Variant report

Variant rs537014
Chromosome Location chr11:104951863-104951864
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:104948000-104953200 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr11:104950200-104953400 Enhancers Cortex derived primary cultured neurospheres brain
3 chr11:104950400-104952000 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr11:104950400-104952200 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr11:104950600-104952400 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr11:104950600-104953800 Enhancers HUES48 Cell Line embryonic stem cell
7 chr11:104950800-104952200 Enhancers Fetal Intestine Small intestine
8 chr11:104950800-104953000 Enhancers HUES6 Cell Line embryonic stem cell
9 chr11:104951000-104952000 Weak transcription H1 Cell Line embryonic stem cell
10 chr11:104951000-104952200 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr11:104951000-104953600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
12 chr11:104951200-104952000 Active TSS Duodenum Mucosa Duodenum
13 chr11:104951200-104952400 Enhancers Primary monocytes fromperipheralblood blood
14 chr11:104951400-104952000 Enhancers Right Atrium heart
15 chr11:104951600-104952000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr11:104951600-104953000 Enhancers H9 Cell Line embryonic stem cell
17 chr11:104951800-104952000 Enhancers HUES64 Cell Line embryonic stem cell
18 chr11:104951800-104952000 Enhancers Monocytes-CD14+_RO01746 blood
19 chr11:104951800-104953200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell

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