Variant report

Variant rs557518706
Chromosome Location chr1:173607642-173607643
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173606800-173607800 ZNF genes & repeats Cortex derived primary cultured neurospheres brain
2 chr1:173606800-173608000 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr1:173606800-173609600 Active TSS H1 Cell Line embryonic stem cell
4 chr1:173606800-173611400 Active TSS ES-WA7 Cell Line embryonic stem cell
5 chr1:173607000-173607800 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
6 chr1:173607000-173607800 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
7 chr1:173607000-173607800 Enhancers Right Atrium heart
8 chr1:173607000-173609200 ZNF genes & repeats hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr1:173607200-173607800 Enhancers Pancreas Pancrea
10 chr1:173607400-173607800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
11 chr1:173607400-173608400 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr1:173607400-173608600 Enhancers K562 blood
13 chr1:173607400-173609200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr1:173607400-173624600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
15 chr1:173607600-173609000 Active TSS H9 Cell Line embryonic stem cell

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