| Tag | Content |
|---|
EnhancerAtlas ID | HS177-24547 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chrX:53316520-53317670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chrX:53316842-53316853 | AGTGACTCATC | + | 6.02 | | JUND | MA0491.1 | chrX:53316842-53316853 | AGTGACTCATC | + | 6.32 | | ZNF263 | MA0528.1 | chrX:53316896-53316917 | AGGGGAGGGGAAGAGAGAGAA | + | 6.22 | | ZNF263 | MA0528.1 | chrX:53317006-53317027 | AGAGGAAGGGGAGGAGAAGAG | + | 6.88 | | ZNF263 | MA0528.1 | chrX:53317565-53317586 | CCCCCACCCCCTCCCTCCTTC | - | 8.05 | | ZNF263 | MA0528.1 | chrX:53317486-53317507 | TCCTCCTCCCACTTCTCCTCC | - | 8.41 |
|
| | 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 |
| GH0XI053286 | chrX | 53315206 | 53318307 |
|
Enhancer Sequence | GCGTTTGTGT TTGTTCACCC AGAAGCTCCC TGGTTCCCTG ACACTTGCAA CCACAGCCAC 60
ACGCTCCAGC CACACGCTCA CACACACTGA CATTCAGTGG CACACAGCAA CAAACGCAGC 120
AGCAACCAGA TATGGTTCTC TGCAGACCCC CTGACATGCA GGGCCACGCG CCAGCATGCA 180
GTGTTGCACT TTGCTCTTCA CAGCCACGCT GCCATGCAGC AGTGCACACC CACATGCATA 240
AACACAGAGG TGCTGCCCGT AAGGCTCAGG GCAGGAGTCG AAGCTTCACT GAGCTCTGTG 300
CAGCCTCCCT CCCCAGCTGC CAAGTGACTC ATCCCCAGGG CTGCTAATTA AAGCCAGGAC 360
AGAGGGGACA GAGGCAAGGG GAGGGGAAGA GAGAGAAGGC AAGTTTATTT CGGTGCCAAC 420
CAGGCACTCA GCCAGCTTAG GGGTCACCCA CTTCCTGGGG CTGGGCCAGG CGGCGGCAGA 480
ACACAGAGAG GAAGGGGAGG AGAAGAGAAA CCTCTTACCC CTTCTTGCCC TTCTTTAGCT 540
TCCTGGAAAG TTACCTCCTC CTCTCTCCCA CTGTCAAAAT CCAGCTCTGA CTCCTCTAGA 600
CTTCTGTCCT CACAAACTGG CTGTCTACAC CATCATCACG CTCCCATTTG GGCTGGCCCG 660
AGCTGGCTCA TCTGTGTCTG CAGCAACCCC AGACTGTGAA GCAGTAAGTG GCAAGGTTCC 720
AGGCAAAGGA AGTGGTAGGA ACAGGGCAGG GTGGGCAACC GGGCTGAGCC AAATGGGAGG 780
CATCATGGGA GGTGATGCAG CTGGATGGCT CTGGGGATGG GTAGTGTCTT GGACATGTGG 840
ATGGGGGAGC CACAGACGGT TCATGAGGTC TTGGCCATCC CAGATTGCCA AGAGGTGAAA 900
ACAAGAGATT ATCTAATCCA AACTCCTGTA GGACAGATTG GAGCACTGAG GCCCACAGTG 960
GGAGGCTCCT CCTCCCACTT CTCCTCCAAC TGCAGTGGCT CCCGTTGCCA TAGGGACGTC 1020
CCTGTCTCCG CGGGTGTCAG CGGCTCCCCC ACCCCCTCCC TCCTTCCCTA GCAACAGGCC 1080
ACCTCCTCCT GCTTTCATCC TTGCGTGCCT AGCAACCCCA GCCTGGTCCC CAGGGCCAAC 1140
AAGTTCAGGC 1150
|
