| Tag | Content |
|---|
EnhancerAtlas ID | HS043-19481 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr18:32185300-32186190 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr18:32185742-32185753 | CTTGAGTGGTT | - | 6.32 | | PHOX2A | MA0713.1 | chr18:32185794-32185805 | TAATTAAATTA | - | 6.62 | | PROP1 | MA0715.1 | chr18:32185794-32185805 | TAATTAAATTA | + | 6.32 | | PROP1 | MA0715.1 | chr18:32185794-32185805 | TAATTAAATTA | - | 6.62 | | Phox2b | MA0681.1 | chr18:32185794-32185805 | TAATTAAATTA | - | 6.62 | | RUNX1 | MA0002.2 | chr18:32185903-32185914 | GTCTGTGGTTT | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATGTGTGTTT GAGCTTTTTA AACAAGCTTT GCTTTCTAAT AAGGTAATAT AAGAATGTAA 60
TTAAAACAAA ACAAAGTCCC TCCACCAATC AGTGTTGCAA CATTTGGGTA AATTTTAGAG 120
CTTGACAATT TTCAAAGCAG AGACATTACT CCAGGCTTTC TGCCAAACCA TTACTGGTAA 180
TCTGATGACA AGGGATGAAG CAAATGAAAG TGCTGCTGCC TGGCTTAGTT AGATATGCAT 240
TTTCTAGAAG AGAAGCCAAC AGATTTCTTA TGCAAACCAT CAAAATTGCA ACTCAGGCAC 300
ACACACACAC ACACACACAC ACACACACAC ACACACAGTG CTTTTACAAG TCTAGGAATA 360
TACACATTAA AACACAACTC CATGCTTAAG GGCAATGCAG AAGTAGCAGA CACAGCTAGG 420
GTTGACTGGA TCCTTTCTTT ACCTTGAGTG GTTTTAATAA ATAGCAACAT TTCTCTCAAT 480
GGCTGCAGTA CAAATAATTA AATTACTTAT ATCTGGACAG GATTTAGCAT TGCCTTCACA 540
TGGTTAAATT CCAACTACTA CCCAAAATCT CTCATTGATA AGTGGGTGAT TTGGGCTGCT 600
ATTGTCTGTG GTTTATTTAA ATGATTTAAA TAAACATCTA TTCTCCTATA GTGTTAAAAA 660
ACAATTTATG TACTATTAAT GAAAAAAATC CACTTCAGTT AGTAACTATG AATGACCTTC 720
AAGATAGGGA TATAAGAAAG TAATCAAATC AGGGATGTTT TATAAAAGGA AGACTTTGGA 780
GTTTAATAAG TTCTGTGGAG GGGAAAAATA CTGAGTAAAT AACTGGGTAT TTGCATGCAT 840
TATTTTGACA ACGGGAGGGC TCTATTTTTT TTACCTATTT CTTTAGAAAT 890
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