Tag | Content |
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EnhancerAtlas ID | HS060-22525 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr21:42758190-42759610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr21:42758800-42758821 | TCTTAGTTTCTGTTTCTGGTT | + | 6.44 | Stat6 | MA0520.1 | chr21:42759133-42759148 | GTCTTCCTGAGAAGT | + | 6.63 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACAATAAAGC GAAGCACAAT AAAAGGAGGT TTGCCCGTGC ACACTCTCTC CACATCTGAG 60 CCTTCTCAGG TATAAGTGCT GCCTTCAAGA GAGAAAAAAA TTTATGTTTT CTTAGAGCAA 120 ACTGCATGAG AGAACAGGGT CACAGGAGTT TAGAGGAGCA ATGAAAACTG TCATTGTGGC 180 TGTGAGAGGC TGGGAGTGTG AAAGAGTAGG GAGTAAGAAC TGTTATGGCA GAGGGAAAAT 240 TCGGATCAAG ACCAGTCTGG GAATCCATCC CGAAACATCT CCTTCTCCAT CACCTTCCCA 300 CCCTCCTTGG CCCCCTGTAG TCTGTCCTAG ACCTCTCTCC TGCAGATCGG GGCCTCCAGG 360 TCCCACAGGC TCCCTGGAGC CCCAGGGTCC TGCCCTACCC AACCTGGCTG AGGCCTCCAG 420 GTGGCCTGTC TGAGCACCAG GAAGCCATTG CTGGGAATTC CTCGATTCTT TGACATTGTC 480 CTCCACGTTC CTGGGCTTGT GAAGGAACAT CCTCCTCCAT GTTCCTGGAA CTTCAGCCTT 540 TGCTTGGCTC AGGAGCCTGA ACTCCCCAGG ATGTCCAGGA GTGTCCGAAG GAGAGAATAC 600 AGTCACAGGT TCTTAGTTTC TGTTTCTGGT TGGGCCAGTA AAGCCCCTTC CTCATCCCAC 660 TTTTCCACTT ACTACTAAAG ACAGAAACCA AAAACCATGG CTTCAGGCTG CTAAAAACCT 720 AAAACAAAAC AGAACAACAA CAACAACAAA ATAAGGCAGG TTGGACAAGC TTAGTCATAG 780 AGTCAAAGCT TCCTGCACGC AATCGTGTGC CTTTCTGGAG TCCCACCACG CTTTCCCTTC 840 GTATTTTTGT GTCTCTTCTC AGATTCTTCA TTGTCTTTGA TTTCCAAAGG CACTGCCAAG 900 GTCAGACTGC TGGTCATGTG CACCCTGTGT TCCTCCCCTC CCGGTCTTCC TGAGAAGTCA 960 TGGAAATCTT AGCTCCTCCA GCAAGAACAC ATGTGTCTTT CATTTGAAAG ATTCATGCCT 1020 CTCCTCCATG TGAAAGCCGA TTAATGCTCA TAAGGAAGGG GGTGGGCTCT ATTCTTGGCC 1080 GATTTGTCTC CCCAGACTGT CCCTGTGAAA GGTCTTTCTG TATTCACGGC CTCATTGTAC 1140 GACTCCACTT TCCCGGCAAC AAGTGCTTGG CAGTGTTCAC CCACCAAATG TGTTAGTTTT 1200 CAACTGCAAT TGATCACTTT CTCCTTCTTG AAAGTCTTCT TCGCTGGCAT CTGGGCACAT 1260 TGACCCTGGT TCTTTCTCTC CCTCCTGTTG GTCTCTCCTT AAGTGAATTG TTCCTCACTT 1320 CCCTGACCTC CAAATGTTGC AATGCCCTAG AGATCCATTC TTCCCATTGA AAACTCTCCC 1380 TGCTATGTCC CTGAACTACA GCCCAGTCTC ATGACTGTAA 1420
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