| Tag | Content |
|---|
EnhancerAtlas ID | HS092-15402 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:114755720-114757620 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr13:114756098-114756119 | CTCAGACCCAGGGACAGCACC | + | 6.49 | | TP53 | MA0106.3 | chr13:114757471-114757489 | CACATGCTCACACATGTC | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_00138 | chr13:114756345-114761325 | Adipose_Nuclei |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 114756646 | 114757228 | | chr13 | 114755819 | 114755916 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I113990 | chr13 | 114755935 | 114757552 |
|
Enhancer Sequence | ACCAGGCTAT GGGGATGGTG AGGTTGGGAA GCGCCTGGAG GAAGACACTT CCAAGGTAAA 60
CAGGGTCTGC CAGCCTGATG CGCAAGGGTG TTCCCAGCAG AGGAAGAGCT GGAGCTGTGA 120
TGCGGGGCGC ACGGCCTAGG AGGAGCTGAG CAAGGTTGGA CAGTGGTGCA GGGAGCAAGC 180
TGATCATGGA GGGCCTGGTC AGCATCTTTC AGAACCTGGG TCTTGTGTGT GATGACCTCA 240
CCCTCTCCGA GGCTCCCTGA CTCTGGCCTC TGCTGTGTCG GTTCCTGCTA TGAGAGGGCT 300
GGGAAGAGGC TGGCTGATGC CAGACCCACT GTCTTGGCCA CCCTGAGGCC TTGTGCCATC 360
TTCACAGTAT CCAGGGACCT CAGACCCAGG GACAGCACCT CGCACACTTG CTGGGGGAGA 420
AGACGCTGTG GTGGGTGGTG GCCCATGAGT GTGTACATGT GTGGTTGTCT GCACATGTGT 480
GTGCATGCCT GCACATGGGC CTGCACATGT GAGCGTGTTG TGTTCAACTG CACATGTGTG 540
CAGGTATTGT TGCCTTGCCT GTCTGCACAC ACATGTACCT GTATGTTCAT TTCACACATG 600
TATTGCTGGG AACATGTGTG TACATGGCTA TGCATACATG TGTATGTGCC TGTGTGTTAG 660
TGTAGGCCTG GAACCCACGT ACACCCAGGG CATGTGGGGC TGGAGAACAG GCGTGGCCAA 720
GCTCACAGAT GGGCAGCTGC ACGGACACCC AGGGCATGTG GGGCTGGAGA TCAGGCGTGG 780
CCAAGCTCAC AGATGGGCAG CTGTGCGGAC ACCCAGGGCA TGTGGGGCTG GAGAACAGGC 840
GTGGCCAAGC TCACAGATGG GCAGCTGCAC GGACACCCAG GGCATGTGGG GCTGGAGATC 900
AGGCGTGGCC AAGCTCACAG ATGGGCAGCT GTGCGGACAC CCAGGGCATG CGGGGCTGGA 960
GAACAGGCGT GGCCAAGCTC ACAGATGGGC AGCTGCGCGG ACACCCAGGG CGTGTGGGGC 1020
TGGAGAACAG GCGTGGCCAA GCTCACAGAT GGGCAGCTGC ATGGACACTC AGGCAGGACT 1080
CATGTGTTTC CAGGCCAAGG CACACTTGAC ACTTCTGGGT TAAATCAGGG GAATGAAAAG 1140
AAGAAAATCT AACAGGCATA ACTCCAGGCA CATTCCGCTC TATTTCCATT CTGAGTGGGA 1200
CTCAAGGGCC CTGTCATATG ATCTCCAAGA GCAGATCCGA GTTCTACCAG ACACTGGCAT 1260
AGAAACAAAC GCAGCTGCTT CACCCCCGTG GGCTTTTCTT GTCTCTGCCT CTCCTGAATC 1320
ACAGACCTCA AACCACTGTC CCCATGTGGT CTAACTGGGC TTATCTGGAT TGCTATTTCA 1380
ATTCTGTAAA GCAATTCAAT GTCACAGATA ATGATACATA CTGCATATAG ATTTGAAACA 1440
CACGGTGTGC CTGGCACTGT TTCAAATATA TATGCAGTAT CGTTATCTGT GACATTGAAT 1500
TGCTTTACAG AATTAGATGG CATGTGTGTA CCCACATATA TGCATGCTGA CACATGTGCC 1560
CAAAGACATA CATGCATACT CACACGTGCC CTCATGTTTC CACACATGCA CAAATTCATG 1620
CATGCTCACG TGTCCCCACA CACACATGCT CACACATGTA CCCACACATT CACTCTCATA 1680
CATGTCATGT CCATACATTC ACACACACTC ACACACGTCC ATTCATGCAC TCACACGTGT 1740
CCACACATTC ACACATGCTC ACACATGTCC ACATTCACAC ATCCACACTC ATACATGTCA 1800
TGTCCACACA TTCACACACG CTCACACATG TCCACATTCA CACGCTCACA CATGCCTACA 1860
CATATGCACA CATCTCATAC GTGTGTCCGC ACACATGCAA 1900
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