| Tag | Content |
|---|
EnhancerAtlas ID | HS034-29967 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr8:144965010-144966180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr8:144965185-144965203 | CTTTCACTCCCTCCTTCC | - | 6.15 | | NR2C2 | MA0504.1 | chr8:144966154-144966169 | AAGGGTCAGGGGTCA | + | 6.65 | | ZIC3 | MA0697.1 | chr8:144965254-144965269 | GACCCCCAGCTGTGC | + | 6.17 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_24284 | chr8:144964965-144965874 | Colon_Crypt_2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 144965203 | 144965609 | | chr8 | 144965491 | 144965890 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I143890 | chr8 | 144964954 | 144966339 |
|
Enhancer Sequence | CAGCACAGTC CCATGCCCCG CTGCCTCCGA AAGCTCCCTC GTCTCTGGCA GTGGGGGCCA 60
CGTCGGGGCT GTGATCTCCG CTGCAGCCAG AGAGCTGTGG TGGGCAGCGT CCCCAGCGTC 120
CCCTGTGTTC AGGTGGGCTG CGACACCGGG CCCCTCCTGA CGTCCTGGCA CCCGCCTTTC 180
ACTCCCTCCT TCCTTGTCAC CCCCAGAAGC ACTCCTCCTC GCAGCCCCTG ACGCAGGCTC 240
TGCCGACCCC CAGCTGTGCA GCCAGCTGGG CCCCCAGGAC CGCCAGTTCC ACCTCCCGGA 300
ACTACCTTCC TTCCTCCACC GCACACTGGC CAGGGAGGGG CCGTCAGATG TTAGCAAACT 360
CTTCCTGCCC AAGAGGCCAC ACCTGCCAGC CCACTCTCAA AATCAGCCCT GGAGAAACTC 420
CCCAAGCAAG AAGGGGTGTG GACTCCAGAA ACCGCCCAGT GAGGCCCCGG TAGGGGGAGC 480
TGTGGGCGGT GGGCTCTGCG CTTGCTGCTC CCCGGCCTGG TCTGCAGACC ATCATCCACC 540
CCTTCACCGC AGGCCACTGC CGCGGTCGAT GGTGGCTTTG AGGAAAACCC TGGCTGGGTG 600
ACCAGTTGTG ACAAGAGCTG GAGGCTAACA TCGCCGGGCC CCTCCTCCAG CCACTGTCCT 660
CTAAGCCCTG GGGCTGCAGG AAAGCAACCT GGGAAGCCCA CCTCCCTCAA ATGCATATGG 720
GGGGATCCAT GGCGCCCTGG CCCCCAGGAC AGACCCTGTA GCCTGCCAGA CAGCGGGGCA 780
GCCGTGAACG TGCAGTGGGG GCGTGGGCCG CATCAGGCAC AGACACGGCT GAGCGGCAGG 840
TGCTGTGGAG GCAGCCAATC AATGAGCCAG TGGACTTTCA CATGAACAAG GGGCGTGACC 900
AGGCCGGAAG CAAGGGTGAG AGTTTGTTTA GGAAAAGTAC CAGACCTGCT AGTGCAGGGA 960
TGCAGGCGGG GTGCCCAGCA TCCCGGGGGC CAGGCCAGGG CCTTGCTGCT GGTGGCTGTG 1020
AAGGAAAAGG AGACCAAAAA TATACAAGAA AATCCAGTGC TTTGGAGAAT GGAGGTGAGA 1080
GGAGGCCGGG AACCGCGGAC TCGGGTTCCC CGGAGTTGGG GTGAAGGGGA AGATCTCACA 1140
CAGAAAGGGT CAGGGGTCAG GGAGGCCACG 1170
|
