Tag | Content |
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EnhancerAtlas ID | HS023-07310 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr14:50333570-50336360 |
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 | ATCACTTTAC TATTCTATAT ATTTCACCTT TATTGTTTTA TGAATTAGTG ATCGGCATAG 60 TATCCAGTGC TAAGTCAGTT ATGCACAACC TCGAATCAGC CGTTTGCTTT TTTTTTTTTT 120 TTTTTTTTTT TTGAGACGGA GTCTCGCTCT GTCGCCAAAG CTGTAGTGCA GTGACGCGAT 180 CCCAGCTCAC TGCAAGCTTC GGCTCCCGGG TTCACGCCAT TCTCCTGCCT CAGCCTCTCG 240 AGTAGCTAGC TGGGACTACA GGAGCCCGCC ACCACGCCCA GCTTTTTTGT TTGTTTTTTC 300 AGTAGAGACG GGGTTTCACC GTGTTAGCCA GGATGGTCTC GATCTCCTGA CCTCGTGTTC 360 CGCCCGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCGC GCCCGGCCAG 420 CCGTTTGCTT TTTTAACAGT GCAAAAAACA AGGCCGTGTC TGGCTATATG GGGCTTTGCT 480 TGTTCAAAAT GTAACCTCTA TACGGCCGCG CGCAGTGGCT CACGCCTGTA ATCCTAGCAC 540 TTTGTAAGGC CCCGGCAGGC GGATCACTTG AGGGCAGGAG TTCGAGGCCA GCCTGGCCAA 600 CATGGTGAAA CCCCATCTCT ACTAAAAATA CAAAAATTAG CCTGGCCTGG TGGCGCGCGC 660 CTGTAGTCCC AGTTATTCAG GAGGCTAAGG CAGGAGAATC GCTTGAACCC GGGAAGAGGA 720 GGTTGCAGTA AGCCGAGACG TGCAACTGCA TTCCAGTCTG GGCAAGACTC CGTCTCAAAA 780 AAAAAAAAAA AAAAAGTAAC CTGTATGAAA GTTAATTTTG TGGCACTGAA CATTGGAGTA 840 GATAATAACC TCATCTGAAA TGGGATGTCT CAATCTGTCT ACAAAAAACT CCATGCCATA 900 GAGCTCAAAA GTTTGTAAAT TAGTCCTTTG GAGACGTTAA AGAGCATGGA GTCATACGAA 960 AAGGCTTTCT GCCCTGGTAA GGGAAGAAAG CTTGTGGGCA GGTTGAGTCT GGTCCTTGAG 1020 TTCTCAGCTC TCACCAGGGA AGGGGTACCA GACAAAGCTG AGGCTGAACT TGAGCCGCAC 1080 AGGCCCTGAT TGCTGGGCCG TGAGAGAACA CCCGAGGAGG GGGCCCAACG CACCTGAAGA 1140 AAAGACGACG TGGAGGTCAT AAACGACCAA GAGAAAGGGG CGCACCGCGG ACACTATCGC 1200 CAGCCGGACC CCAGATCAAG AGAAATAGAA GAGGAGCCGG GGTCTCCAAA CACTACAGGC 1260 TGGGGTCCCA GGGCAAGGGA CTGGGCCGCC GGCGGAAGCG TCGGGGAGAG GCGGGACTGT 1320 CGGCGGGGTG TGGGAGAGGC GGGGCGTGGG AGAGGCGGGG CGTGGGAGAG GCGGGGCCAC 1380 CAGCAAGTGG GCGGGCGGGA GGCGGGGCCG CAGTTGGGGT GTGGAAGAGG TGGGGCAGCC 1440 AGCAACTGGG AGGGGAGGGA GGCGGGGCCG CCGGCGGGGC GCGGTGAAGA GGCAGGCTGC 1500 CAGAGTGCCT GGCCGACAAA TTACCCAGCG TGAGCTCGGT CACCTGGGTG TGGCGGTTCA 1560 ACCCTGAGCT ACGTCCTCCC ACGGCGCCCG GAGTTTCCCC ACCCTTGACA CAATGCCTAT 1620 TCGCAGCTCG CTGCAGCGGA GTCATCTACT GCTGCTGGCA GGATTTTCAT TGCGACGGGT 1680 TGTTATGTGC ATTTCAGGAC ATACCCCGTG GGTTGTCCCT GATTCAGTTA CATTTAATAA 1740 ACGAGCGGTG GATTAACCGG AATTACAGTT TGACAGAAAA CACGTTTTCT TCTCGACAAC 1800 ACCCTGCGTG TAGGAAGAGC CTTTAATATG GTTGATACAC AATATTTAAT CGATCCAGAA 1860 ACACATTTCT TGTGACAGGC TTTTAAATAT CAGAATAAAT CCTAAGAGTG AACAGTTGAA 1920 GTTACTTATC CAATGTTACA CTGCTAGGCC TATAAATAAA CTTGCGGGGT CTATTTTCTC 1980 CCATTTGAAT ATGCTTTGAT TTCCATATGA CAGTTCTGCC GAAATGTTTT GACATTTTAG 2040 ATCTTAGTAG AACTCCATTA CAACACGACT ATTTATTACG TTGATTCTGA TCTGACGTGT 2100 AATAAATCAT GTCCCCAAAC CAAAACTCCA TACATTAATA TCCTGATATT TAACACACTT 2160 TATCCAACTA TTGATTCTAT CTGTTCACAC CAATGTGGTA AAAGCTTTAT GTTGTATTTA 2220 ATTTATTCAT TTTGAAAATA TTTAAAATGC TTCATTTTCA TTAGCTAACT TTGAAGAGTG 2280 CTTCTTTTGT TTGGGGACTC TGTAGATTTA GGCTAATGTC ACCATTCAGA ATAATTGGCA 2340 AATTGATTTG CCTTTCTTTG ACTTTCTATT CTCCAAGCTG ATTATACGCT GAGGTTAACA 2400 CATTTGAACT GGCCGGCCGG TTGGGTGGCT CACGCTTGTA ATGCCAGCAC TTTGGGAGGC 2460 GGAGGTGGGT GGATCACCTG AGGTGAGGAG TTCGAGACCA GCCTGGCCAA CATGGTGAAA 2520 CCCTGTCTCT ACTAAAAATA CAAAAAATTA ACCGGGCGTG GTGGCGGGCG CCTGTAATCG 2580 CAGCTACCCG GGAGACAGAG GTTGCAGTGA GCCGCGGTCG CGCCATTGCA CTCCAGCCTG 2640 GGCAATAAGA GCGAAACTCT GTCTCAAAAA CAAATATATA TGTGTGTGTA TATATATATA 2700 TATATATATA TATATATATA TATGTGTGTG TGTGTGTGTG TGTGTATATA TATATACATA 2760 TATATTTGAA CGTGCCTAGA TTGTGGTAGG 2790
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