Tag | Content |
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EnhancerAtlas ID | HS080-22682 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr22:31201640-31203190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr22:31202572-31202586 | AGGAAATGACTCAT | + | 8.12 | Zfx | MA0146.2 | chr22:31201701-31201715 | GTGGCCTAGGCCTG | + | 6.29 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 31202097 | 31202898 | chr22 | 31202323 | 31202855 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I030805 | chr22 | 31201958 | 31203090 |
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Enhancer Sequence | TACCTCAAAT TTGTGTTTAT GTTCAAACTG TGAAGGCCAT GAAAGGACTC AATAGCTTGA 60 GGTGGCCTAG GCCTGCTGGA GGTGGTGTTC CCAAGGTAGG GACTTTTCTT GGGTCTGTTG 120 TCATCCAGGA ACATTGGCTG GTCAACCCTG GAGCTTGGGT AAAAGGACAA AGGAAATGTT 180 CCCTCCAGGA GAATGGAGCC TAGATGCCAA AGGCCGTGAG GAGTCTGTTC AGAGAAACCC 240 CTTCCAAGAA AGGTTTTGTG GCAAGGGAGG TTTTGTTACA TGGAGAGGCT TCTCTGTCCT 300 GAAATTCTAT CTTTCTGATA CTGGGTTTCC TCCAACGATA TGTGTCTCTT CCTTCTTCTG 360 TCCTGTATGC CCTATGGTAA TAGCAGCTAA AATGGGAAGG TGCTTGTTTC AGGCCAGGCT 420 TTCCTGCAGT AACTCAGTCA TCATCATGAC CCTGTGAGAG GAGAACCACT GCCATCCTTA 480 TTATACAAAT GAAGAGACTG AGGCTCAGAC AGGTCGCAGT GCCCAAGGTC TGACTCTGGC 540 CCTGCCTCTA CAGCATGAGG AGAGGACCTC ACAGATGAGC TGATGACACA GAAAGGAGGG 600 GCAGCAGAGC CGGAGTCACC CCAATCTCCA GGCTCACAAT CCAGTGCTCT CTCCTCACAT 660 TGGGGTGAGA GCGCCCCATC GCTTAGTGGC AAGAGGAGGA AGAATAAGCA GGGTTTAGGG 720 CCAGCCAGGC AGAATCACAA TGGGGAAGAG CTGGTGTCAG GTACCTTCCC TTCCTGGCCT 780 GCCACATCAT CCTGTCTCCA GGATGGGGCT TGTGATCTCA GCAGCTGGGG CAGCAGCCGC 840 AGCAGTAAAC AGGGCTAGAA GGTGGAGCAG AGCCCTTGGA AATCAACTAG GCCAACCTCT 900 CATAATATGA ATGAAGAGCT TGAGGCCCAG AGAGGAAATG ACTCATCCAT GGAGGTGTTG 960 GGGGGAGGAG AGAGATCTTT ATTCCACTGC CCTGGACAGG AACCCCTCCT AATGGACTGC 1020 TCCTCAGTGC CTCTGTGGGA AGCCTGGGTG TTGCTGGTGG CTCTGTCAGA AAGGGCTGCC 1080 CAAGTCCAGG GACCTCCATG GACCCTAGAG ATACCACTGA GCTGGACAGC TCCTTTTTCT 1140 CCCTCCCCAC CTAGCAGCTC CATCTGGCCC CTGCTGGCAC AGGATTGCCG TTCGCAGACT 1200 GCATTGATTT CCATTTCCCG GGTGATGAGA TAATTTAAAG GTTATTCAGT TGAGTTTTTG 1260 CTTCCCTTGA CTTGAGTCCT TTCTCCAAGA GCACCTACTG CCAACAGCCT GAGTTCCAGG 1320 CATTGAAATA AAAAGATGCA ATTGTTGCCC ATAAACTTGA ATTGTTTAAG AGGCATGTGT 1380 GAACTTTTAT AGCTGTTTTG CACACATACC CTGCCTCGAT GGTTACTTAA TGAGCTTACC 1440 CGTGAGGTTG CTCTTTCCAC TGAATGGCAT TTCATGATGC TGAACCTTGC GCCATTCCTG 1500 CAGGTGCGCT CCTTTTCCTA GGTTGCCATT TTCAGTTACT GGCCCCATCT 1550
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