Tag | Content |
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EnhancerAtlas ID | HS187-10206 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:25900560-25903250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr17:25902556-25902571 | GGGTCTTTGTGACCT | - | 6.34 | MAFF | MA0495.3 | chr17:25901087-25901102 | CTGCTGAGTCATCAC | + | 6.26 | MAFF | MA0495.3 | chr17:25901087-25901102 | CTGCTGAGTCATCAC | - | 6.28 | MAFG | MA0659.1 | chr17:25901084-25901105 | AAACTGCTGAGTCATCACAGC | - | 6.36 | MAFG | MA0659.1 | chr17:25901084-25901105 | AAACTGCTGAGTCATCACAGC | + | 6.6 | MAFK | MA0496.2 | chr17:25901085-25901104 | AACTGCTGAGTCATCACAG | - | 6.43 | MAFK | MA0496.2 | chr17:25901085-25901104 | AACTGCTGAGTCATCACAG | + | 6.82 | NFAT5 | MA0606.1 | chr17:25902820-25902830 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr17:25902820-25902830 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr17:25902820-25902830 | ATTTTCCATT | + | 6.02 | NFE2L1 | MA0089.2 | chr17:25901086-25901101 | ACTGCTGAGTCATCA | - | 7.11 | Nfe2l2 | MA0150.2 | chr17:25901088-25901103 | TGCTGAGTCATCACA | - | 6.16 | SRF | MA0083.3 | chr17:25902359-25902375 | AGACCATATAGGGTAA | - | 6.07 | STAT1 | MA0137.3 | chr17:25902306-25902317 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr17:25902306-25902317 | TTTCTGGGAAA | + | 6.32 | Stat4 | MA0518.1 | chr17:25902306-25902320 | TTTCTGGGAAAGGG | + | 6.56 | ZNF263 | MA0528.1 | chr17:25903111-25903132 | CCACCCCCATTCCCCTCCTCC | - | 6.69 | ZNF263 | MA0528.1 | chr17:25903114-25903135 | CCCCCATTCCCCTCCTCCTTC | - | 8.34 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_04008 | chr17:25902760-25905903 | Brain_Anterior_Caudate | SE_06005 | chr17:25902206-25906661 | Brain_Hippocampus_Middle | SE_28854 | chr17:25902569-25908528 | Fetal_Intestine_Large | SE_39231 | chr17:25899481-25906485 | IMR90 | SE_39962 | chr17:25896150-25907770 | K562 | SE_51370 | chr17:25892863-25902462 | Skeletal_Muscle | SE_51370 | chr17:25902797-25906905 | Skeletal_Muscle |
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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 |
GH17I027565 | chr17 | 25892921 | 25908255 |
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Enhancer Sequence | TCGAATCTTG TTCAAATAAG GCAAAGGAGC TGTAACCAAT CCAGCTGTTT CTGTACCTCA 60 CTTCTATTTT CTGAAAGTAG GTAGAAATTA ATTTACTTCG AAAAAAATAA TTTCCCCTGA 120 AAGGTAGCTG CTGTATCCCA AGGCTTTGCC AGGTTAACAA GTGGACAGCA TGGAATATTT 180 GGAGGAGGTT TGGAATCGTG CGCACGTGGG TTTCAATTCT GCTCAGCCAC TTGTTAAGCT 240 GTGAAGTCTC TGAGCCTCAG TAAGATGGAC TTAACTCCAT CTACTTGCGG AGTTGATTAA 300 AGATAAAATA ATGTATACAA AGCCCTAGGC ATATTGTTCT GGCAAATAGT TTGTAATAAT 360 AAATGTAGTT ACTTTGAGAA CTTGAAACTT GGTATGGGTG AGGAGGAGAT GAATAAAAAG 420 AAAGAAAAAG