Tag | Content |
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EnhancerAtlas ID | HS051-28352 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chrX:44112180-44113380 | 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 | CTCATCTCAT TGGGACTGCT TAGACAGTAG GTGCAGCCCA CGGAGGGCGA GCTGAAGCAG 60 GGTGGGGCAT CGCCTCACCC GGGAAGCACA AGGGGTCAGG GAACTCCCTC CCCTAGCCAA 120 GGGAAGCCGT GAGGGACCGT GCTGTGAGGA ACAGTGTACT CTGGCCCAGA TACTATGCTT 180 TTCCCATGGT CTTTGCAACC CTCAGACCAG GAGATTCCCT CAAGTGCCTA CACCACCAGG 240 GCCCTAGGTT TCAAGCACAA AACTGGGCAG CTGTTTGGGC AGACACCAAG CTAGCTGCAG 300 TTTTTTTTTT TTTTCATACC CCAGTGGCGC CTGGAACACC AGTGAGACAG AACTGCTCAC 360 TCCCCTGGAA AGGAGGTGGA AGCCAGGGAG CCAAGTGGTC TAGCTCAGTG GATCCCCCCA 420 GCAAGCTAAG ACCGATGGCT TGAAATTCTC GCTGCCAGCA CAGCAGTCTG AAGTCGATCT 480 GGGACGCTGG AGCTTGGTGG GGGGAGGGGC GTCCCCCATT ACTGAGGCTT GTGTAGGCGG 540 TTTTCCCCTC ACAGTGTAAA CAAAGCTGCC AGGAAGTTGT AACTGGGCGG AGTCCACCAC 600 AGCTCAGCAA TGATTTTGTA GCCAGACTAC CTCTCTAGAT TCCTCCTCTC TGGGTAAGGC 660 ATCTATGAAA GAAAGGCAGC AGCCCCAGTC ACAGGCTTAT AGATAAAACT CCCATCTTCC 720 TGGGACACAG AACATGGGGG AAGGGGTGGC TGTGGGCACA GCTTCAGCAG ACTTAAACGT 780 TCCTCCTGCC AGCTCTAAAG AGAGCAGCAG ACCTCCCAGC ACAGTGCTCG AGCTCTGCTA 840 AAGGACAGAT TGCCTCCTCA AGTGTGTCCC TGACCCCTGT GCCTCCTGCT AGGAGACACC 900 TCCCAGCAGG GGTTGACACC TCTTAAAGGA GACCTCCGAC TGGCATCTGG AGGGTGCCCC 960 TCTGGGACGA AGCTTCCAGA GGAAGGAACA GGTAGCAATC TTTGCTGTTC TGCAGCCTCC 1020 ACTGGTGATA CCAAGGCAAA CAAGGTCTGG ATTGGACTTC CAGGAAACTC CAGCAGACCT 1080 GCAGCAGAGA AGCCTGACTA TTAGAAGGAA AACTAACAAA CAGAAAGGAA TAGCATCAAC 1140 ATCAACAAAA AGGATGTCCA AATGAAAACT CCATCCGAAG GTCAACAACA TCAAAGACCA 1200
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