Tag | Content |
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EnhancerAtlas ID | HS072-01557 |
Organism | Homo sapiens |
Tissue/cell | GM19193 |
Coordinate | chr4:103680380-103681870 |
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 | chr4:103681637-103681651 | AACTTCCCCTTTCC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09424 | chr4:103677687-103683205 | CD14 |
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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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Enhancer Sequence | CCTCATAGAC TCTTTCTATG TTGGCCATGC TGGTCTTGAA CTCCTGGACT CAAGGGATCC 60 TCCTACCTTG GCCTCCCAAA GCTCTCACGT ACCAGCACCC ATTGGCTTAA TTATTTCAGT 120 AAAATCAGGC AAGGAGGAAC CCTACAAAAT AAACACAGGC ATTCTCAAAG CAGATATAAG 180 TGAAAACTCA GAGTATACTG TGGTCAGCTG TGTTCTCTAT CACAAGTAGT TTGTCAACTT 240 AAAATAAAGT ACTAAAGTTT GGGAATGATC TACTCTAAAA ATACATCGGA CAATGGTCAA 300 TGTCATTTAC AACATTCACC TCCTTTCTGA TACACATCTC AGGAAAAAAA AAAAAAAAAC 360 TACTAAGTAC CAGGTCAGAA ATTTGGCACA ACCCTAGATG ACCACCTTGT CATGCAAATA 420 AACTTAGAAT GGTGCTCCTG AAAGTCAGCC ACAGTGCTTC AAAAACACAT GATTTTTTAA 480 AACACCAAAC TAAGCATACC ACATAGTATA GAGACCAGGC TATGGAGTTG AGACCACCTG 540 GGTTAGAATT CCATTTCTTT CCATTTAGTT GCTGTCACCT TCCTAATTTC TCTGTGTTCC 600 ATAATTCCAT ATTATCCATA AAATTCAGAT ATGAACACTT ACTATACAGA GTTGTTATGA 660 GGATTGGACA ATGTATGCAT CCCACAAGTA GATCAATTAC AAGTACATTT TGCCCCAAGT 720 AAAGACAACA CGTGGGAACG CTGTGCAAGA GGGAACAGCA AAAGCAGTTG GAGGATGGAA 780 GTCAGTTTGC AAACCTATGC GCACAGGCAG CCAAACACGA AAACGTTCCC CACAAGTAGT 840 CTGTAAATTG GAGACTCCAT TGGGATACAC ACACACACAC ACACACACGC CCTGAGAGGA 900 AATAGCACCT TTCTTCATCA CCAAGTTAGC CTTAAAAATT ATTTACCCGT TGTTAGCCAC 960 ACTAGCACTG ACAAACCCAA CTTTACTCTT GTAGGTCATT CTCCACAACG TCTGTGCTGC 1020 GTCAATCCCA AATCTGACTC CCTGACGCTT AACAGCGAAA ATAAAAAACC GAGACATTAC 1080 TCAATAGAGT TAACCCTTAC TTAACAAAAC GCTGTTGTCC CCTGTGGCGT GCAGACAGTA 1140 GAGACAGTAA TTCCCGACCT TATGCTTGTC AGTGACGGCA TGCCCTTTGT ATACACGCTT 1200 CAGTAGAGAA CGACTGCAGT AAGTAAACTG CTAGTAGCAA CACTGTTCCC CTATCTAAAC 1260 TTCCCCTTTC CAGAGTTACT GATGTCCCAA CATGGGTCGG TCGCTCAGTC TCCGTCAAGC 1320 CCGTACCCCA TAGCTTGGGC ATTTCCCCCC GCAGATCACA AGATGCAAAG GGGAAGTTAC 1380 TACCAAACCG ACGAGAATGG CCCAGAGCTG GGGGCTGCCA GGCGGTTCCT GGGCCCCTCT 1440 CAGCACCAGA AGAAGGCGGG CGCAGGCTCG CCGCGGGTCG GCCGCACGCC 1490
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