| Tag | Content |
|---|
EnhancerAtlas ID | HS101-46988 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chrX:44111980-44113630 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chrX:44112729-44112745 | CACAGTGTAAACAAAG | + | 6 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH0XI044252 | chrX | 44111957 | 44113570 |
| Enhancer Sequence | ATGATGTTCC TACTCTGAAA GGAAATTATT TAAAACATTT CTTAGCTGTT CTTGGTATTT 60
ATTCTCAATT CCTGGCACAA AAGATCTTTT TCTGGGGGTG GCTGGCAAGA TGGCCGAATA 120
GGAACAGCTC TGGTCTGCAG CTCCCAGCGA GATCAATGCA AAAGGAGGGT GATTTCTGCA 180
TTTCCAACTG AGGTATCCGG CTCATCTCAT TGGGACTGCT TAGACAGTAG GTGCAGCCCA 240
CGGAGGGCGA GCTGAAGCAG GGTGGGGCAT CGCCTCACCC GGGAAGCACA AGGGGTCAGG 300
GAACTCCCTC CCCTAGCCAA GGGAAGCCGT GAGGGACCGT GCTGTGAGGA ACAGTGTACT 360
CTGGCCCAGA TACTATGCTT TTCCCATGGT CTTTGCAACC CTCAGACCAG GAGATTCCCT 420
CAAGTGCCTA CACCACCAGG GCCCTAGGTT TCAAGCACAA AACTGGGCAG CTGTTTGGGC 480
AGACACCAAG CTAGCTGCAG TTTTTTTTTT TTTTCATACC CCAGTGGCGC CTGGAACACC 540
AGTGAGACAG AACTGCTCAC TCCCCTGGAA AGGAGGTGGA AGCCAGGGAG CCAAGTGGTC 600
TAGCTCAGTG GATCCCCCCA GCAAGCTAAG ACCGATGGCT TGAAATTCTC GCTGCCAGCA 660
CAGCAGTCTG AAGTCGATCT GGGACGCTGG AGCTTGGTGG GGGGAGGGGC GTCCCCCATT 720
ACTGAGGCTT GTGTAGGCGG TTTTCCCCTC ACAGTGTAAA CAAAGCTGCC AGGAAGTTGT 780
AACTGGGCGG AGTCCACCAC AGCTCAGCAA TGATTTTGTA GCCAGACTAC CTCTCTAGAT 840
TCCTCCTCTC TGGGTAAGGC ATCTATGAAA GAAAGGCAGC AGCCCCAGTC ACAGGCTTAT 900
AGATAAAACT CCCATCTTCC TGGGACACAG AACATGGGGG AAGGGGTGGC TGTGGGCACA 960
GCTTCAGCAG ACTTAAACGT TCCTCCTGCC AGCTCTAAAG AGAGCAGCAG ACCTCCCAGC 1020
ACAGTGCTCG AGCTCTGCTA AAGGACAGAT TGCCTCCTCA AGTGTGTCCC TGACCCCTGT 1080
GCCTCCTGCT AGGAGACACC TCCCAGCAGG GGTTGACACC TCTTAAAGGA GACCTCCGAC 1140
TGGCATCTGG AGGGTGCCCC TCTGGGACGA AGCTTCCAGA GGAAGGAACA GGTAGCAATC 1200
TTTGCTGTTC TGCAGCCTCC ACTGGTGATA CCAAGGCAAA CAAGGTCTGG ATTGGACTTC 1260
CAGGAAACTC CAGCAGACCT GCAGCAGAGA AGCCTGACTA TTAGAAGGAA AACTAACAAA 1320
CAGAAAGGAA TAGCATCAAC ATCAACAAAA AGGATGTCCA AATGAAAACT CCATCCGAAG 1380
GTCAACAACA TCAAAGACCA AAGGTAGATA AATCCACAAA GATGAAGAAA AACCAGCACA 1440
AAAAGGCTGA AAATTCCAAA AAACCAGAAC ACCTCTTCTC CTCCGAAGGA TCACAACTCC 1500
TCGCCAGCAA GAGAACAAAA CTGGACGGAG AATGAGTTTG ATGAATTGAC AGAAGTAGGC 1560
TTCAGAAGGT GGGTAATAAC TAACTCCTCT GAGCTAAAGG AGCATGTTTT AACCCAATGC 1620
AAGGAAGCTA AGAACCTTGA AAAAAGGTTA 1650
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