Tag | Content |
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EnhancerAtlas ID | HS044-04143 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr14:50333910-50335760 |
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 | GATCTCCTGA CCTCGTGTTC CGCCCGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT 60 GAGCCACCGC GCCCGGCCAG CCGTTTGCTT TTTTAACAGT GCAAAAAACA AGGCCGTGTC 120 TGGCTATATG GGGCTTTGCT TGTTCAAAAT GTAACCTCTA TACGGCCGCG CGCAGTGGCT 180 CACGCCTGTA ATCCTAGCAC TTTGTAAGGC CCCGGCAGGC GGATCACTTG AGGGCAGGAG 240 TTCGAGGCCA GCCTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAAAATA CAAAAATTAG 300 CCTGGCCTGG TGGCGCGCGC CTGTAGTCCC AGTTATTCAG GAGGCTAAGG CAGGAGAATC 360 GCTTGAACCC GGGAAGAGGA GGTTGCAGTA AGCCGAGACG TGCAACTGCA TTCCAGTCTG 420 GGCAAGACTC CGTCTCAAAA AAAAAAAAAA AAAAAGTAAC CTGTATGAAA GTTAATTTTG 480 TGGCACTGAA CATTGGAGTA GATAATAACC TCATCTGAAA TGGGATGTCT CAATCTGTCT 540 ACAAAAAACT CCATGCCATA GAGCTCAAAA GTTTGTAAAT TAGTCCTTTG GAGACGTTAA 600 AGAGCATGGA GTCATACGAA AAGGCTTTCT GCCCTGGTAA GGGAAGAAAG CTTGTGGGCA 660 GGTTGAGTCT GGTCCTTGAG TTCTCAGCTC TCACCAGGGA AGGGGTACCA GACAAAGCTG 720 AGGCTGAACT TGAGCCGCAC AGGCCCTGAT TGCTGGGCCG TGAGAGAACA CCCGAGGAGG 780 GGGCCCAACG CACCTGAAGA AAAGACGACG TGGAGGTCAT AAACGACCAA GAGAAAGGGG 840 CGCACCGCGG ACACTATCGC CAGCCGGACC CCAGATCAAG AGAAATAGAA GAGGAGCCGG 900 GGTCTCCAAA CACTACAGGC TGGGGTCCCA GGGCAAGGGA CTGGGCCGCC GGCGGAAGCG 960 TCGGGGAGAG GCGGGACTGT CGGCGGGGTG TGGGAGAGGC GGGGCGTGGG AGAGGCGGGG 1020 CGTGGGAGAG GCGGGGCCAC CAGCAAGTGG GCGGGCGGGA GGCGGGGCCG CAGTTGGGGT 1080 GTGGAAGAGG TGGGGCAGCC AGCAACTGGG AGGGGAGGGA GGCGGGGCCG CCGGCGGGGC 1140 GCGGTGAAGA GGCAGGCTGC CAGAGTGCCT GGCCGACAAA TTACCCAGCG TGAGCTCGGT 1200 CACCTGGGTG TGGCGGTTCA ACCCTGAGCT ACGTCCTCCC ACGGCGCCCG GAGTTTCCCC 1260 ACCCTTGACA CAATGCCTAT TCGCAGCTCG CTGCAGCGGA GTCATCTACT GCTGCTGGCA 1320 GGATTTTCAT TGCGACGGGT TGTTATGTGC ATTTCAGGAC ATACCCCGTG GGTTGTCCCT 1380 GATTCAGTTA CATTTAATAA ACGAGCGGTG GATTAACCGG AATTACAGTT TGACAGAAAA 1440 CACGTTTTCT TCTCGACAAC ACCCTGCGTG TAGGAAGAGC CTTTAATATG GTTGATACAC 1500 AATATTTAAT CGATCCAGAA ACACATTTCT TGTGACAGGC TTTTAAATAT CAGAATAAAT 1560 CCTAAGAGTG AACAGTTGAA GTTACTTATC CAATGTTACA CTGCTAGGCC TATAAATAAA 1620 CTTGCGGGGT CTATTTTCTC CCATTTGAAT ATGCTTTGAT TTCCATATGA CAGTTCTGCC 1680 GAAATGTTTT GACATTTTAG ATCTTAGTAG AACTCCATTA CAACACGACT ATTTATTACG 1740 TTGATTCTGA TCTGACGTGT AATAAATCAT GTCCCCAAAC CAAAACTCCA TACATTAATA 1800 TCCTGATATT TAACACACTT TATCCAACTA TTGATTCTAT CTGTTCACAC 1850
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