Tag | Content |
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EnhancerAtlas ID | HS112-01600 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr1:223913640-223915460 |
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 | CTTTAAGACT ATGTGACAGA AAGGTGCCAC TGGAACCCAG GGCCTCGTGG GTTTCCTCCG 60 TCTCTCGGGA GACCAGGATC CGAGTGAGAA AGTTTCCCAC GTTCATTCTT GTTGGGCCCA 120 TTCTCAGGAT GATGTTTCTC CTGTATTTTG CTACCCCAGC CCAAGCAAGA CTAGTAGTTC 180 AGCTTTGTGA ATCCCCTCAG GAAGTCAGGA AAATAGATAC TGTCTTTGGG CTTCCTCCAG 240 GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA GGAATTTAAG ACAGGAATTG GCAGCCGAGG 300 GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG TGATGAGAGC AGGGATGGGG 360 AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG CCATCAGGAA GGAGCAGCCA 420 CCTCTGCTGG GGTACTGGAG ATAAAAACTC TGATATTGAC TAGTGACCGT GGGGGCGATG 480 GCCCAGGAGG GTCAGGGCTG CAGGGAACAG GGACACAAAA ACGACAAAAC ATGCAACAGG 540 TTATGTCCTT CTGGTCCAGG GCACGGCTGA GACAGGCAAG GGACTAGAGA GAGGAAGAGT 600 GAATGTCAAG CCCCAGCACC CTCGCCTCCC TCCCATCCTC CCTTTTAGGG CCTCCCTTCT 660 GGCAGATAGG GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA CACGTGGTTT GGATCACTGG 720 CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG GAGGCTGAAG ACTTCTTGTT 780 AATAAGGGTG GGGCATGAGT AAAATGGAGG ATCTGCCCCC TCCCCTCCCA GCCCCTGATA 840 CAAATGAAGG ATGATTGTAC ATGCATGGGG AATTCCACTT TGGGGGTATC CTTTTCTGGG 900 CTGCTGCCAG ACTCTGAAAT GAGTAACAAA GGGATGGCCC AGGGTGACTC ATCAGCTACC 960 CTCTCGCAGG CCTAGCACGC TGGCGGGGTG TGCATTTCCT CTAGAGAAGC CCCTCCCTGC 1020 CAGTTTCAGA GGGATGGCCC TGAATTGGCT TTTCAGAGGT TCCTTCTCCT CCCTTCCAAA 1080 GCGAAGACCC ACAGCTGCCT GAAAATGTGG CTCTCCGCCT TCTTGGGCTG CCTAGGACCT 1140 TGAGAGATGT GTCTCTCTGG GACAGGGTGT CAGGTCTGCT GGAGATTGTT AAAATGCTGT 1200 TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA GCAGTCTTCA GTAGCTTGGT CTGTTTATCG 1260 TGTATCTAGC TGTCAGCATG CAAAACAAAA GAACAAAAGG TCTAAAGAAA TATAACGCAA 1320 AACAGGTACG ATTTGAGATC CATCAGGGTT TCTCAACCTT GGCACAACTG ACTGGATAAT 1380 TGTTCATTGT AGGGGGCTGT CCTGTGAATT ATAGGATGTT TAGCTGCATC CTTGGCCTCT 1440 ACCCACACAC CCCCGTGTGC CACTCAAAAA TGTCTGCAGA CCTTGCCAAA TGTCCCCTGG 1500 GGGCTTGGCG GAGTTGGGGG GTGCATGGAA TGCCCCCAGT TGAGAACCAC TGGCAGAGCA 1560 GGAGTGAAGG GGGAGGTACT GTGGGGGTCA CTGGGCACAC AGAATGCCAT TTGGGGAGCC 1620 TGGTGCAAGG GAGTGGCCGG ATGGGAGGTA GGAATAGCAG TGGTAATCAG TAGGTGAGTT 1680 GCTGAAGACA AACTAAATAT TCTTTCCAGC ATTGCTTCAA TCTAATCCAG CCGCAAGTAT 1740 GAGTAAATAC TGTAGGAAAG GAGAAAACAT TGCATGTACG GGGTCAGGGC AGCATTGCTG 1800 GGATATTTGA GCCTGTGGGA 1820
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