| Tag | Content |
|---|
EnhancerAtlas ID | HS017-04628 | Organism | Homo sapiens | Tissue/cell | CD14+_monocyte | Coordinate | chr10:98140610-98142030 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr10:98140794-98140812 | CCTCTCTCCCTTCCTTCC | - | 6.73 | | IRF1 | MA0050.2 | chr10:98141821-98141842 | AATTTCTTTCTTTTTTTTTTT | + | 6.04 | | Nr2f6(var.2) | MA0728.1 | chr10:98142006-98142021 | CGATCTCTTGACCTC | - | 6 | | ZNF263 | MA0528.1 | chr10:98140790-98140811 | CCCACCTCTCTCCCTTCCTTC | - | 6.34 | | ZNF263 | MA0528.1 | chr10:98140794-98140815 | CCTCTCTCCCTTCCTTCCTCC | - | 6.95 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTAATCCCAG CTCCTCAGGA GGCTGAGGCA GGAGAATCGC TTGAAGCCAG GAGGCGGAGA 60
TTGCGGTGAG CGGAGATTGC GCCATTGCAC TCCAGCCTGG GCAACAAGAG CGACACTCTG 120
TCTCCAAAAA AAAAAAAAAA GAATGCAGAA GAGATGAAGC CGCCCAACAC CCAGCACTGA 180
CCCACCTCTC TCCCTTCCTT CCTCCAAGTC CTTCTGCAGA TGACTCACAG GTCCTCACCC 240
CTGCTCTGAT CCTCTTCCCT GTGCTCTAGT TTCCTATTGC AAATGTGGAG CTGCCCTGCC 300
TGTGAGGCTC TGCTACATCC TCCTCTGAGG TGGCTCCTGC CCCCTGCCCT GCTGCCCTGG 360
TCCTCCAGCC GCCTGGCCCT CCCAGCTCTA CACTGCCTGG CATGGCTTGG TCAGATGACA 420
AGTTTAGGCT TCCCCTGCTC AAGAACCTGC AAACAGTCCC CCTTCCTGTT TCATCGGGTC 480
CCTACTCTTC AGCCCAGCGT TTAAGGTCCC TCATGACCTG GCCTTCTCCA ACTTGGCCCA 540
TCTCGTGCCC TTGGCTTCCC AGCATGGGTC AGGGCTCCAT GCAGGCCCAT CTCATCTCTG 600
TCTCTGTGCT CTGTTGAGAA CTTAACCTGT GCTCACACTG CCTCCCCTAC TGGGGACCCT 660
GATTACTTTC TCTCTAATCA TCCTATCTCC ACCTCCATGT CTTCCATCCT TTAAAACCTG 720
GCTTAGACCA CCCCAAATCC TGCAAAAAGT CTTCACCCAC TGCTCCAGGC AACCATGGGC 780
TTCTCTTCTT CAAACATTAG CCCTTGTTGC ACCAGCCCAC CCCACAGTGC TCCAGGCTGG 840
GACTTAGCAG GGTGTGTATT CCTGGCTCCC TAGCTGGCAT GTAAGCTTGT CCAGGGTTGG 900
GGTCATTTCC CTGGCAGCAG CTCTGAGCCT AGTAGTGTAC TGTGCCCACA GCAGACACTC 960
AAAACAAAAA ACATGACTTG CTCAGTGAGA GACTGCCAAA AAAAAAATGC ATGGAGATGG 1020
AACTCTGGGT ATCTATAAAA TCAACAAATA ATTGGGTCAT TTCTATGCCA AGCATTAAGA 1080
CTATAAAGAT AACCAAAGTA CAGTTCCTGC TTGTAAACAG TTCACCCTCT AATATGACGT 1140
GACATGCAGG ACCTGCTACA CAGTTTGCAA GGCTCAGTGC AAGATTTGCA CTTTGTTGAA 1200
ACACTATTAT GAATTTCTTT CTTTTTTTTT TTGAGACGGC ATCTTGCTCT GTCACCCAAC 1260
CTCTGCCTCC CTGGCTCAAG CGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTACA 1320
CATGCGCCAG CGCGCCCAGC TTATTTTTTG CATTTTTAGT AGAGACGGGG TTTCACCACG 1380
TTGGGCAGGA TGGTCTCGAT CTCTTGACCT CGTGATCCAC 1420
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