Tag | Content |
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EnhancerAtlas ID | HS022-04391 |
Organism | Homo sapiens |
Tissue/cell | CD4+ |
Coordinate | chr14:69285930-69288180 |
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: 27 | ID | Coordinate | Tissue/cell |
SE_02903 | chr14:69285849-69286635 | Bladder | SE_10217 | chr14:69287381-69288209 | 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 | TCTGTGAGGA GGTCCTACAG AAGGAGAAAT ATGGAGAAGT GGGTGACCCA AGATGATGGC 60 TCACACACCT CTCCCAGGAG GGCCAGCCCC ATGCCTAGCT AGGCAGTTCC CTGGCTAGGA 120 CGTCAGCTCT TACTCACTCT TTCCAGAGAG CAGCTAATTA GCCTCCCAGC AGCCAGGAGC 180 TCTCCAGATG AAAGGTGCTT AATACAAGCT CAAGGCGTAA CTCCCATATG TATAACTAAG 240 GTTCCCTGAG GTGAGGAAGG CCCCAGGGCG GAGAGACAGG CCAGATCAGG GCCTCGCCTT 300 CTTTATGACG GAGGTTCCCA GGGAAGGGAG CCGGCTGGGG TGGCAGTGAG CCTGAGAAAG 360 GGCTCGGGGT GGTGGGTGTG CGGCTTCAGA GGGAGCCCCT CCCTGGGAGT GGGCGGGGCC 420 CGGTGGCTGA GGAGGCAGAG TGAATGCTTC AGGGCCCAAG CTGCCTCCCA GAGTGGGAGC 480 TCCAGGTCAG AAGACAGCTT AGAACTGGGT GGGTCAGAGC GAGGGCTTTG CTGCTGGGCT 540 GCCAGGTCAG AATCCCAGCT CTGCTATGGC CATTCCATGT CCCAGAGCCT CAGCTTCCTC 600 CTCTGTAAAA CGGAGATAAT GATAACATTG ACCTCACAGC TATTTACTGA CAGCACTTAG 660 TACAGACAGG ACCTGGCACC CACTACGTAA AGAATGAGGA TTTGTACATT TGTTCATTTA 720 ACAGATATTT ATTGAGTACC TGCTATGTGC CAGGCACTGG GTGTTAGAAA TACAGTCATG 780 AACAAAACAG ATCCATTTTC CCTTGATTCT GTAGGGAAGA TAGACCACAG ACCCCAGAAC 840 CAAGAGATCG GTAATACACT GCCTGGCAGT GACCTGCGCT GTGGGAATCG GGTATGAGGA 900 TGGGGTCAGG TGTCCAATAC AGCGGCAGAA GAGCAGGTAC CCAGGCAGAT ATGGGCAGAT 960 TAAGAAACGA ACCAGGGTTG AAGGGCCAAC CCAAAGTGCG CAGCAAATCA GAGGCGGGAG 1020 CCTGGGCCTG CAGCATAGGA ATGTTCACCC ACAGCTGCTG AAGCAGCCGC AGCAGCTCCC 1080 TCTGCCCCTG ACTAAGGGGT GTGCCCAGCG AAGCCACCTG CCCTCACCTC CCCCTTGGCT 1140 CCTGCCCCTG ACTCCCGCAG TCTGGAGTCC AGCAAGGCAA GGGAACTGAC ACAGCCCCCA 1200 GGGTCACGAT GGCTTCCATT CTTTGACATT CACCAGTGTC ACTGGCTGAG CTCAGGCTAC 1260 ACGGCCATCT TCTCTTTGAA GCCTCCAAAC CAGCTGGTGA AGTCAGTAGC ACCCCTGTGT 1320 TTTTTATCAA GGTAAGGTTC ACATAACATA AAATGAAGCA TTTTAAAGTG AACACTTCAG 1380 TGGAATTTAG TATATTTACA GGGTTGTGGA ACCTCCGCCT CTGTCTAGTT CCAAAACATT 1440 TTTATCACCC CAAAAGGAAA CCCATACCCA CTAAACAGTT GCTCTCCTTT CCCTCCTCCC 1500 CCAGGCCCTG GAAACCACCC TCTACTTCCT GTCGCTATGG GGTTGCCTAT TCTGGATACT 1560 TCACCTATCC AGAGCTTTTG TGTCTGGCTT CTGTCACTTA GCATCATGTT TTCGAGGTTT 1620 ATCCAGGTTG TAACATGTAT TGTTATTACA CCTTGGTCTA TGGCTAAATA ATGTTCCATT 1680 GTCTGTAAGC ACTCCCATCT TACAGATGAG GAAACAGTCC CGAGGCGCTG AGACTCCCAG 1740 CTTGAGTCCA CACCGGAGAG ACATGGTCCG TGCAAGCCTG CTCCCCAGAT GGCCCCATCC 1800 TGGCACTGCC GTCTGGGAGG AGGCTGCCCC TGGGGGCATG CTGGTCCCTG AGTGGTGACC 1860 TGACCCCTTC TGAGGTTCAC TTCTCAGCGC AGGTTCACTT CTCAGCGCAG GTTCACAGGC 1920 GAGGGTGCTC TGGCCTCCCA GTCACCCTGA TCCAGGCAAG ACCATAGCGT GGCCGCAGGG 1980 GCCGCCTCCT TGGGGGAATT CCAGCCCCTG GCCAACCACA GACCATAGCA CTCCCGGGGG 2040 TTGAACCGTT TCTCACAACT GGGTTGTGAC AGCTGGGAGG TGCTCAACCC TGGGGGCCAG 2100 CCTGGTGGCA GGCCGGGTTG GGAACGCTGT TCCCAGCCAG CTTCCCTAGG CAACATGGCC 2160 AGCCCCGTCC AGCAAGTGGA CCACTCAGAT GGCAGGCATG TACTGAGCAC CCACTGTATA 2220 CCAGCCAGGC ACCACGAGGC CTCCAAGGAG 2250
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