| Tag | Content |
|---|
EnhancerAtlas ID | HS078-02018 | Organism | Homo sapiens | Tissue/cell | H2171 | Coordinate | chr1:227073900-227075100 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr1:227073977-227073992 | TTCTATTTTAGGCTC | - | 6.12 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I226886 | chr1 | 227073902 | 227074101 |
| Enhancer Sequence | TGAGTTCCTC ATTGCAGTGT TCCAAGCATC ATTTCTCATA TTTCAAAGTT AATTTTGTTT 60
TGCTTCTCTT TCTGAAGTTC TATTTTAGGC TCCCCTCACC CCGATACTTC CCCTGAAGAT 120
TTATTTTTAG TTTTCCTTTT CCTTTTCGGG CAAGGATGTG CAGAGGCCAT GCTGAGGTCT 180
TGCAGCCCTG GGAGACTTTT GGGTTGTAGC TGCCTATAGC TGCCGAGTAG CCCCAGGGAG 240
TAGTGGAAGG GCAGATCCCA TCTGGCCAGA ATCATGGGCA CTGCCTGTCC CCAAAGATGC 300
CATAAGCTTT TAGACAGCGG CTTCAGGCTT TTCTCCCAGG TAAGGGGTTG AACCCCTAAC 360
GATGGAAAGG AAATTAAGCT GGGCATTACC TATTTTAAAA CTGTTTACAC ACAGGTGCCT 420
CACAGCATTT TTTGTTCAGG CCGCTGCCAT CCATGGAGCA GGTAGATAGA AGTGCAGAGT 480
GCCCAGGCTA GAGGGATGGG ACAGGGACAG TGCAGGGAGG GAGCTGAGCC CCCTTCCAGC 540
GGGGGCAGCA GAGGGGAAAG CCATGGGAGG GGCTGCAGGA TGTGTCCTGA GCTGAAGCTT 600
ATCAACAAGT AATGAGTACC AGCTGGGCAT TGTGGTGCAC GCCTGTGGTC CCAACTACTT 660
GGGAGACTGA GGCAGGAGGA TCGCCTGACC CCAGGAGTTC AAGTCTAGCC TGGGCAATGT 720
AAGACCCTGT CTCTAAAAAA ATAATAATAA AATAAGTAAC AATTACCTGT GTAACTGTGA 780
CGAGGCAGGG TTTGAACATT GCCGCTGGGA GGTTGGCAGA TGGTGGGAAG CAGGGTGGAG 840
GGCTGCTGGT TTGGAGCAGA GGATACAGAT TGCATGGGGT CAAGCTAGAA ATTGCGTGGC 900
AGATGTGAAG AGCTGGCCCC ACTGCGGGCA GTAGGTGTCT GGTGGCCAGT CCCAGAGGCT 960
GTGAAGAGGG GCTCAGCCAT CTGTCTAGTA GGGCTTCCTT GGAGGTTCCA CGATACAGGC 1020
AGATGGTGGT GGCCCGGGCA GCCAGGTGGT GGCTGGGATG AAGAGGGTTG GCAGGTCCCA 1080
GAGGCAGCCC CTTCCCCTTT TGGCTGTGTG TGCAGCAGGG CCGTGGAGGC TGCTTTTAGT 1140
CCAGGTAGAC CAGGGCCACG CTGAGGTCCC AGTGGGCTGA GCTGGTGACT GATGAGTTGG 1200
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