| Tag | Content |
|---|
EnhancerAtlas ID | HS148-04384 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr12:76652560-76653730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK1 | MA0028.2 | chr12:76653566-76653576 | ACCGGAAGTG | + | 6.02 | | ERG | MA0474.2 | chr12:76653566-76653576 | ACCGGAAGTG | + | 6.02 | | ETS1 | MA0098.3 | chr12:76653566-76653576 | ACCGGAAGTG | + | 6.02 | | FEV | MA0156.2 | chr12:76653566-76653576 | ACCGGAAGTG | + | 6.02 | | FLI1 | MA0475.2 | chr12:76653566-76653576 | ACCGGAAGTG | + | 6.02 | | Nkx3-2 | MA0122.3 | chr12:76653261-76653274 | TTTAAGTGTTTTT | - | 6.64 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_37058 | chr12:76652136-76654864 | HSMMtube | | SE_51771 | chr12:76652596-76654254 | Skeletal_Muscle_Myoblast | | SE_63569 | chr12:76652453-76654324 | HSMM |
|
| | 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 |
| GH12I076258 | chr12 | 76652269 | 76654821 |
|
Enhancer Sequence | TGGCAGAACA ACAATATGTG AACAGCAAGA GAGAAAATGT AAGACTAATT GCTTCAGGAA 60
AGATAACTTT GGTACTGCAA TTTAGCCATG AGGGACAAGT CTTAGTGGAC AGCTGGTTCT 120
TCATCCATCG GAAGACTGTG GTCATCTGTT CATTCTACTC TTTCTTCTCT GTGGATGAAG 180
TTTTCCGTCA TTGTCTTCAC ACTACCTTGA CTTTCTCTGG ATTCTATTGA CTTAGACAGA 240
TTACTGGCTC CTAGTGGACT ACTGCATCTG AGCAAATGCT TACTCCCTAT TTAATTGTAC 300
CTGTCTTTAC CTATTTATTC AGAGGAGCCA GCTGCCCTGG ACCCCATCCC AATCTCTGTC 360
AAAGGTCACT CTACTTCCCA ACCCAATGTA TCCCACATTC CTAGAAGACA GAGGCTAGGG 420
AGAGATTAGA AGAGAGAGGT TAGAATGCCA GGATTAAAAG GCAGCTTGTT TTCTTCTTTT 480
TCACATGTCA AACTGTTAAA TGCCATTAGG CCAACTCACT TCCCAGCATG TGACAAGGAC 540
ACTGCTGGCA GGGAACATCT CCTTTCTCTG ACCCTCTTTT GCTCTTCTTA ATCCTCAAAT 600
ATTGAAGTTT TTATCTTCAG CAAATGAAGA GGTAATTTAA ACTGCTTACA GAGAGAAACC 660
GAATGGGGGA AAGGGTATAT GTTGTTAGTA ACCCCCCACA GTTTAAGTGT TTTTAATTGT 720
ACATATAGGT TTTCTGTTAG AAAATGACTA GAATTTTCTA AGGCAGCACT GCCTAATAGA 780
AATATAGTGT GAGCCACACA ATATAATTTT TAAGTTTTTA GTAGTCATTA AAACAAGTAG 840
AAAGATACCA GTGGAATTTT AATAACTGTA TTTCTATACT GCTGCTCCTT CTATTGAATC 900
TAACTTAAAA TTCCATGTAA CCCTCACATG TGGGTATGAA AAACATTAAC AGGAAATGCT 960
AATATAGGGA GTCAGTGAAG CTGGGGTAGG AAATTGATGA TGTGATACCG GAAGTGATCT 1020
GGCAGGGCTT TAAAGTAATG CCAGAGGTCC TTCCAGGCAG TTCTCAACTT GCTCCTTGGC 1080
TGTTCTCCTG ACACTTAAGT CAGAGCATTC TGTAGCTGTA TTTTACAGAA CTGTAATTGC 1140
ACAGATTGTT CCTCTTACAA GAGAAATATC 1170
|
