| Tag | Content |
|---|
EnhancerAtlas ID | HS176-18616 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr19:8488190-8489290 |
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 | ACCTCGGCCT CCCAAAGTGT TGGGATTACA GGCATGAACC ACTGTGCCTG GCCTCTTCTC 60
TGAATTTGCT CTCCCAAACT TTTTCACAGT TTCCCAGAAC AAGCTCCAAA CTGACATGAT 120
TCTTCCTCAA GATTCTCGTC ACTTCTGTTT CCCTGGGTTG GTTTCCGGAC AAAGGGTTCC 180
TTTTTTGTTA ACTTTGTTTG TGTGTGTACT TGGGGGAGGG TGGGATCGGG GTATGGGTTC 240
AGAAAGGAGG CAGGCAGGCA TGCCCTTTTG CCATTGCAGG AGGAAATAGC AGTCCAGGGA 300
CAGGACTGTT GAGAAAGCAG CCATGAGCAG CCTGTTGGGC TCTTTTTAAA GCCGCCCAAC 360
TCCACCCCGC AGCATGAGAA TCTGAGAAAA GGATAGAAAA CAGTCATTTC CAGGCAGGCG 420
TGGTCGCTCA TGCCTGTAGT CCCAGCACTT TGGAAGTCCA AGGCTGAAGG ATCGCTTGAG 480
CCCAGAAGCT CAAGACCAGC CTGGTCAACA TAGTGAGACC CCCCTCTCTA GAAAAAGTTA 540
AAAAATATTA GCTGTGTGGC GTGGTGCCAC CTGTAGTCCC AGCTACTCGG GAGACTGAGG 600
CAGGAGGATC GCTCGAGCTA GGGAGTCCGA GGCTGCAGTG AGCTGTGATT GCACCACTGC 660
ACTCCAGCCT GGGTGACTCA AAAAAAAAAA AAAAAAAGAA AGAAAAAAAA ATACAGTCTC 720
TCTGAGAGGA AATTGGCGTT GTCTGGAAAA TAGCTCTTCT TTGTGTGACC TCACAGTCTG 780
CCTTCTGGCC AGAAATGTTT GGGAAACAGT GACTCATGGC TGTTTGGCCT CTGGGCCACG 840
CCCCCTGCCT CCTGAGCTGC CCTGGGAAGG ACCCGGCATC CCCAGAGACT GGGCCAGGGC 900
TGGAGACTTT TCCGAGGCAG CTTTCTGCAG ATGCTTTTTA TTTCTATTTC CCCCTCACAA 960
GGGCAGAGGA GCAGGTGAGC ACTTCTCTCT GGATGCACAG GTTTCTCAGG TAGCACGGGC 1020
TTCAGGTGTG ATTAGATCCA GGGGCCCGCA AAGATGTCCT TAAGAATCTA CCTTTCCCAG 1080
GCCTTGCGCA GTGGCTCACG 1100
|
