Tag | Content |
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EnhancerAtlas ID | HS182-01078 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:78518390-78519990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr1:78518694-78518707 | CTGATTTGCATAT | + | 6.5 | STAT3 | MA0144.2 | chr1:78518480-78518491 | CTTCCCAGAAG | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 78518795 | 78519048 | chr1 | 78518410 | 78518800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I078052 | chr1 | 78518561 | 78518710 |
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Enhancer Sequence | CATCTTAGAA ACTATGAAAT TTGAGGCTCT GTTTGCAAGC ATAGTCACTT CCTAAATGAG 60 TTACAGCATA TGAGGAGCTG CTTCCTGAGG CTTCCCAGAA GCTGCTTCCT TTTCTCAACT 120 TGCTGACACT AGCACTGAGC TCTTTTGAAA GTCAATATTC TGTATTTATG TGGTACTTCT 180 AGAAGACATG AAATGTTCTG CAGACTTTAT CATTTCCCAG CAGTGCAAAT AACTGGCAAG 240 TGGAACTGTT ATCTTTCTGG TTCACAAATG GGAAACTAGG ACGAATAGAG AAAATAGGGT 300 TTTACTGATT TGCATATAGC ACCCCCTGCC CTGGAAAAAC AAGTTACAAA AATCTACAAA 360 AAATGAAAGA ATTGGGAATT GGGTGTGAAT ATTACTATTG AGGTCTGAGG AATATGAAGT 420 AAGCCCGTCA AAATTGAGTA GAAAAAGTGT GAGAAGCAGT CCCTGACATC TGGTAGGGGC 480 CTTGGCACTT GCAGGAAGGC CTTGGCATTC TGTTGCACAT AAACAATTGC ACAGCATGTC 540 AACAGCAGAT AAGACTGCTC TGACTGTGGT AATTTCTCCT ACCTTACAGA TAGGTTTACT 600 AAGATTCCTG GTCATAGAAT TGCACCCATT TCCTGACAGC ACCCTATCCA GAACAAACCC 660 ATGCTTTGGA CCCTCTCCCA AATCACCTAA CACAAGCCCA AATCCTTTGT AATGTCTCTT 720 TCTGAAACCC CCAGGATTTC CCATAGAGTG CTGTCACCCT CCTCACAAGG AGCAATAAAC 780 TGCAGGTGAG AATCCCTGGT GGTCTTTGCC TGGAAGGTGT TGGCAGTTGT CACTTGTCAC 840 TGTTGGGTTA TTACAATGCA GATTCTAAAG AGGCAGCCTG AATTTGGTTT CCCTGACTCC 900 ACTCATCCTC TTTTAGTATT TTAATGCTGT GATCATACCA GTCTAATCTT AGCACTTTGG 960 AAGGCTGAGA AGGGAGAATC CTTGAAGCCA GGAGTTTGAT TGACAACAGC CTGGGCAACA 1020 TAGTGGTACC CTGCCTCTTA AAAAAAAAAA AAAAAAAAAG CCAAAAAAAA AAAAATTAGC 1080 CAGAGGTGGT GGTACGTACC TGTAGTCCCA GTATTCAGGA GGCTGAGGTG GGAGGATCAC 1140 TCAAGCCGGA GTTTGAGGCT GCAGTGAGCT ATGATTGTGC TGCTACACTC CAGCCTGGGC 1200 AACAGAGCAA GACTGTCTAA ACAAACAAAA ACCTGCAAGG GGCTCCTCAT TACTTACAAA 1260 CCAATTACTA CCAGCCAAAC AATGTCTCAT ATTCCTGTCT GCCTCTTGAG TCCTCTCCTA 1320 TGCCCACTGT TCCAATCTCA CTTCTTAATA ATCCCCTTTA CATTCAACAA TATTTAACTG 1380 TTTCATTCCA TTGTGCTTTT TCTCATGCTG TTCTTTGTTC CAGTAACTCC TACTCACTTT 1440 TCTAGTCCTG TAATTTCCTC CAAGAAGCCT ACCCTGTGAA TCCAGAAATC TGGATACCTG 1500 CTATTGCATG ATTTTTAACA TAGCATTTGC ACATAAGATT GAATTTAGTT ACTCCTCTGT 1560 TTCTTCCTGA GGGCTGGGAC TTTTTTCCTT TTTAAATCTT 1600
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