Tag | Content |
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EnhancerAtlas ID | HS017-00511 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr1:25466310-25467740 |
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) |
EWSR1-FLI1 | MA0149.1 | chr1:25467070-25467088 | GGAAGGAAGCCCGGCAGG | + | 6.35 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I025140 | chr1 | 25466725 | 25467101 |
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Enhancer Sequence | GCCTGGACTT AAGCGATCCT CCCACCTCAG CCTCCTGAGA AGCTAGGACC AGAGCCATCC 60 ACCCATGCCA AGCTAATTTT TAAATTTTTT TGCAGAAACG AGGTCTCACT ATGTTGCCCA 120 GGCTAGTCTT GAACTCCTGG GCTCAAGCGA TCGTCCCACC TCAGCCTCCC AGAGTGTTGG 180 GATTACAGGC ATGAGCCACC GTGCCTGACC AAGATCTTTA AATAGTAATA AAACAGACAT 240 TTATTAAGTG CATCTCATGT GCTGTGCGCT GTTCCAAGTG CCTACACTCC CCATCTCAGT 300 TAAGCACACA CCACCCCACG GGCAGGCAGC TGCTATCATT ATCCCTTTCT CATGGTGGGG 360 AAGTGAAGAT CAGAAAGGCT GAATAACTTG CTCAAGATCA CAAGTCTGGA CTTGACTGCA 420 GGCCTGGCTG ATCCCAGAGC CCAGATCAAG AGTCTCCCCT GGTGCCTCTC CCCTAAAACC 480 ACCTCAGAAA CCCCCTGGTG TGTAACTCTA AACCATGCCT GCGGCAAACT CAGCCCATTT 540 CCTCTTCTCG CATCTTAAGC CCAGATGGGG TCTGAGTGAC ACTTATCTCA TACCCTGTCA 600 TAGAGCTGGA GCCCCACAGG AATGTGGAAC TCCCCATGGA CAGAGGGCAG GAGGAAGTGA 660 CCGCCGGCCC GAAGGGGGCT TGGTCCACTG GGTCCAAAGG TGCCGTCTGG CCCTGGCTGC 720 CACATGCCTC GTGTCCACAA AGCAGAAGTC ACAGGGACAG GGAAGGAAGC CCGGCAGGCA 780 GACTGTCATC ACAGGTGGTG TGTCCTCCTA TCCAGGGACA AGCAGAACTA GCCAAGATTG 840 CCTTCTCCAC GCAGCCTCTC CTGATTCCAC ACTTGTGACT TCATGTTCCC AGAGCGCTGT 900 GCTGGCACGT GTGCTATGAT CTTGACTCTG TATGCACCCC GACGCCCAGC TACAAGCAGC 960 TCTACCCTTA CCTAACCTTT AAATTGCTCG ATTGCCTCAT CTGTAAAAAC AGGGATGTTA 1020 ATAGCACCTG TTTCACGGGG TTATTGGAAG GTGTGTGTAC ATACACACAC ACACACACAC 1080 TCATCAATAT AGATGAGTAT AGATTGTGTG TATGTATACA TGCTTAGAAC AATTCCTGGC 1140 ATATAGTAAG TGCTTAATGA ACATTACCTA TTCTTATTCA TGTTAAGTGG CTATGACAAT 1200 GTGCCAGGGA AGGACATCAC TTGTAATGAC GGGGGATAAC ACCTCTTACA AAATCAAGTT 1260 GAGGTTCCCC AAAACTGGTC TGTGAAACAG CCTCCAGGGG GCTGTTTGTT AAAGAGACAG 1320 ATTCTGTGGT CCCACTCCTA GATCTAATGA TTTTAAGTCT CTGAGATGGA GCCCAAGAAT 1380 TAATATTCTT ACAACCTGTC CAGGTGATTA GAACAATCAG CCAGGGGCTG 1430
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