Tag | Content |
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EnhancerAtlas ID | HS062-14028 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr6:37758630-37760110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr6:37759279-37759290 | GGATGACTCAT | + | 6.62 | JUNB | MA0490.1 | chr6:37759279-37759290 | GGATGACTCAT | + | 6.62 |
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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 |
GH06I037791 | chr6 | 37758778 | 37759775 |
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Enhancer Sequence | TTAGGGACTA TGACAATGCT TTGTGTCTTT ATACCTCTAG TATCCCCCAT AATGCCTGGC 60 ATACAGGGGC CACTCAATAC ATGCTTATTG AAGGTTTGAA TGGATAAGTG AACAAATAGA 120 TCCAGAAATT CACACTAAGA TTGCTTTCAA GCCTTGATTT AGACTGGCTA CCAAGTGGGA 180 TTTATTGGGA TGGAGAAACC AGCTTGGGGA CAATGGGGTT GCTGGGTATC AGTAATGAAT 240 GATCCGCTGA CAGGCTCTCA CCTCAGCCAG GAGGGTTTGG GCCCAGTAGA CAATCAGGTT 300 GAGTTAGAGA GTACATGTCA GGGAGCAGGG AGAAAGGGGC TGCTGGAAAG AGAAAGAGGA 360 CTTGGGAGCA GGTGCCTAAG GGAGGGTAGG GGAACCATTT GGTCAAGGAA TGGAAGTCTC 420 GCTGGGACTA TCAAATGTAG AGGCTCTGGG GGCTGGGCAT AGTGGCTGGA TCAAGAGGTC 480 AGCCAGGGCA CCTGGGAGAT AACACTGCCA TCCCTGTTCT CCTGTAGACC CAGGGGCTGG 540 ACAAGCAAGT TTGCAAAGAA TATGCAGCAG CCAGGCAGGG GAGCCACTCT GGGATTCCTG 600 CCCCCGCCTC CAGAAGGCGG GGTTTGTTCT CCAGCTCATT CATTCTTTGG GATGACTCAT 660 TACTGAGTTG TCATGTTGTC ATCGAGTGCA GAGTTACAGG GAGGAGGGGC AGCCTGTCTC 720 GCCCATCTGT GCACAGGCAG TCCTGGCAGC ACTGCAACTG GAGAGTTCCC AGGCTGGCCA 780 CATGGGGGCG GGGGGAGCCA GGCCTGACAT CCTGGCCATC TGGGCGACTC CAGTTCTGGG 840 AAGAGCACTG GACTGGGAGT CAGGGGCCTG ACTTCCTGGG CCTCCTACAC CCTGGCCACC 900 CTCTGTGCCT CAGCTAATTC CAAAACAGAA ATGATGATAC CTCTCCTGCC TAAAACCAGG 960 ACGTCTCATC CCTCATTTGT GTTTATACCT TAATTTGTGT GTCAGAGAAA TCTCCCTGGT 1020 AGTTAGCCAT ACTCCAGTTT TGTTCGCCCG GAGGACTTAG GGCAACTAGT TTTCTTGAGA 1080 TTACATCTTG CAGATCCATC CCAGGTGCAG ATAGGGGATG AGAGAACACT GCGGTGCCAG 1140 GCAGGCCCTG TGCGAAATGT TTCGCTCTCA CCAACCCTGT AGCCCTCACA ATCACCTTTT 1200 AGGATGGACT TGAGAATGAG GGGCATCTTT TCTGTTTGTT AACTTTTTTT TTTTTTTTTT 1260 TTTTGAGATG GAGTTTCACT CTTGTCGCCC AGGCTGGGGT GCAATGGCGT GATCTCAGCT 1320 CACTGCAACC TCCACCTCCC AGGTTCAAGT GATTCTTCTG TTTCAGCCTC CCAAGTAGCT 1380 GGAATTACAG GCATCTGCCA CCACATATGG CTATTTCTTT TTTTTTTTTT TTTTTTTTTT 1440 TTGTATTTTT AGTAGAGATG GGGTTTCACC ATGTTGGCCA 1480
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