Tag | Content |
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EnhancerAtlas ID | HS094-38326 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr7:56158800-56160520 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:56160184-56160199 | TGAACTCCTGACCTC | - | 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 | GAAGGCTGAG GCAGGAGGAT CACTTGAACC CAGGAGGTGG GGTTGCAGTG AGCTGAGAGT 60 GCACCAGTGC ACTCCAGCCT AGGTGACGGA GTGAGTGAGA CTCTGTCTCA AAAAATAAGA 120 CAAAACAGGC TGGGCGCAGT GGCTCATGCC TGTAATCCCA GCACTTTGGG AGGCCGAGGC 180 AGGAGGATCA CGAGGTCAGG AGATCGAGAC CATCCTGGCT AACACGGTGA AACCCTGTTT 240 CTACTAAAAA ATACAAAAAA TTAGCCGGGC GTGGTGGCAG GCACCTGTAG TCCCAGCTAC 300 TCAGGAGGCT GAGGCAGGAG AATGGTGTGA ACCCGGGAGG TGGAGCTTGC AGTGAGCTGA 360 GATCATGCCA CTGCACTCCA GCCTGGGCAA CAGAGTGAGA CTCCATCTCA AAAAAAAAAA 420 GACAAAACAA AACAAAATCA GATGCAGGAT TTGAGGAATG CAGAAAACCA ACAGGGAAAA 480 GGGCAGATAG AAAATAGGCC CAACCTGCCA CTCAGCAGTG CCAAAGCTGC CTCCAACCCC 540 CTTTCCCCCA CTGCTTCTGG GCCTAAGAAG GCCTGGTCTC ACAAAGGAGC CAATTTGCTG 600 ACCAGCCAAC AGCAGCTCTG GCTGCCTCCG GGATTGGGCA GGCTGTTCCA GGAATCCTGG 660 TGGCCCCACT ACTGGGTGCC TGGTTACCAG AAGAAGGTTT AGAATAACAA GTCCCCTCTG 720 CTGGTGCCAG GCCCCTGGGC TGCTCACACA CAGGCCTTCT CTGCCTGCCC CATCAGCAAC 780 TTGGCGGAGC CCGGGACTGT CTGTTTCCCA TAAAAACAAG CCCATTTGCT GGTAAGTCCT 840 AAGTCCTCAC AATGGGCACC TTTGCCTCAT CACCTCCCAA AGCTGGGTAG CGCTAGCTCT 900 CTCCTCTCCC CCAGCCCTCC ATGAGCAGAA AGTACACTTG GACCCCCATA TGAGATGCCA 960 GCCTAGGCGC AAGCCTCCAG TCCTTGGCAC AGCCAGCTTG GCCAACTTGT GGCTGCACTC 1020 ACCTTTCCTG GGGGGCTGAG GAGGCGGTTA TCTTGCCCCA GCCCCAGCTC TGACTGGGGC 1080 CAACTTTGTG CCTCTGTCTA CTGCCCCACC CACCCCTCAC ACCTTTCCCA AGACCCCTGT 1140 GGACAGGGTC ACCACATGGG AGTAGGTGGC CCAGTCCTTT TTTTAGACAG AATCTCGCTC 1200 TGTCGCCCAG GCTGGAGTGC AGTGGTGAGA TCTCAGCTCA CTGCAACTTC TGCTTTCCGG 1260 GTTCAAGCGA TTCTCTTGCC TCAGCCTCCT GAGTAGCTAG GACTACAGGC ACGAGCCATC 1320 ATACCCAGCT AATTTTTGTA TTTTTAGTAG ATATGGGGTT TCACCATGTT GGCCAGGCTG 1380 GTCTTGAACT CCTGACCTCA AGTGACCCTC CCACCTTGGC CTCCCAAAGT GCTGGGATTA 1440 TAGGCATGAG CCATCGCGCC TGCCTGGCCT GGTACTTTTT GGCACATAAC TTCCCTCCCC 1500 TGAACTCTGA GTCCAAAAAC CAGATCAGTC CCGGGGACCT CTTTTCTGTA GAAAATTCCT 1560 GCAGATGGAG GTTTCAAGGG TCAATGCTGC CACTCTCCCT GGTCCATCCG CCTTCAGAAA 1620 AGAGACATGG ATGGAATGGA TGTGGGGGTT TCTATCTTCT CCACCCCCAG TCCTCCCCGC 1680 TCCCTGCCTA TCACCTGGCT TTTGTCCATC ACTGGGCTAG 1720
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