Tag | Content |
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EnhancerAtlas ID | HS049-03644 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr18:31738720-31740120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arntl | MA0603.1 | chr18:31739517-31739527 | GCACGTGACC | - | 6.02 | RREB1 | MA0073.1 | chr18:31739867-31739887 | GGGAGGGGAGTGGGGTGGGG | - | 6.03 |
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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 |
GH18I034158 | chr18 | 31738918 | 31739902 |
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Enhancer Sequence | AATATATTTC TTCTGATAAT TAAATAGGGC CCAGGACAGT GTTTTGTAGA ATTAAACCAG 60 CTGTCTGCTA ATAGAAGAGG CGTGGCAGAC GGTATAAAAG GAAGCGTTTT CCATCCTCTA 120 GACCATTTAC TCTGGAAGAT GCTGAGATAC AAAATGTAGA ATGGAAAGCC AAATAAAGGC 180 AGGCATGGTA ATGGAACAAG GACAAATGTT GGACGTCTGC CCTCTCACTT CCTGTTTGTG 240 GGAGACAAGC GGTGGCAGCT GCTGGGTTAG AGTCCCTGGA AGAGATGCTG GGGCAAAAGA 300 GAGCTCGGGT TGCTGTTTCT ACTTCAGCGG CGGCGGCTGG AGCAGCGGGT ACAGGTGAGG 360 TTGCCCTGGC GGTGTCCATA GCAACGCTGG AGGGGGTGGC AGGGAGAAAG GCGCCCTCCA 420 CCCTGTCAGC CTCCTCCTCG CCTCCCCCGA CCTGCAGGCG CGCTAAGCGC TCCGGGCGCC 480 GCGCTCCGCG AGGGGGAGCA GTGCTCCCAA CCCGCGACCC TCCGCCTCAG ACATCACAGT 540 TGCCGCGGCA ACGGCCGGAG GAGGAAGGCC AAGGCTTTTC TCCCGCTGAC GTCCCCCGCC 600 ACCAGTACCC AGAGTGCTGG GGCCTGGATG AGATCTGCGT CCGCTTCACC CGAGCATGAG 660 CTTGGGTCTC TCGGAGGAGC AGGAGACGCG GGCTCGAAGC CGCGGGCCTG ACCCTGATCC 720 GTGGATGCCG CCGCCGCCTT CTCCTCCCCT GGGTGGTGGG GGACAGGGCC TGGGAGGCAC 780 GGTCACGCCG AGTTTGAGCA CGTGACCTTC CAAGAGCTTG AGAGTCCCCT AGAGAGCAGG 840 CCCCACCCCA ATCCATCCCG CCTCGCCGGA GGGGTCCCTC TGGCTTTAGT CCTTCTCTTC 900 TAATTCCCTG TATGTCCCGA CCCGACCAAC GGCAGCACAC TCTCCCAGTC CCTTCACTCC 960 CACCTAGAAT TATCTTCGAG GACTATAACG CCGGATCCTT TCTCCCTTTT TTCTGCCCTT 1020 CCCGGGTGTC TGGGGAGCAA AGGAAGGGTC AGAGGCCTTC AGAAAAGGTT GCCCGCTCAG 1080 ACAAGACCAG AGAGCACCCA GGACCCGACC CCGCTCGCTG TAGGCCTCTC AGCGGGAGAG 1140 GGATGCGGGG AGGGGAGTGG GGTGGGGTGG AGTTGTCAGC TGGCCATATC CAGTCATCCC 1200 TGGCCAGGTA AACTAAGTGC TCAGTAGGGG CACCCGTAAT GGACTTCAAA ATTGCATACA 1260 GGAACAGATT TTGCTCAGAG CCCAACTGAA TCCTGTTTTT ATTTACTGGA GCAAAACAAA 1320 CCCAGGCGGA GAAGGGTGTC TTTTCTGGCA GCTAAGTCAA CGGGGACTCT TGCCTCGCTT 1380 TCCAATATAT CAAAAGGAGG 1400
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