Tag | Content |
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EnhancerAtlas ID | HS073-14260 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr9:21095770-21097380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr9:21096524-21096545 | CAAGTGAAAAGGAAACTAAAT | - | 6.39 | MEF2C | MA0497.1 | chr9:21096345-21096360 | GTCTATTTTTGGTTT | - | 6.4 | NR2F1 | MA0017.2 | chr9:21096025-21096038 | CAGAGGTCAAAGG | + | 6.74 | TFAP2A | MA0003.3 | chr9:21096603-21096614 | TGCCTGAGGCA | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 21097000 | 21097199 | chr9 | 21096003 | 21096822 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I021094 | chr9 | 21094434 | 21097557 |
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Enhancer Sequence | ACAAACCCAG AAGAATCTAG ACAGACAGGC CTTGCTAGGC TTCCTCACTC AGTCTATTAG 60 CATTAGATCA TGCCCTTTTT GTCCAGTCAT TTTTCTACAT AGCTGTCCAA TTCTTCATTA 120 ACCTAAGCAT AAAAATGGTA TCTTTGGGCT TTCATTCTGA AGGCTCCCAT GTCACATGAA 180 ACTACTATAC AATTAATTTG TATGGCTTTT TGCCTATTAA TCTGCCTTTT GTCAGATGAT 240 TTTTCAGTGA AGCTTCAGAG GTCAAAGGGC TAATTTTCCC CTGGCCCCTA CAGCTGCCCA 300 CCCAACATTT CTTACCAGGT GCTACCTGGA CTCCCTCTGC TAGAAGCTCC ACATTGGCCC 360 TATCCAATAC AGTCTTCAGT CACCCTCCAG CCTGGGTTTA CTTTTCCCTT TGGATACCAG 420 GCATTTCTCT GAGCTGTATG TTATTTAATC CTCACAACCA TACTCAGGGG TAAATGCAGC 480 CAGGCCTAGG GTTAAGAAGA GAATACACAG ACAACACACT TACAGCAGCT GCTGAATAAG 540 CACCAGCTCC ATTCCCTTCA CAAACACGTG GACATGTCTA TTTTTGGTTT TTCTGTGGGT 600 GCTTCCTATC TTGGAAGCAG TTTCTGGTGC TTCTACAAAG TGAAACCAAA ACCCTGTACA 660 TCATTAAAAC TTACAACCAA TTACATTTTT ATTTCATCAT CAGGGGCTGT ACGATGAACC 720 AGGTGGTGCA AAAATAACAA TGAGGGTGAT GCAACAAGTG AAAAGGAAAC TAAATGTGAA 780 TTGTCGAATT GGAATTGAAG AATGGAGCGG GTATTCCCCT TTGCCCTGGT GCTTGCCTGA 840 GGCAAGTGCT GCTTATCTTC ACAAAGCAGA AGATTCTTCT GGCTGCCTGG AAGATGCCTC 900 TGTTATTTTA GTGAAAACAT TTAGCTCCTC GAAAGGTAGA GAGAACCAAG AGGTAAAGTG 960 TGCCATTGTA GACAGCTGGT GTGTGTGCCA GGTAGCAGTG CTTCTGTCTA CATCCTGGGA 1020 TATTTGCTGC GAAATGATTG GCTCAGTCAC CAAGTGAATG GCTCTTTCTG CCTCTCCCTT 1080 GTGAGTAGTT GAGCTGGCAT TAAAAAGTTC CTGGCTAGTT CTTTTGAAAT TACCTCACCT 1140 TCCTGCAGAC CTAGAACATT AGGGAATAAT CCTCTAATCA GTTTCAAATA GGAGAGCTCA 1200 CATGTAAGCA GCCTTATTTA AGTGCCAGGC ATCATTCTGA GCATGTTATA TAAATTAAAC 1260 AATTAATCCT CACCACAGTT TTATGAGGTA GGACTGTGGT TATCTTAATT TTACAGATAA 1320 GGGAACTGGG CAACGAGAGG TCTGTTTCCT TTCCCCGTTA TGACATCCCA AAATAGCATT 1380 TTGCTCCTTG AGTTCTAGTA GGAACATTCA AGGCCTGGTT GGCCTTTCCC ATCTCTCACT 1440 CTGGACCCCT GGAGGGAAGA AAACTTGGTC TTATTCCTAG CTCTCATTTT TCACTTATTT 1500 CTTATTTTTA GAAAATGTGC AATTCTGCCA ACTCTTTGCT TTAGCTCTTG CTTTCAAATG 1560 ACTTGCACAT CTCTGTCCTT TCTCCCCTTT TCCAAAATTT TCAATGTCAT 1610
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