Tag | Content |
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EnhancerAtlas ID | HS078-13669 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr5:156937920-156940110 |
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 | TTTTGTCAAG GATGGAATAA GCAGGTTGCA AGCAATAGAC TACAGACGTT CTTGGTAATC 60 TTCAGGGTTT TGTCCAAACC AGAGATCCTG AAATTCTATA CCCAAGATCT GACTCGACCT 120 CCTCGAGGCT AGAGCTACAT CTAATCTTTA TGATCTGGCA TTTTTCACCT CATACAAATA 180 TAAGCAGGAG GAGGGTTTTC TTTAAAGCTA AACCACTGGA AGGTGTGGAT ACAACGGGTT 240 CTTTGATGGG TCCACCCTAC AAATACTGAG CCAGTGACTT AATAAAAAGC CCCATGTATG 300 GAGAGGACAT AATGAGCAGG AGATACCATC TTTATCCAAA ATTGGTAGGT ACTGCCCCAG 360 CTGAAAAGAA TAATCATAGC ACCAACATTT TTCCACCACT TTTTACGTAC TAGGCACTGA 420 GGCTTAGAGA AGTTAAGGAA CTTGCCCAAA GTCTCAGCAA GAAGATGGTG GAGCCAGGAT 480 GAAGGCCCAA ATTACAACCT CAGAGCCTAT TTGTGACCCT TTACTACTTC AGTGCTGCAG 540 TACCTACACA TCCAGATAAT CCACTCGCTC CAAGAAACGC TGGTCAAGAT GGGCTCCAGA 600 TTCAGTGAAA TATCAGTTTA TTTCAACAGA AATTTTGATT TTTCTGTTTT GTGCCAGTTC 660 AATCGTTACA GAAAATAAAA GGTTCAGATT CCAATTTGAA TTTGCTTTAC TAGGGAGCTT 720 TTGAAGGAAG TAAACTTGGC TTTTTTTCAC AGTTACAGAA AAACATTTTG GATTGGGTTC 780 ATGACTCAGC ACGAGTCCAA TTCATTCCAG TTTTAGTTCA ACAATAGTTC AGTTCAAGTA 840 GCTAGGTCAG CAAGCTCCAG AGAAGTGGGC GTGGCTTCCC TTACCCGCCA GGAGTGACTA 900 ACACCAGCCG CGAGGAGAGA GCCAAGACGG CTGCACAGGA TGCATGGGCC ACCCAGGCTT 960 AGGGCTTTCA GTAAGGACTG GGGCTTGCTG GTGCCTCTCT TCTCCCTTCA CTTGTCACCA 1020 GCGCCCTTGG TTCCATCACA TACCCCACAG AGGGGATACC CAGCCAAGTC CGAACCTGCC 1080 AGGTCTCCAA ACAATAGATG TCACATGGGG GAAAGCAGAG TCAGCCTCCC ATATTCTCCC 1140 CAGGGAAACA AGCTTCCCTT GTTTTCCCAG ATGTCAAATG TTTGGGTTGT AGGATTATTT 1200 AAATGTTATT CTTGAGTGAG TCAGGAGCTA GAGGGAGGAC TGGACTGTGT CCCTAGAGTC 1260 TGTCCTTCCA GGAAATGCCA GTGTTTGACT TTCACCTGTC ACTGACCACT GACCTTTGTT 1320 TCCAGAGCCA TCTAGGGCAG AAAAAAACCA TGGGCATGGA AACTGCCATC TGATGACTTC 1380 AGAACTAATA CATTTGCCTA TTAATCCCTA AAACATATTT TAAGTGATCT CCTATATTCT 1440 CTAGTGTTTA GGAAAAAATG ATTTTCCCTT TAGACCTGGA ATTCATGAAT CCCTAGCAGG 1500 CCCAAAGTTA AGCTTCATCA ATGTTATGAG TATTCTAAAA TTGTGCAATA AACGTTACCA 1560 GATTCTCAAA GAGACTTTTG ATCCCAAACA CATGAAAAAC TACTTTTAAA AACTATATAC 1620 TACTAGCCTA CCAAGAGGCT ACTGTCATTC TAGGTTACCT ATTCTGCATT TTGTACTATA 1680 ACAAATATCT TCTTTCATAT ACACAATGTA CTTCCAAGTC CCAGACCAGC CCGTTCTAGT 1740 AAAATTCAAA AATGTAGGTA TTTCCGAAGA GCATCTTGTA AAAGGTCCTG ACCTAGGAAA 1800 GTTAACCACT GCACATCCTT CCTAAGAGAC AAGACATAAT TTTAGGATAA CTTTACAGAT 1860 GGAGACTTTA TAGATTAGCC CCAAGCAACC CACTTCTCAG ACAATCCGCT TCTCAAGCAA 1920 CCCACTTCTC AAACAGCCCA CTTCTCAACT TTTAAGGCTG TGTGTCTTTC CCACCCTGAC 1980 CTACCTCAAT TCCCTCCTAA GTCAGAGAAT CCCTGGGCTT TGTATCTGGA AGGAACCTTA 2040 AAGAACCTTA AAGGATTCTT AAACTGGGCT CTTCCATGCC CCAAGCTGCT CGGGAGCCAC 2100 TGCAGGGGTA AGAGGAAGGG GTCAGAAGGA CAGTGTTCTG GGTCCTCACC CCAGCTCCCA 2160 CTTAGAGCAG TCTGTTTTCA TCTAACTTTT 2190
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