Variant report

Variant rs73717487
Chromosome Location chr6:4292605-4292606
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:4288600-4294400 Weak transcription Fetal Muscle Trunk muscle
2 chr6:4288600-4295600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr6:4288800-4295200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr6:4289000-4294600 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr6:4291400-4293000 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr6:4291400-4293000 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr6:4291600-4292800 Enhancers HUES64 Cell Line embryonic stem cell
8 chr6:4291600-4293000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr6:4291600-4293000 Enhancers Placenta Placenta
10 chr6:4291600-4293000 Enhancers HUVEC blood vessel
11 chr6:4291800-4293000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr6:4292000-4293000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr6:4292200-4294200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
14 chr6:4292200-4295000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr6:4292200-4295200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr6:4292200-4295600 Weak transcription HUES6 Cell Line embryonic stem cell
17 chr6:4292600-4292800 Enhancers iPS-15b Cell Line embryonic stem cell
18 chr6:4292600-4293400 Enhancers K562 blood

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