| Tag | Content |
|---|
EnhancerAtlas ID | HS049-05299 | Organism | Homo sapiens | Tissue/cell | Fetal_spinal_cord | Coordinate | chr22:35944540-35946030 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr22:35944683-35944694 | CTTGAGTGCTT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 35945312 | 35945817 | | chr22 | 35945502 | 35945747 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I035548 | chr22 | 35944431 | 35945010 |
| Enhancer Sequence | ATAAGGGAAG GAGTGAGCAG GCAACTCTCT AGGCATCATT CAGATAACCC CCCAACTGAG 60
GTACTTCTAT ACAGAGAAAC CCATGCCACT CCCAGCCCTG CTGCCGCCTT GAGGCCAAGA 120
CTGAGGCTGC GGGGTGGCCC CTCCTTGAGT GCTTTCTCTT CCAGGCTGGC TTTTCCGAGC 180
ATCTGACCCA GACAGCAGTC AAGTTCTCCG CTCCACCCCG AGTTTTGGAG AAGGGGCATG 240
TAGATAGGAG AGCCCTGGGT CGACCTGTGT TCGAATCCTT GCTGGGCCTC TTGGCTTAAA 300
TGTGTGACCA GAGGCACATG CATCCTGTCT GAGTCTCAGC CTCCCCAGCC ACACAGTGGG 360
CTTAACCTCA TACCCCGCAG GGAGGCTGTG AGGACTGCAA GAAGGCTTGT GGCGGGAGCT 420
TCCAGCACGT GACGGGTATT GCATTGGTGT CAGCTCCCCC AGCCTTGGGG AGGGGACTGG 480
GTACCCGCTG CAATGAATAA GGCTAATGAC AGAGGGAAGG AGAGGGGAGA TGTAGAGAGG 540
AAGCACATGC ATATTTTCAG CATTAATTTT CAGTGACACA AGTAATACCC AAACACACCC 600
TCCTGCAAAC GCTACAGATA AAGCTAATGC CCCTTTGACC CATGTCCCCA ATCCCAGGCT 660
CCTGCCCCTG CCCCGGAGGT GGCCACCCTG GCAGTCTGGC ATGGAGCCTT CCGGGCCTCC 720
GTGACTACAC CGGCATTCGT ATTTGTATCC CCACAATGGA GAGTATTTTT GTCTGTCTCT 780
TTTTTATGGC GCATATCATT CTGAGCACAG CTGTCTGATG CTTGTTTTTT TTTCACACAC 840
CAACCCGTGC CTCATTTTCC AACCTGGTGG AACCTCATTT TTTCAACCTC ATTTTCCTGC 900
TGCTCAGGAA ATTCTGAAAG CCATTAATTC CACTGCCAGC TCTTCTTCCA GCTGCCAGAC 960
GGGCCGATCT CTGATGCTTG GCATCGCAGT CTCGCATTTG AATATGTCAA GGCCACGAGT 1020
CCTCAGGGGC CCCGGATTAG CCTAACGGGA TGGGGTTTGG CAGCCCAAGC AGGAAGAGTT 1080
GCCAAGCTGA CGCTGCCTCG CAAGTGCCTT TCAGAAGAGC CCACACTGCA GTTCCCTCCA 1140
TCACCTCCCA TCCATTCAGG CTTCCTTGGT TAACACTGAC TGTGTGCCAG GCCCTGGGGA 1200
GACCAGGACG AGTGGGTGAT GGAACCCTTC TCTGTGCCCG AGCTGTTTGG AGCACACCTT 1260
TGATCTGGAC ACCATTCTGA ATGTGCCATG TGCCATTAAA TGGGGGTAAA TGATGTGCTC 1320
TGGGGGTGCA GAGGAAGGTG GCAGCCATTC TGCCAGAAGC TGGAACTGGT TGCTTCTCTT 1380
CTCAAGAATT TGGGCCAATT GCTGATTCCT CTGGGCCTCA GTTTCCTCAT CTGTGAGACA 1440
GGGATCTTGT CACACCACAA GGCTATCAAG AGTTTGAGCA AAAGTGGTTG 1490
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