Variant report

Variant rs4849133
Chromosome Location chr2:113681441-113681442
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113671600-113683000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr2:113674400-113683000 Weak transcription Gastric stomach
3 chr2:113677200-113681800 Weak transcription Stomach Mucosa stomach
4 chr2:113678200-113683400 Enhancers Fetal Intestine Small intestine
5 chr2:113678800-113683400 Enhancers Rectal Mucosa Donor 31 rectum
6 chr2:113679000-113681800 Weak transcription Primary T cells fromperipheralblood blood
7 chr2:113679200-113682400 Enhancers Sigmoid Colon Sigmoid Colon
8 chr2:113679600-113682800 Weak transcription Primary T killer memory cells from peripheral blood blood
9 chr2:113680600-113681600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr2:113681000-113681800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr2:113681000-113682400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr2:113681000-113682400 Enhancers Colonic Mucosa Colon
13 chr2:113681000-113683000 Enhancers Rectal Mucosa Donor 29 rectum
14 chr2:113681200-113681600 Flanking Active TSS K562 blood
15 chr2:113681200-113682200 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr2:113681200-113682400 Enhancers Fetal Intestine Large intestine
17 chr2:113681200-113682600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
18 chr2:113681200-113683800 Enhancers Primary hematopoietic stem cells short term culture blood

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