Variant report

Variant rs7227343
Chromosome Location chr18:29069580-29069581
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29065400-29071800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr18:29065600-29070200 Enhancers HMEC breast
3 chr18:29066600-29071000 Enhancers Placenta Amnion Placenta Amnion
4 chr18:29067600-29076800 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr18:29068000-29070200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr18:29068000-29070400 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr18:29068000-29072000 Enhancers Hela-S3 cervix
8 chr18:29068200-29070000 Enhancers NHEK skin
9 chr18:29068200-29070200 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr18:29068200-29071000 Weak transcription NH-A brain
11 chr18:29068400-29071600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr18:29068400-29071600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr18:29069000-29069600 Enhancers Esophagus oesophagus
14 chr18:29069000-29069600 Enhancers Rectal Mucosa Donor 29 rectum
15 chr18:29069000-29071600 Enhancers Rectal Mucosa Donor 31 rectum
16 chr18:29069200-29072200 Enhancers Stomach Mucosa stomach
17 chr18:29069400-29070000 Enhancers A549 lung

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