| Tag | Content |
|---|
EnhancerAtlas ID | HS177-03650 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr11:2799900-2800580 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr11:2800506-2800523 | GGGAACACGGTGTTTCC | + | 6.06 | | MEF2A | MA0052.3 | chr11:2799999-2800011 | GCTAAAAATAGA | + | 6.92 | | MEF2B | MA0660.1 | chr11:2799999-2800011 | GCTAAAAATAGA | + | 6.44 | | RFX5 | MA0510.2 | chr11:2800047-2800063 | GGTTTCCCTGGCAACG | + | 6 | | RUNX1 | MA0002.2 | chr11:2799920-2799931 | CTCTGTGGTTT | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_31950 | chr11:2798532-2803653 | Gastric |
|
| | 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 |
| GH11I002777 | chr11 | 2798271 | 2803546 |
|
Enhancer Sequence | CCACCACTGC CCTTTGAAGT CTCTGTGGTT TGAAGCGGGC TGTTATCTTG CCGAACAGCA 60
AGTCCGTCTA CATGGACTTT ATCTGAAAGT AGCTGAGAGG CTAAAAATAG AGGAGTTTCA 120
GTTGGGCAGG GAGTGCGTCT GCCGCCCGGT TTCCCTGGCA ACGCCTGGCT CTGGCCTGCT 180
TCCATCTCGG CTGCAGCCGG GCAGGCGGGG CAGGCACAGC CCGGCCCAGG CTCCTGCTCC 240
TGCCCCACCC GTCCTGGCCC CCAGGACCTG CAGCGTCACC CTCTCCCCAC CTGGCACCAT 300
CTGCCCATGG CCTGGGGCGG CCGTGGGGCC CTGAGACCAG CAAATTGGGT CATGCAGAAA 360
GAGCGAAGGC TGGTGTTCAG GTGCCTGGCC CCATGGGGCT GTGTGACCAC AGTACCCTGA 420
GTCCCATGGG CCTGGCCACC CTCTGTCAGC ACAGACCTGA GCAGGGCTGG TGCAGACCTT 480
TGCCAGGCAG ATGGCCCAGT GGGAGATAGC GCCCATCTGG CAGGACAGGA AGCAAGACCC 540
GGGAGAGGTC AGCTCACAGG ATTGGCAAGC TCAGAGGCCC AGAAGCCTTG GCCTCTCTGC 600
TGCCCGGGGA ACACGGTGTT TCCCTGGCTT TCTCTTTGCG CAAGGGCTGG GTGACTCCTG 660
GCTGGCACAC CCAGTACAGC 680
|
