Tag | Content |
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EnhancerAtlas ID | HS091-29465 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:239171700-239174150 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr2:239172612-239172633 | GGAAAAAGAGGGGGAGGAGGA | + | 6.08 | ZNF263 | MA0528.1 | chr2:239172618-239172639 | AGAGGGGGAGGAGGAAGAGGA | + | 6.11 | ZNF263 | MA0528.1 | chr2:239172577-239172598 | GAGGAAGGAAGAGGAGAGGAG | + | 6.13 | ZNF263 | MA0528.1 | chr2:239172571-239172592 | GAAGAAGAGGAAGGAAGAGGA | + | 6.1 | ZNF263 | MA0528.1 | chr2:239172576-239172597 | AGAGGAAGGAAGAGGAGAGGA | + | 6.23 | ZNF263 | MA0528.1 | chr2:239172640-239172661 | GGAGCAGAAAGGGGGTGGAGG | + | 6.23 | ZNF263 | MA0528.1 | chr2:239171802-239171823 | CCCACCCCCTCCCCCACCCCC | - | 6.26 | ZNF263 | MA0528.1 | chr2:239172653-239172674 | GGTGGAGGGTGAAAAGAAGGA | + | 6.54 | ZNF263 | MA0528.1 | chr2:239172615-239172636 | AAAAGAGGGGGAGGAGGAAGA | + | 6.64 | ZNF263 | MA0528.1 | chr2:239172583-239172604 | GGAAGAGGAGAGGAGTGGGGG | + | 6 | ZNF263 | MA0528.1 | chr2:239172609-239172630 | GAAGGAAAAAGAGGGGGAGGA | + | 7.21 | ZNF263 | MA0528.1 | chr2:239172668-239172689 | GAAGGAGGGGAGGAGGAGGGG | + | 7.33 | ZNF263 | MA0528.1 | chr2:239172567-239172588 | GGAGGAAGAAGAGGAAGGAAG | + | 7.5 | ZNF263 | MA0528.1 | chr2:239172624-239172645 | GGAGGAGGAAGAGGAGGGAGC | + | 8.75 | ZNF263 | MA0528.1 | chr2:239172564-239172585 | GAAGGAGGAAGAAGAGGAAGG | + | 9.24 | ZNF263 | MA0528.1 | chr2:239172621-239172642 | GGGGGAGGAGGAAGAGGAGGG | + | 9.53 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_23101 | chr2:239171015-239172295 | Colon_Crypt_1 | SE_23101 | chr2:239172391-239173998 | Colon_Crypt_1 | SE_23739 | chr2:239172492-239173253 | Colon_Crypt_2 | SE_24713 | chr2:239171194-239173278 | Colon_Crypt_3 | SE_28235 | chr2:239170362-239173208 | Fetal_Intestine | SE_29205 | chr2:239170289-239173310 | Fetal_Intestine_Large | SE_31544 | chr2:239171094-239173874 | Gastric | SE_37617 | chr2:239170986-239172881 | HSMMtube | SE_43918 | chr2:239166296-239177085 | MM1S | SE_50608 | chr2:239171348-239173468 | Sigmoid_Colon | SE_52761 | chr2:239170932-239173329 | Small_Intestine | SE_65405 | chr2:239170980-239173309 | 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 |
GH02I238261 | chr2 | 239170608 | 239173300 |
