Tag | Content |
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EnhancerAtlas ID | HS016-00011 |
Organism | Homo sapiens |
Tissue/cell | CD14+ |
Coordinate | chr1:25466410-25467780 |
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 | AGGTCTCACT ATGTTGCCCA GGCTAGTCTT GAACTCCTGG GCTCAAGCGA TCGTCCCACC 60 TCAGCCTCCC AGAGTGTTGG GATTACAGGC ATGAGCCACC GTGCCTGACC AAGATCTTTA 120 AATAGTAATA AAACAGACAT TTATTAAGTG CATCTCATGT GCTGTGCGCT GTTCCAAGTG 180 CCTACACTCC CCATCTCAGT TAAGCACACA CCACCCCACG GGCAGGCAGC TGCTATCATT 240 ATCCCTTTCT CATGGTGGGG AAGTGAAGAT CAGAAAGGCT GAATAACTTG CTCAAGATCA 300 CAAGTCTGGA CTTGACTGCA GGCCTGGCTG ATCCCAGAGC CCAGATCAAG AGTCTCCCCT 360 GGTGCCTCTC CCCTAAAACC ACCTCAGAAA CCCCCTGGTG TGTAACTCTA AACCATGCCT 420 GCGGCAAACT CAGCCCATTT CCTCTTCTCG CATCTTAAGC CCAGATGGGG TCTGAGTGAC 480 ACTTATCTCA TACCCTGTCA TAGAGCTGGA GCCCCACAGG AATGTGGAAC TCCCCATGGA 540 CAGAGGGCAG GAGGAAGTGA CCGCCGGCCC GAAGGGGGCT TGGTCCACTG GGTCCAAAGG 600 TGCCGTCTGG CCCTGGCTGC CACATGCCTC GTGTCCACAA AGCAGAAGTC ACAGGGACAG 660 GGAAGGAAGC CCGGCAGGCA GACTGTCATC ACAGGTGGTG TGTCCTCCTA TCCAGGGACA 720 AGCAGAACTA GCCAAGATTG CCTTCTCCAC GCAGCCTCTC CTGATTCCAC ACTTGTGACT 780 TCATGTTCCC AGAGCGCTGT GCTGGCACGT GTGCTATGAT CTTGACTCTG TATGCACCCC 840 GACGCCCAGC TACAAGCAGC TCTACCCTTA CCTAACCTTT AAATTGCTCG ATTGCCTCAT 900 CTGTAAAAAC AGGGATGTTA ATAGCACCTG TTTCACGGGG TTATTGGAAG GTGTGTGTAC 960 ATACACACAC ACACACACAC TCATCAATAT AGATGAGTAT AGATTGTGTG TATGTATACA 1020 TGCTTAGAAC AATTCCTGGC ATATAGTAAG TGCTTAATGA ACATTACCTA TTCTTATTCA 1080 TGTTAAGTGG CTATGACAAT GTGCCAGGGA AGGACATCAC TTGTAATGAC GGGGGATAAC 1140 ACCTCTTACA AAATCAAGTT GAGGTTCCCC AAAACTGGTC TGTGAAACAG CCTCCAGGGG 1200 GCTGTTTGTT AAAGAGACAG ATTCTGTGGT CCCACTCCTA GATCTAATGA TTTTAAGTCT 1260 CTGAGATGGA GCCCAAGAAT TAATATTCTT ACAACCTGTC CAGGTGATTA GAACAATCAG 1320 CCAGGGGCTG GGCACGGTGG CTCACGCCTG TAATCCCAGC ACTTTGGGAG 1370
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