Tag | Content |
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EnhancerAtlas ID | HS161-12765 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr5:156937900-156940440 |
Target genes | Number: 13 | Name | Ensembl ID |
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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) |
KLF13 | MA0657.1 | chr5:156938779-156938797 | GAGAAGTGGGCGTGGCTT | - | 6.7 | KLF14 | MA0740.1 | chr5:156938782-156938796 | AAGTGGGCGTGGCT | - | 7.22 | NFE2L1 | MA0089.2 | chr5:156938698-156938713 | TCATGACTCAGCACG | + | 6.39 | Nfe2l2 | MA0150.2 | chr5:156938696-156938711 | GTTCATGACTCAGCA | + | 6.08 | SP1 | MA0079.4 | chr5:156938783-156938798 | AGTGGGCGTGGCTTC | - | 7.75 | SP3 | MA0746.2 | chr5:156938783-156938796 | AGTGGGCGTGGCT | - | 6.54 | SP4 | MA0685.1 | chr5:156938781-156938798 | GAAGTGGGCGTGGCTTC | - | 8.33 | SP8 | MA0747.1 | chr5:156938783-156938795 | AGTGGGCGTGGC | - | 7.22 | Stat4 | MA0518.1 | chr5:156939184-156939198 | CTTCCAGGAAATGC | + | 6.29 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_10243 | chr5:156938517-156940062 | CD19_Primary | SE_10863 | chr5:156909781-156978888 | CD20 | SE_25805 | chr5:156937459-156940635 | Duodenum_Smooth_Muscle | SE_27121 | chr5:156937942-156939406 | Esophagus | SE_30832 | chr5:156937914-156939656 | Fetal_Muscle | SE_36955 | chr5:156931578-156947133 | HSMMtube | SE_40934 | chr5:156937927-156939997 | Left_Ventricle | SE_42416 | chr5:156938057-156939558 | Lung | SE_46096 | chr5:156937729-156940502 | Osteoblasts | SE_48834 | chr5:156938047-156939349 | Right_Atrium | SE_50178 | chr5:156937844-156939424 | Sigmoid_Colon | SE_51718 | chr5:156937592-156941329 | Skeletal_Muscle_Myoblast | SE_52470 | chr5:156937841-156938690 | Small_Intestine | SE_52470 | chr5:156938691-156939525 | Small_Intestine | SE_53856 | chr5:156937978-156939461 | Spleen | SE_54595 | chr5:156937459-156940544 | Stomach_Smooth_Muscle | SE_63503 | chr5:156937579-156941330 | HSMM |
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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 |
GH05I157510 | chr5 | 156937713 | 156941293 |
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Enhancer Sequence | CATCCCTGGA TAGTCTCAGG TTTTGTCAAG GATGGAATAA GCAGGTTGCA AGCAATAGAC 60 TACAGACGTT CTTGGTAATC TTCAGGGTTT TGTCCAAACC AGAGATCCTG AAATTCTATA 120 CCCAAGATCT GACTCGACCT CCTCGAGGCT AGAGCTACAT CTAATCTTTA TGATCTGGCA 180 TTTTTCACCT CATACAAATA TAAGCAGGAG GAGGGTTTTC TTTAAAGCTA AACCACTGGA 240 AGGTGTGGAT ACAACGGGTT CTTTGATGGG TCCACCCTAC AAATACTGAG CCAGTGACTT 300 AATAAAAAGC CCCATGTATG GAGAGGACAT AATGAGCAGG AGATACCATC TTTATCCAAA 360 ATTGGTAGGT