Tag | Content |
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EnhancerAtlas ID | HS091-03858 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:207871620-207872530 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:207872413-207872432 | CTCTGCCACCTGCTGGCCT | - | 6.62 | Gfi1b | MA0483.1 | chr1:207872377-207872388 | GGCTGTGATTT | - | 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 |
GH01I207698 | chr1 | 207872301 | 207872450 |
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Enhancer Sequence | ATTTAAGAAT CATTTCAGTA AATTCTTTAA ACCATCAGTA ATGAAATTTG TAATAGGACT 60 GAAAGTGTAA AAATCAGCAT TTTAAAAAAA TCCAGTCATA TATCGTCTGG CTAGTCATGG 120 GCTCTGGGCT CTGAGCTGGG GTTCTGATGG CTGCTGTTAA TATTTCCAGC AAGGTCATTA 180 CCTTGTTTAT GTCCACCTAG TGCTCTTCAC AGGGTGCACA TCTCTACACG GGAGCTGACC 240 AGCATGGGCA ACAAAGCACC TGATCCCAAA ATGTAACACA GAATCTTGGC AGGCTCCAAA 300 AGCCAGCACC CAGTAAGAGT TAGGAGGGCA TCGGGGCCCA ACAGACATTG AGAATTTTCA 360 ACAATTGCGT ACAAAAATTA TGTCCTCTCT TCTTTCCTTT TTCCCCTAGA ATATTCGTGC 420 TTACTCTTCA GCAGCCCAAA TTGCCCTTTT GAGCCTTCTT CACGCCATCA CAGATGTGGA 480 GATGAAAGGA CAATCTCTGT TCTCTCGCCA GCTATTTCCC ACTTTACCAC TCCAAACTGG 540 GAGCTGTTTT ACTTGCTGTT CCAGGGTCAG AGTTACGAAG GCATTGCATT AGAAGACTGG 600 GTTTCTAATA ATGACAATGA GTAATCAGTG AAACTCCAAG CCTGGGTCCT GGGTCAAGGA 660 GATGGTGGCT ATTTTGTGAC CACCTTTTTC AATTCAAGCA GGACTATCAT GTGACCAAGC 720 TACTGCATTT TGCCACTCTA TATTGCTCCC TTCTGGAGGC TGTGATTTTT CCAGAATAAC 780 GTAGCCTGTG CAACTCTGCC ACCTGCTGGC CTCAGGTCCT CAAAATCCTG AAATTGGGGC 840 TGGGCCTTAG ATTGTGAACT AAGTGTCCTC TTGGCTGAAA CAGCTCGCTA TTCACTCCTA 900 TTTTCTTCTT 910
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