Tag | Content |
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EnhancerAtlas ID | HS134-10396 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr11:67652270-67653290 |
Target genes | Number: 21 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr11:67652689-67652702 | GGTAACAGCTGCA | - | 6.39 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 67652342 | 67652599 | chr11 | 67652691 | 67653133 | chr11 | 67652705 | 67652961 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I067883 | chr11 | 67650905 | 67656465 |
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Enhancer Sequence | TTTATTGGCT CTGAGATCTG AAGCCAGTTT TTTTGTTGTT GTTGTTGTTG AGTATACGGG 60 ATTGTCAGGC AGATCTGGCT GAGGAAAGGA GACTGTGGGC AGCAAGTTTA GAGGCGTGAC 120 TGAAAGTTGC GCTGCGACCT GAGCTGCTGA ATCAGCTTTC TAGTTACTAT GGGCAAAGCC 180 GTGTTTTCTT TTTGATGTCC TTTGCAGTGG ATCACAGCTA TCTGCTGAGG TGAGTAGCCT 240 GCTTTCCTGG TAGATGGCTT TATGTACATG CACAGTAGCA AAGGCGTACT TGCTGTCACT 300 GTAAATGTTA ATACGTTTAT TCTACTTTAT CGGAGAGCCT GAGTGAGGGC GATCAATTCA 360 GCCTTTTGTG CTGAGGTGTT CGCTGGTAAA GCTTGAGCTT ACAACACATC TGTCTCCGTG 420 GTAACAGCTG CACTGGCTTT TAATACTTCC TGCTTGAGGA AGCTGCTCCT GTCTGTGAAC 480 ACGGCGGCAT CTGCCTTTTC CAGGGGCACA TCTTGAAGAT CAGATGGGCC AGTTTCGATA 540 GTTTCTAACA GTTCTTGACA GTCATGAGCA GGAATAGTGC AGTCTGGGTC AGGATGTAGC 600 GAAGCTGGAT TGAAACACTT TGTGGGAGAG AAAGTCAAAC CAGGCTGATC TAACAGTAAA 660 CTTCGAAACT GCAAGATGCG AGCATTTGAC ATCTATTTGC CAGAAGCACT TCGTAGTAAG 720 GTCTTTACAG CATGAGGAGC TGTAAGGGTT AAATTTTGGC TTAGAGTTAA CTTATCATCT 780 TCTTGGACTA GGCTTGCTGT AGCCTCTATG GCTCGCAGAC AACTTGGCCA TCTAGAGGCC 840 ACAGGATCTA GCCTCTTAGA TAAATAGGCC ACTGGGCATC TTTAGGGTCT TAGAGCCTGA 900 GTCAGCACCT CTTTAGCAAC TCCTTGGCTT TTATGGAGAT ATTAGGGAGG GCTAAAGCAG 960 GGGCTTCAGT TAATGCTAAA TTAATGGGCT ATTTCATTCT GCACTTCTTG GATAGCCGCC 1020
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