Variant report

Variant rs76879297
Chromosome Location chr12:32532348-32532349
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:32475600-32532400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr12:32494200-32533800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
3 chr12:32520800-32532400 Weak transcription Fetal Intestine Small intestine
4 chr12:32522600-32535800 Weak transcription Fetal Brain Female brain
5 chr12:32522800-32532400 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr12:32530600-32532400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr12:32530600-32534000 Weak transcription HSMM muscle
8 chr12:32531000-32533400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr12:32531600-32532800 Enhancers HUES48 Cell Line embryonic stem cell
10 chr12:32531800-32532800 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr12:32532000-32532400 Enhancers Ovary ovary
12 chr12:32532000-32532600 Enhancers H1 Cell Line embryonic stem cell
13 chr12:32532000-32532600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr12:32532000-32532800 Enhancers ES-WA7 Cell Line embryonic stem cell
15 chr12:32532000-32533000 Enhancers ES-I3 Cell Line embryonic stem cell
16 chr12:32532200-32532400 Enhancers iPS-20b Cell Line embryonic stem cell
17 chr12:32532200-32532400 Flanking Active TSS HepG2 liver
18 chr12:32532200-32532600 Enhancers HUES6 Cell Line embryonic stem cell
19 chr12:32532200-32532800 Enhancers H9 Cell Line embryonic stem cell
20 chr12:32532200-32532800 Enhancers HUES64 Cell Line embryonic stem cell
21 chr12:32532200-32532800 Flanking Active TSS K562 blood

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