| Tag | Content |
|---|
EnhancerAtlas ID | HS098-08072 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr10:99551050-99552230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr10:99551914-99551933 | CCGCCAGCAGAGGGAGCAG | + | 6.07 | | EWSR1-FLI1 | MA0149.1 | chr10:99551844-99551862 | CCTCCCCTCCTGCCTTCC | - | 6.52 | | Klf1 | MA0493.1 | chr10:99551265-99551276 | AGCCACACCCA | + | 6.14 | | ZNF410 | MA0752.1 | chr10:99551537-99551554 | TATTATCATGGGATGGG | - | 6.34 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_47588 | chr10:99551106-99552760 | Pancreas |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH10I097793 | chr10 | 99551137 | 99551273 | | GH10I097791 | chr10 | 99551561 | 99551710 | | GH10I097792 | chr10 | 99551821 | 99552010 |
|
Enhancer Sequence | GGTGGGAACT GGACACACAT TATCTCTAAT TCCCACAAAA GCTTTCTAAG TTAGGAATGA 60
AGTTTCTTCT ATGGGTGAGA ATATAGTGAT TCAAAGGGAT GAAGCATCTT GCCCAAGGCC 120
ACCAGCCAGG GGGTGTCCAC AGTGCTGTCT GGTCCCAGAG CCTGGCCTTT CCCACCACAC 180
CAGGCCATTC CCCACCCCAG ATACAACCCA GTTTCAGCCA CACCCAATCC AGCCTTGGCT 240
TTGAAGCCAC ACAGGACTGG CTACGGTAAG GAGACCTCCT TGGTTGTAGG ATTAAAAGTA 300
ATGTATGAGG CACAGGGCAT GAGAAAGGTA GGGACTTTCA GAGCCACACT GACCTGGGTT 360
TGGGTTCTGA CTTTGCTTCG TGCCTCAGTT TTCTCATCTG TATGGTAGGA GCAATCATGT 420
CCATGGGGCA GGACAACTAC AAGGATTAGA TGAGGTGTGT ACGCAGCAGG TATGCAGCAC 480
TGGCTGTTAT TATCATGGGA TGGGGCCAGG TAGCCCTGAG GCTGGGCCGA GAGAAGGCTG 540
CCCTCCCTGG GAGTAGTGTG TTCTCATGGT GGAAGCAATG TCCCCCCTTC CTGGTCTGAG 600
GACTCCCATC CGGGTTGTGT TCAGCAAAGA CAGGGAATCC AAGTGATGGT GCTGCTTTGC 660
CAGCCCTGTA GGTAGGGCTG AGGCCAGGCC CCCACGCTTG AGGGCCAGAC TCGGCCAGGC 720
TACGGACTTT CCCTAACCTC CCCGCCCTGA CTCTTCCTAG GCTCAGGGGG TCCAGGCTGG 780
GAGCTCCCCG GAGCCCTCCC CTCCTGCCTT CCCAGTGTCT CCCATGTCTC CGGCAAGGAG 840
GGATCTGCAT GCACTTGTCT GCTTCCGCCA GCAGAGGGAG CAGGTGCTGT GTCTGGGAAC 900
CAGGGAGGCT CCAGGTGAGG TGGCTGCCTG GCAGGGGGTC CTCTTGTCCT GGAAGCCCCT 960
TAGCCCAGTG GGTGACTTGG TGATTTGGAG CAGAGCTGGC AAGGGTGGGG GCTGCATCCT 1020
AGAGCTCCTC CGAAAAGACC AGTCTCAGCT CTCTAGAGCC CAGGAGATGG GGCCATGTTC 1080
AAGGAAGGGA AGGGATGGGG TTTCCTGGGC CTGAGATCTC AGATCTCGGC CCCCGCCTCC 1140
CTTGCAATCC AGGGAGGCAA AGAAGTCATT GCTGCACTCC 1180
|
