Tag | Content |
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EnhancerAtlas ID | HS179-00107 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr1:8476720-8479700 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr1:8477190-8477206 | AATTGTTTATTTAAGG | - | 6.15 | Foxq1 | MA0040.1 | chr1:8477190-8477201 | AATTGTTTATT | + | 6.02 | Pou2f3 | MA0627.1 | chr1:8477353-8477369 | GTCTATGCAAATGACA | + | 6.09 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_00045 | chr1:8465614-8485937 | Adipose_Nuclei | SE_02022 | chr1:8477510-8478261 | Aorta | SE_03407 | chr1:8479298-8480064 | Brain_Angular_Gyrus | SE_04978 | chr1:8478743-8481068 | Brain_Cingulate_Gyrus | SE_06073 | chr1:8479138-8485793 | Brain_Hippocampus_Middle | SE_07042 | chr1:8478805-8485534 | Brain_Hippocampus_Middle_150 | SE_07921 | chr1:8477474-8483841 | Brain_Inferior_Temporal_Lobe | SE_11329 | chr1:8474464-8493359 | CD20 | SE_18764 | chr1:8477368-8486022 | CD4p_CD25-_Il17-_PMAstim_Th | SE_23717 | chr1:8479176-8479684 | Colon_Crypt_1 | SE_25808 | chr1:8476636-8485754 | Duodenum_Smooth_Muscle | SE_27457 | chr1:8477725-8478732 | Esophagus | SE_28078 | chr1:8478132-8486070 | Fetal_Intestine | SE_29095 | chr1:8478033-8485919 | Fetal_Intestine_Large | SE_31622 | chr1:8477645-8478284 | Gastric | SE_31622 | chr1:8479255-8479634 | Gastric | SE_40658 | chr1:8476604-8477230 | Left_Ventricle | SE_40658 | chr1:8477420-8481421 | Left_Ventricle | SE_41679 | chr1:8477672-8478706 | LNCaP | SE_42166 | chr1:8477479-8478781 | Lung | SE_42166 | chr1:8478827-8481118 | Lung | SE_45677 | chr1:8477327-8485510 | Osteoblasts | SE_47251 | chr1:8465934-8485673 | Panc1 | SE_48103 | chr1:8477498-8481110 | Psoas_Muscle | SE_48600 | chr1:8477483-8479198 | Right_Atrium | SE_48600 | chr1:8479269-8481116 | Right_Atrium | SE_50481 | chr1:8479223-8481104 | Sigmoid_Colon | SE_51176 | chr1:8473915-8486131 | Skeletal_Muscle | SE_52725 | chr1:8477578-8478762 | Small_Intestine | SE_52725 | chr1:8479134-8481145 | Small_Intestine | SE_53408 | chr1:8477393-8478777 | Spleen | SE_54752 | chr1:8475052-8485774 | Stomach_Smooth_Muscle | SE_58576 | chr1:8455425-8501956 | Ly1 | SE_60758 | chr1:8454848-8500160 | DHL6 | SE_62661 | chr1:8450826-8509851 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I008416 | chr1 | 8476605 | 8477230 | GH01I008417 | chr1 | 8477394 | 8478781 |
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Enhancer Sequence | TTTTCTGTTT GAAATATTTT GCAATAATTA GAAAAACAAA ATCAAGCCCT AATAGTGAAA 60 CTTTACAATT TTAACAGAAT AAAGACAGTA TCATTTTAAG AATGATATAC TATGCAGGCT 120 CAGAATTCTG CAAGTCTGCA TTACTGTAAA TAGCGGTGCT TCCTAAACTT TACAGTACTT 180 TGGAATCCTC TGGGGGGTCC GTTAAAATGC AGATTCTGGC TCAAGAGACA AGGACAGGGC 240 CTGAGAATCT TCCATTTTAA CCAGTGATGA GAGTGCTGGC CTGAGGAGCA CACTGTGAGC 300 AGTGAGGATA GACAACGTTT GTAGAAGAGG GACAAGGTTT AAAAACAGAG ATCTTCTAAT 360 GTACTGGTAT GTGGCCGTGA CACATTTGCA CATTCTCAGT AGCATCAACC GACTAAGGAA 420 GTCCATACTT TGTTATGCAA CATTAGATTA AGCATTAATG AGGCTAGGAA AATTGTTTAT 480 TTAAGGTTAT AACCTGAAAT