| Tag | Content |
|---|
EnhancerAtlas ID | HS050-36808 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:65066970-65068140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr2:65067626-65067641 | TTCTATTTCTAGCCC | - | 6 | | SOX10 | MA0442.2 | chr2:65067900-65067911 | AAAACAAAGAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_00723 | chr2:65063555-65069256 | Adipose_Nuclei | | SE_09303 | chr2:65064566-65069966 | CD14 | | SE_10494 | chr2:65066427-65068370 | CD19_Primary | | SE_11245 | chr2:65064554-65070071 | CD20 | | SE_45951 | chr2:65063316-65068513 | Osteoblasts | | SE_53747 | chr2:65066675-65067868 | Spleen | | SE_62791 | chr2:65045447-65101119 | Tonsil |
|
| | 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 |
| GH02I064836 | chr2 | 65063814 | 65069733 |
|
Enhancer Sequence | ATGATATCGT GTATTTCATC AATTCTAGGA TGTGCAGCTT TTTGCATCTT AATCTCTCTG 60
AAATTGGGCT ATGTCTTACA GTTGATATGG GGGTAGGAGA TGGTGTATTC CCACTCCTAG 120
ATCGACTGTA GTGCCTCTAG GAGTGCCCTG CCAGAGAAGC CCACACTCCA CCTCCTGAGC 180
CAGGGTGGCC ATATGACTTG TCCTGGCCAA TGGAGTGTGA AGCAAGCAAC ATCTATCACA 240
TCCGGGCTGC ACTTTCAAAG GCAACTGTCG TTCAGCTCAT GCTCCTTTTC ATCCACGTCA 300
GCAGCCAGCA AAGTTCCAGA TGGAGGCTGT TTCGTGGGCC CTGTCCCACA GTAAAGAGGA 360
TGTAGAGCTG AGCTGCAGCT GGTGGGCATT GAACAGAAGC ATAAACCTTT CTTCTTTAGC 420
CATTGAGATT GGGGTTCTGT GTTTTGACAG CACAGTCTAG CATATCCTGA CTGGTATTTC 480
ATGCTCCAGT TAATTGACAG ATTCCTTTTT CTTTCTTAAT ACATAGTGGT GTAACTCACA 540
ATTGTTGGTA TTGTTGATTC AATGAAACAC GGTAGTGCCT CTTACAGACT AATGTAGGTA 600
AATCACTTAG CACAATGCCT GGCCCACAGT AAGTGTTCCA TTCATGTTAG CCATTGTTCT 660
ATTTCTAGCC CTCTGCATGT AGCCAATGTT TAATACATGC TTGGAGGATG ATACTGATGA 720
CACATGAGAT CAGAACCCCC CTTAGATCCC TTGTGGCATG AGAAAGAGTA TCGTAAAAGA 780
CAAAATTACA ACAAATTTAG TTTAAAGATC TCAACAAGCT TTGTTGCAAT TCTAAAATTG 840
GGCAACACTT CGTTCCATAA AACAGAATAA GTGTCCAATG AACTGAGGAG AAGAGGCTGG 900
CTTTACAGAC AGAAAAGGCT GAAGAAAGCA AAAACAAAGA ACAAAAAGCA GATTGATCAT 960
TTCAAAGTTA CTTGCCTTGT AAGGCGGGAC AGGGAGATGG AAGAGTAGAA AAATCACTGA 1020
TCAGTGAACC TTGTGTTACT TCGGGCTAAC TTTTGCATGT AAGGATTAAG GCAGAGGAAA 1080
CTTCATTATC GTGCCAACTG AAGATTGAAA CTGGCCTGTT TGGAAAATTG GCTGTTACCT 1140
TATTTCTCAG AAGGTCAGAT AACTTAGTTT 1170
|
