Tag | Content |
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EnhancerAtlas ID | HS145-11798 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr19:42303310-42304000 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr19:42303689-42303707 | GGAGGGAAGGAATGAATG | + | 6.96 | EWSR1-FLI1 | MA0149.1 | chr19:42303685-42303703 | CGAAGGAGGGAAGGAATG | + | 7.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34052 | chr19:42302164-42304254 | HCC1954 |
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| 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 |
GH19I041798 | chr19 | 42301133 | 42303673 |
|
Enhancer Sequence | ACCATGATTG TAAGCTTGCT GGGTCTCACC AGAAGCCGAG CAGACGCTGG TGCCATGCCT 60 GTATAGCCTG CAGATCCCTG CATCAATTAA ATCTCTTTTC TTTATAAATT ACCCAGCCTC 120 AGACATTTCC TTATAGTAAC AAAAAATAGC CTAACACATT AGCCTAACCT AGAACTAAAT 180 CCCTTGTGTC AACAGAGTCA GTGCCAGGAA TGTCCGGGCC TCCCTCTCAG ATGCGCACCA 240 CTGCCCTCAC TCGACCTGAA ATCCTGTGTT TCCTGATGTG TCAGTGACAC TCCCACAGGA 300 GGATAAAACA CTCCCCACTC ACACCCTGCA CCAGCGCAGG GCCCAGTGAG AGACACACAC 360 TCAGTAGTTC TCTGACGAAG GAGGGAAGGA ATGAATGATG AATAATTCTT AAACTCTTCA 420 GAGACCGGAT CTTGGATGCA GAATCCTATA AGGTTCTGGC CACACCTGTT TCCTGTCCCT 480 CCAGGGGCCG GGATCCTTGT TGCATTCCTC TAACCCCTGC CCCTAAAGCT ACCCCAAGAA 540 CCGCATCTCA TGGGACTCTG GCACAGCTCA CCTGTGGGAA GGTTTTCAGG TCTCCCTGGT 600 CCTGGTTTGT GGGCGGCAGG TCACCCAGGC GCCGAGGCAA GAGACCAAGG ACACGAGCTG 660 TTCCAGTATA ATAAAATATA AAACAAGAAA 690
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