Tag | Content |
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EnhancerAtlas ID | HS139-29126 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:70321240-70323470 |
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 | GGCAGCTTGA GCATGTCCTG TCCTCTTCTG GATGGAGGAC TGGAAATTGA TGAGGCCCCT 60 ATGCAGTTGC TGATTCTTGT CACTGCCCTG TTCCTGCCTC CAGCTGTTAG GCCATAGCCA 120 CTGCCATAGT TGGGAAGAGC TGGAACAGGT TGACAAACAC CTGTTGTGTC ATAGCCATAG 180 TATTTGTATC ATGTGTTTAG AAGGCTGGTC TCCCCCGGTC CCCAATCCCC TCCCTTGCCC 240 CACTCAAATA TAGACACACA CACATGCACA CACGTACATG ACCACCACGA GCTCTCCTCC 300 AGCCAGTAGT TTGGACAGTG AATCACCACT CTTGGGTTCA CCCCTAGAGC AGCTACTTAC 360 TCCCTGTGAC CTGAAAAGTA AGCAGTATTT ACCAAGAGCT TCAGGTTTGT GAGTTGAACC 420 CACCTCACCC CTTGCTACTC TTGGCTACCC CAAGTGGTGA ACCACATACT GTCCAGCATC 480 CCTGGGCCTG CCACCTCCTG CCAGTGAGAC AGCGCCCAGT CAGACATACA AATAGGCAGT 540 CACAGCAAGA GAAGCCTTCC ACTACCAAGT CCTCTGCTCA CCTCACCTAG CCTGGCCACC 600 TGAGGGGCCT TCCTAAAATT CAGATCTAAA CACATGTGTC CCCCGATCAA AGGCCTTCAA 660 GTCCCACCTC ACCCCCATGG TCTATGAAAG AAAACCCAAA CTGTTCAGCA CAGTTTTCCA 720 GGCCCTTGAA CATCTGTTCC CCACCAGCCT CACCAGTGCA AGGCCTAACA AGTCTCCTGC 780 CACTACCTTC AGCCTTCCAT ACAAAATAAC TGGCAGTCCC CCCAAAGTCA TTCTGTGTGG 840 GCATCCTTGC CTGTGGGACA TCATTGTTTC TTCACTCTTC TGATCCTGGC TGTGCTCTTC 900 TTCCTTACCT CCCTGGGGTT CTGGGGTTCC TGTTCTTTGA GCATCAACAT TCTGCAAGGA 960 AAATCACACT GTGCTGAGAA TTGGGAGACC TGAGTTCTAG TCCTGGCTCT GGCATCAGCT 1020 CACTGGGAGA GCTTGGACAA ATTCCTCCCT CTTTCTGGGT CTTAGTCCTC CATCTGAGAA 1080 GACGGGATAA GTTCAGACCC ATGATTCTCT GGCTGCCTTG GAAAATAAGG CTTCCTTTGT 1140 GGGCACCCAT CCCAGCTTCT GCCTCCTGCC ACAGGGCTGA CTTCTGACAC ACAGGCCTTC 1200 TGTAAATACT CTAACAGAGA AAAGCGGAAG TTGACAAAAA ACTGGCAGCA ACAAGCCCCA 1260 GCTTGGCATT TTGGGTAACT ATTCATAGGC ACTTGATTGA GGAGGAAGTA GAAAGGAAGA 1320 ACTGCAGTGA GATTTGCTCG GAACATCCCT GATCTATTAT TGTGCCTGTC GCTTTAGACT 1380 TTTTCTTACT TATTTATTTT ATTTATTTAT TTTTAAGACG GGGTCATTCA CTCTGTGGCC 1440 TGGGCTGGAG GACAATGGTA TGATCACAGC CCACTGCAGC CTCAAACTCC TGGGCTCAAC 1500 CAATCCTCCT GCTTCAGCCT CCCAAGTAGC TGGGATTATA GGCTATCACT TTAGACTTTG 1560 AGGGGAAGAT GTAAGGACAG TAGAGGGGAA GAAGACAGAC ACTCCAGAGA AGGTTACACA 1620 CGAGGAGAAG TTAATCCCTA AAAGCAGGCC CAAGCCCTCG CCCCTCCTTT CCCCTGCCCT 1680 CCTGCCCTCA AAGCAAGGGC TTTGGGAGAG GGCTTGGCTG CCCTGATTTT CCCCTATACC 1740 TTGTGTCCAC TGAAGTAGGG AGATAGTAAC TGTGCTGCCC TCCTTCTCCT CCCAGGGGTG 1800 GATTGTGCCT CCAAACATCT GCCACTGGGC TGAGTGAGCC TTGGTAGGGA GCTGAGACCA 1860 CCGTCCTTCA GCGTCAGCAA ACTCATATCA TGTCAGCTAG CCACTCGAAT GGTGCAAGAT 1920 GCCAAACTGG TTATTCCCTG AGCAGTTCAG TCACAGTAAG GTGACTCTAA ATGGACGGTC 1980 TGCACATTTT TCATCTTGTC TGTAATGACT TTTATTGCTC AATTGTTCTT TTTTATTTTT 2040 TTATTTTTTA TTTTATTTAT TTATTTATTT ATTTATAATT TTATTTATTT ATTTATTTAT 2100 TTTGAGGCAG GGTGTCACCG TATCGCCCAG GCTGGAGTGC AGTGGTGTGA TCTAGGCTCA 2160 CTGTAACCTC CGCCTCCTAG GTTTAAGCAA TCCTCCCACC TCAGCCTCCC AAGTAGTTGG 2220 GACTACAGTC 2230
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