Tag | Content |
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EnhancerAtlas ID | HS050-30972 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr18:13235300-13236770 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr18:13236478-13236490 | TCTATTTTTAGC | - | 6.92 | MEF2B | MA0660.1 | chr18:13236478-13236490 | TCTATTTTTAGC | - | 6.44 | MEF2C | MA0497.1 | chr18:13236477-13236492 | TTCTATTTTTAGCAG | - | 7.06 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_04090 | chr18:13235339-13238726 | Brain_Anterior_Caudate |
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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 |
GH18I013235 | chr18 | 13235510 | 13236675 |
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Enhancer Sequence | GTAGATGCTT TCTCTTTAGA CGAGATGTCT CTATCATAAC CTTGATTCTC CTAAGCTGTT 60 TTCCTCTGTT CTTGGGATCA GGAAAAGTTC AAAGTAGAGA AAATTATGGT CTGTGAATCT 120 TTTTTCCATC TTTTCAAAGA AGACTAAATG TTCGACAGCT ACCTGGAAGT CTGACTCACC 180 CTCCAGGCAT CTGACTGTGC TTTTATTCTG GTATTAGTTT TGTTGCCTTG GATTTAAAAT 240 CCACAAGGAT TGTGAAAACC AAGTGCGGAA GAAGGAGAAA AAACTGAAAA ACCCCCCACA 300 TTCTAAATAG TGGTGAGGAC TCCTAGCAAA TTCATTCCTA TTGATGGCTT TTAGCCTGTG 360 TAATAGACCA CTAGCCATGT TGCATATGCG ATCGGCTTTG GTTGGATGAG TCGACTTTAT 420 TTCCCTCCCA GTCTGAGGAC ACATCTGCAG TCCTGCCCCT GGGGGAAGTG CACATCCAGC 480 CCTGGGGTGG GTTGCTTTTC TTGCAGGCTG GGTGCTGATC CTTGCCTCCG TTAGGAATCT 540 GTTTGAACCT CCACCCGGAG AACAGACTGG AAGGAAATAC ACCAGGACAT TAAAAATAGA 600 GGTCTTGGCA TATAGTGCTA AGGATGGTTT AAAAAATTCT GTCTTTTCAT CTTTTCCATA 660 TTTTCTACAA TGATCATGTG TTCCTGTTTT TATAATGAGA AAATTCCCAG TTAACTAGAT 720 TTGCTAAGGG TGTGGAATAA AAAGTCACTT TCTGAAAAAT TGTGGAAAAC AATTTGATGT 780 GTGTCTTTTT AAGCATTTTG GAAGCGCGGT GGAGTTGCTA TGGGGATAGC AAGGTTTACT 840 CTCTACAGAG AGTGGTTCCA TCTGGCACCC GTCGCTCCCG AGCTGGGCTG GGCAGTTCTG 900 TGCAGAGCAG TTTCTCGTTA GATGTGGAAA CAGTTACACA GAGAAGCACT GTTCCATCTT 960 TTCCCCCTGG AACCATCATT TTGCTTTGAT CTAACAATAG AAAAACTTTT TTTTTTTTTT 1020 TTTTTGAGAC AGAGTTTTGC TCTTGTTGCC CAGGCTGGAG TGCAGTAGTG CGATCTCGGC 1080 ACACTGCAAC GTCTGCCTCC CGGGTTCAAG CGATTCTCCT GCCTCAGCCT CCTGAGTAGC 1140 TGGGATTACA GGCATGCACC ACCACCCCAG GCTAAGTTTC TATTTTTAGC AGAGTTAGGG 1200 TTTCTCCATG TTGGTCAGGC TAGTCTCAAA CTCAGGTGAT CCGCCCTCAG GTGATCCGCC 1260 CTCCTTGGCC TCCCAAAGTG CTAGGATTAC AGGCGTGAGC CACCACGTCT GGCCTAGAAA 1320 AACATGTTAA ACTCCTTTCT GTACCCTCTG CTTCCTCTGG GTGCTGGCGT TGCCTGTGTG 1380 GGGCTCGGTC CGTGTTTCTC AGTCTGGAGG GTTTCTGAGC TGCTGTTGGA GTGGGGGTGT 1440 CTCCTGCACC TGGTGTTCCA TGTCGGACTT 1470
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