Tag | Content |
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EnhancerAtlas ID | HS154-12443 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr2:70321180-70323180 |
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 | GTCCCCTCTT CCATAGGGAC TTGCATCTCA GAATTCCTCT CCTTTGTCCT TTCTCTTTGG 60 GGCAGCTTGA GCATGTCCTG TCCTCTTCTG GATGGAGGAC TGGAAATTGA TGAGGCCCCT 120 ATGCAGTTGC TGATTCTTGT CACTGCCCTG TTCCTGCCTC CAGCTGTTAG GCCATAGCCA 180 CTGCCATAGT TGGGAAGAGC TGGAACAGGT TGACAAACAC CTGTTGTGTC ATAGCCATAG 240 TATTTGTATC ATGTGTTTAG AAGGCTGGTC TCCCCCGGTC CCCAATCCCC TCCCTTGCCC 300 CACTCAAATA TAGACACACA CACATGCACA CACGTACATG ACCACCACGA GCTCTCCTCC 360 AGCCAGTAGT TTGGACAGTG AATCACCACT CTTGGGTTCA CCCCTAGAGC AGCTACTTAC 420 TCCCTGTGAC CTGAAAAGTA AGCAGTATTT ACCAAGAGCT TCAGGTTTGT GAGTTGAACC 480 CACCTCACCC CTTGCTACTC TTGGCTACCC CAAGTGGTGA ACCACATACT GTCCAGCATC 540 CCTGGGCCTG CCACCTCCTG CCAGTGAGAC AGCGCCCAGT CAGACATACA AATAGGCAGT 600 CACAGCAAGA GAAGCCTTCC ACTACCAAGT CCTCTGCTCA CCTCACCTAG CCTGGCCACC 660 TGAGGGGCCT TCCTAAAATT CAGATCTAAA CACATGTGTC CCCCGATCAA AGGCCTTCAA 720 GTCCCACCTC ACCCCCATGG TCTATGAAAG AAAACCCAAA CTGTTCAGCA CAGTTTTCCA 780 GGCCCTTGAA CATCTGTTCC CCACCAGCCT CACCAGTGCA AGGCCTAACA AGTCTCCTGC 840 CACTACCTTC AGCCTTCCAT ACAAAATAAC TGGCAGTCCC CCCAAAGTCA TTCTGTGTGG 900 GCATCCTTGC CTGTGGGACA TCATTGTTTC TTCACTCTTC TGATCCTGGC TGTGCTCTTC 960 TTCCTTACCT CCCTGGGGTT CTGGGGTTCC TGTTCTTTGA GCATCAACAT TCTGCAAGGA 1020 AAATCACACT GTGCTGAGAA TTGGGAGACC TGAGTTCTAG TCCTGGCTCT GGCATCAGCT 1080 CACTGGGAGA GCTTGGACAA ATTCCTCCCT CTTTCTGGGT CTTAGTCCTC CATCTGAGAA 1140 GACGGGATAA GTTCAGACCC ATGATTCTCT GGCTGCCTTG GAAAATAAGG CTTCCTTTGT 1200 GGGCACCCAT CCCAGCTTCT GCCTCCTGCC ACAGGGCTGA CTTCTGACAC ACAGGCCTTC 1260 TGTAAATACT CTAACAGAGA AAAGCGGAAG TTGACAAAAA ACTGGCAGCA ACAAGCCCCA 1320 GCTTGGCATT TTGGGTAACT ATTCATAGGC ACTTGATTGA GGAGGAAGTA GAAAGGAAGA 1380 ACTGCAGTGA GATTTGCTCG GAACATCCCT GATCTATTAT TGTGCCTGTC GCTTTAGACT 1440 TTTTCTTACT TATTTATTTT ATTTATTTAT TTTTAAGACG GGGTCATTCA CTCTGTGGCC 1500 TGGGCTGGAG GACAATGGTA TGATCACAGC CCACTGCAGC CTCAAACTCC TGGGCTCAAC 1560 CAATCCTCCT GCTTCAGCCT CCCAAGTAGC TGGGATTATA GGCTATCACT TTAGACTTTG 1620 AGGGGAAGAT GTAAGGACAG TAGAGGGGAA GAAGACAGAC ACTCCAGAGA AGGTTACACA 1680 CGAGGAGAAG TTAATCCCTA AAAGCAGGCC CAAGCCCTCG CCCCTCCTTT CCCCTGCCCT 1740 CCTGCCCTCA AAGCAAGGGC TTTGGGAGAG GGCTTGGCTG CCCTGATTTT CCCCTATACC 1800 TTGTGTCCAC TGAAGTAGGG AGATAGTAAC TGTGCTGCCC TCCTTCTCCT CCCAGGGGTG 1860 GATTGTGCCT CCAAACATCT GCCACTGGGC TGAGTGAGCC TTGGTAGGGA GCTGAGACCA 1920 CCGTCCTTCA GCGTCAGCAA ACTCATATCA TGTCAGCTAG CCACTCGAAT GGTGCAAGAT 1980 GCCAAACTGG TTATTCCCTG 2000
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