| Tag | Content |
|---|
EnhancerAtlas ID | HS050-30463 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr17:79694210-79695310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr17:79694216-79694226 | GTCACGTGAT | - | 6.02 | | FOSL1 | MA0477.1 | chr17:79695136-79695147 | CATGAGTCACC | - | 6.62 | | Foxd3 | MA0041.1 | chr17:79695167-79695179 | GTTTGTTTGTTT | + | 6.32 | | JUND | MA0491.1 | chr17:79695136-79695147 | CATGAGTCACC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr17:79695075-79695090 | TGAACTCTTAACCTC | - | 6.53 | | TFEB | MA0692.1 | chr17:79694216-79694226 | GTCACGTGAT | - | 6.02 | | YY1 | MA0095.2 | chr17:79694583-79694595 | GCAGCCATCTTG | - | 6.74 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24622 | chr17:79694215-79694862 | Colon_Crypt_2 | | SE_24986 | chr17:79694274-79694842 | Colon_Crypt_3 | | SE_27510 | chr17:79694061-79695025 | Esophagus | | SE_41699 | chr17:79694211-79694856 | LNCaP |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I081727 | chr17 | 79694338 | 79695210 |
|
Enhancer Sequence | TAAATAGTCA CGTGATGCTT CAGGTCATCT GACATCCTGC CCCCCACCCC TTAGTAAAAT 60
GCCTGCTGTT TTATTCAAGC AGCTACCACC CCACCCCAGT CCTTGGGCCT CAAGGGCACC 120
AGGGCCTGAC CCCAGCTCCC AGCATGAATA GGGTTGGTTT AAACCAGTCG GCATGGCCCA 180
CAGTGACTGG TTTAGGCATG GGCCTGTCAC CCACACTGGG CCAATGATAT GTAAGATGTT 240
TATTGTAGCT TCCGGGATGG AAACTTCTCT GCCAGCTTGT GGGTTGGGCA AGGACGACAC 300
TCCGGGCCCT ACCGGCGGAA GCTCTGCTCC TGTCGTGCGT GGACCACGCA GCAAATGGCC 360
TTGGAGGCTG CTGGCAGCCA TCTTGTGACC ATGAGGCAAG TCAGCGCAGG CCGAAGCTGA 420
CGACGCGAAG ACAATGAGGA GAGGGAGAAA GAGCCGATCT TTGGTGTGTA TTGGCTGTGA 480
CGTGCTGCCG CCTCTCTGGA GACCGGGTTC ATTATACTTT TCCTGGTATC TTCTCATGTT 540
TGCTCTGCTG GCTTTGGGCC CGAGTTTTAC CTCCTGGGTG TATTGTGTGT GCCTGTTTTG 600
TGGTGTTGGT TTTGCTCCTG GGTTTGTTGA CCCTTGGGTG TCTGCTCTTT TTTTTTTTTT 660
TTTTTTTTTT TGGGACAGAG TCTCACGCTG TCACCCAGGC TGGAGTGCAG TGACCTGATC 720
TTGGCTCACT GCAGCCTCTA CCTCCTGGGT ACAAGCGATT CTTCTGCCTC GGCCTCCTGA 780
ATAGCTGGGA TTACAGGTGC CTGCCACGGC TAATTTTTTT ACTTTTAGTA GAGATGGGGT 840
TTTGCCATGT TGGCTAGGCT GGTCTTGAAC TCTTAACCTC AGGTGATCTG CCCACCTCCG 900
CCTCCCAAAG TGCTAGGATT TATAGGCATG AGTCACCGTA TCCAGCATTT TTTGCTTGTT 960
TGTTTGTTTT GAGACGGAGT CTCGCTGTGT CACCCAGGCT GGAGTGCAGC GGTGTGATCT 1020
CGGCTCACTG CAAGCTCCGC CTCCCAGGTT CACACCATCC TCCTGCCTCA GCCTCCTGAG 1080
TTGAGTATCT GGGACTGCAG 1100
|
