Variant report

Variant rs113972880
Chromosome Location chr19:43866951-43866952
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43862800-43873200 Weak transcription Gastric stomach
2 chr19:43864600-43867600 Strong transcription Primary neutrophils fromperipheralblood blood
3 chr19:43864600-43868000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr19:43864600-43868200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr19:43866000-43867000 Bivalent Enhancer Fetal Stomach stomach
6 chr19:43866200-43867000 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
7 chr19:43866200-43867000 Enhancers Colonic Mucosa Colon
8 chr19:43866200-43867000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
9 chr19:43866200-43867000 Enhancers Osteobl bone
10 chr19:43866200-43867200 Enhancers NHLF lung
11 chr19:43866200-43867400 Enhancers Rectal Mucosa Donor 31 rectum
12 chr19:43866400-43867000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
13 chr19:43866400-43867200 Enhancers Rectal Mucosa Donor 29 rectum
14 chr19:43866400-43868200 Weak transcription Spleen Spleen
15 chr19:43866600-43868000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
16 chr19:43866800-43868000 Weak transcription Sigmoid Colon Sigmoid Colon

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