Tag | Content |
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EnhancerAtlas ID | HS098-47346 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:180225840-180228550 |
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: 30 | 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_07221 | chr5:180228215-180232669 | Brain_Hippocampus_Middle_150 | SE_09403 | chr5:180224222-180239890 | CD14 | SE_11617 | chr5:180223963-180241038 | CD20 | SE_13619 | chr5:180226362-180227355 | CD34_Primary_RO01536 | SE_13619 | chr5:180228138-180232603 | 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 | TCTTTTCAAA ATCCAAAAAA TTCTCAATTC TGAAATACAT CTAGGACCAA GAACTTCAAA 60 ACTATGAAAA TGGAAGTACA AAGTTACTCA TTGACTGCTA GCATCCCATG TCAAGCCCTC 120 CAGCCCTTTA ACCTGAACTC ATTCCTTCGT AGGAAACACT GTTTTAAGTC TGGACTCTTG 180 ATGTAGTTTC CCAGCTGGTC CACCTGTCAC TAATCTTGCT TCCCTCTCAC AAACCTTCCC 240 AACAGCAACA GCGCATCCTT CCTGACAAGT ACACCTGGTC ACGACATTAA CTTGCTTTAA 300 AAACCATCAG AGGCTGCACT GCCCACAAAC TCAAACTCAA ACTCATTATG ATGACATCCA 360 AAGCCCTTCA GACAGACTGT CTGAAACATC CCTTTTCAAC CTTACCTCCA ACCACTAACC 420 CCATGGACCC TGCACTCTGG CCTCAGCAGG CTGCTTTTTC CCCAGTAAGC ATATACCTGG 480 ACGCTGCTGT GTCTCTGCTC CAGCTGGTCC CTCATCCTGG AATTTGACCC ACAGCGCCAC 540 CTGCCAGCCA CCCACACATC CTTTCAGGCC ACTTCAGGTG ACTCCTTCTG TAACATCACA 600 GACAGAGCCA GGCCTCCCTA TGACTACACT CCCACAGCAC TCTCTCCACG CTGTAACAGA 660 ATCTGTGGCC ACGCTGACCT GACTCCCACC TTCCTCCTTA GGAAAAAAGA CTCTATGACC 720 TCTGTGCCCA CCACAGTGCT TGGCACATGT ATGAGGTTCA AGTGGCTGGA TGGAAGACTG 780 CTTGCACTAT TACCGAAATC AGGGAGAAAG ATGGCCAACG CAGCAGCAAG AGAGTGAAGT 840 GTGACATTTT CCAGAGATGA CCGCACATAT CCCATTCCAT ATGCTCTTCT TACAAGTGAT 900 AAAGACACTC CTGCCTCCAG AGCTGAGGGT CTATGTTCCC TCCCTTTGGT TCTGGGAAGA 960 GATGCTATGT GACTTGTGAG ACTAACTCAT AAAAGGCAGT AGTTTCCACC TGGTCCTCTT 1020 AAGATGCTGA CTCCTAGGAC CCTGCTATAT GGACAGGACA CTGCTACATG GACAGGACCC 1080 CCATAGGTAT TCCAACTGAC CACCCCAGCT AAGGTCCCAG CTGACAGCCA GCATCAACCG 1140 CTAGACACAG GAGACAGCCC TCCAGATTAT CCCAGCCCCA GCTGACTGCA ATGGCGTGAA 1200 AGACCACAAG CAAGAACCAC ATAGCTGAGA TGTTAATAAA ATGATTCTGT TGTTGTAAGC 1260 CACTAAGTTC TGGGGTGACT CATTATGCAG CCATCAGTAC CTGAAGCAAT GAGAGAAACA 1320 GACTCTAGAT AATCTTGACA AGCAGGGCAA GTGCCCTCCC TGCCCTCTGT GCTCAGCTCC 1380 AAGTCCAAAC ACTGAGGCCC TGTCTCCACT CATGTCTCCT TCCTTAGTAG GTATCTACTC 1440 CTGCATAATA AATTACCTCG ATATTTAGTG GCTTAAAACA ATAGTTATCA CTTACTCCTC 1500 ACAGTTTCTA TTGGTCAGAA ATGTGGACAG TGCAGCACAG AGGAGATGAC GTGTCTCTGC 1560 TCCACTATGC CTGAGGCCTT GCTGAAAGAC TCAAAAGCTG AGGGCCAGAT GCCCCTAGAG 1620 GCTCTCACAT TCTCTCACAT GTCTGTAGGA TGATGTTGGC AGCAGCTGAG ACCTTATCAG 1680 CAGGAGTGCT CACTAGAACC CCTCTATGTG GCCTGGAAAT GTCCTGGAAG TGGTGGCTGC 1740 ATTCCAAAGG TGAGTGTTCC AAGAAAGCGG GCAAGCCAGG TGAAAGTGTA TCCTGTTCCT 1800 GATTCAGCCT TGGATCAGGT CTGTCTTACT CACTGGTCAA GGGAACCACA AGTCCCTATT 1860 GACATGCAAG GGGAGAGAAT CATAAACCCC ACCACTAGGT GGGAAGTGGA CAATGTCAAA 1920 CTATAACTAC ATGTGGAAGG GGATACTTAC GGGTGAGGCC CTTGAGGGAA AATACAATCT 1980 GCTACACCTT CCTTTTTAAA TAGAACAACT GCCCTTAATC CTGACCTGAG TTCCTAATGA 2040 TGTCATTTAT GAGACTGGCA TGCAAGGCAC AGACTCAAAA CTGGCTTTGA CTTTCTAGAG 2100 TTTTCACAAC TCCTTTAGGG AGGTGACACA GCCAATCCAC ACCACCAGGT ACAAAGACAT 2160 CTGCACCATG GTGGGAGATG AGAAGTGAGT CTTTTCAGTA CAAAACCCTT CAGCTAAAAC 2220 CGAGGTGGCT CTGGGTAGGC GCCACCTGCC CCTATGGGGC TCACTCAGTT TCTGAAGCAT 2280 TTGAAGGACT GCCTAGGAGC TGTGAGATCC TTTCTAACAC TCTGATACCA TGGTGTTCTC 2340 CAGCCTATTT CCTTTATCTG GCAAAAAATG TTTCTTAAAT AGCAAGTGAA CACCAGATAG 2400 TCAACTTCCA ATCATGAGCA ATAAGCGAGA AGTTATATTT AGCTGTAAAA TTAAGTACAG 2460 AAGTGGAAGA AATGGTAACA GATTTTCCCT TCTATCTCTG CTTTGCTTAA AGTTAAAAAG 2520 CACTACGTAA AAATTCCAGA AAATATAGAC ATGTCACAGG TAATGGAACT CTAACTGAAC 2580 TGCTTTCATG TTCGTTCTTA GACCTTGGCT GGACTCCTGT ATCATGTACC AGGCCCATAA 2640 TTTCAGGACG GAAAAAAAAG AAAGGTAGTC AGAGAAGATA CACTAAATAA TTCAAGAGTT 2700 GAGAGAATAA 2710
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