Variant report

Variant rs13390848
Chromosome Location chr2:172957643-172957644
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:172949800-172960800 Bivalent/Poised TSS Fetal Brain Female brain
2 chr2:172950400-172959000 Weak transcription Hela-S3 cervix
3 chr2:172953600-172957800 Weak transcription Muscle Satellite Cultured Cells --
4 chr2:172954400-172962600 Bivalent/Poised TSS Brain Germinal Matrix brain
5 chr2:172956000-172958000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr2:172956800-172957800 Bivalent Enhancer H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr2:172957400-172958400 Flanking Bivalent TSS/Enh Cortex derived primary cultured neurospheres brain
8 chr2:172957400-172958800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
9 chr2:172957600-172957800 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
10 chr2:172957600-172958200 Bivalent Enhancer H1 Cell Line embryonic stem cell
11 chr2:172957600-172958200 Flanking Active TSS K562 blood
12 chr2:172957600-172958600 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
13 chr2:172957600-172958800 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
14 chr2:172957600-172959000 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
15 chr2:172957600-172959600 Bivalent Enhancer Primary T cells fromperipheralblood blood

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