Tag | Content |
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EnhancerAtlas ID | HS062-09119 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr2:70321080-70324240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr2:70322458-70322472 | GAAAAGCGGAAGTT | + | 7.52 | SPIB | MA0081.2 | chr2:70322460-70322472 | AAAGCGGAAGTT | + | 6.22 | SPIC | MA0687.1 | chr2:70322458-70322472 | GAAAAGCGGAAGTT | + | 6.05 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_00419 | chr2:70320579-70323660 | Adipose_Nuclei | SE_03004 | chr2:70321146-70322478 | Bladder | SE_03004 | chr2:70322550-70323235 | Bladder | SE_08976 | chr2:70321798-70322424 | Brain_Mid_Frontal_Lobe | SE_11876 | chr2:70321479-70323498 | CD3 | SE_12913 | chr2:70321429-70323132 | CD34_Primary_RO01480 | SE_14144 | chr2:70321089-70323275 | CD34_Primary_RO01549 | SE_15476 | chr2:70321454-70322985 | CD4_Memory_Primary_8pool | SE_15969 | chr2:70321496-70323314 | CD4_Naive_Primary_7pool | SE_16420 | chr2:70321615-70323401 | CD4_Naive_Primary_8pool | SE_16927 | chr2:70321482-70323289 | CD4p_CD225int_CD127p_Tmem | SE_19261 | chr2:70321074-70323298 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_21576 | chr2:70321103-70323265 | CD8_Naive_7pool | SE_21995 | chr2:70321100-70323359 | CD8_Naive_8pool | SE_23504 | chr2:70321633-70323217 | Colon_Crypt_1 | SE_24093 | chr2:70321585-70323230 | Colon_Crypt_2 | SE_25188 | chr2:70321908-70323278 | Colon_Crypt_3 | SE_25929 | chr2:70321003-70323419 | Duodenum_Smooth_Muscle | SE_36506 | chr2:70321922-70322715 | HMEC | SE_38843 | chr2:70321606-70323276 | HUVEC | SE_45109 | chr2:70321874-70323353 | NHLF | SE_47654 | chr2:70321627-70323285 | Pancreas | SE_49034 | chr2:70321392-70323244 | Right_Atrium | SE_49786 | chr2:70321672-70322541 | Right_Ventricle | SE_54943 | chr2:70321024-70323255 | Stomach_Smooth_Muscle | SE_60350 | chr2:70310849-70332853 | Ly4 | SE_64604 | chr2:70321838-70323251 | NHEK |
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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 |
GH02I070093 | chr2 | 70320605 | 70324187 |
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Enhancer Sequence | GAGATAATAA GGAACCAATA GTAAGCTGAA CGTTAAAGAT ACAGGTAAGA GAAGACTATG 60 GCTCTAGCCA TAGTCTGTTG GACTGCTGGA ATTTAACTCT GTCCCCTCTT CCATAGGGAC 120 TTGCATCTCA GAATTCCTCT CCTTTGTCCT TTCTCTTTGG GGCAGCTTGA GCATGTCCTG 180 TCCTCTTCTG GATGGAGGAC TGGAAATTGA TGAGGCCCCT ATGCAGTTGC TGATTCTTGT 240 CACTGCCCTG TTCCTGCCTC CAGCTGTTAG GCCATAGCCA CTGCCATAGT TGGGAAGAGC 300 TGGAACAGGT TGACAAACAC CTGTTGTGTC ATAGCCATAG TATTTGTATC ATGTGTTTAG 360 AAGGCTGGTC TCCCCCGGTC CCCAATCCCC TCCCTTGCCC CACTCAAATA TAGACACACA 420 CACATGCACA CACGTACATG ACCACCACGA GCTCTCCTCC AGCCAGTAGT TTGGACAGTG 480 AATCACCACT CTTGGGTTCA CCCCTAGAGC AGCTACTTAC TCCCTGTGAC CTGAAAAGTA 540 AGCAGTATTT ACCAAGAGCT TCAGGTTTGT GAGTTGAACC CACCTCACCC CTTGCTACTC 600 TTGGCTACCC CAAGTGGTGA ACCACATACT GTCCAGCATC CCTGGGCCTG CCACCTCCTG 660 CCAGTGAGAC AGCGCCCAGT CAGACATACA AATAGGCAGT CACAGCAAGA