Tag | Content |
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EnhancerAtlas ID | HS026-03600 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr10:13597850-13598770 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr10:13597863-13597874 | ATATTTACATA | - | 6.62 | RFX1 | MA0509.2 | chr10:13598318-13598334 | TGTTGCCATGGCAATG | + | 6.14 | RFX1 | MA0509.2 | chr10:13598318-13598334 | TGTTGCCATGGCAATG | - | 6.17 | RFX2 | MA0600.2 | chr10:13598318-13598334 | TGTTGCCATGGCAATG | - | 6.66 | RFX2 | MA0600.2 | chr10:13598318-13598334 | TGTTGCCATGGCAATG | + | 6.67 | RFX5 | MA0510.2 | chr10:13598318-13598334 | TGTTGCCATGGCAATG | + | 6.92 | RFX5 | MA0510.2 | chr10:13598318-13598334 | TGTTGCCATGGCAATG | - | 7 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGATGAGGAA CAGATATTTA CATAGGTTTA CCTTACCTCT TCAAAAACTA ATATTAGTAT 60 TAATTCCAGA GGGAAAAACA GTCACTTACA GTGGAGAATC ATGGCCAACA CCTTCTTAAT 120 CAAATGACCA AACATAATAC TAACATAGAA CAGGCAAGCC CCAACATTGA GGCTTAGCCC 180 AGAAGGGTTC TTGGCTTTGC CTGGGAAAGA ATTCAAGGGT TAGCAGGTGG TGTTAAACAG 240 CAACTTGGCA GCATACAGCA GCAGGAAAGG TGCAGCTCCT TGTGAAGCAG GGTTACCCCA 300 AAGGCAGTGT GCCAAGAGAA GCAGCTTGGA GGTGGTTCTG CACTAATATT TATGCCTGTT 360 TTAACTATAC ACAAATTAAG GGGCAGTTTA TGCAGAAATG TCTAGGATGA GGGTGGTAAC 420 TTCCAGGTCA TCAGGCCGTT GCCATGGAAA GGCCTTGTAA TGTCCAGGTG TTGCCATGGC 480 AATGGTAAAC TGATATGGCA TACGGATGGG TGTATCTTAT GGAAAGCTGC TTCCCCTGGG 540 AACCTGTTTT TGCTAGTCCT CAATTTGGTC CTGAATCTGA GCCCTGCCTC TGGAGTCAAG 600 TTTTGCCTCC TACCTCAATA TCACTGGTAA TGGGACAAAT AGACATCAGA ATCCCCTGAT 660 GGAATGCCAT GGGAACACAG CATCACTTCC ATGATTCACA ACCCAAATCT AGTCATGAGA 720 AAACACTGGA AAAACCAAAA TGGTGGGATA TTCCTCAAAA TAACTGTTCT ATAGTCATCA 780 GACTTGTCAA GTTCATGAAA ATCGAGGAAA GAGTCAAGAA CGATTTCAGA TGGAAGGAGA 840 GTAAAGAGAT ATGACAAATA AATGCAACGT ATAATTGTGG ACTAGCTCCT CTTGTATTAA 900 AGAGATTATT GGGACAACTA 920
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