| Tag | Content |
|---|
EnhancerAtlas ID | HS052-28175 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr4:6750820-6752180 |
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 | ACCTCGTGAT CCTTCTGCCC TGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCCCCG 60
CGCCTGGCCC CATGTGTCAG TCTTAATAAT AACATAGCAA TAACAATAGT AACAGCAGCA 120
GCAACCCTTT GCAGATGAGC CTCGGGGTTA AAATGCACTT TCTCTAATTC TCTAATATTA 180
TCTCATTGGC TGCTCTTGAG AGCTCTGAGA GGTAGGAATT CTCATCTGCT TTGACAGATG 240
GGGAAAATGA GGCACACTTC AGCCAGGCAC CTCCTCACAC TACAGGGCAG ATCCAGCCCA 300
TGCAAAGCTG GGCCTAGTTC CTGGGTGGGG CTGTGTCAGG ACAGCTGGGC ACGGACGGAG 360
CTTTCACCCA CGCTGGGGCG CCTGCTCAGC GAGGCTGCCT GGTGGGGCGG TGACTGCATG 420
ACAAACTTGC TGTGTGGCCT GGACGTCAGG GCGGGAGTAA CAGCTCCAGG AAGGCCAGAG 480
TTCAGCCCAG TCAGCCCACT CGGCCCCACT GTTCGGGCTG CCCTCTGAGC ATGTGTCATC 540
CTGCCAGGGT CCCTCCCACT GCGACCTGTC TTCCTGGCAG CTGCTGTTCA GGAGTTCTGC 600
ACCCCGCCCT GGGTGTCCTG CCAAAGCCAA GGTGGCCGTG CGGTCAGAGG CAGCGTCCTC 660
TGCCCTCCCT GTCTCCCTGC CTGTGTGTGC CCCTCCTTCC ATGGCCGGGA GCCTTTCTCC 720
TTTCCCTTCT CATTTTGCCA GACTCCCACC CTACTGTCAC AACCTGCCAA AGAGGCACTG 780
CTCCAGGCAG CTCCTGGACT CGCCCAGATG CAGCCAGACC CTCTGCTGCG CTCACTGCAT 840
CGTCGTGGAT GTAGCTGTCT CTCTGCCTTT CTGGACATCC TGACTGTGGC AGAGGTCCCC 900
AGCCCCACGG GAGGTGGGGT GGGCAGGGTC GGGGGGTCCA TGTCCCCTTT TCTTAGGTGA 960
GGGGAGTCAC TTGAAGCCAG GGCAGGTGTG GGGATGGGGG CCCCAGACTT GAGCACGTGC 1020
CAGGCAGAGG GAAAGGGAGC TCCGGAGAGG TCGAGTCAGG GTAGGGGGCT TGATGGCCAC 1080
ACCCAAGCCA GAGAGGAAGC CGGAGGCTGC GAGCCAGCCC TGAACCCGGC AGCCTCTGCC 1140
GTGATGAACC AGGGCGACCC CTCTACCCAG CGGCTCAGCC GACACCCTCA GAAACTCAAT 1200
TTTATTTAAC CAGCACATAT CATGTGCACT CTGGACCAGG AGTGGTTCAC TTACTCCTCA 1260
CAAGCAGGCT GCCAGCAGCA GGGACACGGG CACAGAGGGG CTAGGGAACT TGCCCAAGGT 1320
CACACTGCTG GTCGGTGGCA GAACTGAGAT CGGAGCACTG 1360
|
