Tag | Content |
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EnhancerAtlas ID | HS139-28084 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:25328180-25329310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr2:25328598-25328608 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr2:25328598-25328608 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr2:25328598-25328608 | AATGGAAAAT | - | 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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| Number: 1 | ID | Chromosome | Start | End |
GH02I025105 | chr2 | 25328288 | 25329350 |
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Enhancer Sequence | CTGGCTAATA TTTGTTTTTA GAAGAGACGG GGTTTCACCA TGTTGTCCAG GCTGGTCTTA 60 AACTCCTGGG CTCAAGTGAT TCACCCGCCT CAGCCTCCCA AAGTGCTGGA ATTACAGGCG 120 TGAGCCACCA CGCCCAGCCC TCAATCTGAA TTTTTATGGC ATGGGTCAGA GCTGCTTTCC 180 TGTTCTACAT AAGTTGATTT AACCAGAAGA GAGTCTTCCA ACTTTCCTTC CAAGGACCAA 240 GAGTAGCAAC CTATACAGAT TCCCTTCTCT TTCCTCTCCC TGGGAGCCAG CTGCCTTTGA 300 CACATTACAC ATATACTAAC TGAGGGGAAA GTCCTTTGTC AAGTTGCTCT GGCAACAGCT 360 TCAGATACTG TTTTAGTTGT CCTGTTTAAG AGAACTACAG CCTAGAAGAG AACATCTGAA 420 TGGAAAATGA ACCAGCCACC ATGCATCCCT GGGGGCCACT GGAAGCAGGT GGCCACCACC 480 TCTAGCTTCC CCCACAGGAA ATCCTAGCCC AGGGTAGGTG TTCTGTCAGC TACAGCATGA 540 AAAATTCAGT GTCCTGCAGA TTCCCCATCG CAGTGAATCA TCGCATCAGC CAGAGAGCAA 600 GCTGACTAAT GATTGCTATG CTGCAGACAA TGAAGATGAT ATAAGGACAA GCTATTGTCA 660 GTGAGTTAAG TCAAATATTT GCAGTAGCTC CAGAGTGCAG CTTGGAAGGC AGCCTTTTCT 720 CTTGCTGTCC CTGTCTGATG CTCTTTCCAG CTCTCTGTGC CCAGACCTTC TTGAGCCTTC 780 CTGAGAAGAG TGTCCTTTTG CTCCTCATCG TTTTAGACCT GCTAGCATGC TAGTGCATGA 840 CATTATCTTA GAGTCTAGCC CGGGAGTTCC AAACAGGTCT TCACAGGGAT TCAGGGCTTT 900 GTGAGGGGAA AGGGGGCCTA GGAGAGGAGG AATAGAAGTC TCTAGGCCCT TTACTGCTAC 960 TTCATCCAGT AGCCACCTCT GGAGTTTTTT TTTTTTGAGG CAGAGCCTCG CTGTGTCACC 1020 CCGGATGGAG TGCACTGGCA TGATCTCGGC TCACTGCAAC CTCCGCCTCC GAGGTTCAAG 1080 TGATTCTTCT ACTTCAGCCT CTCCAGTAGC TAGGATTAGA GGTGTGTGCC 1130
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