| Tag | Content |
|---|
EnhancerAtlas ID | HS127-24226 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr4:185541030-185542370 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Pou2f3 | MA0627.1 | chr4:185541441-185541457 | GTTTATGCTAATTAGG | + | 6.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTTTGTCCC TGTTCCTGGC ACAGAGTTCC CTAAACCCTT GGCATTGCCT GAGTGATGGG 60
AGTCTTTTTT TTTTTTGAGA CAGAGTCTTG CTCTGTCACC CAGGCTGGAG TGCAATGGCG 120
TGACCTCGGC TCACTGCAAC CTCTGCCTCC CAGGTTCAAG CGATTCTCCT GCCTCAGCCT 180
CCTGAGTAGC TGGGATTACA GGTGCCTGCC ACAATGCCTG GCTAATTTAT TTTTGTATCT 240
TTAGTAGAGA TGAGGTTTCA CTGTGTTGGC CAGGCTGGTC TTGGAACTCG TGACCTCAAG 300
TGATTCACCC GCCTCAGCCT CCCAAAGTGC TGGAATTACA GGTGTGAGCC ACCACGCCAG 360
GCCTGATGGG AGTCTTGTTA TTCATAATGA ATTCCTTTTG ATCACACCTG TGTTTATGCT 420
AATTAGGTGA TCTAGCGTGT GGCCCCTAGA TACTCAGGAT GCGGCTGGTC ATCAGAAAGA 480
CTAATGTTTA AAAGGTTGGA ACTTTCACTC TGTCCCTGAC CTTTGCCTCA TGCAAGGGAA 540
AGGGGAAGCT GGAGATTGAG CTGTATAGAA ACTCCAGGCT GGTGAATACA TCGGTGTTGG 600
AAGGCTGGTG CCCGGAATGT GGCAGGGCTG CTCGTGCCCC TCCCCGACGC CTGGTCCTAT 660
GCCTCTCTTC CATCTGGCTG TTCCTTAGTT GTATTATTTA AGTTTGCACA TGTAAGTAAA 720
GTGTGTTCCT GAGTTCTGTG ACTGATTCTA ACATGTTATG AAACCTGAGG AGGAAGTTGT 780
GAGGAAGGCA TCCCCACAGC ATTGACAAGA ATGAAACACG GTTATAATTC AGCATCTATC 840
AGGCTGCTCT CTGGCCCCTT CCTCATTGCT TAAAGTCTCG TAGCACCTGA CACCGACCAT 900
TTGCATTCCC ATTATTCCTA TAGACAGCAT CTCTGACATT AGAATCATAA GACTTTTGTT 960
TGAGGATGCT TAAGATGTTT TTCTGAGACC CTGAATTCCA GTGAAGCAGC TGCAACCAAC 1020
CGCTTTGAAG ACCCCCACAG AGGAACCAAA TCAGTGTGAG AATACAGCTT CTTCATCTTC 1080
CTGTCCCATG ACTTCACACC GCACTATTCA GCCAATCCAC CATCTCCACA CTTCCGCCCA 1140
CTCCAAAACC CTTAAAAGCC CAAGCCCAGG CTGGACGTGG CGACTCAGGC CTATAATCCC 1200
AGCACTTTGG GAGGCCAAGG CGGGCGGGGT GGATTACAAG GTGAGGAGAT CAAGACCATC 1260
CTGGCCAACA TGGTGGAAAT CCTGTCTCTA CTAAAAATAC AAATATTAGC CAGGTGTGGT 1320
GGTGGGCGCC TGTAATCCCA 1340
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