Tag | Content |
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EnhancerAtlas ID | HS064-01327 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr1:223913690-223915010 |
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: 2 | Chromosome | Start | End |
chr1 | 223914239 | 223914747 | chr1 | 223913851 | 223914937 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I223722 | chr1 | 223910120 | 223916233 |
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Enhancer Sequence | GTTTCCTCCG TCTCTCGGGA GACCAGGATC CGAGTGAGAA AGTTTCCCAC GTTCATTCTT 60 GTTGGGCCCA TTCTCAGGAT GATGTTTCTC CTGTATTTTG CTACCCCAGC CCAAGCAAGA 120 CTAGTAGTTC AGCTTTGTGA ATCCCCTCAG GAAGTCAGGA AAATAGATAC TGTCTTTGGG 180 CTTCCTCCAG GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA GGAATTTAAG ACAGGAATTG 240 GCAGCCGAGG GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG TGATGAGAGC 300 AGGGATGGGG AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG CCATCAGGAA 360 GGAGCAGCCA CCTCTGCTGG GGTACTGGAG ATAAAAACTC TGATATTGAC TAGTGACCGT 420 GGGGGCGATG GCCCAGGAGG GTCAGGGCTG CAGGGAACAG GGACACAAAA ACGACAAAAC 480 ATGCAACAGG TTATGTCCTT CTGGTCCAGG GCACGGCTGA GACAGGCAAG GGACTAGAGA 540 GAGGAAGAGT GAATGTCAAG CCCCAGCACC CTCGCCTCCC TCCCATCCTC CCTTTTAGGG 600 CCTCCCTTCT GGCAGATAGG GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA CACGTGGTTT 660 GGATCACTGG CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG GAGGCTGAAG 720 ACTTCTTGTT AATAAGGGTG GGGCATGAGT AAAATGGAGG ATCTGCCCCC TCCCCTCCCA 780 GCCCCTGATA CAAATGAAGG ATGATTGTAC ATGCATGGGG AATTCCACTT TGGGGGTATC 840 CTTTTCTGGG CTGCTGCCAG ACTCTGAAAT GAGTAACAAA GGGATGGCCC AGGGTGACTC 900 ATCAGCTACC CTCTCGCAGG CCTAGCACGC TGGCGGGGTG TGCATTTCCT CTAGAGAAGC 960 CCCTCCCTGC CAGTTTCAGA GGGATGGCCC TGAATTGGCT TTTCAGAGGT TCCTTCTCCT 1020 CCCTTCCAAA GCGAAGACCC ACAGCTGCCT GAAAATGTGG CTCTCCGCCT TCTTGGGCTG 1080 CCTAGGACCT TGAGAGATGT GTCTCTCTGG GACAGGGTGT CAGGTCTGCT GGAGATTGTT 1140 AAAATGCTGT TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA GCAGTCTTCA GTAGCTTGGT 1200 CTGTTTATCG TGTATCTAGC TGTCAGCATG CAAAACAAAA GAACAAAAGG TCTAAAGAAA 1260 TATAACGCAA AACAGGTACG ATTTGAGATC CATCAGGGTT TCTCAACCTT GGCACAACTG 1320
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