Variant report

Variant	rs370067589
Chromosome Location	chr14:71918884-71918885
allele	-/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv498021	chr14:71874708-72128721	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv976298	chr14:71917066-71925965	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71900000-71927200	Weak transcription	Primary B cells from cord blood	blood
2	chr14:71905600-71919200	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr14:71906400-71927000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr14:71907000-71930000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr14:71907000-71930600	Weak transcription	HSMM	muscle
6	chr14:71907200-71921400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr14:71907400-71921400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr14:71908200-71935400	Weak transcription	Primary T cells from cord blood	blood
9	chr14:71911800-71921600	Weak transcription	Brain Angular Gyrus	brain
10	chr14:71912800-71920000	Weak transcription	Right Atrium	heart
11	chr14:71912800-71921600	Weak transcription	Aorta	Aorta
12	chr14:71913200-71927000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr14:71914000-71927000	Weak transcription	Primary B cells from peripheral blood	blood
14	chr14:71915800-71919200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr14:71915800-71938600	Weak transcription	Small Intestine	intestine
16	chr14:71916000-71921600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr14:71916200-71919200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr14:71916400-71921400	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr14:71916400-71932000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr14:71916600-71919200	Weak transcription	NHEK	skin
21	chr14:71916600-71921600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr14:71916600-71921600	Weak transcription	Fetal Heart	heart
23	chr14:71916600-71932800	Weak transcription	Colon Smooth Muscle	Colon
24	chr14:71917200-71921400	Weak transcription	Stomach Mucosa	stomach
25	chr14:71918600-71919800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr14:71918800-71919800	Enhancers	Osteobl	bone
27	chr14:71918800-71920200	Enhancers	Muscle Satellite Cultured Cells	--
28	chr14:71918800-71920200	Enhancers	HMEC	breast
29	chr14:71918800-71920200	Enhancers	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links