Tag | Content |
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EnhancerAtlas ID | HS055-06994 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr5:156937800-156940440 |
Target genes | |
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 | GGATATTTTA TTATAAAATG TCTCCCACTC ATTTTGGAAG TAAATGAGTA TAAATGACAT 60 AAAAGTGCAC AGATATGCTT ACTCTTCAAA TTTTCTTCCC CATCCCTGGA TAGTCTCAGG 120 TTTTGTCAAG GATGGAATAA GCAGGTTGCA AGCAATAGAC TACAGACGTT CTTGGTAATC 180 TTCAGGGTTT TGTCCAAACC AGAGATCCTG AAATTCTATA CCCAAGATCT GACTCGACCT 240 CCTCGAGGCT AGAGCTACAT CTAATCTTTA TGATCTGGCA TTTTTCACCT CATACAAATA 300 TAAGCAGGAG GAGGGTTTTC TTTAAAGCTA AACCACTGGA AGGTGTGGAT ACAACGGGTT 360 CTTTGATGGG TCCACCCTAC AAATACTGAG CCAGTGACTT AATAAAAAGC CCCATGTATG 420 GAGAGGACAT AATGAGCAGG AGATACCATC TTTATCCAAA ATTGGTAGGT ACTGCCCCAG 480 CTGAAAAGAA TAATCATAGC ACCAACATTT TTCCACCACT TTTTACGTAC TAGGCACTGA 540 GGCTTAGAGA AGTTAAGGAA CTTGCCCAAA GTCTCAGCAA GAAGATGGTG GAGCCAGGAT 600 GAAGGCCCAA ATTACAACCT CAGAGCCTAT TTGTGACCCT TTACTACTTC AGTGCTGCAG 660 TACCTACACA TCCAGATAAT CCACTCGCTC CAAGAAACGC TGGTCAAGAT GGGCTCCAGA 720 TTCAGTGAAA TATCAGTTTA TTTCAACAGA AATTTTGATT TTTCTGTTTT GTGCCAGTTC 780 AATCGTTACA GAAAATAAAA GGTTCAGATT CCAATTTGAA TTTGCTTTAC TAGGGAGCTT 840 TTGAAGGAAG TAAACTTGGC TTTTTTTCAC AGTTACAGAA AAACATTTTG GATTGGGTTC 900 ATGACTCAGC ACGAGTCCAA TTCATTCCAG TTTTAGTTCA ACAATAGTTC AGTTCAAGTA 960 GCTAGGTCAG CAAGCTCCAG AGAAGTGGGC GTGGCTTCCC TTACCCGCCA GGAGTGACTA 1020 ACACCAGCCG CGAGGAGAGA GCCAAGACGG CTGCACAGGA TGCATGGGCC ACCCAGGCTT 1080 AGGGCTTTCA GTAAGGACTG GGGCTTGCTG GTGCCTCTCT TCTCCCTTCA CTTGTCACCA 1140 GCGCCCTTGG TTCCATCACA TACCCCACAG AGGGGATACC CAGCCAAGTC CGAACCTGCC 1200 AGGTCTCCAA ACAATAGATG TCACATGGGG GAAAGCAGAG TCAGCCTCCC ATATTCTCCC 1260 CAGGGAAACA AGCTTCCCTT GTTTTCCCAG ATGTCAAATG TTTGGGTTGT AGGATTATTT 1320 AAATGTTATT CTTGAGTGAG TCAGGAGCTA GAGGGAGGAC TGGACTGTGT CCCTAGAGTC 1380 TGTCCTTCCA GGAAATGCCA GTGTTTGACT TTCACCTGTC ACTGACCACT GACCTTTGTT 1440 TCCAGAGCCA TCTAGGGCAG AAAAAAACCA TGGGCATGGA AACTGCCATC TGATGACTTC 1500 AGAACTAATA CATTTGCCTA TTAATCCCTA AAACATATTT TAAGTGATCT CCTATATTCT 1560 CTAGTGTTTA GGAAAAAATG ATTTTCCCTT TAGACCTGGA ATTCATGAAT CCCTAGCAGG 1620 CCCAAAGTTA AGCTTCATCA ATGTTATGAG TATTCTAAAA TTGTGCAATA AACGTTACCA 1680 GATTCTCAAA GAGACTTTTG ATCCCAAACA CATGAAAAAC TACTTTTAAA AACTATATAC 1740 TACTAGCCTA CCAAGAGGCT ACTGTCATTC TAGGTTACCT ATTCTGCATT TTGTACTATA 1800 ACAAATATCT TCTTTCATAT ACACAATGTA CTTCCAAGTC CCAGACCAGC CCGTTCTAGT 1860 AAAATTCAAA AATGTAGGTA TTTCCGAAGA GCATCTTGTA AAAGGTCCTG ACCTAGGAAA 1920 GTTAACCACT GCACATCCTT CCTAAGAGAC AAGACATAAT TTTAGGATAA CTTTACAGAT 1980 GGAGACTTTA TAGATTAGCC CCAAGCAACC CACTTCTCAG ACAATCCGCT TCTCAAGCAA 2040 CCCACTTCTC AAACAGCCCA CTTCTCAACT TTTAAGGCTG TGTGTCTTTC CCACCCTGAC 2100 CTACCTCAAT TCCCTCCTAA GTCAGAGAAT CCCTGGGCTT TGTATCTGGA AGGAACCTTA 2160 AAGAACCTTA AAGGATTCTT AAACTGGGCT CTTCCATGCC CCAAGCTGCT CGGGAGCCAC 2220 TGCAGGGGTA AGAGGAAGGG GTCAGAAGGA CAGTGTTCTG GGTCCTCACC CCAGCTCCCA 2280 CTTAGAGCAG TCTGTTTTCA TCTAACTTTT ATAGTAGATA TTGGCATAAG ATTTCATTTT 2340 TTAAAATTCC ACCAGGAAAA TAAAAATAAC AAAAAAAAAC CACACATTGA TTTACGACAG 2400 CCTTTCTATT TATAAGCTGA AAACAGAACA AAAGAAAAAA AAATGCAACA CAAAGAAAAT 2460 GAGTTACTTG CCTAAGGGTA CGTAGTTCAG GGCTCTGTCA TGACCGCCCT GGGCCTCTAT 2520 GGCACTGCTC ATTCCCTTTC AGAAGATGGC TGGGGCAGCC AATCCAGCAG AAGGCAGCTC 2580 CAGTGCCCTT GGAAGTGCTG GCACCTGGCA CCTTTCCCAC AAAGTACACA CCTGGTCTCA 2640
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