| Tag | Content |
|---|
EnhancerAtlas ID | HS034-10498 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr15:85277800-85278940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr15:85278456-85278474 | CATTCCTTCCCTCTTGCC | - | 6.17 | | Nr2f6(var.2) | MA0728.1 | chr15:85277817-85277832 | TGAACTCCTGACCTC | - | 6.22 | | SPIC | MA0687.1 | chr15:85278529-85278543 | CACAAGCGGAAGTA | + | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09489 | chr15:85276550-85282505 | CD14 | | SE_11419 | chr15:85276610-85281334 | CD20 | | SE_18983 | chr15:85276517-85281348 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_50869 | chr15:85277323-85279318 | Sigmoid_Colon | | SE_53113 | chr15:85277860-85279325 | Small_Intestine | | SE_63014 | chr15:85263877-85307023 | Tonsil |
|
| | 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 |
| GH15I084733 | chr15 | 85276588 | 85280661 |
|
Enhancer Sequence | GTTGGCCAGG CTGGTCTTGA ACTCCTGACC TCAGGTGATC GCCTGCCTTG GCTTCCCAAA 60
GCAGTGGGAT TACAGGTGTG AGCTACCGTG CCCGGCCAAC TCTTTCTTTT CTTTTTTTAT 120
TTGAGATAGG GTCTCACTTT GTCGCCCAGG CAGGAGTGCA GTGGCACGAT TATGGTTCAC 180
TGCAGCCTTC ACCTGCTGGG CTCAAGCAAT CCTCCCACCT CAGCCTCTCA AATAGCTGGG 240
ACTACAGGCA TGTGCCACAA TGCCCAGCTA ATTTTTTTAT TGAGACTGGG TTTCTCCATG 300
TTGCCCAGGC TGGTCTTGAA CTCCTGGGCT CCAGCAATCC ACCTGCCTTG ACCTCCCAAA 360
GTGTTTGGAT TACAGGCGTG AGCCACAATG GCCAGCCTCC CCTGTCTCTA TTCTTCCGGA 420
TTTCACCACT GTGACATTCT GCACTCACCA CTTCCCCCAC CCCACCTTTT TTTTTTTTTT 480
AATGCTTTTC TCCTGTAGCT CCCATGACCA CCAGAAGTTA CCCAACCAGG CAGATCAGTA 540
TCCCTTATCA GCTCACCAGT CCTGAATAAT CCCTGACATT TGCATCTTCC TAGATCCCCT 600
CTTTGAGACA GTGTGTTACA ACTTTTCCTT TTTCCTCACC CCTCCCCCCT TGGTGACATT 660
CCTTCCCTCT TGCCTGCGGT TACTTCAGAG TCAGCACCTG CACCCACACT TGACTCCTCC 720
CCTCCAGCTC ACAAGCGGAA GTATCTTCCT AGCTAAAGCC AGCCTCTCTG CGTTTGCTCT 780
CGATCTCTCC CCTCCCACCA TTTGGCCCCC CTTAGGGGAC AGAACAGATC ATGACTGATG 840
CACCTTCAGC CTCTCCTGCT TTACTTTAAA ATCTTGTCAT CCTTTAAAAT TCTTCCTTGC 900
CCTCATCCGC CCTCCGCATA GTTACTGCCC TCTCTCTCCT CCCTCATTTC TGCCATCAAG 960
CCCAAGCTCT CATGAAGCAT TCATTTAATC TTCACAGCAG CCCATGAGGA TGGTGTCAGT 1020
ATTGTCCCTA TAAAACAGAA GTGGAGTACA GTTGCTTTAT TAAACAAGGT CACCCGGCAG 1080
GGGTTTGAAG GCAGAGAACT GGGCTTAGGG TCTGTGCCCT TGACCACTAT GTCATACCAT 1140
|
