Variant report

Variant rs386644504
Chromosome Location chr2:31503706-31503707
allele CT/GA
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:31486600-31510000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr2:31492400-31507800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr2:31492800-31510600 Weak transcription Aorta Aorta
4 chr2:31494400-31505600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:31495800-31509800 Weak transcription Esophagus oesophagus
6 chr2:31497000-31510400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr2:31501400-31505600 Weak transcription HUVEC blood vessel
8 chr2:31502000-31505600 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr2:31502200-31504200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr2:31502600-31504600 Weak transcription Placenta Placenta
11 chr2:31502600-31505400 Weak transcription Fetal Adrenal Gland Adrenal Gland

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