Tag | Content |
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EnhancerAtlas ID | HS180-04378 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:208355840-208357180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:208356950-208356970 | GAGGGGGGGGTCTTTGGGGG | - | 6.08 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23661 | chr1:208355735-208357908 | Colon_Crypt_1 | SE_31633 | chr1:208355878-208357061 | Gastric | SE_33895 | chr1:208356937-208358912 | HCC1954 | SE_54968 | chr1:208355867-208359565 | Stomach_Smooth_Muscle | SE_58948 | chr1:208347899-208379506 | Ly3 |
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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 |
GH01I208176 | chr1 | 208349541 | 208359979 |
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Enhancer Sequence | AATTTTTTGG CAGTTCCATA GCTACTGAAA GCGTCTTGCT CTGCCCATGC GAGTGGCAAT 60 GTTGGGACAC TGCATTCATG GAATGGAGCT CCGGAAGGGC CTTATGAGGC CGTCTCCTCA 120 TTTTGCAGAT AGGAAAACTG AGGCGTATTT GCCATCACTC TGCTTGTTTG TAGCAAAACA 180 GGGGCTCTCC TGCTTTCCCC TGTAGTTCTG AGCAAGAAAA GGGGTTTGAA GGGCAGCCTT 240 TCAGCTGGGC AGAGCTGTGC GGGGAGTTTG CATCCAGTAC TGCTGGGTTC TAGCCCATTC 300 CTAGGTTGGG CAGCTCAGCC TCTCCTAGAG GAGACTCTGG CTGCTGAGTG ACCCGGTGAA 360 TTAATGCAGC TTCTGGCTAG GGGTAGGGGA CAGTAAAAGC CAAGGAGCCA AGATCAGAAA 420 AAGGAATAGC TTCTTCCCAT GTGGAATCAA GCTGGGGCTG CCAACCTCCT AGTCAAGAAA 480 GAAAGCTTTT CCTCTCTCTT CCTCCTGTTT ACCCACAGCG ACTGGGGGAG GCTGTACAGA 540 GAGGCAGGTT GAATGTATTC AGTCTGGGAT AGGGAGGGAA AGTTCCTCTG GGGCTCCCCC 600 TTCGTCTAGG GGAGAGGTCA GAAGAACAAA GGTCACAGAT GGACCTGCCA TGATATGGGA 660 GGAGGCACAT GTGTTGCAGT GAGCCATGGA GGGTGGGGGC ACAAGAGTTT GGCAACTCAG 720 ACAGGGGAGA AGCCACTGAT GGCTTATAAA CCAGACAAGG TTCATCCTGA ATCCGGAGGG 780 AGGGCAGTGA GAGCCCCATG AACTCACTTT CTTGAATGTC ACTAACATTT CATTTCACCC 840 TCACTCTGCC TTCCTGTCTC TTTTTTTCTC TTTCTCCCTT AACCTTCCTC AGCAGGGGAT 900 GGGGGAGTAG AGGGAGCCGG AAAGGAGGTC TGCAGGCCTC GTTGACTCTG CTGACCATCC 960 ACAGCCAGGA GCTGTTGCTG ACAGAAAAGA AATGAAGGGG CAGAGATGGG AGGGAAACCA 1020 GATGTCCGCA GTTGCAGCAC CATTCTGCGC AGCGTCCCCA CTGGGGTCCC TGCTGTAGAC 1080 GAGAAGCCAG AGCCAGGTGC CAGAGAGGGA GAGGGGGGGG TCTTTGGGGG TGGGGGACGG 1140 TGCTGGGCCC CACTCCTGCT TATCTACCCC TCAGTTTCTT TTACCTGGGA AACAGATCAC 1200 CAAGAGAGGC CCGTCTGATG CTTTAAGCTG GGAATTTGGT TTATTCTGGG GCAGATGAAA 1260 AAGAAATTGC ACTGTAGCAT CTTACAAAAC TGCCCCCTTT TCAACTGGGA CTGAGAGTTG 1320 GAGACTTTTC CTTTAGGCTT 1340
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