Tag | Content |
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EnhancerAtlas ID | HS095-02935 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:223913440-223915610 |
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 | GTCATGGCCT CCTGATGTTT CCCACAAAGG GCCAGAGGCC CTTCAGTGCC AAGGAACGTG 60 GACTCTCTCC TATCCCAGCA CATACACGTG CTTCCAGTAC CTTGTGATCT CTAGCCATAA 120 GTTTCCACTC ACCCATCTGC GAAATGGGAA CAATGACGAT GTTTGCGTCC TTTCTTTTTC 180 TTTTCCTACA ATGCAGGGAA CTTTAAGACT ATGTGACAGA AAGGTGCCAC TGGAACCCAG 240 GGCCTCGTGG GTTTCCTCCG TCTCTCGGGA GACCAGGATC CGAGTGAGAA AGTTTCCCAC 300 GTTCATTCTT GTTGGGCCCA TTCTCAGGAT GATGTTTCTC CTGTATTTTG CTACCCCAGC 360 CCAAGCAAGA CTAGTAGTTC AGCTTTGTGA ATCCCCTCAG GAAGTCAGGA AAATAGATAC 420 TGTCTTTGGG CTTCCTCCAG GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA GGAATTTAAG 480 ACAGGAATTG GCAGCCGAGG GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG 540 TGATGAGAGC AGGGATGGGG AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG 600 CCATCAGGAA GGAGCAGCCA CCTCTGCTGG GGTACTGGAG ATAAAAACTC TGATATTGAC 660 TAGTGACCGT GGGGGCGATG GCCCAGGAGG GTCAGGGCTG CAGGGAACAG GGACACAAAA 720 ACGACAAAAC ATGCAACAGG TTATGTCCTT CTGGTCCAGG GCACGGCTGA GACAGGCAAG 780 GGACTAGAGA GAGGAAGAGT GAATGTCAAG CCCCAGCACC CTCGCCTCCC TCCCATCCTC 840 CCTTTTAGGG CCTCCCTTCT GGCAGATAGG GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA 900 CACGTGGTTT GGATCACTGG CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG 960 GAGGCTGAAG ACTTCTTGTT AATAAGGGTG GGGCATGAGT AAAATGGAGG ATCTGCCCCC 1020 TCCCCTCCCA GCCCCTGATA CAAATGAAGG ATGATTGTAC ATGCATGGGG AATTCCACTT 1080 TGGGGGTATC CTTTTCTGGG CTGCTGCCAG ACTCTGAAAT GAGTAACAAA GGGATGGCCC 1140 AGGGTGACTC ATCAGCTACC CTCTCGCAGG CCTAGCACGC TGGCGGGGTG TGCATTTCCT 1200 CTAGAGAAGC CCCTCCCTGC CAGTTTCAGA GGGATGGCCC TGAATTGGCT TTTCAGAGGT 1260 TCCTTCTCCT CCCTTCCAAA GCGAAGACCC ACAGCTGCCT GAAAATGTGG CTCTCCGCCT 1320 TCTTGGGCTG CCTAGGACCT TGAGAGATGT GTCTCTCTGG GACAGGGTGT CAGGTCTGCT 1380 GGAGATTGTT AAAATGCTGT TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA GCAGTCTTCA 1440 GTAGCTTGGT CTGTTTATCG TGTATCTAGC TGTCAGCATG CAAAACAAAA GAACAAAAGG 1500 TCTAAAGAAA TATAACGCAA AACAGGTACG ATTTGAGATC CATCAGGGTT TCTCAACCTT 1560 GGCACAACTG ACTGGATAAT TGTTCATTGT AGGGGGCTGT CCTGTGAATT ATAGGATGTT 1620 TAGCTGCATC CTTGGCCTCT ACCCACACAC CCCCGTGTGC CACTCAAAAA TGTCTGCAGA 1680 CCTTGCCAAA TGTCCCCTGG GGGCTTGGCG GAGTTGGGGG GTGCATGGAA TGCCCCCAGT 1740 TGAGAACCAC TGGCAGAGCA GGAGTGAAGG GGGAGGTACT GTGGGGGTCA CTGGGCACAC 1800 AGAATGCCAT TTGGGGAGCC TGGTGCAAGG GAGTGGCCGG ATGGGAGGTA GGAATAGCAG 1860 TGGTAATCAG TAGGTGAGTT GCTGAAGACA AACTAAATAT TCTTTCCAGC ATTGCTTCAA 1920 TCTAATCCAG CCGCAAGTAT GAGTAAATAC TGTAGGAAAG GAGAAAACAT TGCATGTACG 1980 GGGTCAGGGC AGCATTGCTG GGATATTTGA GCCTGTGGGA GGGGAGCTTC AAGCTTCCCA 2040 CTAGCATTGG GAGGAACACA GCAAAGGAGG AGAAGGGCCC TCCCTGCTTC TTGGAGAATG 2100 GTTCCACTGG CAGGCCATTC CGTCTGCTCA GCTTCCTAGC TCAGGTGCCT TTCCAAACCA 2160 CACATCAGCA 2170
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