Variant report

Variant rs10518054
Chromosome Location chr4:69314799-69314800
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69308400-69317800 Weak transcription Primary T helper naive cells fromperipheralblood blood
2 chr4:69311800-69321200 Enhancers HUES64 Cell Line embryonic stem cell
3 chr4:69312000-69320000 Enhancers HUES6 Cell Line embryonic stem cell
4 chr4:69312000-69321400 Enhancers HUES48 Cell Line embryonic stem cell
5 chr4:69312200-69315200 Weak transcription H9 Cell Line embryonic stem cell
6 chr4:69312200-69318200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr4:69312800-69318200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr4:69313200-69318200 Weak transcription H1 Cell Line embryonic stem cell
9 chr4:69313600-69316600 Weak transcription HMEC breast
10 chr4:69313600-69316800 Weak transcription NHEK skin
11 chr4:69314000-69314800 Enhancers Primary T cells from cord blood blood
12 chr4:69314400-69316400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr4:69314400-69321400 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr4:69314600-69314800 Flanking Active TSS ES-I3 Cell Line embryonic stem cell
15 chr4:69314600-69315200 Enhancers iPS-20b Cell Line embryonic stem cell
16 chr4:69314600-69316800 Enhancers iPS-15b Cell Line embryonic stem cell

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