Tag | Content |
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EnhancerAtlas ID | HS187-20479 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr5:180225860-180228330 |
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) |
FOS | MA0476.1 | chr5:180227113-180227124 | GGTGACTCATT | + | 6.02 | FOSL2 | MA0478.1 | chr5:180227112-180227123 | GGGTGACTCAT | + | 6.14 | JUN | MA0488.1 | chr5:180227873-180227886 | CTAATGATGTCAT | + | 6.05 | JUNB | MA0490.1 | chr5:180227112-180227123 | GGGTGACTCAT | + | 6.32 | POU4F2 | MA0683.1 | chr5:180227280-180227296 | CTGCATAATAAATTAC | + | 6.75 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_00208 | chr5:180226338-180232837 | Adipose_Nuclei | SE_04432 | chr5:180227786-180229455 | Brain_Anterior_Caudate | SE_06373 | chr5:180228060-180239464 | Brain_Hippocampus_Middle | SE_09403 | chr5:180224222-180239890 | CD14 | SE_11617 | chr5:180223963-180241038 | CD20 | SE_13619 | chr5:180226362-180227355 | CD34_Primary_RO01536 | SE_14652 | chr5:180226061-180232679 | CD4_Memory_Primary_7pool | SE_17640 | chr5:180224285-180240076 | CD4p_CD25-_CD45RAp_Naive | SE_18207 | chr5:180224315-180232594 | CD4p_CD25-_CD45ROp_Memory | SE_18943 | chr5:180224402-180232678 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19487 | chr5:180224404-180232635 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20552 | chr5:180226045-180232629 | CD56 | SE_21228 | chr5:180226799-180232526 | CD8_Memory_7pool | SE_23037 | chr5:180225369-180239518 | CD8_primiary | SE_25888 | chr5:180226182-180232829 | Duodenum_Smooth_Muscle | SE_26659 | chr5:180226632-180228299 | Esophagus | SE_28199 | chr5:180225732-180231148 | Fetal_Intestine | SE_29359 | chr5:180225635-180232008 | Fetal_Intestine_Large | SE_31515 | chr5:180227197-180228261 | Gastric | SE_37805 | chr5:180225251-180231922 | HSMMtube | SE_40819 | chr5:180226144-180232486 | Left_Ventricle | SE_42229 | chr5:180225896-180228353 | Lung | SE_50139 | chr5:180226026-180232582 | Sigmoid_Colon | SE_51462 | chr5:180227840-180239845 | Skeletal_Muscle | SE_52103 | chr5:180226153-180230967 | Skeletal_Muscle_Myoblast | SE_52459 | chr5:180226161-180232564 | Small_Intestine | SE_62365 | chr5:180226988-180260779 | Tonsil | SE_63877 | chr5:180226077-180231374 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 180226966 | 180227821 | chr5 | 180227892 | 180227963 |
