Tag | Content |
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EnhancerAtlas ID | HS093-21074 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr3:5053130-5055650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr3:5055440-5055461 | CTCTCCTCCCCCTCCTCCTCC | - | 10.77 | ZNF263 | MA0528.1 | chr3:5055240-5055261 | TTCTCCCTGTCTCCCTCCCTC | - | 6.11 | ZNF263 | MA0528.1 | chr3:5055428-5055449 | CTCTTCCTCCACCTCTCCTCC | - | 6.1 | ZNF263 | MA0528.1 | chr3:5055449-5055470 | CCCTCCTCCTCCTCTGCCTCA | - | 6.32 | ZNF263 | MA0528.1 | chr3:5055411-5055432 | GCCTCTGCCTCCTCCTCCTCT | - | 6.66 | ZNF263 | MA0528.1 | chr3:5055405-5055426 | TTCTCTGCCTCTGCCTCCTCC | - | 6.82 | ZNF263 | MA0528.1 | chr3:5055384-5055405 | CTCCTCCTCTCCTTCTCCTCC | - | 7.02 | ZNF263 | MA0528.1 | chr3:5055452-5055473 | TCCTCCTCCTCTGCCTCATTC | - | 7.05 | ZNF263 | MA0528.1 | chr3:5055390-5055411 | CTCTCCTTCTCCTCCTTCTCT | - | 7.07 | ZNF263 | MA0528.1 | chr3:5055423-5055444 | TCCTCCTCTTCCTCCACCTCT | - | 7.44 | ZNF263 | MA0528.1 | chr3:5055437-5055458 | CACCTCTCCTCCCCCTCCTCC | - | 7.71 | ZNF263 | MA0528.1 | chr3:5055387-5055408 | CTCCTCTCCTTCTCCTCCTTC | - | 7.81 | ZNF263 | MA0528.1 | chr3:5055417-5055438 | GCCTCCTCCTCCTCTTCCTCC | - | 8.21 | ZNF263 | MA0528.1 | chr3:5055420-5055441 | TCCTCCTCCTCTTCCTCCACC | - | 9.4 | ZNF263 | MA0528.1 | chr3:5055443-5055464 | TCCTCCCCCTCCTCCTCCTCT | - | 9.75 |
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| Number of super-enhancer constituents: 18 | ID | Coordinate | Tissue/cell |
SE_10738 | chr3:5051999-5055734 | CD19_Primary | SE_13436 | chr3:5052379-5054562 | CD34_Primary_RO01536 | SE_14396 | chr3:5052261-5054273 | CD4_Memory_Primary_7pool | SE_14396 | chr3:5054408-5055730 | CD4_Memory_Primary_7pool | SE_20744 | chr3:5052146-5054794 | CD8_Memory_7pool | SE_23149 | chr3:5054024-5054531 | Colon_Crypt_1 | SE_23149 | chr3:5054634-5055622 | Colon_Crypt_1 | SE_26553 | chr3:5052394-5054493 | Esophagus | SE_26553 | chr3:5054680-5055750 | Esophagus | SE_34822 | chr3:5054195-5055937 | HeLa | SE_35840 | chr3:5054419-5055887 | HMEC | SE_39863 | chr3:5052339-5055899 | K562 | SE_46580 | chr3:5054692-5056958 | Osteoblasts | SE_56679 | chr3:5054636-5056538 | u87 | SE_62573 | chr3:5014508-5068965 | Tonsil | SE_64232 | chr3:5054459-5055786 | NHEK | SE_65389 | chr3:5053220-5054152 | Pancreatic_islets | SE_65389 | chr3:5055003-5055636 | Pancreatic_islets |
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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 |
GH03I005010 | chr3 | 5052088 | 5055974 |
