| Tag | Content |
|---|
EnhancerAtlas ID | HS176-12075 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:114755780-114757580 |
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 | CAGGGTCTGC CAGCCTGATG CGCAAGGGTG TTCCCAGCAG AGGAAGAGCT GGAGCTGTGA 60
TGCGGGGCGC ACGGCCTAGG AGGAGCTGAG CAAGGTTGGA CAGTGGTGCA GGGAGCAAGC 120
TGATCATGGA GGGCCTGGTC AGCATCTTTC AGAACCTGGG TCTTGTGTGT GATGACCTCA 180
CCCTCTCCGA GGCTCCCTGA CTCTGGCCTC TGCTGTGTCG GTTCCTGCTA TGAGAGGGCT 240
GGGAAGAGGC TGGCTGATGC CAGACCCACT GTCTTGGCCA CCCTGAGGCC TTGTGCCATC 300
TTCACAGTAT CCAGGGACCT CAGACCCAGG GACAGCACCT CGCACACTTG CTGGGGGAGA 360
AGACGCTGTG GTGGGTGGTG GCCCATGAGT GTGTACATGT GTGGTTGTCT GCACATGTGT 420
GTGCATGCCT GCACATGGGC CTGCACATGT GAGCGTGTTG TGTTCAACTG CACATGTGTG 480
CAGGTATTGT TGCCTTGCCT GTCTGCACAC ACATGTACCT GTATGTTCAT TTCACACATG 540
TATTGCTGGG AACATGTGTG TACATGGCTA TGCATACATG TGTATGTGCC TGTGTGTTAG 600
TGTAGGCCTG GAACCCACGT ACACCCAGGG CATGTGGGGC TGGAGAACAG GCGTGGCCAA 660
GCTCACAGAT GGGCAGCTGC ACGGACACCC AGGGCATGTG GGGCTGGAGA TCAGGCGTGG 720
CCAAGCTCAC AGATGGGCAG CTGTGCGGAC ACCCAGGGCA TGTGGGGCTG GAGAACAGGC 780
GTGGCCAAGC TCACAGATGG GCAGCTGCAC GGACACCCAG GGCATGTGGG GCTGGAGATC 840
AGGCGTGGCC AAGCTCACAG ATGGGCAGCT GTGCGGACAC CCAGGGCATG CGGGGCTGGA 900
GAACAGGCGT GGCCAAGCTC ACAGATGGGC AGCTGCGCGG ACACCCAGGG CGTGTGGGGC 960
TGGAGAACAG GCGTGGCCAA GCTCACAGAT GGGCAGCTGC ATGGACACTC AGGCAGGACT 1020
CATGTGTTTC CAGGCCAAGG CACACTTGAC ACTTCTGGGT TAAATCAGGG GAATGAAAAG 1080
AAGAAAATCT AACAGGCATA ACTCCAGGCA CATTCCGCTC TATTTCCATT CTGAGTGGGA 1140
CTCAAGGGCC CTGTCATATG ATCTCCAAGA GCAGATCCGA GTTCTACCAG ACACTGGCAT 1200
AGAAACAAAC GCAGCTGCTT CACCCCCGTG GGCTTTTCTT GTCTCTGCCT CTCCTGAATC 1260
ACAGACCTCA AACCACTGTC CCCATGTGGT CTAACTGGGC TTATCTGGAT TGCTATTTCA 1320
ATTCTGTAAA GCAATTCAAT GTCACAGATA ATGATACATA CTGCATATAG ATTTGAAACA 1380
CACGGTGTGC CTGGCACTGT TTCAAATATA TATGCAGTAT CGTTATCTGT GACATTGAAT 1440
TGCTTTACAG AATTAGATGG CATGTGTGTA CCCACATATA TGCATGCTGA CACATGTGCC 1500
CAAAGACATA CATGCATACT CACACGTGCC CTCATGTTTC CACACATGCA CAAATTCATG 1560
CATGCTCACG TGTCCCCACA CACACATGCT CACACATGTA CCCACACATT CACTCTCATA 1620
CATGTCATGT CCATACATTC ACACACACTC ACACACGTCC ATTCATGCAC TCACACGTGT 1680
CCACACATTC ACACATGCTC ACACATGTCC ACATTCACAC ATCCACACTC ATACATGTCA 1740
TGTCCACACA TTCACACACG CTCACACATG TCCACATTCA CACGCTCACA CATGCCTACA 1800
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