Variant report

Variant rs4401475
Chromosome Location chr4:76975924-76975925
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:76965000-76977400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr4:76974600-76976000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr4:76975000-76976200 Enhancers Fetal Intestine Large intestine
4 chr4:76975200-76976400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr4:76975200-76976400 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr4:76975400-76976400 Weak transcription H1 Cell Line embryonic stem cell
7 chr4:76975400-76976600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr4:76975400-76979200 Weak transcription HMEC breast
9 chr4:76975600-76976000 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr4:76975600-76976000 Weak transcription HUES48 Cell Line embryonic stem cell
11 chr4:76975600-76976000 Weak transcription HUES6 Cell Line embryonic stem cell
12 chr4:76975600-76976000 Weak transcription HUES64 Cell Line embryonic stem cell
13 chr4:76975600-76976000 Weak transcription iPS-20b Cell Line embryonic stem cell
14 chr4:76975600-76976000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr4:76975600-76976000 Weak transcription Primary monocytes fromperipheralblood blood
16 chr4:76975600-76976000 Enhancers GM12878-XiMat blood
17 chr4:76975600-76976800 Weak transcription Cortex derived primary cultured neurospheres brain
18 chr4:76975800-76976000 Enhancers Fetal Intestine Small intestine
19 chr4:76975800-76976200 Weak transcription iPS-15b Cell Line embryonic stem cell
20 chr4:76975800-76976600 Enhancers Primary B cells from cord blood blood
21 chr4:76975800-76977400 Enhancers Primary B cells from peripheral blood blood
22 chr4:76975800-76977800 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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