| Tag | Content |
|---|
EnhancerAtlas ID | HS052-18039 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr19:1909040-1910550 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr19:1910475-1910488 | GAATGTTCTGGAA | - | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 1909082 | 1910160 | | chr19 | 1910172 | 1910548 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH19I001909 | chr19 | 1909068 | 1910290 |
| Enhancer Sequence | TTGCAGTGAG CTGAGATCAT GCCACTGCAC TCCAGCCTGG GCAACAGAGT GAGACTCTGT 60
CTGAAAAAAA AAAAAATGTG GGCTGGGCAT GGTGGCTTAC GCCTGTAATC CAACCTCAGG 120
CCTGCGGTGC GAGTCTGTGG GGGCAGATGC AGGTGGGGGA AGGCTGGCCA GCTGAGACTG 180
TGGTTTGGGG GTGTTCAGGT GGGGTGGATG CCAGAGATGT GGGAGCCAGA GGCGCTGTCC 240
CCCAGGGCCC TGTGAGCAGT CCCTGCAGGC TGGCTGTCCC CACGCCTGCC TCTCTGCTGT 300
GCTGTCTGCC CGCCTAGGGC AGGCTCCCTT CTAATGGGCG GATCCCGAGA GCTGGGGGCC 360
CCACCAGCCC TTCCTCTCCA GTGGAGTGGC CCTACTGCCT CATGTCCACC TGTGCCAGCA 420
GCAGGGATGG TAATGGCTCT ACTATCTCCT GTCCTCACCT GTGCCAGCAG CAGGGATGGT 480
AACGGCTTTA CTGCCTCCCG TCCTCACCTG TGCCAGTGGC TGGGATGTCT TCACCTGTGC 540
CAGCAGCAGG GATGTCCTCA CCTGTGCCAG CGGCAGGGAT GGTAACAGTG CTGGTGATGT 600
CAGGCCGGGA GGTTCTCACC CGAGAGCCGC CTTGGCACAC TGCCCGGCAG TCAGGGATGT 660
TAGCAGGAGC CCCGGGAGTG ATCCCAGCTC TTCCCGCAGC CCCACTCCAG CCAGGGCCTC 720
CTCTGTGACT GAGTAAGCAG GGACACCCCA GTGGCTGCCT GCTCCACCCG ACAGCCAGGG 780
CCCACCACAG CTGCAGGAAT GTGGTCAAGG GATGGGAAGT CGGGCCCACC AGGGGAGGGG 840
CTGCGCTCCG GGGCTTACGT TTCGTGGCTT GTCTTCTGAG GTCTCTCTTT TCCTAGCCCT 900
TGGCCGACTA GGGGGCGAGT GTTTACAGAA ACCACTGGAG GTGGGTGTTC CGTGTCAGTG 960
CCAGGCTGTG TGCTGTTCTG GGAGGGGGCC CCGTGTCCCC CACACTTGGC ATGCTTGCTT 1020
TCTGTCACTG CATAGCAGAC TCCGTGCATC TGTGGGCTTA ATACAACACC CGCCAGCTCC 1080
CGGTTCTGTG GGTCGGGGCC TGAATGTGAC ATGGCTGGCT CCTCTCTGCG GGGTCTCACC 1140
GGGCTGGAAC CCAGGTGTCA GCCAGGGCTG TGTTGTCATC TGGAGGCTCA ACGGGGGTGG 1200
CATCTGCTTG CAACTCACGC AGGCGTTGGC GGAATTCAGC AGCTTGCGGC CGGGGGACCA 1260
AGGGTCCTGC TCAGTTCCTG GCCACATGGC CCTTCTGTCT GGAAGCCAGG CGCCGCCTGT 1320
CCCCGCTTCT GCTTCCAGGC TCTGGCTTCT GGAGATGCAG AGATCACATC AGTGGTTGCC 1380
TGGGTTGCTG TGTGTGTTGT AGGGTGGTGA GACAAGTTTT CTCTTAGGGG TGATGGAATG 1440
TTCTGGAATT TTATAGTGGT GATGGTTGCA CAACTCCAAG TGTCCTAAGA GCCACTGAAT 1500
AGGACACTTG 1510
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