Tag | Content |
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EnhancerAtlas ID | HS048-13718 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr16:1140600-1141930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr16:1140887-1140904 | AAGGTCCCCCTGACCTG | + | 6.44 | MYC | MA0147.3 | chr16:1141466-1141478 | GAGCACGTGGCT | - | 6.04 | ZNF263 | MA0528.1 | chr16:1140701-1140722 | CACCCTGCCCCCTCCTCCCCC | - | 6.23 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_02040 | chr16:1138505-1142465 | Aorta | SE_34486 | chr16:1137094-1142491 | HCT-116 | SE_57352 | chr16:1139041-1142134 | VACO_400 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 1141470 | 1141592 | chr16 | 1141244 | 1141378 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I001088 | chr16 | 1138813 | 1141793 |
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Enhancer Sequence | GGAGGGGACG GCACTTCCTG AGGGTGGGGC TGGGAGGTCC GGAGTCTTCA CACAAAAACG 60 GCGGCTGTGT TGGGAGATGG CCCCTGACCC CCATCTCCTG CCACCCTGCC CCCTCCTCCC 120 CCGGTTCCTT TGCCCGACGC CCACTGCCGG TTGCCCCCAG GCCTGGCCCA GTGGTGGGTG 180 GTGGGGATGA CTGAGCAGCC CCTCAGGCTG GGGCCCCACA GCAACAGGGA GGGTCACTGT 240 TCCCAGCTGC TTCCTCCCAG CCAGTGTGTG CTGCCAGATG GACAGACAAG GTCCCCCTGA 300 CCTGGGGGCT GCAGCCCGTG CCCTCCTACC TCCCTCCTCG GCTGGCCCCA CCCTGCAGGG 360 TGCACCCTGA TGTTGGGGGC TGTCCTCTCA CAGACCCTCC TGGGGCAGGC TGTGGGCCCA 420 GCTGCTCAGA GATTGGTCAG TACTGGTGGG GGCCCCTGTG GGGAGGGAGT GGGGGCAGGG 480 CAGGCCCTAA AGAGGGGGAT GGGCGAGCCG GGCACTCCAT GGGCCGGGAT GTCCCAGAGT 540 GGACAAGGAT CAAGGGGCCG TGGGGGCACC TGGGACCCCG CATCCCTTCA TCTGTTCGGC 600 ACCCATGGGC CCCCATGAGC CCACGCTGGG TGCACCTGTG GGGGCTCTCC TGCCCCCACC 660 CGGGGATGCT TTATGGAAGG CCTTGTGAGG GTTCCAGGCA GCATGGCTGA GCTGCTCCTG 720 ATGCTGCTCC TGCCCGGGCC CAGTGGCCGC GCTGCCACAA ATAGCACACC AAGGAGGAGG 780 AGGCGGTGCG TGGGAGGCTG GGCCGGAGGG GCTGGGAAGA GGGGGAGGGA GGCCCAGGTC 840 AGGTGGAGGT GGTTCCAGAG ACAAGTGAGC ACGTGGCTGG GAGAGCTTCC GGGAGGGGCC 900 ACAGCTGCTC CAGCCGGGGA GGGTAACAGA GGCTTCCAGT GACCAGAGCT GGGCCAGCCT 960 CTTGCCTGGA GGGACCGACC CACCCACACT CCCAAATGGG GCCCTCTCTG CCCCCACAAC 1020 TGCAGCCAGG CCATGTGGAC CTGACTTTCA TCCCTGTCTA AGCATAAGGC AACTCCGTGG 1080 GGGTCTGAGG CTTCCTCCGG CTCTGGTGCC CATCAGGGTC CAATCTTCCT CCAGCCCCCA 1140 CACATTCAGA CAGACTGAGG ACCCATGAGC CCCCAAAACT GACCCCCTGC GCTCAGCCGC 1200 GTGTTTCCTG CCAAGGACAA GCCACCACTA GAGCAGCCCC ACCCTCCCGG CCACCGTGAG 1260 TGCTGGGTGC CCCTCACACC GCCTGGAAGT GACCGTCTTC CTTCCACCCT TTTGGCCTCC 1320 CCTGGGTCCA 1330
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