Tag | Content |
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EnhancerAtlas ID | HS092-27707 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr3:5035460-5037930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PLAG1 | MA0163.1 | chr3:5037301-5037315 | CTCCCTTGGGCCCC | - | 6.47 | TFAP2C | MA0524.2 | chr3:5036567-5036579 | TGCCCTGGGGCT | - | 6.11 | ZNF263 | MA0528.1 | chr3:5037156-5037177 | GGAGGAGGATAAGAAGAGGAG | + | 6.95 | Zfx | MA0146.2 | chr3:5036813-5036827 | CCAGCCCAGGCCTG | + | 6.19 |
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| Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
SE_00456 | chr3:5035625-5037887 | Adipose_Nuclei | SE_00991 | chr3:5036303-5037749 | Adrenal_Gland | SE_01935 | chr3:5035983-5037705 | Aorta | SE_02322 | chr3:5035786-5038149 | Astrocytes | SE_13436 | chr3:5035896-5039074 | CD34_Primary_RO01536 | SE_14396 | chr3:5035814-5039433 | CD4_Memory_Primary_7pool | SE_20744 | chr3:5035797-5039174 | CD8_Memory_7pool | SE_23149 | chr3:5036486-5037186 | Colon_Crypt_1 | SE_25981 | chr3:5035829-5037703 | Duodenum_Smooth_Muscle | SE_26553 | chr3:5034816-5035987 | Esophagus | SE_26553 | chr3:5036006-5038016 | Esophagus | SE_31556 | chr3:5036424-5037381 | Gastric | SE_34579 | chr3:5035914-5038390 | HCT-116 | SE_34684 | chr3:5035830-5038073 | HeLa | SE_35840 | chr3:5034761-5038436 | HMEC | SE_36983 | chr3:5035644-5038035 | HSMMtube | SE_38020 | chr3:5035054-5038305 | HUVEC | SE_39863 | chr3:5035873-5039236 | K562 | SE_40764 | chr3:5035935-5037778 | Left_Ventricle | SE_42278 | chr3:5036027-5037799 | Lung | SE_44737 | chr3:5035847-5037824 | NHDF-Ad | SE_45042 | chr3:5035912-5037599 | NHLF | SE_45785 | chr3:5034236-5039113 | Osteoblasts | SE_48124 | chr3:5034960-5035738 | Psoas_Muscle | SE_48124 | chr3:5036024-5038582 | Psoas_Muscle | SE_48683 | chr3:5036274-5037527 | Right_Atrium | SE_49557 | chr3:5036486-5036815 | Right_Ventricle | SE_51119 | chr3:5034783-5038500 | Skeletal_Muscle | SE_51934 | chr3:5035924-5037409 | Skeletal_Muscle_Myoblast | SE_55004 | chr3:5036132-5037763 | Stomach_Smooth_Muscle | SE_55854 | chr3:5033941-5038736 | u87 | SE_62573 | chr3:5014508-5068965 | Tonsil | SE_63719 | chr3:5035924-5037609 | HSMM | SE_64232 | chr3:5034870-5035821 | NHEK | SE_64232 | chr3:5035854-5037849 | NHEK | SE_65389 | chr3:5036040-5037714 | Pancreatic_islets | SE_67463 | chr3:5033941-5038736 | u87 |
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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: 1 | ID | Chromosome | Start | End |
GH03I004993 | chr3 | 5034759 | 5039068 |
