Tag | Content |
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EnhancerAtlas ID | HS161-01389 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr1:202002830-202005540 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB1 | MA0018.3 | chr1:202004082-202004094 | GGTGACGTCAGC | + | 6.14 | CREB1 | MA0018.3 | chr1:202004082-202004094 | GGTGACGTCAGC | - | 6.14 | Foxq1 | MA0040.1 | chr1:202003046-202003057 | AATAAACAATT | - | 6.02 | IRF1 | MA0050.2 | chr1:202005141-202005162 | GTTTCCTTTTACTTTTCTTTT | + | 6.23 | IRF1 | MA0050.2 | chr1:202005162-202005183 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | NFAT5 | MA0606.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_23058 | chr1:202003070-202004639 | Colon_Crypt_1 | SE_23723 | chr1:202003133-202004433 | Colon_Crypt_2 | SE_24689 | chr1:202003019-202005179 | Colon_Crypt_3 | SE_25977 | chr1:202003098-202005224 | Duodenum_Smooth_Muscle | SE_26730 | chr1:202003201-202004852 | Esophagus | SE_27624 | chr1:202002753-202007729 | Fetal_Intestine | SE_28545 | chr1:202002635-202005490 | Fetal_Intestine_Large | SE_31432 | chr1:202003030-202004833 | Gastric | SE_31432 | chr1:202005212-202005566 | Gastric | SE_33417 | chr1:202002752-202008344 | H2171 | SE_33792 | chr1:202002877-202005297 | HCC1954 | SE_34304 | chr1:202003057-202005125 | HCT-116 | SE_34741 | chr1:202002989-202005297 | HeLa | SE_41626 | chr1:202003359-202004353 | LNCaP | SE_43434 | chr1:202002760-202004009 | MCF-7 | SE_43434 | chr1:202004034-202004676 | MCF-7 | SE_50066 | chr1:202002922-202004883 | Sigmoid_Colon | SE_52354 | chr1:202003018-202004869 | Small_Intestine | SE_56834 | chr1:202002917-202004651 | VACO_400 | SE_57376 | chr1:202003233-202004124 | VACO_503 | SE_57376 | chr1:202004143-202004423 | VACO_503 | SE_57945 | chr1:202003251-202004112 | VACO_9m | SE_57945 | chr1:202004146-202004634 | VACO_9m | SE_65333 | chr1:202002930-202005541 | Pancreatic_islets | SE_67013 | chr1:202002752-202008344 | H2171 |
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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 |
GH01I202033 | chr1 | 202002815 | 202007566 |
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Enhancer Sequence | AATTGTAACC CATTGCCCAC CCTAGCCCTG CCCGCCTTCC TATCTTCTTT CTTGGTTTTA 60 TTTTTCTCCA TAGCATTTAT CATGCTCAGA CACACAAAAT ATTTATCTAT TTTTGCTGTT 120 TGTAATTGTC TTTCTCCCCC CACTAAAATG AACACTCCGT GAGGGCATGG CATTTTGCCT 180 GCTTTGCTCA CAATGTGTAT CCCACTGAAG ACATCCAATA AACAATTTAT CGAATAAATG 240 AATGCATCTA CCTGATACCT CATCAAGAAA TTGATGACCA CTAATTATCA TCTTTGAACC 300 TCTGATTGGT GACCTCTGGC AAGGCTGAGG ACCTTTAGCT CTAATCAATG GGCAAAAGGT 360 TGACCTCTTT GCTACTGATT GGCTTTTCCT TTTCATTATA CCCTTGGGCT GGATGGGGAA 420 GCTGTGTGAA TCAACGCTTC ATAAGCCTTC CTCTCTGAGA ACTAGGGCTT CCAAGGAATT 480 GGATATGAAA AGGCAGAGAG GAAGGAGGAG GATATGAGAT GCCAGACGGG