Tag | Content |
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EnhancerAtlas ID | HS105-66811 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr5:167899310-167900370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ETV6 | MA0645.1 | chr5:167900245-167900255 | AGCGGAAGTG | + | 6.02 | SPIB | MA0081.2 | chr5:167900243-167900255 | GAAGCGGAAGTG | + | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 167899413 | 167899903 | chr5 | 167900241 | 167900341 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I168471 | chr5 | 167898355 | 167900278 |
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Enhancer Sequence | GTGCATGTGT CTTTTCCAGG ACCTTCAGGA AACAAAGCCG GGAAATGTGA AATGACCCCC 60 TCAAGCTCAC ATAAATAATA AATGGCTACA GCTAGGATGC TAATTCCATC TTTCAACTCC 120 AAAATCTCTA TTTTCTTTCA GCTCCAGCTT CTGTTTCACG GTGGCGTTAC CACAGCACAC 180 CACATGAGGC CCTAATTGTA GAGCCGTAGA ATCCTTGGTC TTGAAGAATG AAGTCACAAA 240 TTCCTGTGGT TTCTCTGCAC AGGGTGGGGA GAAAGGCAGG ATACTAGGAT ACTACTCTGA 300 AAAAAGACAG CAAACCTCAC TGGGTTTGGT CCTCCCACTC CTAAAGGCAA CGGTTGCCTT 360 TGAGTACAGA CCTTTTTGCA ATATGCACAT GTGCTTTCTG TATCTCAAGA AGGCTAATGA 420 CTAAGATTCT TCTAGTTAAC TATCCCCTTG CTAAGCAGTC TCCAGCCACG CTGGCCTTTC 480 TTTTTCTCCT TCCCTCCACC AGCACTTTGC AGTCCTAATT CCTTCTGCCT GGTGCACTCT 540 TCCTCCATGT CTTCACATCG ACTTCACATA GCCAGCTTCT TCTCACCCTT CAGGTCTCAG 600 CTGGAGCCTC ACCCCTCAAG ATCCCTCTCC ACCCTGGAGC ATAAGTTCTT AAAGCAGGGA 660 CCTCATTTGC CTTGTTTTTG TTAGGTCTGA TGTAGAGTGG GTTCTTAATA TTTGTGAAAT 720 GAATTGAATG AATGGATGTG ATGAAAAATC TGCCTCAAAG GTGTATTTAG TCTCTACATC 780 TTTGTCATTC TAATCAGGAA GCCGGAAAGG CTCTGTGTAG AACAGAAGTA CTAAAAGCTG 840 GTTTTGTCAG GTGCCAGGGT GCAGACCCCC CTCCCATCCA GCTCAGGACA TCACCCCCTG 900 CCCCCAAACA CACTTGTGAC TCCACAGCAT AAAGAAGCGG AAGTGATTGG GAGCTAACAC 960 ACACATAATG TTTAAATTCG CTGAAGAGCC AGGCATGGTG GCAGTGAGCC GGGATCACGC 1020 CACTGCACTC CAGCCTGAGC AACAGAGTAA GACTCCATCT 1060
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