Tag | Content |
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EnhancerAtlas ID | HS043-02435 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:117005400-117006880 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr1:117005900-117005910 | TCTAATTAAA | + | 6.02 | GATA2 | MA0036.3 | chr1:117006685-117006696 | TTCTTATCTCT | + | 6.32 | Gata1 | MA0035.3 | chr1:117006685-117006696 | TTCTTATCTCT | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TTATTCAGGG AAGAAAGCAA ATGGGAGCAT CTGGGATCAT GAGGGTATCG TGTTGGAGTG 60 AGCTGGGCTA AGACTCCCCA TGACCCATCC CTGGCCACAG CCAAAGGGCT GGCTCGAGAC 120 TCCTCCCCAG CCTCTCCATT CCCAAGGCAG CACAGATTCC TGCTTCACGA TTGGCAGGTT 180 CAAGTATGAT CGCTCTACCC TTGGCCTCAT TTCCTCAATG CCCTGCCCTC CTTTATTCCT 240 CTGCTTTCCT GGCTTCAGTG TTTCTACCAG CATTTTCAAT ATAGAAGGGG ACTCATCAGA 300 TCAGCTTCTA CCAGGGCTGA TATTTAACTT GCTGAGGAGC CAACAGTTGT GACATTAAGA 360 AAGAACAGTA AGAGCAACGG TGTCACTGAA AACAAGGATA ACTAGTGGGC TATTTTATGC 420 ACAAATGGTC CTTTGCCATT CCCATCAAGC TGAAAACAAA TATCCTGAAA CTATTGATCA 480 GCAGCCAGTT AAATTAAATA TCTAATTAAA AGAGAACTAG AGCTGTTTTA AAATCAGACA 540 CTTCAAACAC TTGCCAGTCA GAACATGATG AAACTGGGGG TTTTAACTCA GTAGCAGCAG 600 CAAATAAAAT ATTTACAGAT CTAAGCTGAA ATAAATGCAT AGATTCTCAT TTTTAAGGAG 660 GATGCACATA GTGCTATTTC AAACACACCC TGGCGAATAC TTGATGCCTC TGATTTAGAG 720 AATGTGCGGG GAGCACCATT TGTCAGGAAA TGGGATAGAA CCATCCAATG TTTCCAAGTG 780 TGATCATTTC TAATGGAACA GGGAGAACTC TACAAATGGA ATTCAAGTAG GATTGCCAGA 840 TGAAATACAG GAGAATGAAT TGTCTTTTGA ATGTATGTCC CAAATATTGC ATGGGACATA 900 CTTATACTAA AATTTTATCT GTTTACCTGA AATTCAAATT TAACCAGGCA TGCTGTATTT 960 TTATTTGCTA AATCTGGCAA CCCTAAATCC AAGATTGTAA GTAACCCCGG TGACCTGGGA 1020 GAATAGTTGG GTGACCAGCA GAAGAGAATC CTGGAGTGGT TCAAGTGCTG CAAGGGTGTC 1080 GTGTGAGAAT TCGAGCTTCC GTCTCTTCAT TTGTACAGGG GAGAATGATA CTGTGCAGAG 1140 CTGCTGCTGT AAGGATTATC TGTGAAGTCA TAAATCACAT AAATGTCTGT CACATTTCCT 1200 GTATGCAGGA AATAGCAGTC ACTATTGGTA TGTAGAGGGC CTATAGCCAA CGAGCGGCAA 1260 ACAATAAGCC CTTAATATAA ATTGGTTCTT ATCTCTAAAA GAAAGAGAGC TGTTAGGTAA 1320 GAGTGGCCAT CATTTATGAG CACCTATCAT ATATATCAAG CACTTTGCCA CATTGTCTTT 1380 TTTTTTTTTT TGGATAGAGT CTCACTTTGT TGCCCAGGCT GGAGTGCAGT GGCATGATCG 1440 TGGCTTATTG AAACCTCAAC CTCCCCAACT CAAGAGATCC 1480
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