| Tag | Content |
|---|
EnhancerAtlas ID | HS127-17066 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr2:88991500-88994010 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr2:88993965-88993976 | TGATTGAATTA | - | 6.14 | | IRF1 | MA0050.2 | chr2:88992973-88992994 | TCCTCCTTTCAGTTTTTCCTT | + | 6.06 | | NFAT5 | MA0606.1 | chr2:88991835-88991845 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr2:88991835-88991845 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr2:88991835-88991845 | AATGGAAAAT | - | 6.02 |
|
| | 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 |
| GH02I088693 | chr2 | 88993052 | 88994248 |
|
Enhancer Sequence | GGTGAGCACT TCGAAACGTG GGGCGCGGGG CGCATGTCCT TGGCGTGATG GGCTACTGTT 60
GCGCGTTGTG GGTGCTGCCG GGGCGCGCCT AGCTCCTGGC AGGGCGGGAG CTGAGTGAGA 120
GGGTAGAGGG TGTGCACTTT ACCCGAGTTT AGACCCCTCT TCCCTGCTCC TTAAAGACCT 180
TTTAGATGTG GAATCGGTTG GGGGCGAATC TTCTAATACT TGAGCTTTCT AAAGACTCCT 240
TGTCCAGCTG GAACAGTTTG CAAAGTGGAG CCTGGTGCTG TCTGATGTTT GGAATGGGGG 300
CTAGAGGCAC TTGCCTTGTG GCCTCCTTAT CAATAAATGG AAAATGGTGG GCTTTGGGGC 360
TGCGGAGAGG TTTTCATTTC TCTTTACTGA CCCGGAAGCC GGCGGAGAGT TGGTTTGCTA 420
GTGCTTTGAA ATTTCAGTCG AAGGAGGTTC TGGGCTTGGT GCGCGCCGGC CCCTGAGTGT 480
ACTCTTGGAG GGAAGGGAAG ACCCGGGGCT TCAAACTTCC TTCTTTCCAT AGGGCTGGGT 540
GGACTAAGTC TGGAGGATGC TGGTTTATTT TTTAAGGCGG GTCTGCAGAG ATGTTTAGCT 600
GTTATTCAGT CAGGTCGTGG TCCCTACTTG TTTGTTAAGT GGCAGGTGTG GTGCTGTTAG 660
TGGAGTTTTT TTAATCCAAG TGGTTTTGCT GTCACCAATC AAGTATCTTA ATTATAATAA 720
GGAAGCCAAG TGGAGTATGT CTGCCCTGTG GTGTAGTTTC CTTGGTCTTA TTGGCTTTTT 780
ATCTCTCGTT TCTACTTATT AGAAAGTGGT ATTAGAGTCT CTTTTCTTCT CCGATAATAG 840
TTCTTTACAT TTGTTAATGC TTTACAAAAT TATTTTGCTT AGATGATGTT GGATGAGCTT 900
CACCACAGCC TGTTTGAGTG GGAGTGGACA ATGTGGTAAC CTGTGGCTCA GCCAGTTCTG 960
TAGAAGGGAT GTTCCAGTGT GACCTTCTAC TCTTTCCACT GCTACCCTGT TCTGGTGTAG 1020
CTTGTTGTAA GTCTGATTGG CAATAGGATT TTCTATGGGG ATTAACAGAG ATAATGTAAA 1080
ATGTGTTAAT TTGACCCTAC CTTTGGGATT CAGTGCCTCC GTTGTAAAAT TGAGACAATA 1140
AGCTGAAATT TCAAAATATC TGCATACAGT GAATAGCTAA TAGATAAATG TAATCCACAT 1200
GAGAATACAA TTAGAAAAGC CCCATATCTA AGTTGTCCTG TTAATGAATT TACATTAATA 1260
TTTGGTGGCG CATCTCCCTG ACCTTTGTGT TATAGTCATG TATTTGATTA AATAAAAATC 1320
TGCAAGCCCT GACCTTAGGC TAGAGCCCCA AAACACTGGA TTCTGACCAC ATCATTTCAT 1380
GAAGTTAGGT AATTTTGGGG AGATCTACAG TGACCTTTTG GGGGCACCTG TTAAAATCAT 1440
ATATGCCCTT CAGGGTTTGG CTTAAAGGCC ATTTCCTCCT TTCAGTTTTT CCTTAGCATC 1500
CTAAGGAGAG GAAGATTTCT CTTCCGTGAT TCTGTAGCAC TTCATGCCTC TTATGTGCTT 1560
TATGTTGTAT CTCATGTTTT GGTCATCTGT GTGTTCGTTT CTTCCAGCCC CTTAAAGGGT 1620
AAGCTCCTGG AGGGTAGTTA ACCTTCATTT AGCATTGGTC ACAGTGGGTC CTGCCCAGTA 1680
CATGTTTGTT CAATTGTGTG CAGTGTGGAC ACAAATACGA AAGTGTTGGG GTTATTGGAG 1740
GTTCTTTGTG TAGAATCTCT GGGGAGTAGG GCTTCCTGTT CTCTAGTCCA TTGGAGTTCC 1800
AATATGGTGA CCACTTCCGT GTCTGAGTGG ATGGAAAACA TGGAGAGTTC TCAGGTGAAT 1860
CCTTTGTATA GCCACCTTGG GCCCAGCTCT GTCTGTTTCT GTGGGTGTAG CCACCCAGGA 1920
TGGGTCGACA TGCAGAACTA GGCTCTTCTG AATGTCTGTA GCCTCATCCC TTTGTTCTCT 1980
TTGGAGCCTG GGCTTTGTTT TTTTACTAGC TTGGTTGAGG AAGCTGATGG GCAGTGGTTC 2040
TAGTTGGTTA GCAGAAGTAG TATTTCCAAA GTTACTCCAT TCGACAAGCT GAGTGAAGTT 2100
CTGATGTTGC ACATACATGT GGTTTAATAT TGCCCATTAG AATGGGGCCA CTCCTCTAGC 2160
AGGGCCTGCT TGGCAGTCTT CTGCTGTTGG GCCACCTCAT AGGCAGCCTT TGGTCACCTC 2220
TGGTTGGCTT TGGCAAGGGC ACTGATTTCC TGGGCCAGTC ATTTGATTCC AAGGCAGCAG 2280
GGATCACATG GGTGAAGAGC TTTAGGTCTG GCAGGGCCTT GCAATTCCTG GTCTCTTTCA 2340
AAAGGCAAAG AACGAGCCTT ATACAGAGCT TGTCTGATTC ATCCGAATTC ACCTCTGTGC 2400
CACCTGCCTG CTGGGGACTG TGAGTGACAT GAATGTATGG CTAAGCTTGG TAACCAGGAA 2460
TTTGGTGATT GAATTACTGT AAAGCTAGAG TTCCTAGCTT CAGGTCATAT 2510
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