Tag | Content |
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EnhancerAtlas ID | HS197-18199 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr6:33047130-33048440 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr6:33048395-33048406 | AAGAGGATTAG | + | 6.62 | EWSR1-FLI1 | MA0149.1 | chr6:33047974-33047992 | AGAAAGAAGGAAGGGAGG | + | 6.59 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_10221 | chr6:33045246-33047933 | CD19_Primary | SE_11036 | chr6:33035108-33052434 | CD20 | SE_62504 | chr6:33024195-33049547 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr6 | 33047501 | 33047612 | chr6 | 33047384 | 33047475 | chr6 | 33047658 | 33047736 | chr6 | 33048097 | 33048189 |
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Enhancer Sequence | TGGGAAAGGC TGCCAAAATT GTTCATGTAA AAATTACATC AATGCTGTCT TCCTCGGTGC 60 TGCCTATGCA GCTGGCAGCC ATCTCTTCCT CCACATCATG GCCTCCCTCA GACTCCTCAT 120 GAAGGATAAG ATCCTCAAAA AGAGGACCAA CAAGTTCATG AGGCACCAAT CAGACTGAAA 180 TGTCAAAATT AAGCATAACT GGCGGAAACC CAGAGGTCTT AACAGTAGGG TTCGTAGAAG 240 GTCCAAGGGC CAGATCTTGA TGCCCAACAT TGCTTATGGG AGCAACAACA ACAACAAAAA 300 AAACATGCTG CCCAGTGGCT TCCAGAAGTT TCTGGTCCAC AGCCTCAAGG AGCTGAAAGT 360 GCTGCTGATG TGCAACAAAT CTTACTGTGC TGAGATCGCT CACAAAATTT CCTCCAGAAC 420 TGCAAAGTCA TCATGGAAAG AGTCACCCAG CCGGCCATCA GAGTCACCAA CCCCAGTACC 480 AGGGTGCACA GCTAAGAAAA TGAGTAGAAA GTTCATGTCC ACGTTTTGTG TGTAAATAAA 540 ACCATAAAAA CTGCCAAAAA AAATTACATC AATGCCTCTA AACCCAAAGG ACTCTACCCC 600 CACAGGTCCC TGGTTGTTGT GGTGATTTTC ATTGTGTAAA ATACTTTCCA CATCTTTTGA 660 CACCAAGTCT TTCTGCAGCC ATGTTTGAAA ATTAACTTTC AGGCTACAGA GTCTTTCTTA 720 TACCAAAGTT GAAGAAAGTT TTAAGAAATA TATTTCTACA TCTCCTACAT GCAAAACAAC 780 AGGAGCAAGT TGAGGAATTC TCAAGAAACT GGTCGAGAAG AGAGAGCGCT TAGCTATGGA 840 AAAGAGAAAG AAGGAAGGGA GGGCTTCCTG GAGGAGGTGG CATTTGAACC AGGACTGACA 900 TCAGGATGGA AATGTCAGTC AGGGAGTTAA GTAGGGGGAG CAGCTCCGCC CTCCACGTCC 960 CCAGCTCCTC CCGCCCCTGT TTTTTCTCCC AGTGACCCCA CGTGAAACGT CTCCGCCTCC 1020 TCCAGCCACC AGCAGAAGGG ACTGCCTTCC CCTCAGTGCT CGCCCCTCCC TAGTGATCAC 1080 TCAGTGCCCC TGAGCTCATT CTTTTCAGTA AATTCTCTCT CTGCGTGGTG AGAAAACAGG 1140 CCTGGAGAGG CTCTGCGACC CGCTTAGGAC CACAGAACTC GGTACTAGGA AAACTCCTAT 1200 TTTAAAATCC AGCCCTGGGT GGGAAGATTT GGGAAGAATC GTTAATATTG AGAGAGAGAG 1260 GGAGAAAGAG GATTAGATGA GAGTGGCGCC TCCGCTCATG TCCGCCCCCT 1310
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