| Tag | Content |
|---|
EnhancerAtlas ID | HS068-04197 | Organism | Homo sapiens | Tissue/cell | GM18526 | Coordinate | chr4:1683520-1685000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr4:1684160-1684172 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr4:1684160-1684172 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr4:1684159-1684174 | TTCTATTTTTAGTAG | - | 6.57 | | NKX2-3 | MA0672.1 | chr4:1684558-1684568 | TTCAAGTGGT | - | 6.02 | | Nkx3-2 | MA0122.3 | chr4:1683887-1683900 | ATAACCACTTAAT | + | 7.34 | | Zfx | MA0146.2 | chr4:1684231-1684245 | CCCGCCTCGGCCTC | + | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCCTGGCCA AGAAATTCAA ATCGTAAAAT GAAGATTATC ATTGTAACCA CTCCACTGGT 60
GAGAACAGGC TGCACCATAT CACCACATGG AAAAAGATAA ACTGCACCAA GTAATTTCAT 120
TGTGAGGTAA AGAACACAAG GTGAGCTCTG GACAGCTGCA CAAAGCCCCG GGTTCAGACA 180
CCAGTTGGGC CCACTCACTA GCCAGGCCAA GGAACTTCAC CTGGACAAGT AACCGCCTCT 240
CCAGGCCTGG GTTCCTTGGA AACTGAAAAT GAGAAGAAAC CACCCACTTC ATGAGGCTCC 300
AAGGAATCAG ATTAAACTAC ATAACACATG TGAGAGTTCC TGAGTCCCTG ACACACATTT 360
TCAAATTATA ACCACTTAAT AACAAATGCT TAACAGATTG TGAAATTCAA TTTTTCTTTA 420
ATATCATTGC AGAAAATGCC AAAAGAGTTT ATATAAAAAT TTTTAATTTC CTTTTTTTTT 480
TTTTTTTTGA GACAGAGTCT GGCTCTGTCA TCACGGTGGC GTGCAGTGGC GCCATCTTGG 540
CTCACTGCAA CCTCCGCCTC CTGGGTTCAA ATGATTCTCC TGCCTCAGCC TCCCGAGTAG 600
CTGGGATTAC AGGCACGCAC CACCACACCC AGTTAATTTT TCTATTTTTA GTAGAGACGG 660
GGTTTCACCA TGTTGGCCAG GATGGTCTCG ATCTCCTGAC CTCGTGATCT GCCCGCCTCG 720
GCCTCTCAAA GTGCTGGGAT TACAGGTGTG AGCCACCGCG CCTAGCCTTA ATTTCCTTTT 780
TTAGAAAAAC ATTTTCCCTG TTCCCAATGC ACCGGTGAAA AATACCTGTT TTCTTAGTTC 840
TTTTATCTAC CAGCTAAAAA TGTGTACTCT CTCGGATTAG AGCCTCTTCC TATTTCTGTT 900
TCCTGTGCAC ATCATTGCAT GTGAGCAACT ACCTCTATAA CTAGAAAGGC CTCACTATAG 960
AGCAACTACC TCTATAACTA GAAATGCATG CACTAAAAAA AAAAAGAAAA AATTACTTTG 1020
GCATTTTCTC TTATATACTT CAAGTGGTAA CAAAAACGTT CTGTGGTCCC CACGTGCAAT 1080
CTAAGAAACA TAAGGACGCA TCCAAAGGGG CGGGACAATT ACCAAGGCCT CAGTGAGTGT 1140
GACCCTCAAA GTCGCAACAC AGAACACAAC AGAGGGACAA AGCTGCAGAA TCAAAAGCTC 1200
TAAGTTCACG GGACAGCACG GGGAATCAAC TATCAAGCCA CAGAAGGGGA TCAGGACTGC 1260
CAGTACCCAG CGCACAAGGA GGACTCAAGG AGGCGGGACA ATGGCGCCGG ACGAGGGAAA 1320
ACTACAATTG TCTGAAAGAA CTACCACCTA GTTTTCCTGC GCTAACTAAC CCAATTTAAA 1380
GAAAAGTCAC TGTTTCTAAA CAATGTCAGT TTCCATTTTG GGGTAATATT GAAGAGCTTC 1440
AAATAAATCA AAACCGTTTC CCAGCCTACC TTCAGGGTGC 1480
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