:92477691..92480563,2	MCF-7	breast:
3	chr15:92477044..92480938-chr15:92480980..92485155,5	MCF-7	breast:

Variant related genes	Relation type
SLCO3A1	TF binding region
ENSG00000176463	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12901800	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12906515	1.00[JPT][hapmap]
rs4244911	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4398089	0.82[ASN][1000 genomes]
rs4420511	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4932515	0.86[CEU][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4932518	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6496877	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs6496878	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6496880	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7163871	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7164216	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7179615	0.82[ASN][1000 genomes]
rs7179786	0.82[ASN][1000 genomes]
rs8027634	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs8028706	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8031009	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8032981	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8037251	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8037463	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8040407	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048635	chr15:92073294-92557339	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer 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	14 gene(s)	inside rSNPs	diseases
2	nsv870094	chr15:92367354-92631647	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv534110	chr15:92397220-92592961	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:92462800-92482600	Weak transcription	HMEC	breast
2	chr15:92463800-92482400	Weak transcription	Esophagus	oesophagus
3	chr15:92464600-92483000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr15:92466400-92482200	Weak transcription	Pancreas	Pancrea
5	chr15:92466800-92480200	Weak transcription	Fetal Brain Female	brain
6	chr15:92469400-92483000	Weak transcription	Gastric	stomach
7	chr15:92469400-92485800	Weak transcription	Aorta	Aorta
8	chr15:92470400-92483200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr15:92470600-92479800	Weak transcription	NHLF	lung
10	chr15:92471200-92483600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr15:92471800-92481400	Weak transcription	Brain Anterior Caudate	brain
12	chr15:92472800-92482400	Weak transcription	Spleen	Spleen
13	chr15:92473600-92479800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr15:92473600-92483200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr15:92475200-92479800	Weak transcription	Brain Angular Gyrus	brain
16	chr15:92475200-92480200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr15:92475400-92479800	Weak transcription	Brain Hippocampus Middle	brain
18	chr15:92475400-92482600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr15:92475400-92483000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr15:92475400-92483000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr15:92475400-92484600	Weak transcription	Primary T cells from cord blood	blood
22	chr15:92475800-92482200	Weak transcription	Brain Substantia Nigra	brain
23	chr15:92477400-92479800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr15:92477400-92483400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr15:92477600-92481800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr15:92477600-92482800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr15:92477800-92480000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr15:92477800-92482800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr15:92477800-92483200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr15:92478000-92480000	Weak transcription	Left Ventricle	heart
31	chr15:92478400-92481800	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr15:92478600-92481400	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr15:92478800-92479800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr15:92478800-92480800	Enhancers	Lung	lung
35	chr15:92478800-92481800	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr15:92478800-92488000	Enhancers	Fetal Heart	heart
37	chr15:92479000-92479800	Weak transcription	Right Ventricle	heart
38	chr15:92479000-92480400	Enhancers	Duodenum Mucosa	Duodenum
39	chr15:92479000-92483000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr15:92479000-92483400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr15:92479000-92491200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr15:92479200-92480000	Weak transcription	Stomach Mucosa	stomach
43	chr15:92479200-92480600	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr15:92479200-92480600	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr15:92479200-92480800	Enhancers	Ovary	ovary
46	chr15:92479200-92480800	Enhancers	Right Atrium	heart
47	chr15:92479200-92482600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr15:92479200-92483000	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr15:92479200-92483200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr15:92479200-92483400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links