| Tag | Content |
|---|
EnhancerAtlas ID | HS062-00021 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr1:2312740-2314840 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:2313353-2313372 | GGCTGCCCCCTGGTGGATG | - | 6.92 | | MAX | MA0058.3 | chr1:2314106-2314116 | AGCACGTGGT | - | 6.02 |
| | | 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 |
| GH01I002381 | chr1 | 2313039 | 2313840 |
| Enhancer Sequence | CGGTCTGGGC AGGAGGAATG CCTGGAGAAG GCGCTGGAGG AGCAGGCAGC TCACTGGCCA 60
TGGTCTGCCC GTGCCTGCAG GTGTCAGCAG CGTGGACGAG GCCAGGGGAC TGCTGCCACC 120
AGTGACACTG CCCAGAGCAC CCCGTGGGGC AGCAAGCACC AGCACACAGC AGTGTCCCCA 180
GGGAGCTCAA GCCACGGGCC TGCCTGGGGA GGGTGTGCGG GCCTCGGTTG GCAGGCGGTC 240
CCAGGGCCTG CCCAGGTCTC CCAGTCCTCT GGGCCTGGAC GGCAGAGGAG TGGGGAGGTC 300
ATGTTATAAC CCCAGGGAAT GTAGGTCACG CGAAGGGTTT GGCACCAAGA CTCTCGCAGA 360
AATCCTCTGC AAAACCCTCT GCAGAATTCA AGGTTTTACC ACCAAGGGGA GAAACCATCC 420
CAAGCAGAAA GGCCTGGGGG GCCGCTTGGG GGCCCGGCTC TCAGGAGTAC CCAGCCAGCC 480
CTTGGGCCCA GTGGCCATCC CAGGCCATCC TCCCCCGTCC AAACTCATGG CTTGGGAATA 540
AGCTCTGGGC TCCCGGGGAG GAGCTGCCTC CCTCCAGCAA GGCCCGGGCC AGTGTGGTGC 600
CGGGACAGGG CTGGGCTGCC CCCTGGTGGA TGCGCTGAGC ACCCTGGTGC TGTCAGCCCA 660
GGAGGGAGGG CGCCGTCCCT TGCCTGGTCC TCTCTCTTGG CCCAGGGCGC TGGTGACCAG 720
CAAGCAGTGT GGACCCGAGT TGGCGCCTGG GTAGTAGCCA GGGGACCTGT GGGACAGAAC 780
AGCCTCTGGG GACAGGGCTA GGCTGGGAGT GGGGGTGGGG AGGACAAAGC TGTCCATGGT 840
CCTCTGGAAG AACAGGAGCT GCTTCTCGCC CGGCCCAGGC CGGAGGGGAT GGCCCTGTCT 900
GGCAGCAGGC GGCACCTCTG TGTCCCTGGG CCATGAGACA GGCCCTGACC AGGTCCTCCT 960
GAATCTCAGG GAACATGAGG ATTGGGTGAG TGGCTGGGGG CCCCCAGGGC TGTGTTGCCC 1020
TGGTGAGGGA GCCTGCCATC CTAGCACCTC AGCTTCCTCA CCTATGCCCT GCTCGGACTG 1080
GTGGGGATCA TGAGCCAATG CACCGAAAGG CTGACAGCAG CGCCTGGCAC CCAGGAAGTG 1140
AAACCACACA CCCGAGCCCA AGCTCCAGAG CTGTGCACCA GCGCCGGCCC CAGCTTTGCC 1200
CTAGCCCTGC AAGGCGAGGG AATCGTCATG GTGGCAGTGG GGTGGGGGCC CGGGTGTGCT 1260
CGGGTGGGAA GGGGCGGGCA GAAGAGAATT CTGCCCAGGG ACTCCCTTAG GCGCACTCTC 1320
CCACTGCCAC TCTGGACAGT GAAGACAAGG GAGCAGTGGC TGCCCCAGCA CGTGGTGAAG 1380
TCTGGTCCTG TAGGATGGAC ACAAGTCCCC AGGGGAGAAG AGGCTACAGC ATCTCCTGCA 1440
TATGGCTCAG GTGAGAACCC GCAGCACCAG CCCAGGCCAG CAGGGGCAGC AACGACGCTG 1500
ACATGGGCTC CCGTGGTCCA GCAAGGACAC TGCCAATGGT CAACTGCCCT GAGCAGGGCT 1560
GGCAGACCCC GGAGTGGGTA TGGGTGGCAC TTTTACCCAA GCAGGATGCT GTTTCAAGAG 1620
CAGGGAGGGT GGACATGCAT GCGGAGGGGA GCCACACTGC ACCTCCCGCC TGACCACCCC 1680
TCCAGGGGCC CCACATCTGA CCACCTCTGA GGCCCTGCTG CGGGCAGCTG TGCCAGCCAG 1740
GATGAGTCTC CCATCCCCAC CCCCAACTCC TCCATCCCCA TGTGGCCCCA TGCCAACTGC 1800
CAACCCATCA CCTCTCAGTT CCCAGCACCC CCCTTCCTTG CCCACTTTTG CCTGACGGGA 1860
ACTGGACCCT GTCAACGTTT CTCCTTTGCC AACAAGTGCA ATGCCAGGCT TTGTCAACAG 1920
AGAACAAGGC GGGACTGTGG GAGGTAGTGT TTCTACTTTA ACTCCTATGG CCAGGGCCAG 1980
TGGCCTGTGG AACACCCCAG AGTCTGGTCT CTGGCAAGCG TCTCCTGCAC CTCAGGGGGA 2040
GTTTCCTGAG AAGTAGCTTT GGCCCCTGGC ACCCTAGAAA ACCTCTCTAC CACCTGGGCT 2100
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