Tag | Content |
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EnhancerAtlas ID | HS197-14104 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr3:5053590-5056230 |
Target genes | |
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: 2 | ID | Chromosome | Start | End |
GH03I005010 | chr3 | 5052088 | 5055974 | GH03I005014 | chr3 | 5056086 | 5056486 |
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Enhancer Sequence | TCTTCCTCTG TCTTGCACTG GTGGGTTCAT GTTTCACTTC TCCACCAGGG CGGTGGGTGG 60 AGGCCACGAG GGCTGTCCCA TCACCTCATG TTTGGCAGCT GTGGTGGGCC TGGGTGGGAG 120 AAGGGTGTCT GGTTCTGGTT CTGCTGTCAG GAGAGGGCCT CTCCACCTGG CCAGCCCTGG 180 TTTCCTCTTT TGCACCCTGG GGAGAGTCAT CTCCCTCACA GTGTTGGGAG GTGGAAATTG 240 GTGATCATGG CTAAGGTGCA TGGAGCATCT ATTATGTGCC AGGGATGTGG GATTTATCTC 300 ACGTAAGCCT CCTGACAACT CTGTTTTACA CATGGGAAAA CAAGTTCAGC GAGATGAAGT 360 GGCTTGCCGG TGGCCACCAG GTAGTGATGG GTGGAGGAGG CAGCATTTGA ACCCAGGTAC 420 TCAGCCCCCA GATCATGGGC TCTTAACCAC ATCCCCACAC CATCTTCCTA AAAAGTAACA 480 TCTGTACCAC ACCCTTGGAA CTAGCAGCAA CAGAAGCTGC AGACTTTTGG AAAGGGAAAG 540 TAGCTCCTCC ATTCCACCCC CACCATATTT TGATGACAAC TATGGACTCG ATGCTCCTGC 600 TTTCTTATCT CACAAAGGTG GGAAGGCAAC AGTCTGTGTT TTCACTGGCA CTCTCCCGTG 660 TCCTGATAGA GGAAGTAGTA GCTCAGACAA GTTAAGGAAG TTGACCAGGG TCACACAGCT 720 GGTCTGTGGC AGCAGGGAGA GTTAAATGCA TGTTAACTTG TTCAGTTATT GAGCACCTGC 780 TGCATACCAG CCTGCATGTC AATTGCTGGG TATGCTGTGG GATACTGCCC TCTCAGGTCT 840 TACAGCTAAA GGAAGGGTGT TGATGGTGGA AATAGTGTGT TGACAGATTT TTTTTTTTTT 900 TTTTTTGAGA TGGAGTCTTG CTCTGTCACC CAGGCTGGAG TGCAGTGGCG TGATCTCGGC 960 TCACTGCAAC CTCTACCTCC TGGGTTCATG CAATTCTCCT GCCTCAGCCT CCTGAGTAGC 1020 TGGGATTACA GACGTGTGCC ACCACGCCAA GCTAATTGTT GTATTTTTAG TAGAGACAGG 1080 GTTTCGCCAT GTTGGTCAGG CTGGTCTCAA ACTCATGGCC TCAAGTGATC CACCTGCCTC 1140 GGCCTCCCAA AGTGTTGGGA TTACAGGCAT GAGCCACTGG GCCAGGCCAA GTGACAGATC 1200 TTTATAGCTG GGCTGGTCCT GCTCCACAGA GCTGTCTCCC TTGGGCTGTT GACATTGAAA 1260 TGACAAACAC TGGGCAGCCA ACTCACCATT AATTGCCAGG ATGAATGGAG CCATCCCAGC 1320 TACAGAGCTC TGGCAGCTAG ACCCTATGGC CACAGCAGGT CTTTTGGAGT GACTTTGAAT 1380 GGCTTCCCAT GCCCCTACTG TTTCTTGCTT TCTCCTGATA ACACCCAGCT GCTGTCAGGC 1440 CTATGGGCAA GGAGAGGCCT CCTGGGGCTG GTAGGGTCTG GGTGGGGCCC TGACTCATCG 1500 CCACCAGTGA GCCTTTGTCT GAACACTTCC CCTCCAGAGC ACAGGGATAG CCATTCGGAA 1560 ACCAAGGTGA AAAAGAGGGT GGAGCCCAGT CTGGGATTTG AGACTGATTA TCTACATCAC 1620 TGGGACCCTT TTGGTCTCCA GGTTTCCTCC TTCTCCCTGT CTCCCTCCCT CCCTCCATAA 1680 GTGGACATTC ATTCAGGCAG AGCCAACCAG GTAGTTGCCT AAGCTGGAGC TGCTGAAGTC 1740 TCATCTCAAA TTTGTTAAGA TCAGTCACCT TCTTCCCCCC ACTCTCAGCT CCTGCTCCTC 1800 CTCTCCTTCT CCTCCTTCTC TGCCTCTGCC TCCTCCTCCT CTTCCTCCAC CTCTCCTCCC 1860 CCTCCTCCTC CTCTGCCTCA TTCCTCGGGT CACTGTGACT TCTGCTTAAT TTCCCTTCCC 1920 CTCTCTTTCC CTCTCTGCAC TCCCCACTTA ATTTTTCACT CACTTCACTG ATGAGGAGTA 1980 CCACTTTTTC CTTTTCGATT ACTTTTCTCC CTGTTTACAT GTTAATAAAA AGTTACTTTT 2040 CTTTTTTTCC AAAACAGGGT CTCACTCTGT CACCTGGGCT GGAGTGCAGT GGTACAATCT 2100 CAGCTCACTG CAGCCTTGAC ATCCCGGGTT CCAGCCATCC TCCCACCTCA ACCTCCTGAG 2160 TAGCTGGGAC TGTAGGTGCA CGCCACCACG CCTGGCTAAT TTTTGTGTTT TCGTAGAGAT 2220 GGGGGCCTTG CCATGTTGCC CAGACTGGTC TTAAACTCTC GGGCTTAAGA GATCCTCCTG 2280 CGTCATCCTC CCAATGTGCT GGGACTACAG GCGTGAACCA CTGCGCCCAG CCAGAAAAAG 2340 TTACTTTTCT CCTTGGCTTC AAACTGATAT TCGAAGGCTA TTTTCTCTTT CAAGAGACAT 2400 TCATTTCATG TGCTTTGAAC ATACATATTT GTTGCAAAAA ATATACTCTG GTTATCCTTC 2460 TCTTGCAGAA AAGAAACACA TGCCATTAGT TTTATTTACT TGTCAGTGTG TTGTGAAGGA 2520 AGGCCAGAGT CCAGATCAGC TTCTCTTCTT TGCAGGTCTG TCTGCTGAAA GTCATCAAGA 2580 CACTTTCCAA CTCATTGTTT CCAACGAGGG GCGCAGGCTG GGAGCGCTGA GGGGCTGGCT 2640
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