Variant report

Variant rs199990535
Chromosome Location chr7:70387991-70387992
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:70373200-70400200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr7:70384800-70390200 Weak transcription HUES64 Cell Line embryonic stem cell
3 chr7:70384800-70390200 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr7:70384800-70390200 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr7:70385000-70388000 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr7:70385000-70388000 Weak transcription Fetal Lung lung
7 chr7:70385000-70390200 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr7:70386200-70388200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr7:70386400-70388000 Weak transcription Fetal Intestine Small intestine
10 chr7:70386400-70388200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr7:70387000-70388000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr7:70387200-70388200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr7:70387800-70388600 Enhancers Fetal Kidney kidney
14 chr7:70387800-70388800 Enhancers iPS-18 Cell Line embryonic stem cell
15 chr7:70387800-70388800 Enhancers Fetal Intestine Large intestine

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