Variant report

Variant	rs11844909
Chromosome Location	chr14:69220580-69220581
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:69218946..69221608-chr14:69261319..69263953,3	K562	blood:
2	chr14:69218982..69221313-chr14:69251306..69253828,3	MCF-7	breast:
3	chr14:69218627..69226949-chr14:69256316..69264627,15	K562	blood:
4	chr14:69218392..69222531-chr14:69227666..69230740,3	K562	blood:
5	chr14:69215425..69218916-chr14:69220182..69222789,4	K562	blood:
6	chr14:69219042..69221394-chr14:69250873..69253733,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000185650	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs7151054	0.82[YRI][hapmap]
rs73277299	1.00[AMR][1000 genomes]
rs8021099	0.82[YRI][hapmap];1.00[AMR][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	nsv456332	chr14:69216412-69230080	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv564963	chr14:69216412-69230080	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69201200-69222600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:69202800-69224600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr14:69212600-69229200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:69214400-69221000	Weak transcription	Right Atrium	heart
5	chr14:69214600-69224600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr14:69215600-69222400	Weak transcription	Pancreas	Pancrea
7	chr14:69215800-69221000	Weak transcription	Spleen	Spleen
8	chr14:69215800-69222400	Weak transcription	Right Ventricle	heart
9	chr14:69216600-69224200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr14:69217000-69222600	Weak transcription	Placenta	Placenta
11	chr14:69218400-69221200	Enhancers	Colon Smooth Muscle	Colon
12	chr14:69218600-69230800	Enhancers	Fetal Muscle Leg	muscle
13	chr14:69218600-69231600	Enhancers	Fetal Heart	heart
14	chr14:69218800-69221200	Enhancers	Rectal Smooth Muscle	rectum
15	chr14:69218800-69221800	Enhancers	Fetal Stomach	stomach
16	chr14:69218800-69222800	Weak transcription	Lung	lung
17	chr14:69218800-69225600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr14:69218800-69230800	Enhancers	Fetal Intestine Small	intestine
19	chr14:69219000-69221000	Enhancers	HepG2	liver
20	chr14:69219200-69221200	Enhancers	Adipose Nuclei	Adipose
21	chr14:69219200-69226000	Enhancers	Fetal Intestine Large	intestine
22	chr14:69219400-69221000	Weak transcription	Left Ventricle	heart
23	chr14:69219400-69221000	Weak transcription	Ovary	ovary
24	chr14:69219800-69222400	Weak transcription	Stomach Mucosa	stomach
25	chr14:69219800-69223400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr14:69219800-69223600	Enhancers	Fetal Lung	lung
27	chr14:69219800-69225400	Enhancers	NHDF-Ad	bronchial
28	chr14:69220000-69221400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr14:69220000-69221600	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr14:69220200-69220600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr14:69220400-69220800	Weak transcription	Fetal Muscle Trunk	muscle
32	chr14:69220400-69221000	Weak transcription	K562	blood
33	chr14:69220400-69221000	Enhancers	NHLF	lung
34	chr14:69220400-69221200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr14:69220400-69221200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
36	chr14:69220400-69221200	Enhancers	Osteobl	bone
37	chr14:69220400-69226800	Enhancers	Fetal Kidney	kidney

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