GGAGGGTGGG 540 GGGGACAGGT CCCAGAAGAG GTCAGCTGGG ACCCAGGCAG GATGGCATTG TGGCTGCGGG 600 TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC CTCAGTCAGC CTTGACTGCT GGGTAATCCG 660 TGGTAAGTAC CCACTGCTCC TGCCTCAGCT TCCCCACCTC TCACATGTGG TTGATCCTCA 720 CAGCCATCTC TTGGGGTTGT TCTGAAGATG AAATGAGATC ATCTATGTAA GAAGCTGGCA 780 CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC GTATGGTCTG TCCTTATTTG GGGAATGGGG 840 GTGGAAGGCG CCCAGCAGGG CATGGGGCGT GGTATGGCAG AGCCAGGACT AAGGGTCTGT 900 AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG ATTTCCCATG TTCTCACCAT CTACAGAGTC 960 ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC TCACACTAGG TGGAGGAGCC 1020 CTCACAGATC TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA GCACCAGGGC CCTGGGACCA 1080 GCTGGTGGTT TCCACCAGAG CAGCCTCGGG GTGAATTTAG TCAGGAATGT GCCCTCAGCT 1140 CAAGAGAACC CTCCCCAACC TTCCACTCCC CATACCCACC CCCGACCGCA GGTTCCCCAC 1200 CCACCCGTGG CCTGGCCAGC AGCAACCTCC ACTAGCTCGC TAGCTCAGTG ACGGTGACGT 1260 CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT TCACCTCTCC CTGGGGAGAC 1320 TGGATTACCT CACCCTGGGA GCAGAGTGAA TGATTAACCA GCTTCATCCT GGAGGGCCTC 1380 AAAGGCCCGT CCTGGGGTGT AGGCCTACAG GGCAAGGGGC TGCATGGTCA CATACCCTAG 1440 TATGCGGGTT CACATACCCC AGCCGGGGCT GGGGTATGTG ACCGCCCCGT CCTTGGCCAC 1500 TGCCCTCTTA TCTGCATCAC TGCTCACAAG TGTCATAAAA ATTTGTCTAC AGCATATATA 1560 AATATACATA TGACGTGGAA GGCTTCCGAT GGCAAATAAC ATTTTCCATT TTGCCTAAGC 1620 TTGGGTGGCT TTTTATTCAT CTATTGTTGT TTTAAGTACA CATTTCCATC TAAACTTAGA 1680 TGTATGTTTA GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT CCCAGTACCT TTTAGGGGGT 1740 TGAGGCGGGT GGATCATTTG AGGCCAGCAG TTCAAGACCA GCCTGGCCAA CATGATGAAA 1800 CCTCGTCTCT ACTAAAAAAT ACAAAAATTA GCTGGGTGTG GTGGCAGGCG TCTGTAATCT 1860 CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CACTTGAACC TGGGAGGCGG AGGCTGCAGT 1920 GAGCTGAGAT TGCACCATTG CACTCCAGCC TGGGCAACAG AGTGACATTC TGTCTCAAAA 1980 ACAAAAACAA AAACAAAACA AAAAAAATAA ACTTAGATGT ATATTTAAAA ATTGCTTTTT 2040 ACCCCTGAAG GTCTCAGCAT CCTACCTGCT CTATTCATTA GTGTTTAGAT TACCCATGAC 2100 ACCAGAAGGA CTTCCCAACC CAGAAAAAGA TCCAGGAGTT GATATAAAAT ATAGAACTAC 2160 TATAATATTA GCAACTTGGA GCAGCAAGTT CTTGACTTGG GAAAGTAGGA ATTCCTCTCA 2220 TTAAGAGATG TTTGCCCACA GGGAATGCTG CATAGAAAAG AATTTGGCTG GAACTCTTTT 2280 TTTCCACTAT GACTCCATTC ACACTTGAAT TGTTTCCTTT TACTTTTCTT TTTCTTTCTT 2340 TCTTTTTTTT TTTTTTTTTT GAGACAGAGT CTCGCTCTGT CACCCAGGCT GGAGTGCAGT 2400 GGCATGATCT CAGCTCACTG CAACCTCCGC CTCTCAGGTT TAAGCGATTC TCCTGCCTCA 2460 GCCTCCAGAG TAGCTGGGAT TACAGGCGCG CACCACCATG CCCGGCTAAT TTTCACATTT 2520 TTAATAGAGA TGGGGTTTTG CCATGTTGGC CAGGCTGGTT TTGAACTGCT GACTTCAACT 2580 GATCCACCTG TCTGGGTCTC CCAAAGTGCT GGGATTACAG GCGTGAACAC AGCATGTTTC 2640 CGTTTTCAAA ATAAGATATG TCCTAATTGC TGTGAATTTT TAAAAGAGAA TTATTTTCCA 2700 TGACACATTC 2710
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