| Tag | Content |
|---|
EnhancerAtlas ID | HS041-04786 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr12:13062990-13063580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:13063334-13063352 | TCTTCCTTCCTTCATTCA | - | 6.78 | | EWSR1-FLI1 | MA0149.1 | chr12:13063338-13063356 | CCTTCCTTCATTCATTTC | - | 6.84 | | RREB1 | MA0073.1 | chr12:13063058-13063078 | AGGGGGTGGGTGGTTTTGGG | - | 7.2 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_02173 | chr12:13062824-13063862 | Aorta | | SE_23547 | chr12:13062912-13063768 | Colon_Crypt_1 | | SE_24533 | chr12:13063058-13063688 | Colon_Crypt_2 | | SE_28138 | chr12:13062026-13064517 | Fetal_Intestine | | SE_28922 | chr12:13061553-13064754 | Fetal_Intestine_Large | | SE_34394 | chr12:13062863-13063891 | HCT-116 | | SE_38847 | chr12:13061711-13063715 | HUVEC | | SE_57272 | chr12:13062902-13063968 | VACO_400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I012908 | chr12 | 13061782 | 13064421 |
|
Enhancer Sequence | AGTACTCCTG CTCATAGGGA CCTATTCATT GGTCTCCAGG GTTTACACTG ACCTTTAAGT 60
CTAATCACAG GGGGTGGGTG GTTTTGGGAT AGGAATGAGG AACCTCCAAG GCCATGTTCT 120
TAGCTCCAGC TAAAAATAGG TCTTTCCTTT GCTCTTAAGC CTGAGGTGTG GAACTTCCTG 180
GTGCTACTCA CTGCAGCTAT GGTCCCTGTC TAGGGCACTT GGAAGTCTGA AGGGAGGCGG 240
AGGAGGGCAG GAGGGGTTAT TTAACCACCC AGCCCCTCCT GTCCGTTCCG TGGCTTCACT 300
CCATCACCTC ACTCCTGTAC TTCCTGTTCT CATTCACTGA TGAGTCTTCC TTCCTTCATT 360
CATTTCAAGG GCCACTGTCA GCTTTCTCCC TTAAAATGCT TCTCTGGCCT CCATGCTTTG 420
CTGCTCACTT TCCTCCCTGG GTCCCCTGAG CCACCCCATC CCATCAAATC CTTCCTGAGC 480
CCTTCCACAG TTGGAACCAA CAACCTCTGA AGCTTTGCTC GCAGTCCAGA TGAACCAAGT 540
CGCTGTGCTT TCCTGCCTGT GCCTGTGCTC CAGGTGTGTC TGTCCTCTGC 590
|
