| Tag | Content |
|---|
EnhancerAtlas ID | HS101-27401 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr20:44105690-44107260 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr20:44106585-44106601 | CTTTGTTTACTCTGTG | - | 6.23 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGTTAATCT AGTTAGCAAT TCCTATAACC TTTTTTCAAG GTTCTTACCT TTCTTGCATT 60
GGGGTTAGAA CATGCTCCTT TAGCTTGGAG GAGTTTGTTA TTACCCACCT TCTGAAGCCT 120
ACTTCTGTCA ATTTGTCAAA CTCATTCTCC GTCCAGTTTT GTTCCCTTGC TGGCGAGGAA 180
TTGTGATCCT TTGGAGAAGA GGTGTTCTGG TTTTTGGAAT TTTCAGCCTT TTTGTGCTGG 240
TTTCTCCCCA TCTTCGTGGA TTTATCTACC TTTGGTCTTT GATGTTGATG ATCTTTGGAT 300
GGGCCTTCTG AGTGGACGTC CTTTTTGTTG ATGTTGATGC TATTCCTTTC TGTTAGTTTT 360
CCTTCTAACA ATCAGGCCCC TCAGCTGCAG GTCTGTTGGC GTTTGCTGGA GGTCCACTCC 420
AGACCCTGTT TGCCTGGCTA TCACCAGCAG AGGCTGCAGA ACAGCAAAGA TTGCTGCCTG 480
TTCCTTCCTC TAGAAGCTTT GTCCCAGAGG GGCACCCGCC AGATGCCAGC CAGAGCTCTC 540
CTGTATGAGG TGTCTGTCAG CCCCTGCTGG AAGGTGTCTC CCAGTCAGGA GACACGGAAA 600
TCAGGGACTC ACTTGAGGAG GCAGTCTGAC CCTTAGCAGA GCTCAAATGC TGTGCTGGGA 660
GATCTGCTGC TCTCTTCAGA ACCGGCAGGC AGGCTGAAGC CACATCCACA GCTGCCCCTT 720
CCCCCAGGTG CTCTGTCCCA GGGAGATGGG AGTTTTACCT ATAAGCCCCT GACTAGGGCT 780
GCTGCCTTTT TTTCAGAGAT GCCCTGCCCA GAGAGGAGGA ATCTAGAGAG GCAGTCTGGC 840
TACAGCGGCT TTGCCGAGCT GTGTTGGGCT CTGCCCAGTT TGAACTTCCT GGTGGCTTTG 900
TTTACTCTGT GAGGGGAAAA CTGCCTACTC AAGCCTCAGT AATGGTGGAC GCCCCTCCCC 960
CTACCAAGCT TGAGAGTTCC AGGTCAACTT CAGACTGCTG TGCTGGCAGT GAGAATTTCA 1020
AGCCAGTGGA TGTTAGCTTG CTGGGCTCCA TGGGGGTGGG ATCCGCTGAG CTAGACCACT 1080
TGTCTCCCTA GCTTCAGCCC CCTTTCCAGG GGCGTGAATG GTTCTGTCTC ACTGGCATTC 1140
CAGGCACCAC TGGGGTATGA AAAAAAAATC CTGCAGCTAG CTCAGTGTCT GCCCAAATGG 1200
CCACCTAGTT TTGTGCTTGA AACCCAGGGC CCTGGTGGTG TAGGCACCCA AAGGAATCTC 1260
TTGGTCTGTG GGTTGTGAAG ACCGTGGGAA AAGTGTAGTA TCTGCTCCAG AGTGCACTAT 1320
TCCTCACGGC ACAGTCCCTC ATGGCTTCCC TTGGCTAGGG GAGGGAGTTC CCTGACCTCT 1380
TGTGCTTCCC AGGTGAGATG ATGCCCTACC CTACTTCTGC TCGCCCTCCG TGGGCTGCAC 1440
CCACTGTCTA ACCAGTCCCA ATGAGATGAG CCACGTACCT CATTTGAAAA TGCAGAAATC 1500
ACCTGCCTTC TGCATTGATT CACTGGGAGC TGCAGACTGG AGCTGTTACT ATTCGGCCAT 1560
CTTGAAAGCT 1570
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