Tag | Content |
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EnhancerAtlas ID | HS034-27110 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr6:159273150-159276140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr6:159274110-159274130 | ACCCCATACACCCCACCACA | + | 6.14 | RREB1 | MA0073.1 | chr6:159275925-159275945 | TGGTAGGGGGTGGTGGGTGG | - | 7.57 | TCF3 | MA0522.2 | chr6:159273513-159273523 | AACACCTGCT | + | 6.02 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_10307 | chr6:159273179-159276502 | CD19_Primary | SE_11101 | chr6:159269935-159278161 | CD20 | SE_12189 | chr6:159273267-159276491 | CD3 | SE_14386 | chr6:159269967-159276559 | CD4_Memory_Primary_7pool | SE_16462 | chr6:159273351-159276594 | CD4_Naive_Primary_8pool | SE_17999 | chr6:159269964-159278117 | CD4p_CD25-_CD45ROp_Memory | SE_18987 | chr6:159273136-159277721 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20282 | chr6:159273082-159276574 | CD56 | SE_20897 | chr6:159272786-159276642 | CD8_Memory_7pool | SE_21904 | chr6:159273108-159276540 | CD8_Naive_7pool | SE_22378 | chr6:159270210-159277819 | CD8_primiary | SE_23109 | chr6:159273079-159276256 | Colon_Crypt_1 | SE_23789 | chr6:159273267-159275641 | Colon_Crypt_2 | SE_23789 | chr6:159275700-159276183 | Colon_Crypt_2 | SE_25058 | chr6:159273048-159276283 | Colon_Crypt_3 | SE_27140 | chr6:159273240-159276220 | Esophagus | SE_27853 | chr6:159268889-159276361 | Fetal_Intestine | SE_28795 | chr6:159268853-159276331 | Fetal_Intestine_Large | SE_34137 | chr6:159273141-159276469 | HCC1954 | SE_34397 | chr6:159270023-159277893 | HCT-116 | SE_34769 | chr6:159269432-159276667 | HeLa | SE_35994 | chr6:159268630-159276489 | HMEC | SE_40070 | chr6:159273143-159276574 | K562 | SE_51056 | chr6:159273219-159276293 | Sigmoid_Colon | SE_52705 | chr6:159273298-159276322 | Small_Intestine | SE_58403 | chr6:159210147-159292283 | Ly1 | SE_63169 | chr6:159270185-159292330 | Tonsil | SE_64395 | chr6:159270254-159276320 | NHEK | SE_69169 | chr6:159273396-159276424 | H9 |
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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 |
GH06I158847 | chr6 | 159268541 | 159279766 |
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Enhancer Sequence | AAGAAGTGTC ATGGAGGTCT TTTATTTTCA ACAATATAGA AACATTTTTG GATGAACTTT 60 GTCTCTCAGG TTTTGGAGAA TTAAAATGCC TCCCTTATCC CATCCCTGCC ACACTCTAGG 120 ACATTGATTC ATGTTCCCAA AGAATAATGG TTAGCTTACT GTATGCCAGC TACTATTCTT 180 AGCTCCTTAC ATGAACTAAT CCTTTTAATC CTCACAACTA CACTATGAAG CGGATGCTAC 240 TATTGTCCAC TTTATGGGGG AAGAAACTGA GGCACAGAGA GGTTAGCTTG CCTCGGGACT 300 CTGTCTCTGC TGAGATTGGA AGCAGAAGAC TAGTTCCAGA ATTCACACTC CTAACCCTAC 360 TACAACACCT GCTCTCAAAC AGAGAAGGGA AAGGAAGTCC TGGCGTTTGC ACTCTCCTTG 420 ATCTTGTGCT GGTCTGGTCT GGACATGGAC CAAGGCTTGG GGGCCTTGCA CACGTAAGTG 480 AGTGCAGATG CCCGGCCCAG CCCCAGGGCT CCCTTGTCCT TGAGCTGGGG CCACGCTGAG 540 GCTGAGGCTG GCCTCCATGG CTTGACTTGA