| Tag | Content |
|---|
EnhancerAtlas ID | HS051-28328 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chrX:41112050-41113420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chrX:41113118-41113137 | TGCTGCCCTCTAGAGGCCG | - | 6.91 | | Foxd3 | MA0041.1 | chrX:41113318-41113330 | GTTTGTTTGTTT | + | 6.32 | | ZNF263 | MA0528.1 | chrX:41112147-41112168 | TCCTTCCTTTCTGCCTCCTCA | - | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 41112099 | 41112200 | | chrX | 41112416 | 41113113 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI041253 | chrX | 41112254 | 41113453 |
|
Enhancer Sequence | TGCTCCAGGG ACGTGCACAC ACACCCTCTG CCTGGCACAC CACAGCTGAC AAGGGCTGAC 60
AATAGTCAAT TTCATCAGAG TGCTTTTCTC ACCTAGATCC TTCCTTTCTG CCTCCTCACC 120
ACACCCCTTT ACCCACAAAC AGTGGGAGGG GAGCCCTGGA CACTCTCAGC TTCCTCCTGC 180
CCCTGAGTTC CAGCGATCAA AGATAAAATT GAAAACATTA GCTATGCCCA CTGCTCCCTG 240
GTGGAAGGCA GCCACCTTCT GAGGAGGTCC CATGGGAGAG TGAGTCCCCT CCCCGTGCAT 300
AACCCGACCC CCAAATTGGG GGCTCTTCAG ACCTCATCAG ATCCTGCACA GGCCCCCCAG 360
GATAGGTGCT TGGGGTGCAG CAGCTGGCCA AGGCGCTGTG CCTTGTTGTC TAGGTGGTGT 420
GCCCACCCGG GCTCCCGGTC CCGCCTGGTC ACAAGCATCC CCGCGTCAGC TGATGAACAC 480
CCCTGTCCAG CAGGTGCCAG ACACCCGAAA TCAAGAGGAG TGTCCTGTGC TCCAGGAGCC 540
TGAGAGGTGG CAAAGTCCCC GGGGGGAGGC GTGATGGTAG GGAAGGCTTC TGACATACCT 600
CTGCAGGGGC CAGGGCCCTG AGTCCCGGGT CCCCATGGTG TGTTTCTGTG TGAAGTCAGT 660
GGCACTGCCA GCGCCGTGGT CATATTACCT AGGCCACAGC TGCCAGGCCT GCAAGCTCTT 720
TCCTACTTCC CTTAGGTGCC CAGACCCAAA GTCAAGAGGA CCTTGACCCG TGGGGGTCGT 780
GGGGAATGAA AACCGTCCTG CGAACTTGAA CTTCACTAGG GAGGCGGCGC TCTCTCTGCC 840
CCGGTTCTAT CACGCGCATC CGTTAGGAAC TAAGCGGCAC CTGCGCGAGG CTAGGCTTGT 900
TGACATATTT CTTGCTGGCG GCGTCCTCTC GCGTGGAGCA CGACTGCGCA AAGCGCCGAC 960
AGTCCCCCGA GCGAGGACGG CAGCGAGACT CCGAAGCCCC CTTAGCAACC AAGCCGGTGC 1020
CGCTGCCCTT GCGCCGGGAC TGCAGCCGGG TCTTCCGAAG TGAGGATATG CTGCCCTCTA 1080
GAGGCCGCGG GGTGACATGG CCCATGAGGC TGTCTGGGCA GGGTGGGTTC GGGTGGGAGG 1140
AACCAAGGTG GACAAGCCTC GAAGTAAGAG ATCTGTTCAA GGTCACAGGG AGTCGGGACT 1200
CATGCGGAGG CACAGATCCA AGCTCTCTGT ACTGGGCCCT TTGGTATTCT GTTGGCTCCT 1260
ATTTTTTTGT TTGTTTGTTT TTTGTTTTTT GTTTTAGATG GAATCTCTGT AGCCCAGGCT 1320
GGAGGGCAGT GGCGCGATCT CGGCTCACCA CAACCTCCAC TGCTGGGATC 1370
|
