Tag | Content |
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EnhancerAtlas ID | HS146-01320 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr1:223913420-223915700 |
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 | TTTTCTTTGG TCACACAATG GTCATGGCCT CCTGATGTTT CCCACAAAGG GCCAGAGGCC 60 CTTCAGTGCC AAGGAACGTG GACTCTCTCC TATCCCAGCA CATACACGTG CTTCCAGTAC 120 CTTGTGATCT CTAGCCATAA GTTTCCACTC ACCCATCTGC GAAATGGGAA CAATGACGAT 180 GTTTGCGTCC TTTCTTTTTC TTTTCCTACA ATGCAGGGAA CTTTAAGACT ATGTGACAGA 240 AAGGTGCCAC TGGAACCCAG GGCCTCGTGG GTTTCCTCCG TCTCTCGGGA GACCAGGATC 300 CGAGTGAGAA AGTTTCCCAC GTTCATTCTT GTTGGGCCCA TTCTCAGGAT GATGTTTCTC 360 CTGTATTTTG CTACCCCAGC CCAAGCAAGA CTAGTAGTTC AGCTTTGTGA ATCCCCTCAG 420 GAAGTCAGGA AAATAGATAC TGTCTTTGGG CTTCCTCCAG GAGCTAAGAA AGGAGAGTTC 480 CTGAAGAGCA GGAATTTAAG ACAGGAATTG GCAGCCGAGG GCAAGGTTCC ACCTCCTCCT 540 CCCTTCTTCT GTGGGGTCTG TGATGAGAGC AGGGATGGGG AGGAAGAGGG TGGGTTTGCC 600 TGCGCCTGGG GGGAGGGCAG CCATCAGGAA GGAGCAGCCA CCTCTGCTGG GGTACTGGAG 660 ATAAAAACTC TGATATTGAC TAGTGACCGT GGGGGCGATG GCCCAGGAGG GTCAGGGCTG 720 CAGGGAACAG GGACACAAAA ACGACAAAAC ATGCAACAGG TTATGTCCTT CTGGTCCAGG 780 GCACGGCTGA GACAGGCAAG GGACTAGAGA GAGGAAGAGT GAATGTCAAG CCCCAGCACC 840 CTCGCCTCCC TCCCATCCTC CCTTTTAGGG CCTCCCTTCT GGCAGATAGG GCAGGGAGAA 900 GGGAAAGGAA AGGCCTGGGA CACGTGGTTT GGATCACTGG CTGTGGCTCA CAGTTCTGAT 960 GTGTGTGCAG TTTAGGGAAG GAGGCTGAAG ACTTCTTGTT AATAAGGGTG GGGCATGAGT 1020 AAAATGGAGG ATCTGCCCCC TCCCCTCCCA GCCCCTGATA CAAATGAAGG ATGATTGTAC 1080 ATGCATGGGG AATTCCACTT TGGGGGTATC CTTTTCTGGG CTGCTGCCAG ACTCTGAAAT 1140 GAGTAACAAA GGGATGGCCC AGGGTGACTC ATCAGCTACC CTCTCGCAGG CCTAGCACGC 1200 TGGCGGGGTG TGCATTTCCT CTAGAGAAGC CCCTCCCTGC CAGTTTCAGA GGGATGGCCC 1260 TGAATTGGCT TTTCAGAGGT TCCTTCTCCT CCCTTCCAAA GCGAAGACCC ACAGCTGCCT 1320 GAAAATGTGG CTCTCCGCCT TCTTGGGCTG CCTAGGACCT TGAGAGATGT GTCTCTCTGG 1380 GACAGGGTGT CAGGTCTGCT GGAGATTGTT AAAATGCTGT TGTCTCAGGA AGGGTGAAAT 1440 TTAGCCAGGA GCAGTCTTCA GTAGCTTGGT CTGTTTATCG TGTATCTAGC TGTCAGCATG 1500 CAAAACAAAA GAACAAAAGG TCTAAAGAAA TATAACGCAA AACAGGTACG ATTTGAGATC 1560 CATCAGGGTT TCTCAACCTT GGCACAACTG ACTGGATAAT TGTTCATTGT AGGGGGCTGT 1620 CCTGTGAATT ATAGGATGTT TAGCTGCATC CTTGGCCTCT ACCCACACAC CCCCGTGTGC 1680 CACTCAAAAA TGTCTGCAGA CCTTGCCAAA TGTCCCCTGG GGGCTTGGCG GAGTTGGGGG 1740 GTGCATGGAA TGCCCCCAGT TGAGAACCAC TGGCAGAGCA GGAGTGAAGG GGGAGGTACT 1800 GTGGGGGTCA CTGGGCACAC AGAATGCCAT TTGGGGAGCC TGGTGCAAGG GAGTGGCCGG 1860 ATGGGAGGTA GGAATAGCAG TGGTAATCAG TAGGTGAGTT GCTGAAGACA AACTAAATAT 1920 TCTTTCCAGC ATTGCTTCAA TCTAATCCAG CCGCAAGTAT GAGTAAATAC TGTAGGAAAG 1980 GAGAAAACAT TGCATGTACG GGGTCAGGGC AGCATTGCTG GGATATTTGA GCCTGTGGGA 2040 GGGGAGCTTC AAGCTTCCCA CTAGCATTGG GAGGAACACA GCAAAGGAGG AGAAGGGCCC 2100 TCCCTGCTTC TTGGAGAATG GTTCCACTGG CAGGCCATTC CGTCTGCTCA GCTTCCTAGC 2160 TCAGGTGCCT TTCCAAACCA CACATCAGCA GGGAGACAGT GGGAACATCT CAGGTCCAGG 2220 GTACCTTGGG AACTGCAGAG CAGCTGGGTG GCCTGACACT GGCATTTCTC AGTGTTGGCT 2280
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