Tag | Content |
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EnhancerAtlas ID | HS133-21889 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:5036010-5038910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PLAG1 | MA0163.1 | chr3:5037301-5037315 | CTCCCTTGGGCCCC | - | 6.47 | SRF | MA0083.3 | chr3:5038003-5038019 | TGACCTTATTTGGAAA | - | 6.01 | 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: 35 | 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_23149 | chr3:5038072-5039086 | Colon_Crypt_1 | SE_25981 | chr3:5035829-5037703 | Duodenum_Smooth_Muscle | 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 | chr3:5036024-5038582 | 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 | chr3:5035854-5037849 | 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: 2 | Chromosome | Start | End |
chr3 | 5037242 | 5038218 | chr3 | 5038569 | 5038695 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I004993 | chr3 | 5034759 | 5039068 |
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Enhancer Sequence | TATGTCTGTG TGTATGAGAT CTCTCTGATA TATATATATA TATCAGACTG TGTGCTAAGT 60 ACTGTACTAG GCACTATGCA TACATTATCT GGTGCAATCT CCATTTTTAC ATTTACAGAA 120 ATTGAGACTC AGTGAGATTA AGTGACTCAC CCAAGGTCAC ACAGCAAGCA GATGGCACAG 180 ACAGGATTTA ACTCAACATA TGACTCAAAA GTCCTTGCTG AAAGAGCCCA GGATGTCAAA 240 ATGGACAGAG GCATGAGGAG GGAAGAGGGT CAGAGATAAG CTTCCCACTC TGTGCACACT 300 GCTGAATTAC CCATTAGGTA GACCTAGTGT GTGCTGAAAA CACTGGGAAA GCAGCCCCAG 360 CTTCCTTCCA TCTCCCCAAA ATTGGAAAAT AATTTCTTTT TGATATTTCA AAGAAAAACA 420 TGGAGATCAT CTTATGATTA AAATCAAGGG CTTATTGGGG TTTCTCTAAA TTTATTTTAA 480 GCTTTGTGTT TTCAGTTTGC ACTTCGTATG GGGAGGAAGG ATCAAAATGC TCATGTCTCA 540 GGACCTTAGG GCTTAATTGC CCTGGGGCTT AGAGCCTCTC TAGACCTTAT CCAGCAAGGT 600 GACGCTAGCT CTCCAGAGTC TGAGTGGGAG GCAGCATGGA CACCCACCTG GCCCCTGCTT 660 CCCCTGGGGC TCACGTGGCT GTGTGAGGGG TGTTTCTTAG GGCAGTGGCC TCAGCTCCCC 720 TGACCCGTGG CTTCTCACAG TCTGCCTTTC AGACAAGGCG CTCACTGTCC CAGCATGTTC 780 CAAGCCACCG GCTCAAGTCC CAGCCAGCCC AGGCCTGTTG CAATGAGTCA GCCTTTCACT 840 GGGGAAAAAC GTGGTGACTG GCCTCCAAGT CATTTTTTCC AGCTTGGCCC TTGTCCTGGG 900 CTGGGTTTGG GGAGACCTTC ATTTTTCCCT TTGGGATTCG GCTGCCTACG AGGTATTCCC 960 AAGGGTCCCT AGGAAGCAAG GGGGCTGGAA TTCCTTTGGG GCAGGTTGAG TTGCTGCAGT 1020 TCAGCCAAAT GAGGGTCCCT