Tag | Content |
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EnhancerAtlas ID | HS187-07563 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr14:69285440-69289590 |
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 | GTACCTACCT CACTGGGCTG TTCTGAAGAT TACTGATAAT AGCTACCACT TAGCAAGTGC 60 TTGATCCGTG CCAGGCAGCA CACTAGAGGC TTCCCATCCA CTCCATGAGG TCATGTGCAG 120 AAGTACTGGT CCCATGCCAG CAAGGAGTAG GGCTCCATCA CAGTTGTTAA CGCATGACAC 180 CCCTACTGCT CTGCACACAT ATATTTATGT AGTCCTACGG CCCTACTGCT CTGCACACAT 240 ATATTTATGT AGTCCTACGG CCCTACTGCT CTGCACACAT ATATTTATGT AGTCCTACGG 300 CCCTACTGCT CTGCACACAT ATATTTATGT AGTCCTACGG CCCTACTGCT CTGCACACAT 360 ATATTTATGT AGTCCTACGG CCCTACTGCT CTGCACACAT ATTTAACAGG CGAAGGGGCT 420 TAGCAAGCTC TTGGCACATA ATAAGCACTC AATAAACGGT GGGCTTCATC ATTAGCCAGA 480 GAGAAGGGAC TCTGTGAGGA GGTCCTACAG AAGGAGAAAT ATGGAGAAGT GGGTGACCCA 540 AGATGATGGC TCACACACCT CTCCCAGGAG GGCCAGCCCC ATGCCTAGCT AGGCAGTTCC 600 CTGGCTAGGA CGTCAGCTCT TACTCACTCT TTCCAGAGAG CAGCTAATTA GCCTCCCAGC 660 AGCCAGGAGC TCTCCAGATG AAAGGTGCTT AATACAAGCT CAAGGCGTAA CTCCCATATG 720 TATAACTAAG GTTCCCTGAG GTGAGGAAGG CCCCAGGGCG GAGAGACAGG CCAGATCAGG 780 GCCTCGCCTT CTTTATGACG GAGGTTCCCA GGGAAGGGAG CCGGCTGGGG TGGCAGTGAG 840 CCTGAGAAAG GGCTCGGGGT GGTGGGTGTG CGGCTTCAGA GGGAGCCCCT CCCTGGGAGT 900 GGGCGGGGCC CGGTGGCTGA GGAGGCAGAG TGAATGCTTC AGGGCCCAAG CTGCCTCCCA 960 GAGTGGGAGC TCCAGGTCAG AAGACAGCTT AGAACTGGGT GGGTCAGAGC GAGGGCTTTG 1020 CTGCTGGGCT GCCAGGTCAG AATCCCAGCT CTGCTATGGC CATTCCATGT CCCAGAGCCT 1080 CAGCTTCCTC CTCTGTAAAA CGGAGATAAT GATAACATTG ACCTCACAGC TATTTACTGA 1140 CAGCACTTAG TACAGACAGG ACCTGGCACC CACTACGTAA AGAATGAGGA TTTGTACATT 1200 TGTTCATTTA ACAGATATTT ATTGAGTACC TGCTATGTGC CAGGCACTGG GTGTTAGAAA 1260 TACAGTCATG AACAAAACAG ATCCATTTTC CCTTGATTCT GTAGGGAAGA TAGACCACAG 1320 ACCCCAGAAC CAAGAGATCG GTAATACACT GCCTGGCAGT GACCTGCGCT GTGGGAATCG 1380 GGTATGAGGA TGGGGTCAGG TGTCCAATAC AGCGGCAGAA GAGCAGGTAC CCAGGCAGAT 1440 ATGGGCAGAT TAAGAAACGA ACCAGGGTTG AAGGGCCAAC CCAAAGTGCG CAGCAAATCA 1500 GAGGCGGGAG CCTGGGCCTG CAGCATAGGA ATGTTCACCC ACAGCTGCTG AAGCAGCCGC 1560 AGCAGCTCCC TCTGCCCCTG ACTAAGGGGT GTGCCCAGCG AAGCCACCTG CCCTCACCTC 1620 CCCCTTGGCT CCTGCCCCTG ACTCCCGCAG TCTGGAGTCC AGCAAGGCAA GGGAACTGAC 1680 ACAGCCCCCA GGGTCACGAT GGCTTCCATT CTTTGACATT CACCAGTGTC ACTGGCTGAG 1740 CTCAGGCTAC ACGGCCATCT TCTCTTTGAA GCCTCCAAAC CAGCTGGTGA AGTCAGTAGC 1800 ACCCCTGTGT TTTTTATCAA GGTAAGGTTC ACATAACATA AAATGAAGCA TTTTAAAGTG 1860 AACACTTCAG TGGAATTTAG TATATTTACA GGGTTGTGGA ACCTCCGCCT CTGTCTAGTT 1920 CCAAAACATT TTTATCACCC CAAAAGGAAA CCCATACCCA CTAAACAGTT GCTCTCCTTT 1980 CCCTCCTCCC CCAGGCCCTG GAAACCACCC