Tag | Content |
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EnhancerAtlas ID | HS083-01790 |
Organism | Homo sapiens |
Tissue/cell | HCC1954 |
Coordinate | chr3:58035280-58039100 |
SNPs | Number: 4 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr3:58037766-58037777 | CCACACCCTGC | + | 6.62 | NFE2L1 | MA0089.2 | chr3:58038185-58038200 | ATGGCTGAGTCATGT | - | 6.2 | Nr2f6(var.2) | MA0728.1 | chr3:58037833-58037848 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6(var.2) | MA0728.1 | chr3:58035975-58035990 | TGAGCTCTTGACCTC | - | 7.23 | Zfx | MA0146.2 | chr3:58035998-58036012 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_00762 | chr3:58032174-58039716 | Adipose_Nuclei | SE_01957 | chr3:58034706-58035838 | Aorta | SE_01957 | chr3:58036187-58037788 | Aorta | SE_01957 | chr3:58037976-58039178 | Aorta | SE_23194 | chr3:58034815-58035733 | Colon_Crypt_1 | SE_23194 | chr3:58038002-58038849 | Colon_Crypt_1 | SE_26498 | chr3:58033363-58039459 | Duodenum_Smooth_Muscle | SE_27681 | chr3:58033703-58037597 | Fetal_Intestine | SE_27681 | chr3:58037756-58039153 | Fetal_Intestine | SE_29426 | chr3:58033550-58039244 | Fetal_Intestine_Large | SE_30574 | chr3:58034058-58035832 | Fetal_Muscle | SE_30574 | chr3:58036943-58038968 | Fetal_Muscle | SE_36024 | chr3:58033449-58039332 | HMEC | SE_37989 | chr3:58025669-58040227 | HUVEC | SE_41579 | chr3:58034780-58035730 | LNCaP | SE_41579 | chr3:58036203-58037368 | LNCaP | SE_41579 | chr3:58038029-58038806 | LNCaP | SE_45969 | chr3:58032377-58039419 | Osteoblasts | SE_47269 | chr3:58019885-58040171 | Panc1 | SE_56289 | chr3:58032310-58039346 | u87 | SE_64106 | chr3:58033450-58035902 | HSMM | SE_64106 | chr3:58036259-58039158 | HSMM | SE_65730 | chr3:58034390-58037100 | Pancreatic_islets | SE_65730 | chr3:58037283-58039024 | Pancreatic_islets | SE_67942 | chr3:58032310-58039346 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 58036837 | 58037638 | chr3 | 58037994 | 58038685 | chr3 | 58038147 | 58038335 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I058046 | chr3 | 58032437 | 58041425 |
