| Tag | Content |
|---|
EnhancerAtlas ID | HS183-06573 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr5:151043790-151045920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr5:151044192-151044207 | GCATGACACAGCACT | + | 6.05 | | Nfe2l2 | MA0150.2 | chr5:151044190-151044205 | TAGCATGACACAGCA | + | 6.42 | | Sox3 | MA0514.1 | chr5:151044080-151044090 | AAAACAAAGG | - | 6.02 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_00092 | chr5:151038273-151068423 | Adipose_Nuclei | | SE_01149 | chr5:151043071-151046423 | Adrenal_Gland | | SE_01642 | chr5:151042218-151046437 | Aorta | | SE_02262 | chr5:151041396-151046427 | Astrocytes | | SE_02923 | chr5:151044536-151045486 | Bladder | | SE_04484 | chr5:151042099-151045872 | Brain_Anterior_Caudate | | SE_06414 | chr5:151042387-151046453 | Brain_Hippocampus_Middle | | SE_26088 | chr5:151041964-151045717 | Duodenum_Smooth_Muscle | | SE_29587 | chr5:151041938-151046411 | Fetal_Muscle | | SE_36971 | chr5:151041906-151046573 | HSMMtube | | SE_38049 | chr5:151042120-151046517 | HUVEC | | SE_41057 | chr5:151042040-151046468 | Left_Ventricle | | SE_42445 | chr5:151042141-151046441 | Lung | | SE_44210 | chr5:151040216-151046312 | NHDF-Ad | | SE_44814 | chr5:151042088-151044887 | NHLF | | SE_44814 | chr5:151044918-151045739 | NHLF | | SE_45698 | chr5:151038109-151046489 | Osteoblasts | | SE_46698 | chr5:151044255-151044741 | Ovary | | SE_46698 | chr5:151044745-151046367 | Ovary | | SE_48812 | chr5:151042092-151046409 | Right_Atrium | | SE_50590 | chr5:151042155-151046444 | Sigmoid_Colon | | SE_51537 | chr5:151042176-151046199 | Skeletal_Muscle | | SE_51808 | chr5:151042907-151045924 | Skeletal_Muscle_Myoblast | | SE_53114 | chr5:151042069-151046071 | Small_Intestine | | SE_53749 | chr5:151042268-151046445 | Spleen | | SE_63597 | chr5:151042907-151046136 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 151044528 | 151044718 | | chr5 | 151044761 | 151045856 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I151662 | chr5 | 151042044 | 151047160 |
|
Enhancer Sequence | AGGTACCTGC AGGGAAGGAG GCAGGGGAGG GCCTGAGGCA TGGAAAAGCT CCACACCCAG 60
CCTTGGGAGG CAACCGGGGA GTTAGCCTGC CCCAGAGCAT GGAGGAAAGG ATATTTAAAG 120
CAGGACAAAA AGCCAGAATC CCAGGTCTAC CCCTAGCTCT GCCACTGACT GCTCTGAGAC 180
TCAGAGAACA GCAGTGCACC ATTCGGAACC TCAGTTTCTC CTTCCAGCAA AGAGGAGGAG 240
