Variant report

Variant rs6933617
Chromosome Location chr6:167721910-167721911
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167717800-167724000 Weak transcription Fetal Brain Female brain
2 chr6:167720200-167722200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr6:167720200-167723200 Weak transcription Rectal Smooth Muscle rectum
4 chr6:167720200-167723200 Weak transcription Stomach Mucosa stomach
5 chr6:167720400-167726400 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr6:167720400-167727600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr6:167720600-167722800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
8 chr6:167720800-167722000 Enhancers HepG2 liver
9 chr6:167721200-167722400 Enhancers Liver Liver
10 chr6:167721600-167724400 Enhancers Fetal Intestine Large intestine
11 chr6:167721800-167722000 Genic enhancers Fetal Intestine Small intestine
12 chr6:167721800-167728000 Enhancers Fetal Brain Male brain

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