Variant report

Variant rs372393516
Chromosome Location chr4:7170592-7170593
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:7105800-7176000 Weak transcription Right Atrium heart
2 chr4:7161000-7172800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr4:7162800-7172800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr4:7167400-7170600 Enhancers Fetal Intestine Large intestine
5 chr4:7167400-7170600 Enhancers Fetal Intestine Small intestine
6 chr4:7167800-7182800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr4:7169000-7171200 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr4:7169400-7170800 Weak transcription Esophagus oesophagus
9 chr4:7170000-7172400 Enhancers Primary Natural Killer cells fromperipheralblood blood
10 chr4:7170400-7171000 Enhancers Spleen Spleen
11 chr4:7170400-7171400 Enhancers Primary B cells from peripheral blood blood

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