Variant report

Variant rs61903593
Chromosome Location chr11:59632273-59632274
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:59629000-59633600 Weak transcription K562 blood
2 chr11:59629600-59633000 Enhancers Primary neutrophils fromperipheralblood blood
3 chr11:59631400-59633800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:59631600-59634200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr11:59631800-59632600 Enhancers Stomach Mucosa stomach
6 chr11:59631800-59633200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr11:59631800-59633400 Enhancers HUVEC blood vessel
8 chr11:59631800-59633400 Enhancers NHEK skin
9 chr11:59631800-59634200 Enhancers HMEC breast
10 chr11:59632000-59632600 Enhancers Primary B cells from cord blood blood
11 chr11:59632000-59633400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr11:59632200-59632800 Enhancers Brain Cingulate Gyrus brain
13 chr11:59632200-59633000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr11:59632200-59633600 Enhancers Fetal Adrenal Gland Adrenal Gland

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