Tag | Content |
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EnhancerAtlas ID | HS042-03240 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:182708600-182709510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:182708834-182708849 | CTTGGCCTTGACCTC | - | 6.3 | RREB1 | MA0073.1 | chr1:182709098-182709118 | CCAACACCCAACCCCCAACC | + | 6.01 | TBX20 | MA0689.1 | chr1:182708854-182708865 | CTTCACACCTC | - | 6.02 | TEAD1 | MA0090.2 | chr1:182709078-182709088 | CACATTCCAT | + | 6.02 |
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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 |
GH01I182738 | chr1 | 182707891 | 182709380 |
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Enhancer Sequence | CAGTCACAGG CATACACACA GTTTCTGGCA TTTATGAAGA ATTGGGGTTT CTTTTAAGAG 60 GAAAAAAAAG AATAAACCAA ATTGTTCATT CCTTTTCTAA AGTATTGTAT ATTGGCTTTG 120 TATTTGAGGA CTGCCTTGTT ATCTTCATGT TTTCAGGCCT CCCCCTGTCC CATAGCCTAG 180 GGGGAATCGC CATGGCCCTG ATTTGTGTAT GTAGACAGTG CTGTTTCCAT TCCTCTTGGC 240 CTTGACCTCT GCCTCTTCAC ACCTCCTCCC ACTCACCCAG CCAGCGGGCA GCCCACCCAG 300 AAGCCCTTGC GCCAGCAGTT ACCTGGCAAC AGCGACAATC ACGCTAACAG GCAGCAACAC 360 AGCAGCAGAG ACCAGAGAGC TCTGAGTCTT CCAGAATCTA AGCAGGGAAG GGAAGGGGGG 420 CAAACGGCTG TTTTTATCAA TGGCTTTTCG TCCCTACCCA TACTGTTTTC CTGTCTCACA 480 CATTCCATGC TCCAGCTCCC AACACCCAAC CCCCAACCCC CAATTTCTAT CATCGCCTGG 540 GTGAAACTAG CCTCCAATCC AGAGTTTAAT AACAGCCACA GAGATTCATA TGGAATTGTG 600 TACTTGGGGA GACCCAATAA TCATCCCCCT TAATTCCAAT GCAGAATGCT CAGGAGTTAA 660 TCAATCCTAG TTTCCATCTG TGCACATGTT GTGTTGCAGT CCAAGGATGT ACTTGACCAC 720 CCAACTGGCC TGCTGTAATA GAGACCTAAG TGCTGTGTAC TCAGAAACAT TGACAAGCTA 780 TTATCTTACT TCTTGCCTCC CTGGCCACAA TTCTACAGTA AGTGCTACCA GAGAGTGGGG 840 CATAAGCATA CCAGTTAGTA ATAGCTAATA TTTACTGATA CTTATTCTGT TCTAGGCTCT 900 GTGCTGAGCA 910
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