Tag | Content |
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EnhancerAtlas ID | HS098-31432 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:128165290-128166460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:128165606-128165624 | GCGTCCTTCCCGCCTTCC | - | 6.01 | KLF16 | MA0741.1 | chr2:128165572-128165583 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr2:128165812-128165823 | GGGGGCGTGGC | - | 6.62 | KLF5 | MA0599.1 | chr2:128165572-128165582 | GCCCCGCCCC | + | 6.02 | RREB1 | MA0073.1 | chr2:128166244-128166264 | GCCCCCACCACCACCACCCC | + | 6.45 | SP3 | MA0746.2 | chr2:128165811-128165824 | TGGGGGCGTGGCG | - | 6.57 | SP8 | MA0747.1 | chr2:128165811-128165823 | TGGGGGCGTGGC | - | 6.11 | TFAP2A | MA0003.3 | chr2:128165379-128165390 | AGCCTCAGGCA | + | 6.32 | ZNF263 | MA0528.1 | chr2:128165526-128165547 | TCCTCCTCCTCCTCCCCCACC | - | 6.27 | ZNF263 | MA0528.1 | chr2:128165532-128165553 | TCCTCCTCCCCCACCACCTCT | - | 6.49 | ZNF263 | MA0528.1 | chr2:128165472-128165493 | CTCCCTCCCTCCTTCTGCTCC | - | 6.59 | ZNF263 | MA0528.1 | chr2:128165529-128165550 | TCCTCCTCCTCCCCCACCACC | - | 7.31 | ZNF263 | MA0528.1 | chr2:128165580-128165601 | CCCTCCTCTTCCCCCTGCCCC | - | 7.81 | ZNF263 | MA0528.1 | chr2:128165523-128165544 | GCCTCCTCCTCCTCCTCCCCC | - | 8.62 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09644 | chr2:128164535-128166940 | CD14 | SE_23461 | chr2:128165153-128165765 | Colon_Crypt_1 | SE_23461 | chr2:128165766-128166677 | Colon_Crypt_1 | SE_24012 | chr2:128165266-128166623 | Colon_Crypt_2 | SE_24894 | chr2:128165065-128166599 | Colon_Crypt_3 | SE_28345 | chr2:128164776-128166852 | Fetal_Intestine | SE_29146 | chr2:128164682-128166773 | Fetal_Intestine_Large | SE_43376 | chr2:128165019-128166813 | Lung | SE_50833 | chr2:128165107-128166882 | Sigmoid_Colon | SE_52838 | chr2:128165093-128165615 | Small_Intestine | SE_52838 | chr2:128165639-128166869 | 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 |
GH02I127406 | chr2 | 128164514 | 128166975 |
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Enhancer Sequence | ACCACCTTAA GCCACAGTGT AGACTTTCCA TAGGCCAAAA CCTGGATCAC CAAGACAGTG 60 TGCCCCAGGC TGCAGGCCAC ACTCCTGGGA GCCTCAGGCA ACCTTGTGCA GGCCTGACTT 120 CGAGACACTC TGAGCATGAG CTGGTTCCTG GGTAGCCTCC CCTCTACCTC TCCCCGCTTG 180 CCCTCCCTCC CTCCTTCTGC TCCTGTCTCT CCTCATCCCC TCCCCGAGTT GCTGCCTCCT 240 CCTCCTCCTC CCCCACCACC TCTCCCCGTC TCCGAGTTGC CTGCCCCGCC CCCTCCTCTT 300 CCCCCTGCCC CTCTCCGCGT CCTTCCCGCC TTCCCCCTCC TCGTCTCCCC CCTCCCCGCC 360 CGCGCCGTCT GCGTCCCTCC CGGGCCCAGA CGCGGCGCGG TCAGGGGGCG CTGACTCACA 420 GGCTGACTCA GCTGCAGGCG CGCTGCCAGG CGACGCAGCG GGCGGGTGGC CGGGCGCCGG 480 CGGGCTCGCA GCCGGGCTGC TGGCAACGGT GCCGGCGGAG GTGGGGGCGT GGCGCGGGAT 540 GGGCGGCGCG GGCCCTGCCG TGGTACCGCC TGGCAGCGTC CACCCCGCCG CTGGGGCGCC 600 CTGGAGGCTC CTGGCCCTCC GTGGGGCCGT GACACCGGCG CTGCGGGGAG CGGTGGCCTC 660 GCAGAGGCTG GGCATGGGAG GACGGCCGCC CCGGGTAAAG GACAGGGCCC TGGAAACGCG 720 GGTCTGCCGG GAGCAGGGGA CAGGAAGGAG ACCGCGGCTC TCCCAGTCCT GCTGCCCCGG 780 GCCTCCAGAC GGCCAGACTC TCCCCACACC GGCCTGGAGG GGGACGCGCC GACCCCAGCT 840 GGGAGGGGTG GCTGGCTGCG TAGATCCGTT TGGGCCGCCT GCCTGGAAAG GCCCAGGTCC 900 GGGCCTCGTC CTCCTCTTCA CACTCTCCCC CGATCTCCAA CCACCTTCAC CCTCGCCCCC 960 ACCACCACCA CCCCCAGCTC CTCCTGGCCG CCTGCGGTCC AGCTGAGGCC CGCCTCCTCC 1020 AGGAAGTCTT CCTGGAGAGC CTGTCCTGGG TTAGGCCCGC CCAGAGCCAC CTGGGGCGAC 1080 TTATTTCATG GCACCTTCGA CCTTGCTCTC TGTCTGTTTT GTGTCTGGCT TCATCACCAA 1140 ACTGAGCCTC TTGGGGGCAG TGACCGGGTC 1170
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