| Tag | Content |
|---|
EnhancerAtlas ID | HS184-06977 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:129723070-129724500 |
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: 2 | Chromosome | Start | End |
| chr11 | 129723853 | 129724184 | | chr11 | 129723312 | 129724437 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I129852 | chr11 | 129722635 | 129725772 |
|
Enhancer Sequence | TGAAGAGGAA TTTTCCTTCA CTCTGCCCCA TTCCAACAAG ATCCACCCAC TCCCACTGTT 60
TCCTTCGCAT CCACTCCGCT CCACTGCGGC CCTCCAGGAA CAAGCAGTGA TGACAGTAAC 120
AAGTGTTCTT CCTCAGGACC AGCCCCACCT GGGGGGAATG AGGGGTCTTA ATCTGCAACT 180
GACAATTACC ACTTGTCATC AGTGGCCTAT GGCTTCTTGG AGAGAGTGAA GCAACATCGC 240
TTCTCTTGGA GGAAGCAAAG CTTCACAGGG CTTTGTTGGT CTCATCCTGC TGAATGTCCC 300
CACTCACCAT TCAGGCATCA GAGAGGCCTC CCGTGAGAAG TGACAGGGAC CTGTGGCTTA 360
AAGGATCAGG ACAGCATCAA CCTTGCCTAA ATAAAGCTAG GACAATTACA ATATTTGGCC 420
CCTTGACTGG GTGAAAATGG TACTCATTCA ACAGCTCTCT GGCACTCCTA CCACAAGCCA 480
GGAAGTCACT GTTCCAGGCA TAGGAGATAC ACTGGGGAAC CACACAGCCG CTGCTGTCAC 540
AGGGCTTCCA TTCTAGTGTC ACTGGGACTT TTCCTGGGTC ATTTCCACAA CTTCCTGACT 600
CTGTGTGTGG GAATTCAAAA AGGGTCTGGC TTGAGAAACA AGTATCTGGG AAACGGAGTC 660
CAAAATGTCA TCATGGAGGA TTTCTTCTAG GCTTCCCCAA GAACACTTTG GGTACCAGGC 720
ATAAAGACAA ATCTTTTGCC TTCCAAATTA GCTGATAAAA GTAGAAGGGA TAAGAACTAA 780
GAGCTATCCT GTGTCGCAGT TTCGTCATTT TCTGGCCCAC ATCCTGGGGC CTCTGCCTTG 840
TTTACCCGGT GTTTTAAAAC ACACAGCTGG GAGGGGCGCA GGGCTTGCAG AGCTGGCTCT 900
GTGCCCAGGA AGGACACGCA CTCAAAATCA GCCCTGCAGA CACGCACCTG GGAGCCGCTT 960
CCCTCCCTTG GCACGTACAG GTATCTTCAT TACCAGTGTG TCTCTGCTCA GATTCTGCTT 1020
TCAGCCTAAT TGTTTCTGTC TGGGATTTCT TTCACTGCTC ACTTGGCAGG GAAGCCCAGA 1080
GATTATTCTA TCAGCCACAC TCCGACTTAA GTGATGATGT CTTGCTCATC TCTGCTCCTG 1140
GACAAACCTC CTGGGGATCT ATGTGTGTGT GGTTGTGTTC ATTGATTCTT CTACCCTCAA 1200
CCCCAAACCC CTAAAAGGAA CAACAATGGC AAGATGTCTA CACAGGTGAC TCAGCACACA 1260
CCCTACTTTA TACTGAAGCA GCTGCACCTG AGGCAGCAAA GTAGCTCTGC TGACCCGCGG 1320
GCCACCCTCA CCTCACCCCA TCTCCGCTTC GCTCATGCCT TTGGGTTATT CCTTGCTCCT 1380
ATTTGTCTTA GAGCTACTCT TCCCTCTAAA ACATCCATCC TCATTTCCCT 1430
|
