| Tag | Content |
|---|
EnhancerAtlas ID | HS180-22089 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr18:217770-218570 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr18:218141-218156 | AGGGTTCAAAGTGCA | + | 6.23 | | Hnf4a | MA0114.3 | chr18:218142-218158 | GGGTTCAAAGTGCACT | + | 6.34 | | MEOX2 | MA0706.1 | chr18:218073-218083 | AGTAATTAAC | + | 6.02 | | NR2C2 | MA0504.1 | chr18:218483-218498 | CGAGGGCAAAGGGCA | + | 6.54 | | PHOX2A | MA0713.1 | chr18:218240-218251 | TAATTAAATTA | - | 6.62 | | PROP1 | MA0715.1 | chr18:218240-218251 | TAATTAAATTA | + | 6.32 | | PROP1 | MA0715.1 | chr18:218240-218251 | TAATTAAATTA | - | 6.62 | | Phox2b | MA0681.1 | chr18:218240-218251 | TAATTAAATTA | - | 6.62 | | TEAD1 | MA0090.2 | chr18:218458-218468 | ATGGAATGTG | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTAAGCCAC GGCAACCTTG GGGAAAAAGT GGTTCAAGCA AGTGAGACAG TAAAGTGTGA 60
AGGTCCTGAC AGGAAAGGGA AAGACAGGAC CAAGAGGCCT GCTGTGGTTA AAGCAGAGGG 120
GAGGCATGGC CACACAGGAG AGTATGAGCC AGACCAAGGA GGTCTTTTAG GCCCTGGGAA 180
GGAGTTTGGA ATAGGCACTC ACTGGGAGAT TTTAAGCAGA TTAGACTTGG ACAATTATTT 240
TAAAGATCAC TGGCTGATGC ATGGAGCACT GACCACAACT AGAGAGATTA GTTAAGAGGT 300
CACAGTAATT AACAACTCTG GTCACAGGGT CACACTAGTC ACAAATACTG AGTGCTAACC 360
ACATGCCCTG TAGGGTTCAA AGTGCACTGT CTTATTTAAT CCTCAGAATA ACCCTGTGAA 420
ATGGGTACTG TTACTATTTA ACAGATGAGG AAAGGGAACT GGCGGTTTAA TAATTAAATT 480
AGCCTTAGTT GCCTAGTAAG TAAGTGGTAG AGGGAATCGA ACCTATGCAT TCTGACCAGA 540
GGCCTCTTGC CTTTAAACCA CTACTCTTCA ATTCCTATTT AAAGCCATGA GACTGCGGTG 600
TCACCCAGAA GGTTCTAGAT AAAGAGGCTA AGACCAATTC CTGATGTTAC TCCAAAATTT 660
GAGTTAGGCA GAGGATGAGG AGGCTGAAAT GGAATGTGAG GTGGAGTGGG CAACGAGGGC 720
AAAGGGCAAA CAGAAGAACC ATGGATTTGG ATTCTCATGG ACGCCAAGAG AAGAAAACAT 780
TAAGGGGAAC AGGATAGGTT 800
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