Variant report

Variant	rs11573644
Chromosome Location	chr9:110057387-110057388
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:110044182..110049393-chr9:110054071..110058486,10	MCF-7	breast:
2	chr9:110056937..110059349-chr9:110068583..110071542,3	MCF-7	breast:
3	chr9:110052754..110054534-chr9:110055786..110058633,2	K562	blood:
4	chr9:110054445..110058128-chr9:110059472..110062917,7	K562	blood:
5	chr9:110056091..110058326-chr9:110068652..110070391,2	K562	blood:
6	chr9:110050921..110052628-chr9:110056459..110059114,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000119318	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11573664	0.88[AFR][1000 genomes]
rs11573708	0.82[YRI][hapmap];0.88[AFR][1000 genomes]
rs11573721	0.85[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869351	chr9:109593212-110191170	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv530948	chr9:109760752-110413602	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv831682	chr9:109937181-110075453	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv508560	chr9:110006490-110060539	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv519266	chr9:110049477-110085255	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110047600-110067200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:110048000-110058400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr9:110048400-110058000	Enhancers	Primary T killer memory cells from peripheral blood	blood
4	chr9:110048600-110058000	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr9:110048800-110058600	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr9:110048800-110059200	Enhancers	HepG2	liver
7	chr9:110048800-110061000	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr9:110048800-110067800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr9:110048800-110069600	Weak transcription	Fetal Brain Male	brain
10	chr9:110049000-110058800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr9:110049000-110061200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr9:110049000-110061400	Weak transcription	NH-A	brain
13	chr9:110049000-110063000	Enhancers	Liver	Liver
14	chr9:110049000-110063200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr9:110049000-110063200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr9:110049200-110059200	Weak transcription	Fetal Intestine Small	intestine
17	chr9:110049200-110067000	Weak transcription	Fetal Muscle Leg	muscle
18	chr9:110049400-110067800	Weak transcription	Primary hematopoietic stem cells	blood
19	chr9:110049800-110058000	Weak transcription	Stomach Mucosa	stomach
20	chr9:110050200-110063200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr9:110051200-110058400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr9:110051200-110066000	Weak transcription	Fetal Intestine Large	intestine
23	chr9:110051200-110067000	Weak transcription	Thymus	Thymus
24	chr9:110051600-110079200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr9:110051800-110057600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr9:110052000-110066800	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr9:110052200-110061200	Weak transcription	Dnd41	blood
28	chr9:110052600-110063200	Weak transcription	Placenta	Placenta
29	chr9:110052600-110067000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr9:110052600-110067000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr9:110052600-110068600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:110052600-110068600	Weak transcription	Brain Germinal Matrix	brain
33	chr9:110052600-110068800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr9:110052600-110069200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr9:110052800-110061200	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr9:110052800-110066000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr9:110053400-110068600	Weak transcription	Stomach Smooth Muscle	stomach
38	chr9:110053600-110061200	Weak transcription	Hela-S3	cervix
39	chr9:110053600-110063200	Weak transcription	Fetal Thymus	thymus
40	chr9:110053600-110063400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr9:110054000-110057800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr9:110054600-110057400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr9:110054600-110057400	Enhancers	Psoas Muscle	Psoas
44	chr9:110054600-110058400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr9:110054600-110058600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr9:110054800-110057400	Enhancers	Spleen	Spleen
47	chr9:110055000-110057400	Enhancers	K562	blood
48	chr9:110055000-110057600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr9:110055000-110058200	Enhancers	Fetal Heart	heart
50	chr9:110055200-110057400	Enhancers	Right Atrium	heart

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