| Tag | Content |
|---|
EnhancerAtlas ID | HS051-18217 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr22:19717640-19719140 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr22:19718333-19718352 | CAGGCACCAGAGGGCGCTC | + | 6.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 19717835 | 19718265 | | chr22 | 19718399 | 19718941 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I019729 | chr22 | 19717312 | 19719321 |
| Enhancer Sequence | TGGGCCCCTC TGTGACCTCA GACTCTTCCT TCTAGGCAGG AACAGGTTGG GGGTCCCGTC 60
TCCAAGCCCT GCCTGGACCC CGCACCTCCA GTCCCAGGCT AGCTGATTCA GGGCTCCTTG 120
CCCTGCAGCC CAAGGGCCCT CTCACCACCA TTGCCCACCC CACCTCCCTG GGCTCCTGGG 180
ATCTCAGCCT TAGGTCAAGG CCCAGCCCTG GTGCACCCTC CCCCATGGGC CAGGCCCTCC 240
ATGCCTTTGC CCGCGCCAGT CCCTCCACGG GGCACGCCCT TCCCGCTGTG GCTACTCCTC 300
AATCTTAGAG GCCCCTCCCA AGCCCATTCT CACAGAGCTT CCTAGGCCTG CCCTGGCCTG 360
ACACATAGTG CAGGACAGTG TCCAGGCCTG TGTCCCCAAG ACCCATCTGG GGTTCAAGCC 420
ACATCTTGGG CCTATACACA GCCAGCTAGT GAGTGAGCGA GCGAGTGAGT GAGGCCCTGC 480
AAGATGGTCA TCTGTCTTGT CCCGCAAAGG CCAAGACAAA CGCCGTGTCA GCGGCAGCCT 540
CTCCAACCCA GTCTGTGATG GCCAGTGGTG GTCAGTGAGG GCTGGGCCGC GAGGCTCACA 600
GCTCAGGCCG CACCCGCCGG TTTCACAGAC CGGCCAGGAA GCTCCCAGGG CGAGGGCCTA 660
GTCGTGTCCT CCCCATGGGC GAGCAACCCT AGGCAGGCAC CAGAGGGCGC TCGCGGTCTG 720
CAGAAAACGC TGGCTAAGGG GGGAGCGCGG AAAGAGGTGG GCACTGTGGG TGCAGACAGC 780
TGGGGTCCGC GGAGAAACGA AGGCCTGGAG CGGGGGCGCT GGGTTGTCCA GGCTGGCGGC 840
GAGCTGCACC GAGTGGGACG GGCAGGCTGC CCCTAGTGAG GGCGGGGAGG GTGTCGCCGC 900
GTGGCGGCTG ACAGACGGGG CGGGATGAGC GTAGCCCCCG CCCCTGCCCT GGTGCACTGA 960
CAGCCTGTCA GCCGGGAAGA TAAGGGACTT CTTCCGCTGG GCGTGGGGTG GGGGTCAACC 1020
CAGGTGCGCT GTCCCCCTCC CGCTGGTGTT TGCTCGGTAA ACACTTATTG GGCCCCGGGC 1080
TGTGCACACC GCCGCGGGGG AGGGGCGGGC GACCTGAAGG CCTGGACTCC ATGGCCTCTG 1140
CCAGGGATGC CGGGTCCATG GGCCATCAAT GATGCAGGAA AAGAGGCTCT GTCACCTCTG 1200
GCCCCGCCTG GAGAGAGTTG CCTGTGGGGT CCTTCGTGGG CCCCCTCCAG CCTGGGGTGG 1260
CCCTAGCCTC AGCTTCAGAG CTGGGCTGAC CCCCGACTAG CCGAGGCATT AATGGGGCCC 1320
CGTGGAGGAG GTCCTGGGAA GGTCTGGGGA GCTGAAGTCC TGGCCACGTG GGGGGGACTG 1380
CACCCCCTGC CCAGACGGAG CAACAACATT GGGGTGGGTG GCGGGGCCCT GGGGGCCCAT 1440
AGCTCAGCGC AGCGTCTGCG CCCACCCCCT GTGTTTCCGA TGGAAGACAG GCTGAAGGTG 1500
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