Tag | Content |
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EnhancerAtlas ID | HS034-18809 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr20:47139360-47140730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESX1 | MA0644.1 | chr20:47139524-47139534 | GTTAATTGGT | - | 6.02 | IRF1 | MA0050.2 | chr20:47139728-47139749 | CCCAGCTTTCTCTTTCTCTCT | + | 6 | REST | MA0138.2 | chr20:47139884-47139905 | TGAGCTGTCCTAGGTGCTGAA | - | 9.26 | ZNF263 | MA0528.1 | chr20:47140278-47140299 | CCTCACTTTCTCCCCTCCTCC | - | 6.53 |
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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 |
GH20I048523 | chr20 | 47139801 | 47139970 |
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Enhancer Sequence | ACTTCCTATT GCATGGTGGG ATATACAGGC TCACCCACAG CCCCATGGTG AACCCACCCC 60 ACATCCGCTG TGAAACCCCT AGTAAGGACC AGACCAATCA TTCACACCCA GTGGAGTGCA 120 GGCAGCCAGC TCTGAGAACC AACTGTGAAA TGTTCAGAAA TTTTGTTAAT TGGTGTTAAA 180 CCTCTGGTAG TTTGAAATCA GCCATGTTGG GAGTATTTAT ACCAGGAAAA CTGGGCTTTT 240 CTTGACCCTA AAGTGCTGGT TTATCGGCCC AGCACTGAAG TTATACCTCA CGCACAGCCC 300 TGACTTTTGG ATGGAAACTA CCGTTATCCT ATTTGGGGTC GCTTCCCAGT GGCTCCCATG 360 TCCAAGACCC CAGCTTTCTC TTTCTCTCTT CACCCACTTT GGATTGGGAG CCTCAAAACC 420 ACTGTGCTGA AACCACTTCT AGGCATCAGC ACCATTCACT AACAGCACAC TGGCCTTTGT 480 TCTAAGACAG GGATTCAGCA GTTACATAGA TGTGCACTGA GCACTGAGCT GTCCTAGGTG 540 CTGAAATGAT TTCATCAGGA GCAATCAGAG GCTGCCTAGT CCAGGAATCT CAGACATTTG 600 ACCCTGGCTG AATGCCCTTA TTGGAGCAGG AAAGAAGTGC AACAGTTTGC AATAAAATAG 660 GCCCCTCATT TGCCATCCAG GGACACACAC AAAGAAGCAA CAGTGAACAG TCAGTACTTC 720 ACCCAGATTC AAGCAACACA TCCCGACCTA TGTGGTATCC TCCCTGTGAC ACAGGAACGG 780 GGTGGGAGAG GAGTTCTCTA GCCACTTGCC TCCCAAGCTC ATCCATGGGA AAGCATCTTG 840 CTCCCAAGCT GTCAGGGAGA ACCACAAAAC CCCCCTCAGC CGGCAGGAAG CTTGCCCCAC 900 CCTCTTCCCC ATTCACCCCC TCACTTTCTC CCCTCCTCCA CTGACACTCC TCAACTCCCT 960 GGACTGTCCA CTCAGCCCCA GACCTTCTCT CTTCTGCCCC CACTGTGTCG TGACTGTCAG 1020 CCATTCCTCC CTAGTCCAGA AATGTCCATG AGGGTGAGAG AGCAGGGGGA GGACAGGACC 1080 CTCCAGGATG ACCTGGCCTC AGAAAAAGAG CATCTAAAAC ACATCGGAGG CATCGCCTTG 1140 TGAAGCTTCA ACTGCCAGCA AGTCCCATCC ACAGATTCTG TCTTCTTTGC ACAAACAGCA 1200 TCTGCCTCCT TCCTGGCTTG TTGTTATCAG AATCTCAAGA GATGCCAGAC CCCAGGAAAT 1260 GTGGACAGAG GGGCTCTGAT CTGTCTCATC TGTTTGACTA TTTGATTAAT ATCCTCCCTT 1320 GCTCTGCCTT CCCCACCATT TCATCATCAG GCCCAGCCAC AGGCTTGGCA 1370
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