| Tag | Content |
|---|
EnhancerAtlas ID | HS051-13874 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr19:15666290-15667770 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:15666824-15666843 | GGGCGCCCCCCGGTGGCCT | - | 6.19 |
| | | 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 |
| GH19I015555 | chr19 | 15666212 | 15667930 |
| Enhancer Sequence | ACACTGTCTC TACTAAAAAT AAAAAAAAAA TCAGACGGGA GTGGTGGCAC GCGCCTGTAG 60
TCCCAGCTAC TCGGTAGGGC GAGACAGGAG AATCGCTTGA ACCCGGGAGA CGGAGGTTGC 120
AGTGAGCCAA GATAGTGCCG CTGCACTCCA GCCTGGGTGA CAGAGCGAGA CTCGGTCTGA 180
AAAACAAAAA CAAAACTTTT TTTTTTGATT GAGTGCTTCC TGTGTGCTCT TTCCATATAT 240
TCCCATTTAA TCCTCATACT GACTTGTAAG ATCACTTTTT ATTATTCCGT TTAACAGAGG 300
TAGAAACTGA GCCCCCGAAT GAAGTGACTT ACCCAAGATC ATTCGGTGCG GCCTCAGCGC 360
TGGCGCTGAG TCCTCTTCTG CCCCACCCCT CAGGCTCCCA GTCCTGGTCT AGATCCCTAG 420
CCACGTAGCG TAGAAGGGGG CGTCGACGGG GGTTGGGCTA GAGTTGGAGC GGGGAGGAGA 480
TGAGCTAAAG CGGGGCTGGC TGTGCGAGAG GCAGTAGCAG CGGCGTGTGT CCTGGGGCGC 540
CCCCCGGTGG CCTGTGCTGG GGTCGTCGGC CGGGATCCCC TGTTCGACGT ACTCCGGGGC 600
TGAATGGGAA ACAGACAGTC CCAGACCCTA CGTGAGCCAC CCGGATCTTG CAGGTGCTGC 660
CTCTCCTACA CCCCCCTCCC AACCGAGGGT CTCCAAGAGC GCATCCTTTG CCAAACATCT 720
CCTGGGCCCT TTTCGGCGCA ACCTCGCCAT CCACTAGCAA ACGAAGTTAG CCTTGAGATC 780
CGACATATGT GGGCTCAATC TAGGCTCTTC CTTCCTAGGG GCGGCCTTGG GCACGTGACT 840
GTCCCTCTCT GCACCTCGGC TTTTTCTTGT CATGCGAATA GTCCGGTATC ATCATGCTTG 900
TAATGCACAC TGAGTTTCCG CCAAGGGCCA CGAGGGTGAA TAAATGAGAA TGAGAAGGGG 960
AGGAGTAAGG TCCCTGGGTC CCCGGAGCCC TGTTACACGT ACTGCAAGTG TAATTCTCAA 1020
AACACCGAAG TCTGGTCCTG TCGCTGGCGG CTGTGGGACC TCCTTCCTCC TGAGTGTGAA 1080
GAACGCTCCC TCTGCTGGAC AATTTGGAGA TCCATTCTCT ATTCGTTCAA TTTTGTGTCC 1140
GTGCACGTTT GAGCGTGCAT GTGTGACCGC GTATGTGTTT GGGTGCATTT GGGTAACAGT 1200
GTGTGCATGT GTTGTAGTGT GCACACGAGT GTGTGTAAAC GTGTATGTGT CGGTGTGACT 1260
GTGTGTGCGC ATATGGATGG GTGTGTTGGA AGGAGAGGAG AGGAGAACTC CACTCACTGA 1320
GTCACTGTAA CTATCCACAC ACACCAGGCT GTGTTCCTGC TCATGGCTGG AGCCACTGTC 1380
AGAGCCCTTG CCTCTGTCCC CAGGTCTGAC CTGTGCGGTG CAGGCAGGAC ATTCTGGAGA 1440
AATCATGCCC TTGGAGGAAG CTGTCAGTAA TGACTGGTGG 1480
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