| Tag | Content |
|---|
EnhancerAtlas ID | HS044-02398 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr11:47939130-47940260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr11:47939366-47939377 | CATGAGTCACT | - | 6.14 | | MEF2A | MA0052.3 | chr11:47939257-47939269 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr11:47939257-47939269 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr11:47939256-47939271 | TTCTATTTTTAGTAC | - | 7.16 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_34924 | chr11:47933567-47942831 | HeLa | | SE_59342 | chr11:47871465-47957002 | Ly3 |
|
| | 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 |
| GH11I047912 | chr11 | 47933805 | 47946963 |
|
Enhancer Sequence | GATGCAGTGC AATGGCACGA TCTTGGCTCA CTGCAACCTT CGCCTCCTGG ACTCAAGTGA 60
TTCCCATGCT TCAGCCTCCT AAGCAGCTAG GACTACAGGT GCAGGCCATC ATGGCCAGCT 120
AATTTTTTCT ATTTTTAGTA CAGGTGGAGT TTCACCATGT TGGGACAGGC TGGTCTTGAA 180
CTCCCGGCCT CAAGTGATCC GCTAGCCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG 240
AGTCACTGCG CCTGGCTCAG ATTCACATTT TCTTCCTTGT TTATTCACAT TTGTGAACAG 300
CTGGCCAAAA TCAGGCGGTG GCTTGGAGTT GCAGAGGGGG CAGGATTGGA CCCAGGACCT 360
TGTCTGTAAA GCACTTCAGC CAGCCTCCAG TCCTTGAGTG GTGCTTTGCA ATCTTGTGAA 420
GCATTACATG TGAAAAGCCT ATCCAGCCTG CTACCCGCCC CAGACCCTTT ACTGGCCAGA 480
GGAATGTGAT GCTCCGATTG GCCAACCCTG AGTCACATGC CCACTCTTGG AGCGGAAAGT 540
GAAGTGAACT CCAGGAAATG AATTTCTTTG AGGAGCAGAG CCTGAAAAGG GTGTGTAGCT 600
GGTGCCCTGA TAATAAGCCG GGGATGAAGA CACCAGAACG AAGGGTAAAT GGATGCCAGG 660
TGGCAAAACC ACACATGCCC ACCCTTCTGG TTGCTAAGCA ACATTTTGTT TTTCTGCTCT 720
GGTTCCTCTT CTGTTCTGCA AAGCTCGCCT AGCACAAGGG CTGACCATTC TGGAGTTGGA 780
AGAGGGCCAA ACCCAGGGGC CTTGAGTGAA GTGTAAAGAG ATCTGGGCTG GAGATTTGGG 840
TTTTAGTCCT GATATTGCCA CGTACTTTCT TCCCTCCCTG AGTCTCAGTT TTTTCTTCAG 900
CTGTAAGACG AGGAGACTGA ATAGAATCTC TGTGGGGTCC TTGCAATTTA CTAGGCTGGG 960
TTCTGGGCAA TGTCACAGGC AGTGGGGGCC TCCTGTGCCT CTCATATTAT ATCTTAGAAG 1020
TGAAGGCAGC TTTCTCTGAA CATGGGCAAT CCCTGCCATG GAACGTGGCT TGCTAGAAAG 1080
TGCCTCAATC TTGGCATTAG ATGATTTGTT TTGGTTTCTG ATCTTAATTT 1130
|
