| Tag | Content |
|---|
EnhancerAtlas ID | HS095-22177 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr4:8102520-8103650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr4:8103219-8103237 | CATTCCTTCATTCCTCCC | - | 7.25 | | GLI2 | MA0734.2 | chr4:8102780-8102795 | GGACCACCCAAGGTG | + | 6.21 | | Klf1 | MA0493.1 | chr4:8103449-8103460 | TGGGTGTGGCC | - | 6.62 | | MEF2A | MA0052.3 | chr4:8103256-8103268 | GCTATTTATAGT | - | 6.11 | | MEF2B | MA0660.1 | chr4:8103256-8103268 | GCTATTTATAGT | - | 6.74 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_48053 | chr4:8096819-8131182 | Psoas_Muscle | | SE_51150 | chr4:8097377-8105418 | Skeletal_Muscle | | SE_53616 | chr4:8101591-8104078 | Spleen |
|
| | 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 |
| GH04I008100 | chr4 | 8102057 | 8104217 |
|
Enhancer Sequence | AACAAGCTGA TTAGCCCAGT GTCTGCCTGG AAATGATGTT GACATCCAAC AGTGCAAGAG 60
TGACGACTAC ATTTACTGTG GGGCATGCAT TGGAAGGAAT TTGGGAGGAT ATTGACATGA 120
ATGTGAGGAA TCTGCATGGT GAGGAAAGTG CCCACACACT AAATTGAAGC GAACGAATCA 180
GGTATACGGC ATGCCTTCAC ATTTTAAAGA GACTCAGACC AGGGGAAAGC TGGGAGGAAT 240
ATACACCCAG ATGGGAACAG GGACCACCCA AGGTGCTGTC CACCCGCTGC TATTTTTCTA 300
TATTGGTGAG TGGAAGACGG AGATGCCAAT TCACATCAAA ACACAAGAAA ACAGAGAACC 360
CCAGGGGCCT GAGTGAGCCT TAACCTGGGC GAGGGCTCCA GGGCTGGCCG GGCATCGCAG 420
CTCCGAGTCT TGGCCCAGCC CGGCTCAGGA TCCCCTTCTG TGAATAACAG GGGGATGAGG 480
CAGACGTCAT CTGAGATTCC TCCTGCCGGG ACTTTCACAA CTCTGCCATG TGATCTTGAC 540
ACTCGTGCCC TGTGCGGCTT AGGCTGTGCG GAACAAGGAG TGCCCTGGGC CAGGGCCAAG 600
GCCCACCTGT CTAGAGCTTC CCTTTGATGC TGGAGGCCCA GGGCTGTTTC TCATAAACGC 660
CTGGAACGCC CAGGAAGCAC GTGTGCAGGC ATCTTGCACC ATTCCTTCAT TCCTCCCAGA 720
CCGCCTAGAA CAGGCGGCTA TTTATAGTCC CAGATGGATG CATCCTCAGG GACAACTCCA 780
CCTGCCTTAC ATGCGCAGCT CACGGGCTCT CCTCCCGGAC ACACGTCCTT CCCTCCCTGC 840
CTGTTTTCTT GGCTCTTGCT AACATTGTGG ACTTGCTCAG TTCCACTTCC AATAGGACCA 900
GAAAATGCCC GCTCTCCCGA GGGCACACAT GGGTGTGGCC TCATCTTTTC ATCATTGCAT 960
TAACAACACA TCACAGTTAA AACATATTCC CAAAGCACAG AGCTCAGCCA CCCTTTGAAG 1020
GCCAAGTAAA CCAGATTTGT TTTTCCAGGC ATTCTGTGCT ATGCGTTTGA CGTATTTATG 1080
TTCTGCATGT ATTCCCATTT GTAGAGTAAG GACAGAGCCA GCTGGATCTC 1130
|
