Variant report

Variant rs62113714
Chromosome Location chr19:43832652-43832653
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43821200-43837800 Weak transcription Right Atrium heart
2 chr19:43822800-43833600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr19:43827800-43833400 Weak transcription NHEK skin
4 chr19:43829200-43833600 Active TSS Hela-S3 cervix
5 chr19:43830000-43832800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
6 chr19:43830200-43835000 Weak transcription Esophagus oesophagus
7 chr19:43830400-43833400 Weak transcription Primary monocytes fromperipheralblood blood
8 chr19:43831000-43833400 Weak transcription Rectal Mucosa Donor 29 rectum
9 chr19:43831800-43833200 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr19:43832000-43832800 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
11 chr19:43832000-43832800 Genic enhancers Primary neutrophils fromperipheralblood blood
12 chr19:43832000-43833400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr19:43832200-43832800 Enhancers Colonic Mucosa Colon
14 chr19:43832600-43833400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr19:43832600-43833600 Weak transcription Rectal Mucosa Donor 31 rectum
16 chr19:43832600-43833800 Weak transcription Sigmoid Colon Sigmoid Colon

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