Tag | Content |
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EnhancerAtlas ID | HS060-14487 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr17:29819880-29822540 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr17:29820068-29820083 | GGGTCTGAGTGACCT | - | 6.19 | Foxa2 | MA0047.2 | chr17:29820241-29820253 | ACAATGTAAACA | - | 6.04 | IRF2 | MA0051.1 | chr17:29820765-29820783 | CTTCTGATTTCACTTTCC | - | 6.11 | Nkx3-2 | MA0122.3 | chr17:29821412-29821425 | AAAAGCACTTAAA | + | 6.03 | Stat4 | MA0518.1 | chr17:29820597-29820611 | CGTTTTCCTGGAAG | - | 6.23 | ZEB1 | MA0103.3 | chr17:29822033-29822044 | CCCACCTGCCC | + | 6.14 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_06379 | chr17:29813394-29821502 | Brain_Hippocampus_Middle | SE_07497 | chr17:29817777-29820336 | Brain_Hippocampus_Middle_150 | SE_08278 | chr17:29815213-29821731 | Brain_Inferior_Temporal_Lobe | SE_10805 | chr17:29817070-29824218 | CD19_Primary | SE_11703 | chr17:29813711-29825938 | CD20 | SE_12102 | chr17:29817986-29823996 | CD3 | SE_16137 | chr17:29819875-29822921 | CD4_Naive_Primary_7pool | SE_20248 | chr17:29815152-29824244 | CD56 | SE_21841 | chr17:29819960-29822928 | CD8_Naive_7pool | SE_22545 | chr17:29814997-29825864 | CD8_primiary | SE_24147 | chr17:29817805-29820206 | Colon_Crypt_2 | SE_24147 | chr17:29820264-29821556 | Colon_Crypt_2 | SE_24147 | chr17:29821672-29822661 | Colon_Crypt_2 | SE_25099 | chr17:29818074-29821575 | Colon_Crypt_3 | SE_25099 | chr17:29821619-29822785 | Colon_Crypt_3 | SE_31907 | chr17:29813274-29822908 | Gastric | SE_50658 | chr17:29814990-29824072 | Sigmoid_Colon | SE_52727 | chr17:29814991-29823464 | Small_Intestine | SE_60298 | chr17:29814235-29825308 | Ly4 | SE_62782 | chr17:29813392-29838946 | Tonsil | SE_65467 | chr17:29815265-29821243 | Pancreatic_islets | SE_65467 | chr17:29821417-29822613 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr17 | 29820298 | 29820473 | chr17 | 29821482 | 29821571 | chr17 | 29820270 | 29820692 | chr17 | 29819921 | 29822027 | chr17 | 29821000 | 29821600 |
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Enhancer Sequence | ATGACAAGAG CTCAGATTCT CAGAACCCCC CTGAGCACCC AGACAACCTT GGTGGTTACT 60 TCTTCACTTT TTCGCATGAC CTGGAAAGGA GATGAGACGG GGAGGAGAAC ATAGGCAACC 120 AGAAGGACGT GCAGCCTACA AGGGTCGTAT GAAGGTCAGA GGGGTGGCTG TGATGGCCCA 180 GAGCTGTGGG GTCTGAGTGA CCTCCAGCCC AGAACCGCCC AGCAGGCCAG TGCTAGTCAT 240 GCCAGCACTT CCAAACCCAC TTCTTGACTG ACCTTAAGAA ATGGGAAGTT TTCCAACTGT 300 TGGTCACATT TTTAATTGAT CTAACCTGCT TCATCTTCCC AGACAAGTGG GTTCTTTCCC 360 AACAATGTAA ACATTAATTC AGATGAAAAC AAAGCTCTGT AGAAGTTATT AATATCTGTG 420 GCTCTGCTCA TGGGAGCCTT TCTCTTTTGA GGTACCAGAA