Variant report

Variant rs35761487
Chromosome Location chr2:111793008-111793009
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:111786000-111795800 Enhancers Primary monocytes fromperipheralblood blood
2 chr2:111787400-111795600 Weak transcription H1 Cell Line embryonic stem cell
3 chr2:111787800-111825400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr2:111788200-111793400 Weak transcription Fetal Thymus thymus
5 chr2:111788200-111799200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr2:111790800-111793600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
7 chr2:111790800-111799200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr2:111790800-111800200 Weak transcription Spleen Spleen
9 chr2:111791200-111794600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:111791200-111795600 Weak transcription Gastric stomach
11 chr2:111791200-111795800 Enhancers Monocytes-CD14+_RO01746 blood
12 chr2:111791400-111793400 Weak transcription Primary B cells from cord blood blood
13 chr2:111792400-111796600 Weak transcription Fetal Lung lung
14 chr2:111792400-111797200 Weak transcription Fetal Heart heart
15 chr2:111792800-111797200 Weak transcription Fetal Intestine Small intestine
16 chr2:111792800-111801600 Weak transcription Fetal Intestine Large intestine
17 chr2:111793000-111796600 Weak transcription Fetal Kidney kidney

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