GAAGCCTTCC 720 ACTACCAAGT CCTCTGCTCA CCTCACCTAG CCTGGCCACC TGAGGGGCCT TCCTAAAATT 780 CAGATCTAAA CACATGTGTC CCCCGATCAA AGGCCTTCAA GTCCCACCTC ACCCCCATGG 840 TCTATGAAAG AAAACCCAAA CTGTTCAGCA CAGTTTTCCA GGCCCTTGAA CATCTGTTCC 900 CCACCAGCCT CACCAGTGCA AGGCCTAACA AGTCTCCTGC CACTACCTTC AGCCTTCCAT 960 ACAAAATAAC TGGCAGTCCC CCCAAAGTCA TTCTGTGTGG GCATCCTTGC CTGTGGGACA 1020 TCATTGTTTC TTCACTCTTC TGATCCTGGC TGTGCTCTTC TTCCTTACCT CCCTGGGGTT 1080 CTGGGGTTCC TGTTCTTTGA GCATCAACAT TCTGCAAGGA AAATCACACT GTGCTGAGAA 1140 TTGGGAGACC TGAGTTCTAG TCCTGGCTCT GGCATCAGCT CACTGGGAGA GCTTGGACAA 1200 ATTCCTCCCT CTTTCTGGGT CTTAGTCCTC CATCTGAGAA GACGGGATAA GTTCAGACCC 1260 ATGATTCTCT GGCTGCCTTG GAAAATAAGG CTTCCTTTGT GGGCACCCAT CCCAGCTTCT 1320 GCCTCCTGCC ACAGGGCTGA CTTCTGACAC ACAGGCCTTC TGTAAATACT CTAACAGAGA 1380 AAAGCGGAAG TTGACAAAAA ACTGGCAGCA ACAAGCCCCA GCTTGGCATT TTGGGTAACT 1440 ATTCATAGGC ACTTGATTGA GGAGGAAGTA GAAAGGAAGA ACTGCAGTGA GATTTGCTCG 1500 GAACATCCCT GATCTATTAT TGTGCCTGTC GCTTTAGACT TTTTCTTACT TATTTATTTT 1560 ATTTATTTAT TTTTAAGACG GGGTCATTCA CTCTGTGGCC TGGGCTGGAG GACAATGGTA 1620 TGATCACAGC CCACTGCAGC CTCAAACTCC TGGGCTCAAC CAATCCTCCT GCTTCAGCCT 1680 CCCAAGTAGC TGGGATTATA GGCTATCACT TTAGACTTTG AGGGGAAGAT GTAAGGACAG 1740 TAGAGGGGAA GAAGACAGAC ACTCCAGAGA AGGTTACACA CGAGGAGAAG TTAATCCCTA 1800 AAAGCAGGCC CAAGCCCTCG CCCCTCCTTT CCCCTGCCCT CCTGCCCTCA AAGCAAGGGC 1860 TTTGGGAGAG GGCTTGGCTG CCCTGATTTT CCCCTATACC TTGTGTCCAC TGAAGTAGGG 1920 AGATAGTAAC TGTGCTGCCC TCCTTCTCCT CCCAGGGGTG GATTGTGCCT CCAAACATCT 1980 GCCACTGGGC TGAGTGAGCC TTGGTAGGGA GCTGAGACCA CCGTCCTTCA GCGTCAGCAA 2040 ACTCATATCA TGTCAGCTAG CCACTCGAAT GGTGCAAGAT GCCAAACTGG TTATTCCCTG 2100 AGCAGTTCAG TCACAGTAAG GTGACTCTAA ATGGACGGTC TGCACATTTT TCATCTTGTC 2160 TGTAATGACT TTTATTGCTC AATTGTTCTT TTTTATTTTT TTATTTTTTA TTTTATTTAT 2220 TTATTTATTT ATTTATAATT TTATTTATTT ATTTATTTAT TTTGAGGCAG GGTGTCACCG 2280 TATCGCCCAG GCTGGAGTGC AGTGGTGTGA TCTAGGCTCA CTGTAACCTC CGCCTCCTAG 2340 GTTTAAGCAA TCCTCCCACC TCAGCCTCCC AAGTAGTTGG GACTACAGTC ATAAGGCACC 2400 ACACTGGCTA TTTTTTTGTA TTTTTAGTAG AGACAGGGTT TTACCGTGTT GCCCAGGGTG 2460 GTCTCGAACT CCTCCAAGCG ATCCACCTGC CTCAGCCTCC CAAAGTGCTA GGATTACAGG 2520 TGTAAGCCGG CGTGCCCAGC CTGCCCAATT TTTCAGTCAA GAAAACATAC ATGAAGCCTG 2580 GCACGGTGGC TCACACCTAT ACTCCCAACA CTTTGGAAGG CCAAGGCAGG AGGATCAGTT 2640 GAGGCCAGGA GTTCGAGACC AGTCTGGGCA ACATAGTGAA ACCTTGTCTC TATTATGTTT 2700 AAAAAAAATA AAAATGTAAA GGCCAGGAAC GGTGGTTTAT GCCTGTAATC CCAGCACTTT 2760 GGGAGGCCAA GGCGAGATGA TCAGTTGAGG CCACGAGTTC GAGACCAGTC TGGGCAACAT 2820 AGTGAGACCT CATCTCTATT ATATTAAAAA AAATAGGGAC CAGGCATGGT GGCTCATGCC 2880 TGTAATCTCA GCACTTTGGG AGGCCGAGGC TGGCGGATCA CGTGGTCAGG AAATCAAGAC 2940 CATCCTGGCT AATACGGTGA AACCCTGTCT CTACTAAAAA TACAAAAAAT TAGCCGGGCG 3000 TGGTGGCTGG TGCCTGTAGT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATGGCGTGAA 3060 CCCGTGAGGC GGAGCTTGCA GTGAGCCAAG ATTGCGGCAC TGCACTCCAG CCTGGGCTAC 3120 AGAGCGAGAC TCCGTCTCAA AAAAAAAAAA AAAAAAGTAC 3160
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