Tag | Content |
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EnhancerAtlas ID | HS048-03349 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:212658890-212660250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:212659447-212659458 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr1:212659447-212659458 | GGGTGACTCAG | + | 6.02 | MAX | MA0058.3 | chr1:212659946-212659956 | AGCACGTGGT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35302 | chr1:212655268-212663203 | HeLa |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 212659054 | 212659720 | chr1 | 212659085 | 212659948 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I212481 | chr1 | 212655167 | 212663350 |
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Enhancer Sequence | TAGCAGGAGC TCCCTCTGAT TTACCTTCAG GTAGTCCAGA GATGTGTGGC CAGGGTCTAC 60 TCATCAGCAA TAACCATACG CGGCTCTTTA TTGAGTGCTT TGTAGAATGC TGGGTACAGT 120 GCTAAGCACT TCACTGGCAC TCTCATTTCT TTCCCATAAC CATCTGATGA AATAGTACTA 180 CTTTCCCTGT TTTGTGCATA AAGAGATAAA GGCTTAGAGA GGTCAAGTGG CTTGGCCGAG 240 GTCACTGAGT AAGCCAGTCG ACAGGTGGCC CTAGAAACTG TCTGTGAATA TATATGTGTG 300 CTCTGAAAGG ACAGGGACCA TGCCTCCCCA TAAGCTCTGA CTCCCTAAGG GTAGGACTGT 360 TCCCCCCTCA GTAGCTTCCC TCCCCACCTT GCTAGCCTCC CTGAAGTGCC CAGGGCAACA 420 TGTGGCACAG CAGGGGTGCT CTGTTGCATG CTTGCTGACA GTCACGGACA GGGGACCAGC 480 CTCTTGCCAA AGAGAGAAGG CCTGTGGGAG CCTCAGACCA CAGAGGAGTG ACTGCGTGGA 540 TGCACCAGAC CATGGCTGGG TGACTCAGCG GCTGGCTGAC AGATGGATGA ATGGACGTCA 600 GTCCTATGGT GTGGCCCTTC CCTTTTCTCC CCGGAACAAT AACACATCCT GGCTCCGTGA 660 TTTCGTCGCC ATAGGAACTG GAAAACATTT GATAACATGG AGCCTCTGGG ACAGGTGGGC 720 TGAGCAGGTC TGAATAAAAA CAACCCTTTC CTGCCCCTTC ACCCAGAATC CAGGCATCTG 780 GTCTATTTGC AGCAGGTTAG GTAAATAGCC TGGGGGGAAC CATGCAGCCA CCTGAACTGA 840 CCGACCTTGT CCAAACTAGG AAGTCAGGGA AGTCACTGTC TATGCTGGCA GGACCTGGCA 900 CAAATTCCTG GTAGGAGGAA ATGGGGCCTC AGGCACCCTG TCTGGACATT CTGAGTATCC 960 TATGGTGTGC CTGTCCCCAG CACATGTGGG CTCTGTCCTG GACACTGTGG GGAATTAGAA 1020 GAAGGAAAGA AGGGGGACAG GGCTCCAGGC TCAGAAAGCA CGTGGTCTGC TAGGGGGCAG 1080 GGCACATATA GAAACAGTCC TATTAGGTCC CAGTCCTAGC ACAGATGGGG AATTACACGG 1140 ATCAGTAGGG AAGGAGTTGG GAGGTAGGTT CTGGGAGGGG ATGGGGTTTG GTGGAATGGA 1200 CCAGAATTCT CCATTCCCCA GCAAGCCCTA ACCAAGTGTG GCACCGTGCT CACATGCACA 1260 ATCTGGGTCC TGGGGTGACT GCTGGGGGCC AGGGCACTGC ATTCTCTTAC TGGCTTGGCC 1320 GTCTCAGCCT TCTCTGCCTG ATGCTTTTTG GTTCTACGGT 1360
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