| Tag | Content |
|---|
EnhancerAtlas ID | HS048-23819 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr21:43106140-43107090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr21:43106714-43106732 | AAAAGGGAGGAAGGAAGG | + | 6.96 | | EWSR1-FLI1 | MA0149.1 | chr21:43106718-43106736 | GGGAGGAAGGAAGGAAAA | + | 7.63 | | MYCN | MA0104.4 | chr21:43106497-43106509 | AGCCACGTGGCC | + | 6.37 | | MYCN | MA0104.4 | chr21:43106497-43106509 | AGCCACGTGGCC | - | 6.37 | | Nr5a2 | MA0505.1 | chr21:43107021-43107036 | CTTGACCTTGGACTT | - | 6.29 | | ZEB1 | MA0103.3 | chr21:43106297-43106308 | GGGCAGGTGGG | - | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_26552 | chr21:43097474-43106561 | Esophagus | | SE_31726 | chr21:43097723-43106451 | Gastric | | SE_33831 | chr21:43096898-43106559 | HCC1954 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 43106400 | 43107000 | | chr21 | 43107000 | 43107014 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH21I041686 | chr21 | 43107001 | 43107150 | | GH21I041677 | chr21 | 43097525 | 43106367 |
|
Enhancer Sequence | CTCTCCCTGC TCAAGACAGG TGACCTCCAC AGTGAGGTGT CCATGCCTAT GGTCATGGTC 60
ACCAGCTGAC ACCCTCAGAA AGTCACCCTC AGGGTGCAGA GCACGGGGCC TGGGGTAACT 120
GCCTGGCTCC GCTCCCTGGT CTGGAATCAG CAGTGTGGGG CAGGTGGGCA GTGGGGTATG 180
GACTTGAAAC TGCTTTCCCA GTGCAGAGCT GCTTTCAAGG CCCTCACTCT TAGCTTGAAC 240
AGCAACCATG ACTGTTTCCC AAAAGGGAAG GAAAAATGTC TTTGCTGCTA TCAATAGCCA 300
AATGGATCAC GAATCCCTGG GTCCTGGTGT TTGCACATCA TGTCATCTCA AGGACCAAGC 360
CACGTGGCCA TTCTTGGGAT AACATTGGGT TTTTTCTACT CCAAAGGGGT AGATCCGTTT 420
GTTATACTTT GCATTTTGTA GCTTACTGAA TGCTTGCTAC AGGCAAGCCC TCGGGTAGTG 480
CAGGAGGGGC TGGGAACTCC TCAAGGGCAG GGAGCAGGGC TTTTTGCTCT AATTGCCTAG 540
TGTCTAACAC ACTGTCTGAT AAATGGTGAA TGGAAAAAGG GAGGAAGGAA GGAAAACAGC 600
ACTCTAAGTT TCAAGGAACT TAAAACCTCT TGCTAGGGTT GAAATGGTTG TGCCCCCCTC 660
AAAGCGATAT ATTGAAGCCT AACCTCCGAT CTGCTGATAT TAGGAGGCAG GGCCTTTGGG 720
AGGTGGTCGG CTCTTGAGGG TGGAGCCCTC ATGAATGGGA CAAGCGCCCC TATAATGAGA 780
TGAAAAGATC AGATTTCTCC CCTCCCCCCG AGTGAGGACA CAGCGAGAAA GTGCGCTCTT 840
TGAACCAGAA AGCCCTCACC AGACGCCGAA TCTGCTGGTG CCTTGACCTT GGACTTTCAG 900
CCTCCAGAAA TGTGAGAAAC AAATGTCTGT TGTTTATAAG CCCTTCCAGC 950
|
