Tag | Content |
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EnhancerAtlas ID | HS068-00018 | Organism | Homo sapiens | Tissue/cell | GM18526 | Coordinate | chr1:2498710-2500020 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr1:2498977-2498988 | AGCCACACCCT | + | 6.02 | SREBF1 | MA0595.1 | chr1:2498769-2498779 | ATCACCCCAC | + | 6.02 | ZNF143 | MA0088.2 | chr1:2499672-2499688 | CAGAGCATTGTGGGAG | - | 6.58 | ZNF263 | MA0528.1 | chr1:2499508-2499529 | AGGGGAGGCCGAGGGGGAGGG | + | 6.37 | Zfx | MA0146.2 | chr1:2499103-2499117 | GAGGCCGAGGCCTG | + | 6.31 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCCCCCCAT CACTCTGCAA CAGCTGAGGA GCCCCAGGCC CCCAAGAGTC CAGCACCGCA 60 TCACCCCACT GCCCTCCGTG AGGCCCTCCA CACAGCCCCG ACCTGGGTCT CCATGGATCC 120 CCACAGGGTC AGCCCCACAC CCCAACCTCC CGGCAGGGCC GTCTCCAGGG GACTGTCCAG 180 AAACCCCCAA AGATGCTTCC CTTTTCTGTT GATGGGAGCC CCTGGGCACA GAGGATGGGA 240 CAGCGGCTGT GGGTACCCGA GGGCTGGAGC CACACCCTAA GGGATGGAGG GCAGGGTCCG 300 GGGCCCAGTT AAGGGCTCCC CCTCCACTCC TGCGCCTTCA AGGTCGGCCT GCACCTCCCC 360 TGCTCTGTGC CAGTGCAGGC CAGGCAGGGG GCTGAGGCCG AGGCCTGGCC ATTGCCCTCC 420 TGGTCACGAT CTGGTGAAGG ATTTGAGTCC AGAAGCCAAA CGTCTACAGT CGTGTGGTGC 480 GGACACTCAG GATGGACTGC CCAGGCCATG GGGGGCTCTG AATGAAGAGG AACCTGCGGG 540 GGCGAGGTGG GCTGCGCGTC TGCAAGAAAG TGCATGAGTT GAGTGCTGCT GCAGAGGGAA 600 GCTGGGGTCC ACCGCTGGTG AGCGGGGAGG GGACGGGACA CAGAACCGGC CGTGGCCCAC 660 CCCGAGACGG AGGCGCAGAC ACCAGGCCCG TTCTGTGCTC TGGAGGCTTT GGGCAGCTGT 720 CAGGCTAGTG GACGGTGTGC AGAGCAGATG GAGGCGTGAG GAGGCGGCTC CGGGGTCACC 780 TAGGTGGGCA GCCCTCACAG GGGAGGCCGA GGGGGAGGGC AGGAGGGCGG AGCAGGCGGC 840 GGTGCAGGAG GCCCGTGGAA CTTGGAGGGC TCTGTGTCCA GCTCTCATGG CCCAGGGCGG 900 GGGCAGCTCC AAGGCCTCGG GCTTGGGGAC AGAAGGGAGA GGACTTGGGG GTTGGGGGTG 960 GTCAGAGCAT TGTGGGAGGG ATCTGGGGCA GCTGGGGCTT CCCAGAGGGT GAGGTGTCTG 1020 CTGGGAATTG GGGCAGCCCC AGGCGTCCCC AGGCCTCCAG CCCAGCCCCG GTTCCTCCCC 1080 GCTGCAGGCC AGGGTATCAA TTGCCTGCTG GGAAACCTCA GGGTGCCTCT GTCTCAAGTG 1140 CCTGCCCCTG ACACTCCTGG CCCTGGGCTC CCCCCGCCTC CCCGTCCGTC TGCTTTCCCC 1200 ACCTCCTCCC CTCCCCTGGC CGTCTTTCTG CCTCGGGGAT GGCGTCACCT CTCACCCCAA 1260 ATCAGGACCC TGGGCCCCAG CTCTGTTCCC CACCTCACCT TCCTTGTGAC 1310
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