Variant report

Variant rs72996199
Chromosome Location chr6:143621586-143621587
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:143603200-143622200 Weak transcription Brain Hippocampus Middle brain
2 chr6:143605600-143622000 Weak transcription HepG2 liver
3 chr6:143607600-143622200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr6:143608600-143624200 Weak transcription Aorta Aorta
5 chr6:143608800-143624200 Weak transcription Ovary ovary
6 chr6:143608800-143629400 Weak transcription NHEK skin
7 chr6:143609400-143622400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr6:143610000-143626000 Weak transcription Fetal Intestine Large intestine
9 chr6:143613800-143624400 Weak transcription Fetal Intestine Small intestine
10 chr6:143615400-143643400 Weak transcription HSMM muscle
11 chr6:143616800-143624400 Weak transcription K562 blood
12 chr6:143618800-143634600 Weak transcription Psoas Muscle Psoas
13 chr6:143619600-143623600 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr6:143620600-143629600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr6:143620800-143622400 Weak transcription Liver Liver
16 chr6:143621200-143624200 Weak transcription Left Ventricle heart
17 chr6:143621200-143629000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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