Tag | Content |
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EnhancerAtlas ID | HS023-07525 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr14:69285330-69289650 |
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 | GCTTTAGAAT CAATCAAATC AATCCAACTC TATTCCTGAC TCTGTGATAG CCAGTAAGTG 60 GTTTAACTTC TCTGAGCCTG TTTCCTCATC TGAGAAATGG GAATAGCATG GTACCTACCT 120 CACTGGGCTG TTCTGAAGAT TACTGATAAT AGCTACCACT TAGCAAGTGC TTGATCCGTG 180 CCAGGCAGCA CACTAGAGGC TTCCCATCCA CTCCATGAGG TCATGTGCAG AAGTACTGGT 240 CCCATGCCAG CAAGGAGTAG GGCTCCATCA CAGTTGTTAA CGCATGACAC CCCTACTGCT 300 CTGCACACAT ATATTTATGT AGTCCTACGG CCCTACTGCT CTGCACACAT ATATTTATGT 360 AGTCCTACGG CCCTACTGCT CTGCACACAT ATATTTATGT AGTCCTACGG CCCTACTGCT 420 CTGCACACAT ATATTTATGT AGTCCTACGG CCCTACTGCT CTGCACACAT ATATTTATGT 480 AGTCCTACGG CCCTACTGCT CTGCACACAT ATTTAACAGG CGAAGGGGCT TAGCAAGCTC 540 TTGGCACATA ATAAGCACTC AATAAACGGT GGGCTTCATC ATTAGCCAGA GAGAAGGGAC 600 TCTGTGAGGA GGTCCTACAG AAGGAGAAAT ATGGAGAAGT GGGTGACCCA AGATGATGGC 660 TCACACACCT CTCCCAGGAG GGCCAGCCCC ATGCCTAGCT AGGCAGTTCC CTGGCTAGGA 720 CGTCAGCTCT TACTCACTCT TTCCAGAGAG CAGCTAATTA GCCTCCCAGC AGCCAGGAGC 780 TCTCCAGATG AAAGGTGCTT AATACAAGCT CAAGGCGTAA CTCCCATATG TATAACTAAG 840 GTTCCCTGAG GTGAGGAAGG CCCCAGGGCG GAGAGACAGG CCAGATCAGG GCCTCGCCTT 900 CTTTATGACG GAGGTTCCCA GGGAAGGGAG CCGGCTGGGG TGGCAGTGAG CCTGAGAAAG 960 GGCTCGGGGT GGTGGGTGTG CGGCTTCAGA GGGAGCCCCT CCCTGGGAGT GGGCGGGGCC 1020 CGGTGGCTGA GGAGGCAGAG TGAATGCTTC AGGGCCCAAG CTGCCTCCCA GAGTGGGAGC 1080 TCCAGGTCAG AAGACAGCTT AGAACTGGGT GGGTCAGAGC GAGGGCTTTG CTGCTGGGCT 1140 GCCAGGTCAG AATCCCAGCT CTGCTATGGC CATTCCATGT CCCAGAGCCT CAGCTTCCTC 1200 CTCTGTAAAA CGGAGATAAT GATAACATTG ACCTCACAGC TATTTACTGA CAGCACTTAG 1260 TACAGACAGG ACCTGGCACC CACTACGTAA AGAATGAGGA TTTGTACATT TGTTCATTTA 1320 ACAGATATTT ATTGAGTACC TGCTATGTGC CAGGCACTGG GTGTTAGAAA TACAGTCATG 1380 AACAAAACAG ATCCATTTTC CCTTGATTCT GTAGGGAAGA TAGACCACAG ACCCCAGAAC 1440 CAAGAGATCG GTAATACACT GCCTGGCAGT GACCTGCGCT GTGGGAATCG GGTATGAGGA 1500 TGGGGTCAGG TGTCCAATAC AGCGGCAGAA GAGCAGGTAC CCAGGCAGAT ATGGGCAGAT 1560 TAAGAAACGA ACCAGGGTTG AAGGGCCAAC CCAAAGTGCG CAGCAAATCA GAGGCGGGAG 1620 CCTGGGCCTG CAGCATAGGA ATGTTCACCC ACAGCTGCTG AAGCAGCCGC AGCAGCTCCC 1680 TCTGCCCCTG ACTAAGGGGT GTGCCCAGCG AAGCCACCTG CCCTCACCTC CCCCTTGGCT 1740 CCTGCCCCTG ACTCCCGCAG TCTGGAGTCC AGCAAGGCAA GGGAACTGAC ACAGCCCCCA 1800 GGGTCACGAT GGCTTCCATT CTTTGACATT CACCAGTGTC ACTGGCTGAG CTCAGGCTAC 1860 ACGGCCATCT TCTCTTTGAA GCCTCCAAAC CAGCTGGTGA AGTCAGTAGC ACCCCTGTGT 1920 TTTTTATCAA GGTAAGGTTC ACATAACATA AAATGAAGCA TTTTAAAGTG AACACTTCAG 1980 TGGAATTTAG TATATTTACA GGGTTGTGGA ACCTCCGCCT CTGTCTAGTT CCAAAACATT 2040 TTTATCACCC CAAAAGGAAA CCCATACCCA CTAAACAGTT GCTCTCCTTT