| Tag | Content |
|---|
EnhancerAtlas ID | HS073-11759 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr5:141735890-141737270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr5:141737219-141737232 | GAACATTCTAGAA | - | 7.34 | | RUNX1 | MA0002.2 | chr5:141736665-141736676 | AAACCACAGAG | - | 6.14 | | ZNF263 | MA0528.1 | chr5:141736724-141736745 | GCCCCCGCTTCCGCCTCCTCC | - | 6.29 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_34287 | chr5:141734813-141741679 | HCT-116 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I142355 | chr5 | 141735231 | 141745153 |
|
Enhancer Sequence | GTAGATGTGA AATAATCCTG TTCATTCATT TTTGAGAATC TAAGCCCCCT GTGGGCAGGA 60
ACCGTATCTG TGTTGTTCCT GCGGTGCGGG GGCTTAGAGT AGTGACCAGC ACTTAGTAAA 120
ACATACTCAT TAAATGACTG AATGAACGAA ATCCCAGGAG GCCAGTTGAG TAGTTTTTTT 180
TTTTTTTTTT TTTTTTCCTG GTCCCGACCA TCTGATTCTC ATTACTTCTA CAGCTCGGGA 240
AGTCTCTGCT TTGGCATTTT ATAAACCTCC TGTGCGTACG TCGACATTTT AACCATAAAT 300
CCAGAGTTTT GGGACTGCAA AACTCGAGGC CAGGGGATTG GGGGAGGGGG ATAACTACCC 360
GGAGGTCCGA AGCCCGGCGG AGCTGCCCTG GGGTTGGGGG GAGGGACGGG AACCCTCGGG 420
AGGACGCCCC TCCGCCCCCT GCCCACCCCC TCGGCGGGAC ATGGCCCCGG GCCGGGACGT 480
CCTTCAGATT GGTGCGCCGC CGCCGCGGCC GTCTCCTCCC GTCGGGCGGG GTGGGGGGTG 540
GTGAGGGACG CGATCCAGGT CGTGGCCTGG CGGCGGCTCC GGCCACAGCC CCCGCATTCC 600
GGCCGCGCGC CCCCGGAGGT GACGCCTTGA GGAAGCTGTA TTTTTTTGGG GGGGAGCCGC 660
AGGGAACCGT TGGGAGAGGG GCCCTGTGTG TGTCCCTTTA AGAGCCGGAG CGCTGCCTCC 720
GCCTCGCAGG CGCCCGGAGC CTCACAAAAG AACAGGATGT TGTTGATTTG TCACCAAACC 780
ACAGAGAGGA AATGATTGTA AATTTCCTTT AAACATCCCC ACCGCGCTCC GGCCGCCCCC 840
GCTTCCGCCT CCTCCGCCCC CGCCCGGTTC GGCACAGCGG GGCCTCAGCG CTCCCGCGGG 900
GCGCCTGCTC CCCGGCCGGG CCACGGGCCG AGCGGCTCCT GGGCGCCTGC GGGAGGAGCC 960
CCCGGCCCGG CCGCTGCCCC AGCTCGCGTT CCAGTTGCTT TTTCTACAGT TGCAGCGGAG 1020
GAAGGTCCTG GGCTTTTGTG TGAGCCCGCG CGCCGCCCTT CTCTCCGGGA GCGAATGGGA 1080
ACCGCGCGCG GGGAGCTCCG TGCTGTGTCT AGGGAGCGCC TTAGCGCGCC ATCCCCGTTT 1140
AGCCTCGCAG CTTCCCTGTA GAGGCAACAA CCGTTATCTC CTTCGTTAGG GTCTGGAGGG 1200
AAACTGAGGC CCAGGTTAGT TACGTGAGCC GAAAGTCACC AGCTCTTGGA ACGCTTTGGG 1260
GGCTCTTGGA ACACACCATG CAGGTTTAGG TCACCCCAGA CCTTATATTT GTGAATCAGT 1320
GAGCGACCGG AACATTCTAG AATCCCCAAG TCATCAAAAG TGGCAATTTA CATTGCGAAG 1380
|
