| Tag | Content |
|---|
EnhancerAtlas ID | HS012-18959 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr4:6750950-6752350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr4:6751894-6751905 | GGCCACACCCA | + | 6.62 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23558 | chr4:6750750-6753976 | Colon_Crypt_1 | | SE_24593 | chr4:6750774-6753042 | Colon_Crypt_2 | | SE_27608 | chr4:6750727-6755682 | Esophagus | | SE_42068 | chr4:6750932-6751798 | LNCaP | | SE_42068 | chr4:6751840-6753045 | LNCaP | | SE_51051 | chr4:6747543-6755479 | Sigmoid_Colon |
|
| | 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 |
| GH04I006746 | chr4 | 6748122 | 6755667 |
|
Enhancer Sequence | GCAGATGAGC CTCGGGGTTA AAATGCACTT TCTCTAATTC TCTAATATTA TCTCATTGGC 60
TGCTCTTGAG AGCTCTGAGA GGTAGGAATT CTCATCTGCT TTGACAGATG GGGAAAATGA 120
GGCACACTTC AGCCAGGCAC CTCCTCACAC TACAGGGCAG ATCCAGCCCA TGCAAAGCTG 180
GGCCTAGTTC CTGGGTGGGG CTGTGTCAGG ACAGCTGGGC ACGGACGGAG CTTTCACCCA 240
CGCTGGGGCG CCTGCTCAGC GAGGCTGCCT GGTGGGGCGG TGACTGCATG ACAAACTTGC 300
TGTGTGGCCT GGACGTCAGG GCGGGAGTAA CAGCTCCAGG AAGGCCAGAG TTCAGCCCAG 360
TCAGCCCACT CGGCCCCACT GTTCGGGCTG CCCTCTGAGC ATGTGTCATC CTGCCAGGGT 420
CCCTCCCACT GCGACCTGTC TTCCTGGCAG CTGCTGTTCA GGAGTTCTGC ACCCCGCCCT 480
GGGTGTCCTG CCAAAGCCAA GGTGGCCGTG CGGTCAGAGG CAGCGTCCTC TGCCCTCCCT 540
GTCTCCCTGC CTGTGTGTGC CCCTCCTTCC ATGGCCGGGA GCCTTTCTCC TTTCCCTTCT 600
CATTTTGCCA GACTCCCACC CTACTGTCAC AACCTGCCAA AGAGGCACTG CTCCAGGCAG 660
CTCCTGGACT CGCCCAGATG CAGCCAGACC CTCTGCTGCG CTCACTGCAT CGTCGTGGAT 720
GTAGCTGTCT CTCTGCCTTT CTGGACATCC TGACTGTGGC AGAGGTCCCC AGCCCCACGG 780
GAGGTGGGGT GGGCAGGGTC GGGGGGTCCA TGTCCCCTTT TCTTAGGTGA GGGGAGTCAC 840
TTGAAGCCAG GGCAGGTGTG GGGATGGGGG CCCCAGACTT GAGCACGTGC CAGGCAGAGG 900
GAAAGGGAGC TCCGGAGAGG TCGAGTCAGG GTAGGGGGCT TGATGGCCAC ACCCAAGCCA 960
GAGAGGAAGC CGGAGGCTGC GAGCCAGCCC TGAACCCGGC AGCCTCTGCC GTGATGAACC 1020
AGGGCGACCC CTCTACCCAG CGGCTCAGCC GACACCCTCA GAAACTCAAT TTTATTTAAC 1080
CAGCACATAT CATGTGCACT CTGGACCAGG AGTGGTTCAC TTACTCCTCA CAAGCAGGCT 1140
GCCAGCAGCA GGGACACGGG CACAGAGGGG CTAGGGAACT TGCCCAAGGT CACACTGCTG 1200
GTCGGTGGCA GAACTGAGAT CGGAGCACTG ACTGTTTGGA GCCACAGTCC AAAGCGCTGC 1260
TGCCCAGCTC TTCCCCAGGG AGCCACTGCA GGTGGAAACT GAACCCCGAA GAGCAGGGGG 1320
CTGGACTGGG GTCGAGACTG CTGGCGTGAA CCTGACGGAT CGCCATGGCC CAACCCCTTC 1380
CTGGCTGTGT GGCCTTAGAC 1400
|
