Tag | Content |
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EnhancerAtlas ID | HS129-01580 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:100511520-100512920 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:100512000-100512015 | TGAACTCCTGACCTC | - | 6.22 | SPIC | MA0687.1 | chr1:100512572-100512586 | GACTTCCTGTTTTC | - | 6.11 |
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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 |
GH01I100046 | chr1 | 100511766 | 100516245 |
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Enhancer Sequence | TAATTTTATT CTTCTGTATA TGGATATCCA CTTTTCCTAG CACCATTTAG GAGACTATCC 60 TTTTCCCAAT GTATACTTCG GTGCCGTTGT CAAAAATGAG TTGACTGTAA ATGCATGGAT 120 TTATTTCTGG GTTCTCTATT GTGCTCTATT GTCTATGTAT CTGTTTTTAT ACCAGTATTA 180 TGCTGTTTTG GTTACTATCA CTTTGTAGTA TAATTTGAAG TGAAGTAATG TGATTCCTCC 240 AAGCCTCGTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT GAGACAGAGT CTAGCTCTGT 300 CGCCTAGGCT GGAGTGCAGT GGCGCAATCT TGGCTCACTG CAACCTCTGC CTCCCTGGTT 360 CAAGTGATTC TCCTGCCTCA GTTTCCCGAG GAACTGGGAT TACAGGTCCC ACCACCACGC 420 CTGGCTAATT TTTGTATTTT TAGTAGAGAC GGGGTTTCAC TTTGATGGCC AGGCTGGTCT 480 TGAACTCCTG ACCTCAGGTG ATCCGCCCGC CTTGGCCTCC CAAAGTGCTG GGATTACAGG 540 CGTGAGTCAC TGTGCCCAGC CTCCAGCCTT GTTCTTTTTG CTCAGGATTG CTTTGGCTGT 600 TCTGGCTCTT GTGGTTCCAT ATAAGTTTTA GGATTTAAAA GAAAAAATTC TGTGAGGAAT 660 GTCATTTGTA GTTTGATAGT AACTGCATTG AATCTGTAGA TTGCTTTTGG TAGTATTAAA 720 ATTTTAACAG TATTGATTCT TCCAATTTAT GAACATGAAA TATCTTCCCA TTTGTGTGTG 780 TGTCCTCTTC AATTCGTGTC ATCAATGTTT TGTAGTCTGT AGACATCTTT CACTTCTTTA 840 AGTTTATTCT TAGGTATTAC ATCTGTAGCT ATTGTAAGTG GGATTATTTT CTTGGTTTCT 900 TTTTCAGATA TTTGCTGTTG GCATATAGAA ATGGTACTGA TTTTTGTATC CTGCAACTTC 960 AGTGAATTTG CTTCCATTCT GATAGTTTTT TGGTGGAGTA TTTAGGGTTC TCTCTATATA 1020 AGGTCATGTC ATCTGTAAAG AGGGACAGTT TTGACTTCCT GTTTTCTAAT TTGCATGCCT 1080 TTTATTTCTT ACTCATGCTT AATTGCTCTA GTTGGTACTT TCCAGTACTT TGTTGAATAA 1140 GAGTGGCGAA AGTGGGCATC TTTGTCTTGT TCCAGATCTT TGAGGAAAGG CTTTCAGGTT 1200 TTCCCTGTTC AGCATGATAG CTCTGTGTCT GTCATATATG GCTTTTATCA TATTGAGGTA 1260 TGTTCCTTCT ATACCATTTT TGAGAGTTTT TATGAAGCAG TGTTGAATTT TAGTAAATGC 1320 TTTTTCATCA TTAATTGAAA TGATCATTTT ATTTTCCTTC ATTCTTTTGA AATGATGTAT 1380 CACCTTGATA GATTTATGTA 1400
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