Tag | Content |
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EnhancerAtlas ID | HS030-00125 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:7668400-7669860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr1:7669072-7669083 | TGTGGATTGGA | - | 6.62 | JUN(var.2) | MA0489.1 | chr1:7669132-7669146 | CTGAGTCACTTCCT | - | 6.23 | NFE2L1 | MA0089.2 | chr1:7669128-7669143 | AGTGCTGAGTCACTT | - | 6.51 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 7668813 | 7669345 | chr1 | 7669462 | 7669554 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I007608 | chr1 | 7668605 | 7669456 |
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Enhancer Sequence | AATTGGACAG AGCCAGGGCA GAGCCTCCCA GGCCTAGTTC CTGGGGAATG CTCAGGGCCA 60 GGGAACCCTC CTCTGGAGCA GGCACATGTC CTTAGCACTC ACCTTCCCTA CTAAGAGCCA 120 GGGCCTGAAA GGAGACAAAA AAGGCCTGAG AAAGAAGCTG GGGCCCAGGA CTGCATAACA 180 CCAGTGCCTG TTTCACTGTC CCCAGCCCAG GGAAAGGGAT TGGGGCTCCA TGAGAGGCTG 240 ATGGCAGGGA AGGAGCCATG CAGGAGCCCC ATTTGGCTTG TGTCTGTCCC CTTGGCATCT 300 CTTTCTCCTT AGAAAATCTG ATTGCTTGTA GCTTCCACAC TGGCCATCAG TTTGATCTGA 360 GCTCAAGGGT GCAGCAGAGG CTCACCTTGT TCTGCTTAAA TAATGCAGGT AGTGAAGTTA 420 TTGACAATCT GTCATCTGCT TGAAAGTGGC TTCGACAGAG CCAGAAGCGT GGGAGGGCCC 480 CAGGGGCCTC AGCCGGCCAC AGGTCCAGTC TCTGGCTGAA CAGGGGCTCT TCAAGAAGGG 540 CCAGGCCCTT GGCATGGTCC AAGATGAATG GATGGGAGCT TGAGCCCTAC CTGGCCTTTT 600 CTAGAAGGAC ATTCTATGGG GAAATTCTAA GCAGAAGTGA GGGCAGGAGC TGTCTGGCTA 660 GGAGGCCTGC GTTGTGGATT GGAAAGGAGT CTCCTGATGC AGGCTGGGCC CCCCGCAGGG 720 GTGGGGGCAG TGCTGAGTCA CTTCCTGCCA GAGGACAGGG TCTGAACTCC CAGGACATTC 780 TGGCCCCTTC CCACTACCGG CCTAGCCCTG CCGCCTGTGC CTTGCCTCCT GGCCTCCTAG 840 CCACAGACAG GGGTTTATGA TGAGCCGGCT TGCTCATCCT TGAGCCTGGG TTGGATTTTT 900 TTTTAATGTT TAAAAATTCC CCACAGCATG GCAGGTGCCC GGCTGCTGGG TCACCCCATC 960 GGCTGTTCTG TCATCAGACA TCATGTTTAC CCATCAGACG CTGTTTTCCT GACACTCAAC 1020 ACTCAAAATA ATGATCTCGC TGGAGCACCT TCATGAATGA TTCATGAGGC TCTGCTCAAC 1080 TTTGGGTGTT AACAGCAAAT CAAAGCCCCT CAGTGAGGGC AGCAGAGCAG CAGCCAGAAG 1140 GCAAGCCCTG GCCCCAGCCT CCAGGCCCCC AGGGATGCTC AGGGCCTGCC ACCCCTCTCT 1200 CAGGCTCCAG TCCAGCCCTG CAGGAGTGAG CCAGCCTCAG CCAGGCCATG GCACAAAAGG 1260 GGAGGGGAGC AGGGTCCTGG CTGTCACCCA TGTCCTGGTG ACCTTGCTGA GGACATTGGA 1320 GCTCCAGCCT CAAGTCAGAT CCCCTGGACC CCAGATCTCT TCCACCCACA GGTGGTGTGA 1380 CCTTGAGCAG GTCACTTTGC TTCTCTGAGC CTCTCTTTCC TGTCTGCAAA GCCAGGTGGG 1440 AACTGCCCTC CCGCAGGGCA 1460
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