| Tag | Content |
|---|
EnhancerAtlas ID | HS193-01235 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr1:59058000-59059180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:59058962-59058980 | CATTCCTCCCTTCTTTCC | - | 7.45 | | EWSR1-FLI1 | MA0149.1 | chr1:59058938-59058956 | TCTTCCTTTCTTCTTTCC | - | 7 | | GATA2 | MA0036.3 | chr1:59058202-59058213 | ACAGATAAGAA | - | 6.14 | | Gata1 | MA0035.3 | chr1:59058202-59058213 | ACAGATAAGAA | - | 6.62 | | ZNF263 | MA0528.1 | chr1:59058966-59058987 | CCTCCCTTCTTTCCCTTCCCC | - | 6.21 | | ZNF263 | MA0528.1 | chr1:59058000-59058021 | CCCTCCCTCTATTTCTGCTCC | - | 6.22 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_26866 | chr1:59057282-59058915 | Esophagus | | SE_34091 | chr1:59057499-59059363 | HCC1954 | | SE_36047 | chr1:59057392-59059297 | HMEC | | SE_64419 | chr1:59057676-59059263 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I058591 | chr1 | 59057374 | 59059501 |
|
Enhancer Sequence | CCCTCCCTCT ATTTCTGCTC CATCCCAGAG AAATTCAGAA CCTGCCAAAA GGCAAGAGAA 60
GTCCTTGAGT AGAAAAATAA GACTCAACAA TTATTGAACT CTCTGTGATA TAGGCTCAAG 120
GATTATCTTA TTCTCACAAA TACACTGTGA ATTTAGGTGC TGTTATTAGC TCCACTTTCC 180
ATCTGATGAA GTCAAGGCTT AGACAGATAA GAAACTTGCC CAAGATCCTA CAGCTAGTAA 240
GGGATGGATT CAAGATCGAA ACCCTGGTGT TTTTGTCTCT GAAGTTCATG CTCTTAAACA 300
GCAAAGCCTA CCTCAGCCCC TGAACTGGGA GCTCCCATGC CAGCTGCATG CCTGGCAGCC 360
TGCCTGATAG AGCAGGACTG GGCAGGCTGA TTAATGAGGG GAACGACCTG GGGAAGGAAT 420
GAGGTCACAT TCCAGGAGGC TGAGGCAAGG CTGTTCACGA ATCACTTCAA AATACTCACT 480
CTCTTGGAAA AATACTAGCA GGGTTGGATA CTCATGCCAA ATAAGAAAAC TAGATATACA 540
AAATGGATAT TAGGACTGAG CATAGTATTC AACCTTCCAG GGCCATAGGC CTAAAGGGGA 600
CCAATTGCTC AGCCATGGGT CATAGCCTTC CAAGGACTCG TTCATGTCCT GCCCCCTTCC 660
CATACCTATC CCTGGTCTCC AGAAGATCAG ATGGCCTTCC CTCTGACTTC CACCCCTCTT 720
TGTATGTGAC TTAAGCACAT AACATGTGCT TGAATTATTA ATAAATTCAT TGGCTTTAAA 780
GATATTTTTT GGGCACCGAC TTGATGTCAG GCACTGTGCT AGGAGTAGTG AATATGACAT 840
ATTAGTTACC CCCTTGGCCC TTACAATCTA GTGAGGAAGG TAGACATTAA ACTGGAGATG 900
AACATTTTGA TAGGATAGGG TGCTATAGGA ACTAACATTC TTCCTTTCTT CTTTCCCTTC 960
CCCATTCCTC CCTTCTTTCC CTTCCCCATT CCTCCCTTTT TCTATTATCT CCTTCCTTCC 1020
AGAAATACTT ATTAAGAACC TACTATGTGC TAGTATCAGT CGAGGTGCTA GAGAAGAAAG 1080
CAGTGAACAA CAGAGATGCT TGCCCCCTTG GAGCTTATAT CCCAGTGATG ACTGGGGAAT 1140
TTGACTTGGG ATAGGAACAA CTTGTGAAGG AACTTGTGAG 1180
|
