| Tag | Content |
|---|
EnhancerAtlas ID | HS080-21838 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr20:52329780-52330920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr20:52330524-52330542 | CCCTCCTTCTCTTCTTCC | - | 6.19 | | IRF1 | MA0050.2 | chr20:52330640-52330661 | ATTTTCTTTCTTTTTTTTTTC | + | 6.07 | | ZNF263 | MA0528.1 | chr20:52330515-52330536 | TTCTCCTCGCCCTCCTTCTCT | - | 6.22 | | ZNF263 | MA0528.1 | chr20:52330524-52330545 | CCCTCCTTCTCTTCTTCCACA | - | 6.3 | | ZNF263 | MA0528.1 | chr20:52330512-52330533 | CTCTTCTCCTCGCCCTCCTTC | - | 7.53 | | Zfx | MA0146.2 | chr20:52330872-52330886 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_47117 | chr20:52321104-52330553 | Panc1 | | SE_58495 | chr20:52322247-52381586 | Ly1 | | SE_59791 | chr20:52322434-52378313 | Ly4 |
|
| | 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 |
| GH20I053713 | chr20 | 52329823 | 52330630 |
|
Enhancer Sequence | TCTCGGCTCG CTGCAACCTC CGCCTCAGGG GTTCAAGCAA TTCTCCTGCC TCAGCCTCCG 60
GAGTAGCCAC CACCATGCCT GGGGCAGGAT TCTGCACCAA TTCTTCCCCA AACCCAGGTC 120
CCCTCCTTCC TGCAGCCCCT TCCCCTCCCA GGGAGCCTGC CTGTCAACCC CAGTGAGTCC 180
CTCGGGTCTA GTTGTGTTTG CTGGACTTCA TTCATGCACT CAACAAACAC TGAGCACCCC 240
TCTGCACCTG ATCCTGCCAT CGGCAGCAGG GGACAATGAT GACCATGACA GGGGACCATT 300
GCCCTTGCTT GCTATAACCT TCCCCAAATG GGATAAAGAG GTATCCCCCG CACCAGGTGG 360
ACCAGGGCTG TGGGTGGACA AGGGCTCCTG CGCAGAACCA TCAAATTCTT CCTTTCAACC 420
CCAGCCCAAG GTGGGTCCTG GTGCTTCCCA TAGTACCAAG TGTGCCTGGC AGAGGTGGAG 480
AAAACTCCCA GGGGTCGGGG AGACACTGGG ACCCCTGAAA CGCCCCTCCC CTCTGCCTTG 540
TGCGGAGTGG TCCCCAGTCA CCTGGCTTGT ACTAAAGACC CAGCACCTCC AACTACTGTG 600
GAATGCGACA GGTCAGGTGA GAATGACGAA AGCTGAGCAG CGGAGCTGGG GGAGGGGATT 660
GCACCACAGA CCCCTCAACT CCCACACCCG CCCTCGGCCT TTCTTCCGCA CAAGCTCCTC 720
TTGTCCGCTG TGCTCTTCTC CTCGCCCTCC TTCTCTTCTT CCACAGGTGT CCCAGAGGCG 780
CTGGCTCCAC TTCCCTCCTT CACGTTTTTC CCTCTTAACT CTCTTCCCTG GTCTCTATCT 840
CCAGAGATCT GAATTTCCTT ATTTTCTTTC TTTTTTTTTT CTGGGACAGT CTCTGTCGCC 900
CAGATTGGAG TGTAGTGGCG CAATCTGCAA CCATCGCCTC CCCGGTTCAA GCGATTCTCC 960
TGCCTCAGCC TCCTGAGTAG CACGGATTAC GGGCACGCGT CTCCACACCC AGCTAATTTT 1020
TGTATTTTAG TAGAGACGGG GTTTCACCAT GTTGGCCCGG CTGGTCTTGA ACTTCTGACT 1080
TGAGGTGATC CACCCGCCTC GGCCTCCCAA AGTCCGAGGC GGGTGGATCA CCTGAGCCAC 1140
|
