| Tag | Content |
|---|
EnhancerAtlas ID | HS170-01809 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr17:80821620-80822500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr17:80822048-80822062 | AAAAGATGAGTCAT | + | 6.98 | | JUN(var.2) | MA0489.1 | chr17:80822053-80822067 | ATGAGTCATCTCTT | - | 7.95 |
|
| | Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
| SE_02968 | chr17:80821858-80822934 | Bladder | | SE_25397 | chr17:80819939-80826250 | DND41 | | SE_26549 | chr17:80820742-80825557 | Esophagus | | SE_30394 | chr17:80821782-80822882 | Fetal_Muscle | | SE_31064 | chr17:80820818-80825358 | Fetal_Thymus | | SE_31475 | chr17:80822162-80823087 | Gastric | | SE_34549 | chr17:80820514-80823679 | HCT-116 | | SE_40359 | chr17:80820637-80822627 | K562 | | SE_41612 | chr17:80822272-80822927 | LNCaP | | SE_55429 | chr17:80821461-80822939 | Thymus | | SE_65913 | chr17:80820992-80823609 | Pancreatic_islets | | SE_69083 | chr17:80820876-80822073 | H9 | | SE_69083 | chr17:80822074-80823443 | H9 |
|
| | 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 |
| GH17I082862 | chr17 | 80820508 | 80825709 |
|
Enhancer Sequence | ATGCAGCTGG CCTCAGATCC TGTTGGGAGA GCAGGATTGG TGAGGAACCT GGAGAGGAGT 60
AGGAGGTGCT GCCTGATAGC AGAGGTGGGT GATGGGGGCA GAGAGGGTAG CAGGGGCCCA 120
GTTCAGTCCT GTCTGGTTTT CACGTGGAGC TTTTTATAGA GTTGTGCTTC TCAAGCCTTT 180
CAAATGCCTC ACAGCGGCAG TCCGACGTGC AGTCAGTGAC AGCTGAGTAG ATTACCACCC 240
TCAGGACTAA ATGCAAAATC ATCTTCACTG GGTGCAGCAT TTACAGTTTT GGTGCTGGAA 300
CCTCCTAACC AGTGTTCTTA GGGGCTGTCT TACCAGTGAA GGGAGCTGCC TGCTGTTGAC 360
GCTCCACAGG AGGTTTGCGG CATGGCTGCC ATCTGTGTTG TGGCCTGGGA CTTTCTTAGA 420
GAGTGGGTAA AAGATGAGTC ATCTCTTGTG TGATTTATCA GCTTCACTTG TGCTTCCAGG 480
GCTCTTTGAA GCGTCTCACT TTTTAATTTC ATGAAGAAAC AAATGTAGTG CAGAGAACAG 540
AAAGCTGCTG TGTGACCTGC GGGTGCCCAG CCTGTGGGGC TTCCTCATCG CCCCCATCCA 600
GGCAGATCGA GTGCCGGCTC TCTGTGCTCT CCAGGAGGTG GCCTTTCACA GCAGGGACGT 660
TCTGTGCTCT TATTTTAACA ACTGTAAGAA TCTGAGCTTG GTGACAGTTG GGTGACCCGG 720
GCTCTGTGTC TTCGTGTTGG CCAGGGTGTG TCATACACCT GGCCTGGCCT GCGTGCCTCA 780
CGTGTGGTGG GGATTTGTGA CTGTCCCCAG CACCTTGACA GAGGGTCCTT GACTCTGCGA 840
CCCTGCACAG TGGGTGGTGG CAGGTGGGAT CTTGGTTCAC 880
|
