Variant report

Variant rs2294236
Chromosome Location chr6:167727314-167727315
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167720400-167727600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr6:167721800-167728000 Enhancers Fetal Brain Male brain
3 chr6:167722800-167727400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:167723800-167728400 Enhancers HepG2 liver
5 chr6:167725200-167730200 Weak transcription Duodenum Smooth Muscle Duodenum
6 chr6:167725400-167730600 Weak transcription Rectal Smooth Muscle rectum
7 chr6:167726400-167728200 Enhancers Fetal Brain Female brain
8 chr6:167726800-167727800 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr6:167726800-167728000 Weak transcription Placenta Amnion Placenta Amnion
10 chr6:167726800-167730200 Weak transcription Fetal Intestine Small intestine
11 chr6:167726800-167730200 Weak transcription Thymus Thymus
12 chr6:167727000-167727600 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
13 chr6:167727000-167727600 Enhancers HUES6 Cell Line embryonic stem cell
14 chr6:167727000-167728200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr6:167727200-167727800 Enhancers HUES48 Cell Line embryonic stem cell
16 chr6:167727200-167728400 Enhancers iPS-15b Cell Line embryonic stem cell
17 chr6:167727200-167729000 Enhancers iPS-20b Cell Line embryonic stem cell

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