Variant report

Variant rs145069014
Chromosome Location chr6:162603675-162603676
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:162591200-162607600 Weak transcription Right Atrium heart
2 chr6:162599600-162607800 Weak transcription Right Ventricle heart
3 chr6:162600600-162607600 Weak transcription Left Ventricle heart
4 chr6:162600800-162607600 Weak transcription Skeletal Muscle Male skeletal muscle
5 chr6:162601400-162606200 Enhancers Primary monocytes fromperipheralblood blood
6 chr6:162601400-162607600 Weak transcription Skeletal Muscle Female skeletal muscle
7 chr6:162601800-162603800 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr6:162602000-162603800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr6:162602000-162603800 Enhancers Adipose Nuclei Adipose
10 chr6:162602200-162603800 Enhancers Primary hematopoietic stem cells blood
11 chr6:162602200-162603800 Enhancers HUVEC blood vessel
12 chr6:162602800-162603800 Enhancers NHEK skin
13 chr6:162602800-162604400 Enhancers Sigmoid Colon Sigmoid Colon
14 chr6:162603200-162606200 Weak transcription Fetal Heart heart
15 chr6:162603400-162603800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr6:162603400-162608200 Weak transcription Fetal Adrenal Gland Adrenal Gland
17 chr6:162603600-162604000 Enhancers Monocytes-CD14+_RO01746 blood

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