| Tag | Content |
|---|
EnhancerAtlas ID | HS044-08393 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr21:44043950-44045700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr21:44045502-44045515 | AGGGACAGCTGGA | - | 6.16 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 44044600 | 44044710 | | chr21 | 44044839 | 44045000 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH21I042624 | chr21 | 44044701 | 44044770 |
| Enhancer Sequence | CCAGACAGGG TCTGTGCTTC TCCCCTAAGC CCCGGTGCCC TCATGCAATC CAGTCCCTCC 60
CTGGAGTTCT TTGCTCCGTG TCTGTCTCCA CGCCAGGCCT CTATGAGGAT GAGCTGTGGT 120
TACTCAACCA GGATCTCGAG GCCCCAGCTC AGTGTCCAAT ACACGTCAGC ATTCAAAATC 180
ATACTACTGA ATGAATGAGT GAACAGATGG TACATCAACC TATTTGCTAT TTTTCTTCAC 240
AAGGGCATTG CATAGAGCTC TTCGGTTCAA GATTTAGCCA TTGTCATATA CCCACTGCTG 300
GTGAACTTGA AGGCATCACT TTCCTCCACT CTTGTACCAG CCTGCCAGTG ACTGAACTTG 360
GTGCAGGATG GGTCACTGCC ATATCAGAGA TGCCAGCTGG CCTCCCCTGT CTACCTGGTC 420
ATCACACAGG GCAGGAGGAA TCCGTCAGCG TCTGGTGCCA CGTGCCTCTC ATTAGAAGGC 480
TGAGCCCATC TACTGCCCAG ACACTGCTGC CTTTTTTCAC GACTTCCTTT AAAACAAATG 540
AATTCCTATG ATGTGTCTGG CATCATGCTG GGTGCTGCAG CGATTACAGA GGGAAAAAAG 600
ATATACTTCC AGTCCTCAAG GAGTTTGCGG TCCAGTAGGG GGATAACCAC ATCTAGATCA 660
TGTAAACCAA AAGTAAAATC CTAAGGCCCT CCCCCACCTC CACCCAACCA TCTAAACGGA 720
CTTCCTCCTC AGCCAGGGCA GTGTTAAAAT TTAACCTGAA AGCCTGGTTC AGGCCATGAA 780
GGACGTGGGG ATCGGACATG CCTGATTATG TTTACCTCTC CAGCATTAAC GTCAACACAG 840
ACCTTAAGAA ACATTTCACA GCGTGTTCTC CCTGAAGCCT GACAGCTAGA AGCTTCATCT 900
GCATGAATAA ACTTTGGTCT TTGCAGTGTC TTATCGCAGC CCAAACATTC CTTTCTATTG 960
ATCCCAGGTC TTTAGACAAA CTCAACCAAT TGTCAACCAG AAAATGTTTA AATTCACCTA 1020
TAGCCTGGAA GCCCCCTACT CTGAGTTGCC TCACCTTTCT GAACCAAACC AATGTCTTTC 1080
TTAAATGTAC TTGATTGATG TCTCATGCCT CTCTAAAATG TATAAAGCCA AGCTGCATCC 1140
CGACCACCTT GGGAACATGT TCTCAGGACT TCCTGAGGCT GTGTCACGGG TGTGCGTTCT 1200
CAACCTTGGC AAAATAAAGT TTCTAAATTA ACTGAGACCT GTCTTAGATT TTCTGGGTCT 1260
ACAACCCTGC TGTACCAGCA GAGTCAGGGG ACAGCCAGAG AAAGAGGTTC AGGGGGACGA 1320
AGCACCCCCA GCAGGGCCAA GTCACCTTCT ACAGCTCGAC TCGCTCAGCC ATCCAAGACC 1380
ACTTGGCTTT TTTTTTTTTT TTCCTGCACA AGCTGTGCTT TGAAGTGTGT GGGGTCTTAA 1440
AAATCCTGCC CATTCTATTT TGATCAGGCT TCTGTCATCT GCATTGCCAT CCTGGGACAA 1500
GTTGTCAGTC ACTGTCTCCC TGAAATGCAC GTGGAGATGC ACAGGCTAAT CTAGGGACAG 1560
CTGGATACAT GACTAATATT ACCGAGGAGC TAACGAGAGC CTGTGACGTT GAGATGCTGA 1620
GGAGATGGAC TGGTCGTAAG CGTTCCCCAG GTTTATAGCC TTCTTTTCAG CACCCCTCAT 1680
GCCTTCCTGT GGTTGTCAGC ATCCCGGATT ATCCTGATCA TGGGGCAAAG AGAATGGGGG 1740
CTTTCCCCAG 1750
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