Tag | Content |
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EnhancerAtlas ID | HS164-12609 |
Organism | Homo sapiens |
Tissue/cell | Raji |
Coordinate | chr9:21096010-21097280 |
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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I021094 | chr9 | 21094434 | 21097557 |
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Enhancer Sequence | TTTTCAGTGA AGCTTCAGAG GTCAAAGGGC TAATTTTCCC CTGGCCCCTA CAGCTGCCCA 60 CCCAACATTT CTTACCAGGT GCTACCTGGA CTCCCTCTGC TAGAAGCTCC ACATTGGCCC 120 TATCCAATAC AGTCTTCAGT CACCCTCCAG CCTGGGTTTA CTTTTCCCTT TGGATACCAG 180 GCATTTCTCT GAGCTGTATG TTATTTAATC CTCACAACCA TACTCAGGGG TAAATGCAGC 240 CAGGCCTAGG GTTAAGAAGA GAATACACAG ACAACACACT TACAGCAGCT GCTGAATAAG 300 CACCAGCTCC ATTCCCTTCA CAAACACGTG GACATGTCTA TTTTTGGTTT TTCTGTGGGT 360 GCTTCCTATC TTGGAAGCAG TTTCTGGTGC TTCTACAAAG TGAAACCAAA ACCCTGTACA 420 TCATTAAAAC TTACAACCAA TTACATTTTT ATTTCATCAT CAGGGGCTGT ACGATGAACC 480 AGGTGGTGCA AAAATAACAA TGAGGGTGAT GCAACAAGTG AAAAGGAAAC TAAATGTGAA 540 TTGTCGAATT GGAATTGAAG AATGGAGCGG GTATTCCCCT TTGCCCTGGT GCTTGCCTGA 600 GGCAAGTGCT GCTTATCTTC ACAAAGCAGA AGATTCTTCT GGCTGCCTGG AAGATGCCTC 660 TGTTATTTTA GTGAAAACAT TTAGCTCCTC GAAAGGTAGA GAGAACCAAG AGGTAAAGTG 720 TGCCATTGTA GACAGCTGGT GTGTGTGCCA GGTAGCAGTG CTTCTGTCTA CATCCTGGGA 780 TATTTGCTGC GAAATGATTG GCTCAGTCAC CAAGTGAATG GCTCTTTCTG CCTCTCCCTT 840 GTGAGTAGTT GAGCTGGCAT TAAAAAGTTC CTGGCTAGTT CTTTTGAAAT TACCTCACCT 900 TCCTGCAGAC CTAGAACATT AGGGAATAAT CCTCTAATCA GTTTCAAATA GGAGAGCTCA 960 CATGTAAGCA GCCTTATTTA AGTGCCAGGC ATCATTCTGA GCATGTTATA TAAATTAAAC 1020 AATTAATCCT CACCACAGTT TTATGAGGTA GGACTGTGGT TATCTTAATT TTACAGATAA 1080 GGGAACTGGG CAACGAGAGG TCTGTTTCCT TTCCCCGTTA TGACATCCCA AAATAGCATT 1140 TTGCTCCTTG AGTTCTAGTA GGAACATTCA AGGCCTGGTT GGCCTTTCCC ATCTCTCACT 1200 CTGGACCCCT GGAGGGAAGA AAACTTGGTC TTATTCCTAG CTCTCATTTT TCACTTATTT 1260 CTTATTTTTA 1270
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