Tag | Content |
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EnhancerAtlas ID | HS098-46839 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:156937810-156940440 |
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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I157510 | chr5 | 156937713 | 156941293 |
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Enhancer Sequence | TTATAAAATG TCTCCCACTC ATTTTGGAAG TAAATGAGTA TAAATGACAT AAAAGTGCAC 60 AGATATGCTT ACTCTTCAAA TTTTCTTCCC CATCCCTGGA TAGTCTCAGG TTTTGTCAAG 120 GATGGAATAA GCAGGTTGCA AGCAATAGAC TACAGACGTT CTTGGTAATC TTCAGGGTTT 180 TGTCCAAACC AGAGATCCTG AAATTCTATA CCCAAGATCT GACTCGACCT CCTCGAGGCT 240 AGAGCTACAT CTAATCTTTA TGATCTGGCA TTTTTCACCT CATACAAATA TAAGCAGGAG 300 GAGGGTTTTC TTTAAAGCTA AACCACTGGA AGGTGTGGAT ACAACGGGTT CTTTGATGGG 360 TCCACCCTAC AAATACTGAG CCAGTGACTT AATAAAAAGC CCCATGTATG GAGAGGACAT 420 AATGAGCAGG AGATACCATC TTTATCCAAA ATTGGTAGGT ACTGCCCCAG CTGAAAAGAA 480 TAATCATAGC ACCAACATTT TTCCACCACT TTTTACGTAC TAGGCACTGA GGCTTAGAGA 540 AGTTAAGGAA CTTGCCCAAA GTCTCAGCAA GAAGATGGTG GAGCCAGGAT GAAGGCCCAA 600 ATTACAACCT CAGAGCCTAT TTGTGACCCT TTACTACTTC AGTGCTGCAG TACCTACACA 660 TCCAGATAAT CCACTCGCTC CAAGAAACGC TGGTCAAGAT GGGCTCCAGA TTCAGTGAAA 720 TATCAGTTTA TTTCAACAGA AATTTTGATT TTTCTGTTTT GTGCCAGTTC AATCGTTACA 780 GAAAATAAAA GGTTCAGATT CCAATTTGAA TTTGCTTTAC TAGGGAGCTT TTGAAGGAAG 840 TAAACTTGGC TTTTTTTCAC AGTTACAGAA AAACATTTTG GATTGGGTTC ATGACTCAGC 900 ACGAGTCCAA TTCATTCCAG TTTTAGTTCA ACAATAGTTC AGTTCAAGTA GCTAGGTCAG 960 CAAGCTCCAG AGAAGTGGGC GTGGCTTCCC TTACCCGCCA GGAGTGACTA ACACCAGCCG 1020 CGAGGAGAGA GCCAAGACGG CTGCACAGGA TGCATGGGCC ACCCAGGCTT AGGGCTTTCA 1080 GTAAGGACTG GGGCTTGCTG GTGCCTCTCT TCTCCCTTCA CTTGTCACCA GCGCCCTTGG 1140 TTCCATCACA TACCCCACAG AGGGGATACC CAGCCAAGTC CGAACCTGCC AGGTCTCCAA 1200 ACAATAGATG TCACATGGGG GAAAGCAGAG TCAGCCTCCC ATATTCTCCC CAGGGAAACA 1260 AGCTTCCCTT GTTTTCCCAG ATGTCAAATG TTTGGGTTGT AGGATTATTT AAATGTTATT 1320 CTTGAGTGAG TCAGGAGCTA GAGGGAGGAC TGGACTGTGT CCCTAGAGTC TGTCCTTCCA 1380 GGAAATGCCA GTGTTTGACT TTCACCTGTC ACTGACCACT GACCTTTGTT TCCAGAGCCA 1440 TCTAGGGCAG AAAAAAACCA TGGGCATGGA AACTGCCATC TGATGACTTC AGAACTAATA 1500 CATTTGCCTA TTAATCCCTA AAACATATTT TAAGTGATCT CCTATATTCT CTAGTGTTTA 1560 GGAAAAAATG ATTTTCCCTT TAGACCTGGA ATTCATGAAT CCCTAGCAGG CCCAAAGTTA 1620 AGCTTCATCA ATGTTATGAG TATTCTAAAA TTGTGCAATA AACGTTACCA GATTCTCAAA 1680 GAGACTTTTG ATCCCAAACA CATGAAAAAC TACTTTTAAA AACTATATAC TACTAGCCTA 1740 CCAAGAGGCT ACTGTCATTC TAGGTTACCT ATTCTGCATT TTGTACTATA ACAAATATCT 1800 TCTTTCATAT ACACAATGTA CTTCCAAGTC CCAGACCAGC CCGTTCTAGT AAAATTCAAA 1860 AATGTAGGTA TTTCCGAAGA GCATCTTGTA AAAGGTCCTG ACCTAGGAAA GTTAACCACT 1920 GCACATCCTT CCTAAGAGAC AAGACATAAT TTTAGGATAA CTTTACAGAT GGAGACTTTA 1980 TAGATTAGCC CCAAGCAACC CACTTCTCAG ACAATCCGCT TCTCAAGCAA CCCACTTCTC 2040 AAACAGCCCA CTTCTCAACT TTTAAGGCTG TGTGTCTTTC CCACCCTGAC CTACCTCAAT 2100 TCCCTCCTAA GTCAGAGAAT CCCTGGGCTT TGTATCTGGA AGGAACCTTA AAGAACCTTA 2160 AAGGATTCTT AAACTGGGCT CTTCCATGCC CCAAGCTGCT CGGGAGCCAC TGCAGGGGTA 2220 AGAGGAAGGG GTCAGAAGGA CAGTGTTCTG GGTCCTCACC CCAGCTCCCA CTTAGAGCAG 2280 TCTGTTTTCA TCTAACTTTT ATAGTAGATA TTGGCATAAG ATTTCATTTT TTAAAATTCC 2340 ACCAGGAAAA TAAAAATAAC AAAAAAAAAC CACACATTGA TTTACGACAG CCTTTCTATT 2400 TATAAGCTGA AAACAGAACA AAAGAAAAAA AAATGCAACA CAAAGAAAAT GAGTTACTTG 2460 CCTAAGGGTA CGTAGTTCAG GGCTCTGTCA TGACCGCCCT GGGCCTCTAT GGCACTGCTC 2520 ATTCCCTTTC AGAAGATGGC TGGGGCAGCC AATCCAGCAG AAGGCAGCTC CAGTGCCCTT 2580 GGAAGTGCTG GCACCTGGCA CCTTTCCCAC AAAGTACACA CCTGGTCTCA 2630
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