CAAGGTGCCC ACCTGGTCTC GCTCCACCTC CCCCTGCTCA 1080 TATAAGCAAA AGTAGAGGCC ACAGAGGGTA AGTTCTTATG GCCCTTACGG TTGTGCCCAG 1140 TCATGGGGAG GAGGATAAGA AGAGGAGTTA TAAAATAAAG TCCACCTTTG GCATCTTTCA 1200 CAGGCCATGC TAGCGCAGCA ACCTCAGGTA CCTGGAGCTT GAGGCACACT TGGCCTCTTA 1260 TCAACTAGTG GTGCCTTCCT GAAAGATGAT GCTCCCTTGG GCCCCTTGAA TTTTAAAGCA 1320 AGCACCATTA CCTTCGGTGA ACCTTCCTGC CCCCAGCTCT ATGCCAGGGT TCCGGTTTCA 1380 GAGCTATTCG CCTTACCATC CCTTCTGACT CACCTCTGGC TTCCCAGGGC TTCGTGAGGC 1440 CTCCCCTGCA TGGCCAGGCT GATGTGGATT CTCCCTAGTG TGACTGGGTG GGAGGGAGGA 1500 AGAGGCAATG ACCATTAGTC AAAGGGTGGT GAGGGTGCGT GAGGGCAGGG CTTTGGCCCT 1560 CACGGATCCC GCAGTAAATT CACTCTCTCC GGAGGAAACA TTGACCTCAC TGCTGCTGAA 1620 GCCCTTACTT AGAACTTCCT ATTCATTTTT GCAATTAGCA AAGATTAACC TCTCAATAAT 1680 TCATTCATTC AGGGCACAGA TAGTTATTGG TACCTTTACA TGCCAGGTAC TGGGCTTTGG 1740 GGCTACAATA GTGCACAGAA GAGTCATGCT CCTGTTTCCT GAAGCCGATA GTCTGAGAGG 1800 GACACAGATA GCAACCTGAT AATTACACAG ATAGATACCA ACAATCCAGT ATCAATATGC 1860 AAGAAGAGCA CAGAAGAGCA GACAACAGTG CCTGGAGTGG TCTGGGGTGT TCAGGGAAGG 1920 TTTGCCTGAA ATAGACGGGT AAGTGGGAGT TGTCTGGTTG AGATGGGGGT CCTGACCCCA 1980 AGTACCTAGA TAGTGACCTT ATTTGGAAAT AGGGTTTTTT ACAGAGATAA TCAAGTTAAC 2040 ATGAGGTCAT TAGGGTAGGC CCTAATCTTG ACTGGTATTC TTATCAAAAG GGGAAATTTG 2100 GACACAGAGA CAGACATGCG CACAGGAAGA ATGTCACGTG AAGATGAAAG CAGACATCAG 2160 GGGGATGCTG GCTGCTTACA AGCCATGGAA TGCCGAAGAT AGTGAGCCGA CACCAGGAGC 2220 TAGGAGAGAA GCCTAGAACT GACGCTCCCT CACGGCCTCC AAGGAACCAA ATCTGCTGAC 2280 ACCTTGATTT TGAATTTTTA GCTTCCAGAA CTTGAGATCA CACATTTCTG TTGTTTAACC 2340 CACCCCAGCT GTGGTCTTTT GTCAAGGTAG CCGTAGCAGA CAAACTCAGT TTTCCAGCAG 2400 AGGAAACTGC ACATGCAAAA GCCCTGGAAG TGAGGGCAGG GGAGGCGGGT TTGAGAAAAG 2460 AGGCCACCCT GGCTGAAATG CAGAGTCAAA AATTCCTTCA TCCAGACTGA CAGGGAAGCA 2520 GATCAGTGTG GGCACCTCAG GCGACTATTA AAATAGCAAT AAAAATAACT ACCTCGAAGG 2580 TGTGTAGAGT GTACCAGATA AGCCTGGGGA GGCAGGAAGT GACTAGAGCT ATGCAGGGGC 2640 TTCCCTGTAG GGGTAGAAGT GGAGCCTTTA ACCTTAAGAC AGAGGAGAAG CTAGCAGGGT 2700 ACGCAGGCGA CCTAGAGCCT CGTTTGAGGT GTGTGACTTT GGGAAAATGG CCGTCTGTCT 2760 CTGTGCCTTA GTTCTTCGAT CTCTTCCCTT ATCTGGGACA TTCTGTGACC ATATGACTAG 2820 CAGTGTGCTC TGTGTTGCTG TCTCCTGTGT GGTGAGCCGG TGCGAAGGAA GAGAAAAGAA 2880 TGAAAATAGC ATTGGACACA 2900
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