| Tag | Content |
|---|
EnhancerAtlas ID | HS177-10236 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr18:32185290-32185960 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr18:32185742-32185753 | CTTGAGTGGTT | - | 6.32 | | PHOX2A | MA0713.1 | chr18:32185794-32185805 | TAATTAAATTA | - | 6.62 | | PROP1 | MA0715.1 | chr18:32185794-32185805 | TAATTAAATTA | + | 6.32 | | PROP1 | MA0715.1 | chr18:32185794-32185805 | TAATTAAATTA | - | 6.62 | | Phox2b | MA0681.1 | chr18:32185794-32185805 | TAATTAAATTA | - | 6.62 | | RUNX1 | MA0002.2 | chr18:32185903-32185914 | GTCTGTGGTTT | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACATGTCCAA ATGTGTGTTT GAGCTTTTTA AACAAGCTTT GCTTTCTAAT AAGGTAATAT 60
AAGAATGTAA TTAAAACAAA ACAAAGTCCC TCCACCAATC AGTGTTGCAA CATTTGGGTA 120
AATTTTAGAG CTTGACAATT TTCAAAGCAG AGACATTACT CCAGGCTTTC TGCCAAACCA 180
TTACTGGTAA TCTGATGACA AGGGATGAAG CAAATGAAAG TGCTGCTGCC TGGCTTAGTT 240
AGATATGCAT TTTCTAGAAG AGAAGCCAAC AGATTTCTTA TGCAAACCAT CAAAATTGCA 300
ACTCAGGCAC ACACACACAC ACACACACAC ACACACACAC ACACACAGTG CTTTTACAAG 360
TCTAGGAATA TACACATTAA AACACAACTC CATGCTTAAG GGCAATGCAG AAGTAGCAGA 420
CACAGCTAGG GTTGACTGGA TCCTTTCTTT ACCTTGAGTG GTTTTAATAA ATAGCAACAT 480
TTCTCTCAAT GGCTGCAGTA CAAATAATTA AATTACTTAT ATCTGGACAG GATTTAGCAT 540
TGCCTTCACA TGGTTAAATT CCAACTACTA CCCAAAATCT CTCATTGATA AGTGGGTGAT 600
TTGGGCTGCT ATTGTCTGTG GTTTATTTAA ATGATTTAAA TAAACATCTA TTCTCCTATA 660
GTGTTAAAAA 670
|
