Variant report

Variant rs550332534
Chromosome Location chr21:46803623-46803624
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46787600-46806800 Weak transcription Right Atrium heart
2 chr21:46793400-46806400 Weak transcription Esophagus oesophagus
3 chr21:46798200-46807600 Weak transcription H9 Cell Line embryonic stem cell
4 chr21:46800200-46805200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr21:46800800-46805800 Weak transcription Pancreas Pancrea
6 chr21:46802800-46804000 Enhancers Fetal Muscle Leg muscle
7 chr21:46802800-46808800 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr21:46803000-46804000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr21:46803200-46804200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr21:46803200-46807400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr21:46803400-46803800 Enhancers HUES48 Cell Line embryonic stem cell
12 chr21:46803400-46804000 Enhancers H1 Cell Line embryonic stem cell
13 chr21:46803600-46803800 Flanking Active TSS iPS DF 19.11 Cell Line embryonic stem cell
14 chr21:46803600-46804000 Bivalent Enhancer Fetal Stomach stomach
15 chr21:46803600-46804000 Enhancers K562 blood
16 chr21:46803600-46804200 Enhancers HUES6 Cell Line embryonic stem cell
17 chr21:46803600-46804200 Flanking Active TSS HepG2 liver

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