Tag | Content |
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EnhancerAtlas ID | HS147-04051 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:192752580-192753640 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr1:192753574-192753585 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr1:192753574-192753585 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr1:192753574-192753585 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr1:192753574-192753585 | TAATTAAATTA | - | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTCTCTGTC AAAGGGAAGG TCTAGGGTTG GAGGCTGTTG TTCAAATTCT TTCATCCCAC 60 AAGGTGTTCC CTTGATGTAG TATTCTCCCC CTTTTCCTAT GGATGTGGCT TCCTGAGAGC 120 CAAGCTGTAG TGATTGTTAT CTCTCTTCTG GGTCTAGCCA TCCAGCAAGT CTACGCACTC 180 CAGGCTGGTA CTGGGAAGGG ATTGTCTGCA CAGAGTCCTA TGATGTGAAC CATCTGTGGG 240 TCTCTCAGCC ATGGATACCA GCACCTTCAG TTTCGCCAGT GGGTGTGTGT GTTCAGAAGA 300 GGATCTCCCT TTCCTACTTC CGCAGTTGGG GCATTCACAG TATTTGGGGT GTCTCCCAGG 360 TCCTGCAAGA GCAGTCTGCT TCCTTCAGAG GATGTGTGGG TCCTCTCAGG ATTGCTGGTT 420 TGTTCTTGCA GTTGATCTGG AGCTAAAATT CATGATGTGA GCCTCTGCAG GCTGCTCTGT 480 CTGTCCGAGT CAGAGCTGCA ATCTCCATAC CTTCATTTAA ATTCAGAAGC TACACGTCTT 540 CCAACTAGTC TCATCGTGCA TAGACTTGAC CCGCCCATTG AGTATGTTCC ACACTCCGTA 600 CCTGGTGTAC GAAATGTGTG GCATGTACAC ACATGGATTT TAGCAGGATA CATGGCTAAG 660 AAGCACTGCT AGTCCAGAAT GTGAATCCAT ATGTGTAGTA TGAATACAAA GTTAACTGGT 720 AACAGTGAAA AAAAAGAGTT TTGAAAAGAC AGGATTTTTG ACTAATTGAT CCTAAAAACA 780 AATTTATGAA ACAACTATAA TATGAACAAT ATATATAACT TTTTGGAATT TAAAAAGGCT 840 ATTTATTCAT ATAATCACAT TTTTAAAAAA TAAAATATCA CATATATTAA ATACACGAGA 900 AGACAGAAAT TAATATTTAT GGAACATCCA GCATATGCCT AGGCACCATC TGCAATAAAG 960 ATTATTTTAT AGTTGAGGGA ACATGGACCC AGACTAATTA AATTATTGCC TCAGATATCA 1020 AAGATAGTAA ATAATACAAT AAGGATGTAA ACCTCATGTT 1060
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