| Tag | Content |
|---|
EnhancerAtlas ID | HS093-00205 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr1:11025050-11026410 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:11025700-11025715 | GAGGTCAGAAGCTCA | + | 6.15 | | RARA | MA0729.1 | chr1:11025700-11025718 | GAGGTCAGAAGCTCAAGA | + | 6.01 | | SPIB | MA0081.2 | chr1:11025389-11025401 | AAAGGGGAAGTG | + | 6.07 | | ZNF263 | MA0528.1 | chr1:11025271-11025292 | AGAGGAAGAGAAAGAGGAGGA | + | 7.36 |
|
| | 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 |
| GH01I010964 | chr1 | 11024590 | 11026962 |
|
Enhancer Sequence | GGTAAATGAC TAAGCCAAAG GCATGTGGCC ATTTCTGAGA CTAGATGTGA GAGCTGGTCT 60
AGCTCATTCC GGTACAAGGC GGACTTCAAA GATGTCAAAC CAATGGGTCC CTCTGCCCCT 120
CCCAGGCTGC CCTCATTCAG CCACATAAGA AGAACCCAAG TCTAAGCTTT GCGGTGGGGC 180
CTGAGAAGGG TGACGGGGCT GTCAGAGAAG GGCGACCACA GAGAGGAAGA GAAAGAGGAG 240
GAGCAGGGTA GTTCCCAAAA TTCCTTCCCC CACTCCAGAC CACAGCCCCA CTCAGGAAAA 300
ACTCTGGACT GGGTCAAGGA AGGGAGCACA AAGAAATGGA AAGGGGAAGT GGAGGTGAGG 360
AAAAGACAAG AAAAAAAAAA CTGTGAGCCA AACTGTGCGG CTGGTTGTCC CCTTGCAGGA 420
CCCCTGGAGT GAAATTTAAG TAACAAGAAT GCTGGCACAG TGGCTCATTC CTATCATCTC 480
AACACATTGG GACACCGAGG CGGGAGGATG GCTTGAGCCT GGGAATTCCA GACCAGCCTG 540
GGCAACATGG TGAAACCCCA TCTTCTACAA AAAGTACAAA AATTACCTGG GTGTAGTGGT 600
GCATGCCTGT AGTCCCAGCT ACTCTGGGGG CCGAGGTGGG TGGATCACTT GAGGTCAGAA 660
GCTCAAGACC AGCCTGGCCA ACAAGGTGAA ACCCCGCCTT TACCAAGTAG TCTCAGCTAC 720
TTCAGAGGCT GAGGCAGGGG AATCGCTTGA ACCTGGGAGG CGGAAGTTGC AGTGAGCCGA 780
GATTGCGTCA CTGCACTCCA GCCTGGGTGC CAGAGCGAGC CTCCGTCAAA AAAAAAAAAA 840
AAAGGAAAAA GAATACAAAA ATATCTTGCT TCTGTAAATT TTAGAGTCAC ATGGTCTCGT 900
GAGCCCATAA TGGGCCTGTG CAAGTGAGGG CTGTCAGTCA GTCTTTGCAA CTCCTCAGCA 960
CCATTTATTC ACTTCATTCA GCACTTACTG AGTACCTACT GTGTGCCAGG CCCTGAGGCA 1020
AGCCTGTGGG TGTGACTGCC TCACCCCAGA GACTCCAGGT CCAGCAGGAT ATGGTGTGTG 1080
AGTGGGCACA TTATGAGTCA GTGTTGGCAA TGATAGAAGC AGGTCTACTG CACAGAGAAG 1140
GGGGGATTCT CAGGAGGACT GCCTGGAGGA GGCAGCATCT GAGCTGGGCG GCCTTTTAAT 1200
ATCTATGCCC ATAAACTCCA TGAGGGCAGA GACTTCTGGT CTCCCTCAGC TCAGTTTCTG 1260
CAGAGGAATA ATGGTGCAGT GTCTCCTTAC TTGATATCTG AGCTCAGGCT TAGCTCCTTA 1320
AATCTCCCTT TAAAAAAAAA AAAAGAAAAG TTTCCCAAAC 1360
|
