| Tag | Content |
|---|
EnhancerAtlas ID | HS051-02367 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr1:226288030-226289110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr1:226288394-226288409 | CTCGGTGGGTGGGCG | - | 6.05 | | IRF1 | MA0050.2 | chr1:226288606-226288627 | AAAAGAAAAAAGAAAGCACAA | - | 6.26 | | NRF1 | MA0506.1 | chr1:226288406-226288417 | GCGCATGCGCA | + | 6.32 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23364 | chr1:226288328-226288640 | Colon_Crypt_1 | | SE_23849 | chr1:226288300-226288591 | Colon_Crypt_2 | | SE_65669 | chr1:226287955-226288637 | Pancreatic_islets |
|
| | 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 |
| GH01I226100 | chr1 | 226287902 | 226289101 |
|
Enhancer Sequence | ATGTGTGGGG GTTTTGTTTG TTTTTTGTTT TTGTTTTTGT TTTTGTTTTC AGAGGGAGTC 60
TCGCTCTGTC GCCCAGGCTA GAGTGCAGTG GCACCATTTC GGCTCATTGC AACCTCCACC 120
TCCCGGGTTC AAGCGACCCC AGACTCCCGA GTGGCTGCGA TTACAAGCAC CCGCCACCGC 180
GCCCGGCTGC ACTCTAGCCT GGGCAACAGT GCAAGAGTCC GTCTCAAAAA AAAAAAAAAA 240
AGAGTAATAG ACTGTATTTC CCGAAGTATA TTCATGGCCT TGGATGTTGT TAACAAGCAT 300
TAAGATTTTA AAAGGGCCCG AGGTCAAACC ATTTAGGAAG AATGCCTAAT TCCCACAGTT 360
AAGGCTCGGT GGGTGGGCGC ATGCGCACAG GATCCTCGCC GTCAGGCACC TGCGGAACAC 420
ACTTGGAAAT CGCTTTTTCC GGAGGCCCAA TTTCATTTCA TTATACACCA CACCACACTG 480
TGCTGGGCTG TGGAGGAAGA ACGGGAAGCA GTTTTGGTCC AGTCCTCCAG GACCTAGTTT 540
TAGGAAGAGG GTGGCAAGGC AAAAAAAAAA AAGAAAAAAA GAAAAAAGAA AGCACAAATC 600
CAATTACAGT TATGAGTTTA TGACAAAGTT TCTATAAATG ACGGACCGCA TACAGACAGG 660
GCCCCATAAG ATTATGATGG AGCTGAAAAA TTCCTATGGC CTAGTGATGT CATAGCCTTC 720
TTAAGTCTTA GCGCAACCAA TGCATTACTC ACGTGTTTAT GGTGACGCTG GTGTAAACAA 780
ACCTACTGCA CTGCCAGTCA TATAAAAGTA TAGCAGAGGG GTCCCCAACC CGTGGATCAG 840
TACTGGTCCA TGGTCTGTTA GGAACCGGGC GGCACAGCAG GAGTTGAGCG GCGGGCCAGC 900
CCCCAAAGAA AGCTTCATCA GTACTTACAG CCACTCCCCA ACACTGGTTT TGCTGCCTGA 960
GCTCCGCCTC CTGTCAGATC AGCAGAAGCA TTAGATTTTC CTAGAATCGG AAACCTATTG 1020
TGAACTGCAT ATGCCAGGGA TCTAGGTTGT GCACTCCTAA TGAGAATCTA ATGCCTCATC 1080
|
