| Tag | Content |
|---|
EnhancerAtlas ID | HS089-02609 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr11:65662810-65664120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:65664012-65664030 | CTTTCCTTCCTCTCTGCC | - | 6.34 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_40472 | chr11:65663663-65664738 | K562 | | SE_44975 | chr11:65662742-65671764 | NHLF | | SE_47245 | chr11:65653835-65672695 | Panc1 | | SE_56176 | chr11:65662492-65672275 | u87 | | SE_64549 | chr11:65662910-65664927 | NHEK | | SE_67476 | chr11:65662492-65672275 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 65663074 | 65663440 | | chr11 | 65662976 | 65663055 |
|
Enhancer Sequence | GGTCTCGATC TCCTGACCTC ATGATCCACC TTCCTTGGCC TCCCAAAGTG CTGGGATTAC 60
AGGCGTGAGC CACCATGCCT GGCCTTAAAC TAGATTCTTA ACGCAACTTT CCATGAAAAA 120
CTGAAGCCCA GAGAGGATAA CTTACTTATG GTTCCAGAGC AGGACTTAGA ACCCATAGAA 180
CTCACTCACT CTATTCCACA TTGAGTGACA GGCCAGATGA GAGAGACCAT TTCACCAAAA 240
GGATCCAACT CACAGCTCAC AGCCCTACCT GGAGAACCCA GGATCAAAGG GTCACCCTCA 300
GGACCAGGCT GAAGGAAGGA CGCACAGGAG GGTTTACCCC TGGCCCGCTT CTGCGGCTCA 360
TACCACAGTC CCTCCTCACC ACAAAGGCCA GACATTCTGT TCTGGGAAAC CTGTCTCTGG 420
CTGATCTCTC ACCTTTCCCA GGGCCCTAAC CTCTCTCCCC ATCCTCTACC TGCCGACCAA 480
GCTTTTTAAC CTCATCCCCT GTAGTCTCCC ACACCAAAAT GCCCCAGGGA GAGGAAAGAT 540
GAGCCACTCC TTTAAAGACT CGCCATCTCT TACTCACTTA TTTTGGTAAG GGCTTTGGGG 600
AGCCAAGAAT TGTCAGTTCC CTCTACTTTG AGCCTTCTGT TAGCTTCCAG TGAGACAGCG 660
TGGCTTGGTG ATTAGTTTTG GGGGTTTTAT TTTATTTTGT TTTTTCGGTA GAGACAGGGT 720
CTCTCTATGT TGCCCAACCT AGTCTTGAAC TCCTGGCCTC AAGTGATCCT CCTGCCTAGG 780
TCTCTCAAAG TGCTGGGATT ACAGGCATGA GCTACTGCAC CTGGCCCTGG TTTGGTGGTT 840
AGGATCTGAC TTTAGAGTTG TATAGACCTG GGGCCAAGGC CAGTCCTGTG TCATTACTCA 900
CTACTTGTGT GATCTTGGGC AAGTGACTAC CCTTCTGTGC CTTCATTTCT TTGGTGGAAG 960
ATGGGGAAAA CCAGAGTACA TTCCCCAGAG AGATTTTGTG AGGATTAAAT GAGACAGGGA 1020
AACTGAGACT GAGGGAGTAG CTGAAGGGAA CCCTCTTGTT CCTGTTCTCT CCCAGACAAC 1080
ATAAGCGCCC CCTCTATGCA TGTCAGCAGG TGGAGACCCC CTCACCATTC CGTGTGCGCA 1140
CCTTACATGT TCTTGCCTCC GCCTCCATCC TTGCTCCTGC CACCCCCGCT ACCTGGAATG 1200
TCCTTTCCTT CCTCTCTGCC TCTGCCAGTC CTACCCATCC TTCTAGGCTA ATATGCCACC 1260
TTTTCCAGGA AGCTTTCCCT GATCTGGAAG TGACTGTTGT ACCCTCTGGG 1310
|
