Variant report

Variant rs7604485
Chromosome Location chr2:144577612-144577613
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:144564000-144577800 Weak transcription Fetal Brain Male brain
2 chr2:144574600-144582200 Weak transcription H9 Cell Line embryonic stem cell
3 chr2:144574800-144591000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr2:144575000-144581600 Weak transcription HUES64 Cell Line embryonic stem cell
5 chr2:144575000-144581600 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr2:144575000-144582400 Weak transcription iPS-20b Cell Line embryonic stem cell
7 chr2:144575200-144581600 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr2:144575200-144582200 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr2:144577000-144577800 Enhancers Primary B cells from cord blood blood
10 chr2:144577000-144578800 Active TSS NHDF-Ad bronchial
11 chr2:144577000-144579200 Weak transcription Fetal Stomach stomach
12 chr2:144577200-144578000 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
13 chr2:144577400-144577800 Flanking Active TSS GM12878-XiMat blood
14 chr2:144577400-144582200 Weak transcription HUES6 Cell Line embryonic stem cell
15 chr2:144577400-144582600 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr2:144577600-144578200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
17 chr2:144577600-144578200 Active TSS Fetal Muscle Leg muscle

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