Tag | Content |
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EnhancerAtlas ID | HS020-24609 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr2:70321030-70323960 |
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 | GGGAAAATAT TGTTTTGTTT TATTGTTTTT GAAAGGAACC TCACTAACAG GAGATAATAA 60 GGAACCAATA GTAAGCTGAA CGTTAAAGAT ACAGGTAAGA GAAGACTATG GCTCTAGCCA 120 TAGTCTGTTG GACTGCTGGA ATTTAACTCT GTCCCCTCTT CCATAGGGAC TTGCATCTCA 180 GAATTCCTCT CCTTTGTCCT TTCTCTTTGG GGCAGCTTGA GCATGTCCTG TCCTCTTCTG 240 GATGGAGGAC TGGAAATTGA TGAGGCCCCT ATGCAGTTGC TGATTCTTGT CACTGCCCTG 300 TTCCTGCCTC CAGCTGTTAG GCCATAGCCA CTGCCATAGT TGGGAAGAGC TGGAACAGGT 360 TGACAAACAC CTGTTGTGTC ATAGCCATAG TATTTGTATC ATGTGTTTAG AAGGCTGGTC 420 TCCCCCGGTC CCCAATCCCC TCCCTTGCCC CACTCAAATA TAGACACACA CACATGCACA 480 CACGTACATG ACCACCACGA GCTCTCCTCC AGCCAGTAGT TTGGACAGTG AATCACCACT 540 CTTGGGTTCA CCCCTAGAGC AGCTACTTAC TCCCTGTGAC CTGAAAAGTA AGCAGTATTT 600 ACCAAGAGCT TCAGGTTTGT GAGTTGAACC CACCTCACCC CTTGCTACTC TTGGCTACCC 660 CAAGTGGTGA ACCACATACT GTCCAGCATC CCTGGGCCTG CCACCTCCTG CCAGTGAGAC 720 AGCGCCCAGT CAGACATACA AATAGGCAGT CACAGCAAGA GAAGCCTTCC ACTACCAAGT 780 CCTCTGCTCA CCTCACCTAG CCTGGCCACC TGAGGGGCCT TCCTAAAATT CAGATCTAAA 840 CACATGTGTC CCCCGATCAA AGGCCTTCAA GTCCCACCTC ACCCCCATGG TCTATGAAAG 900 AAAACCCAAA CTGTTCAGCA CAGTTTTCCA GGCCCTTGAA CATCTGTTCC CCACCAGCCT 960 CACCAGTGCA AGGCCTAACA AGTCTCCTGC CACTACCTTC AGCCTTCCAT ACAAAATAAC 1020 TGGCAGTCCC CCCAAAGTCA TTCTGTGTGG GCATCCTTGC CTGTGGGACA TCATTGTTTC 1080 TTCACTCTTC TGATCCTGGC TGTGCTCTTC TTCCTTACCT CCCTGGGGTT CTGGGGTTCC 1140 TGTTCTTTGA GCATCAACAT TCTGCAAGGA AAATCACACT GTGCTGAGAA TTGGGAGACC 1200 TGAGTTCTAG TCCTGGCTCT GGCATCAGCT CACTGGGAGA GCTTGGACAA ATTCCTCCCT 1260 CTTTCTGGGT CTTAGTCCTC CATCTGAGAA GACGGGATAA GTTCAGACCC ATGATTCTCT 1320 GGCTGCCTTG GAAAATAAGG CTTCCTTTGT GGGCACCCAT CCCAGCTTCT GCCTCCTGCC 1380 ACAGGGCTGA CTTCTGACAC ACAGGCCTTC TGTAAATACT CTAACAGAGA AAAGCGGAAG 1440 TTGACAAAAA ACTGGCAGCA ACAAGCCCCA GCTTGGCATT TTGGGTAACT ATTCATAGGC 1500 ACTTGATTGA GGAGGAAGTA GAAAGGAAGA ACTGCAGTGA GATTTGCTCG GAACATCCCT 1560 GATCTATTAT TGTGCCTGTC GCTTTAGACT TTTTCTTACT TATTTATTTT ATTTATTTAT 1620 TTTTAAGACG GGGTCATTCA CTCTGTGGCC TGGGCTGGAG GACAATGGTA TGATCACAGC 1680 CCACTGCAGC CTCAAACTCC TGGGCTCAAC CAATCCTCCT GCTTCAGCCT CCCAAGTAGC 1740 TGGGATTATA GGCTATCACT TTAGACTTTG AGGGGAAGAT GTAAGGACAG TAGAGGGGAA 1800 GAAGACAGAC ACTCCAGAGA AGGTTACACA CGAGGAGAAG TTAATCCCTA AAAGCAGGCC 1860 CAAGCCCTCG CCCCTCCTTT CCCCTGCCCT CCTGCCCTCA AAGCAAGGGC TTTGGGAGAG 1920 GGCTTGGCTG CCCTGATTTT CCCCTATACC TTGTGTCCAC TGAAGTAGGG AGATAGTAAC 1980 TGTGCTGCCC TCCTTCTCCT CCCAGGGGTG GATTGTGCCT CCAAACATCT GCCACTGGGC 2040 TGAGTGAGCC TTGGTAGGGA GCTGAGACCA CCGTCCTTCA GCGTCAGCAA ACTCATATCA 2100 TGTCAGCTAG CCACTCGAAT GGTGCAAGAT GCCAAACTGG TTATTCCCTG AGCAGTTCAG 2160 TCACAGTAAG GTGACTCTAA ATGGACGGTC TGCACATTTT TCATCTTGTC TGTAATGACT 2220 TTTATTGCTC AATTGTTCTT TTTTATTTTT TTATTTTTTA TTTTATTTAT TTATTTATTT 2280 ATTTATAATT TTATTTATTT ATTTATTTAT TTTGAGGCAG GGTGTCACCG TATCGCCCAG 2340 GCTGGAGTGC AGTGGTGTGA TCTAGGCTCA CTGTAACCTC CGCCTCCTAG GTTTAAGCAA 2400 TCCTCCCACC TCAGCCTCCC AAGTAGTTGG GACTACAGTC ATAAGGCACC ACACTGGCTA 2460 TTTTTTTGTA TTTTTAGTAG AGACAGGGTT TTACCGTGTT GCCCAGGGTG GTCTCGAACT 2520 CCTCCAAGCG ATCCACCTGC CTCAGCCTCC CAAAGTGCTA GGATTACAGG TGTAAGCCGG 2580 CGTGCCCAGC CTGCCCAATT TTTCAGTCAA GAAAACATAC ATGAAGCCTG GCACGGTGGC 2640 TCACACCTAT ACTCCCAACA CTTTGGAAGG CCAAGGCAGG AGGATCAGTT GAGGCCAGGA 2700 GTTCGAGACC AGTCTGGGCA ACATAGTGAA ACCTTGTCTC TATTATGTTT AAAAAAAATA 2760 AAAATGTAAA GGCCAGGAAC GGTGGTTTAT GCCTGTAATC CCAGCACTTT GGGAGGCCAA 2820 GGCGAGATGA TCAGTTGAGG CCACGAGTTC GAGACCAGTC TGGGCAACAT AGTGAGACCT 2880 CATCTCTATT ATATTAAAAA AAATAGGGAC CAGGCATGGT GGCTCATGCC 2930
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