ATGGCCATAA TTACTAACGG CCCTTCCAGC TCTAAGGTTT CAGGGTCTCA AAAACAAAGG 300
TCTGTTTGGT GTATTTGATT GTTTCCTAAT TGGCTGAGAA CTGGGGACAC AGAAACTTAA 360
AATCAAAATT CAGCACTTCT GCTATGGGTA GATCAAAATC TAGCATGACA CAGCACTGTA 420
TATTGTCTAT GGACACACAT TTATACATCT ATAAATGCCT AGTAAAGGGT CTAAAAATGA 480
CACACCAATC TGGTGACAGT GCTGCCTTCT GGGGAGGAAT GTGGAAAGGG ACTGGGATTG 540
GCAGTGAGGG TCAACGGGAG CTCTAACCAT CTTCATAGAG CTTTGCTTGT GTATCCTGTA 600
ATGTCTGAGA GGGAGGCCCT TTGGATGTCT CTCCCACTGT CCTCCCTCCC TATTCTCCCT 660
GCTGGCCTTA GACTCCAGAG CATGTGTATA ATTTTTTTCT TTGTTTCCCA GAGCCCCCAA 720
CTACTTGTCC CTAAAGATCC ACAAAGGATC TCCAGGGAAC AATGTGACTC CAGTTGTCTT 780
CTTAACCTCT AGACCTCGCA GCCCCACCCA GCTCACCAAA GAAATCACAC AATGTTTGAA 840
CTGATAGGAA CATTCTCCTC CCCTTCATTG TACTGGTGGA AAACTGAGGC CCAGGGAGGG 900
GCAGGGATGC AGGCAAGGTC ACCTACAGCC CTGGGATGGG AGGAGGAGGA AGCGGGTCCC 960
CTTGCCCAAG CTGGACCCCT TTCCCAGATG TGCTGTTCTT GCACCCCATC TGAAAGCCTC 1020
CCTCCAGGCC CTCTGTTGCA GTGGGATCAA ATTGCTTTGC CTGAGCTCCA GATGTTCCCC 1080
TTTGACTTTT CCCCTCCCTG CCATAATGAG TGACTCAGTT GGATCCCAGC CATGGCAAAA 1140
GCCTGGGAGA GAAGTGGCCG GGAGATTCCC AGAGCCCAGG AGACCCCAGC CCTCAGGATC 1200
ACTGGCAGGG TTGGCAGACT CCAGGCACAC AGGCTGGACA AAGAGCGAGG GGTGAACATC 1260
CTAGAGAGGA AGTTCCCTGA GTATGTGAGT AGGGCAGCCC TTCCTTTCCC CTCTGTGTGA 1320
TGCTCTGCTT CCACAACCCA AGGACGAAGA AAAAACCACT CTGGGAAGGT GCAGGTGTAG 1380
CTTGCTCCAT CTGAGGCTGA GCAGGGGCTC TCACTTCATC ACCACAAGAG AAGTTCAGAA 1440
GGTAGTGACA GGTTATGAAC AGAGTATAAG TCCATGAGGG CAAGGACCAT GCCAGCTCTG 1500
ACTGCTGTTC AATCCCCTGC CTAGAATAGT GCAGGGCACA AAATGCACAC TCCATAAGCA 1560
TTTGCTAACT GGCCAGCTGC CTGCCTGTTC GGCAGTGCAG TTGCACAGGG CCTCATAACT 1620
CGTTTGGACA AGGGACAAGA GCCCTCAAAC TGGGGGCTTG CAAAATAGAC AGGCTTTTTT 1680
GGATAACTTC CAGGGTCAGT TGGGCCCTAT TGGGGCTGAG CCTTAGGAGG GGGCTTAGAC 1740
AGTGCCAGGT GGCTGCTCTG CCCCTGGATG TTCTGCTGAA GGACAGGGGG CGTGTGGCTG 1800
ACCCAACCTT GTCCCCTGCC ACCCCTTGGA GCCTGGTACT CCTTCTTAAT TCACACTCCT 1860
TCATTATCCA GATATCCACG CCTAGTACTT GCAGGATTAT GGAGCTATTT TGAGCTCCTA 1920
CTGACTTTCA CCTCAGCATG AGAGTGTCTT ATCGGTTTCT TTGTCCCAGG TCCACATCTT 1980
TTCTCCAGAT GCCTCATCCT TCTGCTCCAA TCCCCAGGCA AACTGTGGAT GCCAGGGCTT 2040
GGAGCAGTAT AGGCTGCTGA GAGGCTTTCT GGCCATAGCT AGTGCACCTG CCAGCCTTGA 2100
GCTCTGTTCA CTCTAGGGTC TGGGGTCTTA 2130
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