Tag | Content |
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EnhancerAtlas ID | HS051-15493 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:70320940-70323310 |
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: 2 | Chromosome | Start | End |
chr2 | 70320974 | 70321737 | chr2 | 70322001 | 70322909 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I070093 | chr2 | 70320605 | 70324187 |
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Enhancer Sequence | GCGCCACTGC AGTCCGGCCT GGGCAAAAGA GCGAGACTCC GTCTCAAAAA AAAAAAAAAA 60 AAATTAAGTC AAAAAGTTGA GCAGTTGAGC GGGAAAATAT TGTTTTGTTT TATTGTTTTT 120 GAAAGGAACC TCACTAACAG GAGATAATAA GGAACCAATA GTAAGCTGAA CGTTAAAGAT 180 ACAGGTAAGA GAAGACTATG GCTCTAGCCA TAGTCTGTTG GACTGCTGGA ATTTAACTCT 240 GTCCCCTCTT CCATAGGGAC TTGCATCTCA GAATTCCTCT CCTTTGTCCT TTCTCTTTGG 300 GGCAGCTTGA GCATGTCCTG TCCTCTTCTG GATGGAGGAC TGGAAATTGA TGAGGCCCCT 360 ATGCAGTTGC TGATTCTTGT CACTGCCCTG TTCCTGCCTC CAGCTGTTAG GCCATAGCCA 420 CTGCCATAGT TGGGAAGAGC TGGAACAGGT TGACAAACAC CTGTTGTGTC ATAGCCATAG 480 TATTTGTATC ATGTGTTTAG AAGGCTGGTC TCCCCCGGTC CCCAATCCCC TCCCTTGCCC 540 CACTCAAATA TAGACACACA CACATGCACA CACGTACATG ACCACCACGA GCTCTCCTCC 600 AGCCAGTAGT TTGGACAGTG AATCACCACT CTTGGGTTCA CCCCTAGAGC AGCTACTTAC 660 TCCCTGTGAC CTGAAAAGTA AGCAGTATTT ACCAAGAGCT TCAGGTTTGT GAGTTGAACC 720 CACCTCACCC CTTGCTACTC TTGGCTACCC CAAGTGGTGA ACCACATACT GTCCAGCATC 780 CCTGGGCCTG CCACCTCCTG CCAGTGAGAC AGCGCCCAGT CAGACATACA AATAGGCAGT 840 CACAGCAAGA GAAGCCTTCC ACTACCAAGT CCTCTGCTCA CCTCACCTAG CCTGGCCACC 900 TGAGGGGCCT TCCTAAAATT CAGATCTAAA CACATGTGTC CCCCGATCAA AGGCCTTCAA 960 GTCCCACCTC ACCCCCATGG TCTATGAAAG AAAACCCAAA CTGTTCAGCA CAGTTTTCCA 1020 GGCCCTTGAA CATCTGTTCC CCACCAGCCT CACCAGTGCA AGGCCTAACA AGTCTCCTGC 1080 CACTACCTTC AGCCTTCCAT ACAAAATAAC TGGCAGTCCC CCCAAAGTCA TTCTGTGTGG 1140 GCATCCTTGC CTGTGGGACA TCATTGTTTC TTCACTCTTC TGATCCTGGC TGTGCTCTTC 1200 TTCCTTACCT CCCTGGGGTT CTGGGGTTCC TGTTCTTTGA GCATCAACAT TCTGCAAGGA 1260 AAATCACACT GTGCTGAGAA TTGGGAGACC TGAGTTCTAG TCCTGGCTCT GGCATCAGCT 1320 CACTGGGAGA GCTTGGACAA ATTCCTCCCT CTTTCTGGGT CTTAGTCCTC CATCTGAGAA 1380 GACGGGATAA GTTCAGACCC ATGATTCTCT GGCTGCCTTG GAAAATAAGG CTTCCTTTGT 1440 GGGCACCCAT CCCAGCTTCT GCCTCCTGCC ACAGGGCTGA CTTCTGACAC ACAGGCCTTC 1500 TGTAAATACT CTAACAGAGA AAAGCGGAAG TTGACAAAAA ACTGGCAGCA ACAAGCCCCA 1560 GCTTGGCATT TTGGGTAACT ATTCATAGGC ACTTGATTGA GGAGGAAGTA GAAAGGAAGA 1620 ACTGCAGTGA GATTTGCTCG GAACATCCCT GATCTATTAT TGTGCCTGTC GCTTTAGACT 1680 TTTTCTTACT TATTTATTTT ATTTATTTAT TTTTAAGACG GGGTCATTCA CTCTGTGGCC 1740 TGGGCTGGAG GACAATGGTA TGATCACAGC CCACTGCAGC CTCAAACTCC TGGGCTCAAC 1800 CAATCCTCCT GCTTCAGCCT CCCAAGTAGC TGGGATTATA GGCTATCACT TTAGACTTTG 1860 AGGGGAAGAT GTAAGGACAG TAGAGGGGAA GAAGACAGAC ACTCCAGAGA AGGTTACACA 1920 CGAGGAGAAG TTAATCCCTA AAAGCAGGCC CAAGCCCTCG CCCCTCCTTT CCCCTGCCCT 1980 CCTGCCCTCA AAGCAAGGGC TTTGGGAGAG GGCTTGGCTG CCCTGATTTT CCCCTATACC 2040 TTGTGTCCAC TGAAGTAGGG AGATAGTAAC TGTGCTGCCC TCCTTCTCCT CCCAGGGGTG 2100 GATTGTGCCT CCAAACATCT GCCACTGGGC TGAGTGAGCC TTGGTAGGGA GCTGAGACCA 2160 CCGTCCTTCA GCGTCAGCAA ACTCATATCA TGTCAGCTAG CCACTCGAAT GGTGCAAGAT 2220 GCCAAACTGG TTATTCCCTG AGCAGTTCAG TCACAGTAAG GTGACTCTAA ATGGACGGTC 2280 TGCACATTTT TCATCTTGTC TGTAATGACT TTTATTGCTC AATTGTTCTT TTTTATTTTT 2340 TTATTTTTTA TTTTATTTAT TTATTTATTT 2370
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