Tag | Content |
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EnhancerAtlas ID | HS045-05655 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:223913530-223915770 |
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 | CTTCCAGTAC CTTGTGATCT CTAGCCATAA GTTTCCACTC ACCCATCTGC GAAATGGGAA 60 CAATGACGAT GTTTGCGTCC TTTCTTTTTC TTTTCCTACA ATGCAGGGAA CTTTAAGACT 120 ATGTGACAGA AAGGTGCCAC TGGAACCCAG GGCCTCGTGG GTTTCCTCCG TCTCTCGGGA 180 GACCAGGATC CGAGTGAGAA AGTTTCCCAC GTTCATTCTT GTTGGGCCCA TTCTCAGGAT 240 GATGTTTCTC CTGTATTTTG CTACCCCAGC CCAAGCAAGA CTAGTAGTTC AGCTTTGTGA 300 ATCCCCTCAG GAAGTCAGGA AAATAGATAC TGTCTTTGGG CTTCCTCCAG GAGCTAAGAA 360 AGGAGAGTTC CTGAAGAGCA GGAATTTAAG ACAGGAATTG GCAGCCGAGG GCAAGGTTCC 420 ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG TGATGAGAGC AGGGATGGGG AGGAAGAGGG 480 TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG CCATCAGGAA GGAGCAGCCA CCTCTGCTGG 540 GGTACTGGAG ATAAAAACTC TGATATTGAC TAGTGACCGT GGGGGCGATG GCCCAGGAGG 600 GTCAGGGCTG CAGGGAACAG GGACACAAAA ACGACAAAAC ATGCAACAGG TTATGTCCTT 660 CTGGTCCAGG GCACGGCTGA GACAGGCAAG GGACTAGAGA GAGGAAGAGT GAATGTCAAG 720 CCCCAGCACC CTCGCCTCCC TCCCATCCTC CCTTTTAGGG CCTCCCTTCT GGCAGATAGG 780 GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA CACGTGGTTT GGATCACTGG CTGTGGCTCA 840 CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG GAGGCTGAAG ACTTCTTGTT AATAAGGGTG 900 GGGCATGAGT AAAATGGAGG ATCTGCCCCC TCCCCTCCCA GCCCCTGATA CAAATGAAGG 960 ATGATTGTAC ATGCATGGGG AATTCCACTT TGGGGGTATC CTTTTCTGGG CTGCTGCCAG 1020 ACTCTGAAAT GAGTAACAAA GGGATGGCCC AGGGTGACTC ATCAGCTACC CTCTCGCAGG 1080 CCTAGCACGC TGGCGGGGTG TGCATTTCCT CTAGAGAAGC CCCTCCCTGC CAGTTTCAGA 1140 GGGATGGCCC TGAATTGGCT TTTCAGAGGT TCCTTCTCCT CCCTTCCAAA GCGAAGACCC 1200 ACAGCTGCCT GAAAATGTGG CTCTCCGCCT TCTTGGGCTG CCTAGGACCT TGAGAGATGT 1260 GTCTCTCTGG GACAGGGTGT CAGGTCTGCT GGAGATTGTT AAAATGCTGT TGTCTCAGGA 1320 AGGGTGAAAT TTAGCCAGGA GCAGTCTTCA GTAGCTTGGT CTGTTTATCG TGTATCTAGC 1380 TGTCAGCATG CAAAACAAAA GAACAAAAGG TCTAAAGAAA TATAACGCAA AACAGGTACG 1440 ATTTGAGATC CATCAGGGTT TCTCAACCTT GGCACAACTG ACTGGATAAT TGTTCATTGT 1500 AGGGGGCTGT CCTGTGAATT ATAGGATGTT TAGCTGCATC CTTGGCCTCT ACCCACACAC 1560 CCCCGTGTGC CACTCAAAAA TGTCTGCAGA CCTTGCCAAA TGTCCCCTGG GGGCTTGGCG 1620 GAGTTGGGGG GTGCATGGAA TGCCCCCAGT TGAGAACCAC TGGCAGAGCA GGAGTGAAGG 1680 GGGAGGTACT GTGGGGGTCA CTGGGCACAC AGAATGCCAT TTGGGGAGCC TGGTGCAAGG 1740 GAGTGGCCGG ATGGGAGGTA GGAATAGCAG TGGTAATCAG TAGGTGAGTT GCTGAAGACA 1800 AACTAAATAT TCTTTCCAGC ATTGCTTCAA TCTAATCCAG CCGCAAGTAT GAGTAAATAC 1860 TGTAGGAAAG GAGAAAACAT TGCATGTACG GGGTCAGGGC AGCATTGCTG GGATATTTGA 1920 GCCTGTGGGA GGGGAGCTTC AAGCTTCCCA CTAGCATTGG GAGGAACACA GCAAAGGAGG 1980 AGAAGGGCCC TCCCTGCTTC TTGGAGAATG GTTCCACTGG CAGGCCATTC CGTCTGCTCA 2040 GCTTCCTAGC TCAGGTGCCT TTCCAAACCA CACATCAGCA GGGAGACAGT GGGAACATCT 2100 CAGGTCCAGG GTACCTTGGG AACTGCAGAG CAGCTGGGTG GCCTGACACT GGCATTTCTC 2160 AGTGTTGGCT CCATTCTCTT GCTGGCACCC CCAGGTGGGA GACTCTGTTA GCAGGTGTAT 2220 CTTACTATCC CTGGCTCCCT 2240
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