Variant report

Variant rs752833
Chromosome Location chr2:111798824-111798825
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:111787800-111825400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr2:111788200-111799200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr2:111790800-111799200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:111790800-111800200 Weak transcription Spleen Spleen
5 chr2:111792800-111801600 Weak transcription Fetal Intestine Large intestine
6 chr2:111795400-111800000 Weak transcription Primary B cells from peripheral blood blood
7 chr2:111795800-111799600 Weak transcription Gastric stomach
8 chr2:111795800-111800400 Weak transcription Primary monocytes fromperipheralblood blood
9 chr2:111795800-111800600 Weak transcription Monocytes-CD14+_RO01746 blood
10 chr2:111796600-111800400 Weak transcription Primary B cells from cord blood blood
11 chr2:111797600-111799200 Weak transcription Fetal Heart heart
12 chr2:111797800-111801400 Weak transcription Fetal Intestine Small intestine
13 chr2:111797800-111806600 Weak transcription Fetal Kidney kidney
14 chr2:111798400-111799600 Weak transcription Fetal Thymus thymus
15 chr2:111798600-111799200 Bivalent Enhancer Fetal Muscle Trunk muscle
16 chr2:111798600-111800200 Weak transcription Primary T cells from cord blood blood

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