Variant report

Variant rs11119776
Chromosome Location chr1:211803231-211803232
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:211790400-211803600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:211795200-211803400 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr1:211796600-211803600 Weak transcription Spleen Spleen
4 chr1:211798600-211803800 Weak transcription Hela-S3 cervix
5 chr1:211800000-211807200 Enhancers Fetal Heart heart
6 chr1:211800800-211803600 Weak transcription Left Ventricle heart
7 chr1:211802000-211803400 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr1:211802000-211803400 Enhancers K562 blood
9 chr1:211802000-211803600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr1:211802000-211806400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
11 chr1:211802400-211803400 Weak transcription Cortex derived primary cultured neurospheres brain
12 chr1:211802600-211803400 Weak transcription Right Atrium heart
13 chr1:211802600-211803600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr1:211802600-211803600 Weak transcription Fetal Muscle Trunk muscle
15 chr1:211802600-211803600 Weak transcription Fetal Muscle Leg muscle
16 chr1:211802800-211804200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
17 chr1:211803000-211804800 Enhancers Fetal Intestine Small intestine

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