Variant report

Variant	rs11568811
Chromosome Location	chr9:101913015-101913016
allele	C/G
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	chr9:101912686-101913140	HL-60	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:101907167..101909352-chr9:101910696..101913205,3	K562	blood:
2	chr9:101910109..101913329-chr9:101915349..101919610,4	K562	blood:
3	chr9:101911700..101915310-chr9:101917488..101920239,4	K562	blood:
4	chr9:101906889..101909084-chr9:101911405..101913205,2	K562	blood:

Variant related genes	Relation type
RNA5SP290	TF binding region
ENSG00000252942	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10988726	1.00[ASN][1000 genomes]
rs10988727	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10988728	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11568750	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11568795	1.00[ASN][1000 genomes]
rs12683974	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12685067	1.00[ASN][1000 genomes]
rs61052245	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893619	chr9:101835165-101936231	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv831666	chr9:101874985-102018690	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101890000-101914200	Weak transcription	Pancreas	Pancrea
2	chr9:101892600-101914200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:101892800-101921000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:101895000-101914200	Weak transcription	Esophagus	oesophagus
5	chr9:101897600-101913400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr9:101897600-101915400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr9:101898000-101919400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr9:101900200-101914800	Strong transcription	Primary B cells from peripheral blood	blood
9	chr9:101900200-101915200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:101900800-101916800	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr9:101902800-101914200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr9:101902800-101915400	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr9:101903000-101915200	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr9:101903000-101921800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr9:101903200-101913200	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr9:101903200-101915000	Strong transcription	Osteobl	bone
17	chr9:101903400-101914200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr9:101903400-101915400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr9:101903600-101915000	Strong transcription	HSMMtube	muscle
20	chr9:101903600-101915200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr9:101904000-101913400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr9:101904000-101915800	Strong transcription	Placenta	Placenta
23	chr9:101904000-101916400	Strong transcription	Primary B cells from cord blood	blood
24	chr9:101904000-101917200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr9:101904200-101913200	Strong transcription	Skeletal Muscle Female	skeletal muscle
26	chr9:101904200-101914800	Strong transcription	Liver	Liver
27	chr9:101904600-101916200	Weak transcription	Fetal Intestine Small	intestine
28	chr9:101906200-101915000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr9:101906200-101915000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:101906800-101913400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr9:101907000-101913200	Strong transcription	Stomach Smooth Muscle	stomach
32	chr9:101907200-101919800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr9:101907800-101916600	Weak transcription	Fetal Brain Male	brain
34	chr9:101908000-101914400	Weak transcription	Small Intestine	intestine
35	chr9:101908200-101922000	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr9:101908400-101914200	Weak transcription	Brain Substantia Nigra	brain
37	chr9:101908400-101916600	Weak transcription	NHLF	lung
38	chr9:101908400-101918000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr9:101908600-101914200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr9:101908600-101914200	Weak transcription	Aorta	Aorta
41	chr9:101908600-101924600	Weak transcription	Gastric	stomach
42	chr9:101909000-101918600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr9:101909000-101920000	Weak transcription	HepG2	liver
44	chr9:101909200-101918000	Weak transcription	Fetal Stomach	stomach
45	chr9:101909400-101914400	Weak transcription	Right Ventricle	heart
46	chr9:101909600-101916200	Weak transcription	Brain Anterior Caudate	brain
47	chr9:101909800-101914200	Weak transcription	Rectal Smooth Muscle	rectum
48	chr9:101909800-101915800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:101910000-101913200	Weak transcription	Fetal Heart	heart
50	chr9:101910400-101914200	Weak transcription	Spleen	Spleen

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