Variant report

Variant rs10857395
Chromosome Location chr4:143452535-143452536
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:143428800-143453000 Weak transcription Primary hematopoietic stem cells blood
2 chr4:143438800-143462800 Weak transcription Aorta Aorta
3 chr4:143444400-143456400 Weak transcription Primary T helper cells PMA-I stimulated --
4 chr4:143444800-143468400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr4:143451000-143454400 Weak transcription Primary T helper naive cells fromperipheralblood blood
6 chr4:143451200-143453000 Enhancers Fetal Intestine Large intestine
7 chr4:143451200-143453000 Enhancers Fetal Intestine Small intestine
8 chr4:143451400-143455400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr4:143451800-143452600 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr4:143451800-143453600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr4:143452200-143453200 Weak transcription H9 Cell Line embryonic stem cell
12 chr4:143452200-143453400 Weak transcription ES-I3 Cell Line embryonic stem cell
13 chr4:143452200-143453400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
14 chr4:143452200-143453400 Weak transcription Left Ventricle heart
15 chr4:143452200-143453800 Enhancers Fetal Heart heart
16 chr4:143452400-143453400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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