Tag | Content |
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EnhancerAtlas ID | HS164-03797 |
Organism | Homo sapiens |
Tissue/cell | Raji |
Coordinate | chr14:50333760-50336270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr14:50333932-50333946 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
SE_00765 | chr14:50333992-50336201 | Adipose_Nuclei | SE_09576 | chr14:50334033-50337802 | CD14 | SE_10599 | chr14:50334104-50337580 | CD19_Primary | SE_11096 | chr14:50333539-50339390 | CD20 | SE_12440 | chr14:50334282-50335987 | CD3 | SE_13687 | chr14:50334042-50335876 | CD34_Primary_RO01536 | SE_14679 | chr14:50334123-50336212 | CD4_Memory_Primary_7pool | SE_15756 | chr14:50333996-50336021 | CD4_Memory_Primary_8pool | SE_16123 | chr14:50334427-50335886 | CD4_Naive_Primary_7pool | SE_16695 | chr14:50334068-50336069 | CD4_Naive_Primary_8pool | SE_18438 | chr14:50333984-50336198 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19324 | chr14:50334089-50335907 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20104 | chr14:50334006-50337438 | CD56 | SE_21237 | chr14:50334033-50336208 | CD8_Memory_7pool | SE_21722 | chr14:50334033-50336067 | CD8_Naive_7pool | SE_22278 | chr14:50333968-50336018 | CD8_Naive_8pool | SE_22837 | chr14:50333983-50336850 | CD8_primiary | SE_23303 | chr14:50334241-50334973 | Colon_Crypt_1 | SE_23303 | chr14:50335002-50335628 | Colon_Crypt_1 | SE_23303 | chr14:50335787-50336170 | Colon_Crypt_1 | SE_24603 | chr14:50334338-50334959 | Colon_Crypt_2 | SE_24603 | chr14:50335010-50335534 | Colon_Crypt_2 | SE_25036 | chr14:50334350-50336082 | Colon_Crypt_3 | SE_26328 | chr14:50334059-50336156 | Duodenum_Smooth_Muscle | SE_26732 | chr14:50333843-50335723 | Esophagus | SE_26732 | chr14:50335793-50336365 | Esophagus | SE_27777 | chr14:50334068-50336154 | Fetal_Intestine | SE_28725 | chr14:50333995-50336010 | Fetal_Intestine_Large | SE_29997 | chr14:50334173-50335973 | Fetal_Muscle | SE_34956 | chr14:50334024-50336109 | HeLa | SE_52966 | chr14:50334193-50335805 | Small_Intestine | SE_54002 | chr14:50334175-50335700 | Spleen | SE_55560 | chr14:50334310-50335555 | Thymus | SE_59312 | chr14:50327340-50367097 | Ly3 | SE_60830 | chr14:50327790-50364534 | DHL6 | SE_61265 | chr14:50327065-50374962 | HBL1 | SE_62348 | chr14:50327484-50374966 | Tonsil | SE_64446 | chr14:50334201-50336000 | NHEK |
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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 |
GH14I049867 | chr14 | 50334045 | 50337750 |