ACTGCCCCAG CTGAAAAGAA TAATCATAGC ACCAACATTT TTCCACCACT 420 TTTTACGTAC TAGGCACTGA GGCTTAGAGA AGTTAAGGAA CTTGCCCAAA GTCTCAGCAA 480 GAAGATGGTG GAGCCAGGAT GAAGGCCCAA ATTACAACCT CAGAGCCTAT TTGTGACCCT 540 TTACTACTTC AGTGCTGCAG TACCTACACA TCCAGATAAT CCACTCGCTC CAAGAAACGC 600 TGGTCAAGAT GGGCTCCAGA TTCAGTGAAA TATCAGTTTA TTTCAACAGA AATTTTGATT 660 TTTCTGTTTT GTGCCAGTTC AATCGTTACA GAAAATAAAA GGTTCAGATT CCAATTTGAA 720 TTTGCTTTAC TAGGGAGCTT TTGAAGGAAG TAAACTTGGC TTTTTTTCAC AGTTACAGAA 780 AAACATTTTG GATTGGGTTC ATGACTCAGC ACGAGTCCAA TTCATTCCAG TTTTAGTTCA 840 ACAATAGTTC AGTTCAAGTA GCTAGGTCAG CAAGCTCCAG AGAAGTGGGC GTGGCTTCCC 900 TTACCCGCCA GGAGTGACTA ACACCAGCCG CGAGGAGAGA GCCAAGACGG CTGCACAGGA 960 TGCATGGGCC ACCCAGGCTT AGGGCTTTCA GTAAGGACTG GGGCTTGCTG GTGCCTCTCT 1020 TCTCCCTTCA CTTGTCACCA GCGCCCTTGG TTCCATCACA TACCCCACAG AGGGGATACC 1080 CAGCCAAGTC CGAACCTGCC AGGTCTCCAA ACAATAGATG TCACATGGGG GAAAGCAGAG 1140 TCAGCCTCCC ATATTCTCCC CAGGGAAACA AGCTTCCCTT GTTTTCCCAG ATGTCAAATG 1200 TTTGGGTTGT AGGATTATTT AAATGTTATT CTTGAGTGAG TCAGGAGCTA GAGGGAGGAC 1260 TGGACTGTGT CCCTAGAGTC TGTCCTTCCA GGAAATGCCA GTGTTTGACT TTCACCTGTC 1320 ACTGACCACT GACCTTTGTT TCCAGAGCCA TCTAGGGCAG AAAAAAACCA TGGGCATGGA 1380 AACTGCCATC TGATGACTTC AGAACTAATA CATTTGCCTA TTAATCCCTA AAACATATTT 1440 TAAGTGATCT CCTATATTCT CTAGTGTTTA GGAAAAAATG ATTTTCCCTT TAGACCTGGA 1500 ATTCATGAAT CCCTAGCAGG CCCAAAGTTA AGCTTCATCA ATGTTATGAG TATTCTAAAA 1560 TTGTGCAATA AACGTTACCA GATTCTCAAA GAGACTTTTG ATCCCAAACA CATGAAAAAC 1620 TACTTTTAAA AACTATATAC TACTAGCCTA CCAAGAGGCT ACTGTCATTC TAGGTTACCT 1680 ATTCTGCATT TTGTACTATA ACAAATATCT TCTTTCATAT ACACAATGTA CTTCCAAGTC 1740 CCAGACCAGC CCGTTCTAGT AAAATTCAAA AATGTAGGTA TTTCCGAAGA GCATCTTGTA 1800 AAAGGTCCTG ACCTAGGAAA GTTAACCACT GCACATCCTT CCTAAGAGAC AAGACATAAT 1860 TTTAGGATAA CTTTACAGAT GGAGACTTTA TAGATTAGCC CCAAGCAACC CACTTCTCAG 1920 ACAATCCGCT TCTCAAGCAA CCCACTTCTC AAACAGCCCA CTTCTCAACT TTTAAGGCTG 1980 TGTGTCTTTC CCACCCTGAC CTACCTCAAT TCCCTCCTAA GTCAGAGAAT CCCTGGGCTT 2040 TGTATCTGGA AGGAACCTTA AAGAACCTTA AAGGATTCTT AAACTGGGCT CTTCCATGCC 2100 CCAAGCTGCT CGGGAGCCAC TGCAGGGGTA AGAGGAAGGG GTCAGAAGGA CAGTGTTCTG 2160 GGTCCTCACC CCAGCTCCCA CTTAGAGCAG TCTGTTTTCA TCTAACTTTT ATAGTAGATA 2220 TTGGCATAAG ATTTCATTTT TTAAAATTCC ACCAGGAAAA TAAAAATAAC AAAAAAAAAC 2280 CACACATTGA TTTACGACAG CCTTTCTATT TATAAGCTGA AAACAGAACA AAAGAAAAAA 2340 AAATGCAACA CAAAGAAAAT GAGTTACTTG CCTAAGGGTA CGTAGTTCAG GGCTCTGTCA 2400 TGACCGCCCT GGGCCTCTAT GGCACTGCTC ATTCCCTTTC AGAAGATGGC TGGGGCAGCC 2460 AATCCAGCAG AAGGCAGCTC CAGTGCCCTT GGAAGTGCTG GCACCTGGCA CCTTTCCCAC 2520 AAAGTACACA CCTGGTCTCA 2540
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