Variant report

Variant rs11671058
Chromosome Location chr19:51473302-51473303
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:51470000-51473400 Enhancers Esophagus oesophagus
2 chr19:51470000-51474000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr19:51471200-51473800 Enhancers NHEK skin
4 chr19:51471200-51474000 Enhancers HMEC breast
5 chr19:51471200-51474800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr19:51471600-51474800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr19:51472800-51482200 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr19:51473000-51473400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr19:51473000-51477400 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr19:51473000-51480600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
11 chr19:51473200-51473400 Weak transcription Brain Cingulate Gyrus brain
12 chr19:51473200-51473600 Enhancers Brain Hippocampus Middle brain
13 chr19:51473200-51474000 Bivalent Enhancer Brain Inferior Temporal Lobe brain
14 chr19:51473200-51474800 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr19:51473200-51474800 Enhancers Brain Substantia Nigra brain
16 chr19:51473200-51476200 Weak transcription Placenta Amnion Placenta Amnion
17 chr19:51473200-51477600 Weak transcription ES-I3 Cell Line embryonic stem cell
18 chr19:51473200-51479000 Weak transcription H1 Cell Line embryonic stem cell
19 chr19:51473200-51479000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr19:51473200-51480800 Weak transcription ES-WA7 Cell Line embryonic stem cell
21 chr19:51473200-51482400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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