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Enhancer Sequence | TGCAAGCTTC GGCTCCCGGG TTCACGCCAT TCTCCTGCCT CAGCCTCTCG AGTAGCTAGC 60 TGGGACTACA GGAGCCCGCC ACCACGCCCA GCTTTTTTGT TTGTTTTTTC AGTAGAGACG 120 GGGTTTCACC GTGTTAGCCA GGATGGTCTC GATCTCCTGA CCTCGTGTTC CGCCCGCCTC 180 GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCGC GCCCGGCCAG CCGTTTGCTT 240 TTTTAACAGT GCAAAAAACA AGGCCGTGTC TGGCTATATG GGGCTTTGCT TGTTCAAAAT 300 GTAACCTCTA TACGGCCGCG CGCAGTGGCT CACGCCTGTA ATCCTAGCAC TTTGTAAGGC 360 CCCGGCAGGC GGATCACTTG AGGGCAGGAG TTCGAGGCCA GCCTGGCCAA CATGGTGAAA 420 CCCCATCTCT ACTAAAAATA CAAAAATTAG CCTGGCCTGG TGGCGCGCGC CTGTAGTCCC 480 AGTTATTCAG GAGGCTAAGG CAGGAGAATC GCTTGAACCC GGGAAGAGGA GGTTGCAGTA 540 AGCCGAGACG TGCAACTGCA TTCCAGTCTG GGCAAGACTC CGTCTCAAAA AAAAAAAAAA 600 AAAAAGTAAC CTGTATGAAA GTTAATTTTG TGGCACTGAA CATTGGAGTA GATAATAACC 660 TCATCTGAAA TGGGATGTCT CAATCTGTCT ACAAAAAACT CCATGCCATA GAGCTCAAAA 720 GTTTGTAAAT TAGTCCTTTG GAGACGTTAA AGAGCATGGA GTCATACGAA AAGGCTTTCT 780 GCCCTGGTAA GGGAAGAAAG CTTGTGGGCA GGTTGAGTCT GGTCCTTGAG TTCTCAGCTC 840 TCACCAGGGA AGGGGTACCA GACAAAGCTG AGGCTGAACT TGAGCCGCAC AGGCCCTGAT 900 TGCTGGGCCG TGAGAGAACA CCCGAGGAGG GGGCCCAACG CACCTGAAGA AAAGACGACG 960 TGGAGGTCAT AAACGACCAA GAGAAAGGGG CGCACCGCGG ACACTATCGC CAGCCGGACC 1020 CCAGATCAAG AGAAATAGAA GAGGAGCCGG GGTCTCCAAA CACTACAGGC TGGGGTCCCA 1080 GGGCAAGGGA CTGGGCCGCC GGCGGAAGCG TCGGGGAGAG GCGGGACTGT CGGCGGGGTG 1140 TGGGAGAGGC GGGGCGTGGG AGAGGCGGGG CGTGGGAGAG GCGGGGCCAC CAGCAAGTGG 1200 GCGGGCGGGA GGCGGGGCCG CAGTTGGGGT GTGGAAGAGG TGGGGCAGCC AGCAACTGGG 1260 AGGGGAGGGA GGCGGGGCCG CCGGCGGGGC GCGGTGAAGA GGCAGGCTGC CAGAGTGCCT 1320 GGCCGACAAA TTACCCAGCG TGAGCTCGGT CACCTGGGTG TGGCGGTTCA ACCCTGAGCT 1380 ACGTCCTCCC ACGGCGCCCG GAGTTTCCCC ACCCTTGACA CAATGCCTAT TCGCAGCTCG 1440 CTGCAGCGGA GTCATCTACT GCTGCTGGCA GGATTTTCAT TGCGACGGGT TGTTATGTGC 1500 ATTTCAGGAC ATACCCCGTG GGTTGTCCCT GATTCAGTTA CATTTAATAA ACGAGCGGTG 1560 GATTAACCGG AATTACAGTT TGACAGAAAA CACGTTTTCT TCTCGACAAC ACCCTGCGTG 1620 TAGGAAGAGC CTTTAATATG GTTGATACAC AATATTTAAT CGATCCAGAA ACACATTTCT 1680 TGTGACAGGC TTTTAAATAT CAGAATAAAT CCTAAGAGTG AACAGTTGAA GTTACTTATC 1740 CAATGTTACA CTGCTAGGCC TATAAATAAA CTTGCGGGGT CTATTTTCTC CCATTTGAAT 1800 ATGCTTTGAT TTCCATATGA CAGTTCTGCC GAAATGTTTT GACATTTTAG ATCTTAGTAG 1860 AACTCCATTA CAACACGACT ATTTATTACG TTGATTCTGA TCTGACGTGT AATAAATCAT 1920 GTCCCCAAAC CAAAACTCCA TACATTAATA TCCTGATATT TAACACACTT TATCCAACTA 1980 TTGATTCTAT CTGTTCACAC CAATGTGGTA AAAGCTTTAT GTTGTATTTA ATTTATTCAT 2040 TTTGAAAATA TTTAAAATGC TTCATTTTCA TTAGCTAACT TTGAAGAGTG CTTCTTTTGT 2100 TTGGGGACTC TGTAGATTTA GGCTAATGTC ACCATTCAGA ATAATTGGCA AATTGATTTG 2160 CCTTTCTTTG ACTTTCTATT CTCCAAGCTG ATTATACGCT GAGGTTAACA CATTTGAACT 2220 GGCCGGCCGG TTGGGTGGCT CACGCTTGTA ATGCCAGCAC TTTGGGAGGC GGAGGTGGGT 2280 GGATCACCTG AGGTGAGGAG TTCGAGACCA GCCTGGCCAA CATGGTGAAA CCCTGTCTCT 2340 ACTAAAAATA CAAAAAATTA ACCGGGCGTG GTGGCGGGCG CCTGTAATCG CAGCTACCCG 2400 GGAGACAGAG GTTGCAGTGA GCCGCGGTCG CGCCATTGCA CTCCAGCCTG GGCAATAAGA 2460 GCGAAACTCT GTCTCAAAAA CAAATATATA TGTGTGTGTA TATATATATA 2510
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