Tag | Content |
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EnhancerAtlas ID | HS093-16507 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr2:28939960-28940810 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr2:28940106-28940116 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr2:28940106-28940116 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr2:28940106-28940116 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_02169 | chr2:28939958-28940678 | Aorta | SE_41111 | chr2:28938705-28940799 | Left_Ventricle |
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| 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 |
GH02I028713 | chr2 | 28936139 | 28941575 |
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Enhancer Sequence | TCTAACCAAT TTTTATTTTG TTGATGAAAA CTGAAAGCGG AAGCTAGAAG AATGGGGGGA 60 TTGTCCTCTT TTCTATATAT TTTTTTCTTT TTGATGTCCT TTACTTCAAG TTAAGCCTGG 120 TGTTTGCTTT AATCACAGCA GAAAGCATTT TCCATTTCAG GGAAAGGAGA GAACAGGCCA 180 TAAACCCTGT CCCCTGTTTG TTCTCCAACT ACCCATTTTT GTCCTTTGCC CTGCCATGTC 240 TTTTCCCCCT CGTTTGCTTC TCCTTTCTTT GTTGATTTCT CAGTTCTTTT CTGGCCTCAC 300 TCAAAATGGC AGAAATTACG CAACCTAGTA CTTTTTTACA CAAGCTCCTT TAGTGTCAAG 360 GATTCATCAA GTGCCTGCCA TGTGCCGGAA CTGTTCTAGA TGCCGAGAAT ACTACCATGA 420 ATGAAATAGA CAGAAATCCC GGCTGTCATT GGGCTTTGTC TGAGGGCCAT TGGGGAAGGC 480 CTCTCAAAGG AAGTGATAGC TGAGCTGGGA TCTGAGTCAT GAAGAGGAGT GAGCCCAGGG 540 GACAACAGCT GCAAGAGTGT GCCAATGGGA GAGACCAGCC CAGCAAAAAG GAGAAGCATA 600 AGTCTGGTGC ATTCCAGGGA CAGGAAGGAA TGGGGCAGGG TGCCTTTAAG AGAAAAGCAT 660 CAGTTTGGAT GAGGAGGGAT GTAGGGTCGG GAATACAAAA TAAGAGTAAT TATGGCTGGG 720 CACAATAGCT CACACCTGTA ATCCCAGGAC TTTGGGAGGC CAAGGTGGGC GGATCACTTG 780 AGGTCGGGAG TTAGAGACCA GCCTGGCCAA CATGGCGAAA CCCTGTCTCT ACCAAAAATA 840 CAAAAATTAG 850
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