| Tag | Content |
|---|
EnhancerAtlas ID | HS080-02896 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:204683390-204684740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:204684306-204684327 | TGTCAGTTCCTCTTTCCTTTT | + | 6.1 | | KLF4 | MA0039.3 | chr1:204683851-204683862 | CCACACCCTCT | + | 6.02 | | LBX2 | MA0699.1 | chr1:204684088-204684098 | GCCAATTAGC | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_40390 | chr1:204683392-204684345 | K562 |
|
| | 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 |
| GH01I204714 | chr1 | 204683687 | 204684972 |
|
Enhancer Sequence | CTTGTCCCTG TCATCCAGAA GCTCATAGCC CAGGCAGTAG GAGGTATGAT ACAAATTATC 60
TGTTACTAAT AATAAGGGAT CCACATTTGC AAATGGTTTT TATATATGCA TGAATATTAC 120
ATTCAAGGTG ACCCCTATGA TGTCATGCTT TCTTGAGCGG AGAAAGTGAG AACTGGGGCT 180
CGAGAGAAAG AGAGAGAGAG AGAGAAAGAG CTGATCTAAG ACCACGTTTC CTAACACTCC 240
TAGGCCTCCA TATTCACACA TGCCCCAGCC ACAAGGCTGG CAGCTTCTTT CCCACCCTGG 300
GGTTACTGCC TTCCTAATTC ACAGGCTACC TCCTTATAAA GGGGGTCCAC CCCGCACTAT 360
GGAGCACTAC CAGAAGCAAC ACAGTTGTTG TAAGATGCCC ATTGGGAAGG GAGTTGGGGA 420
GGGTGTCTTT CAGATGAGCC CACTGGCCGT GTGCTTGTCC TCCACACCCT CTTCCAGCAG 480
TATCTCGTTT AAGCAACAAG CAGCCCTCTA AACCCTATTT GGAATGTGAG TTACCTGGCT 540
TCAGGGAGAT TACAGGTGTA CAAGGTCACA CAGCTGGCCT GGGAAAGAGC CTGGATGCCC 600
CCGACGTAGA TCTGTGGGTC TTCAGTGCTT TCCCCCACTA GTCCAGACAG GCAGATCTGA 660
GCTGGAAACG TTGGCTTGCC AGGAGGTGTC GGCCTTGAGC CAATTAGCTC TCAGTCTGTG 720
AGCCCTCTTT CCCACCTCCC AACAGTGAGC CTCAATTCCG TACATTCTTT TTCCACTTCA 780
AGGTTGGATT TCCATCTCCT CTCCCCACGT TTGGAAACTG TCCCTAATCA CCAGAGAATC 840
TAATTATCAC TCCTTCTAAG TGATTCTCGG TCTCTGTTAT GCAAATGTGG CTATAATTGT 900
GTCAGGCAGG TTTTGTTGTC AGTTCCTCTT TCCTTTTTCC GCCTCTCTCC CCATCTCCTT 960
TCAAATGGGA GTTGCAGTCT CCCCTCTTTT TATTGTAAAG GCCTCTAAGG TCCCCGGCTC 1020
CCTGAACCAC AAATCGCCTA GATTACCCAC TCTGGATCCC AGGAGCCACA ACAGGCCCGC 1080
CTCAGGGCAA ACAGAAGGAA AAACAAACAG CATTTAGTGG AATTTATTTT ATTTCTTTGG 1140
AGATGCAAAT CAGAAGGTTC CCAATGAGCT CTGGGAAGGG AGCGTCTGTG TGGGGTGGGA 1200
GGAAGTTGGT TCTGTGAACA GCAGCAGAGT CAGGGAAAAC AGGCCCCTGT GCAGCCGGAG 1260
GTGCTGAGGG CATTCAATGT GGGCCTAGGT GTGTGGGACA GGGGTGGGAC GGGTGGGAAG 1320
CCCCACCAAG CCCTAAACCA CTGCATTTGT 1350
|
