Tag | Content |
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EnhancerAtlas ID | HS133-21530 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:40111840-40114460 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr22:40114321-40114342 | AAAACAAAAACGAAACCAAAA | - | 6.77 | IRF2 | MA0051.1 | chr22:40114325-40114343 | CAAAAACGAAACCAAAAA | + | 6.44 |
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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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Enhancer Sequence | CACAGCAGGC AGGGGCCCAG CTGGGACGCT GCCCCAGACC TGCCACTTCC TGGCCCTGGA 60 GCAGTCTCAG CGGCAGCTCG CGAGGGGCCC GGATGCTGGG GACACAGCTG GCTCTCTCCT 120 CGCTCTGCCT TGTCTTGAGC TTGTCCCAAG TCTTGGGAGT CCCCGGGGCT GATACAGACA 180 GTGATGGACC TGGTGGAGTC TTTCACGTCA GACCCTGGCA CACCAGCCTC TCCATGCTCC 240 CGACCCATGT CCTGGCGCTT CCTGCCCCCC CGCCAGGGCC CGTGCAGACC TCTACTGCAG 300 ACCCCAGCCT GCCCTCCCGA GAGCCTCCCA ACTCCTAGAC AAAATAAGCA GGTTCAGATT 360 CCAGGCCTGA AACTTCTAGC TGGGTGAACC TGGGAAAGTT TCTTCCCCAC TCCGAGCCTC 420 GGTTTCCTCA CTTGTCGAAT GTGGGTAACT CTCCTTGTTA CTGTTCTGAC TCCTGCAGTT 480 CCCCCCTCTT GGCTGGAAAT TAGAGCTGGG CAGCCACGGA GGCAGCCAAG GCCGACAACG 540 GCCTGTGCCT CACCTGACTT CTGGCAGATG CGTGACCACC CTTCCGGTCC TCAGTTGTCA 600 CCAAGTCCTT CCCCTGCCTG ATCCTACCAG ATGCCAAGCC CTGAAGGTAC CACATCCGCA 660 CCGCTGCTGC CACATCCCAC CTCACTCTGG GCCCGTCCAT CATGCCACCC CTGGCCCGGG 720 GCCTCACCTG CGCTTTTGAA TAAATGGATG TGAGTGAATG AATGTGATCA TAGAGGCTGG 780 CCTGGCTATC AGCCATGTTG GGGACTCTTC GTGGGTCTCT GGACTGACTT CAGGATTCAG 840 AATCAGGCAG GGGCAGCGTC TTGGTGGGAC AGCCTTGTTC AACAGTCAAC TCAGTTTTCG 900 CGCAGGGTCT TTCTAAAGGC CGTTGTCTAG GGCTGGAGGG CGGGGGAGGC CTCGGACAGC 960 CGGAACTCAG GAATTGGAAC TCAGGAGCTG GTATTTCCTG GGTCTTCACT TTAAGGAAGA 1020 TGTGAGCTGC TAGGAGCTGG GGACTGAGCT GGGCAGTGAG CTAGGAAGAA GGAAGGGACT 1080 TCCTGGAAGA CAGACAGACA AATACACGCA CACACATGCA CACACTGTCT TTTCTGTTTA 1140 ATAGAGGTAT ATAATATGTG CAGCAAGCAG TGTGAAGTGC AAAGCGAACA AATCTCAAAT 1200 ACACAGCCTG ATTAACTTTT CCATATGCGC ACACCCTTGT TCAAGATACG GAATAGCCTC 1260 CCAGAAAGAA GGCCTCCTCT TGCCCCTCCC AGTCAATCCC AGCCCCTTCC CCAGAGGTAG 1320 CCACGTTTTG GTCTCTCTCA CCGTATACTA GTTTTGCCTA TTCTTGAACT TTGTATGCAG 1380 CAAATCACAC AATGCAGCCT TTTGTGCCTG GCTTCTTTCA CTCAGTGCAG TGTCTGCGAG 1440 AGTCAGCCGT GCCGTCATGT GGATCAATAG CTCATTTCTC TATCTCTGAG GAGCTCTTCA 1500 TTGTGCGGGT GTAACACTGC TCACCCTTCC TCCTGTCGGT GGGCATCTGG CTTGTTTCCA 1560 TTCTTTGTCG ACTTTGAATA CAGCTGCTCT GAGCATTCTT GCACTTGTCT TTGGTTGGAT 1620 ATGTGGACTC TTTTCTCTTA GGTAGACACC CAGTGGTGCA ATTGCTAAGT TATAGGATAG 1680 GCCGGTCAGA TTAACCATTG GTGCACTGGT TTAACCACCG GCTCTTTGAG GAGAATGTGG 1740 TGTTGACCAG CTTCCCTGGA GTAAAGAATC CTACCATGGC CAGTCTCGAG CTGCCGAGGC 1800 GAAGTCACTG CACCCAGGTA AATTCCATCG GACCCTGGAG TCCACATGAG CTGGCTCAAG 1860 AACACCTCTG GGCAGCTTTT CCTTAGGAGC GTGTTCAAAT AGAACAGGGC CTGGGAACAG 1920 GATTATTCCT CCAATAAATG AATGTGAGTG AGTGAATGGG ATCACAGGGG CCGGCCTGGC 1980 TATCAGCCAT GCTGTGGACC TCTTGGGGGC CTCTGGAATG ACTTTAGGAT TCAGAATCAG 2040 GCAGGGGCGG CATCTTGGCG GGACAGCCTT GGTCAACCGC AGAGATTGGG CTGTGTGGCG 2100 AAACATGGGT CCATTCTTGA GGGCACCCTT GATGCTTATA TTTACTTGAC AACGGTGTCA 2160 TCCCAGCATA CTCTCTGGGC TAAAGGGCAA GTGTCCACCT CTCACCAGCA GTAAAAGGGG 2220 ACCGTGGGCT GGGCACAGTG GCTTACGCCT GTAATCCCAG CACTTTGGGA GGCTGAGGCG 2280 GGTGGATCAC CTGAGGTCAG CAGTTTGAGA CCAGCCTAGC CAACATGGTG AAACCCTGTC 2340 TCTACTAAAA AAACAAAAAT TAGCTGGGCG CAGTGGCGGG TGCCTGTCAT CCCAGCTAGT 2400 TGGGAGGCTA AGGAGGTTGC AGTGAGCCGA GATTGCACCA TTGTACTCCA GCTGGGCGAC 2460 AAGAGCAAAA CTCTGTCTCA AAAAACAAAA ACGAAACCAA AAATGGGGGA CCGTGTATCT 2520 TTGAGGGCAG CGTGCCCATG GTGGCTGGGA TCAGCCAGCC ACTCCCAAGG TGAACTGTGG 2580 AGGAGAGGTG CCCCACCCCT GCCAGCAGTG TCTCTTTGCT 2620
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