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Enhancer Sequence | GCGAAAGCAA GGGAAACCCA GCTATCCTTA GAGGCTGGAA GCCCACCAGT CAGAAAGGCT 60 AACCCTGTCG TGCTAACCAA AAAGCCACTG AGGGATTTCT TAAGTTAAGA CGAAGGCAGC 120 TTCTAAGAAT CAGGGACTTG TGTTTTCTCC CAAGAGACTT TTGAAAGCAA AACTTGCAGG 180 GACCCCCTCC TTAGAGACAG GAGGTCACAG CTGAGGTATC TGGCCAGATG CAAAGAACTT 240 CCCTCTCTGT TCTTGTTAAC ACTGATAAAA AGGCTTCCTT CCTCATTCTC GGGACCAGCT 300 TTTCACCCCG GGCCGCCGGC CGACTCAACC CCCATACCCC TCTTGTCATA CTATCCTCCC 360 ACCGCCTCCA CCCTCTTGCC ACCCCGGACT TGACCTTGTC CTGGACTGTC CCTTTGACAA 420 AATTCAGGGC CACCCGACTC TTCTTACCTT CGCTGGTGCC TCTTCCTCTG TCTTGCACTG 480 GTGGGTTCAT GTTTCACTTC TCCACCAGGG CGGTGGGTGG AGGCCACGAG GGCTGTCCCA 540 TCACCTCATG TTTGGCAGCT GTGGTGGGCC TGGGTGGGAG AAGGGTGTCT GGTTCTGGTT 600 CTGCTGTCAG GAGAGGGCCT CTCCACCTGG CCAGCCCTGG TTTCCTCTTT TGCACCCTGG 660 GGAGAGTCAT CTCCCTCACA GTGTTGGGAG GTGGAAATTG GTGATCATGG CTAAGGTGCA 720 TGGAGCATCT ATTATGTGCC AGGGATGTGG GATTTATCTC ACGTAAGCCT CCTGACAACT 780 CTGTTTTACA CATGGGAAAA CAAGTTCAGC GAGATGAAGT GGCTTGCCGG TGGCCACCAG 840 GTAGTGATGG GTGGAGGAGG CAGCATTTGA ACCCAGGTAC TCAGCCCCCA GATCATGGGC 900 TCTTAACCAC ATCCCCACAC CATCTTCCTA AAAAGTAACA TCTGTACCAC ACCCTTGGAA 960 CTAGCAGCAA CAGAAGCTGC AGACTTTTGG AAAGGGAAAG TAGCTCCTCC ATTCCACCCC 1020 CACCATATTT TGATGACAAC TATGGACTCG ATGCTCCTGC TTTCTTATCT CACAAAGGTG 1080 GGAAGGCAAC AGTCTGTGTT TTCACTGGCA CTCTCCCGTG TCCTGATAGA GGAAGTAGTA 1140 GCTCAGACAA GTTAAGGAAG TTGACCAGGG TCACACAGCT GGTCTGTGGC AGCAGGGAGA 1200 GTTAAATGCA TGTTAACTTG TTCAGTTATT GAGCACCTGC TGCATACCAG CCTGCATGTC 1260 AATTGCTGGG TATGCTGTGG GATACTGCCC TCTCAGGTCT TACAGCTAAA GGAAGGGTGT 1320 TGATGGTGGA AATAGTGTGT TGACAGATTT TTTTTTTTTT TTTTTTGAGA TGGAGTCTTG 1380 CTCTGTCACC CAGGCTGGAG TGCAGTGGCG TGATCTCGGC TCACTGCAAC CTCTACCTCC 1440 TGGGTTCATG CAATTCTCCT GCCTCAGCCT CCTGAGTAGC TGGGATTACA GACGTGTGCC 1500 ACCACGCCAA GCTAATTGTT GTATTTTTAG TAGAGACAGG GTTTCGCCAT GTTGGTCAGG 1560 CTGGTCTCAA ACTCATGGCC TCAAGTGATC CACCTGCCTC GGCCTCCCAA AGTGTTGGGA 1620 TTACAGGCAT GAGCCACTGG GCCAGGCCAA GTGACAGATC TTTATAGCTG GGCTGGTCCT 1680 GCTCCACAGA GCTGTCTCCC TTGGGCTGTT GACATTGAAA TGACAAACAC TGGGCAGCCA 1740 ACTCACCATT AATTGCCAGG ATGAATGGAG CCATCCCAGC TACAGAGCTC TGGCAGCTAG 1800 ACCCTATGGC CACAGCAGGT CTTTTGGAGT GACTTTGAAT GGCTTCCCAT GCCCCTACTG 1860 TTTCTTGCTT TCTCCTGATA ACACCCAGCT GCTGTCAGGC CTATGGGCAA GGAGAGGCCT 1920 CCTGGGGCTG GTAGGGTCTG GGTGGGGCCC TGACTCATCG CCACCAGTGA GCCTTTGTCT 1980 GAACACTTCC CCTCCAGAGC ACAGGGATAG CCATTCGGAA ACCAAGGTGA AAAAGAGGGT 2040 GGAGCCCAGT CTGGGATTTG AGACTGATTA TCTACATCAC TGGGACCCTT TTGGTCTCCA 2100 GGTTTCCTCC TTCTCCCTGT CTCCCTCCCT CCCTCCATAA GTGGACATTC ATTCAGGCAG 2160 AGCCAACCAG GTAGTTGCCT AAGCTGGAGC TGCTGAAGTC TCATCTCAAA TTTGTTAAGA 2220 TCAGTCACCT TCTTCCCCCC ACTCTCAGCT CCTGCTCCTC CTCTCCTTCT CCTCCTTCTC 2280 TGCCTCTGCC TCCTCCTCCT CTTCCTCCAC CTCTCCTCCC CCTCCTCCTC CTCTGCCTCA 2340 TTCCTCGGGT CACTGTGACT TCTGCTTAAT TTCCCTTCCC CTCTCTTTCC CTCTCTGCAC 2400 TCCCCACTTA ATTTTTCACT CACTTCACTG ATGAGGAGTA CCACTTTTTC CTTTTCGATT 2460 ACTTTTCTCC CTGTTTACAT GTTAATAAAA AGTTACTTTT CTTTTTTTCC AAAACAGGGT 2520
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