Variant report

Variant rs2469553
Chromosome Location chr15:76640162-76640163
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:50 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:76630200-76641800 Weak transcription A549 lung
2 chr15:76636400-76640200 Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
3 chr15:76637800-76640200 Bivalent/Poised TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr15:76638000-76640400 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell
5 chr15:76638200-76640200 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
6 chr15:76638200-76640200 Bivalent/Poised TSS ES-UCSF4 Cell Line embryonic stem cell
7 chr15:76638600-76640200 Bivalent/Poised TSS Small Intestine intestine
8 chr15:76638600-76640600 Active TSS Stomach Smooth Muscle stomach
9 chr15:76639000-76640200 Bivalent Enhancer Primary monocytes fromperipheralblood blood
10 chr15:76639000-76640200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
11 chr15:76639000-76640400 Active TSS Rectal Smooth Muscle rectum
12 chr15:76639000-76640600 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
13 chr15:76639200-76640200 Bivalent/Poised TSS H9 Cell Line embryonic stem cell
14 chr15:76639200-76640200 Bivalent Enhancer Primary B cells from peripheral blood blood
15 chr15:76639200-76640200 Bivalent Enhancer Primary T helper naive cells fromperipheralblood blood
16 chr15:76639200-76640200 Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr15:76639200-76640200 Bivalent Enhancer Fetal Muscle Leg muscle
18 chr15:76639200-76646400 Weak transcription Aorta Aorta
19 chr15:76639400-76640200 Active TSS Rectal Mucosa Donor 29 rectum
20 chr15:76639400-76640400 Bivalent Enhancer Primary B cells from cord blood blood
21 chr15:76639400-76641200 Weak transcription HepG2 liver
22 chr15:76639600-76640200 Bivalent Enhancer Primary neutrophils fromperipheralblood blood
23 chr15:76639600-76640200 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
24 chr15:76639600-76640200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
25 chr15:76639600-76640400 Bivalent Enhancer Primary hematopoietic stem cells blood
26 chr15:76639600-76641800 Weak transcription Hela-S3 cervix
27 chr15:76639800-76640200 Flanking Bivalent TSS/Enh H1 Cell Line embryonic stem cell
28 chr15:76639800-76640200 Bivalent Enhancer H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
29 chr15:76639800-76640200 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
30 chr15:76639800-76640200 Flanking Bivalent TSS/Enh Fetal Intestine Small intestine
31 chr15:76639800-76640400 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
32 chr15:76639800-76640400 Flanking Bivalent TSS/Enh iPS-18 Cell Line embryonic stem cell
33 chr15:76639800-76640600 Bivalent/Poised TSS Duodenum Smooth Muscle Duodenum
34 chr15:76639800-76642000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
35 chr15:76639800-76659800 Weak transcription Gastric stomach
36 chr15:76639800-76682600 Weak transcription Pancreas Pancrea
37 chr15:76639800-76695400 Weak transcription Spleen Spleen
38 chr15:76639800-76727400 Weak transcription Right Ventricle heart
39 chr15:76640000-76640200 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
40 chr15:76640000-76640200 Bivalent Enhancer hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
41 chr15:76640000-76640200 Flanking Bivalent TSS/Enh HUES48 Cell Line embryonic stem cell
42 chr15:76640000-76640200 Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
43 chr15:76640000-76640200 Enhancers Colonic Mucosa Colon
44 chr15:76640000-76640200 Bivalent Enhancer Fetal Kidney kidney
45 chr15:76640000-76640200 Flanking Bivalent TSS/Enh Rectal Mucosa Donor 31 rectum
46 chr15:76640000-76640400 Flanking Bivalent TSS/Enh HUES64 Cell Line embryonic stem cell
47 chr15:76640000-76640400 Flanking Bivalent TSS/Enh iPS-20b Cell Line embryonic stem cell
48 chr15:76640000-76640400 Active TSS Fetal Stomach stomach
49 chr15:76640000-76640400 ZNF genes & repeats K562 blood
50 chr15:76640000-76642000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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