Tag | Content |
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EnhancerAtlas ID | HS048-30625 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:167772830-167773780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr5:167772945-167772956 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr5:167772945-167772956 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr5:167772945-167772956 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr5:167772945-167772956 | TAATTAAATTA | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41838 | chr5:167772972-167774759 | LNCaP |
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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 |
GH05I168345 | chr5 | 167772518 | 167774993 |
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Enhancer Sequence | AGATACATAT CCAGTCATTG ACTTTCCCCT GATTAAGAGA GCAAGCTGTG GAGTCAGAGT 60 GGCTGGGTTA GAATCCCAGC TTCTACTTGT ACAATCTGTG TGACCCTTGA TAAGATAATT 120 AAATTATTGG AGTCTCAGTC TTCCCCAGTG CGAGCCTGCG GGGACCCTGT GTGGTGAGAG 180 AGGCTCTGTC CAACACCACC AGGGCAGGGA GAAACAACTG GCCCCATTTC ATAACAGAAT 240 CAGATGGCCC AGGAGGGACC CCCAAGAGTG TTTGATTGGG ATGCCCAGCC CTGGCTCTCC 300 CTCCACCTGA AGCCCACCGA GATTAATCGG GTACCTATGT CTGATGTCGA AAGGAAGGAG 360 AAGGGTTTGC TGAGGACTGA TCTCAGCAGG TCTGAAGTTA GGCTGAAAAT CTGTGTTTTG 420 CAAGTATAAA CACTGTAAGG AGATACAAGA TACTTAGGAA AGCAGGGAGC AGCCCAGAGT 480 GCGAGCCCAG TGTCACAGAC TCAGAATGAT CCAGGAACCA TACAGGGAAA CAATGCCCGC 540 AGAAAACAGC AGCTGCAGAT GTATTTCCTC CCCTGCTCAG CTCCTCCTGC CCTGCATGAG 600 CAAGACCCTA AGACCCTCAA GAGACCCTCA GAAAATCTGT CCAGTGCCCC AACATCAGAA 660 TGAAGGCATC TGGGGAACAG GTAGAAACAC AGTGCCTGAC ACACCGATGC CCTTAGTAGG 720 CGTGCCTGAA ATGCTTGTTG AGAAAATAAA TGCATGCAGA ATACAAGACT CATTTGAATA 780 CCTCCTGTTT GACTAGGAGC AGAGGAATTC AGGTGAGCCA TTGTTGAGAA ACCTGTATGA 840 CTAGTTAGAA TTAGTTAAAA AGTAAAAGCC GGGACCTCCC AGGGCCCATG CTTGGTATGC 900 TGTGAGTGAG ATTGTTCTGT AAGTTGGTGG TGGCTTAGAA ATGATTGACA 950
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