Tag | Content |
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EnhancerAtlas ID | HS040-20234 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr2:97151200-97152420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr2:97151952-97151970 | GGAAAGCGAAACTTAGCC | + | 6.61 | RUNX1 | MA0002.2 | chr2:97151283-97151294 | AAACCACAGAG | - | 6.14 | SPIC | MA0687.1 | chr2:97152342-97152356 | GTCTTCCTCTTTTT | - | 6.22 | Sox6 | MA0515.1 | chr2:97151896-97151906 | CCATTGTTTT | + | 6.02 | Stat4 | MA0518.1 | chr2:97151946-97151960 | CTTCTAGGAAAGCG | + | 6.17 | ZIC1 | MA0696.1 | chr2:97151220-97151234 | CACCCCCTGCTGTG | + | 6.99 | ZIC3 | MA0697.1 | chr2:97151220-97151235 | CACCCCCTGCTGTGC | + | 7.14 | ZIC4 | MA0751.1 | chr2:97151220-97151235 | CACCCCCTGCTGTGC | + | 6.61 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65729 | chr2:97150674-97152957 | Pancreatic_islets |
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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 |
GH02I096485 | chr2 | 97150742 | 97153281 |
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Enhancer Sequence | TGGCTATAAA ATGAGAATGT CACCCCCTGC TGTGCCCCTC GCACTTCACA CAGATCTGAG 60 AGAAACAAGC TGGCTGCGCC AGAAAACCAC AGAGGCACCA CCTCTAGATT CCTGTGGAGA 120 TCCTACCACC CATTCCTTCA AAGGAAGGGA CTGGGGAGCA GGGCAGCTGG CAGCAGAGGC 180 TAATCTGCTG TGCAGGTCTG TGGAGGAAGG GACCGTGCGC GGTTCTCTTC CCTCTGCCTC 240 CAGGCTTAGG AGTCATCCCC CACACGCGGG ACCCCCAGTC CCCACTGTAG ACTTCTTCCA 300 AGTGGAATTT CTTCAACAGT TGATCAGCAG GGGGGTCAGG GCGTGCAGTG CAGGGGTGGG 360 GGTGGGGGTT GCGAGAGGAG TGCCATCAGG GAGTAATGCT GGCGAGGCCT CATGAGGACA 420 GCACGCTGGG GCCCTGTGTG CGATGGGCGC CAGGGGCAGG TGACATGGTG GACCCGGTCT 480 CCCCCTTCCC TCTCCAATTG ATCTAACAGA AAGCCTGATG TGAAAGTCTG GACGAGGGAA 540 TTTTCCCATA TCTGCAGGAA AGCCCCGTAG CAGGTCCCTG GAGCCAGCCC GGGCAGGCCT 600 CCGCTTACAG GACGCTAAAG ATCCCTGGTT GCAGTTCTAC TTTCTTTTTA CTGCGTGTAT 660 TCTGCCCCTG TGATAATGAT TCATTACACG CTTCCTCCAT TGTTTTACTC CAGTGACCTC 720 ACGTCAAGGG AACCTGTGAT CTCAGGCTTC TAGGAAAGCG AAACTTAGCC GCAGCCTGCC 780 TCTCTCCCAG CCTGCCTTAC AAGCACTGTG AGTTGCTGGC TGGCCGAGGC CCTGGCAGAT 840 CAGACCTCCT GCAGCCCCAG GGATGGCACG GGCACCGCCA CTCACGCAGC CGGTAGAGCG 900 CTCCTAGGGC AGGCCCATCT CGCTTCCCTC TCGCCTCTCC CCCCCGCTTT TGCTTGGGCC 960 AATCCGACCT CCTCACCTCC TCGTAGCTCC CCCAGCACAC CTTGCCTTTG CCATCTCTGC 1020 ATGTGCCGCG CCTGCTGTCT GGAAGACCGG CATCCATTCC CCTCTGCCTT CCAAACTCTC 1080 CCTGTAGGAC CAGCTCAAAA GGCATCTCCT CTTCAGCTGT TCCTGCTGCC AGGGCTAATA 1140 TCGTCTTCCT CTTTTTTCCC CACTAGCGCT TCTTTGTCTA TTTTGGAGAG GTTTTGTTTT 1200 GGATAACTTT TTAATTGAGA 1220
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