Variant report

Variant rs2619891
Chromosome Location chr5:60273799-60273800
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:60254200-60288800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr5:60262400-60288600 Weak transcription Ovary ovary
3 chr5:60262800-60288600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr5:60266200-60317400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr5:60268400-60275000 Weak transcription Aorta Aorta
6 chr5:60269200-60274200 Weak transcription Primary T cells from cord blood blood
7 chr5:60269400-60275400 Weak transcription Skeletal Muscle Female skeletal muscle
8 chr5:60270000-60275200 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr5:60270200-60275600 Weak transcription Gastric stomach
10 chr5:60270600-60274800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr5:60270600-60275400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr5:60270600-60287600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
13 chr5:60272000-60274200 Weak transcription Right Atrium heart
14 chr5:60272200-60275800 Enhancers Fetal Intestine Large intestine
15 chr5:60272600-60276000 Enhancers Fetal Intestine Small intestine
16 chr5:60272800-60274600 Weak transcription Skeletal Muscle Male skeletal muscle
17 chr5:60272800-60275200 Weak transcription ES-I3 Cell Line embryonic stem cell
18 chr5:60272800-60277000 Weak transcription Fetal Adrenal Gland Adrenal Gland
19 chr5:60272800-60288600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
20 chr5:60273000-60274400 Enhancers Pancreas Pancrea
21 chr5:60273000-60288800 Weak transcription Stomach Smooth Muscle stomach
22 chr5:60273600-60274000 Flanking Active TSS K562 blood
23 chr5:60273600-60275600 Weak transcription Spleen Spleen

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