Tag | Content |
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EnhancerAtlas ID | HS170-01817 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr18:2971970-2973930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr18:2972069-2972080 | AAAACAAAGAA | + | 6.62 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00574 | chr18:2966969-2973380 | Adipose_Nuclei | SE_09781 | chr18:2966395-2973802 | CD14 | SE_10621 | chr18:2966529-2973369 | CD19_Primary | SE_11211 | chr18:2965754-2974502 | CD20 | SE_11888 | chr18:2966025-2973515 | CD3 | SE_13797 | chr18:2971877-2973371 | CD34_Primary_RO01536 | SE_14570 | chr18:2966147-2973511 | CD4_Memory_Primary_7pool | SE_15580 | chr18:2968955-2973487 | CD4_Memory_Primary_8pool | SE_16149 | chr18:2968825-2973294 | CD4_Naive_Primary_7pool | SE_16392 | chr18:2965894-2973313 | CD4_Naive_Primary_8pool | SE_16996 | chr18:2966118-2973202 | CD4p_CD225int_CD127p_Tmem | SE_17424 | chr18:2965889-2974201 | CD4p_CD25-_CD45RAp_Naive | SE_17870 | chr18:2953882-2974054 | CD4p_CD25-_CD45ROp_Memory | SE_18346 | chr18:2955510-2974150 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19436 | chr18:2965856-2974074 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20084 | chr18:2966548-2973789 | CD56 | SE_21011 | chr18:2966194-2973557 | CD8_Memory_7pool | SE_21798 | chr18:2969010-2973427 | CD8_Naive_7pool | SE_22207 | chr18:2967244-2973383 | CD8_Naive_8pool | SE_22362 | chr18:2965884-2973987 | CD8_primiary | SE_26140 | chr18:2969941-2973385 | Duodenum_Smooth_Muscle | SE_28431 | chr18:2972309-2973678 | Fetal_Intestine | SE_31871 | chr18:2972028-2972961 | Gastric | SE_32704 | chr18:2970342-2973397 | GM12878 | SE_46307 | chr18:2970914-2973905 | Osteoblasts | SE_51026 | chr18:2971961-2973044 | Sigmoid_Colon | SE_52825 | chr18:2968508-2973013 | Small_Intestine | SE_58874 | chr18:2954099-2995404 | Ly3 | SE_59888 | chr18:2955879-2985795 | Ly4 | SE_62302 | chr18:2955378-2999752 | 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: 1 | ID | Chromosome | Start | End |
GH18I002965 | chr18 | 2965574 | 2973631 |
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Enhancer Sequence | GGAGGTGGAG GTTGCAGTGA GCCAAGATCG CGCCACTGCA TTACAGCCTG GGCGACAGAG 60 TGAAACTCCA TATCAAAAAC AAAACAAAAC AAAAAAACAA AAACAAAGAA AAGAAATCCA 120 TGGTGGAAGT TAACCCAAAG TCCCAAAAGC AATGCCCATG TGTTCAGACC AATACTTTCC 180 TCCAGAAGCT GCTGAAGACC TCACAGAGAA AAACTTGCAT AAATCTAGTC TATGTCAGTG 240 ACAAAAATGA CACCGCCTCA GGATGGGTAA ATCTAAAAAT ATCCCCGTGA GAACAAATGA 300 CAGCCAAGTA GATCATTCTG GAGAATACTG AGCAGCGCAG CAGCAACTCG CGGCAGAGAC 360 TGCTGGTCAT CAGAGGAAGT CAGTGTGAAG TCAGCCGAGG CAGGGGCAAG GGTGCCGTAA 420 CTGCATTATT ACAGAAAACA AAGTGAAACA CAACCACAAA GTTATCCATC TTCTACTAGT 480 CAGCTGACTT TTACGAAAAT GCCCAATATA ATTATGCTAC AGAGCACAGC CTTTAAGGAA 540 AATGGCTGGA AACAATAGTT TAATTTTCCT GTGCTCAATA ATGTACCAGA ACATTAATTT 600 TCTTCAGAAA TAGAACCTGG TACAGAGCAA GAAAAACTAG TGTTCAATTT TATCGTTAAA 660 TTTCAAAATA ACATGTGTGG CTTAAGGAGA TCCTAAAACG GTAAGCAGCA CCCTCAAAAG 720 GGGGCCCCAA CTCCCTTCCT CAGCCCCGAC AACATTCACA TGGCCAAACT TGTTTCAAAC 780 TATCATAGCT CTGTAAAACT AAATGGTTCC TGTTCCCACA TTTCTCTTTA ATGCTTCTCC 840 CTTCATTTCC CAAAATGAAA ATAAAACCTT GTCATGAAAC TTTCTGATAA TTTAATTCTT 900 GTCTGTTCCC ATCAAGGCTA AAATATGCCC AGTTTTGACC TCTGTACATG AGGTGACAGA 960 TGCTGTTACA GGGAACATTT AACCTGACTG GCAAATAGAG AGAAATGCAA TAAGTAAAAT 1020 CATTAAGAAC TGTAATCAGT TCAACATTCT GTTTATAATT AATAATGAAA GATATTAAAC 1080 TATTACTTAA GTTAACCTTT GTGTAATGGT TATACCTATC AGCACAGAAA AAATTCCAGC 1140 TAAATGTTCA TGCCAATTTA GCTATGAAGT TTTAAGATTA CAAATAGCTG TACCTTGAAC 1200 TATTCAAAAT AGATTTTTCT TAAAACAAAA AAAAAAGCAT ACACTTTACA GGCAGGAAAA 1260 TTAACCCTTT TGTAGTGTAC AGTTGTTAGC TGTGACCACA CATTGCTGTA GCCACCACTA 1320 TAATCAAGAT ACAGATCAAT CAGACTGCTC TCCAAAATGC CCAAACCCAT CTGGAGTCAA 1380 TCCCTCTTCC CCACCCATGC CAATCACTGA TCTGCTTTCT GTCCCTAGTC TTGCCATCTC 1440 TGGAATATCA TATAAATAGA ACCATACAGT ATGTACCTTT GGATTCTGGC TTCTTTAGCT 1500 TAGCACAGTC CACGTGACAT TAATCAATAC TGCTGCATGT ATCAGTAGTC TGTTCCCTGT 1560 TAAGTAGTAC CCCACTGCAT GGATGTATCA AATGTTTATC CATTCACTAG CTAGAAGATA 1620 TCTGGGTTGT TTCCAGGTTT CGGCAATTAC AAATAAAACT ACAGGTTGAG TATCCCCCTT 1680 ATCCAAAATG CTCAGGACCA GAAATGTTTT GAATTTTGGA TATTTTCAGA TTTTGGAATA 1740 TTTGCATATA CATAATGACC CAAGTCCAAA CATAAAATTC ATTTATGTTT CATATACACC 1800 TTAAACACAT AGGCTGAAGG TAATTATAGA AAATATTTTC AATTAATTTT GCACACGAAA 1860 CAAAGCTTTA ACTGCATCTT GGCTGGGACC TATCACCAGG GCAAGTGTGG AATTTTCCAC 1920 TTGTGGCATC AGAGAGTTTT GGATTTTAGA GCATTTTGGA 1960
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