Tag | Content |
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EnhancerAtlas ID | HS108-26360 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr22:19205230-19206790 |
Target genes | Number: 20 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr22:19205366-19205387 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr22 | 19206400 | 19206529 | chr22 | 19206000 | 19206200 | chr22 | 19206200 | 19206400 | chr22 | 19206359 | 19206641 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I019217 | chr22 | 19205501 | 19206590 |
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Enhancer Sequence | CCTGTAATCC CAGCTACTCA GGAGGCTGAG GCAGGAGAAT CACTTGAACC TGGGAAGTGG 60 AGGTTGCAGT GAGCCGAGAT CACGCCATTG CACTCCAGCC TGGTGAAGAG CAAAACTCTG 120 TCTCAAAAAG AGAAAAAAAA AAAAAAAGAA AGAAAGAAAA CCTTGGNGCA NCTTAAATAA 180 ATACACACAG GTTGTTTTAA GGGCAAAAAT AAATTTCTNC CATCTGTTTG AGTCAATACA 240 GGATGCCCCA CCTAAGGTTG CCTCAGGACA CTGCTCTCAG TAAACTTTTC ATAATGAGGT 300 TCCACTCCAG ACACTAAAAG CAGCCTCCCT CTGTTATTAT GCGCTCTGGA TTACAGGAGC 360 ATTGCAGTTG AATTTCGCAC CAGGAGGTGG CTACAGATAT CCAATTACAG CAGAGATAAT 420 GAAAGACCAG CAGCTCTACC CAGAAACAGG AAGACAAGAG GCCCCCGCTG GCTCCGGTAT 480 GGTGCAGTGT TAAAGTGGCC CTTCCCCAGT ACCAACATGA AGTCACCTTC AAGGTGTACC 540 AGGTGGCTGG ACTATACCTG GAGAAATGTC TGATGTCTGG GAACCTGGAT GTAGAACCCT 600 AGTAGAATAT TGTGTTGTTT AATATTTTTA TTAGATTTGG ATGGGTAAGT CCAAAGTTGA 660 AACAGAGATT CAAAACAACA TGACCTTCCA TAAATCTCAA AGTATTTCAA AATAAAAAGT 720 TTATTTAAAA AAGTAGTGGC ACAGGCTTGA GGAAACAGTG GACAGAAAAC GAGAGGATGA 780 AATTCAGTAG AGATAAAGGT CAAATCCAGC CCTCAAGCCT TTCGAAAGCA CTGGTCCAGC 840 AGGTTGGCAA TGTGTATGAG GGAGGTGGGA GTTTTAACTG GTCCTATTCT CAGGGCTGAA 900 GCCACTTGTT GGACGAGGGT TTTGTTCCAA CATTGGTCTT GCCCCACCCC TAAACAGTCT 960 GCCTAGCACC TAGGGACAGT GCTGAGGGCA GCAGAGGCAC TATCTGCAAA TGTCTGTGAG 1020 GCTATAACTG GAGAGGAGGC TCTTCCACAG GGCTGTGGGA AGCCCTCCCA GAGGCCGAGG 1080 CAGACTCCCA CCTGCCAGGC CATACCCAAT AATGACCCCT GGCCCCAGCA CTCTGCCCAG 1140 TCTCCAAGGA GGTGCTGGAT AGTCACAGGG GCATAAAGAG CACCTCAACA AAGGGAAGTC 1200 AGCTGAGACA ACCTTGAAAG CTACTTCACC TCTGTCCACG AGGGCTGAGC TGGGCCCAGC 1260 ATGCAGGCAT GACACCAGGT ACTCTCTTCC TGGGCTGCAT ATCCCTGCTT TGGATCCAAG 1320 GGCCAACTCT ATGCCCTTGG CCAGTTAACA GTTCCAAGTC AGCTTACCCT GGGGAATCAA 1380 GCTATTTTTA GGCAAGCTAT TTCTGCAGGG GAGAAGGTTC GTAAGGACTA AGATGTTTTA 1440 TTTATTTATT TATTTATTTA TTTATTTATT TATTTAATTT TTTTGAGACA GAGTCTCACC 1500 CAGTTGCCCA GGCTGGAGTG CAGTGGCGTG CAGTCTCGGC TTTCTGCAAC CTCCACCTCC 1560
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