Tag | Content |
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EnhancerAtlas ID | HS182-20078 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:99677660-99679250 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gabpa | MA0062.2 | chr7:99678659-99678670 | CCCACTTCCGG | - | 6.02 |
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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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Enhancer Sequence | GGAAAAAAAA GAGAATACTT ATTATATGCT AATAAATACC AATTAAGACC ACCACCACAA 60 CTAGTATTTG CGTTGCACCC GTGGAGAGAT GAAAGGGAAT GGTAGGTTCT CAGGTCCACC 120 TCCACCCAGG GTAAGAAAGT TCTAACGTTC TGTCAGCTAA CTTGCTAGAC ACTGTGCTCC 180 GAACTACTTC AGCAGGGGAT CCACATTGCA CAGCTGAGCC ATTAGAAGTC TTCAGGTGAT 240 TCGCTGAAAA TCTATCTCCT TGGACCTTCA CCGCACAGAG ACCTAGTGCA TCACAGAAAT 300 TCAATGACTG GCGACCTGCA GTGGCTCACG CCTGTAACCC CAGCACTTTA GGAGGCTGAG 360 GTGGGAGGAT TACTTGAGCC CAGGAGTTCC AGGCTATGGT GAGCCATGAT GGCACCACGG 420 CACTCCAGCC GGGGGCAACA GAGCAAGACC TTAATACACA CACAAACATT TTAAAAGGAA 480 AAAAAAAAAA AAGGCCGGGC GCGGTGGCTA ACGCCTGTAA TCCCAACACT TTGGGAGGCC 540 AAGGCAGGTG GATCACTTGA GGCCAGGAGT TGCAGACCAG CCTGGCCAAA AGGGCGGAAC 600 CCCGTCTCTA CTAAAAATAC AAAAAATTCG CCGGAGGTGG TGGCGGGCGC CTGTAGTCCC 660 AACCACTCGG GAGGCTGAAG CAGGAGAAGC GCTTGAACCG GGAGGCGGAG GTTGCAGTGA 720 GCCGAGATCG CGCCACTGCA CTCCAGAGAC AGTCTCAAAA ATAAATAAAA ATTAATTTTT 780 TTAAAAAAAG AGCTTCAATA ACAGAATCTT CTCCTTCCAC CCGACTGTCC ATCAAACACG 840 TATAATCAAA TGATGCCCAC TCTCCACAGA TGTCTTTTCT GGAGAAAATA ATACGCTCGT 900 TCCTCTAATT AGCCCATCGG TTTCAGGTTC ATCACTCTGC TATCTTCTCC TGGAGTTTAC 960 AAAAGCCCTT CAGAGTGTAA ACACCGATGT GGATTCAATC CCACTTCCGG AGAGAGGATC 1020 AAACCAGGAA TCTAATACAA CTGAAAACGG AGCCTGAGCC AGGTGTATCA CGCGATGCAC 1080 TGGGCTCCAG CAGGATTACC CCTGGAATCG GCGTCTGCAC CCACTCCCAG CCCTCGTGCT 1140 AACTGCGTAC GCTTAGCAGA ATTTCTCTGA TCCTTGGACC CAGCTGCGTA AAAATAAACT 1200 TCCTCTCCTG CCACGGGCGC GAATAACTGT GTTAACATCA AATAAAAACG TCTGGGAGAA 1260 ATACCAAGTT AGGGTCGCTG TCATTAGCTG CTTTCAAGAG AGAGGCGCCC CTACCGCTCT 1320 GCTGAAACTT TTAAACGCTC CAGCTGGGTC GCCGTTAAAG TCACAAAACC AGAACCGGAG 1380 CCCCATTACT AACCCCTACG CAGGATCCCG CTAGGCTAGG GGGATCCCTG GGGAAGCGGA 1440 GTAGAGGACG GGCTGCAGGG GACGGAGGGG CGCCTCCCCG AACCCTGCTC CGGGCCGGCC 1500 GGGGGACCCT GCGGGCCGCA GTGGCACAGA CACCACCCCC TTCCCCGGCG ACCACAGCCT 1560 CCGTCTCACC GCGAGACCCG GGGACGCGTG 1590
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