Tag | Content |
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EnhancerAtlas ID | HS105-84358 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chrX:16825310-16826750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chrX:16826470-16826491 | TGTTGGTTTCATTTTCATTTG | + | 7.27 | IRF2 | MA0051.1 | chrX:16826469-16826487 | GTGTTGGTTTCATTTTCA | - | 6.21 | SPIC | MA0687.1 | chrX:16826107-16826121 | TACTTCCTCATGTT | - | 6.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chrX | 16825600 | 16826600 | chrX | 16825760 | 16825967 |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI016807 | chrX | 16825255 | 16826934 |
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Enhancer Sequence | ATTAGACATG TCTTACCTCC CTAAATCCCA GAGTTAATCC CTGCTAAAAA TTCTACGTAT 60 CTTTCATGAT GTTTTCTGAA TGCATATTGG TATTTCTAGT GTGCTGTGTA TTTTTAGACA 120 TTTAATTTAG ATTTATTTTG TAACTGCGTC AGAGATCTGT TTGACTTTGA ACTTGCATTT 180 TCCAAAGCTG ATTTATAAAG TGAGGGAAAC AGTGTAATAG AGAGAACATT GACTCTTGAG 240 TTTGGTGGAC CTGGTTTTGA ATTTTCCCAG CCCCTTTTAC TGATTTTAAT ATGATTTTGA 300 GCGAGTTACT TAATCTCGTC AAGTCTCATT TTCTGTACCT GGGAACAATA AGGCCTGTAT 360 CTCAGTGAGG CAGGGAAGGT TAAATGGGGT CACTTTGAGA ATACCTCACA CAGTGTCAGC 420 CTGAGGTGCT AAAGGTTCCC TTTACTTATT TGATAAGTTC CTCCTAGACT GGGAATCTGA 480 GGCAAGCTAA GGATGTCTGT CTAGGAAAAT GCAGAAATAC ACACAACTTT TCCCAACTGC 540 TCCCTCTGAA GGTCCACTCT AGCTCTTGCT GGCAAGGACT GGGTAATTTG TGTCCTCTGC 600 ATATGCCTGG CCCTGGTCAA AGGTGTTTGA GCTCATGTGA GCAAGCAGTA GTTGAAATAA 660 TTAGGAAGTG AATGTGGGTG TTGGTAGAAG GGAAAGAAAC CTAAAAATTT TTTTTTCCTT 720 CTGGTTTTAA TTTCCATGTT CTTAGTTTTG AATGTTTTGA TCCAAAAAGC TATTACAAGT 780 AGTTGATGAA TGCAGAGTAC TTCCTCATGT TCATTTGCAA AAATTTCTAT GATAGTTGTT 840 CTTTGCTCCT GTCATTTATT ATTGATAAAC TGGTGACCTC CCATTTTGAA GGCATCTCTT 900 GGTCAGTTAG TGAGTCCTCT TAGCTCCAAG TATTGAGACA GTGGAAGGAA GATTGCGAAA 960 TATATCCTTT GACCGGAGGG GAGTGGCTAG GGTGAGGGAT TATTCGTGTT TAAGGCTCTT 1020 GTAAACAAAC ACTTGTAGCA CAGTGTTGTG CTTCTCTAAA AGGTACACAT GCTGCTCACA 1080 AGATGCAGAT GTCATAGCTT TTGTGTCTTG ATTTTCTGCA GGGAAGGGTT CTAATAGAAA 1140 TCCATCTGGA AACTACTCAG TGTTGGTTTC ATTTTCATTT GAGATTGGAA TTTAAATAAA 1200 TATTTCCTCC CCTTTTGTTT TTCCAAATAA GGCACTATAT TAGAGCTCTT CATTTTGCTG 1260 TTAAAAAACA TGTTAAAGCT CTTGTAAAGG TAACTCATGG CACCTAACTT AAAAGGTGAA 1320 AACACGCCTG CTGTGAAAGT CTTGTCCCCA CTCACCCAGT TTGTCTCCAG TAATGTTTCT 1380 TTGTGTCCGG CCAGAGATTG GATATACTAC TCTGCTCATA CATTTATACC TCCTCAAGCC 1440
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