Tag | Content |
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EnhancerAtlas ID | HS147-10297 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr11:129722970-129724500 |
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 |
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| 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 |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I129852 | chr11 | 129722635 | 129725772 |
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Enhancer Sequence | CCCACTGGCT TATCTTCATC CTCAAGTCTC AAGCGCTTAT AGAGAGTTTA TGTAGATTCG 60 TAAATTAGCC AGTGGGAGAG AAAAAGCAGC AGAGGGCTGT TGAAGAGGAA TTTTCCTTCA 120 CTCTGCCCCA TTCCAACAAG ATCCACCCAC TCCCACTGTT TCCTTCGCAT CCACTCCGCT 180 CCACTGCGGC CCTCCAGGAA CAAGCAGTGA TGACAGTAAC AAGTGTTCTT CCTCAGGACC 240 AGCCCCACCT GGGGGGAATG AGGGGTCTTA ATCTGCAACT GACAATTACC ACTTGTCATC 300 AGTGGCCTAT GGCTTCTTGG AGAGAGTGAA GCAACATCGC TTCTCTTGGA GGAAGCAAAG 360 CTTCACAGGG CTTTGTTGGT CTCATCCTGC TGAATGTCCC CACTCACCAT TCAGGCATCA 420 GAGAGGCCTC CCGTGAGAAG TGACAGGGAC CTGTGGCTTA AAGGATCAGG ACAGCATCAA 480 CCTTGCCTAA ATAAAGCTAG GACAATTACA ATATTTGGCC CCTTGACTGG GTGAAAATGG 540 TACTCATTCA ACAGCTCTCT GGCACTCCTA CCACAAGCCA GGAAGTCACT GTTCCAGGCA 600 TAGGAGATAC ACTGGGGAAC CACACAGCCG CTGCTGTCAC AGGGCTTCCA TTCTAGTGTC 660 ACTGGGACTT TTCCTGGGTC ATTTCCACAA CTTCCTGACT CTGTGTGTGG GAATTCAAAA 720 AGGGTCTGGC TTGAGAAACA AGTATCTGGG AAACGGAGTC CAAAATGTCA TCATGGAGGA 780 TTTCTTCTAG GCTTCCCCAA GAACACTTTG GGTACCAGGC ATAAAGACAA ATCTTTTGCC 840 TTCCAAATTA GCTGATAAAA GTAGAAGGGA TAAGAACTAA GAGCTATCCT GTGTCGCAGT 900 TTCGTCATTT TCTGGCCCAC ATCCTGGGGC CTCTGCCTTG TTTACCCGGT GTTTTAAAAC 960 ACACAGCTGG GAGGGGCGCA GGGCTTGCAG AGCTGGCTCT GTGCCCAGGA AGGACACGCA 1020 CTCAAAATCA GCCCTGCAGA CACGCACCTG GGAGCCGCTT CCCTCCCTTG GCACGTACAG 1080 GTATCTTCAT TACCAGTGTG TCTCTGCTCA GATTCTGCTT TCAGCCTAAT TGTTTCTGTC 1140 TGGGATTTCT TTCACTGCTC ACTTGGCAGG GAAGCCCAGA GATTATTCTA TCAGCCACAC 1200 TCCGACTTAA GTGATGATGT CTTGCTCATC TCTGCTCCTG GACAAACCTC CTGGGGATCT 1260 ATGTGTGTGT GGTTGTGTTC ATTGATTCTT CTACCCTCAA CCCCAAACCC CTAAAAGGAA 1320 CAACAATGGC AAGATGTCTA CACAGGTGAC TCAGCACACA CCCTACTTTA TACTGAAGCA 1380 GCTGCACCTG AGGCAGCAAA GTAGCTCTGC TGACCCGCGG GCCACCCTCA CCTCACCCCA 1440 TCTCCGCTTC GCTCATGCCT TTGGGTTATT CCTTGCTCCT ATTTGTCTTA GAGCTACTCT 1500 TCCCTCTAAA ACATCCATCC TCATTTCCCT 1530
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