Tag | Content |
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EnhancerAtlas ID | HS089-07180 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr2:24122980-24124180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr2:24123984-24123995 | ATGAGTCATCC | - | 6.62 | JUNB | MA0490.1 | chr2:24123984-24123995 | ATGAGTCATCC | - | 6.62 |
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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 |
GH02I023900 | chr2 | 24122981 | 24125731 |
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Enhancer Sequence | TTTCACTGTG TTGGCCAGGC TGGTCTCAAA CTCCTGACCT CGTGATCTGC CAGCCTCGGC 60 CTCCGAAAGT GCTGGGATTA GAAGCATGAG CCACCACGCC TGGCCTCTTA CTTTTTATTT 120 TATATTTTTA TTATTTTATT TTATTTGAGA CAGAGTCTCA TTGCCAGGCT GTTCTCAAAC 180 TCCTGACCTA AAGAGATCCT CCCACCTCGG CCCCACAAAG CGCCGGGATT ACAAGCATGA 240 GCCACCACGC CCAGCTTTAG TTTTCTTTAT ACTAGCTCAT CCACTCCAAC CTGGTATATT 300 TACAGACTCC CAAGGTTAAA GTGTGCATTA AAGGTCATCT AACTGAATTA CTAATCCAAG 360 ACATTCTTTA CTCCAATTCT GGTCTGTGAA CCAACAACAT GGGCATGATC TATTTGGAAG 420 CTCATTAGAA ATGTAGAATC TCAGGCTCCA CCCTCAGATC CACTGAATCA GAAACCATTT 480 TTAAAAGATC CCCAGGTGAT TCATGTGCAC ATTAGAGTTT GAAAAGCATT ATTATATAAC 540 ATATTCAAGA CGTAGTCACT GGACCGCCTG ACTGCCACCA TCATGAGTCG CATGTGCACT 600 CCTGGGAAGG GCCTGTCTCA ATCGGCTCTG CCCTGTCACT GCAAGGTTCC CACTTGGCTG 660 AAGCTGACAT CTGATGACAT GAAGGAGCAG ACTTACAAAC TGACCAAGAA GGGTCTGCCT 720 CCCTCACAAA TCAGTGTGAT CCTGAGGCTC ATATGGTGTT GCACAAGTAT ATTTTTGTGA 780 CAGGCAATAC AATCTTAAGA ATCCTTAAGT CCAAAAGACT TGCGCCTGAT CTCCCTGAGG 840 ATCTCTACTG TTTAATTAAG CAAGCAGTTG CTATTCGAAA GCATGCTGAG AGGAACAGAA 900 AGGATAAGGA TGCCAAATTC CATCTGATTC TGATAGATGA ATTCACCGAC TGGCTCAATA 960 TTATTAATAC AAGACCAAGC AAATCCTCCC ACCCAACTGG AAACATGAGT CATCCACAGC 1020 CTCTGCCCTG GTTGCATAAG TTTGTCTACG TACTCAAGTA ATAAAATGAT TGTTTATCGA 1080 AAAAAAAGGA GTCACTGAGG AAGCAACATC ATGTATTTTA AGCTAGAGTG TATCTGTGAT 1140 ACAGAAACTA GTACCTATAA ACTACTGTAC CAATTTAGAT AGCCCAGGCC AGCATTACTC 1200
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