Variant report

Variant rs375299928
Chromosome Location chr4:187217939-187217940
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:187212600-187219000 Weak transcription H9 Cell Line embryonic stem cell
2 chr4:187217400-187218000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
3 chr4:187217400-187219200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr4:187217600-187218000 Enhancers ES-I3 Cell Line embryonic stem cell
5 chr4:187217600-187218000 Enhancers H1 Cell Line embryonic stem cell
6 chr4:187217600-187218200 Enhancers Duodenum Mucosa Duodenum
7 chr4:187217600-187218800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr4:187217600-187219000 Enhancers Liver Liver
9 chr4:187217800-187218000 Enhancers HUES64 Cell Line embryonic stem cell
10 chr4:187217800-187218000 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr4:187217800-187218000 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr4:187217800-187218000 Enhancers Duodenum Smooth Muscle Duodenum
13 chr4:187217800-187218000 Enhancers Fetal Heart heart
14 chr4:187217800-187219200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell

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