Variant report

Variant rs56718647
Chromosome Location chr22:21253521-21253522
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:21240200-21270600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr22:21240200-21271000 Weak transcription Right Atrium heart
3 chr22:21242200-21254200 Weak transcription HepG2 liver
4 chr22:21243200-21258200 Weak transcription HMEC breast
5 chr22:21243200-21258400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr22:21244600-21254400 Weak transcription Primary hematopoietic stem cells short term culture blood
7 chr22:21244600-21256000 Weak transcription Primary mononuclear cells fromperipheralblood Blood
8 chr22:21244600-21258200 Weak transcription NHEK skin
9 chr22:21244800-21253600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr22:21244800-21254200 Weak transcription Liver Liver
11 chr22:21244800-21254400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr22:21244800-21254400 Weak transcription Fetal Intestine Large intestine
13 chr22:21253400-21253600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr22:21253400-21258200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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