Tag | Content |
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EnhancerAtlas ID | HS017-29514 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr6:159269580-159272210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr6:159271832-159271847 | TTCTATTTTTGAATT | - | 6.35 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_10307 | chr6:159270489-159272427 | CD19_Primary | SE_11101 | chr6:159269935-159278161 | CD20 | SE_12189 | chr6:159270476-159272674 | CD3 | SE_14386 | chr6:159269967-159276559 | CD4_Memory_Primary_7pool | SE_16462 | chr6:159270366-159272622 | CD4_Naive_Primary_8pool | SE_17999 | chr6:159269964-159278117 | CD4p_CD25-_CD45ROp_Memory | SE_18987 | chr6:159270298-159272689 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20282 | chr6:159270258-159272560 | CD56 | SE_20897 | chr6:159270325-159272691 | CD8_Memory_7pool | SE_21904 | chr6:159270304-159272606 | CD8_Naive_7pool | SE_22378 | chr6:159270210-159277819 | CD8_primiary | SE_23109 | chr6:159269528-159270215 | Colon_Crypt_1 | SE_23109 | chr6:159270311-159272890 | Colon_Crypt_1 | SE_23789 | chr6:159269757-159270124 | Colon_Crypt_2 | SE_23789 | chr6:159270320-159272542 | Colon_Crypt_2 | SE_25058 | chr6:159269583-159270161 | Colon_Crypt_3 | SE_25058 | chr6:159270298-159272906 | Colon_Crypt_3 | SE_27140 | chr6:159269496-159270180 | Esophagus | SE_27140 | chr6:159270275-159272234 | Esophagus | SE_27853 | chr6:159268889-159276361 | Fetal_Intestine | SE_28795 | chr6:159268853-159276331 | Fetal_Intestine_Large | SE_34137 | chr6:159269472-159272352 | HCC1954 | SE_34397 | chr6:159270023-159277893 | HCT-116 | SE_34769 | chr6:159269432-159276667 | HeLa | SE_35994 | chr6:159268630-159276489 | HMEC | SE_40070 | chr6:159270467-159271929 | K562 | SE_51056 | chr6:159270265-159271835 | Sigmoid_Colon | SE_52705 | chr6:159269488-159270224 | Small_Intestine | SE_52705 | chr6:159270267-159272097 | Small_Intestine | SE_58403 | chr6:159210147-159292283 | Ly1 | SE_63169 | chr6:159270185-159292330 | Tonsil | SE_64395 | chr6:159268761-159270224 | NHEK | SE_64395 | chr6:159270254-159276320 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr6 | 159270408 | 159272193 | chr6 | 159270971 | 159271326 | chr6 | 159270643 | 159272155 | chr6 | 159271429 | 159272000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I158847 | chr6 | 159268541 | 159279766 |
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Enhancer Sequence | GGTGTGAGCC ACCGCGCTCG GCCATTTCAC TTCTTATTAA TCACGACCAG TGTTTCCTGA 60 GCACTTACCA CATGTCAGAC ATGGTACTAA GAATGTTATC AGTGTTATTT ACTTAACCTG 120 TACAAATAGA GATAGGGACT ATTATGAACT TAATTTTTAT AGAAAAGAAA CCTGAGAGTA 180 AGAGACATGA AGAAACTTGC CTGAGGTCAT CCAGAAGGAA GAATAAGGAG TCAAGGTGTC 240 TCCAAGGCAA TGCCCTTCCA CCCCGAGCAC CTCTGTGCTG GCCTGAGAAC ATGTTCCAGG 300 AGGCAGAGCC TCACTTCATG