Tag | Content |
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EnhancerAtlas ID | HS002-00614 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:117188350-117189790 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr1:117189630-117189641 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr1:117189630-117189640 | AAAACAAAGG | - | 6.02 |
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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 |
GH01I116645 | chr1 | 117188405 | 117192183 |
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Enhancer Sequence | CCTTCCCCAA ATATCCACTT CTGTTTTCTT TCCTCAGTGT GAGTAAGTGG CTCTAATGAT 60 CCACAAACCT TCCAACCAGC CAAGTCAAGG ACCAGCAGGA GGACTCAGGA AAGTACTGAA 120 ATGCTGGGGA GAACCAGGAC AGCGGCTGAG CACAGCCAGA CAGGGAGGGC AGCCTGGTGG 180 GGCCCTGGAA GCCATGGACG CGACTGCGCT GGGAGTGGGG ATGGGAGGTA GCAGGAGTTG 240 GTGGGTGGGG CACAAAGTGG GAGCCAGGGC CGAATTGCTG CTGATTTGAC CATTTTGCAA 300 AAGGCCAGCC TGGCTGTGGC CTCAGGCCTC TCACTTCCTC TACCCTAATG AGGGGTCATA 360 GAAGTGCCTT CCCACAACTG CAGCATCTCC CTCCACATTT GGGCTCAAAT ACAGAGTGGG 420 GCCGGAGACA GAAAAAGTCT CCGTGACACA CTGTGATTTG TTTCTGCACC GTGTGAACCC 480 TTGGCTCTGT GACACGGAAC ACAAGTTTCA GCAGTTCCTG TCACTTCCCA CAGGCGAAAC 540 AGACAGAGCC TTCTTTTGTC CGGCTTCTGG TGAAACGCCA TTATCGTTAT TTTTAGGAGG 600 AAGATGGAGA ATTGGGGGGG GTCCACACAA AGAGGATGGA TTCAGAAGAC TTCCAGGAAC 660 CTTAAAAGCC TTGGAAACTA ATTGTGCCAG TTCTTTTTGA TGTCTAATTT TACTCCAAAA 720 GTTCCTCTCA GCACAATATA TTAATACTTA TCAGCCAAGA GAAGGTTAGG TTTTGGCTCA 780 CAAACAGTCA AGGAGAGAAT CTCCTTAATT CATTGAGAAG GCAGAAGATG GCGTTAAAGA 840 GTATTCATAG GTAACTAAGA TTGCCAGAGG GAGAATCGAG TGAGTTGTCA GCGGTGAAAT 900 ACAGAGGAGG TAGAGAGAGC TACACTGAGA CAACAAAGGC AGCTTAAGGG AACAAAGCCA 960 GCTAAGGGAA CAAAGCCGGG GTCCCTCAGG TCTGTGGCCA CCGGCTACAG CCAGGACAGC 1020 CTGGTAGCTG AAGAGCACGT CCTTGCCTGT TACATGCCTG TGTTTCAAGT GATGCTAACT 1080 TGCTAATGCA GATGTCTCCC CAAACCCTGC CCCTGGCTCA CCACCCAGTG AGCAATCACT 1140 CACTTTCCCC AGGACACCTT CAGGGAGGTA CTCTGCCAGC ACCGCACACT TAAACGGCTA 1200 ATGCAGGTTC TTCTCTCAGA CGCAGCACAG TTCCTGAGAT GACGTCAGCG CTGCTTGCTG 1260 AAAGCACCAG GCAAGGAGGC AAAACAAAGG AAATCCTAAA GAGCAGGCGA GAGAACAGTG 1320 GAACTGGCAG AGAGAGGCAC TGGTGCAGAT GGAGAGGGCA GCAATAAAAA CTGGGGGACA 1380 CTTAGAGGCA AAGGTATGGC AGGTGACAAA AAAGATGAGG CTGAAGGTCA GGAGAGACCC 1440
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