Variant report

Variant rs11589756
Chromosome Location chr1:211800484-211800485
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr1:211793400-211803000 Weak transcription Fetal Intestine Small intestine
3 chr1:211795200-211802400 Weak transcription Right Atrium heart
4 chr1:211795200-211803400 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr1:211796600-211803600 Weak transcription Spleen Spleen
6 chr1:211798600-211801200 Weak transcription Primary hematopoietic stem cells short term culture blood
7 chr1:211798600-211803800 Weak transcription Hela-S3 cervix
8 chr1:211798800-211801800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr1:211800000-211800800 Enhancers Left Ventricle heart
10 chr1:211800000-211801000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr1:211800000-211802600 Enhancers Fetal Muscle Leg muscle
12 chr1:211800000-211807200 Enhancers Fetal Heart heart
13 chr1:211800200-211800800 Enhancers HSMMtube muscle
14 chr1:211800200-211801400 Enhancers K562 blood
15 chr1:211800200-211802600 Enhancers Fetal Muscle Trunk muscle
16 chr1:211800400-211800800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
17 chr1:211800400-211800800 Enhancers Brain Germinal Matrix brain
18 chr1:211800400-211802400 Enhancers Cortex derived primary cultured neurospheres brain

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