| Tag | Content |
|---|
EnhancerAtlas ID | HS041-00166 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:8110470-8111410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:8111093-8111105 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:8111097-8111109 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:8111101-8111113 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:8111105-8111117 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:8111109-8111121 | AAACAAACAAAC | - | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr1:8110683-8110698 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_34231 | chr1:8110750-8111779 | HCT-116 | | SE_47106 | chr1:8109694-8110692 | Panc1 | | SE_47106 | chr1:8110954-8112532 | Panc1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I008050 | chr1 | 8110751 | 8112532 | | GH01I008049 | chr1 | 8109695 | 8110692 |
|
Enhancer Sequence | TCTTTTTTTT TGAGATGGAA TCTTGCTCAG TCAGCCAAGC TGGAGTGCAG TGGCACGATT 60
TCGACTCACT GCAACCTCTG CCTCCTGGGT TCAAGCGATT CTACTGCCTC AGCCTCCCAG 120
GCAGCTGGGA TTACAGGCAT GCCCCCACCA TGCACAGCTA ATTTTTGTAT TTTTAGTAGA 180
GATGGGGTTT CGCCATGTTG GCTGGGCGGG TCTTGAACTC CTGACCTCAG GTGGTCCTCC 240
CACCTCGGCC TCCCAAATTG CTGGGGTTAT AGGCGTGAGC CACCTTGCCC TGCCTAGACA 300
TTTCTTGTAT TGATTTCTTA GGGCTGCTTT AAGAATGTAC CACAGGCCAG GCGTGGTGGC 360
TCACATGTGT AATCCTAGCA CTTTGGGAGG CCGAGGTGGG CGGATCACAA AGTCAGGAGT 420
TCGAGACTGG CCTGGGCAAT ATGGTGAAAC CCCGTCTCCA TTAAAAATAC AAAAATTAGC 480
GGGCGTGGTG GCACGTGCTT GTAGTTCCAG CTACTCAGGA GGCTGAGGCA GAGGAATTGC 540
TTGAACCTGG GAGGCAGAGG TTGCAGTGAG TCAAGACTGC GCCACTGCAC TCCAGCCTGG 600
ACAACAGAGT GAGACTCCAT TGCAAACAAA CAAACAAACA AACAAACAAA CCATAAAAAG 660
AATGTACCAC AAATTGGGTG GCTTTAAACA ACAGAAATTT ATTCTTTCAC AGCTTTGGAG 720
GCCCGAAGTC CAAGATCAAG GTGTCACCAG GGCCATGCTG CACTCTGGGT GGAATCCTTC 780
CTGGCCTCTT CTGGCTTCTG GCTGTGGCTG GCAATCTTGG CATTCCTTCA CTTGCAGCTG 840
CACGCCTCCC CCGCTGTGCC TCCATCTTCC CATGGTGCCA GTCATAGTGG ATGAAGGGCC 900
CATCCTACTC CAGAATGAGT TCATCTTTAA AAAATTGCAT 940
|