AGAGGAAGGC CTAAACAGAA 480 CTGGAGTGTG GGAGAGTGGG CGGGCTCTCT CTCTTTAGTC ATCTGTGGTC ACCCCCCACC 540 CCCCTGCGCT GTGCAAGCCT GATACCATGG AAAGGGAACC CACATTTCAA ATAGCTGCTG 600 CTGCTCCGGT GAACTTGGGG TAAGGGAGCT GAGGGGTGTC TACCCTCTGC ACCAGACTCA 660 AGTCTCCCTC CTAGAATAGG AGCGAGAATA GCAGCAAGTC CCTGCCCCCT GCTCCCTCGT 720 TTTCCTGGAA GAAATGCCTA CCTAAGACAC AGACACCTGC ATCCCACGCT TTGTCACCCA 780 ATGCCTGTTT CCTTAAGGAG AAAAAATGGG CGCCAGAAAA CTTCTAGGTC TAGATCCTGG 840 CTCTGTTGCT CGCTAGTTGT GGAACTTTGG ACAGGCGACC TCACCCTTCT GATTTCACTT 900 TCCCTGGCCT CACTCTTCAC TCCCTCTGCC TGTGGGCAGG CAGCAGCATG GTTCTGTGGG 960 GTCCTAAGGA CCCCAGGGAG TCACTCCCAC ATTTGGGCAG CAGCTTTGGG TTTAGTCTGT 1020 CCAGTTTAGG GCCCCAGATC GTATATGTGT GTGTGCACAC ACGTGTGTGT TTGCGTGTCA 1080 GGCAGCATTC AGATGGGGCA TCCTGTTCAT CCACCCCCCT GCTTTGGGGT GGCTGAGGGT 1140 TGGGGTGCCC AACAGGTAGA ATGGGGTTGA TAATAGCACC TGCCTCGCAG GGTGATGGTG 1200 AAAATAAAAT GAGCCATGGT GATTTAAGAT GCCCAGTCTA GGTTCTGGCC TTTACTTAGT 1260 TGACACTCGT GGACGGTTAG ATGGTTAGAG AGGCAGGCCA GTTTAGTACC AAAATGCCTT 1320 CAGAGTCAGG CTGTCTCTGG GTTCAGATCC TGGCTCTGCC CCTTGCTATT GGTGGAATCT 1380 TAGACAAGTT ATTTAATTTC TCTGTGCCTC AGCTTCCCCA CCTGTAAAAC GAGGATGAGG 1440 CTAGTACCTC CCTCACAGGG TTCGTGGTAA GAGGATGAGG CTAGTACCTC CCTCACAGGG 1500 TTCGTGGTAA GGCTCAAATA TGTAAATGTA TGAAAAGCAC TTAAAACTGT GCTTTGGGGT 1560 GAGCTGTTAT TCTTAGTTCC TGCAGGCTTC AGCTGGTTTG ATTGTTGTGA CTAATAACCT 1620 TCGCACCTAA CAGAATGTCT TGCCGGGGAG TGTCATGGCC CAAACAGGAA GGTGGCAGCG 1680 GAAAAACTCC ATTACTCAAG GGCCTTTGCA AGAGAAGCAA AACTCTACTT CCTCAGCTTC 1740 TGTGGGTTTT TAAATCTTTT TTTTCAATTT TAATTTTAAT TTTTTTAAAA AAAAAGTAGA 1800 AATGAGGTGT TACTATGTTA CCCAGGCTGA TCTCGAATTC CTGCCCTCAG GTGATCCTCC 1860 CACCGCGGCC CCCCAAAGTG CTGGGATTAC AGGCATGAGC CTCTGCACCC AGCCAGCTTC 1920 TGTGTTTTTA ACAAACCTTG CTCGGGCTCT GCAGATACAG ATTCTGGGTC TGGGGTGAAG 1980 TGACTAGCAT TTGTGTGGCA GTCTGTGAAT GAGATGTCAA GCAGCTTCCG AGGTAACAGA 2040 CTTCTCCCCA GGTTCAGTGA GGGAGACTGT ACCTAGCCTG TCCTTCCAGA GGCTGCTCAC 2100 ACTGCCAGGC TGTGGCTGGC CTGCCAAGGG GAGGATGGCC CTCCACACCT CGGCCCACCT 2160 GCCCTTCACC TCCAGCCAGG GCCTGCCTGT CCATCCACCT GTGCCTAGCT GGAAAAGCTG 2220 GCTTGGAGCA GTGCTGCCCA TCTGCCACTG CCAGCCCCCA GCATCTGCCT TATTAAAATG 2280 CTGAGGCTCT GGCTGGCCAC AAGCCCCAGG AGATTTGGAG AAAAGCCAGA CAAAAAGGTG 2340 CAGGCTGTGC CACCGCCCAG CCACACTGGG TGACTGCCCT TGGTAGTTAA CCACAGAGTC 2400 ATCCAGCTTG GCTGCCCAGA GGTCTATAGC TCCACTCAGG CGAAGCTGGC TAGCCTGGCC 2460 TAGCCTGGCT GGTTAGGTGG GCAGGACAGC CTCCACTTGA CTGATTTTTT TTTTTTTTTT 2520 TTTTTTTTTT GAGACAGGGT TTCGCATTTC TGCCCAGGCT AGAGTGCAGC GATACAATCT 2580 TGGCTCACTG TAGCCTCGAC CTCCTGGGCT CAAGTGATCC TCCCACCTCA GCTGCCTGAG 2640 TAGCTGGGTG CACCACCACT 2660
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