GTGGGGTCTG GGGCACAGCC AACACATCTG GGGGCTTAGA 360 TTATGAAGAA GTGAAGGTAT CCCTTAAAGC AACTTTCCTA GTTTCTTGGA TTGGCTTATG 420 ACTCTAGTTT CTTCTTAATT CTTGCAGAAA TCATAACCCC TCTATTAACA GTATTAAGAC 480 TATGCCATGC TGGCCAGGCA CGGTGGCTCA CACCTGTAAT CCTAGCACTT TGGGAGGCCG 540 AGGCAGGCAG ATCATGAGGT CAGGAGATCG AGACCATCCT GGCTAACACG GTGAAAGCCC 600 GTCTCTACTA AACATACAAA AAAAAAATTA GCTGGGCGTG GTGGCGGGCG CCTGTAGTCC 660 CAGCTACTCG GGAGGCTGAG GCAGGAGAAT GGCATGAACC TAGGAGGCGG AGCTTGCAGT 720 GAGCCGAGAT CGCGCCACTG CACTCCAGCC TGGGCAACAG AGCAAGACTC CATCTCAAAA 780 ACAAAAACAA ACAACAACAA CAACAAACTG ATCTTAAGTA GAGGAAAAGA AGATTGAAGA 840 TTGGAAGAAA ATGACAGATC ATCAAATCAC AAAGAAATGG GGGAATGTGG AATCTGTCCT 900 TGATGACTGC CACTGAATAT TCACACTAAC ATCACAGTGA GGTCCCTGTT CATTTGTGCA 960 GGAGAACATG TACAAACATT TAGGCAGAAC ATACGCAGAG TAGAGTATAC AGACCTCTCC 1020 CTCCTGTTCA GGCTTTTAGC TGGCATTAGG GGTTTGAGAC CTTGGAATGT TGTCAAAGAA 1080 AAACACACTT TAAAAGCCCG TTTCCAAAAG GGTGACAAAC GGGACTGGAT GATGTGTTTA 1140 ACCTCATGAA ATATTGAACT CTTGGATGTA AATCTGCCCA TATCACTAGA GATGAAAGAG 1200 TTATTCCTGT TTTTATGTCT AATTGTGGAA CTGGTGAAAT TTGCATTTCC CTAGAATCAC 1260 TGCCCCTGTT GATAGTTGAA ACACACAGTT TTGAAGAACA GCAAATCATA CTCTAAGAGG 1320 CAGTAGTCCC CTATGTCCTG TCGTTTTCCC TGTTTCTGCC TTCTATAGAC ACCCTTGCCA 1380 CCACTCAGAA ATGTTTGAGA CTTTGTGGAG AAAGTAGACT GGTGAGAATT TCCTCGTACT 1440 TGGAAGGGTT AAGCACTGAG TCGATCTACA GCAAGTGGCA CACCCAGTTT GAGGTCCACG 1500 AGGGTGAAGT AATTTATCTG TGAGTCATAT CACTGAATAC ACTGTTCTAT AGAATGTTGG 1560 TTAGCAACTC ACTTCCAAAC ATCGTGGCCA ATGGTTCTGT TAGACATAAC ATTTGAAAGT 1620 GAGATGAGTT GCTCATGTGG GCTTAGCAAT AGGCAATGAA ACGAATCTGG CATTGAAACA 1680 GACGTGGGTT TTTACAATGG GTTTAGACTG AAAAGAAGTG CTGTGTTGCA TGAGTCCATC 1740 TTCACACTAA GCATGAAAGC CAGAGAAGGA CCATCCGGTG CTCCTGGTGG AGACAGTGTC 1800 TCGGGACACT GCCTGTGAGG TTTTCAGGAT AGGAAAAAGA AGAGAAAAGG AAACCCAGCC 1860 CCTTGGTTTT CTTGTTTTAT AATGTGGCCA TTTCAGAGGC TGTGACTATA GGATTAAATG 1920 CTTAGCAATT GGCAGGACTT TATATTGACT GGTGTTTAAA ACTTAAAATT CAGTTATTCC 1980 AACCACAGAT ACTATTAAAA GAACTCTGGA GTCAAGAGGA ATGAGCAGGC AAGAGGGTGA 2040 GGCTGTGTCT ATGGCTGGAG GAAAGGTGTG ATGAGTTGCT GTTTTGTTGC TAGGCAATAG 2100 GTTTTATGTG ACAACAATTC CTTTCCTTTA AAGAACTAGA GTGCTCTTTT TGTTTAATGA 2160 AAGCATTAGA TTTTCTTGGT ACAAGAGGTA CCCATTGAGT TTACGTGAAT ATGTGGTATT 2220 ATAGTAAACA GTGCTTATGA AAGGGAATGC TATTCTATTT TTGAATTCTT TTGTTTTACA 2280 TTGCCACCTC TAGAAATCAT TTGCCTGAGG AGATGTGGTT TTTTCCTTTT CTCAAATGAT 2340 TTCTGTTGTT TGGCTTGTCT GACTGTAAAC CTCTAAATTA CCCCCAGCTG TTATGAATGT 2400 GCTTCTGAAT TTCTCAACAG ATAGCATAGC ATGTTTGTGT TTGGGGATGT TAGAAGATTT 2460 GCTTTTATAA TTCCAAACTA GTTAACAAAT CCTGATGTAA ATATGTTATG GTATCTTCTA 2520 TATTTCTTCT TTTATTGATC CTATTATAAT GTAAAATGTT GTAGACTGCT TATGGTCACA 2580 TTAAGACAGG GCCATATATC TCTTGCATCC TTATAGCCTT AATACCAATC 2630
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