Tag | Content |
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EnhancerAtlas ID | HS029-04534 |
Organism | Homo sapiens |
Tissue/cell | CUTLL1 |
Coordinate | chr14:69285890-69289440 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NOTO | MA0710.1 | chr14:69286082-69286092 | GCTAATTAGC | + | 6.02 | NOTO | MA0710.1 | chr14:69286082-69286092 | GCTAATTAGC | - | 6.02 | ZNF263 | MA0528.1 | chr14:69287408-69287429 | TTGCTCTCCTTTCCCTCCTCC | - | 6.02 | ZNF263 | MA0528.1 | chr14:69287411-69287432 | CTCTCCTTTCCCTCCTCCCCC | - | 8.26 | Znf423 | MA0116.1 | chr14:69288013-69288028 | TCAACCCTGGGGGCC | - | 6.7 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_02903 | chr14:69285849-69286635 | Bladder | SE_10217 | chr14:69287381-69288209 | CD19_Primary | SE_10217 | chr14:69288257-69289855 | CD19_Primary | SE_10927 | chr14:69286461-69289803 | CD20 | SE_12450 | chr14:69286263-69289248 | CD3 | SE_13798 | chr14:69286668-69287305 | CD34_Primary_RO01536 | SE_19711 | chr14:69278919-69289914 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20000 | chr14:69286486-69289209 | CD56 | SE_23287 | chr14:69285779-69286677 | Colon_Crypt_1 | SE_23844 | chr14:69285825-69286627 | Colon_Crypt_2 | SE_25802 | chr14:69284790-69287321 | Duodenum_Smooth_Muscle | SE_26562 | chr14:69279542-69288565 | Esophagus | SE_27622 | chr14:69285187-69287040 | Fetal_Intestine | SE_28546 | chr14:69285382-69287096 | Fetal_Intestine_Large | SE_29562 | chr14:69285744-69286511 | Fetal_Muscle | SE_31416 | chr14:69285740-69286625 | Gastric | SE_34435 | chr14:69279712-69289129 | HCT-116 | SE_52355 | chr14:69285748-69286963 | Small_Intestine | SE_52355 | chr14:69287471-69288770 | Small_Intestine | SE_54538 | chr14:69278934-69287559 | Stomach_Smooth_Muscle | SE_55116 | chr14:69286790-69287252 | Thymus | SE_56951 | chr14:69286150-69286718 | VACO_400 | SE_59058 | chr14:69250411-69290070 | Ly3 | SE_60527 | chr14:69255025-69290272 | DHL6 | SE_61098 | chr14:69252323-69292163 | HBL1 | SE_61862 | chr14:69255096-69290190 | Toledo | SE_62217 | chr14:69237592-69290254 | Tonsil | SE_65371 | chr14:69285889-69286757 | Pancreatic_islets |
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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 |
