| Tag | Content |
|---|
EnhancerAtlas ID | HS105-38344 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr19:1909030-1910670 | 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 | GAAGTGGAGG TTGCAGTGAG CTGAGATCAT GCCACTGCAC TCCAGCCTGG GCAACAGAGT 60
GAGACTCTGT CTGAAAAAAA AAAAAATGTG GGCTGGGCAT GGTGGCTTAC GCCTGTAATC 120
CAACCTCAGG CCTGCGGTGC GAGTCTGTGG GGGCAGATGC AGGTGGGGGA AGGCTGGCCA 180
GCTGAGACTG TGGTTTGGGG GTGTTCAGGT GGGGTGGATG CCAGAGATGT GGGAGCCAGA 240
GGCGCTGTCC CCCAGGGCCC TGTGAGCAGT CCCTGCAGGC TGGCTGTCCC CACGCCTGCC 300
TCTCTGCTGT GCTGTCTGCC CGCCTAGGGC AGGCTCCCTT CTAATGGGCG GATCCCGAGA 360
GCTGGGGGCC CCACCAGCCC TTCCTCTCCA GTGGAGTGGC CCTACTGCCT CATGTCCACC 420
TGTGCCAGCA GCAGGGATGG TAATGGCTCT ACTATCTCCT GTCCTCACCT GTGCCAGCAG 480
CAGGGATGGT AACGGCTTTA CTGCCTCCCG TCCTCACCTG TGCCAGTGGC TGGGATGTCT 540
TCACCTGTGC CAGCAGCAGG GATGTCCTCA CCTGTGCCAG CGGCAGGGAT GGTAACAGTG 600
CTGGTGATGT CAGGCCGGGA GGTTCTCACC CGAGAGCCGC CTTGGCACAC TGCCCGGCAG 660
TCAGGGATGT TAGCAGGAGC CCCGGGAGTG ATCCCAGCTC TTCCCGCAGC CCCACTCCAG 720
CCAGGGCCTC CTCTGTGACT GAGTAAGCAG GGACACCCCA GTGGCTGCCT GCTCCACCCG 780
ACAGCCAGGG CCCACCACAG CTGCAGGAAT GTGGTCAAGG GATGGGAAGT CGGGCCCACC 840
AGGGGAGGGG CTGCGCTCCG GGGCTTACGT TTCGTGGCTT GTCTTCTGAG GTCTCTCTTT 900
TCCTAGCCCT TGGCCGACTA GGGGGCGAGT GTTTACAGAA ACCACTGGAG GTGGGTGTTC 960
CGTGTCAGTG CCAGGCTGTG TGCTGTTCTG GGAGGGGGCC CCGTGTCCCC CACACTTGGC 1020
ATGCTTGCTT TCTGTCACTG CATAGCAGAC TCCGTGCATC TGTGGGCTTA ATACAACACC 1080
CGCCAGCTCC CGGTTCTGTG GGTCGGGGCC TGAATGTGAC ATGGCTGGCT CCTCTCTGCG 1140
GGGTCTCACC GGGCTGGAAC CCAGGTGTCA GCCAGGGCTG TGTTGTCATC TGGAGGCTCA 1200
ACGGGGGTGG CATCTGCTTG CAACTCACGC AGGCGTTGGC GGAATTCAGC AGCTTGCGGC 1260
CGGGGGACCA AGGGTCCTGC TCAGTTCCTG GCCACATGGC CCTTCTGTCT GGAAGCCAGG 1320
CGCCGCCTGT CCCCGCTTCT GCTTCCAGGC TCTGGCTTCT GGAGATGCAG AGATCACATC 1380
AGTGGTTGCC TGGGTTGCTG TGTGTGTTGT AGGGTGGTGA GACAAGTTTT CTCTTAGGGG 1440
TGATGGAATG TTCTGGAATT TTATAGTGGT GATGGTTGCA CAACTCCAAG TGTCCTAAGA 1500
GCCACTGAAT AGGACACTTG ATAGTTTTTG GTTTTTGAGG TGTCTTTTTT TTTTTTTTTT 1560
TTTTGAGACA GAGTCTCGCT CTGTCACCAG GCTGGAGTGC AGTGGCACGA TCTCGGCTCA 1620
CTGCAACCTC TGCCTCCCAG 1640
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