Tag | Content |
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EnhancerAtlas ID | HS093-23182 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr4:1329020-1330640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr4:1329315-1329326 | AAACCACAGAG | - | 6.14 | RUNX1 | MA0002.2 | chr4:1329397-1329408 | AAACCACAGAG | - | 6.14 | RUNX1 | MA0002.2 | chr4:1329480-1329491 | AAACCACAGAG | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I001337 | chr4 | 1329850 | 1330624 |
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Enhancer Sequence | GAAGTAAGAG TTTTTACACC TAATGCTCTG AGGTGCACTC TGCACTGAGC TGTCCTTCCA 60 GCTGTGTGAG TCTATTTTTT GTCACAGTGC ACAGGTTGCA CACATTCCAG ATCATTCAAG 120 TTGATTCACA AGTGAGTGTA GCAGAGTTAA GTCAGCACCA GCCCTGTGGC ATGTTGAAAT 180 CAGAGTTAAG TCAGCACTGG CCCCACAGTG TGTTGAAATC AGAGTTAAGT CAGCACTGGC 240 CCCACAGTGT GTTGAAATCA CAGAGTTAAG TCAGCACTGG CCCCATGGCG TGTTGAAACC 300 ACAGAGTTAA GTCAGCACTG GCCCCACAGT GTGTTGAAAT CACAGAGTTA AGTCAGCACT 360 GGCCCCATGG CGTGTTGAAA CCACAGAGTT AAGTCAGCTC TGGCCCCCAC AGTGTGTTGA 420 AATCACAGAG TTAAGTCAGC ACTGGCCCCA TGGCGTGTTG AAACCACAGA GTTAAGTCAG 480 CACTGGCCCC ACAGTGTGTT GAAATCACAG AGTTAAGTCA ACACCTGCCC TGCAGTGTGT 540 TGAAATCACA GAGTTAAGTC AGCACCTGCC CTGCAGTGTG TTGAAATCAC AGAGTTAAGT 600 CAGCACCTGC CCTGCAGTGT GTTGAAATCA GAGTTAAGTC AGCACCTGCC CTGCAGTGTG 660 TTGAAATCAC AGAGTTAAGT CAGCACCTGC CCTGCAGTGT GTTGAAATCA CAGAGTTAAG 720 TCAGCACCTG CCCTGCAGTG TGTTGAAATC AGAGTTAAGT CAGCACCTGC CCTGCAGTGT 780 GTTGAAATCA CAGAGTTAAG TCAGCACCTG CCCTGCAGTG TGTTGAAATC ACAGAGTTAA 840 GTCAGCACCT GCCCTGCAGT GTGTTGAAAT CAGAGTTAAG TCAGCACTCA TCCCGCAGCA 900 TGTTGAAATC AGGGAGTTAG ATCAGCACTG GCCTTGCAGC ATGTTGAAAT CAGAGAGTTC 960 CAGCACTCGT CCCGCAGAGT GTTGAAATCA GAGTTAAGTC AGCCCTTGTC CTGCAGGTGT 1020 TGAAATCAGA GCGTTAAGTC AGCACTGGCC TCACAGCGTG TTGAAATCAG AGACTTAAGT 1080 CAGAACTGGC CCCACAGTAT TTTGAAATCA GAGAAGTCAG CACTCCCCCG ACAGTGTGTT 1140 GAAATCAGAG TTAAGTCAGC ACTCACCCCA CAGCATGTTG AAATCGGAGT TAAGTCAGCA 1200 CTCACCCCAC AGCATGTTAA AATCAGAGTT AAGTCAGCAC TCATCCCACA GTGTGTTGAA 1260 ATCAGAGTTA AGTCAGCACT TGTCCCGCAG CATGTTGAAA TCAGAGTTAA GTTCATACTG 1320 GCCTCGCAGT GTGTTGAAAT CAGAGAGTTA AGTCAGCACT GACCCTGTAG CATGTTGAAA 1380 TCAGAGTTAA GTCAGCACTC ATCCCGCAGC ATGTTGAAAT CATAGTTAAG TCAGCACTCA 1440 TCCCACTGTG TGTATCAGTC AACACTTGAG GGAGTTATGC TTTGTGCTGA CCCTTAGTGC 1500 AAAGTGTGTG GGTCACTGGG GGATGGCTGT GGGCCGATGG CACCTGCTTC ACCATGGTCC 1560 ACGTTTTTAA GCTGTCCCAG GAGCTTCCCT GGGAGCATCC CCAGGACCCT CTGCTCTCTG 1620
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