| Tag | Content |
|---|
EnhancerAtlas ID | HS141-09052 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr19:8488140-8489140 |
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 |
|
| | 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 | GGTTTCACCA TGTTAGTCAG GCTGGTCTCC TGACCTCAGA TGACCCACCC ACCTCGGCCT 60
CCCAAAGTGT TGGGATTACA GGCATGAACC ACTGTGCCTG GCCTCTTCTC TGAATTTGCT 120
CTCCCAAACT TTTTCACAGT TTCCCAGAAC AAGCTCCAAA CTGACATGAT TCTTCCTCAA 180
GATTCTCGTC ACTTCTGTTT CCCTGGGTTG GTTTCCGGAC AAAGGGTTCC TTTTTTGTTA 240
ACTTTGTTTG TGTGTGTACT TGGGGGAGGG TGGGATCGGG GTATGGGTTC AGAAAGGAGG 300
CAGGCAGGCA TGCCCTTTTG CCATTGCAGG AGGAAATAGC AGTCCAGGGA CAGGACTGTT 360
GAGAAAGCAG CCATGAGCAG CCTGTTGGGC TCTTTTTAAA GCCGCCCAAC TCCACCCCGC 420
AGCATGAGAA TCTGAGAAAA GGATAGAAAA CAGTCATTTC CAGGCAGGCG TGGTCGCTCA 480
TGCCTGTAGT CCCAGCACTT TGGAAGTCCA AGGCTGAAGG ATCGCTTGAG CCCAGAAGCT 540
CAAGACCAGC CTGGTCAACA TAGTGAGACC CCCCTCTCTA GAAAAAGTTA AAAAATATTA 600
GCTGTGTGGC GTGGTGCCAC CTGTAGTCCC AGCTACTCGG GAGACTGAGG CAGGAGGATC 660
GCTCGAGCTA GGGAGTCCGA GGCTGCAGTG AGCTGTGATT GCACCACTGC ACTCCAGCCT 720
GGGTGACTCA AAAAAAAAAA AAAAAAAGAA AGAAAAAAAA ATACAGTCTC TCTGAGAGGA 780
AATTGGCGTT GTCTGGAAAA TAGCTCTTCT TTGTGTGACC TCACAGTCTG CCTTCTGGCC 840
AGAAATGTTT GGGAAACAGT GACTCATGGC TGTTTGGCCT CTGGGCCACG CCCCCTGCCT 900
CCTGAGCTGC CCTGGGAAGG ACCCGGCATC CCCAGAGACT GGGCCAGGGC TGGAGACTTT 960
TCCGAGGCAG CTTTCTGCAG ATGCTTTTTA TTTCTATTTC 1000
|
