Tag | Content |
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EnhancerAtlas ID | HS177-10348 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr18:43991860-43992780 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr18:43991861-43991882 | AGAGGAGGAAGGGCAGGGGCA | + | 6.69 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH18I046410 | chr18 | 43989998 | 43994222 |
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Enhancer Sequence | GAGAGGAGGA AGGGCAGGGG CACCATGGAG CCCAGCTCCC TGGAGTGGGG TCGATGATGC 60 CAGGCTCCCT GGGCTAAAAG CCTCTTGTCA GCAGAGTAAT TGGATCTGAC TTGCAGCAGG 120 CAGGGAGCAG AGGTATTCGA GTCAGTTGGT GCTATTTTTA AATGCCCTCT CTTCCCCAAG 180 TGCAGATCTC AGCTCAGCGG GAGACAACGG CTCATCTCAC AGCCCTGGGA ATCAAAGCAC 240 AGCCCCCTCC CCTCAAGGTT TAAGTCCTTC CAACCCCATT CTTCAAAATC AGATCTCAAA 300 TTGGGCAACT GCCCACAAAT CCTGCCATGA TCATATGTCC CAGTTTGGGG AAGGATGGAC 360 TCCTGGGGCC ATGGGGTCAA GGGCTGGTTT GGGCTGGTTG CCCAGTTGGC CAGAAGCAGA 420 CCCACAGCCT TGGTTTCTTG GTTGCCTGGC AGCCCCAGAG GGTTACCACT AAGCCTGCAG 480 GCAAACATGT CCCTGCCAGT CTGCTGCTGT CTTGACCCTT GGTAGCAGCT CACAGCTGCC 540 TGTCAGGCTC TGAAAACAGA GCAGAAAGCA GCCACCCTCC TGCCAAATGT CCTGCTAGGA 600 GATGAGCCTC ATACTGAGTG CAGCCCAGGG TAGTGGGAGG AGATCAGGGA GGCCGATGTC 660 CAGTCATGTG CTGATGAGGC TGCCTGGTTG GTCAGTTTCT TCTCACTTGT CACACCTCCT 720 CTCTCCTCCC TACTCCAGTA GCTGGCTGTT AAATGCTCTC CCTCCAGAGG ATGTGGTCAG 780 GCCGGAAGGG AATTGCTGGT GGTCCTGACT ACCCCCACCC CTCCCAACTC TTAGAAAATG 840 ACAAGGCCGC CTCGGGCAGG TACGGAGATG CTGCTAACAG CCAACGCGGA GTGACCACGT 900 TTCATGCTTC AGATGGCACA 920
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