Tag | Content |
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EnhancerAtlas ID | HS098-08613 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr10:121379690-121380970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr10:121380857-121380872 | ATCTATTTTTGGATC | - | 6.99 | NFAT5 | MA0606.1 | chr10:121380734-121380744 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr10:121380734-121380744 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr10:121380734-121380744 | AATGGAAAAT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 121379710 | 121380743 | chr10 | 121380600 | 121380657 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I119618 | chr10 | 121377981 | 121380676 |
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Enhancer Sequence | CTGCCTGAGA CTTTGTCTTC AGTTACAAGT GCAGTGAGTG ACGAGGGGAG GGAAGAGAGC 60 TTTTTGAAGC CATATGACCC TGGCATGTAT TTCTGGGCCT CGCGTAGCAC CTTCCCACGG 120 GTGCTAGAGA GACAGGAGAG GAGGAAAGAG CCTCCCTCTT TCAGTCAAGA GTGCCACCTT 180 GTGATGCCAG CACCAGAAAA GAACTGAACA TCACTCTGGC CCCTGAGCTC AGCCCTGTGA 240 TTCATCCCCA CAGCCCCTCC CTGGCAGTAG GCTCTGTTTG TGGTGCTCTG TAATTAGTTA 300 ATGAACTATC TGAATGATAT TCCTGTAGTC ATTCAACCAG CCCCATCCTC AGGGTGTAAT 360 TGTATTTGAG GTTATTTAAA AACATTATTG TATCCAAATA GAGTTTACAT CAGCAGACAG 420 CATGATTCGT AATTCTGCTA TCCCTGGTGT TTCTAAATTG TGCTATAAAC TGCCTGATGA 480 GTCGTGCAAA AATGGCTGCA CCAACAGAGA ACAGTGGGGC TTCTCTGGCA AAAACCACCA 540 ACTATCTAAG GGGAAGAGTA GTAAAAGCAA CTTGTGGCTA GAACCCAGTT GACTTCAGTA 600 TAGAACAGAT TGTTTTCAAG AGGCCCTCCA CTAATTTGAT CATCATCTTT GGATGAACTA 660 ACTCTTCATT ACCTTTACAA GAAAATGCTT GGAAAGGAAG TGGAAGGCTG ATCTGAAGAG 720 TGGCAGGGGC TGCTTCACTT CCTCTGCAGT TTCCTGGAGC TGCCTTGCTC CGCCTCAGGG 780 AATTTGCTGG GAGAGGCTCT CCAGCATCCA GATCCCCCTG CAAAGGTGTT TCGCGATCTG 840 CAGGAACAGG CCCCAGGAGC ATCCCTTGGG GCCGAATGTG CAGTGGGCGA TGCCCCTCCT 900 GACCCAACAG ATCCAAGACG AGCATGATCA ATACAGTCTT GTGGCCAGCC TTGACAATGT 960 TAGGAATCTC TCCACTATCT TAAAAGCTAT TCATTTCCGA AAATGTGCTG TGTGTTTCGC 1020 AACTAAAAAT GGAATCAAAG TAACAATGGA AAATGCAAAG TGTGTGCAAG CAAATGCTTT 1080 TATTCAGGCT GGAATATTTC AAGAGCTTAA AGTTCAGGAA GAGTCTGTTA CTTTTTGAAT 1140 TAATTTCATT GTCCTTTTAG ACTGTTTATC TATTTTTGGA TCAAGTCCTA TGCCAGGGAC 1200 TTGAACTGCA CTTCGGATGT GTTACCAAGG TTATGGTTAC CCTTTGATGC TGTTCCTGGA 1260 AGAAGAAGGA GTGGTGGCAG 1280
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