Tag | Content |
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EnhancerAtlas ID | HS105-21176 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:125624620-125626000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr12:125625770-125625785 | TGGTCAGGCTGACCC | - | 6.04 | IRF1 | MA0050.2 | chr12:125624835-125624856 | TCTTCCTTTCTCTTTCCCTTT | + | 7.26 | RREB1 | MA0073.1 | chr12:125625224-125625244 | CCACAACACACCAACACTGC | + | 6.25 | ZIC3 | MA0697.1 | chr12:125625025-125625040 | TCACAGCGGGAGGGC | - | 6 |
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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 |
GH12I125139 | chr12 | 125624374 | 125626130 |
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Enhancer Sequence | GCGAGGGTCA TGGCCAAGTG GAATGGACTC CTGGCATTTG AGGGCTTCCC GACTGCAGCC 60 CTCAGGCAGC CATGGCTGTC CCAAGTCCAG CGGGCCTTTG CTCGGGTCAT GGCTGGGATG 120 TCTGGCCCTT CCTGACAGGA GGCTGCTGGG CTCCTGTCTA CTTGGGGACG CCTCATGCAG 180 GAGCTGGTGT GGGGGTGGGC AGGGGGGCGG TGGCTTCTTC CTTTCTCTTT CCCTTTCCTC 240 TACCTTTTCC CCTCTCCCCA GAGGAAATGG TAGCAGGATT TCTTTTAAGA GGATGCTGCT 300 GTATTTTGCC AGCGGGTGGA AGGTGGCGGT ATTAGCTCCC GTGAGCTGCA CGTGGACCCC 360 TGTGTGAAGC GTAGCAGGGC ACAGAGCAGG CGAGACGTTT GCATCTCACA GCGGGAGGGC 420 CGGCGACATC ACATGAAGTG ACAGGCAGGC CCTTGGAAGC CGGTGCTTAG ATCCTTAATT 480 AGTTCACACG TCGACTGAAT TTTCAAGTGA ATGAATTTTA ATTACATCTC AGGTTAAAAA 540 AAAAAAAAGG CGCCAGTGAT CGAGGACTCG TCACTGGGCT CTGTTGCTCC TGAAGTTTCC 600 TAGCCCACAA CACACCAACA CTGCCAAGGG CTCTTCTGGA TTCAAGGTGA AACACATGTG 660 CCATAAATCT TGGAGCTCTG AATGTTTGGA AAGGGCCCGA CTGTGAGAAG AAGTAACACA 720 CCGTCCCGTG CAGATGGCTG GCTCTGAGGA GGAGTTCATG GGAGCTTGGG GACACTCTTG 780 CCTCTAGTTC TAGGAAGCTG GGCCACTTCT GAAGTAATGG CAATATCAAT AAAGTAATGG 840 TCTTTATCAT AGAATAACGT GATAAAATAT ATAGAGAAGT AAAAAAGTAT AAATAAAAGT 900 AAAATCATCA TAAAACATAG TAGCTAGGCA CTTCTGAAGC TGTGTGTGCA CTGATTCATT 960 CACCCAGTGA CTCACAGCCT TATAGCCTAG GTGCTGGCAC CCCTACTTTC ATTCGAGGAA 1020 GTGAACTCAG GTTCAGGAAT TTACCCAGCA TCCCCCAGAT GGGGTGGCAG GAGCCACATC 1080 TTCCCTGAAA ACTTTCTTGC CCAGGGTGTC TGCTGGGATT TAGGAATGGT CTATGCCTGC 1140 ATTTTTATCC TGGTCAGGCT GACCCTGAAC CCTGAGAGAT ACTCTTTTTT ATATTCCCAT 1200 CTGGAATATG CACTGCCGGG GTCAGTGGGG TGTCTGGAGG GCCCTCTCGA GGCCAGCTTG 1260 GATGTGACAC GTGTCGTGGG TCCCAACGGG GCCCAGTAGA GTGTGCAGCG TTAGAAAAAT 1320 GAACATGCTC GGCTGGGCGC GGTGGCTCAC GCCTGTGATC CTAGCACTTT GGGAGGCCAA 1380
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