GGCCACCTCC AGATCCACAC CCTGAAAGCT 600 TGGGACTGGC CTTCTCAGAG AATGGGGCAA AACACTCTGA CGCCAACTAC AACCATCACA 660 AGGAGGTACA TTCTCTGTAA GGGCAAGCCT GGGGCTGCAC CCAAGTAGAC TAGCAGACAC 720 TCATTACAGA GAGAATGTTC TGGCACTCTG GCCCTGCCAA AGGCTACCAG AACACAGAAG 780 GCCCTTTCTT CCAAGGGGCC GAAGGAGGAG CAGGCACACA CCATATGCCT CACTCACCAC 840 ACGAAACCAC ACACCACATA GCACACACGC GTGCACCCTC ATACCACACT GACCCTTCAC 900 CACACACACA CCCATACACC TTCATGTCAC ACATACCACA CACACAGATA TACCACATGC 960 ACCCCATACA CCCCACCACA CACATACAAA CACCACACCA TATACACACA CACACAGTAC 1020 AACATACACA CTCACACACC ATATGCCACA CACATATACT TTACACATAT ACATACCTCC 1080 AAACACACAC CATGCACACA CACGGTACAC CATACACACA CCACACACTA TGCACACACC 1140 ATGTACCACA CACATACCCC TCCAACATCA CATGAACACT ACGCACCCTC CCCCATACCA 1200 CACACATACA CGCACACGTA CCATGCACGC ACACACACCA CAATGTGCTG TTACTTAACA 1260 GGTTTGCCTT CCCACAACTC TATCAGCAAA CCCTTCTGGA GGCGCAGCCC ACACCTGCAT 1320 TCCAAAGAAC GCAAATCCCT TCCCTGCCCG ATGAAAGGCC CCTCCCACAG TGAGTCACAG 1380 AAACTGCAGC CGAGCAGGCA GTGGTGGGCC CCACCCTTCT CACAGGAAGT GAGAAAGAGT 1440 AAATATGTAG TTTTTCTTTG AGGGCCAATG CACATGTTAA ATGGGTGATT AAGAAGACAG 1500 AGAGCTGCTT AAAAGGTCAT GGGAGAAGTA CAATGTCTGG GGACTTGGCA GTAGCCTGGC 1560 AGAGACCGCA GGAATCCTAT AGAGTCTTTT ATGGACAGGG CTCTGAAATT CCAGAGCCTG 1620 CAGGAGGTAC CTTCCCCTTT GACTCGGCGG GGCTGTACCA CTAAGAATGC ACTGAGCATT 1680 GGGTGCACTT GGGATACCTG AGCTGTGGGG CCAGAGAGGC AGCCCTAGGG GAGAATTCCG 1740 GAGTTGGGGC TGGGTTCTTT CAGCATAAAA AATCAAAGTG TCGCTTCTTT AATGAACCTC 1800 CCGGCAAGGT CTTCCCTGAA GACCTTGAAC AAGTGTTCTT AAACAAGTGT TCCTTTATGC 1860 AATTAAAGGC CAGGGAAGCT GGGGTCTGAG AGGCCATGGA GCCATTGGGA TAATAGTGAC 1920 AGTTCGGCTA CCATTCAACT GGGCTTCTGA TGAATCATGC TGGGGGCAAG GACTCCAAAT 1980 CACCAGCTCT ACTCTATACT CGAATCAGTA GGCAGTTCAG ACAGTCTTGG GGGATTTGGG 2040 CAAACGAACG CTCCACTTAG AATCTCTCCA GAAAGACAAA GGGGGTGCCT AACAAACAAT 2100 TCAAGGACTG TGGGAAACCA ATGATCATCA AGGGCTCAGT TGTACAGTGT AAACCAAAAA 2160 GTATCTGAGA CAGGTCTCAA TCAACTGAGA AGTTTATTTT GCCAAGGTTA AGGACAGGCC 2220 AGGGAGGAAG AAACACGGAA TCACAGAAAC AGTCTATGGT CTGTGTCGTT CTTCCAAGAT 2280 GATGTTGAGG GCCTCGATGT TTAAAAGGGA AAAGTGGGCT GGAGAGGAAA GAGGAAGGGC 2340 ATGGGAATCT ACTTGTTGCA AGGGAAAAGG AGCAGGAAGA GGAACAATCA GTTACGTTTC 2400 CTCTAGCAGT CTGTAAATTG GTGCTTTACA TAAGATGAGC ATAGAGTTTA GCTGCCTGTG 2460 GTGGGGATAT CTAGCCTTTT ATCTGTAGCT ATCTGCTTAG GCACAAACAG AAAGGCAGCT 2520 TCTTGCATGA CTCAGCTTCT AGTTTAATTT TTTCCTGTTG CCAAGAAAAA ACTGGGGTCC 2580 TGAGAGTTTT TCTTTTCCTT TCACAACAGG AAGAAACAAA CTACAGAGCC CCTAGGTATA 2640 CTGGGGCCAC CTGGGGTCTT GTTAAAAATG TGCATTTGGG GGAGGGGCGG AGAGTCTGCG 2700 TTCCCCCCAT GCAGTGCCCA GGCTGCTGCT CTGTAGGCCA CACTTTGAAT ACTGAGAGTA 2760 CCAGAGAGGA CTTGGTGGTA GGGGGTGGTG GGTGGATTCT GGTACAGTTG GAGGGAGGAG 2820 GCTTCCTGGG GTGAGGGCAC TGAGATGGGT CCTGGTGGTA AGATTGTGTG GGGAGGAGAA 2880 TAAAGGTACC CCAGATCAAC CTTGTGGGGC AACAAGTGAC CTGACAAACT CCCATCATGT 2940 ATGGCCACTG TCCCCCATTC AAGGCCAGGG ACCGTTGGAG GAGTTGGAAA 2990
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