Variant report

Variant rs13054904
Chromosome Location chr22:23410918-23410919
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:23400800-23411600 Strong transcription Right Atrium heart
2 chr22:23408000-23411400 Enhancers Fetal Brain Male brain
3 chr22:23409000-23411200 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
4 chr22:23409200-23411800 Enhancers Left Ventricle heart
5 chr22:23409400-23411400 Bivalent Enhancer Adipose Nuclei Adipose
6 chr22:23409600-23411000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr22:23409800-23411000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr22:23409800-23411200 Weak transcription Brain Angular Gyrus brain
9 chr22:23409800-23411200 Weak transcription Fetal Brain Female brain
10 chr22:23410000-23411000 Weak transcription Brain Cingulate Gyrus brain
11 chr22:23410000-23411400 Weak transcription Lung lung
12 chr22:23410000-23411400 Enhancers Hela-S3 cervix
13 chr22:23410000-23411600 Weak transcription Primary B cells from peripheral blood blood
14 chr22:23410200-23411600 Enhancers Right Ventricle heart
15 chr22:23410200-23411600 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
16 chr22:23410400-23411400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
17 chr22:23410400-23411800 Weak transcription Primary B cells from cord blood blood
18 chr22:23410800-23411200 Weak transcription Spleen Spleen
19 chr22:23410800-23411800 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood

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