Tag | Content |
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EnhancerAtlas ID | HS113-03489 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:223913450-223915840 |
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 | CCTGATGTTT CCCACAAAGG GCCAGAGGCC CTTCAGTGCC AAGGAACGTG GACTCTCTCC 60 TATCCCAGCA CATACACGTG CTTCCAGTAC CTTGTGATCT CTAGCCATAA GTTTCCACTC 120 ACCCATCTGC GAAATGGGAA CAATGACGAT GTTTGCGTCC TTTCTTTTTC TTTTCCTACA 180 ATGCAGGGAA CTTTAAGACT ATGTGACAGA AAGGTGCCAC TGGAACCCAG GGCCTCGTGG 240 GTTTCCTCCG TCTCTCGGGA GACCAGGATC CGAGTGAGAA AGTTTCCCAC GTTCATTCTT 300 GTTGGGCCCA TTCTCAGGAT GATGTTTCTC CTGTATTTTG CTACCCCAGC CCAAGCAAGA 360 CTAGTAGTTC AGCTTTGTGA ATCCCCTCAG GAAGTCAGGA AAATAGATAC TGTCTTTGGG 420 CTTCCTCCAG GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA GGAATTTAAG ACAGGAATTG 480 GCAGCCGAGG GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG TGATGAGAGC 540 AGGGATGGGG AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG CCATCAGGAA 600 GGAGCAGCCA CCTCTGCTGG GGTACTGGAG ATAAAAACTC TGATATTGAC TAGTGACCGT 660 GGGGGCGATG GCCCAGGAGG GTCAGGGCTG CAGGGAACAG GGACACAAAA ACGACAAAAC 720 ATGCAACAGG TTATGTCCTT CTGGTCCAGG GCACGGCTGA GACAGGCAAG GGACTAGAGA 780 GAGGAAGAGT GAATGTCAAG CCCCAGCACC CTCGCCTCCC TCCCATCCTC CCTTTTAGGG 840 CCTCCCTTCT GGCAGATAGG GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA CACGTGGTTT 900 GGATCACTGG CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG GAGGCTGAAG 960 ACTTCTTGTT AATAAGGGTG GGGCATGAGT AAAATGGAGG ATCTGCCCCC TCCCCTCCCA 1020 GCCCCTGATA CAAATGAAGG ATGATTGTAC ATGCATGGGG AATTCCACTT TGGGGGTATC 1080 CTTTTCTGGG CTGCTGCCAG ACTCTGAAAT GAGTAACAAA GGGATGGCCC AGGGTGACTC 1140 ATCAGCTACC CTCTCGCAGG CCTAGCACGC TGGCGGGGTG TGCATTTCCT CTAGAGAAGC 1200 CCCTCCCTGC CAGTTTCAGA GGGATGGCCC TGAATTGGCT TTTCAGAGGT TCCTTCTCCT 1260 CCCTTCCAAA GCGAAGACCC ACAGCTGCCT GAAAATGTGG CTCTCCGCCT TCTTGGGCTG 1320 CCTAGGACCT TGAGAGATGT GTCTCTCTGG GACAGGGTGT CAGGTCTGCT GGAGATTGTT 1380 AAAATGCTGT TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA GCAGTCTTCA GTAGCTTGGT 1440 CTGTTTATCG TGTATCTAGC TGTCAGCATG CAAAACAAAA GAACAAAAGG TCTAAAGAAA 1500 TATAACGCAA AACAGGTACG ATTTGAGATC CATCAGGGTT TCTCAACCTT GGCACAACTG 1560 ACTGGATAAT TGTTCATTGT AGGGGGCTGT CCTGTGAATT ATAGGATGTT TAGCTGCATC 1620 CTTGGCCTCT ACCCACACAC CCCCGTGTGC CACTCAAAAA TGTCTGCAGA CCTTGCCAAA 1680 TGTCCCCTGG GGGCTTGGCG GAGTTGGGGG GTGCATGGAA TGCCCCCAGT TGAGAACCAC 1740 TGGCAGAGCA GGAGTGAAGG GGGAGGTACT GTGGGGGTCA CTGGGCACAC AGAATGCCAT 1800 TTGGGGAGCC TGGTGCAAGG GAGTGGCCGG ATGGGAGGTA GGAATAGCAG TGGTAATCAG 1860 TAGGTGAGTT GCTGAAGACA AACTAAATAT TCTTTCCAGC ATTGCTTCAA TCTAATCCAG 1920 CCGCAAGTAT GAGTAAATAC TGTAGGAAAG GAGAAAACAT TGCATGTACG GGGTCAGGGC 1980 AGCATTGCTG GGATATTTGA GCCTGTGGGA GGGGAGCTTC AAGCTTCCCA CTAGCATTGG 2040 GAGGAACACA GCAAAGGAGG AGAAGGGCCC TCCCTGCTTC TTGGAGAATG GTTCCACTGG 2100 CAGGCCATTC CGTCTGCTCA GCTTCCTAGC TCAGGTGCCT TTCCAAACCA CACATCAGCA 2160 GGGAGACAGT GGGAACATCT CAGGTCCAGG GTACCTTGGG AACTGCAGAG CAGCTGGGTG 2220 GCCTGACACT GGCATTTCTC AGTGTTGGCT CCATTCTCTT GCTGGCACCC CCAGGTGGGA 2280 GACTCTGTTA GCAGGTGTAT CTTACTATCC CTGGCTCCCT GGTATGCGTT ACAGTTCAGA 2340 CTCCCAAGCA CAAGCTCCCT GTTTTGTCAC ACCTGTATCT AGTGTGTAAC 2390
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