Tag | Content |
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EnhancerAtlas ID | HS145-11499 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr19:8545590-8546850 |
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) |
SPI1 | MA0080.4 | chr19:8545641-8545655 | TAATTCCGCTTTTT | - | 6.16 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_53813 | chr19:8545583-8546506 | Spleen | SE_55325 | chr19:8545221-8546962 | Thymus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 8546261 | 8546416 | chr19 | 8546107 | 8546246 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I008480 | chr19 | 8545621 | 8545870 |
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Enhancer Sequence | TTTTCTTGCT AAGAGCCTTC AGCTTCTTGC CACTCTGCAG CACCTCTCGC CTAATTCCGC 60 TTTTTGGAGT GGCACATGAG TGGCACAGAG AGGTGGATGT GGGCTTCTTG CCTTTGAGGT 120 CACTTCATGT GGCCACAGGA AACTGTTCCT GTCCTGACCG GCAGGGCGCC ACCTCTCCCG 180 CTGCGGTTAC ACCTTCTTTC TGATTGGGAC TGTGCGATCT CTGTCCCGGA ATTCCCTCCT 240 GCCGCTGTGA TCAGACCTAC ATGAGTAAGG TGATCTCGTC AGGTTCTCAG AGTGGTTGGG 300 TTGGTTTTTC AAGATTCAAT TCTTGACCTC TTTCCCGTGT CCTTTGCCAT GAGAGGTGAA 360 CCATTGTGGT GCTCCTTTCC ATAGTGCTTT CCTACTCGGT GCCCCTTCCT GTGCCTAGGC 420 AGTAGATCTT TGCACTCCTT TGTGCAAACA GCTGTACTTG CTGCTTCAAA AATTTGGATA 480 GGCCTGTGGT CTTTGGCCTT CAAGGATGAG GTGTAGCTGA GGCGATACTA AGGGTGGCTT 540 GGGACATCGC CAGAGGTCTG TGCATCCAAG TGGCCTAGTG AGGACGCTGG TGGAGACGTT 600 GGTTGCCAGA TGCTGCTCAG GGCATTGGCT CTGCTAGGGG GCTCAGCAGG CTTGGCACAG 660 GCAGCAGGTG TGCGCAGATA GAGCGGCTGG CGGCGGTGGG TGCAGGTCTC TGTGAGGCAG 720 GGGAGGAGCA TGGGCAGAAC AGGCTCCAGT TGTGGTCTGT GGGGAGGCCT GTGAATGCCG 780 ATGGGAGAAT TCCGCCATTC TCTGCAAATC AGTGGCATGT TGGTTGAAAG CTTTTGCAGC 840 TGTCTTGCAG GTGTGTTAGT TGGAAGCTTG ATCTAGTTCA GGGGTGTGCA CGGGAGAATA 900 TAGTCATGGG TTCTCAGTTG GTTTCTGTTT GGGTCAGTAA AGCCCCTTAT CCCTCTTTTC 960 CACTTATTAC TAGAGACAGA AACTTAAAAA CCATGGTTTC AGGCTGCCAA AAAGCCTAAA 1020 ACAGAACAAA GCAAAGTAAG ACGTGTTGGA CAAGCTTGGT CTAGGTGCTG GAAAGCCAGC 1080 CTCGGCTCAG GCATGCCGGG CAGGATCGCA GGCGTCCCGG GAGAATGAGC TGTACCTGCT 1140 GGTAGACTGA AGTCTGTGTC TCTTGGTGAA CTTTCCCACC TTGTCCCACA GCAGTTAGTT 1200 GGGATATAAG AAGCAGCTGT GTGGGGTGCA GGTGCTTTTG TTGTTGTTGT TGTTTGGTGT 1260
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