| Tag | Content |
|---|
EnhancerAtlas ID | HS051-28643 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chrX:129194250-129195410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chrX:129194644-129194663 | CAGCGCCACCTGCTGGACG | - | 7.74 | | KLF16 | MA0741.1 | chrX:129194345-129194356 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chrX:129194346-129194356 | GGGGCGGGGC | - | 6.02 | | SP1 | MA0079.4 | chrX:129194344-129194359 | CGGGGGCGGGGCCAG | - | 6 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24424 | chrX:129193867-129195210 | Colon_Crypt_2 | | SE_32136 | chrX:129193936-129195014 | Gastric | | SE_50613 | chrX:129194129-129195218 | Sigmoid_Colon | | SE_53216 | chrX:129194149-129195076 | Small_Intestine |
|
| | 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 |
| GH0XI130059 | chrX | 129193435 | 129195382 |
|
Enhancer Sequence | AAGGCGGCGG CGCGCGAGGG GAGGGGAGGG CAGGCCGGGT GACTGCGACT CCGCGTGCTC 60
ACCTGCTGGT CCGCGAGGCT GAGGGAGGGG GCGCCGGGGG CGGGGCCAGA GCGCGGCTGG 120
CCAATGGGGG AGCGCATTCG GCGGCCGGCT AAATTCCCCC TGGAAAGTGA AGGGGGCTGG 180
GGTCGAGGGG AAAGTTCGAA GCTCCGGAGC AGCGGAGGGC TTTGGTGGCG GCCAGAACCA 240
TCCGGGGACA GTTGCAGGCG CAGGGGCAAG ATCGGGGGAC CGGAAGACGC CAGCCGCGGC 300
CGCGGCCGCC TCCGCCAGGG ACGGTAGGCC CAACCCTGGC TGCCCCTCCC TTCCCGGGCC 360
CCGCCGGGCC ACTCTCCCGC CATCGCTGGC TCGACAGCGC CACCTGCTGG ACGTCGGCCT 420
CCACGTCCGG CGCGCCGGGG CCCGAAGTTC TCGGAGGCTG GGACCTCAGT CTGGGAGGGG 480
AAGGAGCTCA CTCACCCCAG GTCCAGCGGC TTCAGAGCTG GAGGCAACTG CCTCTTTTGG 540
AGTACAAGAT GGGATCAGAA AGGCCTGTGA CCGTCAGAAT AACTTCTTGT CCCGCCCCAC 600
CCACCGGAGC TGACACTTCC ACCGCACAGC CCCACCCAGG GGTGAGGAAA TAGTGGCGAG 660
GCAGTCCCTG GAAGCGGGCA GCAGCAAAGG GCGGGAGTTC GGGAGTTGCA CGTGGCACCT 720
GGTGACAGCA ACGCACAGCT GGCAAGCAGC CCTGGGCTCC TCATGGACCC TGTGATCCGG 780
GGATGTCTGT TAACACTCCA GGGGCAAAGG AAGTAGCCGC CTGCAGTGTT ATAGGAGCGG 840
GCAGAAAGCT GCCTTAGCTC CCAAGTGTGG ATTGTCCTCC TCCCTCTCCT CTTGCCTGCC 900
ATAGCATAGG GCAGAAGTCT CAGAATTAAA ATCAGGACCA GTTCCTTCTT TCAATAAGCA 960
TTTATTAAGA ACCTACTGTG TGCTAGGCAC TAGGGATATA TCAGTGACTA ACACACAGTC 1020
CCTGTCCTTG AGGAGCTCAC AGCCTATTGG CGGGGAACCC TACATAAACA CGTAATTAAA 1080
GAACTGTACT GTGCTAAGTG CTACCATAAG AGGTATTTAC AAAGTGCTGT GAGGTGGCTC 1140
AGGGCTGTAA TCCCAGCACC 1160
|
