Tag | Content |
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EnhancerAtlas ID | HS184-15301 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:16208560-16209150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:16209036-16209051 | GAGGTCAGAAGTTCA | + | 6.38 | RARA | MA0729.1 | chr19:16209036-16209054 | GAGGTCAGAAGTTCAGGA | + | 6.05 | ZNF263 | MA0528.1 | chr19:16208709-16208730 | CCCTCAGCCTCTCCCTGCTCC | - | 6.66 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23280 | chr19:16208506-16208969 | Colon_Crypt_1 | SE_24812 | chr19:16208468-16209144 | Colon_Crypt_3 | SE_26678 | chr19:16208277-16209524 | Esophagus | SE_27889 | chr19:16208269-16209129 | Fetal_Intestine | SE_28973 | chr19:16208302-16209223 | Fetal_Intestine_Large | SE_31734 | chr19:16208416-16209401 | Gastric | SE_35489 | chr19:16208226-16209840 | HepG2 | SE_46221 | chr19:16208245-16209704 | Osteoblasts | SE_52442 | chr19:16208317-16209080 | Small_Intestine | SE_62472 | chr19:16180149-16231639 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I016091 | chr19 | 16202245 | 16209891 |
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Enhancer Sequence | AAAATCTCCA ACTAGATCCT GAATTTTCGG TATCCATTGT TATTCCTCAT CCTATTTTTT 60 TGTCCAGGTG GGAAGCTCTG TCCCCATTAC TCTCTCTATT CATCCATTCC TCCAAAATGC 120 ACCTCCCCTA AACCACCTCC ACCTTTCCAC CCTCAGCCTC TCCCTGCTCC TAACTGCCGT 180 CCATCCTGAA CTTCTGCAAA AACCATTCCC CTCACACATT GCCATATATA TGCCCTTGGA 240 AAGATTACAG ACTGTGTAGG GGGCTGGTTT TTGTTTGGAG TCTGTGTGTT TGTCCCTGGA 300 ATTTCTCCAG GCATTTCTGG ACTCCACCCT TTGAAGTAAC TATGCAGCCT GTCTATCCAG 360 TTATTCTACC TAACTAAGCA CATAAGTGGA ATTTCAGAGA TTAGTGCTAT GGCCGGGCAC 420 GGTGGCTCAC GCCTGTAATC CCAACACTTT GGGAGGCCAA GGCAGGCAGG TCACTTGAGG 480 TCAGAAGTTC AGGACCAACC TGGTCAACAT GGTGAAACTC TGTCTCTACT AAAAATGCAA 540 AAATTAGCCG GGCATGGTCA TGGGGGCCTG TAATCCCAGC TACTGGGGAG 590
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