| Tag | Content |
|---|
EnhancerAtlas ID | HS184-29911 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr8:101483940-101485070 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr8:101484400-101484421 | ATTTGGTTTCAGTTTGATTTA | + | 6.07 | | ZNF740 | MA0753.2 | chr8:101484053-101484066 | GTGGGGGGGGTAA | - | 6.41 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_22743 | chr8:101483886-101485006 | CD8_primiary | | SE_27991 | chr8:101483399-101488990 | Fetal_Intestine | | SE_28830 | chr8:101483384-101489121 | Fetal_Intestine_Large | | SE_32305 | chr8:101483709-101485077 | Gastric | | SE_32533 | chr8:101483317-101490498 | GM12878 | | SE_34085 | chr8:101482418-101486804 | HCC1954 | | SE_36367 | chr8:101484099-101485072 | HMEC | | SE_47999 | chr8:101483989-101484303 | Pancreas | | SE_47999 | chr8:101484469-101485013 | Pancreas | | SE_62291 | chr8:101421434-101542088 | Tonsil | | SE_65844 | chr8:101484956-101488621 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I100471 | chr8 | 101483587 | 101489609 |
|
Enhancer Sequence | AAGAGAAAGT CATCCCCAAA TAGAGGATAT GGATGCTTAG GTTTCAAAGA AAGGCCAAGA 60
AAGGGTAACC CAGCACAGCT GAGGCAGGTT TTTTTTTGTT TGTTTTGTTT GTGGTGGGGG 120
GGGTAAGGGG GGTGTGGGGT GTGGAGTACT GACTTCTCAC ACTCCTAAGA GGTTGCTAAG 180
CAGGGCATCT TATTAAATGC CCGGCAATGG AAATCAGCCA AGTGTTCCCA GGGAGGGGGC 240
CCTCTCCCAG TCCTGGGCTC CCCTAGGAAA ACAGATCTTA ACAAAGCTCT TGATTATTTT 300
GCCATGTCCA TGATTTAGCA CTTTTTCCTG GCGTTGGAAA ACAGCTGAGA ACATTGAGCA 360
AGTCCTTTTT GCTCATAGAT AATTCCTTTA GTTTGGTTCT TACCACTTGT TTGAAACAGG 420
GACTGGCTCC AGCCCGTTCC TTATACGGAT GGCGCCTCTA ATTTGGTTTC AGTTTGATTT 480
ATGCCAGGAT CTAACTCACT ATGGAGTTCA ACTAAGAATT TTACAAACAC TTTTTGATGC 540
TAATGATATG TGTCTCACAA TCTAGACATC TGGACTTAAT GTCAAACAAA TATTACCCAC 600
CACAAAAACC AGTTGGATCT GTTTGTGGTT ACTTCAGCCC TGAGCAGTTC CTTCTTTAAA 660
GGCTCTGACC TGATAAAGTA GCTTTTGGCC CCATCAGCCT GCTGGCTAGG TGAGATAAAG 720
CGATCCCTGA ACCATTTGCT CCTTTTTCTC AGACCTACAC TCTGAAGCTG GATGGCCCAG 780
CCCCTCCCCA GCACAAAAAC ATTGTGTGAT CCTGTCTGTT GAGATGCTTT TCTCTGGGCC 840
AGATTCTCCA CATAAGCAAT GCAGGATTAG GATATGATGC TTGTTTGCTT GGAGATCCAG 900
GTGGTATTTG GAAGTGGCTT GCACAATCAC ATCCCTATGG GAACTTACCT CCCATGTGCT 960
TTTGGGAAAG TTTCCCACTC AACTCCATCC ACCCTGAATA TAAAATAGAG GTCACAGTGG 1020
TTGATTCACC AGCATTTTCT AACCAAAGTT TCTTTACGCT GTTTTTATAT TACCCACAAT 1080
CCTATTACGG CAATCACACT CACTATGCAT AGAAAGAATC ATTAAACCTT 1130
|
