Tag | Content |
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EnhancerAtlas ID | HS150-03377 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr12:123886490-123887440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HEY2 | MA0649.1 | chr12:123887056-123887066 | GACACGTGCC | + | 6.02 | Npas2 | MA0626.1 | chr12:123887056-123887066 | GACACGTGCC | - | 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 |
GH12I123402 | chr12 | 123886641 | 123886770 |
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Enhancer Sequence | ACAGTCATGA CTCACTGCAG CCTCAACCTC CTGGGCTCCA GCAATCCTCC TCCTTCCTCA 60 GCCTCTAGAG TAGCTGGGAC CAAAGGTGTA CGCCACCACA CCTAGCTTAT TTATTTTTTG 120 TAGGGACAGG GTCTGGATCT GTTGCTTAGG CTGGTCTCTA ACTCCTGTCC TTAAGCGATC 180 CTTCCTCCTG GCTTTCCTGA AGTGTTGGGA TTACAGGAGA GAGCCACTGC CCCTGGCCTC 240 ATTTACATTT TAAAAGACCC CTCTGGCTAC CTTGTGGAGA ACTGAGTGTT CCCTGGGGTC 300 AGAGTGAAAG CCTGGTGACT AGCAAGGGGG CCGGAGCGGG GCCGGGGCCG TGGCTGGGCT 360 GCAGGGCCGC AGTGGGAATG GAGATGGAGA GGAGGTGGCA GGATTTGGGA CTGTCCTTGA 420 GGTTACTCAT TCACCATTGT TCCCAGCACA GACTGCAGCG CCTGGCACAT TGCAGGTGTG 480 GATTGAGTGC CTGGAAAAGC TGCAAGCTGG TTTGGGCCTC TGTGTAGGGG GAATGGGCTG 540 AGCTCAGCAG TTGGTGTCAG GCTCCTGACA CGTGCCATCT GGTTTGGTGA AAGTCTATGC 600 CGTCAAGACA TGCTGGTTTG GGGTGAGCCA CACTGGTTTG GAGCTTCCGA TCTGTCTTCA 660 TTTGGTTCCC TTTTGCTCTG TAGTATCTGT GCAGTGGCAG AGCAGTAGAA CCCAGGGTTA 720 GGGATGGAGG TAGGTGCAGG AGGGGTGGCC TTAGAGGAGA GGTGGATCCA GGGGTGCCCC 780 CTCCCAGTTC TCTGTTCAGG TCTGTATTGA CCCTCGGGAT TGGAGGCCCT CTTCTCATCC 840 ATCGTGGTGG CCTCCATACA GGTGAATCTC AGCGATCCCA AACAGAAGTA TGAGCCATCA 900 GACCAGAGCC ATGTGGACTG CGTGTGTCCC ATCCAAAGGG CACAGCCTCT 950
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