Tag | Content |
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EnhancerAtlas ID | HS197-19539 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr7:47577450-47579780 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr7:47579289-47579300 | AGCCACTCAAG | + | 6.62 | RREB1 | MA0073.1 | chr7:47577563-47577583 | ACCCCCCCCACCCCCCGCCA | + | 6.8 | ZNF740 | MA0753.2 | chr7:47577561-47577574 | GCACCCCCCCCAC | + | 6.74 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_01808 | chr7:47575247-47578158 | Aorta | SE_24231 | chr7:47578561-47579696 | Colon_Crypt_2 | SE_27796 | chr7:47573548-47583706 | Fetal_Intestine | SE_28671 | chr7:47572869-47584643 | Fetal_Intestine_Large | SE_47105 | chr7:47533228-47656720 | Panc1 | SE_52800 | chr7:47578479-47580814 | Small_Intestine | SE_53304 | chr7:47577577-47580606 | Spleen | SE_65257 | chr7:47576666-47578199 | Pancreatic_islets | SE_65257 | chr7:47578623-47579629 | Pancreatic_islets |
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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 |
GH07I047533 | chr7 | 47573007 | 47584707 |
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Enhancer Sequence | CTAACCAGGT AAGGATTTCA AGCAAATATC AAAGCACAGG ACCGCCCGGG GCCTTGCACA 60 CCTGGGGGCT GGGCTGCACC TCCCTATCTC CCAGCCTATC CCTCCCTCAC CGCACCCCCC 120 CCACCCCCCG CCATCCTGCT CCTGGCAAAT CAGGACAATT CACAGCACAT CTGAAGTCCC 180 GTCTTCCTTT ATGGGTCTGC GATTTTAGAA GGAAATTAGA AACCCGAAGT TCAGGAGGTG 240 AAGATGACAG GGTGATGGGA GAAGATGGAC AAGCCAGGAT CCTGAAGAAA GGGTCACTTA 300 GAAACGCCAG GAGGAGAGGC GGGCAAGATC CACAGGCAGA TCCCTCCTTT CAATGCCTGT 360 CGGACTTCAC CAGCCTTCCC GGGGCAGTGG ATCTTGGCTG TCTGCAAGAA GCTTTGTGGC 420 AAGTCTAAAA CTAAAAGAAC ATGTTCAAGA TGAAGCCACT GCCTGTGGTC TACGGTGGGC 480 AGCGGAAGAG ACCCCTGCCT CAGAGCAGGA TAGGGGGCCT TCTAGTCTCA GGCCAGCTAA 540 CCCTGTACTC CTACCACTGG CCTTCACTCC AGGCCCAGCC TAGGAGCAGT GTCCCAGAGC 600 TCAGCCTTTA TGGCTCCAAC ACTCTAACTT CAGATCTACA GCTCCACTTG CAACTCCACA 660 TGCCTTGGAT GTGGGGAGCA GTCTGGGTGG GCTAAGTCGT GGCCTTTATG GCTGACATAT 720 GTGCAAATTC CAGCCATCAA TTCAACTGGC TGACGTTAAC CTCTCAAGTT CTGGCACTAA 780 ATATCCATCT TTCTGTTTCT GCAGTAGAAG AGCAAAGCTG CTCTTCAACT TTTAACTACA 840 AAGGAAAAAA CCTCCTCCTA GAACACACCA TTCTGGGTTC CAATTCCTCA CTAAATCATC 900 ACCTGGCAGA CAAGCAGGCA TTCTCATTTC CCCCTGTCCT TCAAATGACA CCATTATTCA 960 CCTTTTTCTA TATTCATTCC TTCATTCATT TTTCTGTATA CATTCATCAT TTTTTTCCTA 1020 TAGCATATCC AAACTTTAGT CTTTTCAAAC ATTTTTCCCT GAGAACACAT CTGTATCGTA 1080 TTCATTCCAG ATTGCTTCAC ATCTGACACA ATACCAGGTA CATAGCAGTG CCTACAAACA 1140 GCTAAGAACA GGATATGCTG CTGTCATGGT TTACCCAGGG CAAACACGCC CAGAGGTCAG 1200 CTGGATCTAC CACCGCCCTT ACCATGGTGC CCACAGGAAC CGGCCAAAGA AATCTGAATT 1260 CAGCAATGAA CAGATAGCCC CCAGCAGGAT AAAACTCCTC CAACCTGAGT ACCAGGATTC 1320 ATACTCTCTG GGGTCCACCC AGGAACAACG GCCAGGAGCA CAGGCCAGCC CACTGCCTAT 1380 GCAAGCCAGA GTGGAAGGCA AATGGTTGAA GGTGGCTTTT TATTGCAGGG ATACCCTGAA 1440 TCTGCTCTTA CTTATTTAAA AGAGTAGCCA TTCAGAAAAC TCCCACACTT CGTTACTAGT 1500 AACAAATATC GTGCGTGTGA TAAACCTCCC CAGTGAGGAC AACAAACTGA TTTTTCACTG 1560 GCAAGAAACA GTGCTCAATC CTAAGGCGAA TCCGCATTCA TCAGCAGGCC GCCTCTCCAG 1620 CCCCTCTCCC TGCCCCCGAC TCTGACCTCC TCCTGCCAGG CTTGCAATCT AGGCTCTTAC 1680 ACTCCAGGGT CCTTCTGCTC TGCGCCCTTG GGCTCACTTG GGGCTTCTCC CAAGGCAGTT 1740 TCCCATTCTC CTTTCTGGCT GAAAACCGCT GTCCTGGGCT CAGTTGAAGA TCCGCCCCCC 1800 ATCTGACCTC CCAGACTGGT TAATCATCCT CCATGGCTGA GCCACTCAAG GATGGTTGGG 1860 GCCCTGACCC TCTAGTGTGG TCATAAGTCT TGTACCTCCA ATAGGAAGTC CTAACCTTGT 1920 CTGGGATTTT CCACACACAG CACCAAGCAG GAGCAATAAA CACTGGTGCA GGAATGAAAA 1980 CATTCTCCTT TGCTGTATTT CCACCACATC AACACCGGTG TTCACTGCCT GTCTCAGACC 2040 ACACCCTTCT GAGTCCTCCC AGAAGTAAGC TGTAGCTGAG GGTCTGGGGA TGCGAAGGGA 2100 CTCAGAAGCC AGGGCACAGA CTCCTCCAGG CACAGACCCT CACCTCAAAA CTTGGGTGGC 2160 AGACTGGCCT CACTCCATCT TAAAGCCACA GTGAGCTCTG TGCTGCTGCC CAGCTTCCAA 2220 TTTTCTTCGT GCTTTGCCAC AATCCTCTGT GCTTTTTACT CGCCAGGTTG TCTCACCCTA 2280 GCTTCTGACT GCACTTGGTT CCCAGGAACA AAACAAGGTT CTTCCCAGGA 2330
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