Variant report

Variant rs35263478
Chromosome Location chr4:175319925-175319926
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:175316000-175320000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr4:175316000-175320200 Weak transcription NH-A brain
3 chr4:175318400-175320800 Enhancers A549 lung
4 chr4:175318600-175322800 Weak transcription ES-WA7 Cell Line embryonic stem cell
5 chr4:175319200-175320200 Weak transcription Rectal Mucosa Donor 31 rectum
6 chr4:175319200-175323200 Weak transcription Fetal Intestine Large intestine
7 chr4:175319400-175320600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr4:175319600-175320200 Weak transcription Sigmoid Colon Sigmoid Colon
9 chr4:175319600-175320400 Enhancers Rectal Smooth Muscle rectum
10 chr4:175319600-175320400 Enhancers NHDF-Ad bronchial
11 chr4:175319600-175320600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr4:175319600-175320800 Enhancers Muscle Satellite Cultured Cells --
13 chr4:175319800-175320000 Enhancers Hela-S3 cervix
14 chr4:175319800-175320400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr4:175319800-175320400 Enhancers HMEC breast
16 chr4:175319800-175320400 Enhancers K562 blood
17 chr4:175319800-175320600 Enhancers NHEK skin
18 chr4:175319800-175320600 Enhancers NHLF lung
19 chr4:175319800-175320800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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