TAAATAAAAC TTCAGGCTGG AAGCTCATAT TGAATACTAG 540 AATCATTTTT AACCTCTTAA TATTAACAGA AACCTGATTA CTCAGTCTTA AAGCCCTTTC 600 TCAATAGCAT TTATTCTCTG CTGCAGGAAT ATGGTCTATG CAAATGACAT TTTGCCTGAA 660 GAAAAAAGTA CAGTTAATGG CCAGTAGTTA CGTACGTATT TAATAGAATT CATTCCCAGA 720 AATGTGGCTA AGAAAGGTGG TTGATTTTCA TGTTATTTAT TAAATTAAAA ATTTAAATCT 780 CTAATACCTT TCATCCCATT ACTTAAAGTT AAAAACGTCA AAACTGGCTG CCCTTTCACT 840 GGGCCCTTGG TGCCAAACAG TGACACATTT CCAATAGAGA AAATGAAGAT AGAAGGCAGG 900 CTTCCCTTCC CATTAACTTT GAACTTTCAA GTCCCTATCT GTCTTCCTAC AAGACTAAAT 960 TATAAGAAGA GCCTCCTCTT TGGTCCCATC CTATACATAC TTCGGTAGCA CAGCCCTCAC 1020 TTCTCTTCTT AAAAGCCTTA AATGGGTCCC ATCCCCACAC TCACCCATAC ACATTCTTTG 1080 GAGGGAATTC AAGGTCCCCC AAAATCTACC CTGCAGCTAT AATTTGGGCC CAAGTTCTAC 1140 TGCATCCGCT TATGCAACCT CCTTTCCAAC CATGCTCATG TACTTGCTGG GCACGTTTTA 1200 CAATTTCCTG TCTCCGTGCC TTTGTTCATA GTATTTCCTA TGGCTGGAAA GTTGCTTTTC 1260 CTCTACCCTC CCAACCTGGG CCTGTCAAAA ATGAATCCTT CCTTCAAAGC CCAGTTCAAA 1320 CACCGCCCCT CCAATTAGCT TTCCAGGAGC CTCTGTGCTC ACTTTGTGGG GCCTGAACCT 1380 CCACCCACCA GGGCCCTCAG CACATTCTAC CAAGTATGGC AGGTATGTAA ATGTCGTGCT 1440 GGCTCCCTGC AGGGCAGGGA TGGCACCTTG CTTCTCTTTA TAGATACCCT ACCCATTGCA 1500 GTGCTCAGTG GGCACCCAGA ACTTTAAAAA ATTGAACTAT ACACAAAATT TAGTTCTGAT 1560 AATGGGAAGT GAATGAAAAT GAGTTTCCAG TGTAGTAAGT GTCAATGCAC CACCAACTGG 1620 GATTACAAAT GACACAAGCT TAATCTTCAC TGGGCTAGGT GCTCAAAAAT AAAAAGAAAG 1680 AGACGAGAAA GACAGCCAAA GCATGTCCCC TTTCACCTTC CATCTCCCTC CAGGGGCTAA 1740 CACTTTGGGA ACACCTCTTG GCTACCAAGC TGGGGTAGAT CACATTGTCT TCTCACCAAT 1800 CTTAGTTGCA CCAGAGACAA GCAACGGCAG GTCACTGAGG AAGCGCTCCT GGACTACGAC 1860 CCAGTGCCAG CTGAATTTGT CTAAGTAATA GGAGACACAG CTATAAACAA AGGCCAGGAT 1920 TCAAGGGACA ATCATCCAGG TGCCAGACAC AAAAAGTCTT TGGTTCAAAT AACTGATATG 1980 TCCTCAGAGA AGAGATATGT CACCACTGCT TGAATAATTA TCTCATGATT TTGAAGAAAA 2040 CTGCAATGTA TAGACAAATC AAACAAAAAA TTATTTTTGG ATCATCCACG ATTTTGTGTT 2100 ATTCCTAACA TGGATTCACC TTTAGGTAAT TAAGATTCTC TATTAGGCCT CCTACTTTTT 2160 CAGGCATTAC CTTAACATCA AAGCTCATGT ACCATCCATC TACCCAACAA TAAGTGGCAG 2220 GGCTCAAAGC AGAATCAAGA GGCCTAGTTC TCCACTGTCC TCCCAAAAGT TCAGACACCG 2280 GGCGCTCTGT GACTTATACA AATATACTAA CACTTAAGAC TCTGATGTGG TTTATGACAA 2340 ACAGTGGCTT GACAGAGAAG AGGTATACAG CCAAGGTGAA TCTAAAATGC TCCACCCGTA 2400 TTCCTGACTA CATTTCACCT ACTAATTATA TACTTTATAA GCATATTGAG GGGAGGTAAA 2460 TGGTTATAGA GAAACAGAGA ATGGGAAAAA GTATAATAAA CTACAGGATA TTTGCACAAC 2520 CATGACACTA AAAGATTTGA CTTGTAGTTA TTCTCTTGGG TACCCTGAGG TTAACACGTA 2580 ATACCCATTC AACTAAGCCT CTATAAACAG TTGGGTTTTC CGCAATCACA GCCACTATTC 2640 CCACTTCAGT GGGCAGCAGT GTTCAGAGAA AAGCCAGATT TAGCTCTTGT GCAATAAACA 2700 CCAGAAACCA AAAGAGCTAG GAAAGCTGTT TACGTCTATG CCCACCAGGA ACCCTTCTCT 2760 GCTATAACCG CATGAATGAA CTGGTAAGAA TGAGGTCTCA ACAAAGCTTC AAGACGGACG 2820 TTGTTAACTA GTTGCTGCCC TCCAAGTTTT TGGCAAGACA GATTAATGAA AAACAGGTAA 2880 CTTATTTTTA TACAGGCTCA GTATATTTAC AAGCAGAAAG GAATTCTGTA CTTTTCAAAG 2940 CATTTAGCTA CCACCTTATG TAGTATTTAA GGTAGACAGG 2980
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