GH14I068818 | chr14 | 69285016 | 69290030 |
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Enhancer Sequence | AATAAACGGT GGGCTTCATC ATTAGCCAGA GAGAAGGGAC TCTGTGAGGA GGTCCTACAG 60 AAGGAGAAAT ATGGAGAAGT GGGTGACCCA AGATGATGGC TCACACACCT CTCCCAGGAG 120 GGCCAGCCCC ATGCCTAGCT AGGCAGTTCC CTGGCTAGGA CGTCAGCTCT TACTCACTCT 180 TTCCAGAGAG CAGCTAATTA GCCTCCCAGC AGCCAGGAGC TCTCCAGATG AAAGGTGCTT 240 AATACAAGCT CAAGGCGTAA CTCCCATATG TATAACTAAG GTTCCCTGAG GTGAGGAAGG 300 CCCCAGGGCG GAGAGACAGG CCAGATCAGG GCCTCGCCTT CTTTATGACG GAGGTTCCCA 360 GGGAAGGGAG CCGGCTGGGG TGGCAGTGAG CCTGAGAAAG GGCTCGGGGT GGTGGGTGTG 420 CGGCTTCAGA GGGAGCCCCT CCCTGGGAGT GGGCGGGGCC CGGTGGCTGA GGAGGCAGAG 480 TGAATGCTTC AGGGCCCAAG CTGCCTCCCA GAGTGGGAGC TCCAGGTCAG AAGACAGCTT 540 AGAACTGGGT GGGTCAGAGC GAGGGCTTTG CTGCTGGGCT GCCAGGTCAG AATCCCAGCT 600 CTGCTATGGC CATTCCATGT CCCAGAGCCT CAGCTTCCTC CTCTGTAAAA CGGAGATAAT 660 GATAACATTG ACCTCACAGC TATTTACTGA CAGCACTTAG TACAGACAGG ACCTGGCACC 720 CACTACGTAA AGAATGAGGA TTTGTACATT TGTTCATTTA ACAGATATTT ATTGAGTACC 780 TGCTATGTGC CAGGCACTGG GTGTTAGAAA TACAGTCATG AACAAAACAG ATCCATTTTC 840 CCTTGATTCT GTAGGGAAGA TAGACCACAG ACCCCAGAAC CAAGAGATCG GTAATACACT 900 GCCTGGCAGT GACCTGCGCT GTGGGAATCG GGTATGAGGA TGGGGTCAGG TGTCCAATAC 960 AGCGGCAGAA GAGCAGGTAC CCAGGCAGAT ATGGGCAGAT TAAGAAACGA ACCAGGGTTG 1020 AAGGGCCAAC CCAAAGTGCG CAGCAAATCA GAGGCGGGAG CCTGGGCCTG CAGCATAGGA 1080 ATGTTCACCC ACAGCTGCTG AAGCAGCCGC AGCAGCTCCC TCTGCCCCTG ACTAAGGGGT 1140 GTGCCCAGCG AAGCCACCTG CCCTCACCTC CCCCTTGGCT CCTGCCCCTG ACTCCCGCAG 1200 TCTGGAGTCC AGCAAGGCAA GGGAACTGAC ACAGCCCCCA GGGTCACGAT GGCTTCCATT 1260 CTTTGACATT CACCAGTGTC ACTGGCTGAG CTCAGGCTAC ACGGCCATCT TCTCTTTGAA 1320 GCCTCCAAAC CAGCTGGTGA AGTCAGTAGC ACCCCTGTGT TTTTTATCAA GGTAAGGTTC 1380 ACATAACATA AAATGAAGCA TTTTAAAGTG AACACTTCAG TGGAATTTAG TATATTTACA 1440 GGGTTGTGGA ACCTCCGCCT CTGTCTAGTT CCAAAACATT TTTATCACCC CAAAAGGAAA 1500 CCCATACCCA CTAAACAGTT GCTCTCCTTT CCCTCCTCCC CCAGGCCCTG GAAACCACCC 1560 TCTACTTCCT GTCGCTATGG GGTTGCCTAT TCTGGATACT TCACCTATCC AGAGCTTTTG 1620 TGTCTGGCTT CTGTCACTTA GCATCATGTT TTCGAGGTTT ATCCAGGTTG TAACATGTAT 1680 TGTTATTACA CCTTGGTCTA TGGCTAAATA ATGTTCCATT GTCTGTAAGC ACTCCCATCT 1740 TACAGATGAG