Tag | Content |
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EnhancerAtlas ID | HS146-09398 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr20:48643980-48645180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLIS3 | MA0737.1 | chr20:48643982-48643996 | GACCCCCCAGGAAG | + | 7.14 | ZNF263 | MA0528.1 | chr20:48644617-48644638 | GGCGGAGGGAGGGGAAGGGGA | + | 6.04 | ZNF263 | MA0528.1 | chr20:48644644-48644665 | GGGGGAGGGAGGGAGTGGAGA | + | 7.03 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_38189 | chr20:48643039-48652392 | HUVEC |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 48644508 | 48644680 | chr20 | 48644281 | 48645013 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I050026 | chr20 | 48643273 | 48648549 |
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Enhancer Sequence | AGGACCCCCC AGGAAGTGTC CCCTGTCTCC TTTGCTGGGT ATTTTCCTTC CCTGACTCTT 60 GGCCTGTTTC TTTCTTGGTG AGTGTATGTG GGGTGGGGTT AGTGAGAAAG GGAGACCCCA 120 GCTCTGGCGT TGCGGGAGTG TTAGGATCCA AGGCCAGGCC TGCAGCCCTG GGTCCCTCCT 180 GCCTGGGAGG TACCTGGGGA AGTCTGCAGC CTGTCTACAC TGGTGAAGCC TCAGCCCCAA 240 CCAGCCCCCT GCCCTGCACT TGCCAACTGG GCACCGCCAC TGTCGGCACC ACATCCCCAG 300 GGTGTGTAAC AAGTGTCACA GCCTCACCCA GCCTCAGTTT CCTCCCCTGG AAAATGGGGA 360 TAGCCACGAC ACGTGGTGGG GAAGGTTATA TTTACATGAC CTGGGCTGTT ACTCTTATTC 420 CTGCCTCCAG TAAGAAGCCA CGTGGAGTGT CTGCCATGCT GAGGAGAGGG CACCCCTGGC 480 CGGAGCCCAG CTGGATGTCA GGCCTGAGGC TGGATGTCAG GCCAAAGCTG GCTCCAGCCC 540 AGCAGCCTGA CACGAAGGGG AGGGAGGCCT GAGTCGGCCA GACTCCTGAG TCACTGTTTC 600 CCGGCTCTGC CAGGCCAGGC GGGAAAAGGG GGAGCGGGGC GGAGGGAGGG GAAGGGGATA 660 ATCTGGGGGA GGGAGGGAGT GGAGAGTGAG ACACCAGTTG TAACCATTGT TGGGTGGGAC 720 AGACAGAAAG CCACCTGCCA GGGGGGCAAG GAGATTCTGG GGTGTCAGAG TGGGGTCCTT 780 GCACTTCCCT GCATTATAGG CTGCAAACTC CTCCCTCCCT CGCCACCAAC ACATACACAC 840 ACACACACAC ACACACACAC ACACACACAC ACACACACAC TGCACTCAGC TTCACAGCTT 900 TCCTTCTCTT TCTTGAGTGT GTTGACCAGG TTCCAGCCTC AGGGCCTTTG CACTGGCTGT 960 GTTTTCTGCC TGGAACACTT CAAGGTTCTT TCTCAAATCT CAGGCTTCAG CTTAAATGTC 1020 ACCTCTTCAG TGAAGCTGTC CAGGCTGGAG TGCAGTGGTG CCATCATGGC TCACTGCAGC 1080 CCCAACCTCC CCGGGCTCTG GTGATCCTCC CACGTCAGCC CCTCGAGTAG CTGGGACCGC 1140 AGGCGTGCAC CATCATGCCC TGCTAATTTT TGTATTTTTC TGTAGAGATG GGGTTTTGCT 1200
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