Variant report

Variant	rs1050244
Chromosome Location	chr11:47260477-47260478
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:47234544..47240299-chr11:47253173..47262641,20	MCF-7	breast:
2	chr11:47256660..47260798-chr11:47290143..47292249,4	K562	blood:
3	chr11:47257344..47261784-chr11:47428504..47430961,3	K562	blood:
4	chr11:47256660..47261423-chr11:47290143..47292492,5	K562	blood:
5	chr11:47257788..47261523-chr11:47268362..47272495,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000134574	Chromatin interaction
ENSG00000025434	Chromatin interaction
ENSG00000255197	Chromatin interaction
ENSG00000134575	Chromatin interaction
ENSG00000165915	Chromatin interaction
ENSG00000110514	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10838677	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11039143	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11039145	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11039146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11039160	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11039161	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11039177	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11039179	1.00[AMR][1000 genomes]
rs11039185	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11530167	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3729936	1.00[AMR][1000 genomes]
rs3729948	0.90[EUR][1000 genomes]
rs3729953	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3729991	1.00[AMR][1000 genomes]
rs45603841	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4640	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4647718	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4647730	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4647731	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4647738	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4647752	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56023479	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57741802	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs57852039	0.93[EUR][1000 genomes]
rs58528246	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58912703	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61124822	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7110333	1.00[AMR][1000 genomes]
rs7943429	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][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	nsv897323	chr11:47182926-47460306	Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription 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 lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv917316	chr11:47232210-47448882	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47238400-47269400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:47238600-47261000	Weak transcription	Small Intestine	intestine
3	chr11:47240200-47266600	Weak transcription	Fetal Brain Male	brain
4	chr11:47242400-47269200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:47243600-47269200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr11:47246600-47267800	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr11:47247400-47267600	Strong transcription	Thymus	Thymus
8	chr11:47248200-47265200	Strong transcription	GM12878-XiMat	blood
9	chr11:47248600-47260800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr11:47254000-47264600	Strong transcription	Dnd41	blood
11	chr11:47254600-47267800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr11:47254800-47261000	Weak transcription	Ovary	ovary
13	chr11:47255400-47262000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr11:47255400-47269200	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr11:47255600-47264600	Strong transcription	HepG2	liver
16	chr11:47255600-47268800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr11:47255800-47267600	Strong transcription	H1 Cell Line	embryonic stem cell
18	chr11:47256000-47260600	Weak transcription	Fetal Kidney	kidney
19	chr11:47256000-47268000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:47256200-47260800	Strong transcription	Fetal Intestine Small	intestine
21	chr11:47256200-47267800	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr11:47256400-47260600	Weak transcription	Brain Angular Gyrus	brain
23	chr11:47256400-47261000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr11:47256400-47267800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr11:47256600-47261000	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr11:47256800-47260800	Weak transcription	Stomach Mucosa	stomach
27	chr11:47256800-47268800	Strong transcription	Fetal Thymus	thymus
28	chr11:47257000-47260800	Weak transcription	NH-A	brain
29	chr11:47257000-47261400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:47257200-47260600	Weak transcription	Fetal Heart	heart
31	chr11:47257200-47260800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr11:47257400-47260800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr11:47257400-47262000	Strong transcription	HMEC	breast
34	chr11:47257800-47267800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr11:47257800-47268000	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr11:47258000-47262600	Strong transcription	HSMMtube	muscle
37	chr11:47258000-47269000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr11:47258200-47261000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr11:47258200-47263600	Strong transcription	NHLF	lung
40	chr11:47258200-47267600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr11:47258400-47263200	Strong transcription	Osteobl	bone
42	chr11:47258400-47266400	Strong transcription	Fetal Intestine Large	intestine
43	chr11:47258400-47267800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr11:47258400-47268400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr11:47258600-47261200	Weak transcription	Primary B cells from cord blood	blood
46	chr11:47258600-47262400	Strong transcription	NHDF-Ad	bronchial
47	chr11:47258600-47265200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr11:47258600-47267800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr11:47258600-47267800	Strong transcription	Rectal Smooth Muscle	rectum
50	chr11:47258600-47268800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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