Tag | Content |
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EnhancerAtlas ID | HS050-06649 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:244504700-244505540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:244505131-244505142 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr1:244505131-244505142 | CTGAGTCACCC | - | 6.02 | NFE2L1 | MA0089.2 | chr1:244505127-244505142 | AGTGCTGAGTCACCC | - | 6.67 | Nfe2l2 | MA0150.2 | chr1:244505129-244505144 | TGCTGAGTCACCCAG | - | 6.53 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09694 | chr1:244504516-244506059 | CD14 | SE_33040 | chr1:244504843-244505865 | H1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I244341 | chr1 | 244504385 | 244505860 |
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Enhancer Sequence | GACACTCGCA GAGGTTTTCA CAGATGATGT TGCTATTGGA ATCAGTAAAT TGTATTGTGT 60 ATAATACAGG ATGTAACAAT GTCATTCTGG CATTTGTTAT GAATGCAGCC CATGCGCGAG 120 GGAAAATCAC GGGTCCCGCA AGCACACTCT GTAACAATGC CTCTTCCCAG GAGGGGCCCC 180 CCACCAGGCT GACGATTGTC TTCAGGCTCC ATCGATGTTT TCCGTTGTTT AAAGACACAC 240 ATTAACGTAA AGTCTCCTCC CATTCTCTCT GTAAATTACA GCATTCAGAA GAAGTGGCAG 300 CTGCTGTAAT TAAGACACAG TTAATTGCCT ATCTCCTTAA TTGCAGTGAT AGGATTTTGA 360 CAGTTTGGTA AATAAGAATT GTTTGGTTTC CTCTGGCAAC TTCAGCCTCA GTCAGTTCTC 420 TCCTGCAAGT GCTGAGTCAC CCAGTCTGGG GACAAAGGGC TGTGGTCCAA CGGAGACAGG 480 ATGGGGCAGG AACTGCAGGT GAGAGGGGGG CAGTGTTTAT GATTCACCTT AAGTCTCCTC 540 TCTCTCTCTG CAAGAGCCTC CCCACCATTG CCCATTCTGT CGCCCAGTAA GATCCTCCCA 600 GAGTTTTCTC CCAGTTGAAT CAGTCATCAC ATGAGCCTAT GAGACAGGAA GAAACAGAAG 660 CAGAATGCCC GTATTGTGGG GCAATGATCT CCTGCTGCTG ACGGGCACAG GAGGATGGGA 720 CGCTGTCAAC TGAGGATACA GAAGCCCAGA GAGACTAAAC GTACCCAAAG TCAGGGAGCT 780 ACGCTGTGCA AAGCCAGGAT CCCAATTCAG GTCTTCTGAC CCACAGCCTC AAGCACACTC 840
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