| Tag | Content |
|---|
EnhancerAtlas ID | HS050-03286 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:92030270-92031740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:92031439-92031460 | GGAGGAGGTGAAGCAGGAAGC | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_44373 | chr1:92029151-92034320 | NHDF-Ad | | SE_45456 | chr1:92029980-92031594 | NHLF |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 92030478 | 92030600 | | chr1 | 92030600 | 92031000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I091564 | chr1 | 92030086 | 92031533 |
|
Enhancer Sequence | ACCATGAGTT CATAACTGTT GAAGTTGAGT GATAAGCACT GTTTTAGATG TTTGAAATCT 60
TGCGTATTCA TCTACCTGTG TACATACTTA GAATTTTCCA TAATACACAG TTTAAAAATA 120
ATACCAACCC TGTACCAGGA ACTAGGCTGG CATTGACACA CCTAAGCCAT GAATTGGCAT 180
CACAGAAAAA CACTGTCAGA ACTTTTCCTT CATGACTTAC ACATGTGGGA AGGGAGAGGA 240
ACTTGGTGGC AACGCCCTTA ACTCTCCTCT GACTTGATGA ATATGCAGTT TCCTTTGCCA 300
AATTGGAAAT TGAGAGGAGA ATGCAGCCCT GTCTAAACTA GCTTCTCTGC AGAGCTTGTT 360
GAAGGCCGGA ACCATTACTC AGGGTCCAGC TGCACAGCAT TCTCATCCAC CCAGCAACAC 420
ATGCAGAGAG CTGTGAGATC AACATAGGGC CACATGTGGG TTTGAACAAA GAACAGTCAG 480
ACAAAAGCCC TACAGACGCT CCTGACCTCT CTCTTGGCCC CTGGGCCTTC CATGGAAATG 540
CGAACTTTCC TTTGACACTC ACATGACACC CTTTGGCCCT TAACAACAGT CCTATAGAGA 600
GTGGGCAGTG CCCTTTGGCT GCATCAAGGG CAGGGGGCTC AATGCTCTAA ATTGCTGGCA 660
TTCACACCAC AATCTCCTCT TATTTCTAGG CCCCACCCTA TTTATACTTT AGCTTTGTGG 720
CATTTGAGAG TAGAAACATA AATTCAGCTA GACACTCCAC TGCCCAGAGG GGTGACCTTT 780
ATTGTACATG CCTGGGATGT TTTCCCAGGG AATCCAAGAG AAAATGGCTT CATCAGAGAT 840
GTGTGGTACT ATAGAAATGC CTAACCAGGG CCTGCGCCTG GGCACAGGTC TCCCTGGCTT 900
GCACGTGACT TGAATTTGGC TTGCAATGAG GGAGTATTTC TGTGGGGGCC CATTCATTCA 960
CTCATTTACT CAAGCACATG CTGAGCCTCA ACATTAGAAG CTCTGGAAGA TACAAAGAAG 1020
AAAAAGACAA AGTCTTTGCA TGGAAAAGCT CTCAGGTAGG TCGGGGAGAA AGACATATTC 1080
ACAAATAACT TCAATTTAAG GCAAGGTGTG ATCAGACCAT GACTGAGGAG TTCAGAAAAG 1140
GAGAGAAAAT TCCCAACTGC AGTAAAGTTG GAGGAGGTGA AGCAGGAAGC AGATGTTAAA 1200
AGCTGAATAA AATTTTAGGC CGGGCTCAGT GGCTCATGCC TGTAATCCCA ACACTTCGGG 1260
AGTCTGAGGT GGGTGGATCA CCTGAGGTCA AGAGTTCCAG ACCAGCCTGG CCAATATGCT 1320
GAAACCCCAT CTTTACCAAA AACACACAAA AACTTAGCCA GGCATGGTGG CGGGTGCCCG 1380
TAATCCCAGC TACTCGGAGG CTGAGGTGGG AGAATCACTT GAACTCAGGA GGCAGAGGAT 1440
GCAGTGAGCT GAGATCACAG CACTGCACTC 1470
|
