Tag | Content |
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EnhancerAtlas ID | HS134-05252 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:229326370-229327610 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr1:229326988-229327003 | TCATGACTCAGCAAT | + | 7.6 | NFIA | MA0670.1 | chr1:229326713-229326723 | GGTGCCAAGT | + | 6.02 | Nfe2l2 | MA0150.2 | chr1:229326986-229327001 | CTTCATGACTCAGCA | + | 6.7 | SOX10 | MA0442.2 | chr1:229326626-229326637 | AAAACAAAGAA | + | 6.62 |
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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 |
GH01I229190 | chr1 | 229325947 | 229328624 |
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Enhancer Sequence | TATATACTAT GCATCAAGCT TTACTATGTG TTCCTGGGTG CTTTAAAATA TCAACCGATT 60 CAATATTCTT AGCAACCCCA TGAGGTGGGT ACCATAAGGT GCTGAGATGC ACAGAGGTTA 120 ATCTGCCTAG GGTCCCATAG GTAACAGGCA CAGCCAGAAT TCAAACTCAG GTCTTTAGAG 180 CCAAGTTCTG AACCACTGAC CTACAGGGCC ATGCCACAGA GTGGTGACAG ATTGGGACAA 240 GATATGTGCT ATATCCAAAA CAAAGAAGGA CACAAATTTA GAATGTACAA AGAACTTCTG 300 TAAATCAACA GCGTAAAACA GAGAAGCCCA ATAGAAAAAA AAGGGTGCCA AGTGTATGAA 360 CAGGCAATTT ACAGGAGAGG AGATACAAAG GACTGCTGAC AAGCCTTCAG AAGAGAAATT 420 TAAACTCATT ATTATCAGAA AAATAAAAAT AAAACAACAA AACATCACAT TACACCTACG 480 AGATTGGCAA CAAGTCAAAA GCTGGGCATG AGGCTCCAGG AGGCTAATTG CATTGCTGGG 540 GCAGGGATGG AGTGGACGGG TGCAGCCACT CTGGGGAGCA ACTTGGTGGT TGTTATTCCA 600 TCTGGGTATA CTCATACTTC ATGACTCAGC AATCCAGCTC ATTCATATGT ATATTTATGT 660 ATGCAGGTAT TCAGGAGCTG GATATATATG TAAATCTTCC AGGGAAGTTC TCACAGATGT 720 CCTAGAGGGG AATGAATGTG TGAATGTTCT CATCCCAGTT TGGTCCTGGT ACTGGGGAGT 780 TGAGGGGGAC CTAGATACCT GTTTCTAGGT GAAGCAACGT ATACCATGTG GTGGGTACTC 840 ACTGTGGAAT CCTATGCAGT GGTGTGAAAC CACACACTGG GTGTACACAC AAAAACACAG 900 ACAGAGAAAC ATTGTGCTGA GTAAAAAAGG AAACAGAATT ACATCTATAG CACATTACTA 960 TTTATGTAAA TTGAAAAGCA CACACACAAA ATCACAGTAT GTGTTTTATA AAATATATTT 1020 ATTGTCTTTT TTTTTTTTTT TGAGCTAGGG TCTTGCTCCG TCTCCCAGGC TAAAGTACAA 1080 TCATGGTTCA CTGCAGCCTT GACTTCCTGG GCTAAAGTGA TCCTCCCACC TCAACCTCCC 1140 CAAGTACTTG GAACTACAGC CACATGCCAC CATGCCTGGC TAATTTTTAA AAGATTTTTT 1200 TAGAGATAGT ATCTTGCTGT GTTGCCCAGG CTGGTCTCAA 1240
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