Tag | Content |
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EnhancerAtlas ID | HS187-05159 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr11:129723060-129724500 |
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: 2 | Chromosome | Start | End |
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 | AGAGGGCTGT TGAAGAGGAA TTTTCCTTCA CTCTGCCCCA TTCCAACAAG ATCCACCCAC 60 TCCCACTGTT TCCTTCGCAT CCACTCCGCT CCACTGCGGC CCTCCAGGAA CAAGCAGTGA 120 TGACAGTAAC AAGTGTTCTT CCTCAGGACC AGCCCCACCT GGGGGGAATG AGGGGTCTTA 180 ATCTGCAACT GACAATTACC ACTTGTCATC AGTGGCCTAT GGCTTCTTGG AGAGAGTGAA 240 GCAACATCGC TTCTCTTGGA GGAAGCAAAG CTTCACAGGG CTTTGTTGGT CTCATCCTGC 300 TGAATGTCCC CACTCACCAT TCAGGCATCA GAGAGGCCTC CCGTGAGAAG TGACAGGGAC 360 CTGTGGCTTA AAGGATCAGG ACAGCATCAA CCTTGCCTAA ATAAAGCTAG GACAATTACA 420 ATATTTGGCC CCTTGACTGG GTGAAAATGG TACTCATTCA ACAGCTCTCT GGCACTCCTA 480 CCACAAGCCA GGAAGTCACT GTTCCAGGCA TAGGAGATAC ACTGGGGAAC CACACAGCCG 540 CTGCTGTCAC AGGGCTTCCA TTCTAGTGTC ACTGGGACTT TTCCTGGGTC ATTTCCACAA 600 CTTCCTGACT CTGTGTGTGG GAATTCAAAA AGGGTCTGGC TTGAGAAACA AGTATCTGGG 660 AAACGGAGTC CAAAATGTCA TCATGGAGGA TTTCTTCTAG GCTTCCCCAA GAACACTTTG 720 GGTACCAGGC ATAAAGACAA ATCTTTTGCC TTCCAAATTA GCTGATAAAA GTAGAAGGGA 780 TAAGAACTAA GAGCTATCCT GTGTCGCAGT TTCGTCATTT TCTGGCCCAC ATCCTGGGGC 840 CTCTGCCTTG TTTACCCGGT GTTTTAAAAC ACACAGCTGG GAGGGGCGCA GGGCTTGCAG 900 AGCTGGCTCT GTGCCCAGGA AGGACACGCA CTCAAAATCA GCCCTGCAGA CACGCACCTG 960 GGAGCCGCTT CCCTCCCTTG GCACGTACAG GTATCTTCAT TACCAGTGTG TCTCTGCTCA 1020 GATTCTGCTT TCAGCCTAAT TGTTTCTGTC TGGGATTTCT TTCACTGCTC ACTTGGCAGG 1080 GAAGCCCAGA GATTATTCTA TCAGCCACAC TCCGACTTAA GTGATGATGT CTTGCTCATC 1140 TCTGCTCCTG GACAAACCTC CTGGGGATCT ATGTGTGTGT GGTTGTGTTC ATTGATTCTT 1200 CTACCCTCAA CCCCAAACCC CTAAAAGGAA CAACAATGGC AAGATGTCTA CACAGGTGAC 1260 TCAGCACACA CCCTACTTTA TACTGAAGCA GCTGCACCTG AGGCAGCAAA GTAGCTCTGC 1320 TGACCCGCGG GCCACCCTCA CCTCACCCCA TCTCCGCTTC GCTCATGCCT TTGGGTTATT 1380 CCTTGCTCCT ATTTGTCTTA GAGCTACTCT TCCCTCTAAA ACATCCATCC TCATTTCCCT 1440
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