Variant report

Variant rs577220192
Chromosome Location chr4:69317163-69317164
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 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 chr4:69312200-69318200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr4:69312800-69318200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr4:69313200-69318200 Weak transcription H1 Cell Line embryonic stem cell
8 chr4:69314400-69321400 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr4:69314800-69317400 Weak transcription Primary T cells from cord blood blood
10 chr4:69315200-69317200 Enhancers H9 Cell Line embryonic stem cell
11 chr4:69315800-69319800 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr4:69315800-69320000 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr4:69316400-69318400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr4:69316400-69319200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr4:69316600-69317400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr4:69316600-69318400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr4:69316600-69319600 Enhancers HMEC breast
18 chr4:69316800-69317200 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
19 chr4:69316800-69317200 Active TSS Esophagus oesophagus
20 chr4:69316800-69319200 Enhancers NHEK skin
21 chr4:69317000-69317400 Enhancers Placenta Amnion Placenta Amnion
22 chr4:69317000-69317800 Enhancers Colon Smooth Muscle Colon
23 chr4:69317000-69318200 Weak transcription ES-WA7 Cell Line embryonic stem cell

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