Variant report

Variant rs1002822
Chromosome Location chr14:32777753-32777754
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:25 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32768000-32780000 Weak transcription Psoas Muscle Psoas
2 chr14:32769800-32780800 Weak transcription Left Ventricle heart
3 chr14:32772800-32778400 Enhancers Fetal Intestine Large intestine
4 chr14:32774000-32778200 Weak transcription Pancreas Pancrea
5 chr14:32775400-32778400 Enhancers Fetal Intestine Small intestine
6 chr14:32775600-32777800 Enhancers NHEK skin
7 chr14:32775800-32777800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr14:32775800-32777800 Enhancers Hela-S3 cervix
9 chr14:32776400-32778200 Enhancers Liver Liver
10 chr14:32776600-32777800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
11 chr14:32776600-32777800 Enhancers Colon Smooth Muscle Colon
12 chr14:32776600-32778000 Enhancers Duodenum Mucosa Duodenum
13 chr14:32776800-32777800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr14:32776800-32778000 Enhancers Pancreatic Islets Pancreatic Islet
15 chr14:32776800-32778000 Enhancers HepG2 liver
16 chr14:32776800-32778400 Enhancers Stomach Mucosa stomach
17 chr14:32777000-32778400 Enhancers Rectal Mucosa Donor 31 rectum
18 chr14:32777000-32780800 Weak transcription HMEC breast
19 chr14:32777000-32788000 Weak transcription Esophagus oesophagus
20 chr14:32777400-32777800 Weak transcription Small Intestine intestine
21 chr14:32777400-32778400 Enhancers A549 lung
22 chr14:32777400-32780200 Weak transcription Fetal Heart heart
23 chr14:32777400-32791400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
24 chr14:32777600-32780400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
25 chr14:32777600-32780400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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