Variant report

Variant rs1509661
Chromosome Location chr11:34859150-34859151
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:34858000-34859200 Enhancers HUES6 Cell Line embryonic stem cell
2 chr11:34858000-34861200 Enhancers Esophagus oesophagus
3 chr11:34858200-34860800 Enhancers HepG2 liver
4 chr11:34858400-34859200 Enhancers HUES48 Cell Line embryonic stem cell
5 chr11:34858400-34859200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr11:34858400-34859600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr11:34858400-34859600 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr11:34858600-34859200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr11:34858600-34859400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr11:34858600-34859400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr11:34858600-34859400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr11:34858600-34859600 Enhancers HUVEC blood vessel
13 chr11:34858800-34859600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
14 chr11:34858800-34859800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
15 chr11:34859000-34859200 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
16 chr11:34859000-34859200 Enhancers NHLF lung
17 chr11:34859000-34859400 Enhancers Brain Substantia Nigra brain
18 chr11:34859000-34909400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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