| Tag | Content |
|---|
EnhancerAtlas ID | HS177-06007 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr12:133170280-133171040 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr12:133170736-133170750 | AGGTGGGCGTGGCA | - | 7.14 | | SP3 | MA0746.2 | chr12:133170737-133170750 | GGTGGGCGTGGCA | - | 7.12 | | SP4 | MA0685.1 | chr12:133170735-133170752 | AAGGTGGGCGTGGCAAC | - | 6.33 | | SP8 | MA0747.1 | chr12:133170737-133170749 | GGTGGGCGTGGC | - | 6.62 | | ZNF263 | MA0528.1 | chr12:133170577-133170598 | GAAGGAAGAGGAAATGGGAAA | + | 6.12 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I132593 | chr12 | 133170057 | 133171053 |
|
Enhancer Sequence | CACCTGCCTT TCAGGTGAAA TATCAGAGTG TTCAACCCAG ACCATACCAA TGGCACCCGC 60
GCGGAGTGCA GTCACCAGGG AACCGCCCTG CGGCGATGGC CCCGGCGGGG AGAGGGTGGG 120
TGACGTGCGC TGCGGAGCAT CTGCCCTGGT GGAGGTGCAG CCCCACTCAA AAAGGTTCAC 180
CGTGTGAGTT AAAGATGTTT ACTGTGAACC CTGAAGCAAC CACTAAAACA ACAAAACAAA 240
ATTCTGGCTC ATAAGCCAAC AACTGCAATC AAACAGGATC ATCAAACAGA ATCCAAGGAA 300
GGAAGAGGAA ATGGGAAAGG GAGAGCCGGT GACAGCAGCG GGAGCAGAGA GCAGGACGGC 360
GGGCGTGGCC TCTACACAGT GAGACCAATG GGAGCAGAGA ACAGGATGGC AGGCGTGGCC 420
TCTGCATAGT GAGACCAAAG GGAGCAGAGA ACAGGAAGGT GGGCGTGGCA ACTGCACACT 480
GAGACCAATG GGAACAGAGC AGGACAGCAG GCGTGGCCTC CACGCAGCCA CAGCCACACC 540
GGAGCAAGTG GTCAGACAGC CCCAGTTAAG AGCAGAGATT GCCAGGGAGG GTAGGACAGC 600
AAAACCCAAC GCTAAACTGC TCATGAGAAA TGCACTTTAG ATATGGACAC CAATAAGTCA 660
AAAGGACAGG AAAAGCTATG CCATGCAAAC AAAAATTTTT AAAACCTGCA GTGACTATGT 720
CAATATCAAA GTAACTTCAG GGGCCGAGCA CGGTGGCTCA 760
|
