| Tag | Content |
|---|
EnhancerAtlas ID | HS184-16791 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:128165330-128166540 |
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 |
|
| | 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 |
|
| | 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 |
| GH02I127406 | chr2 | 128164514 | 128166975 |
|
Enhancer Sequence | CCTGGATCAC CAAGACAGTG TGCCCCAGGC TGCAGGCCAC ACTCCTGGGA GCCTCAGGCA 60
ACCTTGTGCA GGCCTGACTT CGAGACACTC TGAGCATGAG CTGGTTCCTG GGTAGCCTCC 120
CCTCTACCTC TCCCCGCTTG CCCTCCCTCC CTCCTTCTGC TCCTGTCTCT CCTCATCCCC 180
TCCCCGAGTT GCTGCCTCCT CCTCCTCCTC CCCCACCACC TCTCCCCGTC TCCGAGTTGC 240
CTGCCCCGCC CCCTCCTCTT CCCCCTGCCC CTCTCCGCGT CCTTCCCGCC TTCCCCCTCC 300
TCGTCTCCCC CCTCCCCGCC CGCGCCGTCT GCGTCCCTCC CGGGCCCAGA CGCGGCGCGG 360
TCAGGGGGCG CTGACTCACA GGCTGACTCA GCTGCAGGCG CGCTGCCAGG CGACGCAGCG 420
GGCGGGTGGC CGGGCGCCGG CGGGCTCGCA GCCGGGCTGC TGGCAACGGT GCCGGCGGAG 480
GTGGGGGCGT GGCGCGGGAT GGGCGGCGCG GGCCCTGCCG TGGTACCGCC TGGCAGCGTC 540
CACCCCGCCG CTGGGGCGCC CTGGAGGCTC CTGGCCCTCC GTGGGGCCGT GACACCGGCG 600
CTGCGGGGAG CGGTGGCCTC GCAGAGGCTG GGCATGGGAG GACGGCCGCC CCGGGTAAAG 660
GACAGGGCCC TGGAAACGCG GGTCTGCCGG GAGCAGGGGA CAGGAAGGAG ACCGCGGCTC 720
TCCCAGTCCT GCTGCCCCGG GCCTCCAGAC GGCCAGACTC TCCCCACACC GGCCTGGAGG 780
GGGACGCGCC GACCCCAGCT GGGAGGGGTG GCTGGCTGCG TAGATCCGTT TGGGCCGCCT 840
GCCTGGAAAG GCCCAGGTCC GGGCCTCGTC CTCCTCTTCA CACTCTCCCC CGATCTCCAA 900
CCACCTTCAC CCTCGCCCCC ACCACCACCA CCCCCAGCTC CTCCTGGCCG CCTGCGGTCC 960
AGCTGAGGCC CGCCTCCTCC AGGAAGTCTT CCTGGAGAGC CTGTCCTGGG TTAGGCCCGC 1020
CCAGAGCCAC CTGGGGCGAC TTATTTCATG GCACCTTCGA CCTTGCTCTC TGTCTGTTTT 1080
GTGTCTGGCT TCATCACCAA ACTGAGCCTC TTGGGGGCAG TGACCGGGTC TTAGGTCTTA 1140
GTTGGCCCTT AGGCGCTAGG GCTGAGAAGA CTTAGGCGGA CAGGAGATGA GACTGTGTAT 1200
TCGACGACAC 1210
|
