| Tag | Content |
|---|
EnhancerAtlas ID | HS002-02954 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr13:114487540-114489100 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA | MA0729.1 | chr13:114488540-114488558 | AAGCTGAAAAGTTCAATT | + | 6.26 | | ZNF263 | MA0528.1 | chr13:114487550-114487571 | GGAGGAGAAGGAGAGAAGGGT | + | 6.04 | | ZNF263 | MA0528.1 | chr13:114487547-114487568 | GAAGGAGGAGAAGGAGAGAAG | + | 7.48 | | ZNF263 | MA0528.1 | chr13:114487541-114487562 | GGAGGAGAAGGAGGAGAAGGA | + | 8.74 | | ZNF263 | MA0528.1 | chr13:114487544-114487565 | GGAGAAGGAGGAGAAGGAGAG | + | 8 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 114487568 | 114487897 | | chr13 | 114487898 | 114488634 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I113784 | chr13 | 114487393 | 114488641 |
|
Enhancer Sequence | AGGAGGAGAA GGAGGAGAAG GAGAGAAGGG TTAGAGAGTG AAATGCCCAT TGTGAGCGGT 60
TGGAGGTGGA TTTCTGAGAC CTGAGGATTT TGAGAGCCCA CTGGGGAGTA GCCCCGGCCC 120
AAGCCTCACA GTTCCCTTCG GGTCAGTTGT CCTCCTTATG CAAATTGCTC AGAAAGTAAA 180
GTGAGAGAAA AGACAAGGCA GGTGGCTAGA GGCCCTCAGG ATCTAGGAAT TAGCCTGGGA 240
CGAGCTGCCA CTGCCCACGG CTTCCTGGGT TGCAAGAGAG CCTCTGGCCC CAACACCTGT 300
CCTAGGTTTC GGCACCAAAT GTAAGAGTTA AAGAGGAAAG AAACATGAAA AGTGGCTCAA 360
CCATCAAAGA GAGGTTTATT TTGGAGAATA AACCTGAGAG GGGCTTCTGG TGAATTTAGG 420
TCAGGAGTGT TCTCTCTTAT ATAAGGGTAT TTAAGGGTTT ATGAAGCGGG GAGCTTATTG 480
CAGGAGCAGA ATGTTTCTGG GTGGAGGAGA GTTTTATTGC AGGGTTGGAA TGTTTCTGGT 540
CGGAGGTGTC ATTTGTGGTT TATGGTCATG CTGACATTAG TCAGTAAGTT GATGTTTCTG 600
GGGCTGGATT TAGGCAGTTT TTAGTCAAAG GGAACTTAAA ATGGCAGTGT TTGTCCAAGA 660
TGGTGATGCC CCTGCTCTGT CACTGGCAAA GTGCCCAGGC TGAGAGTCAT TTCCTGAAGT 720
TCACTGCCCT GCACGCAGGC ACTGGCTTTG CCTTCTGATT TCCACCTGCA CTTCTAATAC 780
CATGACAGAG GTTGCCCTCC AGGCAAAACA CTGCAGGGCA GAGAGGGAGG CTTGCGGGCT 840
TCCCTCACCC CCAGCTGCGG TTTCTGACTC AGCTGGCACT AGGGTCTCAT GTTTGCTCCT 900
CGTCCTACCT CTCTTGCTGT TGTCTTTAGC AAATGCATGA GCAAAGAGAG GTCTTAGACC 960
ACTGACAGAG AAATAGACCC ACCGGAGGAG AGAGGCTGGA AAGCTGAAAA GTTCAATTAA 1020
AGAAACTTCT AAGTCAGCAG AAATTTAGAA ATTCAGTCTC CCCAACATGA GCTTTCCCTG 1080
GTTTTGAAAC CCTTAGGTCA TTGGTCAGGG TCAGAAGTAG GAACGGTTGC CGCTGGGCTT 1140
GGAGACCCCA CTCTGGACGT GACTGTGGGT GCTGGACGTC CCCAGGCCTC CCTGTCCTCT 1200
TCTCGATGAA GGGATGATAG GGTTGCCCTC AGGGGCTCAG GAGAGGCAGG AAAAACACCT 1260
GGGATAGTGG CTTGACGTAC TCACACATCC CTGTGTCTTC TCGGACACTC CCGGAGCCAG 1320
ATGCTTCTCG GAGTGTTTTG GATTTTAGGA GGGAACGTGG GGATGGGCCA GACCGTTTGA 1380
TTCCTCCAGT GGAGTCTGAG GCAGTCTCCC ACTTCGTGTT TCCAAAGCAA AGCACACGAA 1440
CATTCACACA ACGTGGGGTA AATGCAGGCT GTGCATGGAC TTCTTCAGAC CAGGGCATGC 1500
TTTGCTGTAA AATGAATTCA AGCATCAAAC CGTGAGGGCT CTGGACTTCG GGATTCTAGC 1560
|
