| Tag | Content |
|---|
EnhancerAtlas ID | HS138-12847 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr14:75405710-75407480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr14:75406896-75406907 | AACAGCTGCAG | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr14:75407436-75407451 | GAGGTCAGGAGTTCA | + | 6.22 | | SOX10 | MA0442.2 | chr14:75406321-75406332 | TCCTTTGTTTT | - | 6.32 | | Sox3 | MA0514.1 | chr14:75406322-75406332 | CCTTTGTTTT | + | 6.02 | | TCF7L2 | MA0523.1 | chr14:75407239-75407253 | TAACATCAAAGACA | + | 6.01 | | Tcf12 | MA0521.1 | chr14:75406896-75406907 | AACAGCTGCAG | + | 6.62 | | ZNF263 | MA0528.1 | chr14:75406177-75406198 | CTCCCTCTCTCTTCCTTCCCC | - | 6.08 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_38122 | chr14:75405657-75410020 | HUVEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 75406346 | 75407402 | | chr14 | 75405775 | 75406286 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I074938 | chr14 | 75405505 | 75410103 |
|
Enhancer Sequence | AAGTCCCTGT CAGCTGTGGC CATTTCTTCT CTGGCTATGA ATGTTCCCGG CATGATGGCG 60
TTCAGATGCT AACTCTCTTG TGGGTTCACC ACAGGGCCAC CTCGCACCAC TGTTCCCTGA 120
TGTGAGAGGT CCCTTCAGCT CTATATCTCT CACCCCACCA CTCAGCCACT GCCCCAACCT 180
CCACCCAACA GCCTACCGAC TGTGGGTCTG CACAGCTGCA GGCCTCCCTC TTGGGAGGAC 240
ATGGACAAGA CAGCTCAAGG ACATGCACCT TCCGCCATGT CCACCTGACC CATGGGCAAC 300
GACTGCTGGG TGCCCCAAGG AGTCCCTGCC CTGTCTGTCT CTGCCTCTTC AATCCTGCCC 360
TCCCCCAACC TCCCTGTCCA GATGGCGCGT GGGCTGATCT CAACAGCAAA TCCAGATCCA 420
GGGAGAGGAG GGGAGGGAGT CAGCACCCCA GGACTCCAGT GACCCATCTC CCTCTCTCTT 480
CCTTCCCCTG TCCTGGTCTT CTGCTTATGG AGACTGAGGA AGGGGGTGCT GGGAGATTTG 540
GGGGCATAGC AGAATTGCTT TAACCATCTC TTAATAAATC CTGTAGGCAA ATGGGCCTAG 600
TCTCAAATGG TTCCTTTGTT TTAGAATATG GGGTACTCAA GGCCCTTTTT CCTTAGCTCT 660
GAGTCCGGCC ACCCATTCGA GCAGCAGAAA AGGCCCACCC AGTACCCTCT GGCACTAGAG 720
CATGGGCTGT CTCTCCCCTC GCATGTGTGG TCCACGAGAG CAGGGTCCTG TGTGTCTGTC 780
CCCACTGGAT CCTGGATGCC TAGTCAGTGT CTAGGACACA GAGGGTGCTC CACAAATAGA 840
TGACAAGCAA ATCCCTCTAG GACCTAAATG GCTGGAACGG CTGCCAATAT AGTCAAGTAG 900
GCCAGCTGGC TCCTTCCTAC CCATTCCTGC TGCGAGGCTC CTGCCCACGG ATGTGGAGTT 960
TTGCTTCTGG CTTCCAGGAG CTTTTCTGGT TTCTGTCTTG CTCTCTACAG GGGTCACTGG 1020
CCTGGGTCGG GAGGCTGCCC GCCATGTGGG TGACCTTATG GAGCCAAAAG CCTTGAAGAT 1080
GCTACCGGGC CTGGGTTGGG GTCCTCAGGG CTGAGCTAGA GGCCTGGCCA GTGGGAGGGG 1140
ATGGGTGCTC TTCCCAGTTC ACAGTGGGTC AAAGGCAACA GCTCAGAACA GCTGCAGCTA 1200
AAGAGAGGAG AGGCAGGAGA GGAAGTGCAT TTCTTTGGCA AAGTATGTCT CCTGGGGCTG 1260
ACTCACACCC GTCTATGACC ACAGCCAGAA GCACATTCTG ACCAGCGTGT CCTGCAGAGT 1320
CCCCAGGCCT CGGTGAACAG GGCACCAAGG ACAGCTGCCT CAGCAGGGCC ACCCCACTCC 1380
GCTGGACATC CCCAGCTCCC CTCAAAGCCC CAGGCAGGCC CCTGTGCCCC TGGGTCCCTG 1440
TGGGTTTCTC CTCAGCAGCC TCAAATGAGG AAGTGAGGCT GAGGAGAGAA TGGGGGAACT 1500
TCTCTTCCCC CAATACATAT AGCAGCATAT AACATCAAAG ACACAGACAC ACAGACACAC 1560
ACACACACAC ACACACACAC ACACACACAC ACACACACCC CTTGCAGGTC AGAAGCAGAG 1620
TGGAGTTTGA TAGTAAGTGG TTTGGATTAA AAAAAAAATA GGCCTGGCAT GGTGGCTCAT 1680
GCCTGTCATC CCAGCACTTT GGGAGGCTGA GGCGGGTGGA TCACTTGAGG TCAGGAGTTC 1740
AAGACCAGCT TGGTCAACAT GGTGAAACCC 1770
|
