| Tag | Content |
|---|
EnhancerAtlas ID | HS012-00664 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr1:156341170-156342130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MITF | MA0620.2 | chr1:156342042-156342060 | AGAGGTCATGTGACCTGG | + | 6.91 | | MITF | MA0620.2 | chr1:156342042-156342060 | AGAGGTCATGTGACCTGG | - | 6.91 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35485 | chr1:156336383-156344399 | HepG2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 156341510 | 156341619 | | chr1 | 156341373 | 156341652 |
|
Enhancer Sequence | GAATTCCTGA CCTCAGGTGA TCCACCCACC TCGGCCTCCC AATGTGCTGG GATTACAGGT 60
GTGAGCCACT GCACCTGGCC CTATTACCCT ACTTTCTGTA TGCAGAGCTC ATCAGCAGGC 120
TATCCCCACC TCACCCTGTT CTAGACCCAA CAAAATGAAG CTCAAAATGC TAAGGATATA 180
GAGAGTGAGG TGGAAACTTG GACTTGGGTG TGAAGCACCA GAGCCCCCAC CCACCCTAGG 240
CAGAAGGGGC TACAGCTCCT CCCTCCCCAT ATTTCATCCA CAGCCCTGGC TAGAAAAGAA 300
GGATAGAGAG TTGGGAGGGA ACAGTCCAGA GTCTGACAGA ACTAAGCTGT TGCGTAAGGG 360
TCTGACCTGG CTGCTTGCCA TGAACCCCTG ACTTGCTTCT CCTCGAAGCC TCCTTATTAC 420
AAAGCTTTCC CTGGAGTCCA GCCTCTTGCC CCTGTGCTGC AATGGTAGGC TCTCCTTGGA 480
CATACAGCAT TTCATCCCTG AATTGCAATA AGAGAGATAT AAAAGGTGGG ATTCCTACTT 540
CTTTTTCTGC CCTAGGTTTC CATTCCTGTG GACTTGGATA CTGTTGTGGG GGAAGGTTGG 600
GGAGGCGGGA GGTGCAAGGT CCCTAGAGCC TGGGGCTTTG ATGAGCCGGG TCCTCACCTG 660
TCCTTGTGCC CAAGGGAAGG GGTCAGGGCC AGAGGGAGGT GCAGCCACTG CCCTTTGATT 720
CGGGAGATGA AAGGGAGTTG TGTGACTGTT GTTGAGCTCC AGGACTGGCC AATGCCAAGA 780
CATGGCTAGT CTGAGGGTCC GTCTGTTTTC TCTGCTGGAA GGACGCTGAG AGCCCATCTG 840
GTTCACCCAC TCAGATGCTG AGAGTGAGTC AGAGAGGTCA TGTGACCTGG CCAAGTCACA 900
CAGCAAGTTA CAGAAGGAGC CAGGCTAGAA CCAGGTCTCT TGATTGCCCA TCTGTGGCCT 960
|
