| Tag | Content |
|---|
EnhancerAtlas ID | HS007-00107 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr1:10926480-10928760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr1:10926893-10926905 | GTCTGTTTACAT | - | 6.44 | | FOXP2 | MA0593.1 | chr1:10926894-10926905 | TCTGTTTACAT | - | 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 |
| GH01I010865 | chr1 | 10925202 | 10927814 |
| Enhancer Sequence | CAGGATCCCA AGTTTCCCCA GCCCAGCGCC CCGTGCAGGA GTGGGGAGGG GGGGCACCTT 60
GAACCTGACC CTTCTGATGT CCAGTGCCCA GGGCCCCAGA GCTTACTGGC TGCTGTAACC 120
AGAAGAAGGC TGGGCAGGAA CCCCATCTCA GGGCCTCAGC CCGCAGCAGG GTCTCCCCAA 180
GACCCTCCTC CTTGCTTCTC AGGATGTGTG TAGGTTTTGG GGTGCTGACT TTTACAGCAC 240
CTTTAGAAGG CCAGGGGCCG GGCAGAGAGA AACTCCAGTG GCCCAGGGAC TGGCCAAGGT 300
CAGGCCCCTC TTTGCCAGTA GTGTCTCTGC ACAAACGTCA CCTCCCTGGC CATCCGAACA 360
GCCCCAGCCG AGTTTTATTT TCTGCAGAGC GCTCGCCTGG AATTATCTTC CTTGTCTGTT 420
TACATGCTTT GGATCGGCAT CCCACCCCCG CAACCTTTGA ATGTAAGTTT GAGAACGATG 480
GGGCCGCGCC TACCTTGCTC CCCATCACAT CCCCCGCCCC TCACGCTGAG CCAATGCTCC 540
CTCTGCCCCA GCTGACTCGA TGGAGGACGG ACAGACGGAC GCTGCAGCCT CCGCCCTCCG 600
CTCGGCCAGC CCCCCGCCTG AGCCCGCTTC GAGGCCGGGT GACCCAGCCT CGCCCCCACC 660
CCGGGACCCC TCCCAACCCC CGCCGCCCCC GCAGCCGCTC GAGGCTGCGC GCCCCCGCCT 720
CCCCGGATCC GTCACTCGCG GAGCTGCCAC AATATTGTGA AGGCTCCGCG CTCCCGCTCC 780
GCGGCGCAGC CCGCAGCCCG CGCGGGGGCC GTGAGGGAGG CGCGGGCGGG CGGGCGCCGG 840
CGATGAATAA TGCATGACCA AGGCGCCCCC TACCGGCGGC CGCGGGCGGC GCGGGGACGG 900
CCCCGCCGCG CCCGAACCCG GCCGGACCCA GGACCCGCAC GTGTCCCTGC CCACCCGGGA 960
GGGAGCTCCT GCCTCTATCC CCGCCTCAAC CCCGACCCGG CCAGGCCCTC CTCCCCCACC 1020
CTCCACGTCA GGGGAGCAGC CTCCTACTCA CGCCAAGACC GAGGAATGAG TTTGGGGAGG 1080
CGGGGGAGGC TGCACAGAGC CCAAGCCAGA GCCCCTTCTT GTGCTCCCGG GTTCGCGGTG 1140
CAGTGGGGAC CAGGACCCCC CCATTCCGTC TCACCCTCAC CCCAGGGCTT CTGGACCAGG 1200
ACTTGCAGCC TCAGAGAAGG ACAGGCTCGG AAGGACAGAG CAGAGAAGGA GATTTCATTC 1260
GTTTATAAAA ATGAGTACAA ACAATTTCAT AAGAGTTTCC AAGTTTCTGC AGAATATTTA 1320
CAACGTTGAG ATATGAAGGC TTTTTTTTTT AAGTTCAAAT GAAATACGGG AAAGCCCACT 1380
GTGTATAGAT GGGTCTGTGT GGTTTTAGAA TAAGGGTCCG GGAAGTGTCT TCCTGGGGTC 1440
TTCTTGGTGG GAGGATTGGA TCTTCTTGGC TGCAGACGAT CTGCTTGGGT GGTAGAGGAC 1500
ACGGTGGGGG GAGCGATGAC CAAGAGCAGG CCCCCGCCGG GCTTGGAGTG TCCCCTAAGA 1560
TGCCTGTGTT CTCTGGGGAT CAGCCTGCAC GCAGTCGCCT GTTCTTCAAG CCTGCCAGTC 1620
CTGCTAACAG GCAGGTAATG AGGAGAGCAG AGGCCTCTTT CAGGCAGCTG CTTTAGCTCC 1680
CAATCACGCA GGCCCCTGGG GAGCTGGGCC AGCCTCTCGG CCTCATGGCC TCTCCTCACT 1740
GAGAACAGAT TCTAATGACA CCCCCCTTCC ATCCCCCGTG GTTCCTGCTG TGCCCTGACT 1800
CCCTGCCCAG CCTTAATAAG CCAGAAGGCA GAAACAACCA TCACAGGGGC TGGGGACCCA 1860
GGGCCATTTG TTGAGCATCT GCTGAGATGC TGGCTCGTGT TGAGATCTCT CGTCCCAGCA 1920
ACACTCCACA CATTCAGATT GCAAGCCCCA TATTACAGAT GAGGAAAGCA AGGCCCAGAG 1980
AGGTGCGGCC ATGGGCCAAA GATCACACAG CTGCTCAGAG ATGAGCCAAG AGGCGTGGAG 2040
CTGGGCAGAG GAACTCCATC CCCCCACCCA GACGCTGCTT TGTGTCCCGG ACCCCATGTC 2100
CAGGAGATCA GATTCAAACC TTGCGCTGGG CTACAAGCCC TCCCCATTGG AGCAGCAGTT 2160
GGTCTGCGTC ACTAAAAATG AGTTGCAAAC TCAATTGCCC TGGGCCTAGA CTGGCAAGGC 2220
AAATGCATGA AGTGGGCCAC ACATGCAAAC ACGTGGTTCC CACAAGAGTT TCCCAAATCG 2280
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