Variant report

Variant rs5998608
Chromosome Location chr22:33134399-33134400
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:33121800-33141400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr22:33128400-33135000 Enhancers Fetal Thymus thymus
3 chr22:33130800-33134600 Enhancers HepG2 liver
4 chr22:33132000-33140600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr22:33132600-33134600 Enhancers Thymus Thymus
6 chr22:33133800-33134400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr22:33133800-33134400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
8 chr22:33133800-33134400 Enhancers Lung lung
9 chr22:33133800-33134600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
10 chr22:33133800-33134600 Enhancers Spleen Spleen
11 chr22:33134200-33134400 Enhancers Skeletal Muscle Female skeletal muscle
12 chr22:33134200-33134600 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr22:33134200-33134800 Enhancers Placenta Placenta
14 chr22:33134200-33135000 Enhancers Adipose Nuclei Adipose
15 chr22:33134200-33135000 Enhancers Fetal Adrenal Gland Adrenal Gland
16 chr22:33134200-33135600 Enhancers Fetal Stomach stomach
17 chr22:33134200-33140200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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