Variant report

Variant rs1611565
Chromosome Location chr6:29864745-29864746
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29856600-29877200 Weak transcription Left Ventricle heart
2 chr6:29856800-29867600 Weak transcription Brain Substantia Nigra brain
3 chr6:29857000-29868800 Weak transcription Brain Inferior Temporal Lobe brain
4 chr6:29857200-29865800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr6:29857200-29867200 Weak transcription Esophagus oesophagus
6 chr6:29857200-29868800 Weak transcription Adipose Nuclei Adipose
7 chr6:29857200-29878400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr6:29857600-29875600 Weak transcription Pancreas Pancrea
9 chr6:29857600-29879400 Weak transcription Stomach Smooth Muscle stomach
10 chr6:29859000-29866000 Weak transcription Primary B cells from peripheral blood blood
11 chr6:29861200-29865200 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr6:29861200-29865800 Weak transcription Rectal Mucosa Donor 31 rectum
13 chr6:29861200-29867000 Weak transcription Duodenum Smooth Muscle Duodenum
14 chr6:29864000-29865200 Strong transcription Fetal Intestine Large intestine
15 chr6:29864200-29865400 Strong transcription Duodenum Mucosa Duodenum
16 chr6:29864400-29865200 Strong transcription Right Ventricle heart
17 chr6:29864400-29867200 ZNF genes & repeats Fetal Intestine Small intestine
18 chr6:29864600-29865200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
19 chr6:29864600-29865800 Strong transcription Aorta Aorta

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