TCTACTTCCT GTCGCTATGG GGTTGCCTAT 2040 TCTGGATACT TCACCTATCC AGAGCTTTTG TGTCTGGCTT CTGTCACTTA GCATCATGTT 2100 TTCGAGGTTT ATCCAGGTTG TAACATGTAT TGTTATTACA CCTTGGTCTA TGGCTAAATA 2160 ATGTTCCATT GTCTGTAAGC ACTCCCATCT TACAGATGAG GAAACAGTCC CGAGGCGCTG 2220 AGACTCCCAG CTTGAGTCCA CACCGGAGAG ACATGGTCCG TGCAAGCCTG CTCCCCAGAT 2280 GGCCCCATCC TGGCACTGCC GTCTGGGAGG AGGCTGCCCC TGGGGGCATG CTGGTCCCTG 2340 AGTGGTGACC TGACCCCTTC TGAGGTTCAC TTCTCAGCGC AGGTTCACTT CTCAGCGCAG 2400 GTTCACAGGC GAGGGTGCTC TGGCCTCCCA GTCACCCTGA TCCAGGCAAG ACCATAGCGT 2460 GGCCGCAGGG GCCGCCTCCT TGGGGGAATT CCAGCCCCTG GCCAACCACA GACCATAGCA 2520 CTCCCGGGGG TTGAACCGTT TCTCACAACT GGGTTGTGAC AGCTGGGAGG TGCTCAACCC 2580 TGGGGGCCAG CCTGGTGGCA GGCCGGGTTG GGAACGCTGT TCCCAGCCAG CTTCCCTAGG 2640 CAACATGGCC AGCCCCGTCC AGCAAGTGGA CCACTCAGAT GGCAGGCATG TACTGAGCAC 2700 CCACTGTATA CCAGCCAGGC ACCACGAGGC CTCCAAGGAG CTCCCTTTCT GATGAGGATG 2760 AGCCACCCCA GAACAGAAAC TGGGTGCTGG GGCCAGGGGC AGGACAGAGG GGTGCTCCGG 2820 AGAACAAGCA CCAGCACTGA GCCTGGGGAG TTCCCCGCTG GCAGCGCCTG ACACAGCCCA 2880 CACCGGGGAT CCCTGGCCTC AGGAAAGCAG GGCTGTCACA TCAAGAAGGC CATGACATAA 2940 GGGCCCCTAC CAACGTCCAG CCTTAGGTGG AGGGCACAGA TATGGCAATA CACAGGACCC 3000 TAGAATGCCT GCCTGGGGAT GCCCACCTTG GCCCACTTGA TGGCCAGTTG AGACTCAGTG 3060 TGCACTGTCC ACACACCCTG TTCTGACACT GACTGCCTAG TGTCCAATTA TTCTTCCATC 3120 TCACTCATTC AGTGCCAGTT ACTCTACTGA GCAATAAGGA TATAACATTT TAAAAACAAA 3180 ACAAACATGT TCCTGTCCTC TAGAAGCTTA AAATAGAGCA AACTGAGAAG GAAACTAATA 3240 ATGACCACCT TGCCAGGGGC AAGGAGACCA GAGGCAGGGC CCTAACCCAC GGGCAGCTGC 3300 AGCTGGAATA TATGAGACAG TGTGTGTGTG CTCACATGTC CACAGCCGAG CTCACCTCCA 3360 GACAGTTATG CACCCCTACC GCTCACCCCA TCCCACCTCA TCCTCACCAA GGCAGGTCTA 3420 CTCAGTAAGT CAGGCTGAAA ACATGAGCCT GGGGAGTTGG GACTTCTTAA CTGCCACCCC 3480 CACCTGCACC CCATCCAGGA TGAAAGAAGC ATTATCCAGC AAGGACATGG CCACTGAAAG 3540 TGCCACCAAG GACCGGCCAA GGGGAGGGGA AGGGCTCCCT ACAGCCCTTC CCCTGCTGGC 3600 TGAGTTGAAT GGCCAGGGAC TTACCCAGGC TGGTACAAAG CCACTGGCCC CAGGGCCATC 3660 CCCTTATAAC ACAGCACTTC CTGGGTGTCA GTGCATGCTG AGTATGTCAC GTGTATTTCT 3720 TAAACCACTA AGATTTTACC AGTGACTTAT CCAAGGTCAC CAGGCCAGTG TGTAGAAAAT 3780 TTGCATTCTG GTGTGAGCCA CTCAAAGGTC CACACCCACA TTTCTACACA TCCCCTAATA 3840 AAAGCCAAGG GGCCCACAAC GCTCCCCTGT GAACCTCACA TGGCTGCCTG TCTAGGGGAA 3900 ATGAAGGAAA TCCCTTCACA CGGAGCCCCT GCCCCAGCCG TGCTCCAGTC CCTCTCTTTT 3960 CCCCTGCCCT AGCTGACCCC ACAGCTAAGC CCACCTTTTG GCATTCAGGG TGCACCTCCT 4020 GCCCCAGGGA ACTCCCAGAT GAGCTGGAGG GAACAGTCTG CACTGGGGCT CTGGGTGGAA 4080 GGGAAGAGGA TGGGGGCTAA CCAGGTCCTG GGCACATAGG GCCTCATGTG GGAAGGAAAA 4140 TGCTCCCTCA 4150
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