| Tag | Content |
|---|
EnhancerAtlas ID | HS088-01159 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:26743320-26744760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:26743696-26743715 | CAGCGCCATCTGGTGGAGA | - | 7.34 | | SREBF1 | MA0595.1 | chr1:26744159-26744169 | ATCACCCCAC | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_32755 | chr1:26743602-26745015 | H1 | | SE_68737 | chr1:26742540-26745575 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 26744058 | 26744178 | | chr1 | 26743535 | 26744048 |
|
Enhancer Sequence | GCTGGTCTCG AACTCCTGAC CTCGTGGTGA TCCGCCTGCC TCGGCCTCCC AAAGTGCTGG 60
ATTTACAGGC ATGAGCCACC ATGACTGGCC CAGCGTGGTG TTATTTAATT TAGACAGGAC 120
TTGGCTTTTC TAAGCAGTAG AATATAAGAA CTGAGTTTCT GGCCTAAAAG TCTAGGAACC 180
TTTCATTCTT ATCCCTGATC AAGCCGGTGG TTGGGTGGGG GCAGGGTGGG ACGGGGAGGA 240
CAAGATGACT GCCCTAAGGA GCTGTGGAGA TAAATCTACC CGAACACTTG AGTTCACAGC 300
TCAGACCAGG TAGCGGGCCA CTCAGTACCT CCTGGTATAG GCGCCCTCGG GCTTACCTTT 360
GGGCAGACAG GCTGAGCAGC GCCATCTGGT GGAGAACTCC AGGCAGGAGC TACAGGGCCT 420
GGCTGTGGCT GAGCAGAGGG GATCAGAGGG ATTGGCTGCC TGCAGCCTTC TGTTCCAGAC 480
ACCCCTTTCA CCAACCTCCT TGACACACAC CCTCCTTGAC ACACACACCA TCGAATAACT 540
GCTTCTGGGA GAACCGGTTG GTTCTCCCTT ACCAAATCTT ACCTCCAGGA ATGAAGCTAA 600
GTTAGGGATG TGACACCACA GGACTGAATC ATTAAAATTA CTTTCATCAG CTGCTTTTTT 660
AAACGTAGCT ACTAGAAAGT TTTCAATTAT ATATGTGACT TGCATCATAA TGAATTGCAC 720
TGGGGAGAGT TAGGCCAGCT GCACTCAGCT CAGCTCTTGC CTCTTATTGC GACTTTAACC 780
AAGGTGCTTA TTAACCCCTC TGCCTCCATG TCCTCAAGCT GTAAAATGAG GGTCTTCATA 840
TCACCCCACT GCACCAGTTT GATATGAGGG TTAAATGAGT TACAACACGT AAAGTGGTTA 900
GAATGCCACT TAGCCTACAG TAAGAATCAA TTAGTAACAG TTATTTTGCA TAGTACTTAG 960
ACATTCAACA AATGCTTGTG CAAGCTAAGA ACCTAGAATT GAGGTAGAGA CCTGCACTAC 1020
AGAATCTTCC GGCTGGAATG GCCCTGGAAG AAGATCTGGA ATAGCCTCTT GCGGAAGAGC 1080
CAAGAACCCC AGCTTTAATC TGCACAACTG TAGCAAGTAC CCTGAAATTC TGTTGCCACT 1140
TCTGGAGAAA GGACACTTAG GTTCCTTTGT GTTGTTTTTT TTTTTTCTCT TCATACTTTT 1200
TTCTTTTATA ATGTTTTCTT TTGTTTTTAA CTCCACATTT CCTAAGTGAC CCCTAAGGCT 1260
CATTCTATCT CTAAGCTTGC AAAGGCATAA ATTGAAGCTG GGATGAGGTA CTTGGTGTGG 1320
GTTGGATAGG GTAAGGCAGG CAATTACTGA GGTATTAAGA AGGGATCAGA AGGCCTAAGT 1380
ACTTTAACTG GAGAGATTCC TTCCCTGTTA TCAAAAAAAG AAAAAGAAAT GCTTGGGGTG 1440
|
