| Tag | Content |
|---|
EnhancerAtlas ID | HS087-10481 | Organism | Homo sapiens | Tissue/cell | HEK293T | Coordinate | chr19:10442200-10443960 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr19:10443176-10443188 | AGCCACGTGCCC | + | 6.18 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAATACAAA AATCAGCTGG CTGTGGTGGC GTGCACCTGT AGTCCTAGCT ACTCGGGAGA 60
CTGAGGCAAG ACAATTGCTT GAACCCGAGG GGTGAAGGTT GCAGTGAGCA GACATCAAGC 120
CACTGCACTC TAGCCTGGCG ACAGAGTGAG ACTCCGTCTC AAAAAAAAAA AAAAAAAAAA 180
AAAGAGTATG CCTTTAGGGA AGCCATTTAA CCTGCATGAA CCTCCTTTTG CAAGATTCAC 240
TGTTTCCAAC AACTCTGTAA GTGAAGTATT AACAAACTCA TGTTGTATAT GAGAAAACTT 300
AGGCTAGGAG AAGTGAAGAG ATCTGCTGGA GGCCATGCAG TTGGGCAGCG CAGCCACCCA 360
TGGGTACCTG ACTGGGGAGC CCACCTTCTA GTAAGCCCCA CGTTGTGTGG GTTCACATGC 420
CTCCCAATTT CCTCCTGCTG ATAAAGCTGC CCTCTTCCAA GCCAGCTCAT TTATTTTTCT 480
TTTTTTTAGA GATAGTGTCT TGTTCTGTCA CCTAGGCTAG AGTGTAGTAG CACAATCATA 540
GCTCACTGCA GCCTCAACCT CCTAGGCTCA AGTGATCCTC CCACCTCAGC CTCCTGCGTA 600
GCTGGGACTA CAGGCACGCA CCACCATGCC TGGCTAATTT TTAAAAATTT TTTGTAGAGA 660
TGAGGGTTTC ACTATACCGC CCAGGCTAGT CTCGAACCCT TGGGCTCAAT ACAGCCTCTT 720
GCCTCAGCCT CTCAAAGTGC TGGGATTAAA GGGATGAGCC ACCATGCCCA GCCTCTCAAG 780
CCAGCTTTGA AGGCAAAGTG CTGGCGCCTG CTGGGACCAG ACACACTGTG CATCTTGCAG 840
GAGAGACAAT GTGTTCCCAG CTGAGAGACT GCAGACACTG AGAGGAAGAC CCAGAAAGAA 900
ACCTGACCAT CCTTAATGAT CCCTGTCCCG ATCTGTCCCC AAATTCAGCC CCTCCCAACA 960
TCCCTGGGGT TCCACTAGCC ACGTGCCCAC CCGGTGTGCT GGTGGGCCGG AGAGCAGGGA 1020
ATCTCAGCAG CAGGAAGCGA GAACCTATTT CACCGCCATA GGGCAGGGCA GTATAGATGC 1080
CATTTCCCTG GGTCCAAAGA GCATTGGGAA GCGCTGCCCC ATGCTGGCCC CATGAGAAGG 1140
GCACTCCTAG CAGGAAGATT AGCCACGAGG GGCTCCATAG AACACAGGCC TCGCTTCCTT 1200
CCTGTAGGTC TGTAGGCTGG TGGCAGAAGA CCCCATTTTC CCAAATTAAT CCTGAGGTTT 1260
TGGGGGCTGA GACCCAGGGG CTGCTGTTAA CTTCCGGATT TATCTCTGAG AGCAGTGAAT 1320
AAACGCGTGA TATGGAGGGG CGTACTCTCC GCAGTCCTGA AACTTCTGGA TGTGAGGTCC 1380
CGCCACCCTG TGGTAGAGTG GGTGGAGAAA AGCATCATCC AAGCAGGGGG CAACTGGTGG 1440
TCCAATGTAC CAGCCCATTC ACAATTCCCC AACAGGACCA AAGCTGTCCG CCCCCTTCCA 1500
TTCCCCGCCC GCTTCCATCA CTTGGTGTCG CCCAAGCCTG TGGTCGCCCC TAGCAACGCC 1560
CTCCCTCACT TCGCAGTCGG TTTCCCCTTT CATCATCGCC CCCCCACGTC CCGCTCTTGG 1620
TCTCTCCCGA TCCCGCGTGG ATCCGGTGCT TGGGCGCCCC CGCCAACGAC CCCCGCGCAC 1680
CTCAGCGTTG GTGTCGCCCG GTTCCCCCCG CGCACGCGCA CCGTGGTATT TCCCGCCACG 1740
CTCCTACACC GCCCCCCCCA 1760
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