Tag | Content |
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EnhancerAtlas ID | HS101-13797 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr14:65531890-65533240 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYCN | MA0104.4 | chr14:65532011-65532023 | GCCCACGTGGCC | + | 6.27 | MYCN | MA0104.4 | chr14:65532011-65532023 | GCCCACGTGGCC | - | 6.27 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27251 | chr14:65531364-65534009 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I065064 | chr14 | 65531552 | 65533106 |
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Enhancer Sequence | GAATGTGTGG CCTGGGCCTC CTATAACCAT TTTTCTACCT AGAAGGAAAC CAGCGTGAGA 60 AGCCAGCACA CACATATGCT CTGAGACTGA GAAACATGGC CCTGATCACA TGGCTCCCGA 120 GGCCCACGTG GCCTCTGGAT TTTCAGTTAT ATGAGACAAT GTGAGTTGGA CTTACTATTA 180 CCTGCAACTG AAAGCAACCT AATACAGTCA TGTCACTTAA TGACGAGGAT ACACCCTGAG 240 AAAAGCAGTC AGGTGATCTC GTCGTTGTGT GAACATCATG GAGTGCACTT ACACAGACCT 300 AGATGGCCTA CCCTACCGCA CACCTAGGCT AGATGGGGTA GCCTGTTGCT CCTAGGCTAC 360 AAACCTGTGC AGCTTGTCAC CGTACTGGAT ACTGTAGGCA ACTGGAACAC AGTGGTAAGT 420 ATTTGTGAAT CTAAACATGG AAAAGGTACA GTAAAAATAC AGTATTATGA TCTCACGGGA 480 CCACTGTCGT ACATGCATTC TGTTGTTAAC CAAAACATGA TGTGGCGTGA CTATATACAA 540 AACTCTACCA CCAATTAGCC CCAAGACCAA GGCTTTACCT GCTGCTTAAA AAGTGCTGAC 600 CACTCTTGCC TCATCTGCCC AAACAATAAC CCCTAAGACA GTCCCTCCTG TTCTACCGCC 660 TCTCATTTGA TCCTTGACTC ACCTTGTAAG GTGGGTGAAG CAGGCGTATT ACCTGCCTTT 720 TACAACTGGA GAAACAGGTT GGAGAGCTTA CGTAAATCAC CCAAGGTTTC CCAGCTGTCA 780 AGTGGTGGTG CCTGAGCCCG AGCCCGTATC TGCTGCCTCC AAAGCCCATG CCCTTCCACC 840 ACCGCAGGCC TCTGAAGGAA GGTGAGAGGT CTCGGGGAAT AGGGGGCACT GGTGAAACAT 900 GCTTGGTTTA CCTCTAGGCT GGATGGCTGA GGCCCTGAAT ACCAGCTGCC ATCTGTCACT 960 AGGTCAGGGA TGGTGACAGC AAATAGGGCA GGCCCCTCAC CCTTCTAATG AGGTCTCCAC 1020 TTGCCACCAA GTGTGTGGCC ACACCAGTGC AGTGTGATGC CGTGTGGCTC AGTGAGGCCG 1080 TGATGAGTCC GTCTTCCCAG GAGCTGACCT GACAGCAGCC AGCTTTCTCC AACCTGGCCC 1140 AGGCACATCT AACAGGTTCC TGCACATCCT CACACTTTCC TGCAGTAACC CTCCTTGCCT 1200 CTGTTTTCCA CCAGCTGGGG AACTGGGGCC AGGTGGCCTC ACGTTCCTCC CTCCCGCTTC 1260 TCTGGCACAT CCAAGAACAA AACCAGGCAG GGCAGGGACA GGGCGCTCAT CATTAGCCCA 1320 GCTTAATGGA AACTTTCCCT TGCCCTCTGC 1350
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