GAAACAGTCC CGAGGCGCTG AGACTCCCAG CTTGAGTCCA CACCGGAGAG 1800 ACATGGTCCG TGCAAGCCTG CTCCCCAGAT GGCCCCATCC TGGCACTGCC GTCTGGGAGG 1860 AGGCTGCCCC TGGGGGCATG CTGGTCCCTG AGTGGTGACC TGACCCCTTC TGAGGTTCAC 1920 TTCTCAGCGC AGGTTCACTT CTCAGCGCAG GTTCACAGGC GAGGGTGCTC TGGCCTCCCA 1980 GTCACCCTGA TCCAGGCAAG ACCATAGCGT GGCCGCAGGG GCCGCCTCCT TGGGGGAATT 2040 CCAGCCCCTG GCCAACCACA GACCATAGCA CTCCCGGGGG TTGAACCGTT TCTCACAACT 2100 GGGTTGTGAC AGCTGGGAGG TGCTCAACCC TGGGGGCCAG CCTGGTGGCA GGCCGGGTTG 2160 GGAACGCTGT TCCCAGCCAG CTTCCCTAGG CAACATGGCC AGCCCCGTCC AGCAAGTGGA 2220 CCACTCAGAT GGCAGGCATG TACTGAGCAC CCACTGTATA CCAGCCAGGC ACCACGAGGC 2280 CTCCAAGGAG CTCCCTTTCT GATGAGGATG AGCCACCCCA GAACAGAAAC TGGGTGCTGG 2340 GGCCAGGGGC AGGACAGAGG GGTGCTCCGG AGAACAAGCA CCAGCACTGA GCCTGGGGAG 2400 TTCCCCGCTG GCAGCGCCTG ACACAGCCCA CACCGGGGAT CCCTGGCCTC AGGAAAGCAG 2460 GGCTGTCACA TCAAGAAGGC CATGACATAA GGGCCCCTAC CAACGTCCAG CCTTAGGTGG 2520 AGGGCACAGA TATGGCAATA CACAGGACCC TAGAATGCCT GCCTGGGGAT GCCCACCTTG 2580 GCCCACTTGA TGGCCAGTTG AGACTCAGTG TGCACTGTCC ACACACCCTG TTCTGACACT 2640 GACTGCCTAG TGTCCAATTA TTCTTCCATC TCACTCATTC AGTGCCAGTT ACTCTACTGA 2700 GCAATAAGGA TATAACATTT TAAAAACAAA ACAAACATGT TCCTGTCCTC TAGAAGCTTA 2760 AAATAGAGCA AACTGAGAAG GAAACTAATA ATGACCACCT TGCCAGGGGC AAGGAGACCA 2820 GAGGCAGGGC CCTAACCCAC GGGCAGCTGC AGCTGGAATA TATGAGACAG TGTGTGTGTG 2880 CTCACATGTC CACAGCCGAG CTCACCTCCA GACAGTTATG CACCCCTACC GCTCACCCCA 2940 TCCCACCTCA TCCTCACCAA GGCAGGTCTA CTCAGTAAGT CAGGCTGAAA ACATGAGCCT 3000 GGGGAGTTGG GACTTCTTAA CTGCCACCCC CACCTGCACC CCATCCAGGA TGAAAGAAGC 3060 ATTATCCAGC AAGGACATGG CCACTGAAAG TGCCACCAAG GACCGGCCAA GGGGAGGGGA 3120 AGGGCTCCCT ACAGCCCTTC CCCTGCTGGC TGAGTTGAAT GGCCAGGGAC TTACCCAGGC 3180 TGGTACAAAG CCACTGGCCC CAGGGCCATC CCCTTATAAC ACAGCACTTC CTGGGTGTCA 3240 GTGCATGCTG AGTATGTCAC GTGTATTTCT TAAACCACTA AGATTTTACC AGTGACTTAT 3300 CCAAGGTCAC CAGGCCAGTG TGTAGAAAAT TTGCATTCTG GTGTGAGCCA CTCAAAGGTC 3360 CACACCCACA TTTCTACACA TCCCCTAATA AAAGCCAAGG GGCCCACAAC GCTCCCCTGT 3420 GAACCTCACA TGGCTGCCTG TCTAGGGGAA ATGAAGGAAA TCCCTTCACA CGGAGCCCCT 3480 GCCCCAGCCG TGCTCCAGTC CCTCTCTTTT CCCCTGCCCT AGCTGACCCC ACAGCTAAGC 3540 CCACCTTTTG 3550
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