Tag | Content |
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EnhancerAtlas ID | HS094-25919 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr22:42378750-42380080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr22:42379934-42379944 | ACTTGGCACC | - | 6.02 | POU4F2 | MA0683.1 | chr22:42379945-42379961 | AAGAATAATTAATGAA | + | 6.81 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 42379304 | 42379957 | chr22 | 42379600 | 42379858 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I041983 | chr22 | 42379621 | 42379770 |
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Enhancer Sequence | TGGGCATGAT GGCACATGCT TGTAATCCCA GCTACTCTGG AGGCTGAGGC AGGAGAATCA 60 CTTGAACCTG GGAGGTGGAG GTTGCAGTGA GCTGAGACTG CACCATTGGA CCCCAGCCTG 120 GGCAACAAGA GTGAAACTCC ATCTCAAAAA AAAAAGAAGA AAAAAAAAAG AGTAGGAAGG 180 GACCTTTGCC CCGTCTCAGT GAGATGTCCA GTCAGTGCTG AAAAAGGAAT CTGGCGTCAT 240 CCTTCTGTCC TCTTCCTCCT TCATCCCCCA ATCAGTCATC CAGTCCTGTC CATTTTACCT 300 CATACGTATC TCTTACGTCT GCCCACTTCT CTCCTCTCTC TTGCTGCCAC CCTATACTGA 360 CTTTCTCTCA CCTGGCTTGC CGTGGCCACC TGACTCTGTG CTGTCAAAGT GCTGACCTGC 420 AGCAAGATAA GCTCAGCTGG GGCTTGGGCC AGAGTATAAA TCATCTGGAA AATCTTGCTA 480 TAAAAAACCT CCACTGAGCT AAACAGTGTG CTCAGTGACA AGGTAGATTT CTCTCCTGAG 540 GCAGACTTCT TATCTCAAGA ACCAGTAGCA AATGGGTCAG GGACCCTGGT AGCTGGGCCC 600 CTATGGGCCA CACTCGGAGT GGCACCAACC CTCCTAGCTC TCTGTCTCCT TTCCTCTCCA 660 ATCCCTTGTC CACCAGTGAC CAAATAATCT TCCCACCTTG CAAAACTTAT CGAGTCACCC 720 AACTTACTTA AAACTCTGTA ACAAACTCTC CTTTAACCTC AGGGTAAGTT TAAACTCGTA 780 GACTGTCCTG ATTGTACCTC TTCAGCTCAT CTCTGACCAC TTCCCATCTA GCATTGTACT 840 CCTCACTCAG AAGAGGCAGT GCTCGTCCAC ATGCCATGCT CTCTCCTACC CTAGAGCTTT 900 TGCATCTGCT GTTCCCTCTG GCTAGAACTC ATGACTCTTT TGAAATCAAC CTTCCGGTTT 960 CAGCTTAGTT GCATTTCTCC AGAAGTCTTC CTTAGTCCCA GAGAGACTGG GTTGGATTCC 1020 CTTGGCAATG CTGTTTCAAT ACCCTGTGGC TATTCTCTTT CACAGTGGTT ATTGCAACAT 1080 ACTATAATTG TCTGCTTATG TTTTGGTCAC TCTCACACTA AGCAGCTCCT TGAGGGTAAG 1140 GATCATGTTT TGTTCACGAT AGTACCTCCA AATTTTAGGA CAACACTTGG CACCTAAGAA 1200 TAATTAATGA ATGAATGCTC TTAGAAAACA TCTCAGAGCA AGCATGGCAA ATCCAACACC 1260 CGTGAGCCAC TTCTCTCCCC AGTGGTGTGC ATGGCAGACT GCTAGTCAGT CATGGCACGT 1320 GTTCAGTGCT 1330
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