Variant report

Variant rs1998258
Chromosome Location chr2:33155182-33155183
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:33152200-33157000 Weak transcription Placenta Placenta
2 chr2:33152400-33156200 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr2:33152400-33156600 Weak transcription H1 Cell Line embryonic stem cell
4 chr2:33152400-33156600 Weak transcription H9 Cell Line embryonic stem cell
5 chr2:33152400-33156600 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr2:33152600-33155800 Weak transcription HUES64 Cell Line embryonic stem cell
7 chr2:33152600-33155800 Weak transcription iPS-20b Cell Line embryonic stem cell
8 chr2:33152600-33156200 Weak transcription HUES6 Cell Line embryonic stem cell
9 chr2:33152600-33156600 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr2:33152600-33156600 Weak transcription Cortex derived primary cultured neurospheres brain
11 chr2:33152600-33157000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
12 chr2:33152600-33162800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr2:33152800-33157000 Weak transcription K562 blood
14 chr2:33152800-33158600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr2:33154000-33155600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr2:33154800-33155200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
17 chr2:33154800-33155200 Enhancers Dnd41 blood

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