Tag | Content |
---|
EnhancerAtlas ID | HS052-18308 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr19:8488320-8489420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr19:8488997-8489008 | AGTGACTCATG | + | 6.14 | IRF1 | MA0050.2 | chr19:8488876-8488897 | AAAAAAAAAAAGAAAGAAAAA | - | 6.59 | KLF14 | MA0740.1 | chr19:8489023-8489037 | GGCCACGCCCCCTG | + | 6.69 | KLF16 | MA0741.1 | chr19:8489024-8489035 | GCCACGCCCCC | + | 6.62 | SP1 | MA0079.4 | chr19:8489021-8489036 | TGGGCCACGCCCCCT | + | 6.12 | SP3 | MA0746.2 | chr19:8489023-8489036 | GGCCACGCCCCCT | + | 6.82 | SP4 | MA0685.1 | chr19:8489021-8489038 | TGGGCCACGCCCCCTGC | + | 6.03 | SP8 | MA0747.1 | chr19:8489024-8489036 | GCCACGCCCCCT | + | 6.92 | Zfx | MA0146.2 | chr19:8489311-8489325 | GAGGCCGAGGCGGG | - | 6.01 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 8488334 | 8488459 | chr19 | 8488784 | 8489136 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I008422 | chr19 | 8487743 | 8490043 |
|
Enhancer Sequence | GATTCTCGTC ACTTCTGTTT CCCTGGGTTG GTTTCCGGAC AAAGGGTTCC TTTTTTGTTA 60 ACTTTGTTTG TGTGTGTACT TGGGGGAGGG TGGGATCGGG GTATGGGTTC AGAAAGGAGG 120 CAGGCAGGCA TGCCCTTTTG CCATTGCAGG AGGAAATAGC AGTCCAGGGA CAGGACTGTT 180 GAGAAAGCAG CCATGAGCAG CCTGTTGGGC TCTTTTTAAA GCCGCCCAAC TCCACCCCGC 240 AGCATGAGAA TCTGAGAAAA GGATAGAAAA CAGTCATTTC CAGGCAGGCG TGGTCGCTCA 300 TGCCTGTAGT CCCAGCACTT TGGAAGTCCA AGGCTGAAGG ATCGCTTGAG CCCAGAAGCT 360 CAAGACCAGC CTGGTCAACA TAGTGAGACC CCCCTCTCTA GAAAAAGTTA AAAAATATTA 420 GCTGTGTGGC GTGGTGCCAC CTGTAGTCCC AGCTACTCGG GAGACTGAGG CAGGAGGATC 480 GCTCGAGCTA GGGAGTCCGA GGCTGCAGTG AGCTGTGATT GCACCACTGC ACTCCAGCCT 540 GGGTGACTCA AAAAAAAAAA AAAAAAAGAA AGAAAAAAAA ATACAGTCTC TCTGAGAGGA 600 AATTGGCGTT GTCTGGAAAA TAGCTCTTCT TTGTGTGACC TCACAGTCTG CCTTCTGGCC 660 AGAAATGTTT GGGAAACAGT GACTCATGGC TGTTTGGCCT CTGGGCCACG CCCCCTGCCT 720 CCTGAGCTGC CCTGGGAAGG ACCCGGCATC CCCAGAGACT GGGCCAGGGC TGGAGACTTT 780 TCCGAGGCAG CTTTCTGCAG ATGCTTTTTA TTTCTATTTC CCCCTCACAA GGGCAGAGGA 840 GCAGGTGAGC ACTTCTCTCT GGATGCACAG GTTTCTCAGG TAGCACGGGC TTCAGGTGTG 900 ATTAGATCCA GGGGCCCGCA AAGATGTCCT TAAGAATCTA CCTTTCCCAG GCCTTGCGCA 960 GTGGCTCACG CCTGTAATCC CAGCACTTTG GGAGGCCGAG GCGGGTGGAT CACGAGGTCA 1020 GGAGATCGAG ACCATCCTGG CTAACACGGT GAAACCCCGT CTCTACAAAA AATACAAAAA 1080 ATTAGCCGGG CGTGGTGGCC 1100
|