| Tag | Content |
|---|
EnhancerAtlas ID | HS037-22166 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chr20:414650-416120 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr20:415419-415436 | AAGGGCAGTGTGACCCT | - | 6.02 | | ESR2 | MA0258.2 | chr20:415420-415435 | AGGGCAGTGTGACCC | - | 6.8 |
| | | 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 |
| GH20I000432 | chr20 | 413492 | 417030 |
| Enhancer Sequence | TTTGTTTTTT TTTTGAGACG GAGTTTTGCT CTGTTGCCCA GGCTGGAGTG CAGGGGTGCA 60
GTCTTGGCTC ACTGCAACCT CCGCCTCCCA AGTTCAAGTA ATTCTCCTGC CTCAGCCTCC 120
CGAGTAGCTG GGATTACAGG CACCCGCCAT CATGCCCGGC TAATTTTTGT ATTTTAGTAG 180
AGACGGGGTT TCACCATGTT GGCCAGGCTG GTCTCGAACT CCTGACCTCA GGTGATCCAC 240
CTGCCTCGGC CTCCCAAAGT GCTGGAATTA TAGGCGTGAG CCACCGCGCC CAGCCCTGAA 300
TCTCAAGTTT GTAAAGTGCT CCACCTCTGT CACTCCAACT CCCAGGAGTC ACTGCTTGGG 360
ATTGAAAGTT TCCGCCCTCG AATCACCTGG TCTTTCTGGT GCAGGAGCAA CCCCGAGGCA 420
ATCTAGGGGC CCTGCTCTAA CGAATTCATT AGCATGAACT CAAATGGGCT GGAAAGGGGT 480
TATGAATAAC AAAAGACACT CACCACTCAC GAAATTCCAA GGGTTGTAGG AGACCCGTGT 540
TAGGAACCCA GGAGAAAGAC CAAATATTTC TTAGTATCCC ACACATACCC TTCCTTTAGT 600
TCTCCAATTA TCATAATTCT ATTCATCCTT CACATTCCAC CCTCACCTTC TATGAAAGTG 660
CCCTGAATTT GCTGCAGGAT AGATTGCTCC TGGAGTGCAG CTCTGGTGTG AGCTTTCAGA 720
GGCAGCGCAG TGCCCTGGGC AGCCTGCGTA ATCCACGACT GTCAGATCAA AGGGCAGTGT 780
GACCCTGGCC CACAGTGGCA GGAGCTGAGT GCCACTGGCT TGGCCCCGGG AACCTGCGCA 840
TCTCCCCTCT GAGCCAAGGA AACAAACAAC ACAGACAACA GTGTCTCCCC GATGGCCCCA 900
TCCCCAGGGT GGAGGCCCTG CACCGGGCAC TGCTCTGCGC GCGCGCTCCC CAGCAGCCAG 960
CAGTGTCTGG AGGATACTGG AAAGCTTGGC AAGAGTAGGC TGAGCAGCTC CTCTGTGGAC 1020
AGAAAGGGCA TGTGGAGAAG CGGCACATCA AGCTCTGGTT AGGATCCAAA ACCAAATGCC 1080
AGCTCCTAGG ATCCCCAGAC CAGGGTGTGA AACACACCAA GAGCACCCCA GACCCGCACC 1140
AGTTGTGTCG ACTGTGACAG TACCCAGAGT GGAAAAAACA TGAACTCAAA CTGTGTTTTC 1200
CTCCACTGCT CTCTCAATAC CAACAGACAT CTGTGGCCAA ATGTGTTGGG GATTTCTCCC 1260
CTGACACCAA GCAAGCAAGC AATTCTGCAG CCTACATCAG CTGGGTATCC TCCAATTCAA 1320
TTCAGTGCTC ACCCTACCTA TAGTATCTGG AAATGGAATC CACAGGTTCA AGGCTCTGTC 1380
CCACAAGACC GCCGCCTCTG CCACAACATT GGACTGACCA CCCTCTTTGG GTGGCATGAT 1440
TTGCCAAGAG TGGCTCACAG AACTCAGGGA 1470
|
| |
|
|
|
