Tag | Content |
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EnhancerAtlas ID | HS060-31240 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr7:22484140-22485560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr7:22485222-22485233 | GCTTCCCGCCC | - | 6.02 | PLAG1 | MA0163.1 | chr7:22485010-22485024 | CCCCTTTGGGCCTC | - | 6.37 | ZNF263 | MA0528.1 | chr7:22484643-22484664 | AGAGGATGAGAAAGAGAAAGG | + | 6.3 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_38354 | chr7:22481760-22486692 | HUVEC |
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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 |
GH07I022441 | chr7 | 22480873 | 22487061 |
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Enhancer Sequence | CTCTTTGCAG ACACACTACT CAAACCCATG GAGAAAATGT CCCATCGGCT GCCCGGGAGC 60 CTCTGCCTTG GCCACTCGCA GCAACCCTGG GAGAAATAAG GGCCTCAGAC AGAACAATAG 120 CATGGATTGT GCCTCTTGCA GGAATTTCAT CTGTCACTGA GTAACAGGTT TTGATCTCAG 180 GCTCGCTGCC AGTTAGGAAG TGAAACCCTT TCCGGAACAC TTGCTGTTTT GTTGGTTTTC 240 CCCTGGAGAT TTAATGATTT CACCTTGGAG GTTTTAGCTG ATGAGCTGTG CTCTGTATGG 300 AGCCTACCCA TGTGAAAAAC CAATCAGGTA TTTCATGGGC TCCCCAGTAT TCTATTTCGT 360 GAGTTTGGAG ACCCACTAAG CCAACAATTG GACACCCCCA CAAGGTGTGC ATTTGCTGTC 420 ACCAGAGCGA GCTCTGGGTC TGTCCGCGTG GCACAAGGAG AGCTGTTAGA TCAGTCGTCT 480 TCTCTAACCC AGAGGCCTAA GTGAGAGGAT GAGAAAGAGA AAGGGCCATT GTTTCTAAAG 540 ACAGGTTCAC CTGAAGAATT TGGACAATGA TGCCGGTTTC AGTTTAAAGG GCCTTTGGGC 600 AGGGTTGGCA TTGGGAACAG GGGCTGAGGG AGCTTCTAGA CTTTTCTGCA TTATGAGCAG 660 AGTAATTACA AATCAGCTCT GCAGATGACA GCACAGACCT CTTTGTGGTG GGTTCTCTTG 720 GGCCAACAGC AGATTTGGAG CCGTGGAAGA ACAGCGAGAA ATCTCTTCAC ATGACCTTCA 780 TGTCTTCCTC CTGTAAACCG CATTGTATTT CTAACTTCAG ATCAAGGGGA CTGACATCTG 840 CAACTCTTCA GGGAGGACAG CTGGGCCATG CCCCTTTGGG CCTCCCATCC TCCCCTCGTC 900 TTGTCAGCCA GTCGTGCTGG GATCTGCCGG CAGCCTTGTG AGAACCGGGC AGGAACTGGC 960 CAGCAAAGGC AGCTATAAAT ACTCCTCTTG GCAGCCAGCT TCACTTGGGA GCCCACAGCT 1020 GAGGGGCGGA GGCCAGCGGG AAGCACCTGC ACCTCTTCAG GGTACATCCG AGCCTGGGCC 1080 TGGCTTCCCG CCCTCCACCT CTGAATGGGG ATTTGGTCGA CCTTTTCCGG CTTGGGGGAA 1140 GTCCCCGTGG TGATCCAGCT TCCCAGATGC AAGAGCAGCA GGGAGGGCAC TGCTCTCCAA 1200 GCAGCCCAAC CCCTTTAAAC TCAAAGTCAG AGCTATATTC TCACAAGGGC TGATGAAACT 1260 GAATAGCTAA GGGTAAATGA GGAGGCAGGA GAGGCGAAGA GGAAGGGAAA TAAGCTCTTT 1320 TATAGAATGC TTTTCTCCTC CTGATTTCAC TTGTGTGGGG AAGCATGAAA CAACCACTAA 1380 TCAGTCTTTC CCCCTGATGA GTCGGAAACT TGACAACTGG 1420
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