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Enhancer Sequence | TGAATCTGTT TCCTTATCCA TCAAATGGGG ATATTAGTGA TCTTGTAGAG ATTGCCGTGA 60 GGATGAAAAG AAATCCTTAT GTAGAATATA CAGCATCTAG CTACAGTCAG GTATGTGGTA 120 GGTGCTCAAG CATTTGCTGA TTAAATGAAT GAAAGGAGCC TGGGCAACAT AGCAAAAACT 180 CTGTCTCTAC AAATAAAAAT TAAAACATTA GCCAGTCATG GTGATACGGA CCTGTAGTCC 240 CAGCTACTCA GGAGGCTAAG GTGGGAGGAT CTTAGCCTGC AGTGAGCCAT GACCACGCCA 300 CTGTACTCCA GCCAAGGTGA CAGAGTGAGG CCCCATCTCA AAATAAAACT TTAATTTAAT 360 TTAAAAATAA AAGAAAATAA AAAAATAAAT GAAAAGAAAG AATGACATTT ATAGGAACAT 420 ATTCACTCTA AAGTGTAAGT AACTGACATA ACATTATTTC CTGAAAGATG CTTTGTAGAG 480 GGAAAAGCTG AAAGAGATCT CATACACACA CACACACACA CACACATATA TATACACACA 540 CACATATATA TATGTCTGTG TGTATGAGAT CTCTCTGATA TATATATATA TATCAGACTG 600 TGTGCTAAGT ACTGTACTAG GCACTATGCA TACATTATCT GGTGCAATCT CCATTTTTAC 660 ATTTACAGAA ATTGAGACTC AGTGAGATTA AGTGACTCAC CCAAGGTCAC ACAGCAAGCA 720 GATGGCACAG ACAGGATTTA ACTCAACATA TGACTCAAAA GTCCTTGCTG AAAGAGCCCA 780 GGATGTCAAA ATGGACAGAG GCATGAGGAG GGAAGAGGGT CAGAGATAAG CTTCCCACTC 840 TGTGCACACT GCTGAATTAC CCATTAGGTA GACCTAGTGT GTGCTGAAAA CACTGGGAAA 900 GCAGCCCCAG CTTCCTTCCA TCTCCCCAAA ATTGGAAAAT AATTTCTTTT TGATATTTCA 960 AAGAAAAACA TGGAGATCAT CTTATGATTA AAATCAAGGG CTTATTGGGG TTTCTCTAAA 1020 TTTATTTTAA GCTTTGTGTT TTCAGTTTGC ACTTCGTATG GGGAGGAAGG ATCAAAATGC 1080 TCATGTCTCA GGACCTTAGG GCTTAATTGC CCTGGGGCTT AGAGCCTCTC TAGACCTTAT 1140 CCAGCAAGGT GACGCTAGCT CTCCAGAGTC TGAGTGGGAG GCAGCATGGA CACCCACCTG 1200 GCCCCTGCTT CCCCTGGGGC TCACGTGGCT GTGTGAGGGG TGTTTCTTAG GGCAGTGGCC 1260 TCAGCTCCCC TGACCCGTGG CTTCTCACAG TCTGCCTTTC AGACAAGGCG CTCACTGTCC 1320 CAGCATGTTC CAAGCCACCG GCTCAAGTCC CAGCCAGCCC AGGCCTGTTG CAATGAGTCA 1380 GCCTTTCACT GGGGAAAAAC GTGGTGACTG GCCTCCAAGT CATTTTTTCC AGCTTGGCCC 1440 TTGTCCTGGG CTGGGTTTGG GGAGACCTTC ATTTTTCCCT TTGGGATTCG GCTGCCTACG 1500 AGGTATTCCC AAGGGTCCCT AGGAAGCAAG GGGGCTGGAA TTCCTTTGGG GCAGGTTGAG 1560 TTGCTGCAGT TCAGCCAAAT GAGGGTCCCT CAAGGTGCCC ACCTGGTCTC GCTCCACCTC 1620 CCCCTGCTCA TATAAGCAAA AGTAGAGGCC ACAGAGGGTA AGTTCTTATG GCCCTTACGG 1680 TTGTGCCCAG TCATGGGGAG GAGGATAAGA AGAGGAGTTA TAAAATAAAG TCCACCTTTG 1740 GCATCTTTCA CAGGCCATGC TAGCGCAGCA ACCTCAGGTA CCTGGAGCTT GAGGCACACT 1800 TGGCCTCTTA TCAACTAGTG GTGCCTTCCT GAAAGATGAT GCTCCCTTGG GCCCCTTGAA 1860 TTTTAAAGCA AGCACCATTA CCTTCGGTGA ACCTTCCTGC CCCCAGCTCT ATGCCAGGGT 1920 TCCGGTTTCA GAGCTATTCG CCTTACCATC CCTTCTGACT CACCTCTGGC TTCCCAGGGC 1980 TTCGTGAGGC CTCCCCTGCA TGGCCAGGCT GATGTGGATT CTCCCTAGTG TGACTGGGTG 2040 GGAGGGAGGA AGAGGCAATG ACCATTAGTC AAAGGGTGGT GAGGGTGCGT GAGGGCAGGG 2100 CTTTGGCCCT CACGGATCCC GCAGTAAATT CACTCTCTCC GGAGGAAACA TTGACCTCAC 2160 TGCTGCTGAA GCCCTTACTT AGAACTTCCT ATTCATTTTT GCAATTAGCA AAGATTAACC 2220 TCTCAATAAT TCATTCATTC AGGGCACAGA TAGTTATTGG TACCTTTACA TGCCAGGTAC 2280 TGGGCTTTGG GGCTACAATA GTGCACAGAA GAGTCATGCT CCTGTTTCCT GAAGCCGATA 2340 GTCTGAGAGG GACACAGATA GCAACCTGAT AATTACACAG ATAGATACCA ACAATCCAGT 2400 ATCAATATGC AAGAAGAGCA CAGAAGAGCA GACAACAGTG CCTGGAGTGG TCTGGGGTGT 2460 TCAGGGAAGG 2470
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