Tag | Content |
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EnhancerAtlas ID | HS170-01965 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr19:35695860-35696950 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr19:35696563-35696581 | CCCTCCTTCCCTCCTCTC | - | 6.33 | EWSR1-FLI1 | MA0149.1 | chr19:35696559-35696577 | CTTTCCCTCCTTCCCTCC | - | 7.22 | GATA2 | MA0036.3 | chr19:35696839-35696850 | TTCTTATCTCT | + | 6.32 | Gata1 | MA0035.3 | chr19:35696839-35696850 | TTCTTATCTCT | + | 6.32 | Gata4 | MA0482.1 | chr19:35696840-35696851 | TCTTATCTCTC | + | 6.32 | ONECUT1 | MA0679.1 | chr19:35696781-35696795 | AATATTGATTTTTC | - | 6.76 | ONECUT2 | MA0756.1 | chr19:35696781-35696795 | AATATTGATTTTTC | - | 6.75 | ONECUT3 | MA0757.1 | chr19:35696781-35696795 | AATATTGATTTTTC | - | 6.92 | SPI1 | MA0080.4 | chr19:35696386-35696400 | GAAAAGAGGAAGTG | + | 6.92 | ZNF263 | MA0528.1 | chr19:35696575-35696596 | CCTCTCCCCTCCTCCTTCTCT | - | 6.54 | ZNF263 | MA0528.1 | chr19:35696559-35696580 | CTTTCCCTCCTTCCCTCCTCT | - | 6.88 | ZNF263 | MA0528.1 | chr19:35696569-35696590 | TTCCCTCCTCTCCCCTCCTCC | - | 7.65 | ZNF263 | MA0528.1 | chr19:35696572-35696593 | CCTCCTCTCCCCTCCTCCTTC | - | 8.15 |
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| Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
SE_10316 | chr19:35694706-35699540 | CD19_Primary | SE_11602 | chr19:35693742-35708404 | CD20 | SE_11952 | chr19:35694362-35699527 | CD3 | SE_14788 | chr19:35693951-35699612 | CD4_Memory_Primary_7pool | SE_15612 | chr19:35695871-35699271 | CD4_Memory_Primary_8pool | SE_15961 | chr19:35695886-35699340 | CD4_Naive_Primary_7pool | SE_16561 | chr19:35696013-35697479 | CD4_Naive_Primary_8pool | SE_20324 | chr19:35695762-35706055 | CD56 | SE_21443 | chr19:35695519-35699393 | CD8_Memory_7pool | SE_21632 | chr19:35696466-35699556 | CD8_Naive_7pool | SE_22136 | chr19:35695876-35699598 | CD8_Naive_8pool | SE_22903 | chr19:35695804-35699515 | CD8_primiary | SE_43856 | chr19:35694166-35699480 | MM1S | SE_62877 | chr19:35694122-35708296 | Tonsil |
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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 |
GH19I035202 | chr19 | 35693414 | 35699474 |
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Enhancer Sequence | GGCGCTGGTG GGAGTGTAGC AGTGAGGACG ACCAGAGGTC ACTCTCGTGG CCATCTTGGT 60 TTTGATGGGT ATTATCTGGC TTCTTTATTG CATCCTGTTT TATCAGCAAG GTCTTTATGA 120 CCTGCATCTT GTGTTGACCT CCTATCTCAC CCTGTGACTC AGAATGCCTT AACCATCTGG 180 GGATGCAGCC CAGTAAGTCT CAGCCTCATT TTACCTGGCC CCTACTCAAG ATGGGGTTGC 240 TCTGGTTCAA ACGCCTCTGA CAGGGTGACA ACTGTGACCA CAACAGATTC ACAAACATGA 300 CATTTTCAGA GAGAGGAAGG TATGCAGGGT GGTGTGATTT GGAAGAGGCT GTGGGCGTAG 360 AGGGATGGGT AATTCAGTTG GGGTGGTCAG GGAGGGCTGC TTGGTGGAGG GGACTCTTGG 420 CTGAGACCTG AGGGCTGTGA AGTTCTTAGA GAAGGGTGTT CCAGGCAGAG GGAACAGCAA 480 GCACAAAGGC CTGAGACGAG AGCTAGCTTG GTATGCAAGA GGAACAGAAA AGAGGAAGTG 540 AGAGTAAGGC GGGGGAGGGA AGGGGCAGGG AATGGAGGCT GTGGAGAGGG GAGGGTTTCC 600 AGGCAGCCCA GGACCCTCAA GGAGAGAAAC GTTGGATGTA GTCTCCCAGG TAGGGTCCAT 660 CTGGCCCTTC CTCCTGGCTC CTGCGGAGTC CGAGTGGCTC TTTCCCTCCT TCCCTCCTCT 720 CCCCTCCTCC TTCTCTCCCT CTCCATTTTC CCTGCAAGGT CTGCAGCCCA ACTCCAGCTC 780 TCCCATTACT ACAGGGGCTG GTGGGTCCTT CTGAGCAAGA AGATGGGGCT CTTTGTCTAC 840 AGTGTCTGTC TATAGTCATT CACCCACTCA TTCATTTAAT CATTCACTCA TTCATTCATT 900 CATTTAGCCA CTCATTTGTC AAATATTGAT TTTTCTCAGG TGTTTTGCCC TCACAGGTCC 960 TGCCGCCTAA AACACTGACT TCTTATCTCT CAAGGCTTTG CTTTCAACAC TGTCTCTTCC 1020 AAGACCTCTC CCTGACCACT CCCAACTTAC TAAACCCCTA TCACCCTGTT AGCTTTTGAA 1080 TGCTCTTCAT 1090
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