Tag | Content |
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EnhancerAtlas ID | HS113-37739 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr9:75885420-75886920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr9:75886206-75886217 | AATGAGTCACC | - | 6.02 | FOSL2 | MA0478.1 | chr9:75886207-75886218 | ATGAGTCACCC | - | 6.14 | JUNB | MA0490.1 | chr9:75886207-75886218 | ATGAGTCACCC | - | 6.32 | MEF2B | MA0660.1 | chr9:75885646-75885658 | GCTATTATTAGC | - | 6.07 |
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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 |
GH09I073271 | chr9 | 75885916 | 75886517 |
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Enhancer Sequence | GGTGGAGAAA AACGTCTATC TAATAAGAAC TAATATTGGG ACATATTTGT TACACCAAAA 60 TTTATCTAAT GTGCAAATCT ATGTCTCACT TACTGATAAC ATAATTTATC AGAACATGTG 120 CAACATAAAG AGAATTTGTA GTACATCCCT TATTACCTTC CTAGACACTC AACACACTTT 180 TACAAACACG GAAAGGTGTT ATTACCAGAG TGCTATAAGA TGGCTTGCTA TTATTAGCTT 240 CACATCTCCG GATGATAAAA TCAGCACTGT TGAGGGGATG CAGAGCAAAG ACAGGACAAA 300 AGAATAGAGT CAGGACAAGT AATACAACTA CTTCTATTTG AATATTTGTG CTAAGCATGT 360 TACTAGATAC TTTATATGCA CTCTCTAATT TCATCCTCAC CATAATCATG TGAAGATCAT 420 ACATAACATT ATAATTTTCA TTTCATGGTT TTAAACACCT GCCTATGATC ATACAACTAC 480 TAAGTGGTAG AACCAGGAAC CCAAACTCAG GAAGTGTGAT GGCAGAGTTC TCAAAACCAC 540 TGCATATCTG CTGAAGACAA TTTCTCTTCT TAAACTAGTC ATTCAACCAA TGTATATATG 600 TTCCCATGTT GTTTATTAAC AGGCTAGCTA GCCCTTTCTC TTCTAAAAAC TTACTGGAGA 660 AGACACCATC TCTCCTTCTA TATATGAGTC ATCACTGGCT CCTCATAGAA CCTTGTGCAT 720 TCCAGTTACG CAAGAAACAT TTCCTGAATA TGTAACCCTC AGTCCAACTG GGAAACCTGT 780 ACATGCAATG AGTCACCCTG TTCATTTATA TAATATCCCT CCCCTCCCAT ATCTTTTCTT 840 TCTTATGTAT TTTCATTTTA CCCTGACAAA TGCATGTTGT TTTTTTAAAA AGTATGCTTT 900 TGTTGTTGAA ACAAGGCTCT TATCCATTCC CCTAGGCATT TTGTCTTCTA ACTTTGAAGA 960 TCTTTCTGCT TTCTCTACTA CAAAACACGA CTCACAAGGC TTTGCCTTTT GCCACTCCCC 1020 TGAGTCTCTG AGCTACAGCT TCACACTGTA GGGGACTGTC CATCCATCTA GAGCACCTGG 1080 GGTTTAAGGT GTAAGCAATT TGACTGTAAT TGCTTCTTTC CAGCAGTTAT TCCTTGAAGT 1140 AGCGAAGGGG GACATTTGGT TGGTTCTCTT TTTCTATCTA CATAAATAGG TATTGGAACC 1200 AAATCCAAAG AGCATGGCGT ATTTAGAAAT AAATGTTACC CCCCTTGAGG AGAGTTTTTA 1260 GCTATGCTTT TGTCTTATTC TTTTCTTGGA TTATGTTTTA GCAGAACCTT AGTTCACTCT 1320 TTCCATTTCC GTTTGATCTG TTGATTCCTC TGGGGGAACT CAAACTTAGG TTTTAATACT 1380 ATATTACTTA AATAAATCAC ACGTTCTTTT TTTTTCTCTC ATATCTCCAT TTTGAATTGA 1440 TGTAATACAG TATTGGACTC AACTACTATT TCTCAAGCTG TAGGTAAAAA GCATTTCAAA 1500
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