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Enhancer Sequence | TTCTCAATTC TGAAATACAT CTAGGACCAA GAACTTCAAA ACTATGAAAA TGGAAGTACA 60 AAGTTACTCA TTGACTGCTA GCATCCCATG TCAAGCCCTC CAGCCCTTTA ACCTGAACTC 120 ATTCCTTCGT AGGAAACACT GTTTTAAGTC TGGACTCTTG ATGTAGTTTC CCAGCTGGTC 180 CACCTGTCAC TAATCTTGCT TCCCTCTCAC AAACCTTCCC AACAGCAACA GCGCATCCTT 240 CCTGACAAGT ACACCTGGTC ACGACATTAA CTTGCTTTAA AAACCATCAG AGGCTGCACT 300 GCCCACAAAC TCAAACTCAA ACTCATTATG ATGACATCCA AAGCCCTTCA GACAGACTGT 360 CTGAAACATC CCTTTTCAAC CTTACCTCCA ACCACTAACC CCATGGACCC TGCACTCTGG 420 CCTCAGCAGG CTGCTTTTTC CCCAGTAAGC ATATACCTGG ACGCTGCTGT GTCTCTGCTC 480 CAGCTGGTCC CTCATCCTGG AATTTGACCC ACAGCGCCAC CTGCCAGCCA CCCACACATC 540 CTTTCAGGCC ACTTCAGGTG ACTCCTTCTG TAACATCACA GACAGAGCCA GGCCTCCCTA 600 TGACTACACT CCCACAGCAC TCTCTCCACG CTGTAACAGA ATCTGTGGCC ACGCTGACCT 660 GACTCCCACC TTCCTCCTTA GGAAAAAAGA CTCTATGACC TCTGTGCCCA CCACAGTGCT 720 TGGCACATGT ATGAGGTTCA AGTGGCTGGA TGGAAGACTG CTTGCACTAT TACCGAAATC 780 AGGGAGAAAG ATGGCCAACG CAGCAGCAAG AGAGTGAAGT GTGACATTTT CCAGAGATGA 840 CCGCACATAT CCCATTCCAT ATGCTCTTCT TACAAGTGAT AAAGACACTC CTGCCTCCAG 900 AGCTGAGGGT CTATGTTCCC TCCCTTTGGT TCTGGGAAGA GATGCTATGT GACTTGTGAG 960 ACTAACTCAT AAAAGGCAGT AGTTTCCACC TGGTCCTCTT AAGATGCTGA CTCCTAGGAC 1020 CCTGCTATAT GGACAGGACA CTGCTACATG GACAGGACCC CCATAGGTAT TCCAACTGAC 1080 CACCCCAGCT AAGGTCCCAG CTGACAGCCA GCATCAACCG CTAGACACAG GAGACAGCCC 1140 TCCAGATTAT CCCAGCCCCA GCTGACTGCA ATGGCGTGAA AGACCACAAG CAAGAACCAC 1200 ATAGCTGAGA TGTTAATAAA ATGATTCTGT TGTTGTAAGC CACTAAGTTC TGGGGTGACT 1260 CATTATGCAG CCATCAGTAC CTGAAGCAAT GAGAGAAACA GACTCTAGAT AATCTTGACA 1320 AGCAGGGCAA GTGCCCTCCC TGCCCTCTGT GCTCAGCTCC AAGTCCAAAC ACTGAGGCCC 1380 TGTCTCCACT CATGTCTCCT TCCTTAGTAG GTATCTACTC CTGCATAATA AATTACCTCG 1440 ATATTTAGTG GCTTAAAACA ATAGTTATCA CTTACTCCTC ACAGTTTCTA TTGGTCAGAA 1500 ATGTGGACAG TGCAGCACAG AGGAGATGAC GTGTCTCTGC TCCACTATGC CTGAGGCCTT 1560 GCTGAAAGAC TCAAAAGCTG AGGGCCAGAT GCCCCTAGAG GCTCTCACAT TCTCTCACAT 1620 GTCTGTAGGA TGATGTTGGC AGCAGCTGAG ACCTTATCAG CAGGAGTGCT CACTAGAACC 1680 CCTCTATGTG GCCTGGAAAT GTCCTGGAAG TGGTGGCTGC ATTCCAAAGG TGAGTGTTCC 1740 AAGAAAGCGG GCAAGCCAGG TGAAAGTGTA TCCTGTTCCT GATTCAGCCT TGGATCAGGT 1800 CTGTCTTACT CACTGGTCAA GGGAACCACA AGTCCCTATT GACATGCAAG GGGAGAGAAT 1860 CATAAACCCC ACCACTAGGT GGGAAGTGGA CAATGTCAAA CTATAACTAC ATGTGGAAGG 1920 GGATACTTAC GGGTGAGGCC CTTGAGGGAA AATACAATCT GCTACACCTT CCTTTTTAAA 1980 TAGAACAACT GCCCTTAATC CTGACCTGAG TTCCTAATGA TGTCATTTAT GAGACTGGCA 2040 TGCAAGGCAC AGACTCAAAA CTGGCTTTGA CTTTCTAGAG TTTTCACAAC TCCTTTAGGG 2100 AGGTGACACA GCCAATCCAC ACCACCAGGT ACAAAGACAT CTGCACCATG GTGGGAGATG 2160 AGAAGTGAGT CTTTTCAGTA CAAAACCCTT CAGCTAAAAC CGAGGTGGCT CTGGGTAGGC 2220 GCCACCTGCC CCTATGGGGC TCACTCAGTT TCTGAAGCAT TTGAAGGACT GCCTAGGAGC 2280 TGTGAGATCC TTTCTAACAC TCTGATACCA TGGTGTTCTC CAGCCTATTT CCTTTATCTG 2340 GCAAAAAATG TTTCTTAAAT AGCAAGTGAA CACCAGATAG TCAACTTCCA ATCATGAGCA 2400 ATAAGCGAGA AGTTATATTT AGCTGTAAAA TTAAGTACAG AAGTGGAAGA AATGGTAACA 2460 GATTTTCCCT 2470
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