Tag | Content |
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EnhancerAtlas ID | HS145-10814 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr18:20045880-20047020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr18:20046683-20046701 | GGAAAAATGGAAGGAATG | + | 6.09 | FOSL1 | MA0477.1 | chr18:20046155-20046166 | CATGAGTCACC | - | 6.62 | FOSL2 | MA0478.1 | chr18:20046156-20046167 | ATGAGTCACCC | - | 6.14 | IRF1 | MA0050.2 | chr18:20046549-20046570 | GTCTTCTTTTACTTTCTTTTA | + | 6.19 | JUNB | MA0490.1 | chr18:20046156-20046167 | ATGAGTCACCC | - | 6.32 | JUND | MA0491.1 | chr18:20046155-20046166 | CATGAGTCACC | - | 6.02 | Myog | MA0500.1 | chr18:20046309-20046320 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr18:20046309-20046320 | GACAGCTGCAG | + | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_48987 | chr18:20045421-20049085 | Right_Atrium | SE_65170 | chr18:20045383-20049854 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I022465 | chr18 | 20045407 | 20052904 |
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Enhancer Sequence | CATATGGCTA CGAATGTGGA GCAAAGCAAT ATGGAAACAA TATGTTCAAC TTTATGACTA 60 GTAACTCATT GGCTCATGGA CAGCTTTGTC CCAGCTTCTC TGGGGGTAGT TTTCCTGCTG 120 CATGGCACAC ATTTGAGGAG CACTGGAAGT CCCACAGTTT TTCCCACACT ACAGTATTCT 180 GAGTATTGCA AGTAGAGATG GAACGGAGAG TGGGTTTGTC AAAATAAGCC AGCCCCACAT 240 TGAAAAAGTC ACGTGTGCTT GGTGCTATCC ACAAACATGA GTCACCCAGG GAGGTATGTA 300 GATGCTTGTG ACAAGAGAGG AGAGGCCTAA AAATAACAGT TCCACTGAAG GGTGGAGCTA 360 CAGGCTGCTG GTGTGTCATG TTTGGCTGCT GCTTCTGAAA ATTCCTTCAG TTAAAGTAGC 420 AAGTGGGATG ACAGCTGCAG ATACCTGGCT TTCAGGAGAG AAGTGTAGCA GGTATCCATT 480 GAGGGGGGAT TTCAGGGTCA TGAACTCCTC CTTATTACTT ATTTCCTGAA GCTGATGTGT 540 GAAAATCCAT ACAAGAATCC CACATCTTTA GTTAAAGACT TTGATCCCCA ATAAATCAGA 600 ACGACAGCAC ATTCGGCTGT TCTCAGTGAC ACATTTGAAG GTTGCTGGAG ATACAAGGAT 660 GCTCAGAGTG TCTTCTTTTA CTTTCTTTTA ACTTTCTCCT GCTGTTCCAT ATACTACATG 720 AGGGCAAGGA CCTTGTTTGT CCTGTTTTCA GTTCCATCCT CGGTGTCTTG CACAGAGCAG 780 GAGCTAAATA AATATTTGCT TAAGGAAAAA TGGAAGGAAT GTGTCTAGCC CAGCCCTCTT 840 AGTTTGCAGG CAAGAATACT GAGCAGGGAG AAGAAACTTG CTCAGGATCA TGCAACCTAT 900 CAGCAGGGGT AGGAGGGAAG CCAGCCTCTG ACTCTCCACC CAGTGCTCTC ACCTTTCCAA 960 CAAGCTAGCA ATGACTCAGT GTGGCTAGAA GTGTCTTGTT GAGGGCAAAG ACCAAACACG 1020 AGGTCTCTGG CTACTAGGCT GAGGTGGACA GTATGGGGCA GCAGTTCTGA GGGGGGCCAA 1080 AAGATAGTGA ACTTCACTGG GAGGAGGTGA CAAAGACAAG GCTTGCCACT GGAGGCTGCC 1140
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