Tag | Content |
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EnhancerAtlas ID | HS127-01534 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr1:117129130-117131310 |
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) |
NEUROG1 | MA0623.2 | chr1:117129519-117129529 | GACATATGTC | + | 6.02 | NEUROG1 | MA0623.2 | chr1:117129519-117129529 | GACATATGTC | - | 6.02 | NFKB1 | MA0105.4 | chr1:117129278-117129291 | AGGGAAATCCCCT | - | 6.15 | NFKB1 | MA0105.4 | chr1:117129278-117129291 | AGGGAAATCCCCT | + | 6.1 | REL | MA0101.1 | chr1:117129280-117129290 | GGAAATCCCC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59077 | chr1:117079459-117152311 | Ly3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 117130518 | 117130699 | chr1 | 117129425 | 117129671 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I116586 | chr1 | 117129425 | 117129730 | GH01I116587 | chr1 | 117130423 | 117131022 |
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Enhancer Sequence | AACGAGGAAA GCTGTTTTAC TCGGTGTCCT CTGAGTTCCA TGTTTACGGT GTTAAAGTTC 60 ACTGTAACAG AGACTTCACT AAATGTGTTG AGGGGGGTCC TTCTAGTCCT TCCGCACTGT 120 CCCACTTAGC TTGATTGTAG TCTCAGAGAG GGAAATCCCC TCAATAAATT TAGGATCCTC 180 CAAGAATCTC TTGGTTTCAG TACAAATGAG GAAAGGAAAA AATGGTGATG ACTAGAGTGG 240 AAATGCAGAG TGGTGGGGGT GATCATGTTC TTTCAGTAGA GAAAATAATC AGAACTGAAA 300 ACAGATGAAA AATAGGAACC AAAAGAACAC TGGTGGGCCT AATGACAACC TTCAATGTTC 360 AAAAGCCCCA GGGACTGGCC TGAAGTCAGG ACATATGTCA CCGAAAATGC CAATGGGAAT 420 CACTTCAGAC CAGAGCTTCC TGTTTAATGC ACCAGCAGAG GTTAGCAGAA AATGCCACCG 480 AGAGGCCAGT GAGAATCTCT GGAAATATAA TAACCTCAGG CAAAGGAGGG GAACAGACTC 540 ACTGCATTCA GCAGGGCACA GGCCACATGT GGAGTTTGGT ATCGGGTTCC ACTGGCTTAC 600 TGAATAGGCC TCCTTAGGAG ACAAGCAATA GTGAAGAAAA CCAAGTCCCT ATGCTTACTC 660 AGGAGGCTTC AATTCTAGTA GAAGAGATAG AAAACAAATG TGTGTGTGTG TATATATATA 720 TGTATTCTAG TATAAAAATA ATAAGACATA GTAACTGATA AGTCAATTAT AAGTAAATAC 780 TTCATAATTA CTTATATATG AATAAGTAAA TTAACAGAAT GTCAGGTGGT GATATGTGTT 840 GTGAAAGGGC CGGGGAAAGG AAATCTAGAG TGATGAGGGG GCTACATTTA AGTTAAAATG 900 AGCTAGGAAT CCCCCTTCAC GGAAGAGCAA GACAAATGAA TATCTATGGC CAACATGTTC 960 CAGGCTGACA GAACAATAAG TACAAAGGCC TTAGGGTGAT CAAGGAAAGC AACCATTTAT 1020 TCCTTATTCA ACCAATATTT ACTAAAAGTA CCATGCCAGT GGCTGAAGAT ATAAGACACA 1080 GCCCTGTCCT CAACATGCTT ACAGAGTAGT ACAGAAGAAA TGCAAACCAT TATTAGGCTA 1140 TGTGTTTTAG AAGGGACCCC TACTGGTATG GGAGAAATCA GGGTAGGCTT CTTGGAGGTG 1200 GTGCTGAATG AAGTCTTAGG GATGGAGTGA AGACAAGGGA GAAGCAGCAG GAAAAACACA 1260 TTTCAGACAA TGAGGGCAGC ACAAGCGAAG GCACGGAGAT GAGGCTCTGG GTGGCAACAC 1320 AGCACCCCCC ATGGCCCATC AAGAAGGACA GGCAGTGACA ACAACGAATT GCAGGGATGT 1380 GAGAATGAGG GGTGGAGAGG CCCTTCAGGC TACACTATGT GAGAAGTTGA AAGGACTAGA 1440 GATCTTTAAC AGAGAAGGGG CATACATTTC ATGTATTTGA AAGGAAATGA CGCAGACTTC 1500 TCTTTGGTTG TTCCAGGGGC AGATCTAAAA AGGGAAATTA CAGGAAAGTG AACTTTTTAA 1560 CAATCAGAGC TGCCCAAAAA TGGAACTGAG GCTTGCGGAC TGAATAGCTC TCCCTCCCTG 1620 GAAGCATTCT GGCAGAGGTT GAGTGCCACC TGTGAGGGAG AGGAATAAGG GCTACACCAT 1680 GGGATCAAGG AAGGGCCAGA GGAGGAATGA TTCAGTTTGG AGATAGGAAA GGCTTGTCTG 1740 GGCGGGCTGG GAGCTAAGGA AGAAGGGGGA TGCAGATGCA TAAAACCAGA AAATGCCTTC 1800 TAGGTAGGAA CTCTGGGTGT GGAGCTGGTG TCAGCCCAAG ATTCAGGGTG CAAACTGCAA 1860 ACCCAGAAGA AGATTCAGGA GCTGCCATGA ACCCTGCCTT GCCACATTTT GCTAACCACA 1920 GCTGCCCTGC TCCTTGGTGA AGATGGTATC CACAGAAGCA GAGTCAAGGA TGCTTCCATG 1980 AGTCTGCCGT CAGCATCAGG ACCCACTGCA GGTAAAATGG ATGGGATTGC AGTGTGCTAG 2040 GGTGATGGTC CGTGTACCTG CACCCATACT CAGCATGCAC CTTGCAGACA GTCTCTCCAC 2100 ACCAGCCCCA CAGATCCCCA CCCACCCCCA GGCAGTCTCT GCACTAAACC CACTGGCCCA 2160 GGACAGCCGT GCCCTGCGGC 2180
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