Variant report

Variant rs17098793
Chromosome Location chr1:76809752-76809753
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:76780200-76813800 Weak transcription Primary B cells from cord blood blood
2 chr1:76780600-76817200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr1:76803600-76817400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr1:76803600-76817400 Weak transcription Brain Anterior Caudate brain
5 chr1:76803800-76817600 Weak transcription Brain Substantia Nigra brain
6 chr1:76804000-76809800 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr1:76806200-76813800 Weak transcription Adipose Nuclei Adipose
8 chr1:76808800-76810400 Enhancers Primary T cells from cord blood blood
9 chr1:76809000-76810400 Enhancers Primary T helper naive cells fromperipheralblood blood
10 chr1:76809200-76810200 Enhancers Primary T helper naive cells from peripheral blood blood
11 chr1:76809200-76812200 Weak transcription Duodenum Smooth Muscle Duodenum
12 chr1:76809400-76818800 Weak transcription Gastric stomach
13 chr1:76809600-76810000 Enhancers Primary T killer naive cells fromperipheralblood blood
14 chr1:76809600-76810200 Enhancers Primary T helper cells PMA-I stimulated --

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