Tag | Content |
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EnhancerAtlas ID | HS148-08030 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr18:21441950-21443060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr18:21442770-21442784 | AGTCCCCTGGGACT | - | 6.32 | EBF1 | MA0154.3 | chr18:21442770-21442784 | AGTCCCCTGGGACT | + | 6.57 | IRF2 | MA0051.1 | chr18:21442158-21442176 | GGAAAACGAAAGCTAACA | + | 6.69 | NEUROG2 | MA0669.1 | chr18:21442378-21442388 | GACATATGTT | - | 6.02 | ZNF263 | MA0528.1 | chr18:21442962-21442983 | GGGGGAGAGAGAGAGAGAGAG | + | 6.3 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35820 | chr18:21440540-21443393 | HMEC |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I023860 | chr18 | 21440821 | 21446901 |
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Enhancer Sequence | CACACACTGC GCCCCACCAT TGCCATGCAT GAGCTACCAG CAAAGGAAAT CACCCACAAT 60 GTTTTTCTCA GTTTTTACCT AATGTCAAAG AATTTTCCTC CAGGGAAATA ACCATTTAAA 120 TACTATCTAT TGCAAATGGG ACATGCGTGC TTTTAAATGC CAATGCTGAG AATTCTTTAT 180 TTTAAGGCAG AAGAAAGCCT CTTTGTTAGG AAAACGAAAG CTAACAAGTG ACTCACAAGC 240 TTATTAAAAG AAACACAGGA TCTGGTGGCA GTTCGACTTT CCTAAGTAGA ATCACATAGT 300 TACACACTCC TCAGGAACTT ACAAACCACT TGCTCTTCCT TTGCTGCAAG AGTTATTATG 360 CCAGAGGCTG GCCACCTCCA TCCATTTTAT GAGGACAGAA ATGCAGGCCT CATGTGGAAA 420 CATGAGGTGA CATATGTTTC TTAGCAAGGG TGGAACTTGC TAACGGGTGG ATTTCACAGG 480 GCCTGGCTCA GGGGATGCCA AATTCTCACA TTAGGAAGAC TAAAATAATA GGGCCTTGTT 540 GGCCTGAGGT CTCTAACTTT GTCTTCTGGG TGAAGGACTG TGGGTTTTGA CATCTGAGTG 600 TGGGAAATGT TGCCTCTCTT CTATGATCCC ACTTCTCTTT CACTTAATAC TCCTCTTTAC 660 CGCTATATGA CGGGCCCATG TGTTGATTAT CTATTGCTAT GTAACAAATT ACTCCAACAC 720 TTCGCAGCTT AAAGCAGTAA TGATTATCTT GGATGAGGAA TTCAGGAGGG GATGGCCCAG 780 AGTCTTCCTA GGTTACTGTC AAGATGTCAA CCAGGGCTGT AGTCCCCTGG GACTGCAGCA 840 TCTGCTTCCA AGCTCACCCA CATGGCTGTT AGCAGGCCTC TGCTTCTGGC TAGCTGTGGG 900 CTGGAAGCCT CCATTTCTCA TCACGTGAGA CCCTCCATAG GCTACCTGAG GGTCCTCATG 960 ACATGACAGC TGGCTTCCCC CAAAGCAACT TATGGGGGGT GGGTAACAGG GTGGGGGAGA 1020 GAGAGAGAGA GAGAAAGAGA GAGAGAGAGA GAGAGCTAGC TCAAGACAGA AGCTGCAGTG 1080 TTTTTGTAAC CTAATTTCAG AACTGCCATG 1110
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