| Tag | Content |
|---|
EnhancerAtlas ID | HS176-12070 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:114487890-114488940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA | MA0729.1 | chr13:114488540-114488558 | AAGCTGAAAAGTTCAATT | + | 6.26 |
|
| | 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 |
| GH13I113784 | chr13 | 114487393 | 114488641 |
|
Enhancer Sequence | AGTGGCTCAA CCATCAAAGA GAGGTTTATT TTGGAGAATA AACCTGAGAG GGGCTTCTGG 60
TGAATTTAGG TCAGGAGTGT TCTCTCTTAT ATAAGGGTAT TTAAGGGTTT ATGAAGCGGG 120
GAGCTTATTG CAGGAGCAGA ATGTTTCTGG GTGGAGGAGA GTTTTATTGC AGGGTTGGAA 180
TGTTTCTGGT CGGAGGTGTC ATTTGTGGTT TATGGTCATG CTGACATTAG TCAGTAAGTT 240
GATGTTTCTG GGGCTGGATT TAGGCAGTTT TTAGTCAAAG GGAACTTAAA ATGGCAGTGT 300
TTGTCCAAGA TGGTGATGCC CCTGCTCTGT CACTGGCAAA GTGCCCAGGC TGAGAGTCAT 360
TTCCTGAAGT TCACTGCCCT GCACGCAGGC ACTGGCTTTG CCTTCTGATT TCCACCTGCA 420
CTTCTAATAC CATGACAGAG GTTGCCCTCC AGGCAAAACA CTGCAGGGCA GAGAGGGAGG 480
CTTGCGGGCT TCCCTCACCC CCAGCTGCGG TTTCTGACTC AGCTGGCACT AGGGTCTCAT 540
GTTTGCTCCT CGTCCTACCT CTCTTGCTGT TGTCTTTAGC AAATGCATGA GCAAAGAGAG 600
GTCTTAGACC ACTGACAGAG AAATAGACCC ACCGGAGGAG AGAGGCTGGA AAGCTGAAAA 660
GTTCAATTAA AGAAACTTCT AAGTCAGCAG AAATTTAGAA ATTCAGTCTC CCCAACATGA 720
GCTTTCCCTG GTTTTGAAAC CCTTAGGTCA TTGGTCAGGG TCAGAAGTAG GAACGGTTGC 780
CGCTGGGCTT GGAGACCCCA CTCTGGACGT GACTGTGGGT GCTGGACGTC CCCAGGCCTC 840
CCTGTCCTCT TCTCGATGAA GGGATGATAG GGTTGCCCTC AGGGGCTCAG GAGAGGCAGG 900
AAAAACACCT GGGATAGTGG CTTGACGTAC TCACACATCC CTGTGTCTTC TCGGACACTC 960
CCGGAGCCAG ATGCTTCTCG GAGTGTTTTG GATTTTAGGA GGGAACGTGG GGATGGGCCA 1020
GACCGTTTGA TTCCTCCAGT GGAGTCTGAG 1050
|
