Tag | Content |
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EnhancerAtlas ID | HS018-13083 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr2:145212300-145215260 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:145213316-145213337 | TCTCTCTTTCTCTTTCTCTCC | + | 6.28 | Pou2f3 | MA0627.1 | chr2:145213258-145213274 | TATAATTTGCATAGCA | - | 6.32 | Sox6 | MA0515.1 | chr2:145213678-145213688 | CCATTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr2:145213323-145213344 | TTCTCTTTCTCTCCCTCCCCA | - | 6.64 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_00013 | chr2:145208646-145220907 | Adipose_Nuclei | SE_03135 | chr2:145208774-145218083 | Brain_Angular_Gyrus | SE_03858 | chr2:145208840-145232427 | Brain_Anterior_Caudate | SE_04763 | chr2:145177825-145243674 | Brain_Cingulate_Gyrus | SE_05778 | chr2:145209021-145234668 | Brain_Hippocampus_Middle | SE_06674 | chr2:145177449-145244019 | Brain_Hippocampus_Middle_150 | SE_07715 | chr2:145204565-145243004 | Brain_Inferior_Temporal_Lobe | SE_08781 | chr2:145212225-145212954 | Brain_Mid_Frontal_Lobe | SE_09144 | chr2:145176556-145221318 | CD14 | SE_11384 | chr2:145208702-145218754 | CD20 | SE_13334 | chr2:145212348-145213153 | CD34_Primary_RO01536 | SE_13334 | chr2:145214186-145214916 | CD34_Primary_RO01536 | SE_20010 | chr2:145209183-145221155 | CD56 | SE_22321 | chr2:145209170-145241141 | CD8_primiary | SE_26195 | chr2:145208502-145218704 | Duodenum_Smooth_Muscle | SE_37250 | chr2:145209337-145212670 | HSMMtube | SE_37250 | chr2:145213365-145215328 | HSMMtube | SE_45982 | chr2:145209246-145221181 | Osteoblasts | SE_53346 | chr2:145211995-145213210 | Spleen | SE_53346 | chr2:145214108-145215274 | Spleen | SE_58795 | chr2:145182294-145230606 | Ly1 | SE_64101 | chr2:145211685-145213287 | HSMM | SE_64101 | chr2:145213483-145214875 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 145213443 | 145214567 | chr2 | 145214152 | 145214623 |
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Enhancer Sequence | TATTCTAAAA GCTTCAACCC TGCTCAGAAT GTAGGGATTT TGTTTGAACC CAGGATTTTC 60 AAAGTTGGGA GAGAATCCAT GAAATGATCC CTCGTTCCTG TAAATGTACA CACATGGGTG 120 TGCCTGCCTA CACCATCAGA GCATCACACA CACACACCCT GCACACACAT CACCACACAC 180 ACCCTCTATG CTAAATCTGC CTTCAATTAA CCAAAAGCAC AATTTTGCCC TGACAGAGAA 240 GATTTCATTT GGTCCACATA TGACTAGGGA GCCGATTTCA TTTCCTGTAA AAAACCCCCT 300 CAAACGCTGC AAAGTTACCT GACTCAGCTG CTTGTAGAAA TCAAATTCAG TCAGAGATAA 360 CAGCTAATCA TTTGTCACAG TAAGAAGCAA TTCCCTGAAA TCGGAAGGGA AAACCTGCCG 420 CTTCAATCCG CAGGTCTGTC AGATTGCTAG AAATTACATT CTGCTCTGAC TAACCTCTGC 480 ACTTGGATTG CTAACAACAA GCAGCCTGCT CTATCAAAAG AGAATATCAT ACAACCAGGA 540 ACCGCTTTTG ATTCGTTCTG TTCCAATAAC CTGAGAAAAG TTTATGGACA TGCCTTGCTG 600 CCTGGACCTC AATTTCCACC AACCTGCACA CTGTTTTGAA TTTATAGCAC TGCAGCTCCA 660 