Tag | Content |
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EnhancerAtlas ID | HS048-29252 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:50262900-50263610 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:50263416-50263434 | CCTTTCTTCCCTCCTCTC | - | 6.03 | RREB1 | MA0073.1 | chr5:50263552-50263572 | TGGGAGGTGGTGGTTTTGGT | - | 6.48 | ZNF263 | MA0528.1 | chr5:50263408-50263429 | TCTCTCTCCCTTTCTTCCCTC | - | 6.11 | ZNF263 | MA0528.1 | chr5:50263417-50263438 | CTTTCTTCCCTCCTCTCCCCC | - | 6.3 | ZNF263 | MA0528.1 | chr5:50263412-50263433 | TCTCCCTTTCTTCCCTCCTCT | - | 7.13 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_54708 | chr5:50258475-50276228 | Stomach_Smooth_Muscle | SE_63234 | chr5:50258906-50266774 | GLC16 | SE_63413 | chr5:50258826-50269335 | NCI-H69 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I050965 | chr5 | 50261318 | 50263948 |
|
Enhancer Sequence | TGAAACCCCG AGGATGCGCT TTGGACTTGG GGACTGAGGG CGTGGTGGGC AGACAGCTGT 60 TGAATCCAAA CAAAGACTAT TCTGGATCTG ACGCCGTTTC GGTTTCCATC TGGGAGTACT 120 TTTCATTTCC TTCTTCCCAT TCCAAAGGAA AGAAATGGAT TAGGAATGGG GCAGTCAGAA 180 TTATGTGTTT ATGGCGGACA GATGGAACAG GAGAGGATGA ACCTTCAGCA ACAAAAGGAT 240 CATTGAGATT TGGTTCCTGG GTGTGCAAAT TTGGAAACAA AATAACCAAG GAAGCTATGG 300 GAATACCAAG ACTCTAGCTA TCGACAATGT TGACTCATAG ACGAATCATC TCTCCTTCTC 360 TACTTTCCTA TCATCAATCA AGAATTGTGG CCCCATCTCA CAAACTGCCG CGGAAGCCAA 420 AATTGCAGGA CATTTTGAGA AACAAGTCTT GAAATCTGCC TGAAACTAAC AAAAGCCACC 480 CGCCAGTCAA CCAGAGTCAG TCGCTCTCTC TCTCTCCCTT TCTTCCCTCC TCTCCCCCAC 540 TCTTCCTCGT CTCCCGCCCC CGCCCCCCAT CTTTCTCCAG CTAGCCTCGC CCCAATTAAC 600 GCCCTACAGC CAGTCAGCCT TACACCTGCT GGAAAAATCT TGGTGGCAGT GGTGGGAGGT 660 GGTGGTTTTG GTTTTTAGCA GAGCGCGGGA GCACCCTGTC ACACCCTCCT 710
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