Tag | Content |
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EnhancerAtlas ID | HS164-10649 |
Organism | Homo sapiens |
Tissue/cell | Raji |
Coordinate | chr6:32628030-32628630 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr6:32628235-32628245 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr6:32628235-32628245 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr6:32628235-32628245 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr6:32628235-32628245 | AACAGCTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_10570 | chr6:32627517-32628440 | CD19_Primary | SE_11111 | chr6:32625538-32631526 | CD20 | SE_62549 | chr6:32627125-32671412 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr6 | 32628153 | 32628241 | chr6 | 32628084 | 32628200 | chr6 | 32628279 | 32628519 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I032660 | chr6 | 32627121 | 32628579 |
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Enhancer Sequence | AGAAGAGAGA AGAGCATTGA TCAGCACAGG GTATCCTGGT GGGCCTGCCA TCTCCCCCAC 60 CCTTCAGGGG CCCCCTGCAG CTTCAGACAG AGAAAGTTGA GGTCCAGGGT GTATTGTCAT 120 CACCTCCCCC AAGATCTGTG CAAAGGTGAA ATCAGCTCAT GAGGACACAG AACTTCAGCT 180 TGATGCAGAT GTGTGGGAGG TGGGGAACAG CTGTTATTCT TCTGGGGAAT ATGAAGGGTT 240 CAGTCTTTTT AGGAAATTGG ATGATATCTC TTCCCGACCA CTAGCAGCCT CTTTCAGTCA 300 CTGGAAAATG CTTACAGGCA GTAGCCACCA TCATGTGGCA CAAAGTGGGC ATCATCCTAG 360 TGTCTAACAT TTAAGCTGTG GTTCTGGCTC CACATTTCAC AAGAAGATGC CACCAAAGTT 420 AAGGCTTGGT TCTGGGGAAC AATGTCTGGA GATTCCTAGA AACTGGCAAA CTTCTCCCCT 480 AAGTCTTGAT CCTCATAGCA GCAAATAGGC CATGAACATG GACCACTGTG GTCAGGTACA 540 CTCAGCTCAT GCTCTTCCCT CTTATACCTG TGCCTCCCCA CACTGGATCA TGGCTGAAAT 600
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