Tag | Content |
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EnhancerAtlas ID | HS002-01163 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:223913510-223915500 |
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 | TATCCCAGCA CATACACGTG CTTCCAGTAC CTTGTGATCT CTAGCCATAA GTTTCCACTC 60 ACCCATCTGC GAAATGGGAA CAATGACGAT GTTTGCGTCC TTTCTTTTTC TTTTCCTACA 120 ATGCAGGGAA CTTTAAGACT ATGTGACAGA AAGGTGCCAC TGGAACCCAG GGCCTCGTGG 180 GTTTCCTCCG TCTCTCGGGA GACCAGGATC CGAGTGAGAA AGTTTCCCAC GTTCATTCTT 240 GTTGGGCCCA TTCTCAGGAT GATGTTTCTC CTGTATTTTG CTACCCCAGC CCAAGCAAGA 300 CTAGTAGTTC AGCTTTGTGA ATCCCCTCAG GAAGTCAGGA AAATAGATAC TGTCTTTGGG 360 CTTCCTCCAG GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA GGAATTTAAG ACAGGAATTG 420 GCAGCCGAGG GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG TGATGAGAGC 480 AGGGATGGGG AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG CCATCAGGAA 540 GGAGCAGCCA CCTCTGCTGG GGTACTGGAG ATAAAAACTC TGATATTGAC TAGTGACCGT 600 GGGGGCGATG GCCCAGGAGG GTCAGGGCTG CAGGGAACAG GGACACAAAA ACGACAAAAC 660 ATGCAACAGG TTATGTCCTT CTGGTCCAGG GCACGGCTGA GACAGGCAAG GGACTAGAGA 720 GAGGAAGAGT GAATGTCAAG CCCCAGCACC CTCGCCTCCC TCCCATCCTC CCTTTTAGGG 780 CCTCCCTTCT GGCAGATAGG GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA CACGTGGTTT 840 GGATCACTGG CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG GAGGCTGAAG 900 ACTTCTTGTT AATAAGGGTG GGGCATGAGT AAAATGGAGG ATCTGCCCCC TCCCCTCCCA 960 GCCCCTGATA CAAATGAAGG ATGATTGTAC ATGCATGGGG AATTCCACTT TGGGGGTATC 1020 CTTTTCTGGG CTGCTGCCAG ACTCTGAAAT GAGTAACAAA GGGATGGCCC AGGGTGACTC 1080 ATCAGCTACC CTCTCGCAGG CCTAGCACGC TGGCGGGGTG TGCATTTCCT CTAGAGAAGC 1140 CCCTCCCTGC CAGTTTCAGA GGGATGGCCC TGAATTGGCT TTTCAGAGGT TCCTTCTCCT 1200 CCCTTCCAAA GCGAAGACCC ACAGCTGCCT GAAAATGTGG CTCTCCGCCT TCTTGGGCTG 1260 CCTAGGACCT TGAGAGATGT GTCTCTCTGG GACAGGGTGT CAGGTCTGCT GGAGATTGTT 1320 AAAATGCTGT TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA GCAGTCTTCA GTAGCTTGGT 1380 CTGTTTATCG TGTATCTAGC TGTCAGCATG CAAAACAAAA GAACAAAAGG TCTAAAGAAA 1440 TATAACGCAA AACAGGTACG ATTTGAGATC CATCAGGGTT TCTCAACCTT GGCACAACTG 1500 ACTGGATAAT TGTTCATTGT AGGGGGCTGT CCTGTGAATT ATAGGATGTT TAGCTGCATC 1560 CTTGGCCTCT ACCCACACAC CCCCGTGTGC CACTCAAAAA TGTCTGCAGA CCTTGCCAAA 1620 TGTCCCCTGG GGGCTTGGCG GAGTTGGGGG GTGCATGGAA TGCCCCCAGT TGAGAACCAC 1680 TGGCAGAGCA GGAGTGAAGG GGGAGGTACT GTGGGGGTCA CTGGGCACAC AGAATGCCAT 1740 TTGGGGAGCC TGGTGCAAGG GAGTGGCCGG ATGGGAGGTA GGAATAGCAG TGGTAATCAG 1800 TAGGTGAGTT GCTGAAGACA AACTAAATAT TCTTTCCAGC ATTGCTTCAA TCTAATCCAG 1860 CCGCAAGTAT GAGTAAATAC TGTAGGAAAG GAGAAAACAT TGCATGTACG GGGTCAGGGC 1920 AGCATTGCTG GGATATTTGA GCCTGTGGGA GGGGAGCTTC AAGCTTCCCA CTAGCATTGG 1980 GAGGAACACA 1990
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