Tag | Content |
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EnhancerAtlas ID | HS078-00756 | Organism | Homo sapiens | Tissue/cell | H2171 | Coordinate | chr1:38582550-38584100 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TP53 | MA0106.3 | chr1:38583486-38583504 | GGCGTGCCTGAGCATGTC | + | 6.36 |
| | 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 |
GH01I038117 | chr1 | 38583122 | 38583462 |
| Enhancer Sequence | CCCTCTGAAT TAGATGAATT CAATGTAGGG ATAGGATGGC AGTAGGTTTC ATTCCACATG 60 CCAACTCTGG CCAAGTATGA ATGGTGCTTG GAGTGGTGTG TTGAGAAGGA TTCAGAGGCC 120 AAGTCTAAAT TCACCAAAAA AGAGACTGTG AGCTCTTAGT GACATTTCCC ATGGGCAAGT 180 GTTTGGATTC TGGGAGGTCA TGTGCTGCAT ACTTACCTAC CTGAAAGATA TGGAATTTGG 240 AGCAGGAACC TGGGTTCCAG TCCTGTCTGC TCCCTTGATT AAGTTACTTA TCCTTCCTTG 300 GCTCAGCTTC CTAGTATAAA GCAGGGAAAA TAAAACCTAT GTCTTTGGGT TATTGTAAAG 360 ATTAGGCAAG GGAAACTTAG GCAAAATCTC TTTGTCATCT GAGAGGGGAT GTCCATTTAA 420 TTGGCATGTC AGTAGGGCAG GCATATTGTC CATTTCACAG GTGAGGAGCT TGAGGCCTGG 480 AGAGGGTGGA TGACCTGAAG AAGAAGCTGG CAGCATCACC AGGCAGGGCT GCATGGCAAC 540 TGGGGCTGCT TCTCTCTCTG CCACTACAGG ATCCTGGCTC CCTCACACCA CCCCCATGCT 600 GATGCCCCAC ACGGGCTGCA ACAAGCCCTG CTGGCCTGGC TCCATTTCTG GGTGTGAAAT 660 TTGGCTGAGT CGGCACCTGG TAGAATGGAG CAATTGCTAT CCTGGAGCCT GGGGCCTGGG 720 ACAGGGCCAA TGCGCAGACC AAGGGTTGAT GGGCGGATCT GACCAAGGGT TGGTGGGTGG 780 GCCTGGCGGG CTTGGCCAGG GAACTCGCCA AAGCTGGGCA GCTGGCAGGA GTGGGGCAGG 840 AGAGGGCCTG GCTTGAGGAC AGCCACTCAG GGAAGCTGAG ACCCAGGGCC TAAGCTCAAA 900 ACAGAGCCCA GCAGCATGAG TGTCTGCCTG GTTGCTGGCG TGCCTGAGCA TGTCGGCCGG 960 TGTCTCCGAG CTTGTCTTTG TGTGTGTGCA CGTGTCTAAG GGTATGCTGG GTGCGTGTGT 1020 TCTTATAAAT GAGTGTGCAT GTCTATCAGT GCAAGAGCTG GTGCACCCAT GTAGTTGTGC 1080 ACATCTGTGT ACCAAGGTGT GTCTGTGTCA GTGTGAGCCT ACACATCTGT GTATAAGCAA 1140 ACTTCTTGCA TGCATACATC TGTCAGTATC CGTGTGTGTC TGTGCATTTC TGCCTGTATC 1200 TGCAAATGTC TGCTTGTGCA CTGTCCATGC AGGTAGGTCC ACACTGGTGT GTGTCTGATG 1260 ACCTCTGTCA GTATCTGCGG ACATGAGTCT GTGCTTTCTG TTAGCATCTG TGCAAGTGTC 1320 ATCTACGTCT ATGAGCATGT TTGTTCTTTC CAGTGCCTCT ATGTGTCTTG TACCTGTATG 1380 TAAATCTGTC CATGCCTGTC GTGAGTGTCT CTGCAGCTGT GCCTGTATGT TGGTGTATTT 1440 TGCAGTGTGT ACATCTAGTG AGGGTATTGG TATTCACTTC AGGATGCAGG CATGGCTGTC 1500 TCAGGGTGAG CAGGATGGAA TCTTCCCTGT GTCTGCAGTG GCTCCCGGTC 1550
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