AATCCCTATT TGCATTATAG TTAGGTTGAA GATTGGGTTT CCTCAGCCTG 480 GCTCCCTCCC CAGCCCCATT AAACATCTCT ATCATCATCT GGGCAAACTG CTGAGTCATC 540 ACAGCCTTGG AGTATGTGGT GGAGAGACAA ACTGAGGACA CCCTTCCGGA CAAGTAGAGG 600 ATTGCTTTGT TCAGATAAGG TGAAGGTTGC TCTTGTGCTT ACCCTGACGG TATCGCCAAG 660 GTGCTCTTAA CAGTCAAATG AGGGCAAAGA TATCCAAACC TCATTTCAGT GGAAGACAGG 720 CTAAGGGAAA GAAAGCAAGA CATGTTGATT GTATAGAAGC TTCTGCATGG CACCATTTGT 780 CTAATCTGCC TCCCCTGCTG GTGCCGTTCT CATCAGTGGT TCCTGTGACA CTTTAGTTTT 840 ATCTTCTGGA AGGCAACCAG GGTTTTGGCC AACCAGTGAT GAGCTTCTTG GTACAGTTAT 900 GTGTCTGGCT TTATTTTGGT GTGATCATGC TAAGTGGTGA TGTGATTCTT GCCTACAGCC 960 CTGAAGATTG AAGAATATAC TGAAAAGCTA CAAAAGCATC TGCCGTCAGC GGGTACAGTA 1020 AAAAACAAAC AAATACAGAA AGGCAGGCAT CTAGCTCCAG CCTTGCTATG GGAGAGAGGG 1080 GTATGGGTTG GGCCTCATAC CTTCAGGACT CAGCCAGTAT CTTCATTAGG GTTAGTTTTG 1140 ACGCTTGAGA CAAGGAATTA CAGCATGTAA ATGGAATGAC AATGAAATTA GTCCTTAAAA 1200 GTAAAATTAG ACACAACTTG CTAAAAATCA GGATTGGCTT AGATTCTCAA GAACTGTGAG 1260 CTTTATAGCA GTCATTTGAT GTGGAATGTC TGGCCTTCTC TGTTACAGAA AATCTGGAAA 1320 ATATAGAAAG GGTTAAAGAC AAAAAAAGGT CTGATCTGGT CCCATAGCTC TTTGAACTCT 1380 CTCTGCTCTA GTGCGCATCT TACTGCATTG TAGTTACCTG TTTAAATGTC TGTCACTCCT 1440 CCCACTGGGC TGTAGGCCAC TTGAGACCAG AGGCATGTCC CATTGGTTTT TTATATTTGT 1500 CCCAGGTTTG GTATTGTTGC TGGATATAGG GGTCCCATTC TGGATCCCAA AAGAGGGTTC 1560 TTGAGTCTTG CACAAAAAAG AATCCTGGGT GAGTCCACAG AATAAAATGA AGGCAAGTTT 1620 ATTAGAGAAG TGGAGAAACA AAAGAATAGC AACCCCGTAG GCAGAGCAGC CCTGAGGGCT 1680 GCTAGTTAGC TATTTTCATG GTTATTTCTT GACCATATGC TAAACTGGGG TAGATTATTT 1740 GTGAATTTTC TGGGAAAGGG GCAGGCAATT CCTGGAACTG AGGGCCCCTC CCCCTCTTTA 1800 GACCATATAG GGTAACTTCT GGGCATTGCC ATGGCATTTG TAGACTGTCA TGGTGCCGGT 1860 GGGAGTGTCT TTTAGCATGC TAATGCATTA TAATGAGCAT ATAATGAGCA GTGAGGAAGA 1920 CCAGAGGTCA CTTGGGATAC CATCTTGGTT TTGGTGGGTT TTGGCTGGCT TCTTTAGCTC 1980 ATCCTGTTTT ATCATGGGGT CTTTGTGACC TGTATCTTGT GACCTTCTCT CTCACCCTAT 2040 GATTAAGAAT GCCTGACTTC CTGGGGATGC AGCACAGCAG GTCTCACCCT CATTTTACCC 2100 AGCCCCTATT CAAGATGGAA TGGCTCTGGT TCCAGTGCCT CTGACAGTGT CATGTGGCTC 2160 AAAGTAGTCA GAGCTGGAGA GGTTTCCTCC CTCCCTGATG AGAGGAAAGG GCACAAGTTT 2220 TGAAGTCCAC TGAGCCTTGA TTCTACCATT CATTCTTTGT ATTTTCCATT GCTTCATAAC 2280 AAATTTAGCA GCTTAACACA CCACCCGCTT ATCATCTCAT GGTTCTCTAG GTGGAGGAAT 2340 CCACTCAGGC TCTGCTTATA TCCCTACTTG GGATCTCACA AGGCTGAGGT CAAGGTGTAG 2400 GCCAGGCCTT CCTCTTACCT GGAAGTTCTG GAGAAGAATC CACTTCACGT TCATTCAGGT 2460 TATTGGCAGA ATCCATTTCC TTGTGGCTGG AGGTCTGAGG TCCTCATTCC CTCAATGGCT 2520 GTCAGCCAGG GGCTACTTTT TTTCCCAGAG GCCACCCCCA TTCCCCTCCT CCTTCAAAGT 2580 CTGCTTTTCA CGCTTCAGGT CTCTTGACTT CTCTGTTACC AGCTCAAGAG AACCCTTTGC 2640 TTTTAAAGGG CTCTTGTGAT TGGATGAAGC CTACTTGGAT AATTTCCCTT 2690
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