TAGTAATGTA GGTAAAATTT ACAAGCTGAC TATCTGCTAC TTCATTGAAA GAAAATTAAG 720 AGTTGATTTT ATAACCACAC GACTGATATT TGCCTTCTGA TACTTTGAGG AAGCATACGG 780 TTTGGAAGCT TCAATTAAAA TGCCAAAAGA GAAAAAACAA ATTGATTAAC TCTCAAAATA 840 CAATTTATAT TTTTTAGAAA TGCTTCCCGG GAGGGAATTA ACTTTATACT CTTCTATGTA 900 AACACTATTT GTGCAGCATA AGTTTAATAA AAATGATACA TCACCTCTCT GTTAGGTTTA 960 TAATTTGCAT AGCAATAGTG AATATGGAAT TTTGGTCAAA ATGTTTCTCT CGTCTCTCTC 1020 TCTTTCTCTT TCTCTCCCTC CCCACATCTC TCCTGCAATA GTACAGGATC GTTGGAAATG 1080 GGTAAGTTTA ATATCTTTCC TAATCCCAAG AAGCCATTAT TATTACTTAA AGTATATCTC 1140 AAGGTAGGTT ATTAACCCCC AAGAAGTTAC AGCTTTGAGT TAGAATCACA TAATCTTAAA 1200 AAAGGACAAC ATATTTTCCA AGCAGTACTT AACCAAATAC TCTTCTTTAA CTCTGACTAG 1260 ATTTATGATG AATACAGATA TTGCAACTCT TATAAGAACT TAAAGATGGC GAACTCAGAG 1320 ATTCAGCATT TAAGAAGGCT GCCTCTAAGA CTAAGACTAA ATCCATCCCA AGTTTGTTCC 1380 ATTGTTTTTT TTTTTTAAAG CATTTTATTT TCCACAGTTG GAATCAGCTG AGGATACAGT 1440 GTGAGCAGTG ACTCTGAATT TCCTTTGCTT TTGTCAAACT GTGTCACAAC CATAAAGTTA 1500 TTTTAACTGA GTTTATTTGC CTAGGCATTT CCTTTCTCTT GTAGTAGTGT AAGAGAAAGG 1560 AAAACAACCA TTTAAAATGT AAGTACAGTT GAGTGGATAT AAGGGACTCT TCCAGCTCCT 1620 ATCGTAAGCA GACAATTCGA TGATAAGTAT GTGGGCTTTT TAAGCTTTAA AAAATATTCA 1680 TAAATCCCTT TTTGGATTCT TTCATTTCAA TTTTCTTCAA GCAATGAGAA TTAGACAAGT 1740 TTATAAATTC TCATTTCTAC CTTTCTTGGG CCAGTCCTGA TTACTCTTAT CATGGTTAAT 1800 ACTGGTTCAC ATGGGGGACT TCCACAAATT CTTTAATATA CTGTGTATCT GGTGTAAAAA 1860 AAATTATGTA AAATACAATA ATTGATGCTA TTAATGTATT TGGTGAGATA ATCTAATAGA 1920 TTTCCTTGAA GTAACTCTAA TAAATTTTTC TTCCTTAGTA AAAACAACCC CTTGGTCTTA 1980 GATTCTGCTC TTGTACAGTC ATCCGTACAG TGGCCAGGGC TTAAGCTCTG GTACTGTATG 2040 AGTATGCAAA CAAGCAGATT TCACAATCAG ATGACACTGA GACTTAGGCT TACTGTGCCA 2100 GACTCTCTTT GGTGACTGTT CTCTCATCTT GGGCCAGCCT AGGGATCTGA GAACCTGCTG 2160 TAGTTAGAAA GAAGTCACCT GACCTCGAAG TTTCCCTCCT GTCTTTTCTC AATCGTTCCA 2220 GCTCTCACAC TCAAGAGTCA GAGCTCTCCA CCACTGTCCT GGCCAGAGCA GCACCCCCCA 2280 AAGGTCTGCA TGTACCTCTG GCAAGATAAA TGCATATAGA AGACAATGCA TTTTTAGTCC 2340 CTATAGACTT TCTATAACGT CTACGTTTCC AGAATCTCAT GTGTGCCTTA AAAACCCTTT 2400 TCTTCTACAT TTAAAAGGAC AGTTTGATTA TATAATAATA CCTGGATTTA TGCATTAATC 2460 CACTGACAGC AGAGCCCGTT AATAGACATT TTTCCACTTG CTCCTCATAA CAAACCTTTG 2520 AAGGGGGGAG CAATTATTAT GAGGATGATT TTATAGATGA GTAAATTGAA TCTCAGAAAT 2580 TTTAACTGAC TTTTTCCCAC ATCACCTCGT GTTAGAATCT GGATCTGATT CCTGACTCCA 2640 GAAACTATTT GTCTCTAGAT TCTATCTGTG CTCTCTTCAT CACCTTGGGT GTACAAATCT 2700 AAGTGAGCAA ACAAAAGCCA AAATAGGATT TTTAACTATT TAACAGAGTA TGGTGGTGTC 2760 AGTATGAAAT CTTGTTCATC TGGTTTAGTG GACATAACTG TGCCTGGGCA GAAGAGAGAA 2820 GGAGGAGAGA AGAACAAAGG CAAGGTCAAG AGCAACTACA CTGAAATTGG GAGAAAAAGC 2880 AAGTTAGATA TAAGGAAGAG GACCTGGTAT GTAACAGGTA TTAATGGGAT CAGTGACATC 2940 CATCATTTGT GAATGGAACA 2960
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