Tag | Content |
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EnhancerAtlas ID | HS048-07848 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr11:120063390-120064610 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:120064332-120064350 | CCTTCCCTGCTTCCTGCC | - | 6.62 | Nr5a2 | MA0505.1 | chr11:120063983-120063998 | GCTGACCTTGAACTC | - | 8.73 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_24076 | chr11:120063824-120064478 | Colon_Crypt_2 | SE_27662 | chr11:120063285-120064772 | Fetal_Intestine | SE_28582 | chr11:120063252-120064954 | Fetal_Intestine_Large | SE_35389 | chr11:120063378-120064804 | HepG2 | SE_52530 | chr11:120063655-120064644 | Small_Intestine |
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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 |
GH11I120192 | chr11 | 120063440 | 120064751 |
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Enhancer Sequence | CGACAGAGCA AGACTCTGTC TCAGAAAAAA AGAAAAAAAA GGAAAAAGAG ATTTTCCTGA 60 TTTGCTAGGG TGCATTCGGT GGTGCCACGT CTAGACAGCT GCCTCCTACC CCAAAGAGTA 120 TCTTCTCAGG GAAGGTTACA TTGTCTCCGG CTCCTGTACT CAGTGGAAGG GCCAGCTTCC 180 TCTGAGGAGA TAAAAGGGTT ACTTTTGTTT CTACTTCTGT AAACTGTAAA TATGTGCTCA 240 GAATCTCCAG GTGACAGGAC AAGCCCCAAT GCTCCACTTT TGGAATTGAT GCCAAAGCTT 300 GACGGAGCTG CCAATTCATG CAAGAAAGTC CACCGGCACC AGACGGGGTG CTCTTGGCTT 360 GTTTCCAGAC CTGCTGCCCT TCCCCAGCTG TAGTTCCGGG GGCATTGCCC CTCAGGGGAG 420 GACTGGTACC AGGCGCCCCT CTGCAAATGG ACACACCAAC GGTAGAACTG GCTTGGGCCC 480 TCCAGAGACA AAGTTCAGGA AAGATCCTCC TCCCATGATC GGCTCCAGAG TGCTCCAGGG 540 CTGGGGCCTG AGGGAGGAGC TACGAGGCCG GCTTGCGGCT GTGGCAGCAT GCTGCTGACC 600 TTGAACTCAC CTTGACTACC ACCAGAGCGG CCCCAGAGGC AGGCAGGGGC CAGTCCTCCG 660 CTGTGTTGGG ACCAGAGGGA GCACACAGAG CCAGAGAAGT CCAGAGTCCT CACCCTTCAC 720 TGGGACAGGA TGGGACCTGG GTCTTGCCAA CCAGCTTGGG CAAAGGTAAA CCTTCTTTGT 780 GTGCCCCAGG GAGGCTCAGA GCCAGCAGTC CCCACTGTAT GGGGCCTGTG CGGGGAGAGG 840 GTTCAGATGT GCCTCACGGC TGCTGCTGGC CGATCCCAAG GTCTTCTTCC ACCAGAGGCA 900 CCTCTGCCTC CTTGGCCAGC AAAGGTTGCC ACATGTGGCC ACCCTTCCCT GCTTCCTGCC 960 TCCCCCCATT TGCACCCCAG GTGTGAACAC TCTTCTCATG GGTGTTTACA TGCCTACTCG 1020 AACACCACAG GCAAGTCCTT GGCCAGCCAG CTCCTTTCCA CCCTAGACCC CACAGGTCAG 1080 GGTCAGGGAC TCCCCACCTT TTATACAGTG GGGAGAGAGT AGAACCTGTG CTCTCAAAGT 1140 CAGAGTGGGC CTGCACTAGA ATCCCAGCTT TGCCAGATAC CATTTGGTCT TGACAACTTC 1200 TTTAACATTT TCTGAACAGT 1220
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