Tag | Content |
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EnhancerAtlas ID | HS094-20908 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr2:69525200-69526480 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr2:69525591-69525602 | ATGTAAACAAA | + | 6.14 | RUNX1 | MA0002.2 | chr2:69525599-69525610 | AAACCACAGAG | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 69525331 | 69525996 | chr2 | 69526102 | 69526289 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I069297 | chr2 | 69524848 | 69527647 |
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Enhancer Sequence | TGCAGGCAGA GCATAAGGCC CACACGAGGG CAATGAAGAT CCCTATGAGG CAAGATGGAA 60 CCAGGAACCA GATTGCGTGC CACAGACATT GCCTGCTCGC GAACTTCAGA AGAGAAAGGG 120 AAGAGCCAGG AAGGTTCACG AAGGGGCACC TGCAAGGATG GATGGGCTGG TAGGATGGGG 180 TTTTCAGATG GGGAACAGCA CATGCAAAGA CACAGAAGTG TGATTTGTCA TGTGCGTCTG 240 CAGGAAAGAC ACTGTCCCCA CGGACATGGA CGTTTGCTCA TGGCATTGGT TAGGACTTAT 300 TTTGACTGAT GATTCACTTT GAAATCAGCC CTGCCAGGGC TCCATGTGGC TTAGGAGCCT 360 GGATAGGGTA AGTCATCTTC CTTGCCCAGC CATGTAAACA AACCACAGAG CAAGGCCAAA 420 CCACCAGGGC GAGTCAGAGC AAGGAGAGGG AAGGCAGCCC TAAGAACCAC TGCGCTTTTC 480 TTCTTCAGAG GCCAAGGAGA AACCCTGGCC CTTCACACAC ATGCGCAACC TCACCATCTG 540 TGTCTGAAAA TGCTGAAATC AACACAAGTG GGAAAGACAG CTACCGGGAA AGGCAGGGGG 600 AACTGCATGG ACCTGTGTCT GCTTATTTCT CCACCTCCTA ACCTCTGATT GACCAAAGTT 660 CCCTGCAAGA CAAAATATCC AAAGCCAAAA GAGAACTCAG TGGCTATTTA GCAAGTATGG 720 TGAGATGCTT TTAAAATGAC TCCCAATAAC CCCCAGCTCC TGGTATTTGT GCCCTGGTTA 780 GTCTCCTCCC CTTGCATGGG GGCTAGACCT ACGGAGCTGC TTCTAATTAA GAGAATACAG 840 CAAAATCATG CTTGGGGTAT AAAAGACTGA CCACCCTCCT GCTCACACTC TCTCTGGCCC 900 CTCCAGTGTG CTCACTCTGG CTGCTACTGT GAGCTACCCT ACAGAGAGGC CCCCATGGCA 960 AGGAACTGAG GTGGCCTCTG GCCAACAGCC AGCGATGAGC TGATTCTCAC CAACACTCAG 1020 CGAGTGCACT TGGAGGAGGA TCCTACCCTG GAGAGCCTTG AGATGACTGC AGCCCCAGCT 1080 GAGGCTTTAA TCGCAGATTG TGAGACCCTG AGCCAGAGAA CCCTGTCAAG CCATTCTGTA 1140 TTCCTAACCC ACAGAAACTA TGAGATAATA AATGTTATTT TGAACCACTA AGTTTCAGGG 1200 GAATCTGTTA TGCAGCAGGA GATAACAAAT ACCTTTCAAT CAGGCTTTCG GGTCTAATAA 1260 ACAAGATCGT GTGTGTGCCT 1280
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