Tag | Content |
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EnhancerAtlas ID | HS095-20012 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr3:5053910-5055900 |
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 | CTGTTTTACA CATGGGAAAA CAAGTTCAGC GAGATGAAGT GGCTTGCCGG TGGCCACCAG 60 GTAGTGATGG GTGGAGGAGG CAGCATTTGA ACCCAGGTAC TCAGCCCCCA GATCATGGGC 120 TCTTAACCAC ATCCCCACAC CATCTTCCTA AAAAGTAACA TCTGTACCAC ACCCTTGGAA 180 CTAGCAGCAA CAGAAGCTGC AGACTTTTGG AAAGGGAAAG TAGCTCCTCC ATTCCACCCC 240 CACCATATTT TGATGACAAC TATGGACTCG ATGCTCCTGC TTTCTTATCT CACAAAGGTG 300 GGAAGGCAAC AGTCTGTGTT TTCACTGGCA CTCTCCCGTG TCCTGATAGA GGAAGTAGTA 360 GCTCAGACAA GTTAAGGAAG TTGACCAGGG TCACACAGCT GGTCTGTGGC AGCAGGGAGA 420 GTTAAATGCA TGTTAACTTG TTCAGTTATT GAGCACCTGC TGCATACCAG CCTGCATGTC 480 AATTGCTGGG TATGCTGTGG GATACTGCCC TCTCAGGTCT TACAGCTAAA GGAAGGGTGT 540 TGATGGTGGA AATAGTGTGT TGACAGATTT TTTTTTTTTT TTTTTTGAGA TGGAGTCTTG 600 CTCTGTCACC CAGGCTGGAG TGCAGTGGCG TGATCTCGGC TCACTGCAAC CTCTACCTCC 660 TGGGTTCATG CAATTCTCCT GCCTCAGCCT CCTGAGTAGC TGGGATTACA GACGTGTGCC 720 ACCACGCCAA GCTAATTGTT GTATTTTTAG TAGAGACAGG GTTTCGCCAT GTTGGTCAGG 780 CTGGTCTCAA ACTCATGGCC TCAAGTGATC CACCTGCCTC GGCCTCCCAA AGTGTTGGGA 840 TTACAGGCAT GAGCCACTGG GCCAGGCCAA GTGACAGATC TTTATAGCTG GGCTGGTCCT 900 GCTCCACAGA GCTGTCTCCC TTGGGCTGTT GACATTGAAA TGACAAACAC TGGGCAGCCA 960 ACTCACCATT AATTGCCAGG ATGAATGGAG CCATCCCAGC TACAGAGCTC TGGCAGCTAG 1020 ACCCTATGGC CACAGCAGGT CTTTTGGAGT GACTTTGAAT GGCTTCCCAT GCCCCTACTG 1080 TTTCTTGCTT TCTCCTGATA ACACCCAGCT GCTGTCAGGC CTATGGGCAA GGAGAGGCCT 1140 CCTGGGGCTG GTAGGGTCTG GGTGGGGCCC TGACTCATCG CCACCAGTGA GCCTTTGTCT 1200 GAACACTTCC CCTCCAGAGC ACAGGGATAG CCATTCGGAA ACCAAGGTGA AAAAGAGGGT 1260 GGAGCCCAGT CTGGGATTTG AGACTGATTA TCTACATCAC TGGGACCCTT TTGGTCTCCA 1320 GGTTTCCTCC TTCTCCCTGT CTCCCTCCCT CCCTCCATAA GTGGACATTC ATTCAGGCAG 1380 AGCCAACCAG GTAGTTGCCT AAGCTGGAGC TGCTGAAGTC TCATCTCAAA TTTGTTAAGA 1440 TCAGTCACCT TCTTCCCCCC ACTCTCAGCT CCTGCTCCTC CTCTCCTTCT CCTCCTTCTC 1500 TGCCTCTGCC TCCTCCTCCT CTTCCTCCAC CTCTCCTCCC CCTCCTCCTC CTCTGCCTCA 1560 TTCCTCGGGT CACTGTGACT TCTGCTTAAT TTCCCTTCCC CTCTCTTTCC CTCTCTGCAC 1620 TCCCCACTTA ATTTTTCACT CACTTCACTG ATGAGGAGTA CCACTTTTTC CTTTTCGATT 1680 ACTTTTCTCC CTGTTTACAT GTTAATAAAA AGTTACTTTT CTTTTTTTCC AAAACAGGGT 1740 CTCACTCTGT CACCTGGGCT GGAGTGCAGT GGTACAATCT CAGCTCACTG CAGCCTTGAC 1800 ATCCCGGGTT CCAGCCATCC TCCCACCTCA ACCTCCTGAG TAGCTGGGAC TGTAGGTGCA 1860 CGCCACCACG CCTGGCTAAT TTTTGTGTTT TCGTAGAGAT GGGGGCCTTG CCATGTTGCC 1920 CAGACTGGTC TTAAACTCTC GGGCTTAAGA GATCCTCCTG CGTCATCCTC CCAATGTGCT 1980 GGGACTACAG 1990
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