Tag | Content |
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EnhancerAtlas ID | HS187-13403 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:70321070-70323850 |
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 | TCACTAACAG GAGATAATAA GGAACCAATA GTAAGCTGAA CGTTAAAGAT ACAGGTAAGA 60 GAAGACTATG GCTCTAGCCA TAGTCTGTTG GACTGCTGGA ATTTAACTCT GTCCCCTCTT 120 CCATAGGGAC TTGCATCTCA GAATTCCTCT CCTTTGTCCT TTCTCTTTGG GGCAGCTTGA 180 GCATGTCCTG TCCTCTTCTG GATGGAGGAC TGGAAATTGA TGAGGCCCCT ATGCAGTTGC 240 TGATTCTTGT CACTGCCCTG TTCCTGCCTC CAGCTGTTAG GCCATAGCCA CTGCCATAGT 300 TGGGAAGAGC TGGAACAGGT TGACAAACAC CTGTTGTGTC ATAGCCATAG TATTTGTATC 360 ATGTGTTTAG AAGGCTGGTC TCCCCCGGTC CCCAATCCCC TCCCTTGCCC CACTCAAATA 420 TAGACACACA CACATGCACA CACGTACATG ACCACCACGA GCTCTCCTCC AGCCAGTAGT 480 TTGGACAGTG AATCACCACT CTTGGGTTCA CCCCTAGAGC AGCTACTTAC TCCCTGTGAC 540 CTGAAAAGTA AGCAGTATTT ACCAAGAGCT TCAGGTTTGT GAGTTGAACC CACCTCACCC 600 CTTGCTACTC TTGGCTACCC CAAGTGGTGA ACCACATACT GTCCAGCATC CCTGGGCCTG 660 CCACCTCCTG CCAGTGAGAC AGCGCCCAGT CAGACATACA AATAGGCAGT CACAGCAAGA 720 GAAGCCTTCC ACTACCAAGT CCTCTGCTCA CCTCACCTAG CCTGGCCACC TGAGGGGCCT 780 TCCTAAAATT CAGATCTAAA CACATGTGTC CCCCGATCAA AGGCCTTCAA GTCCCACCTC 840 ACCCCCATGG TCTATGAAAG AAAACCCAAA CTGTTCAGCA CAGTTTTCCA GGCCCTTGAA 900 CATCTGTTCC CCACCAGCCT CACCAGTGCA AGGCCTAACA AGTCTCCTGC CACTACCTTC 960 AGCCTTCCAT ACAAAATAAC TGGCAGTCCC CCCAAAGTCA TTCTGTGTGG GCATCCTTGC 1020 CTGTGGGACA TCATTGTTTC TTCACTCTTC TGATCCTGGC TGTGCTCTTC TTCCTTACCT 1080 CCCTGGGGTT CTGGGGTTCC TGTTCTTTGA GCATCAACAT TCTGCAAGGA AAATCACACT 1140 GTGCTGAGAA TTGGGAGACC TGAGTTCTAG TCCTGGCTCT GGCATCAGCT CACTGGGAGA 1200 GCTTGGACAA ATTCCTCCCT CTTTCTGGGT CTTAGTCCTC CATCTGAGAA GACGGGATAA 1260 GTTCAGACCC ATGATTCTCT GGCTGCCTTG GAAAATAAGG CTTCCTTTGT GGGCACCCAT 1320 CCCAGCTTCT GCCTCCTGCC ACAGGGCTGA CTTCTGACAC ACAGGCCTTC TGTAAATACT 1380 CTAACAGAGA AAAGCGGAAG TTGACAAAAA ACTGGCAGCA ACAAGCCCCA GCTTGGCATT 1440 TTGGGTAACT ATTCATAGGC ACTTGATTGA GGAGGAAGTA GAAAGGAAGA ACTGCAGTGA 1500 GATTTGCTCG GAACATCCCT GATCTATTAT TGTGCCTGTC GCTTTAGACT TTTTCTTACT 1560 TATTTATTTT ATTTATTTAT TTTTAAGACG GGGTCATTCA CTCTGTGGCC TGGGCTGGAG 1620 GACAATGGTA TGATCACAGC CCACTGCAGC CTCAAACTCC TGGGCTCAAC CAATCCTCCT 1680 GCTTCAGCCT CCCAAGTAGC TGGGATTATA GGCTATCACT TTAGACTTTG AGGGGAAGAT 1740 GTAAGGACAG TAGAGGGGAA GAAGACAGAC ACTCCAGAGA AGGTTACACA CGAGGAGAAG 1800 TTAATCCCTA AAAGCAGGCC CAAGCCCTCG CCCCTCCTTT CCCCTGCCCT CCTGCCCTCA 1860 AAGCAAGGGC TTTGGGAGAG GGCTTGGCTG CCCTGATTTT CCCCTATACC TTGTGTCCAC 1920 TGAAGTAGGG AGATAGTAAC TGTGCTGCCC TCCTTCTCCT CCCAGGGGTG GATTGTGCCT 1980 CCAAACATCT GCCACTGGGC TGAGTGAGCC TTGGTAGGGA GCTGAGACCA CCGTCCTTCA 2040 GCGTCAGCAA ACTCATATCA TGTCAGCTAG CCACTCGAAT GGTGCAAGAT GCCAAACTGG 2100 TTATTCCCTG AGCAGTTCAG TCACAGTAAG GTGACTCTAA ATGGACGGTC TGCACATTTT 2160 TCATCTTGTC TGTAATGACT TTTATTGCTC AATTGTTCTT TTTTATTTTT TTATTTTTTA 2220 TTTTATTTAT TTATTTATTT ATTTATAATT TTATTTATTT ATTTATTTAT TTTGAGGCAG 2280 GGTGTCACCG TATCGCCCAG GCTGGAGTGC AGTGGTGTGA TCTAGGCTCA CTGTAACCTC 2340 CGCCTCCTAG GTTTAAGCAA TCCTCCCACC TCAGCCTCCC AAGTAGTTGG GACTACAGTC 2400 ATAAGGCACC ACACTGGCTA TTTTTTTGTA TTTTTAGTAG AGACAGGGTT TTACCGTGTT 2460 GCCCAGGGTG GTCTCGAACT CCTCCAAGCG ATCCACCTGC CTCAGCCTCC CAAAGTGCTA 2520 GGATTACAGG TGTAAGCCGG CGTGCCCAGC CTGCCCAATT TTTCAGTCAA GAAAACATAC 2580 ATGAAGCCTG GCACGGTGGC TCACACCTAT ACTCCCAACA CTTTGGAAGG CCAAGGCAGG 2640 AGGATCAGTT GAGGCCAGGA GTTCGAGACC AGTCTGGGCA ACATAGTGAA ACCTTGTCTC 2700 TATTATGTTT AAAAAAAATA AAAATGTAAA GGCCAGGAAC GGTGGTTTAT GCCTGTAATC 2760 CCAGCACTTT GGGAGGCCAA 2780
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