Tag | Content |
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EnhancerAtlas ID | HS086-01267 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr1:223913880-223914750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:223914582-223914593 | GGTGACTCATC | + | 6.32 | FOSL2 | MA0478.1 | chr1:223914581-223914592 | GGGTGACTCAT | + | 6.14 | JUNB | MA0490.1 | chr1:223914581-223914592 | GGGTGACTCAT | + | 6.32 | JUND | MA0491.1 | chr1:223914582-223914593 | GGTGACTCATC | + | 6.62 |
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| Number of super-enhancer constituents: 36 | ID | Coordinate | Tissue/cell |
SE_00224 | chr1:223912311-223916909 | Adipose_Nuclei | SE_01908 | chr1:223913738-223914955 | Aorta | SE_02306 | chr1:223913344-223915961 | Astrocytes | SE_04026 | chr1:223913451-223915326 | Brain_Anterior_Caudate | SE_05036 | chr1:223913560-223915403 | Brain_Cingulate_Gyrus | SE_05972 | chr1:223913207-223916372 | Brain_Hippocampus_Middle | SE_07996 | chr1:223913125-223915466 | Brain_Inferior_Temporal_Lobe | SE_09681 | chr1:223912826-223918041 | CD14 | SE_19702 | chr1:223913106-223916325 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_24051 | chr1:223913880-223914466 | Colon_Crypt_2 | SE_26209 | chr1:223912988-223915695 | Duodenum_Smooth_Muscle | SE_26925 | chr1:223913192-223915372 | Esophagus | SE_31491 | chr1:223913141-223916265 | Gastric | SE_34545 | chr1:223913070-223916058 | HCT-116 | SE_34979 | chr1:223912930-223916086 | HeLa | SE_36294 | chr1:223913510-223915892 | HMEC | SE_37129 | chr1:223913319-223916436 | HSMMtube | SE_38254 | chr1:223913007-223915923 | HUVEC | SE_38957 | chr1:223913198-223916265 | IMR90 | SE_41495 | chr1:223912854-223916323 | Left_Ventricle | SE_42269 | chr1:223912507-223916406 | Lung | SE_44530 | chr1:223913197-223916987 | NHDF-Ad | SE_44904 | chr1:223913680-223916262 | NHLF | SE_45872 | chr1:223913083-223917105 | Osteoblasts | SE_49408 | chr1:223912976-223915760 | Right_Atrium | SE_50365 | chr1:223913039-223916033 | Sigmoid_Colon | SE_51879 | chr1:223913896-223915223 | Skeletal_Muscle_Myoblast | SE_53249 | chr1:223913106-223915207 | Small_Intestine | SE_55958 | chr1:223913015-223914574 | u87 | SE_55958 | chr1:223914578-223916004 | u87 | SE_63671 | chr1:223913673-223915261 | HSMM | SE_64794 | chr1:223913313-223915321 | NHEK | SE_65644 | chr1:223913370-223915937 | Pancreatic_islets | SE_67677 | chr1:223913015-223914574 | u87 | SE_67677 | chr1:223914578-223916004 | u87 | SE_68376 | chr1:223892363-223922876 | TC32 |
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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 |
GH01I223722 | chr1 | 223910120 | 223916233 |
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Enhancer Sequence | GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA GGAATTTAAG ACAGGAATTG GCAGCCGAGG 60 GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG TGATGAGAGC AGGGATGGGG 120 AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG CCATCAGGAA GGAGCAGCCA 180 CCTCTGCTGG GGTACTGGAG ATAAAAACTC TGATATTGAC TAGTGACCGT GGGGGCGATG 240 GCCCAGGAGG GTCAGGGCTG CAGGGAACAG GGACACAAAA ACGACAAAAC ATGCAACAGG 300 TTATGTCCTT CTGGTCCAGG GCACGGCTGA GACAGGCAAG GGACTAGAGA GAGGAAGAGT 360 GAATGTCAAG CCCCAGCACC CTCGCCTCCC TCCCATCCTC CCTTTTAGGG CCTCCCTTCT 420 GGCAGATAGG GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA CACGTGGTTT GGATCACTGG 480 CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG GAGGCTGAAG ACTTCTTGTT 540 AATAAGGGTG GGGCATGAGT AAAATGGAGG ATCTGCCCCC TCCCCTCCCA GCCCCTGATA 600 CAAATGAAGG ATGATTGTAC ATGCATGGGG AATTCCACTT TGGGGGTATC CTTTTCTGGG 660 CTGCTGCCAG ACTCTGAAAT GAGTAACAAA GGGATGGCCC AGGGTGACTC ATCAGCTACC 720 CTCTCGCAGG CCTAGCACGC TGGCGGGGTG TGCATTTCCT CTAGAGAAGC CCCTCCCTGC 780 CAGTTTCAGA GGGATGGCCC TGAATTGGCT TTTCAGAGGT TCCTTCTCCT CCCTTCCAAA 840 GCGAAGACCC ACAGCTGCCT GAAAATGTGG 870
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