Tag | Content |
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EnhancerAtlas ID | HS060-10120 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr14:50333850-50335680 |
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: 37 | 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_12710 | chr14:50334684-50334870 | CD34_adult | 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_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_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 | GCTTTTTTGT TTGTTTTTTC AGTAGAGACG GGGTTTCACC GTGTTAGCCA GGATGGTCTC 60 GATCTCCTGA CCTCGTGTTC CGCCCGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT 120 GAGCCACCGC GCCCGGCCAG CCGTTTGCTT TTTTAACAGT GCAAAAAACA AGGCCGTGTC 180 TGGCTATATG GGGCTTTGCT TGTTCAAAAT GTAACCTCTA TACGGCCGCG CGCAGTGGCT 240 CACGCCTGTA ATCCTAGCAC TTTGTAAGGC CCCGGCAGGC GGATCACTTG AGGGCAGGAG 300 TTCGAGGCCA GCCTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAAAATA CAAAAATTAG 360 CCTGGCCTGG TGGCGCGCGC CTGTAGTCCC AGTTATTCAG GAGGCTAAGG CAGGAGAATC 420 GCTTGAACCC GGGAAGAGGA GGTTGCAGTA AGCCGAGACG TGCAACTGCA TTCCAGTCTG 480 GGCAAGACTC CGTCTCAAAA AAAAAAAAAA AAAAAGTAAC CTGTATGAAA GTTAATTTTG 540 TGGCACTGAA CATTGGAGTA GATAATAACC TCATCTGAAA TGGGATGTCT CAATCTGTCT 600 ACAAAAAACT CCATGCCATA GAGCTCAAAA GTTTGTAAAT TAGTCCTTTG GAGACGTTAA 660 AGAGCATGGA GTCATACGAA AAGGCTTTCT GCCCTGGTAA GGGAAGAAAG CTTGTGGGCA 720 GGTTGAGTCT GGTCCTTGAG TTCTCAGCTC TCACCAGGGA AGGGGTACCA GACAAAGCTG 780 AGGCTGAACT TGAGCCGCAC AGGCCCTGAT TGCTGGGCCG TGAGAGAACA CCCGAGGAGG 840 GGGCCCAACG CACCTGAAGA AAAGACGACG TGGAGGTCAT AAACGACCAA GAGAAAGGGG 900 CGCACCGCGG ACACTATCGC CAGCCGGACC CCAGATCAAG AGAAATAGAA GAGGAGCCGG 960 GGTCTCCAAA CACTACAGGC TGGGGTCCCA GGGCAAGGGA CTGGGCCGCC GGCGGAAGCG 1020 TCGGGGAGAG GCGGGACTGT CGGCGGGGTG TGGGAGAGGC GGGGCGTGGG AGAGGCGGGG 1080 CGTGGGAGAG GCGGGGCCAC CAGCAAGTGG GCGGGCGGGA GGCGGGGCCG CAGTTGGGGT 1140 GTGGAAGAGG TGGGGCAGCC AGCAACTGGG AGGGGAGGGA GGCGGGGCCG CCGGCGGGGC 1200 GCGGTGAAGA GGCAGGCTGC CAGAGTGCCT GGCCGACAAA TTACCCAGCG TGAGCTCGGT 1260 CACCTGGGTG TGGCGGTTCA ACCCTGAGCT ACGTCCTCCC ACGGCGCCCG GAGTTTCCCC 1320 ACCCTTGACA CAATGCCTAT TCGCAGCTCG CTGCAGCGGA GTCATCTACT GCTGCTGGCA 1380 GGATTTTCAT TGCGACGGGT TGTTATGTGC ATTTCAGGAC ATACCCCGTG GGTTGTCCCT 1440 GATTCAGTTA CATTTAATAA ACGAGCGGTG GATTAACCGG AATTACAGTT TGACAGAAAA 1500 CACGTTTTCT TCTCGACAAC ACCCTGCGTG TAGGAAGAGC CTTTAATATG GTTGATACAC 1560 AATATTTAAT CGATCCAGAA ACACATTTCT TGTGACAGGC TTTTAAATAT CAGAATAAAT 1620 CCTAAGAGTG AACAGTTGAA GTTACTTATC CAATGTTACA CTGCTAGGCC TATAAATAAA 1680 CTTGCGGGGT CTATTTTCTC CCATTTGAAT ATGCTTTGAT TTCCATATGA CAGTTCTGCC 1740 GAAATGTTTT GACATTTTAG ATCTTAGTAG AACTCCATTA CAACACGACT ATTTATTACG 1800 TTGATTCTGA TCTGACGTGT AATAAATCAT 1830
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