Variant report

Variant rs855662
Chromosome Location chr7:149456974-149456975
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:149448600-149461000 Weak transcription Primary hematopoietic stem cells short term culture blood
2 chr7:149448600-149461000 Weak transcription Lung lung
3 chr7:149448800-149461000 Weak transcription Spleen Spleen
4 chr7:149451000-149462400 Weak transcription Pancreas Pancrea
5 chr7:149451000-149462600 Weak transcription Liver Liver
6 chr7:149451200-149460400 Weak transcription Primary neutrophils fromperipheralblood blood
7 chr7:149451200-149468400 Weak transcription Right Atrium heart
8 chr7:149451400-149461000 Weak transcription Monocytes-CD14+_RO01746 blood
9 chr7:149451400-149461400 Weak transcription Primary monocytes fromperipheralblood blood
10 chr7:149452600-149463200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr7:149453000-149461600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr7:149454600-149460800 Weak transcription Primary T cells from cord blood blood
13 chr7:149455800-149458600 Weak transcription Gastric stomach
14 chr7:149456000-149457200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr7:149456200-149457800 Enhancers K562 blood
16 chr7:149456400-149457000 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
17 chr7:149456400-149457400 Enhancers Placenta Placenta
18 chr7:149456600-149457400 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
19 chr7:149456800-149457000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
20 chr7:149456800-149457000 Enhancers Fetal Stomach stomach

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