| Tag | Content |
|---|
EnhancerAtlas ID | HS040-02555 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:159819580-159820320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr1:159819773-159819783 | AACATATGTC | + | 6.02 | | TFAP2C | MA0524.2 | chr1:159820261-159820273 | TGCCTTAGGGCA | + | 6.04 | | TFAP2C | MA0524.2 | chr1:159820261-159820273 | TGCCTTAGGGCA | - | 6.32 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27216 | chr1:159818257-159820698 | Esophagus | | SE_34829 | chr1:159819258-159820570 | HeLa | | SE_56622 | chr1:159817508-159821445 | u87 |
|
| | 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 |
| GH01I159848 | chr1 | 159818381 | 159820253 |
|
Enhancer Sequence | ATCTGTATCA TGGAAATACT ATACAATCAT GTGCTACTAA ACATTTCTCC CAATTCCATG 60
CCAGTCACAT CATGTTGGTA GCTTGAATTC AGCCATAGTG GAAGCATTGA CATCATGGAA 120
ATCAGCAAAG GCTACAAATC AGGGCTTCCC AGTCCCTACC CCACCCTACA CCCTACTCCC 180
AAAGCCACTG TTGAACATAT GTCACCACAA GTGCTCTCCT CCAGCACTGA ACAAGGTTTC 240
ATGCAGGAGA AATGAACAAA AAACACCAAG GCATCCCTGA AGCAAAATTG TTCAAACAGA 300
AACTTCCTTC CCTCGTTCTC CTGGGGTGGT AAGTACAGTG ACGACTGTGA TCTCAGCATT 360
GGATTTAGGA AATCTCTACC TTCCCTGTTG ACTCACCCTA ACAGGAAGCT GTTCTCAGAG 420
TCTCTATAAA ATCTCTCTTG CTGCTCTTTA GTGAGCCTTT CTTGCCAGAG CCTCACTGGT 480
CCCACCCCCC AAATAGAGGC CAAGTCTGAT CATGGCTCCC TTGTTCCTGG AATAGGGAAG 540
ATTATATCAT TCAACAACCT GCACAGCCAA CTGGCTGCCT CTGTCCCTCA GCACCTTTCA 600
GGAAGCTAAG CTGGAGGCTC CTCAGACAGG GAGCACCCTC CCCAAGTCAT CCTATACCAT 660
CCCCTGCCTT AGGGGATATT TTGCCTTAGG GCAAAAATAT GCCAGGCACA GTGCCCTGCT 720
GAAGATCTCT TCATCTATGA 740
|
