Tag | Content |
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EnhancerAtlas ID | HS047-07189 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr11:129723130-129724500 |
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 | TCCTTCGCAT CCACTCCGCT CCACTGCGGC CCTCCAGGAA CAAGCAGTGA TGACAGTAAC 60 AAGTGTTCTT CCTCAGGACC AGCCCCACCT GGGGGGAATG AGGGGTCTTA ATCTGCAACT 120 GACAATTACC ACTTGTCATC AGTGGCCTAT GGCTTCTTGG AGAGAGTGAA GCAACATCGC 180 TTCTCTTGGA GGAAGCAAAG CTTCACAGGG CTTTGTTGGT CTCATCCTGC TGAATGTCCC 240 CACTCACCAT TCAGGCATCA GAGAGGCCTC CCGTGAGAAG TGACAGGGAC CTGTGGCTTA 300 AAGGATCAGG ACAGCATCAA CCTTGCCTAA ATAAAGCTAG GACAATTACA ATATTTGGCC 360 CCTTGACTGG GTGAAAATGG TACTCATTCA ACAGCTCTCT GGCACTCCTA CCACAAGCCA 420 GGAAGTCACT GTTCCAGGCA TAGGAGATAC ACTGGGGAAC CACACAGCCG CTGCTGTCAC 480 AGGGCTTCCA TTCTAGTGTC ACTGGGACTT TTCCTGGGTC ATTTCCACAA CTTCCTGACT 540 CTGTGTGTGG GAATTCAAAA AGGGTCTGGC TTGAGAAACA AGTATCTGGG AAACGGAGTC 600 CAAAATGTCA TCATGGAGGA TTTCTTCTAG GCTTCCCCAA GAACACTTTG GGTACCAGGC 660 ATAAAGACAA ATCTTTTGCC TTCCAAATTA GCTGATAAAA GTAGAAGGGA TAAGAACTAA 720 GAGCTATCCT GTGTCGCAGT TTCGTCATTT TCTGGCCCAC ATCCTGGGGC CTCTGCCTTG 780 TTTACCCGGT GTTTTAAAAC ACACAGCTGG GAGGGGCGCA GGGCTTGCAG AGCTGGCTCT 840 GTGCCCAGGA AGGACACGCA CTCAAAATCA GCCCTGCAGA CACGCACCTG GGAGCCGCTT 900 CCCTCCCTTG GCACGTACAG GTATCTTCAT TACCAGTGTG TCTCTGCTCA GATTCTGCTT 960 TCAGCCTAAT TGTTTCTGTC TGGGATTTCT TTCACTGCTC ACTTGGCAGG GAAGCCCAGA 1020 GATTATTCTA TCAGCCACAC TCCGACTTAA GTGATGATGT CTTGCTCATC TCTGCTCCTG 1080 GACAAACCTC CTGGGGATCT ATGTGTGTGT GGTTGTGTTC ATTGATTCTT CTACCCTCAA 1140 CCCCAAACCC CTAAAAGGAA CAACAATGGC AAGATGTCTA CACAGGTGAC TCAGCACACA 1200 CCCTACTTTA TACTGAAGCA GCTGCACCTG AGGCAGCAAA GTAGCTCTGC TGACCCGCGG 1260 GCCACCCTCA CCTCACCCCA TCTCCGCTTC GCTCATGCCT TTGGGTTATT CCTTGCTCCT 1320 ATTTGTCTTA GAGCTACTCT TCCCTCTAAA ACATCCATCC TCATTTCCCT 1370
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