| Tag | Content |
|---|
EnhancerAtlas ID | HS037-09570 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr12:120831600-120833050 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr12:120832754-120832764 | GCTAATTGGG | - | 6.02 | | ZEB1 | MA0103.3 | chr12:120832654-120832665 | CCCACCTGCCC | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65438 | chr12:120831662-120833343 | 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 |
| GH12I120394 | chr12 | 120831965 | 120833250 |
|
Enhancer Sequence | AGAGTCCTGA GTTCTGGACT ATGGGCTCCA TGCTTCAGTG AGTTATCTTA TTTTATTTAT 60
TTTCGTGACA AGTTTTTGCT CTGTCACCCA GGGTGGAATG CGGTGGCAGG ATCGCAGCTT 120
ACTGAAGCCT CAGCCTCCCA GGCTCAAGCG ATCTTCCCAC CTCAACCTCC CAAGTAGCTG 180
GGACCACAGG CACGCACCAC CACACCTGGA TAATTTATTT TATTTTATTT TTATGTTTTG 240
AGACAGAGTC TTGCTCTGTT GCCCGGGATG GAATGCGGTG GGGCAATCTT GGCTCACTGC 300
AACCTCCACC TCCCGAGTTC AAGCGATTCT CATGCCTCAG CCTCCTGAGT TGCTGGGATT 360
ACAGGCGTGT GCCACCACGC CCAGCTCATT TTTGTATTGT TAGTAGAGAC AAGGTTTTGC 420
CATGTTGGCC AGGCTGGTCT GAAACTCAAG TGATCCTCCT GCCTTGGCCT CCCAAAGTGC 480
TAGGATTACA GGCATGAGCC ACTGCGCCTG GCCCAGTTAC TTATTTTAGA AGTTATATTT 540
GAGCACCTAT TCTGTGCCGA GCCCTGGCAT GAGCTGTGAA CAGGCCATAT CTATCCTAGA 600
TGTGCACTAA TGGGGCTTTG GAGGGTGGCA ACAGGAGGCC CGGTGAAATC CCCGGTGAGA 660
GCAGCCTTTT CGCCGTGGCC TGCCGTGAAG CACTATGGCA GCACCCACAC CTGCCAGGAC 720
TGAAGGTATT GTCGGGCCCT CTCCTGCTCC CAGCTGCAGC CAAGGCCGTG TGTACAGGGC 780
CCTTTAAGTA GTCTGTGCCC TCCCTAATTA ACCAGCTAAA GAAAGAGCTG GCTTGAAATG 840
GGATTGTGCA GACCCAGCTT TGGGACCCGA GGACGCCGGA TCGGGGATTG TTATGCTAAT 900
CGCCTGAGAT CAGCAGTTCC CGTGCCCTTC AGATGGCAGG TAGCGAGGCC GGGCTCTGCC 960
CAGCGGCTGT GGCTACAGGA GGCCAGGCTT TTCCTCCAGC TTCCGGCTTC CTCTGTTCCC 1020
CTCCTTACCC CGTCAGACTT GCCCTGCCTG TCCTCCCACC TGCCCGTTGG CTGGAAGGCT 1080
TGGCGTCTCC TAGAAATGTC CAGGCCAGCT CCTCCCACCC TCCAAAGAGA AACCTGCTTG 1140
CCTTCAAGCT GGGCGCTAAT TGGGGATGCA GAGGCAGGAA GGAGAAGGTA CCCAGCTCCT 1200
CCTCCTGTAT AACCCATTCT CATCTCCAGG CATGAGAGCC TCATTGGTCC CTCCTGCCCC 1260
CTTGGGCTCT GGAAAACACA CTAGGTGGTG CCTTTGCCGC TTACTAACTA TACCATTTTG 1320
GGCAAGTGAC TGCCTCTCAG AGCCTCAGTT TCCTAATCTG TAAAATAGGT TGATAATAAC 1380
AGTAGCTACC TCAAAGGGTT GAAATGAGAA TAGAATGAGA ACAGGCATCT AACATAGCCA 1440
GTTCAATTGC 1450
|
