Tag | Content |
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EnhancerAtlas ID | HS187-22165 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:159273400-159276330 |
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 | TTTATGGGGG AAGAAACTGA GGCACAGAGA GGTTAGCTTG CCTCGGGACT CTGTCTCTGC 60 TGAGATTGGA AGCAGAAGAC TAGTTCCAGA ATTCACACTC CTAACCCTAC TACAACACCT 120 GCTCTCAAAC AGAGAAGGGA AAGGAAGTCC TGGCGTTTGC ACTCTCCTTG ATCTTGTGCT 180 GGTCTGGTCT GGACATGGAC CAAGGCTTGG GGGCCTTGCA CACGTAAGTG AGTGCAGATG 240 CCCGGCCCAG CCCCAGGGCT CCCTTGTCCT TGAGCTGGGG CCACGCTGAG GCTGAGGCTG 300 GCCTCCATGG CTTGACTTGA GGCCACCTCC AGATCCACAC CCTGAAAGCT TGGGACTGGC 360 CTTCTCAGAG AATGGGGCAA AACACTCTGA CGCCAACTAC AACCATCACA AGGAGGTACA 420 TTCTCTGTAA GGGCAAGCCT GGGGCTGCAC CCAAGTAGAC TAGCAGACAC TCATTACAGA 480 GAGAATGTTC TGGCACTCTG GCCCTGCCAA AGGCTACCAG AACACAGAAG GCCCTTTCTT 540 CCAAGGGGCC GAAGGAGGAG CAGGCACACA CCATATGCCT CACTCACCAC ACGAAACCAC 600 ACACCACATA GCACACACGC GTGCACCCTC ATACCACACT GACCCTTCAC CACACACACA 660 CCCATACACC TTCATGTCAC ACATACCACA CACACAGATA TACCACATGC ACCCCATACA 720 CCCCACCACA CACATACAAA CACCACACCA TATACACACA CACACAGTAC AACATACACA 780 CTCACACACC ATATGCCACA CACATATACT TTACACATAT ACATACCTCC AAACACACAC 840 CATGCACACA CACGGTACAC CATACACACA CCACACACTA TGCACACACC ATGTACCACA 900 CACATACCCC TCCAACATCA CATGAACACT ACGCACCCTC CCCCATACCA CACACATACA 960 CGCACACGTA CCATGCACGC ACACACACCA CAATGTGCTG TTACTTAACA GGTTTGCCTT 1020 CCCACAACTC TATCAGCAAA CCCTTCTGGA GGCGCAGCCC ACACCTGCAT TCCAAAGAAC 1080 GCAAATCCCT TCCCTGCCCG ATGAAAGGCC CCTCCCACAG TGAGTCACAG AAACTGCAGC 1140 CGAGCAGGCA GTGGTGGGCC CCACCCTTCT CACAGGAAGT GAGAAAGAGT AAATATGTAG 1200 TTTTTCTTTG AGGGCCAATG CACATGTTAA ATGGGTGATT AAGAAGACAG AGAGCTGCTT 1260 AAAAGGTCAT GGGAGAAGTA CAATGTCTGG GGACTTGGCA GTAGCCTGGC AGAGACCGCA 1320 GGAATCCTAT AGAGTCTTTT ATGGACAGGG CTCTGAAATT CCAGAGCCTG CAGGAGGTAC 1380 CTTCCCCTTT GACTCGGCGG GGCTGTACCA CTAAGAATGC ACTGAGCATT GGGTGCACTT 1440 GGGATACCTG AGCTGTGGGG CCAGAGAGGC AGCCCTAGGG GAGAATTCCG GAGTTGGGGC 1500 TGGGTTCTTT CAGCATAAAA AATCAAAGTG TCGCTTCTTT AATGAACCTC CCGGCAAGGT 1560 CTTCCCTGAA GACCTTGAAC AAGTGTTCTT AAACAAGTGT TCCTTTATGC AATTAAAGGC 1620 CAGGGAAGCT GGGGTCTGAG AGGCCATGGA GCCATTGGGA TAATAGTGAC AGTTCGGCTA 1680 CCATTCAACT GGGCTTCTGA TGAATCATGC TGGGGGCAAG GACTCCAAAT CACCAGCTCT 1740 ACTCTATACT CGAATCAGTA GGCAGTTCAG ACAGTCTTGG GGGATTTGGG CAAACGAACG 1800 CTCCACTTAG AATCTCTCCA GAAAGACAAA GGGGGTGCCT AACAAACAAT TCAAGGACTG 1860 TGGGAAACCA ATGATCATCA AGGGCTCAGT TGTACAGTGT AAACCAAAAA GTATCTGAGA 1920 CAGGTCTCAA TCAACTGAGA AGTTTATTTT GCCAAGGTTA AGGACAGGCC AGGGAGGAAG 1980 AAACACGGAA TCACAGAAAC AGTCTATGGT CTGTGTCGTT CTTCCAAGAT GATGTTGAGG 2040 GCCTCGATGT TTAAAAGGGA AAAGTGGGCT GGAGAGGAAA GAGGAAGGGC ATGGGAATCT 2100 ACTTGTTGCA AGGGAAAAGG AGCAGGAAGA GGAACAATCA GTTACGTTTC CTCTAGCAGT 2160 CTGTAAATTG GTGCTTTACA TAAGATGAGC ATAGAGTTTA GCTGCCTGTG GTGGGGATAT 2220 CTAGCCTTTT ATCTGTAGCT ATCTGCTTAG GCACAAACAG AAAGGCAGCT TCTTGCATGA 2280 CTCAGCTTCT AGTTTAATTT TTTCCTGTTG CCAAGAAAAA ACTGGGGTCC TGAGAGTTTT 2340 TCTTTTCCTT TCACAACAGG AAGAAACAAA CTACAGAGCC CCTAGGTATA CTGGGGCCAC 2400 CTGGGGTCTT GTTAAAAATG TGCATTTGGG GGAGGGGCGG AGAGTCTGCG TTCCCCCCAT 2460 GCAGTGCCCA GGCTGCTGCT CTGTAGGCCA CACTTTGAAT ACTGAGAGTA CCAGAGAGGA 2520 CTTGGTGGTA GGGGGTGGTG GGTGGATTCT GGTACAGTTG GAGGGAGGAG GCTTCCTGGG 2580 GTGAGGGCAC TGAGATGGGT CCTGGTGGTA AGATTGTGTG GGGAGGAGAA TAAAGGTACC 2640 CCAGATCAAC CTTGTGGGGC AACAAGTGAC CTGACAAACT CCCATCATGT ATGGCCACTG 2700 TCCCCCATTC AAGGCCAGGG ACCGTTGGAG GAGTTGGAAA GTTAAGAGCT TGAAAACTGG 2760 ATTCTGCCTC ACTGGGAGGT TCACTGACAT TTAGTCTTCT CTGAAAGATG GGCATAGTTA 2820 TACCAATCCT ACAGGAGTAG TGTGAAGATT AAATGAGATG ACATATAAAG TGCTTAGGGC 2880 CTGGGGCAGC ATAAGTGGTA GAATATTTGT TCATATTATT ATTGTTATTA 2930
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