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EnhancerAtlas ID | HS148-19137 | Organism | Homo sapiens | Tissue/cell | NHLF | Coordinate | chr9:113531880-113532300 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr9:113531941-113531952 | AATTGTTTATT | + | 6.02 | PHOX2A | MA0713.1 | chr9:113532170-113532181 | TAATTAGATTA | - | 6.32 | PROP1 | MA0715.1 | chr9:113532170-113532181 | TAATTAGATTA | - | 6.14 | Phox2b | MA0681.1 | chr9:113532170-113532181 | TAATTAGATTA | - | 6.32 | REST | MA0138.2 | chr9:113532136-113532157 | CTCAACACCATGGATAGATGC | + | 6.44 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTAATTATCA CTTCTTTAGT TTAGATTTCT CTTTCTTGGG CTTCTTTATA GGATTCTCCA 60 AAATTGTTTA TTTGACGTAC TGCTCAACAG TGAAAATCCT TTTGCTAGAA AGTAGCACGT 120 GTATAATAAA CAGAATGTAA CCAGCAAAAT AAAGTGACAG TAGATTCTAT CAGCTTTTCC 180 TTTAGTACTA CTAACATAAT TTGTGGTGGC CACGGGATAG TTATCATACT TACACAGTGA 240 CACTCAGGCA AATCAGCTCA ACACCATGGA TAGATGCTTG AGAGAAATAA TAATTAGATT 300 AGAAAAATTC TCTGTGTGTG TGACAGCCAT TGTGGTTTTC TGATTACAAA ACCCACAAGA 360 CTCCATTGTA TAAAAAAAGA ACACAGTACT TTCATTGCTA AAACCCAGAA AGTTGGTCAC 420
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