| Tag | Content |
|---|
EnhancerAtlas ID | HS108-07448 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:47938730-47940560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr11:47939366-47939377 | CATGAGTCACT | - | 6.14 | | Foxd3 | MA0041.1 | chr11:47940277-47940289 | GTTTGTTTGTTT | + | 6.32 | | 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 | | Nr2f6(var.2) | MA0728.1 | chr11:47940489-47940504 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 | GATCATGCCA CTGCACTCCA GCCTGGGCAA CAAAGCGAGA CTCTGTCTCA AAAAAAAAGA 60
CCCTGGGCCA TTTGCTATCA TAACATAAAA GCAGTCAGGG GCCATTGTTG GCTGAGTACT 120
GACCTGGGTC ACCTACTCTC TGCATGGCTT TAAGGACTCA CCTCCCCAGT TTGGGCCTTG 180
GTTTCCTTGT CTGAGATATG GAGGAGATGG GTGAATCTTT GCTACTTCTC TTTGCAATCT 240
GTACTTTATG AGTTTAGGAA TCTTGAGAAG TTTGTGAGCC TTCCAAGACT TCCCCCTCCT 300
CCCCTGTTAG CAGGATATTG GAGTTATATT GTCGAGGGGT TTACGTCACT CGATTCACAT 360
TTTCCTTTTT TTTGGGACAG AGTCTTTCTC TGTCACCCAG GATGCAGTGC AATGGCACGA 420
TCTTGGCTCA CTGCAACCTT CGCCTCCTGG ACTCAAGTGA TTCCCATGCT TCAGCCTCCT 480
AAGCAGCTAG GACTACAGGT GCAGGCCATC ATGGCCAGCT AATTTTTTCT ATTTTTAGTA 540
CAGGTGGAGT TTCACCATGT TGGGACAGGC TGGTCTTGAA CTCCCGGCCT CAAGTGATCC 600
GCTAGCCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGTCACTGCG CCTGGCTCAG 660
ATTCACATTT TCTTCCTTGT TTATTCACAT TTGTGAACAG CTGGCCAAAA TCAGGCGGTG 720
GCTTGGAGTT GCAGAGGGGG CAGGATTGGA CCCAGGACCT TGTCTGTAAA GCACTTCAGC 780
CAGCCTCCAG TCCTTGAGTG GTGCTTTGCA ATCTTGTGAA GCATTACATG TGAAAAGCCT 840
ATCCAGCCTG CTACCCGCCC CAGACCCTTT ACTGGCCAGA GGAATGTGAT GCTCCGATTG 900
GCCAACCCTG AGTCACATGC CCACTCTTGG AGCGGAAAGT GAAGTGAACT CCAGGAAATG 960
AATTTCTTTG AGGAGCAGAG CCTGAAAAGG GTGTGTAGCT GGTGCCCTGA TAATAAGCCG 1020
GGGATGAAGA CACCAGAACG AAGGGTAAAT GGATGCCAGG TGGCAAAACC ACACATGCCC 1080
ACCCTTCTGG TTGCTAAGCA ACATTTTGTT TTTCTGCTCT GGTTCCTCTT CTGTTCTGCA 1140
AAGCTCGCCT AGCACAAGGG CTGACCATTC TGGAGTTGGA AGAGGGCCAA ACCCAGGGGC 1200
CTTGAGTGAA GTGTAAAGAG ATCTGGGCTG GAGATTTGGG TTTTAGTCCT GATATTGCCA 1260
CGTACTTTCT TCCCTCCCTG AGTCTCAGTT TTTTCTTCAG CTGTAAGACG AGGAGACTGA 1320
ATAGAATCTC TGTGGGGTCC TTGCAATTTA CTAGGCTGGG TTCTGGGCAA TGTCACAGGC 1380
AGTGGGGGCC TCCTGTGCCT CTCATATTAT ATCTTAGAAG TGAAGGCAGC TTTCTCTGAA 1440
CATGGGCAAT CCCTGCCATG GAACGTGGCT TGCTAGAAAG TGCCTCAATC TTGGCATTAG 1500
ATGATTTGTT TTGGTTTCTG ATCTTAATTT TGTGTTTTTT TTTTTTTGTT TGTTTGTTTT 1560
TGAGACTGAG TCTCGCTCAT CACCCAGGCT GGAGTGTGGT GGCACGATCT CGGCTCACTG 1620
CAACCTCCGC CTCCCGGGCT CAAGCAATTC TCCTGCCTCA GCCTCCTGAG TAGCTGAGAC 1680
TACAGGCGCA TACCACCATG CCCAGCTAAG TTTTGTTTTT AGTAGAGACG GGGTTTCACC 1740
ATGTCGGCTA CGCTGGTCTT GAACTCCTGA CCTCAGATGA TCCACCCACC TTGGCCTCCC 1800
AAAGTTATGG GATTACAGGT GTAAGCCACT 1830
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