Tag | Content |
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EnhancerAtlas ID | HS148-01684 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:223913610-223915720 |
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 | TTTCTTTTTC TTTTCCTACA ATGCAGGGAA CTTTAAGACT ATGTGACAGA AAGGTGCCAC 60 TGGAACCCAG GGCCTCGTGG GTTTCCTCCG TCTCTCGGGA GACCAGGATC CGAGTGAGAA 120 AGTTTCCCAC GTTCATTCTT GTTGGGCCCA TTCTCAGGAT GATGTTTCTC CTGTATTTTG 180 CTACCCCAGC CCAAGCAAGA CTAGTAGTTC AGCTTTGTGA ATCCCCTCAG GAAGTCAGGA 240 AAATAGATAC TGTCTTTGGG CTTCCTCCAG GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA 300 GGAATTTAAG ACAGGAATTG GCAGCCGAGG GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT 360 GTGGGGTCTG TGATGAGAGC AGGGATGGGG AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG 420 GGGAGGGCAG CCATCAGGAA GGAGCAGCCA CCTCTGCTGG GGTACTGGAG ATAAAAACTC 480 TGATATTGAC TAGTGACCGT GGGGGCGATG GCCCAGGAGG GTCAGGGCTG CAGGGAACAG 540 GGACACAAAA ACGACAAAAC ATGCAACAGG TTATGTCCTT CTGGTCCAGG GCACGGCTGA 600 GACAGGCAAG GGACTAGAGA GAGGAAGAGT GAATGTCAAG CCCCAGCACC CTCGCCTCCC 660 TCCCATCCTC CCTTTTAGGG CCTCCCTTCT GGCAGATAGG GCAGGGAGAA GGGAAAGGAA 720 AGGCCTGGGA CACGTGGTTT GGATCACTGG CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG 780 TTTAGGGAAG GAGGCTGAAG ACTTCTTGTT AATAAGGGTG GGGCATGAGT AAAATGGAGG 840 ATCTGCCCCC TCCCCTCCCA GCCCCTGATA CAAATGAAGG ATGATTGTAC ATGCATGGGG 900 AATTCCACTT TGGGGGTATC CTTTTCTGGG CTGCTGCCAG ACTCTGAAAT GAGTAACAAA 960 GGGATGGCCC AGGGTGACTC ATCAGCTACC CTCTCGCAGG CCTAGCACGC TGGCGGGGTG 1020 TGCATTTCCT CTAGAGAAGC CCCTCCCTGC CAGTTTCAGA GGGATGGCCC TGAATTGGCT 1080 TTTCAGAGGT TCCTTCTCCT CCCTTCCAAA GCGAAGACCC ACAGCTGCCT GAAAATGTGG 1140 CTCTCCGCCT TCTTGGGCTG CCTAGGACCT TGAGAGATGT GTCTCTCTGG GACAGGGTGT 1200 CAGGTCTGCT GGAGATTGTT AAAATGCTGT TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA 1260 GCAGTCTTCA GTAGCTTGGT CTGTTTATCG TGTATCTAGC TGTCAGCATG CAAAACAAAA 1320 GAACAAAAGG TCTAAAGAAA TATAACGCAA AACAGGTACG ATTTGAGATC CATCAGGGTT 1380 TCTCAACCTT GGCACAACTG ACTGGATAAT TGTTCATTGT AGGGGGCTGT CCTGTGAATT 1440 ATAGGATGTT TAGCTGCATC CTTGGCCTCT ACCCACACAC CCCCGTGTGC CACTCAAAAA 1500 TGTCTGCAGA CCTTGCCAAA TGTCCCCTGG GGGCTTGGCG GAGTTGGGGG GTGCATGGAA 1560 TGCCCCCAGT TGAGAACCAC TGGCAGAGCA GGAGTGAAGG GGGAGGTACT GTGGGGGTCA 1620 CTGGGCACAC AGAATGCCAT TTGGGGAGCC TGGTGCAAGG GAGTGGCCGG ATGGGAGGTA 1680 GGAATAGCAG TGGTAATCAG TAGGTGAGTT GCTGAAGACA AACTAAATAT TCTTTCCAGC 1740 ATTGCTTCAA TCTAATCCAG CCGCAAGTAT GAGTAAATAC TGTAGGAAAG GAGAAAACAT 1800 TGCATGTACG GGGTCAGGGC AGCATTGCTG GGATATTTGA GCCTGTGGGA GGGGAGCTTC 1860 AAGCTTCCCA CTAGCATTGG GAGGAACACA GCAAAGGAGG AGAAGGGCCC TCCCTGCTTC 1920 TTGGAGAATG GTTCCACTGG CAGGCCATTC CGTCTGCTCA GCTTCCTAGC TCAGGTGCCT 1980 TTCCAAACCA CACATCAGCA GGGAGACAGT GGGAACATCT CAGGTCCAGG GTACCTTGGG 2040 AACTGCAGAG CAGCTGGGTG GCCTGACACT GGCATTTCTC AGTGTTGGCT CCATTCTCTT 2100 GCTGGCACCC 2110
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