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Enhancer Sequence | GGTAATAAAT GGGAATGGAG TTTCACAGGT AGGGTGTGGA GGAATTTATT GTGACAGGAA 60 GCCTGATGGA GCCTCTTGCC TGTGTGCAGC CCCCAGCCAG GTTTCTGAGT TCTGATGAAC 120 TACCAGAAAC TTCCACCACG GCCTGTGATT ACACTGTTGG CCCAATGCCC TGGAAAAATT 180 GGCTTGCTCT CGGGGAACAC TCCAGGAGCT GCAAAGGGGG TGTCAGGACT GTTGTGCAGC 240 TCCCCTTAAA TTGGGGAGGA GGGGTGGCTG ATGTGGAAAC TGTTCATTAG ACTGCTCAGG 300 GTAGTGTGAG AAAACGTGTA ATCTGTGGGC ATCTACCCCT AGCTGCCCCT CTGATCTCAC 360 CCACTACTGT GGGAGGACCC CGTGGATGGG GGCAGAGGAG GGTCTTCTGG ATTTAGACAC 420 TCACAAAACT TCCTTTTACC TTGTTCATTG GAAGAAATAG AAAATGCCTT TTTTTTTTTT 480 TTTTTCTTTT TTTTTGAGAC AGAGTCTCGC TCTGTTGACA GGCTGGAGTG CAGTGGCATG 540 ATCTTGGCTC ACCGCAACCT CTGCCTCCCG GGTTCTAACA ATTCTCCTGC CTCAGCCTCT 600 GGAGTAGCTG GGACTACAGC CACGTGCCAC CACACCCAGC TAATTTTTGT ATTTTTAGTA 660 CAGACGGGGT TTCACCATGT TGGCCAGGAC GGTCTTGAGC TCTTGACCTC GTTATCCACC 720 CGCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC CACCATGCCT GGTCTCTTTT 780 TCATTTTTAA AGGGTAATTT GCTGTGCAGG AGTGGGCTCT CAGACCAGAA GTGGGGACCT 840 GAATGAAATC AAGGACTGAG TATGGTAACT ACAGCCATTT AATTTTATTT GAAGTCTCCC 900 GTAAAATGTT CTGGAAAAAA CAGGGGTTCC AGGGCTGGGT GGGCAGTTTC AATCATGGAC 960 TGGATTTTGT GGTTCAGATT TCTCTGGGCC TGTTGGAGGT TCCCCTTAAG CAATTACCCA 1020 AGGCAGTTCT GCCCAGCTGA AGTACTGATT ACCTGCACAC TATACCAGTG AGGACTCATG 1080 GGTGAGCAGA TGGGAGGCAC TGAGCTTGAT TCTGAAACCC TGGCCTCCAT CCCACCTGAC 1140 ATTCAATGTC AGATTAGAAT TTGGAAGACC CTAAGTCTCC AGATTGGTGC ACTGGGTAGC 1200 TCCTGAAATG GGGTGGCTGA GACAGGTCCT CTGTGCCCCC TTCCACAGCT TCCTCTGGGG 1260 CCCTTCTGCT CACTGGCATG TGCTTCTGGG CAAATAGGCC TCTCCCAGCA TTTGTTTTGG 1320 CTCTGTGAAA TGGGGTAATA TTTGTTCCTA TTGCGGGTGA AGCGCTGCTG TTGGGATGCT 1380 CAGGTAACTC ACTCCGTGGG TAGCTGATAT TGCCTGGGCA AGTGGCATTT TAGAGGAAAT 1440 CTGTGCCATC AAAAGAGTTG GACCTGATCA CACTTTTGCT TTTGAATATG CTTTGTCCCA 1500 GCCTGGCCAT TCGTCACTTG GGACCCCCTG AGTCTCTCTG ACCCCACTGT AAAATGGATA 1560 TGCCATGGAG TTGTCCCAGG AATCAAGGGC AGGTCCTCTC CAGTGAGTGA TGGGCTTGCC 1620 TCTCACTTCT CTAACACCCT TCTGCTTCCT TGTGTAAGAT TTCACTATTA GTGGCTATTC 1680 TCTTTTACAG AAGAAAAAGG GAGACGCATG CCTCTTCCAG TTCACTGTTC ACCATTGCAG 1740 CATATTTATT CCAAGGGACT GGCCGAATCA TCCCTTTCTT TGTTAGAATG TGGTTTTGTT 1800 GCCTTGAGAC AAGTGGCCCG CATGTCTGCA CTGAAGGAGG CTTTGCGCAA TAGCCTTGGG 1860 CACCTCCGGT TCTGCAAGCA TGTACAGTAC TTGCTCTCCT TTCCCTTTCT TTGTATACTT 1920 TTTCTGGTCT GCTACGTGTC CATCTGCATG TGGATAAAGG GTCGTCGTCT TGAGTAGTGA 