| Tag | Content |
|---|
EnhancerAtlas ID | HS048-11421 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr14:56548550-56550040 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr14:56549886-56549901 | AGAGTCCAGAGTTCA | + | 6.13 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTCCATGGAA CATTCTAGGG TGAATCTTAA GAGTGGAGAA GGCCTTGTTT AAGTAGGGTT 60
TGGTTAGCAT CTGGCCTGGA TTTAAATGAT CACATTAGGA GAGCAGCCTG TGAAATTTCA 120
GCTTAATTAA CTATAATATT AACTATTAGT GCAAAGAAAA ATGGGAGAAA GAGAGGAACA 180
CAGTGGGGAA AGGAAAAGGG AGAGGCAGAA GCTGGGAGAC TGACTAGATT CGAGGAAGAG 240
AAGAGGAAAA GTTCAATGCA GGTGCTTAGA GAAAACCATC AAAGATTGGA AGAGAACTAA 300
GGGTTCAGTG ACAGGGAGGC TAAGGGATGA AAAATTCCCA AAGGAAGGCA TCCAAAGTGA 360
GAGATTTCAA TAGAATAATT AGGCTAGATT GCCATAAAAA GACATAAAGG TATTGAGTTT 420
TAGCATCTCG TCCAAAAAGT TTGACACAGT GAAACTTAAG AAATGCAGCA GTGGCTTAAT 480
GGATAGCAGG CATTTTTTAA AATTTGAGGC ATGAGGCTAA ATATGAGCTT GAACATGTGA 540
GAAGAGGTTC CCATTAAAGA CATGGGAGGA AGTGGCATCG TGGACACACA CAGAAAGGTT 600
ATCTTGGAAA GATAAGGGAC ACAGCTTCCT GCCTCTGAGA TCAGAGGAAG GAGGGTGGAA 660
TAAACATGAA GCAAATCTGA TGCAAAGGGT AGAGGAGTTG AGGAAGTTTA CCTAGGATGG 720
CCTCCCTCTT CTCACTAAAG ATTGCTAATG AAAGGAGCTA GGAGCTCTGA AAGTAGAGGA 780
GTGCCACTTT AGATCATGTA CTTGGAAAAG CTGATCTGTA AAAAGTCGTA AATGTCCACT 840
TGGAATGCCT AAGAAGTATA TTTGAGACAC AGAATGAAGA GCAAGAAAAC AATGCTGCTA 900
TGGAGGTGGG GGGAAATGGA AGCTTGTTTT GAAAGCAAGC AATCCCAAAG ACCAAAAAAA 960
AAAAAAAAAA AAAAAAAAAA AGCAGCTTCA CATTCACACT CTAGTTGTGT GCCTAAACTT 1020
CCTTCCTTAC TGATTTTTGC AATAAAATAG TAGACCAATG GTTTGGACAT GTGTATACCA 1080
AAGAGAGCTC TGATAAATTA AAAGTCACCT TGGCAGAAAG CAGTGTTCTG GATCTGGAAT 1140
GCCCATGGTA TATCAAAAGG TTCTTTGCAG AACAACCCCA CAGATCAAGG GTCTGAGGTA 1200
GGAGTTTCTG AGTTATCTAG AGAGCTAGGC TATGGACAGG GCAGGAAATT CCTTCATAAA 1260
TTACCGACGT AGTATTTGCC TTTCCTAAAT GATCATAGAG CAAAGTACAA TGAAAATAGC 1320
ACAGTGCTGG GCTCTGAGAG TCCAGAGTTC AAGTCTGGGA CCCCTACTTA CTATATGGGC 1380
AAGTTACTTA ATCTCTCTGA ATCTGATCTA TAAGATCTAG ATAATCATAC CTACCTCATA 1440
GAACTGTCAG AATTGGATGA CATAATAAAT TCCCCTTCTT CTTTCCCTAC 1490
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