| Tag | Content |
|---|
EnhancerAtlas ID | HS042-03955 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:226287950-226289160 |
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 | GCAAACAACA GGTAAGAGTC CCAAACTGCT GCTTGAAAGA GAAAAATCCC TTTGGAAGAC 60
CACGGTAATA ACTACTACTA ATGTGTGGGG GTTTTGTTTG TTTTTTGTTT TTGTTTTTGT 120
TTTTGTTTTC AGAGGGAGTC TCGCTCTGTC GCCCAGGCTA GAGTGCAGTG GCACCATTTC 180
GGCTCATTGC AACCTCCACC TCCCGGGTTC AAGCGACCCC AGACTCCCGA GTGGCTGCGA 240
TTACAAGCAC CCGCCACCGC GCCCGGCTGC ACTCTAGCCT GGGCAACAGT GCAAGAGTCC 300
GTCTCAAAAA AAAAAAAAAA AGAGTAATAG ACTGTATTTC CCGAAGTATA TTCATGGCCT 360
TGGATGTTGT TAACAAGCAT TAAGATTTTA AAAGGGCCCG AGGTCAAACC ATTTAGGAAG 420
AATGCCTAAT TCCCACAGTT AAGGCTCGGT GGGTGGGCGC ATGCGCACAG GATCCTCGCC 480
GTCAGGCACC TGCGGAACAC ACTTGGAAAT CGCTTTTTCC GGAGGCCCAA TTTCATTTCA 540
TTATACACCA CACCACACTG TGCTGGGCTG TGGAGGAAGA ACGGGAAGCA GTTTTGGTCC 600
AGTCCTCCAG GACCTAGTTT TAGGAAGAGG GTGGCAAGGC AAAAAAAAAA AAGAAAAAAA 660
GAAAAAAGAA AGCACAAATC CAATTACAGT TATGAGTTTA TGACAAAGTT TCTATAAATG 720
ACGGACCGCA TACAGACAGG GCCCCATAAG ATTATGATGG AGCTGAAAAA TTCCTATGGC 780
CTAGTGATGT CATAGCCTTC TTAAGTCTTA GCGCAACCAA TGCATTACTC ACGTGTTTAT 840
GGTGACGCTG GTGTAAACAA ACCTACTGCA CTGCCAGTCA TATAAAAGTA TAGCAGAGGG 900
GTCCCCAACC CGTGGATCAG TACTGGTCCA TGGTCTGTTA GGAACCGGGC GGCACAGCAG 960
GAGTTGAGCG GCGGGCCAGC CCCCAAAGAA AGCTTCATCA GTACTTACAG CCACTCCCCA 1020
ACACTGGTTT TGCTGCCTGA GCTCCGCCTC CTGTCAGATC AGCAGAAGCA TTAGATTTTC 1080
CTAGAATCGG AAACCTATTG TGAACTGCAT ATGCCAGGGA TCTAGGTTGT GCACTCCTAA 1140
TGAGAATCTA ATGCCTCATC TGTCACTGTC TCCCATCACC CCCAGATGGG ATGTCTAGTT 1200
GCAGGAAAAC 1210
|
