| Tag | Content |
|---|
EnhancerAtlas ID | HS034-25418 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr5:176521440-176522330 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr5:176522000-176522018 | GCTTCCTTCCTTCCTTCC | - | 10.05 | | EWSR1-FLI1 | MA0149.1 | chr5:176522004-176522022 | CCTTCCTTCCTTCCTGCT | - | 7.69 | | ZNF263 | MA0528.1 | chr5:176522003-176522024 | TCCTTCCTTCCTTCCTGCTCC | - | 7.23 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_30460 | chr5:176520882-176523067 | Fetal_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I177093 | chr5 | 176520362 | 176528755 |
|
Enhancer Sequence | TTGACTTCAC ATCTCCTTGT CAGCCTCACA GGCCCTCTAC CTCCTTCCTT ATGGTTCCCC 60
CCAGACACAC CCTCAGCCTC CCTTGGACCC TCCCTAGGTC TGCCCCCCAC GTCCACTGCT 120
GTAGGAGGAC AGCCCTTCTG CTTGCACCCA GGCCCAGCCC CGGGGTGCTC TTGCTGGGCA 180
CTCCTGCACC CCACCCATCA GGGCCTCTCC TTGCAGTTCC CCAGCCCCCT CTGCAAGAAT 240
GGCCTCCACT GCTCTTCTGC TCCTCCCCTC CTCTCTACAC AGCTGGGGCC ACCTGGTGCT 300
CCCTGGGAGG CAGGGATTGA GAAATGCACA TTGTGTCATT GGCCCAGGGC CACAGGTCAG 360
CCCCAGGGGC TCAGCCAGAG AAGCCAAAGC AGCCTTCTTC CCAAGCTCCC CGGCTGCACC 420
CGGCCTGCCG CCAGCTCCCT GAATTCCCAG GCCAGTTGGA AGCCAGGCCC TGGTCAAACA 480
GACCCCAGGG CGCCAGCCTG CTTTCCGCAC CCAGAAGCTC TGACCCCATG CGGGGACTAC 540
CGCTGACCCC TCCAGCGGCA GCTTCCTTCC TTCCTTCCTG CTCCGAGCTC TTCCCCTCTC 600
TCCTGTGTCC TGGGCCTGCC CGCTGGAAGG CCTGCCTCTT AGATCCTTGA TACAGTTGCA 660
TCCTTGCAAC TGCTGTGACA GGCAGGGTGT GACCCACTGC TCTGTTTCCC ACAAGACGAA 720
CCTGAGGTTC AGAGACGCTA GGAGACTTTT TCAAGGCCAC ACAGCCTAGC AAGGATTCAG 780
CCCTAGACCT ACGTAGCCCT GGTCCAGTGC TGCTTGTCCT GCACCTGCCT CTGCATGCTC 840
CCTCGTGCAG TTGGAGGGCA GCCTCTTCAC CCCGTCTGCT GCCCTTACAG 890
|