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Enhancer Sequence | TGGAAGGCAA GCAGACACAC GCTAGGATTG GCATCCAAAC AGATGAGGAG ATTGTCACTA 60 AGAACCATCT TATTCCCTGG AAAGAGAAGA TACACTCCAA ACCCCACCCC CTCCCCCACC 120 CCCGGAGATC AAAAGTTGGA CTAACAGAAC CAGCTAGACT TTTAATCAAT AGCAAACGAA 180 GGTTCACTGT CCAGGACGCT GAAGGAGGCT CCCTCTGCTG GGGCCTGAGT GCTTCAGCTC 240 TGCGTTTCAC CTCCCAAGAG ATAAGTCATG ATCATGCTTT TGTTTTCTTC CTTCCAGCAT 300 CTTTTTCTTT TTCAGTGTCA TTCATTAGTT TGGCCACATG TGACCTGGCA TGGATTTTTG 360 CTTAACAAGT TTTGCCTGGG CCTCGGAAAA CCCTTTGTAT GTGCTTCTTT TCCAGCCTGG 420 TCTCGTGTGA CTTTGGCCTC AGCATCCAGT TGGTTTACTG TGGCTTCTTT GGAGTCTCGG 480 TGGCTGGCTG GGCCTCTGCC CTTTGAGCTC ATGCCTCCTC CCAGAGCTGT GGCTTTGCTC 540 CATTGCAGGA CGGAGCTGAA CTTCAGCAGC ACCTTCTGCT TCTGTTTGTG TCCAGCGCCC 600 TCTGCCGGCT CCACCGACCA TTTCTTCTCC CGATCTGCCT CTTAACACTT GTTGCATCCA 660 AACCAATGTT TCCTCAAACT CTGCTGCTTG TGTAGAAGGA TTTTCCCTGT GAATCTTTAG 720 ACCATGGTGC AGAACTTTCT CAAGGGCCTG GCGTTATTCT TTGATTTCCT CCTTCTTGTC 780 TGAGGCTCTC TCTTCAGGCC TCATGTTTTC CTTTGGACAG GATATACAGA ATGTTCCTGG 840 CATCCGTCCC ATCAAGGCCT TGCTGAAGGA GGAAGAAGAG GAAGGAAGAG GAGAGGAGTG 900 GGGGAACAGG AAGGAAAAAG AGGGGGAGGA GGAAGAGGAG GGAGCAGAAA GGGGGTGGAG 960 GGTGAAAAGA AGGAGGGGAG GAGGAGGGGG AGCCCTGGCT GTCCTTGGGC TTTGTGAGCC 1020 AGGCCACACA CAAGGCTTCA TCAAGGAGAG CTTGCAGGCT GTGGCCCATC ATGCCAGGTG 1080 AACCTGTCTG CCAACCTCCC TGCACAGGGC TGAGCTGGAC ACCAAGTTGG CATGGGAGTG 1140 GGTTAGAGAC AGTTCTCAGA TCTCTGAAGG AAGAAAAGTC TCCAGAGGCT GCTTTACATA 1200 TACGGCCCCA GGCCCTGCCC TCCAAGATCC TGGTTCCACA GGGCAGGGTG GTGTCCAGAA 1260 GCCTGCATCT GCAAACTGGC TCTGCCCCAG GCAGCCCCGC GGACACACCT GAGCCACCTG 1320 GAGCTGGAAG TGACGGATCC CTTTTTACCC ATAGAGCCTC CCCAGGAAGC TGTGTGGCCC 1380 TGACTCCAAG GATGGGGGCC TGTGTCCCTG GGCCAAGAGT AGAGGAGGGA GAGGTCTTGA 1440 TCCTCCAGCT TCTAGGTGAC CTGGTTCATT TTAGGAACCC AGCACACTGG TGCTTCTTGG 1500 TCCACTTCCT GTGGTATCTT CTGAGGTCAC TTTTCGGTGA CTACTGCCAG TGGCCCACAC 1560 ATTTTTTTTC TTTCTATTTT TTTGAGACAG GGTCTTTTGC TGTGACCTAG GCTGGAGTGC 1620 AGTGGTGCAA TCATAGCTCA CCGTAGCCTT GAACTCCTAG GCTCAGTGAT CCCCCTGCCT 1680 CAGCCTCTGA GTAGCTGGGA CTACAGGTGC ACACCACCAC ACCCAGCTAA TTTTTATTTT 1740 ATTTTGCAGA GACAGGGTCT TGCTACGTTT TGAACTCCTG GTTTCAAACA GGCTGGTTTC 1800 AGACTCCTGG CCTCAAGTGA TGCTCCTATC TCAGCTTCTC AGAGTGCTAG GATTATAAGT 1860 GTGAGCCACT GCACCTAGCC GGCCCAAGTG TTTTTGGAGT CTTCATGCAT TTGTGGAGGA 1920 GCTGGGAGAA GATGCATGGT GGGGGCAGAA GCCACTCAGA ACATGGGTGC TCCCAAATCT 1980 CACTGGGACT GTTCGCACCT GCTACAGCAC CCTGAGGGGG AGACCCAGAG AGAGGGACCC 2040 AAGTGGGGCT CTGAGGCATG GAGAAAATCC TGTCCCCTGG AGAAGCCTCT AGCACACAGG 2100 CTGGAAGATA GACTTCTGCT GGGATCCAGC CAATGGCATC TCCGGCTTCC ACCCTGACAC 2160 TGGTCCCAGG CAACAGCGCC TCTGTCTGGA CCATTATCCA CTCCGAATGG GTTTATATGG 2220 GAGAATTAAG ACAGGCTCAA TTAGATCAAC AGCTCTCCAG AAAGCCTCAA TTACACCATG 2280 TGCATATCTT AGGAAGTTTT CAGTGTAATT CCATAATTAT TTCATTGCCT GTATATAATT 2340 ACATGTTTTT GTCCATTATC ATGTAATTAT AAAACCAAGA TGCAGTCTTG GCTTTGGCTA 2400 AATAGCTTTT ATATCAAAAA CATGAAAAAG GGGGTGGGTC AAGACCACGT 2450
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