Tag | Content |
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EnhancerAtlas ID | HS060-16530 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:1991800-1993010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr19:1992985-1992996 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr19:1992985-1992995 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr19:1992982-1992997 | CTGGCCCCGCCCCCG | + | 6 | SP4 | MA0685.1 | chr19:1992982-1992999 | CTGGCCCCGCCCCCGCC | + | 6.2 | Zfx | MA0146.2 | chr19:1992814-1992828 | CCCGCCTCGGCCTC | + | 6.01 | Zfx | MA0146.2 | chr19:1992977-1992991 | CAGGCCTGGCCCCG | - | 6.24 |
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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 |
GH19I001992 | chr19 | 1992821 | 1992970 |
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Enhancer Sequence | TCCCCAGCCC CCGCCCTTTG GGCTGCACAG AGCCCAACTG GGGTCCCCTG AGATCCCTGG 60 CCCTGCTCTG TCTACCTGAC ATTTCCTTAG AGAGAGAGAG AAAGTTCTCT CTGGTTTTTT 120 TTTTTCTTTT TTTTTAGCCA GGCGCGGTGG TGGGGGCCTG TAATCCCAGC TACTGTGGAG 180 GCTGAGGCAG GAGAATCGCT TGAACGCTGG AGGCGGAGGT TGCAGTGAGC TGAGATCGTG 240 CCATTGCACT CCAGCCTGGG CAACAAGAGA AACCCCGTCT CAAAAAAAAA TTATTTTACT 300 TTTTTTTTAG AGACAGGGTC TCACTCTGTC ACTCAGGCTG GAGTGCAGTG GCGCCATCTC 360 CACTCACTGC AGCCTCAACC TCCCGGGCTC AGGCAATCTT CCTGCTTTGG TCCCCCAAGT 420 AGTTGAGATT CCAGACATGC ACCAGCGTGC TTGGCTAATT TATGAAATAT TTTTTTTTAG 480 TAGAGATGAG GTTTCACCAT GTTGGCCAGG CTGGTCTCAA ACTCCTGACC TCTGGTGATC 540 TGCCTGTCTC AGCCTCCCAA AATGCTGGGA TTACAGGCAT GAACCACAGT GCCCGGCCTG 600 AATCTTTTTT TAATTTTTTG TAGAAACGGG GTCTCTCTAT GTTGCCTAGG CTGGTCTAGA 660 ACTCCGGGCC TCAAGCAATC CTCCCTACTT GGCCTCCCAA AGTGCTGGGG TTACAGGCGT 720 GAGCCACCGC ACCCTGCCAA TAATTTTTTG AAGTATCACG GAAAAGTCCA AAACACATCT 780 TTTTTTTTCA GGTGGAGTCT CGCTCTGTCA TGCACGCTGG AGTGCAGTGG TGCGATCTCG 840 GCTCACTGCA ACCTCCACCT CCCAGGTTCA TGCAATTCTC CTGCCTCAGC CTCCCAAGTA 900 GCTGGAATTA CAGGTGCCCG CCACCACGCC CGGCTCTTTT TTGTGTTTTT AGTAGAGATA 960 GGATTTCGCC ATGTTGGCCA GGCTGGTCTG GAACGCCTGA GCTCAGGTGA TCTGCCCGCC 1020 TCGGCCTCCC AAAGTGCCGG GATTACAGGC GTGAGCAACC ACGCCCGGCC CAAAACACAT 1080 TTTACTACCA GGCAGGAGCC TGCTGCCTCC CGGGCCCGCC CCCGGCCCCG CCTCCGCCTC 1140 CAGCCTCGGT CCGCCCCACC CCGGCCCCGC CTCCAGCCAG GCCTGGCCCC GCCCCCGCCT 1200 CGTACCGGCC 1210
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