Tag | Content |
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EnhancerAtlas ID | HS049-04232 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr19:51110620-51111960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB1 | MA0018.3 | chr19:51111400-51111412 | AGTGACGTCACC | + | 6.22 | CREB1 | MA0018.3 | chr19:51111400-51111412 | AGTGACGTCACC | - | 6.22 | EBF1 | MA0154.3 | chr19:51111886-51111900 | TGTCCCTGGGGACT | - | 6.15 | RFX1 | MA0509.2 | chr19:51111546-51111562 | TGTCATCATGGCAACC | + | 6.25 | RFX1 | MA0509.2 | chr19:51111546-51111562 | TGTCATCATGGCAACC | - | 6.25 | RFX2 | MA0600.2 | chr19:51111546-51111562 | TGTCATCATGGCAACC | - | 6.2 | ZNF263 | MA0528.1 | chr19:51110877-51110898 | CGCTCCTCCCCTGCCTCCCTC | - | 6.24 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I050608 | chr19 | 51111341 | 51111570 |
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Enhancer Sequence | GGATCTTTGT CTTCGTCACC TCTCTAGTTC GCTCCCATCT GATTCACTGT CTTCTCTCTC 60 TGGTCCTGTC CCCTTTGCCT ACGAATGTAT CCTCTTTATT GCTGTTGATC CCACTGCTGC 120 ACTGTCCTCG CTGCTGCCTT CTCACAGTCC TGTCGCCGTC CCCATCCTCT TTCTCAGTCC 180 CCTGTGCCGT CGGGCGCTCC ACCTGTGACC GTGGGGTCTT TTTCTGTCCC CTCGGTGCCT 240 GTCACAACCC CTCTTGTCGC TCCTCCCCTG CCTCCCTCGC CTCAGGGCCC TTCCCCGTCT 300 CCTTCTCTTC CTGTCATCCC TGGCTCCTTC CCAGCGTCTT TTCTTCCTTC TCCGAATCGT 360 CGTCTGCTCC TCTGGGTTTG CGGCTGTTGG GGACTCTGCC CCTGGGAGAG AGAAATGCGA 420 AACGTATTTC TGGGAGCTGG AAGCTGTTTC CTCCATTTAG TCTCTGGATG TTTTCTAGGT 480 GACCACAGCC TCTTATAGGC CTGTCCTGGG GCAGAGCGGC CACCTTGAGG TCCATCAGTC 540 AGTCTGATCA TCTCTGTAGA ACCTCGAACC TCTCGCCTCG CCTCGCCTGA CGCCGTTTCC 600 TGCCCTTTAT CTCTCCCTTC AGAATTAAAA AAAAAAAAAA AAAAAAAGAC AGTCGGAAGC 660 AGCAGCGCAT GAGCCCCAAT CACCACTCTG AAACAGGTGC GCGCGGTGGC CTGCGGGCTC 720 GCGGGAGCTC ACGCGAACTC ACGCGCGAGC TCACAAGCTG CGGCGGCCGG CTAGGCGACT 780 AGTGACGTCA CCGAGGCTTG TCCCTGCCTT ATTGGCTGCC TTCGACCAGC GCGCGTTTGC 840 TGGAGTAGTC GGCCACGCCT TGCCAATCGC CAGGGGGCGC TCAGCGCTAG AGCTCCGCGA 900 CCCTGGGAGC CCTATAGAGA GACTCGTGTC ATCATGGCAA CCCTGCCCTA CCTAATTGGA 960 TACCTGCTCC AGTTGGTTGG ATCCATTACT CTGATTGGAT GCCTGGCGAG TCAAGGCTTG 1020 TATATAATTG GATGCCGGAA ATTTGGATCT TTTCTACGTT TCGCATTTCT GTCTCTTAGC 1080 CGGATTTCTT CCGCAAGCAC TGGGGATGTG GAGATTGAAA GTAACTTGAG TCTCCGTGGG 1140 GGAGTGATGG GTGTTGGGCA CGGTATGGGA ACCTGGCCCG AGTCTGCGGA CCCGATTGGC 1200 TGCTGTCTCT CAGATACAGG TCCCTTTCGT CCCGCCAAGG GGGGCCATGG AACGTAGGGC 1260 CCTCTCTGTC CCTGGGGACT GGGTGATGTC AGGGGTGATT GGCTACATCG CTCCCCAGAA 1320 GGTGAAATGG AAAAATTGAG 1340
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