| Tag | Content |
|---|
EnhancerAtlas ID | HS050-38196 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:128282390-128283750 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr2:128282960-128282971 | AAGCACTCAAG | + | 6.02 | | RREB1 | MA0073.1 | chr2:128282710-128282730 | GGGGTGGGGGTGGTGTTGGT | - | 6.57 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_19088 | chr2:128282403-128286609 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_27871 | chr2:128282507-128286757 | Fetal_Intestine | | SE_28747 | chr2:128282686-128286988 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TAACTTAAAA ACACAAATGA ATGGAAAAAA AACTATTCTG AAAGTATCAG GAAAGTGTTT 60
TTTTGTTTTT GTTTTTGTTT TTGTTTTTTT TGAGACAGAG TCTTGCTCTG TCGCCCAGGC 120
TTGGAGTGCA GTGGTGCAAC TTCCGCTCAC TGCAACCTCT GCCTCCCGGG CTCAGGGCTC 180
AAAGGATCCT CCCACTTCAG CCTCCTGAGT AACTGGGACT ACAGGTGTAT GCCACCACAC 240
TCGGCTAATT TTTGCATTTT TTTGTAGAGA CGAAGTAGGG GGGTGGGGTA GGGGCGTAGG 300
GGGGTGGGGT ACGGGCATGG GGGGTGGGGG TGGTGTTGGT CTCACTATGT TGCCCAGGCT 360
GGTCTCGAAC TCCTGGGCTC AAGCCATCGG CCGCCTACGC CTCCCAAAGT GCTGGGATTA 420
CAGGCATAAT CCACCGCACC TGGCTTAGGA AAGTGTTTTT AAGCAGTGCA TGCCTGGAAA 480
ACGCTTTGCA GTCATTAGAA TTCACTGTCC TACGTAAGGA AAAGCAATGA ACTCAAAACA 540
GTAAAGGGCT TAACGCTTAA ACAATTATTT AAGCACTCAA GTTTTCTTTT TAATTTTCAA 600
TTTTTGTGGG TACATAGAGG GTGTATTTAT TTATGGTGTA TTTAAGAACT TTTGTAACAG 660
AACGCCCCAA CAGGACTAGC ACACAAAGGG AAAGCAAATG CGACGTGTTT CCCACACCAG 720
GTTCTGCCTC ACTTATCCTT AATCTCAGGT GCCAAGCACC GTGCCAGCAG AGTGGGCCCC 780
AGTAACAGCT TACAGAATAA ACAAACAGTA AAGAAAGGAG ACCAAACTTC GGTGAGGAGG 840
AAGAGGAACG ATCTCAAGGT GGAGGAAAGG CACAAAAACC ACCAGTAAGT GCCAGAAGCG 900
CATTCCTTAC TCTATGCATG CAACTGAAAC ATGGGTCCTG CACTTACGTC CGGTGTTGCA 960
AGCAAGATTA AACCACTCCT AACTAGCAGT GAAAAGTCTA GGAAGGATCC CCCGCCCCAA 1020
CGCCCCTTGG ATTCTCCAAC TACTCAACTA CTGAAAACTC TCTTAACAGA AGACACCTCT 1080
CCTTCCCTGC ACACAATAGG AGCTTAACAT ATGAAAGTGA CTTCCCAATT TCAGCAAAAA 1140
CCTTCGCCGA TTCAGAAGAA AGCTTTCCCA CCAGAATCCC CTCTCCAACG TTCTAGCTTC 1200
GACGCTTGCA GCTGGTCAGA GGGCTCTTGC CCTCCTCGGG CCGGGTCGCG GGAGGGAAGG 1260
TTTCGGGGGG CCTCCTTGCC CCCACCCGCG GGGTGCCAGG CCAAGCCCCG CCGAGTAACT 1320
GCTCCGCCTC CCAGCCCGGT CCCCCAGGTC CCTGCCCCAC 1360
|