1980 TTTTGCTGTG ATGTGATTCC TGTGAGGTCT AGTTGCACAC AGTGATTCCG AAGGTAGACC 2040 CAGCTGGAAA GCTTTTAAAT TGCTGATACT CCAGCCCCAC TCCCCAAGAG ATGCTGATTT 2100 TGTTTTGTTT TGGGGAGGGC AGTTTTTTTG GGTTTTTTTT TTAAGCTTTT TGATGTGTAG 2160 CCAGGGTTGA GACTGAAGTG ATTTTTGTGA GTAACGGAGA AGTGTTAAGG CTTGAGAAGT 2220 TGGAAGAGCC ATGCTTGAGA TAGGACCAAG GTCATATCCC CGGCATTAGC ACAGAGCAAC 2280 CCTGACCTGT TGGAGAGTTG GGCTGGATGG ATGCGGTCAG GGGAGAGACT CGCTTTATTT 2340 TATTTATTTA GAGATACAGT TTCACTCTTG TCACCCAGGC TGGAGTGTAA TGGCACGATC 2400 TCGGCTCACT GCAACCTCTG CCTCCTGGGT TCAAGTGATT CTCGTGCCTC AGCCTCCTGA 2460 GTGGCTGGGA CTCCAGGCAC GCGCCGCCAC ACCCTGCTAG TTTTTGTGTT TTTACTAGAG 2520 ACAGGGTTTC ACCATTGTTG GCCAGGCTGG TCTTGAACTC CTGACCTCAG GTGATCCGCC 2580 CACCTCGGCC TACCAAAGTG CTGGGATTAT GGGTGTGAGC CACTGTGCCC AGCCTCGACT 2640 CGCTTTATTA TATCCACACT TGGAATACAA TTCGGATTGA TTGTAGTGGG GCATTTTATA 2700 ATTAGGAAAA ATTAATCAGG AAAAATCACT CCATGTAGAT TAGTACCACC ATATGAGGGG 2760 ACAAGAATTT CTTCAGATTA GGAACTTCTT CCAACAGGAC TGACAGGGTC CAAAACTACT 2820 CTTGGATCCA GCTTTAAGAT GGACCCAGCC CACTGTTGAG TCCCCTCTGA GGTCTTCTCT 2880 CTGTGGATGG ATTTGATTGT TAACAATGGC TGAGTCATGT GGCACCCAGC CCGGTGAGTA 2940 AGACAGCTGA GTAAGAGGGG AAACAGGGCC TTTGGTCAGA AAAACCAGAC TGACTTCAGT 3000 CTTATCTGTT TAGAGAAGCC CCAGAAGCTG CAAAAATTGC AGCTTCCAGA CTTTAGTGTG 3060 CCGTGGTCAT GACATCGGTG TGGATGGCAG GTTGTCATCT GAGCAGTCAG GGTGGCAGCA 3120 CACAGCTTGC GGGCTGGCTG ATGGCCGAGG TGTGTGAACT GACCTGCCCC AAGTGACTTC 3180 AGTGCTGGGC ACAGCATAGG AGCAGTACTA ATGATATGGA CAGTATGCTC AGAGGACGTT 3240 AGGGAGCACA GCTTTGTGTA AAGGGCATGC CCTGCCCTGT CCGGATTTAA AGCAGCTATA 3300 GCACTGAAAC CCCATGGTCA CCCTCGCATT TCTACACTTC TGCCTGTGCC AAGTCTAGTT 3360 TGTGTGCCTC CTCCATTTTG TGTGTACATG GGGGTATTTT TTTCTGCTAG GCAACTGCTA 3420 TTTATGCCTC TCAGTACTGT ACTTAGTGTG TACCATTCCT GCAAGGTATA GACATTGTCA 3480 GCCCATTTTA CAGATGAGGA AAATGGAGTT TTTGAGAGGG TGAGATCATT CAGTGGCAGA 3540 ATGGAATGTT AACCCAGGTA GTCTAACCTC TCTGCTGTAG ATCTGATGTC CATTTGAACT 3600 TTAGACTTCC CATCTGTGTC TACAGTCTAG CCCTTAAAAA ATGTGATAAA CAGGTTTTTA 3660 GGTAAGTCTG TTAATTTCAG AAAGACATTA TTATTATTTT TTAGAAAGTT AGAGCTTATG 3720 TTAGGGCTCA GTCTATCCTC CTGCCTCAGC TGCCTGAATA GCTGGGACTG CAGGCACATG 3780 CCACCATGCC TGGTTAATTT CTGTGGTATA CATCATTGAT 3820
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