| Tag | Content |
|---|
EnhancerAtlas ID | HS080-02645 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:183385340-183386810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:183385614-183385635 | CAAAGGAAAGTGAAAGTGGAG | - | 7.98 | | IRF2 | MA0051.1 | chr1:183385618-183385636 | GGAAAGTGAAAGTGGAGT | + | 6.25 |
|
| | 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 |
| GH01I183416 | chr1 | 183386008 | 183386935 |
|
Enhancer Sequence | TCAATCCAAA TCTGTTTCTC TTGTAATCTA AAACAACTGG GATTTCCTAG CTTCAGGAAG 60
AAAGGAGCAG TACCTGCTGG GTCATCAAAG ATTCTTAGAG CCACAGAGTT TCATCCCCAG 120
CCCAATGGCT CTTCCCTACT CCTCCTTTCT CTTGGTTCCA AAGGAAAACC CATCATTGCC 180
TGGTCAAGGG AGAGGAGTAA AGCGCATCAA CATAAAGTGC TAGAGGACAT ATGGACAGAC 240
AGGAAAAGAA GGAAAGGGAT GAAGACACCA GCATCAAAGG AAAGTGAAAG TGGAGTGTTC 300
TTAGGGCACT GATAGTCCTT AGAAGACTGA TGACATGCTC TTGTCTACCC TGATGCTGGA 360
ACAGAAGTCC TTATTTAACA GGCAAGTTGG CATTGGTTCT TAATAAAAGA CTTTTGAAAG 420
CTGAAGGAAT GGTGAAGAAG GGATGGCTAT CTCTCAGCCT CCCTCCTTCT ATCGTGTAGA 480
TATGCCTACC CGATTTGCCC TTTGCTCAAA GTAGTTCTAT ATTCTTTCCA TGAGGTTTTT 540
AACAAGCGAG CCCAGTTCAG CGCACCTTTT AAGTTTAAAG ATGAATATTT TTAGCCTAAG 600
CCACCTCGCC CTGTCTTTAC CGCTGTGGTG TGGTTTTCAC TAAACCTCCC TAGGAGGGCT 660
CGCGCAGTCC TCAGGCTCCG GATAAACACG TGTGCCCGCA TCCAGCTCCG GCGCGCCCTG 720
CATTTCAGCA CCGCCGCCTC TGGAGAGCGC CTTGCTGGCG GGCCAGGTCA GGGCCTCCCA 780
CACGCTCTCT CATCCATCCC AGCCCACTCG CTTTTCCCTA CTCCTCGCTT CTCTCAGTTT 840
CAAGAAAAAG CACCCCCAAC TTCTAACTTC TCAATTCCTG CTTCTAAAGT GACCTCCGCG 900
TCCCTCTTTC CGTGTCTAAA CGCTCATGCC CCACGCCTTT GAGTCCTACG AGCAGCTGCG 960
AAGCCGCGTG GCTTCCCACC GGTGGCGCGA GACCTCCAAT AGGCATCTAT CGATCACCTT 1020
TCCCCTACCG CTGCTGGACC CCGAACCAGC CAGCCGGATG CCCCCGCTCG CTCTCTCTGA 1080
CTCCACGCCC CAAAGCTTCT AAGAAACAAA CGCGCGATAA GTCCCCTCCC CCCAACACGC 1140
ACACGCATAT ACTCACACAC AGTCATTCGC ACATTCGTAC ACACACTAGA CGCCTCAAGC 1200
CTTCCGAGTG CCATCGCCAC CCTGGGCAGA GCCTCAGCCA ACTTGGGCCC CGATCCTTCG 1260
GCTCCGGCTC GCGCAGGGCC TCCCGCAGCC TCCGCCCGGC CCCCTCCCCG TCCTAGGCAG 1320
CGGGTCCCTG AGGCCGAACC TAGGCGGAAA AGGGCCCCCT CCCTATTCAC TCAGCATCCA 1380
CCTCGCGCGG GCAATACACG GCCCACAATT CCCAAACACT GGTCCCTGGG CCGCCCAGAA 1440
TCACCAGCCA AATCCGAAAT TAATCTTGAA 1470
|
