| Tag | Content |
|---|
EnhancerAtlas ID | HS051-28309 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chrX:40061720-40062680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chrX:40062477-40062495 | GGAAGGAAGCCAGAAGGG | + | 6.29 | | EWSR1-FLI1 | MA0149.1 | chrX:40062473-40062491 | GGATGGAAGGAAGCCAGA | + | 6.3 | | SCRT1 | MA0743.1 | chrX:40062066-40062081 | ACACACCTGTTGCAA | - | 6.29 | | SCRT2 | MA0744.1 | chrX:40062068-40062081 | ACACCTGTTGCAA | - | 6.06 | | YY1 | MA0095.2 | chrX:40062629-40062641 | GCAGCCATCTTG | - | 6.74 |
|
| | 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 |
| GH0XI040201 | chrX | 40060334 | 40061894 |
|
Enhancer Sequence | CATTGCACTC CAGCCTGGGC AACAAGAGTG AAACTCCATC TCAAAAAAAA AAAAAAAAAG 60
ACAGATATTT TTGGTGCTGC TGCCCCATCT CTTCGTCCCC CTTCCTGCCT TGACCGTGTT 120
GTGTTGAGGA AACTGTCTCT AACCATGTTC TTCCTCTACT CTCACACCAC AACAACTGTC 180
AACACAGAAG ACTTCTGTGA CCAAATGTGG GAGGGGCTTC CCCACACACC AAGCAGCGGG 240
CACCAGCTAG GTGTCCTTGA ATTCAGTTTT GACACTGTCT ACCCGCGGAT AATGTCAGAT 300
CCCACAGGTT GAGGGCTCAG TCCCCAAGAC TGCCCCCCCA CCCCACACAC ACCTGTTGCA 360
AACCCAGGCC TCTGAAACTT CTGACTGACT GGCTTCAAGT TAAAGTTCCC ATGACCCCCT 420
CTTTGGGTTT GATTAATTTG CTGGAGCGGC TCACAGAACT CAGAGAAACA CTTATGTTTA 480
CCGGTTTATT AGAAAGGATA TTGCAAAGGA TACAGATGAA GAGACACGCA GGCGAGATAT 540
GGGAGAAGAT ACGTGGAGCT TCCATGCCTC CCCTAGGCGA GCCACCCTCC AGGAACCTCC 600
ATGTGTGCAG CTATCTGGAA GCTCGCTGGA CCCTGTCCTC ATGGGTTTTT ATGAAAGCTT 660
CATGACATCA GCATCCCTTC CCCCAGGGTA TAGGGGGGCA CTCTGTCATG GCAGAGTCTT 720
AAGACCCACA ATCAGAAAGG TAGGAAAAGA TTAGGATGGA AGGAAGCCAG AAGGGCAGAA 780
CCCTGCCCCT GAGGCCCAGT ACACCCAACG TTATAACAAA AGACTGGAGC AAGGGCGATG 840
GAGTTATAAG CCAGGATCTG CGGATGAAAA CCAATATATA TCATAACACC ACACTGTGCA 900
AGAGCTACAG CAGCCATCTT GGGGCCTAAA GGAGAGGCCA AAATAATCAC AGAAATGCTG 960
|
