| Tag | Content |
|---|
EnhancerAtlas ID | HS136-02805 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr10:98140490-98141870 | 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 | | ZNF263 | MA0528.1 | chr10:98140790-98140811 | CCCACCTCTCTCCCTTCCTTC | - | 6.34 | | ZNF263 | MA0528.1 | chr10:98140794-98140815 | CCTCTCTCCCTTCCTTCCTCC | - | 6.95 | | Zfx | MA0146.2 | chr10:98140536-98140550 | GAGGCCGAGGCGGG | - | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGAGGCCAG GCGTGGTGGC TCATGTCTGT AATCCCAGCA CTTTGGGAGG CCGAGGCGGG 60
TGGATCACCT GAGGTCCGGA GTTCGAGACA CAAATTAGCC AGGCATGGTG GCAAGCACCT 120
GTAATCCCAG CTCCTCAGGA GGCTGAGGCA GGAGAATCGC TTGAAGCCAG GAGGCGGAGA 180
TTGCGGTGAG CGGAGATTGC GCCATTGCAC TCCAGCCTGG GCAACAAGAG CGACACTCTG 240
TCTCCAAAAA AAAAAAAAAA GAATGCAGAA GAGATGAAGC CGCCCAACAC CCAGCACTGA 300
CCCACCTCTC TCCCTTCCTT CCTCCAAGTC CTTCTGCAGA TGACTCACAG GTCCTCACCC 360
CTGCTCTGAT CCTCTTCCCT GTGCTCTAGT TTCCTATTGC AAATGTGGAG CTGCCCTGCC 420
TGTGAGGCTC TGCTACATCC TCCTCTGAGG TGGCTCCTGC CCCCTGCCCT GCTGCCCTGG 480
TCCTCCAGCC GCCTGGCCCT CCCAGCTCTA CACTGCCTGG CATGGCTTGG TCAGATGACA 540
AGTTTAGGCT TCCCCTGCTC AAGAACCTGC AAACAGTCCC CCTTCCTGTT TCATCGGGTC 600
CCTACTCTTC AGCCCAGCGT TTAAGGTCCC TCATGACCTG GCCTTCTCCA ACTTGGCCCA 660
TCTCGTGCCC TTGGCTTCCC AGCATGGGTC AGGGCTCCAT GCAGGCCCAT CTCATCTCTG 720
TCTCTGTGCT CTGTTGAGAA CTTAACCTGT GCTCACACTG CCTCCCCTAC TGGGGACCCT 780
GATTACTTTC TCTCTAATCA TCCTATCTCC ACCTCCATGT CTTCCATCCT TTAAAACCTG 840
GCTTAGACCA CCCCAAATCC TGCAAAAAGT CTTCACCCAC TGCTCCAGGC AACCATGGGC 900
TTCTCTTCTT CAAACATTAG CCCTTGTTGC ACCAGCCCAC CCCACAGTGC TCCAGGCTGG 960
GACTTAGCAG GGTGTGTATT CCTGGCTCCC TAGCTGGCAT GTAAGCTTGT CCAGGGTTGG 1020
GGTCATTTCC CTGGCAGCAG CTCTGAGCCT AGTAGTGTAC TGTGCCCACA GCAGACACTC 1080
AAAACAAAAA ACATGACTTG CTCAGTGAGA GACTGCCAAA AAAAAAATGC ATGGAGATGG 1140
AACTCTGGGT ATCTATAAAA TCAACAAATA ATTGGGTCAT TTCTATGCCA AGCATTAAGA 1200
CTATAAAGAT AACCAAAGTA CAGTTCCTGC TTGTAAACAG TTCACCCTCT AATATGACGT 1260
GACATGCAGG ACCTGCTACA CAGTTTGCAA GGCTCAGTGC AAGATTTGCA CTTTGTTGAA 1320
ACACTATTAT GAATTTCTTT CTTTTTTTTT TTGAGACGGC ATCTTGCTCT GTCACCCAAC 1380
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