Variant report

Variant rs9457276
Chromosome Location chr6:167558001-167558002
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167534000-167573400 Weak transcription Right Atrium heart
2 chr6:167543400-167565000 Weak transcription Spleen Spleen
3 chr6:167550600-167560400 Weak transcription Placenta Amnion Placenta Amnion
4 chr6:167551200-167559600 Weak transcription Primary hematopoietic stem cells blood
5 chr6:167552800-167560800 Weak transcription H9 Cell Line embryonic stem cell
6 chr6:167553000-167558800 Weak transcription HUES64 Cell Line embryonic stem cell
7 chr6:167554800-167559200 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr6:167555400-167558200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr6:167555800-167559600 Weak transcription Duodenum Mucosa Duodenum
10 chr6:167555800-167559800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr6:167556000-167560600 Weak transcription ES-WA7 Cell Line embryonic stem cell
12 chr6:167556800-167559600 Weak transcription Primary B cells from peripheral blood blood
13 chr6:167557400-167558400 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
14 chr6:167558000-167558200 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
15 chr6:167558000-167558400 ZNF genes & repeats H1 Cell Line embryonic stem cell

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