Tag | Content |
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EnhancerAtlas ID | HS197-19268 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr7:23293930-23295320 |
Target genes | Number: 13 | Name | Ensembl ID |
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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) |
MEF2A | MA0052.3 | chr7:23295216-23295228 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr7:23295216-23295228 | TCTATTTTTAGT | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr7:23294573-23294588 | GAGGTCAGGAGTTCA | + | 6.22 |
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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 | GGTAAGAACA CAGTATTCTC CTAAACTACT GGAGACCCAG TTTCTAAACC TTAATGATCA 60 CAGGTGCTTC TGTAAGTGCC AGATGCTGAT CTCATCCCTT GCCACTGCAC TCCATGAGCT 120 GGATGACAGA GACAGTGAGT GTGTGGTCCT ACCCAGTGCC TTCATCAACA TCAACGTCAG 180 CCAGACCTAC TGCAGCAAAC CAGTGGCTCT CCCTTGCTTG GAGCCCTCTT CAAAAGCCAC 240 ATCACCACCT CCTGCTTTTC CTTAGTGTCC AGTTGACTGG ACAGAGAATA CCTTGCTGAG 300 TCTCAGATTT TGCTTTTATT ACTTGGAACT CTTTTGGCTA CTCAAAGAAT AGCCAATTTG 360 ACAGATGTTT GCTGATCAGT CTAATTTAGG CTGACAAGGA TTTCTCAAGC AAATGCTGTG 420 TAGCTGGCGC AAATGCTAAA ATGTGTATAT TTTGGTTTTG CTTTGCTCTT AGTGAAAGAA 480 ATAAGCTCTC TATCTATGTT AAAGAGGACC AAAGGTGCAA ATACATCAAG GGAAATTATC 540 TTGTCAGAAT GGTACATGCT CAAAAAACGG AGTTAATGGC CGGATACCAT GGCTCATGCC 600 TGTAATCCCA GCACTTTGAG AGGCCGAGGC AGGTGTATCA CCTGAGGTCA GGAGTTCAAG 660 ACCATTCTGG CCAACATGGT GAAACCCCAT CTCTACTAAA AATATAAAAA TTAGCCAGGC 720 GTGGTGAGAT GGAGTCTTGC CTTGTCACCC AGGCTGGAGT GCAATGGCGC GATCTTGGTT 780 CACTGCAGTC TTTGCCTCCC GGGTTCAAAT GATTCTCCTG CCTCAGCCTC CCAAGTAGCT 840 GGGATTACAG GCACCCACCA CCATGCTCAG CTAATTTTTG TATTTTTAGT ACAGACGGGG 900 TTTCCCCATG TTGGCCAGGT TGGTCTCAAA CATTTGACCT CGTGGTCCGC CCGCCTCGGT 960 CTCCCAAAGC GCCGGGATTA CAGGCGTGAG CCACCGCGCC CAGTCAGCAT TTGTCTTTCT 1020 ATGCCTAGCT TATTGCACTT AACATCATGG CCTCCAGTTC CATCCATGTT GCTGCAAACG 1080 ATGGGATTTA ATTCTTTTTA TGACTGAGTA ATATTCCATC ACATTTTCTT TATCCATTTA 1140 TCTATTGATG GATACTTAAT TTGGTTCCAT ATCCTGACTA TTGTGAATAC TGCTGCAACA 1200 CAGGAATACA TACATCTCTT TGATGGATTG ATTTCCTTTC TTTTGTATAT ATTCCCAGCA 1260 GTGAGATTGC TGGCTCATAT GGTAGCTCTA TTTTTAGTTT TTTGAGGAAC CTCCATACTG 1320 TTTTCCATAG TGGTTGTACT AATTTACATT CCCACCAACA GTGATATACT GTTGGTGATT 1380 TGTATGACTT 1390
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