| Tag | Content |
|---|
EnhancerAtlas ID | HS050-14431 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:129723040-129724500 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr11:129724313-129724328 | AGGTGACTCAGCACA | + | 6.38 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27353 | chr11:129722906-129725277 | Esophagus | | SE_27846 | chr11:129723063-129724609 | Fetal_Intestine | | SE_35121 | chr11:129721033-129725996 | HeLa | | SE_36539 | chr11:129723345-129724382 | HMEC | | SE_64293 | chr11:129722901-129725891 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 129723044 | 129723175 | | chr11 | 129723853 | 129724184 | | chr11 | 129723312 | 129724437 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I129852 | chr11 | 129722635 | 129725772 |
|
Enhancer Sequence | AGTGGGAGAG AAAAAGCAGC AGAGGGCTGT TGAAGAGGAA TTTTCCTTCA CTCTGCCCCA 60
TTCCAACAAG ATCCACCCAC TCCCACTGTT TCCTTCGCAT CCACTCCGCT CCACTGCGGC 120
CCTCCAGGAA CAAGCAGTGA TGACAGTAAC AAGTGTTCTT CCTCAGGACC AGCCCCACCT 180
GGGGGGAATG AGGGGTCTTA ATCTGCAACT GACAATTACC ACTTGTCATC AGTGGCCTAT 240
GGCTTCTTGG AGAGAGTGAA GCAACATCGC TTCTCTTGGA GGAAGCAAAG CTTCACAGGG 300
CTTTGTTGGT CTCATCCTGC TGAATGTCCC CACTCACCAT TCAGGCATCA GAGAGGCCTC 360
CCGTGAGAAG TGACAGGGAC CTGTGGCTTA AAGGATCAGG ACAGCATCAA CCTTGCCTAA 420
ATAAAGCTAG GACAATTACA ATATTTGGCC CCTTGACTGG GTGAAAATGG TACTCATTCA 480
ACAGCTCTCT GGCACTCCTA CCACAAGCCA GGAAGTCACT GTTCCAGGCA TAGGAGATAC 540
ACTGGGGAAC CACACAGCCG CTGCTGTCAC AGGGCTTCCA TTCTAGTGTC ACTGGGACTT 600
TTCCTGGGTC ATTTCCACAA CTTCCTGACT CTGTGTGTGG GAATTCAAAA AGGGTCTGGC 660
TTGAGAAACA AGTATCTGGG AAACGGAGTC CAAAATGTCA TCATGGAGGA TTTCTTCTAG 720
GCTTCCCCAA GAACACTTTG GGTACCAGGC ATAAAGACAA ATCTTTTGCC TTCCAAATTA 780
GCTGATAAAA GTAGAAGGGA TAAGAACTAA GAGCTATCCT GTGTCGCAGT TTCGTCATTT 840
TCTGGCCCAC ATCCTGGGGC CTCTGCCTTG TTTACCCGGT GTTTTAAAAC ACACAGCTGG 900
GAGGGGCGCA GGGCTTGCAG AGCTGGCTCT GTGCCCAGGA AGGACACGCA CTCAAAATCA 960
GCCCTGCAGA CACGCACCTG GGAGCCGCTT CCCTCCCTTG GCACGTACAG GTATCTTCAT 1020
TACCAGTGTG TCTCTGCTCA GATTCTGCTT TCAGCCTAAT TGTTTCTGTC TGGGATTTCT 1080
TTCACTGCTC ACTTGGCAGG GAAGCCCAGA GATTATTCTA TCAGCCACAC TCCGACTTAA 1140
GTGATGATGT CTTGCTCATC TCTGCTCCTG GACAAACCTC CTGGGGATCT ATGTGTGTGT 1200
GGTTGTGTTC ATTGATTCTT CTACCCTCAA CCCCAAACCC CTAAAAGGAA CAACAATGGC 1260
AAGATGTCTA CACAGGTGAC TCAGCACACA CCCTACTTTA TACTGAAGCA GCTGCACCTG 1320
AGGCAGCAAA GTAGCTCTGC TGACCCGCGG GCCACCCTCA CCTCACCCCA TCTCCGCTTC 1380
GCTCATGCCT TTGGGTTATT CCTTGCTCCT ATTTGTCTTA GAGCTACTCT TCCCTCTAAA 1440
ACATCCATCC TCATTTCCCT 1460
|