CCCTCCTCCC 2100 CCAGGCCCTG GAAACCACCC TCTACTTCCT GTCGCTATGG GGTTGCCTAT TCTGGATACT 2160 TCACCTATCC AGAGCTTTTG TGTCTGGCTT CTGTCACTTA GCATCATGTT TTCGAGGTTT 2220 ATCCAGGTTG TAACATGTAT TGTTATTACA CCTTGGTCTA TGGCTAAATA ATGTTCCATT 2280 GTCTGTAAGC ACTCCCATCT TACAGATGAG GAAACAGTCC CGAGGCGCTG AGACTCCCAG 2340 CTTGAGTCCA CACCGGAGAG ACATGGTCCG TGCAAGCCTG CTCCCCAGAT GGCCCCATCC 2400 TGGCACTGCC GTCTGGGAGG AGGCTGCCCC TGGGGGCATG CTGGTCCCTG AGTGGTGACC 2460 TGACCCCTTC TGAGGTTCAC TTCTCAGCGC AGGTTCACTT CTCAGCGCAG GTTCACAGGC 2520 GAGGGTGCTC TGGCCTCCCA GTCACCCTGA TCCAGGCAAG ACCATAGCGT GGCCGCAGGG 2580 GCCGCCTCCT TGGGGGAATT CCAGCCCCTG GCCAACCACA GACCATAGCA CTCCCGGGGG 2640 TTGAACCGTT TCTCACAACT GGGTTGTGAC AGCTGGGAGG TGCTCAACCC TGGGGGCCAG 2700 CCTGGTGGCA GGCCGGGTTG GGAACGCTGT TCCCAGCCAG CTTCCCTAGG CAACATGGCC 2760 AGCCCCGTCC AGCAAGTGGA CCACTCAGAT GGCAGGCATG TACTGAGCAC CCACTGTATA 2820 CCAGCCAGGC ACCACGAGGC CTCCAAGGAG CTCCCTTTCT GATGAGGATG AGCCACCCCA 2880 GAACAGAAAC TGGGTGCTGG GGCCAGGGGC AGGACAGAGG GGTGCTCCGG AGAACAAGCA 2940 CCAGCACTGA GCCTGGGGAG TTCCCCGCTG GCAGCGCCTG ACACAGCCCA CACCGGGGAT 3000 CCCTGGCCTC AGGAAAGCAG GGCTGTCACA TCAAGAAGGC CATGACATAA GGGCCCCTAC 3060 CAACGTCCAG CCTTAGGTGG AGGGCACAGA TATGGCAATA CACAGGACCC TAGAATGCCT 3120 GCCTGGGGAT GCCCACCTTG GCCCACTTGA TGGCCAGTTG AGACTCAGTG TGCACTGTCC 3180 ACACACCCTG TTCTGACACT GACTGCCTAG TGTCCAATTA TTCTTCCATC TCACTCATTC 3240 AGTGCCAGTT ACTCTACTGA GCAATAAGGA TATAACATTT TAAAAACAAA ACAAACATGT 3300 TCCTGTCCTC TAGAAGCTTA AAATAGAGCA AACTGAGAAG GAAACTAATA ATGACCACCT 3360 TGCCAGGGGC AAGGAGACCA GAGGCAGGGC CCTAACCCAC GGGCAGCTGC AGCTGGAATA 3420 TATGAGACAG TGTGTGTGTG CTCACATGTC CACAGCCGAG CTCACCTCCA GACAGTTATG 3480 CACCCCTACC GCTCACCCCA TCCCACCTCA TCCTCACCAA GGCAGGTCTA CTCAGTAAGT 3540 CAGGCTGAAA ACATGAGCCT GGGGAGTTGG GACTTCTTAA CTGCCACCCC CACCTGCACC 3600 CCATCCAGGA TGAAAGAAGC ATTATCCAGC AAGGACATGG CCACTGAAAG TGCCACCAAG 3660 GACCGGCCAA GGGGAGGGGA AGGGCTCCCT ACAGCCCTTC CCCTGCTGGC TGAGTTGAAT 3720 GGCCAGGGAC TTACCCAGGC TGGTACAAAG CCACTGGCCC CAGGGCCATC CCCTTATAAC 3780 ACAGCACTTC CTGGGTGTCA GTGCATGCTG AGTATGTCAC GTGTATTTCT TAAACCACTA 3840 AGATTTTACC AGTGACTTAT CCAAGGTCAC CAGGCCAGTG TGTAGAAAAT TTGCATTCTG 3900 GTGTGAGCCA CTCAAAGGTC CACACCCACA TTTCTACACA TCCCCTAATA AAAGCCAAGG 3960 GGCCCACAAC GCTCCCCTGT GAACCTCACA TGGCTGCCTG TCTAGGGGAA ATGAAGGAAA 4020 TCCCTTCACA CGGAGCCCCT GCCCCAGCCG TGCTCCAGTC CCTCTCTTTT CCCCTGCCCT 4080 AGCTGACCCC ACAGCTAAGC CCACCTTTTG GCATTCAGGG TGCACCTCCT GCCCCAGGGA 4140 ACTCCCAGAT GAGCTGGAGG GAACAGTCTG CACTGGGGCT CTGGGTGGAA GGGAAGAGGA 4200 TGGGGGCTAA CCAGGTCCTG GGCACATAGG GCCTCATGTG GGAAGGAAAA TGCTCCCTCA 4260 GAGGGTCAGA TGCTCTCAAC CAGTTCCCAC CCCCTGCTGC TGTCACAGAG AACTTCCTTG 4320
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