| Tag | Content |
|---|
EnhancerAtlas ID | HS051-13257 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr18:77402850-77404400 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr18:77404250-77404269 | CGTCTCCATCTAGTGGCCG | - | 6.1 |
| | | 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 |
| GH18I079642 | chr18 | 77402801 | 77404469 |
| Enhancer Sequence | TGCGGTGGAG AAATCCTGGG CTGTCTCAGG TTTCCTCACT CCACACTCTC CCCAAGACAA 60
AGTGGGTAGT TACCGCGCTA GAAGGTGGCC AAGAGCATGT GAGTCTACAG GCAAGTACCT 120
TACTCTCCTG GGGTGAAAAT AATTCGGAGA AAGTAGAATA TATGAAAAGA AAGTGTGGAG 180
TTAAAGAACC AAAGCTCACA GACCATCTCC CCAGTAACCA GAGTTACTTA AATGCTTTGA 240
ATGCCACTTC TCTCATCTAG AAAATAGGGG TGAGGCCTCT AACTTCCCAG GACTGCCGCC 300
CACGTCAAAC CCTACCCCGA GCATGTGAAG CCTCTGAGGC CTGCGATTTT GGCTGACAGA 360
GGCACAGGCG GAGGCCAGGG CAGCGTGGGG AGCAGGAAGC CCCCGTGGCA GAACAAGAAG 420
CTCCCCGTGG GGGAACAGGA ACCCAAGCCC CATGGGGGAA CAGGAAGCAG GTGAACTTGC 480
TGCCTCCCCT CCCAGCTGGT GCGTCCCCAG CAGACAGAGG CCCCAAAACA CCGAGTGACT 540
CAACCTACAA TCAGGCTTGT TTCCAAAACC TTGATTTCCA GGTTTCAAAA TTGTAAGCTA 600
AGCCCCGTCC ATGGCCATGT GCCGCCCAAA GACCCCCCTC AGCCCCTCAG CCTGTATTCT 660
TGCCCCCATA ACTGCAAGCA CTGCCCGGGA TGGCCAGTTC CATAAAGAGC CAGCTTCCTG 720
ATTGCATTAT CCGAGGACGA ACCTCCCCAG GACTGAGGAG TTCGTCCCCC GCGGCTGATC 780
ACACAAATGG ATCAAGGGCC TCCTGCTTGG AGGCCGGAGG GGAGAGCAGG TGAGACAGAG 840
TCATCGATTC CCAGGCAACG TGGAGCACAC ATCTGCGCCT GGAAGGGGGC TGTCCCATTC 900
TCGTGGAAGT CAAGGGATTT TTACTTCATC CTCCCACAGG CATCCTTCCT GCGCTGTTTC 960
AGAGCCTAGA AGCTGGGGTG CCCCACAGGA CTTGGCCATG TCTGCACCTC AACCGACAGT 1020
CACTTAATAT GTTTCTCGAA TTAATTTTAA ATGTAATTTT GCTTTTCCAC TTAGGCTCAT 1080
TGTAAGTAAA ACGAGTGACA TCATGGACTA ATGTGCCTGT TATATTACTC TCTGTAACAC 1140
ATTCGAATTA ATGTATAATA ATACGTAAGA AATAACTAGT AAAATAAAGA ACGTGTGTGC 1200
ACATTCTTCC TAAAGAGCCT CTCTTGCACG GACAGGACTA GGCATAAGGT ATTTGGGGAA 1260
ACTGTCTCGC GAGAAGTGAG GGGCGGAGGC AGGTGTCCGG AGGCCTGCAG GTGCCACGGG 1320
GCTGAGGCCG GCCTCCTGCG CGGAGTCCCT CCCTCTGACC TCCCCGGGGT GCGAGCCCCA 1380
CCTGCAAGGC GGTGGAGAGA CGTCTCCATC TAGTGGCCGC CTGCTTCCAT TACACTGGGA 1440
AGCAAGTTCC TGACCCTGAG GGTCCCGGGT TCCTTTTGGT GATGAAAACC CTCCGGAACT 1500
GAATAGCGGT AATGGCTGCA CAACCTTGTA AATATACTAA AAACCCCTGA 1550
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