| Tag | Content |
|---|
EnhancerAtlas ID | HS002-05206 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr2:43206360-43207540 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr2:43206415-43206426 | TGCTGTTTACA | + | 6.14 | | ZEB1 | MA0103.3 | chr2:43207250-43207261 | GGGCAGGTGGG | - | 6.14 | | ZNF263 | MA0528.1 | chr2:43206384-43206405 | GAGGCAGGAGGAGAGGAGAGA | + | 6.16 | | ZNF263 | MA0528.1 | chr2:43207050-43207071 | TCTCCCCTTCCCTCCTCCCCA | - | 6.85 | | ZNF263 | MA0528.1 | chr2:43207047-43207068 | GCCTCTCCCCTTCCCTCCTCC | - | 7.4 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27836 | chr2:43203983-43208787 | Fetal_Intestine | | SE_28610 | chr2:43200706-43208896 | Fetal_Intestine_Large |
|
| | 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 |
| GH02I042973 | chr2 | 43200849 | 43208785 |
|
Enhancer Sequence | GGTCCACAAA GGGCTGTGTA TCAAGAGGCA GGAGGAGAGG AGAGAGAGTG AGTGATGCTG 60
TTTACAGCAG GACCAGCTCT AGTGCTTGTT ATATGCGTAC GTGATCCTGT TTGATCATCC 120
TAAACAGTGA TGAGAGCAGG GTGCTATTAC TATGGCCATT TCATAAACGA GGAAACTGAG 180
GCATAAATCG GGCCACTTGT CCAAGTCCTG GAGCTGGGAA ACAGCAGAGC AGGGGCAGTC 240
TGATTCCTGA CCTGGGTCCG GTATAACTCT GTTATCTGCA GGGAGCAGGG CAGAGGGGCA 300
ATGCAGGAAG GGGAAGGGGC TCCATGCAGC TGCGGGTTGC AGAGAAGAGG CCCAGCGAGA 360
CCAGGCCTCT GGCTCAGGGC ATGCCTTTGA GGTGGAGGTG GGGTGGGAAT CTGGCTTCTT 420
CTCGATAGGG AAGGAGAATG TGTGTGCTGG CCTCTGGGTG TCAGGCAAGT GTGTCCCAGG 480
CTGGCTTGCT CCCACAGCCC CCACCTCCTC TTCCCCTGGG GCTTTACCGG TGAGAAGTCA 540
ATATTGATGT TTTATGACCC AAGATAAACA CACATTTTTT TCCTCCCATG GAGGGTTTAT 600
CTGGTCTAGA GGGTTAATCA ATGACCACTT GGAGGTGGGG GAAGCCTCTG AGAAGAAAGC 660
AGCTATTCAA TTCCAGCCCT TTACCCAGCC TCTCCCCTTC CCTCCTCCCC ACTACCACCT 720
CCCCTCCCAC CCTCTAGTGG GGACTGACCT GGCCCTGCAA GTGGGTGGGG GCAGGACATT 780
TGGGAATCTG AGGCTGGAGT CCATGTGGGT GCGTTCAGGG GACTGTTAAG TAGGATGCAT 840
CCAAGGAGAG TGTCCCTAGA GCTGTGTTTG CCCTGAGCAC GGTGTTGGCA GGGCAGGTGG 900
GCCCTGCATG TGGCTGTCAT GGGACCAGCC TGGTTAGGAG TGGGAAAGAG AAAATAAGTC 960
TCGTGTCACA GAGCACTCAG AGATGACACA AGATAATGCG GGTTGCTCCT CTTGAGAACA 1020
GGGGCACTGG AGCACAGTGT GGGGCCCGAC CCTGCCTCTT ACCTGCTGTA TGGCCTTGGA 1080
CAGGTGGCTT CACGTCTCTG GGCCTCAGGT GCCTCCTGTC TCCTCTAGGG TGGTTTTGAG 1140
AATCAAACGA GATCCTGTAC TTGCAGAGGA GAGAACGCAA 1180
|
