Variant report

Variant rs578056984
Chromosome Location chr2:132986694-132986695
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:132976800-132996200 Weak transcription NHEK skin
2 chr2:132984000-132994800 Weak transcription K562 blood
3 chr2:132985400-132986800 Weak transcription H1 Cell Line embryonic stem cell
4 chr2:132985400-132986800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr2:132985400-132986800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr2:132985400-132986800 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr2:132985400-132986800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
8 chr2:132985400-132986800 Weak transcription Liver Liver
9 chr2:132985400-132986800 Weak transcription Fetal Brain Male brain
10 chr2:132985400-132986800 Weak transcription Psoas Muscle Psoas
11 chr2:132985400-132987000 Weak transcription NH-A brain
12 chr2:132985400-132987600 Weak transcription HSMMtube muscle
13 chr2:132985400-132987600 Weak transcription HUVEC blood vessel
14 chr2:132985600-132987400 Weak transcription Osteobl bone
15 chr2:132986600-132986800 Enhancers Aorta Aorta
16 chr2:132986600-132988400 ZNF genes & repeats Primary T cells from cord blood blood
17 chr2:132986600-132988600 ZNF genes & repeats HUES48 Cell Line embryonic stem cell

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