| Tag | Content |
|---|
EnhancerAtlas ID | HS052-28598 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr4:58029470-58030640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr4:58030343-58030362 | TCGCCGGCAGAGGGCACCG | + | 6.38 | | HSF1 | MA0486.2 | chr4:58029667-58029680 | TTCTAGAAGCTTC | + | 6.28 | | MEF2A | MA0052.3 | chr4:58030255-58030267 | TTTATTTTTAGA | - | 6.07 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 58029987 | 58030295 | | chr4 | 58030392 | 58030600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I057163 | chr4 | 58029321 | 58030930 |
|
Enhancer Sequence | AAACATTCCT GGAGGCCCAC TTTACTGTGA TATTACAGAT GAGGAAACAA CCCAAAGGAG 60
CTGACATATT TAAGACCCAA AGTGACTTTG ACCCAAAGCC TGCCACCCAC ACCATTCCAG 120
ACCCCAAAGA CTAGTCTGCT TTTTATTTTC ACACTTATTG GAGACTTTCT TTCATTTGCC 180
CATGGTAGTG TTTCTCTTTC TAGAAGCTTC TTTATTGTTT TAAGATGAAA AAATTCATGA 240
CCAATTTCCA GAACCTCAAA ACACAAAGCA ACTGCTTATT TTCCTGAGCT GCTGCGTGAG 300
TCAGTGATTC CCAGTGTTGC TGTGCCTGAA AACCCACCAC TAATGTCAGC GCCTTGTGCT 360
GTTGAGTTGC ACGCGGCGCC CCTGCAGTCC AGGGCTGGGG CTAGCCCGGC GAGCGCGCGG 420
CAGGCAGAGC ATTCCCGGAC GAGTCCGGTA GATGGTAGCA TTGTGCAGCC GATGCGTCCT 480
CTCCCAGCTT GCGTCTCATT TTTCCCTCTC CCCCTTTCCT GGGCTCAGCG GTGAGGCTCA 540
GGTACCGGCG CCGCCCTGAT GCCTACTATG CCGCGCCATC TCCAGATGGT CCGCACCTGG 600
CGGGTCACGA CGAGTCTCAA TCCACAGCAT GGGGCTGACT CGGACTCAGG AGTTTTTGTG 660
GCTCCAGGCG TAACCGTTGC TTTGGATAAA ATTGGTCCAG TTCACTTGAC CAAGGAGAAG 720
TGCAGAGGAG GATAAACGTC CCCATCCCAG TGGTGTCCTC TCCCGACTCC TTTCGTGTAG 780
TGAGCTTTAT TTTTAGAGAC TCCCGCGCCT GCCAGCCGCT CATGCTCGGG TTCCCCAAGC 840
GGAGGGGCTC CGCGTGCAGT GTGATGCCCA CTGTCGCCGG CAGAGGGCAC CGTCGTCACA 900
CACTGCGCAG GAGCCGGCGC GGGAAGGCGG CGGGGCTGTC CTTCCCGGTC AGCGTCCTAC 960
GCGTGACCTT GGGACCCGCA AATGTCTGCG CCGGAGGCAT TGCCTCTTCC CGACTATGGG 1020
GGATACTGCA CGGGGCTCCC GATGGCCTCT TCCACGCCTG GCCCTTCACT TCTTGAAGCT 1080
CACCCTTTTC TTATTTGATC TTTCTAGAAC TGGCGCTCTC TCCCTTCAAA TTCTGTCCCA 1140
CCTTGGCTAG GTTCTGGTTC TGAGACTTCT 1170
|
