Tag | Content |
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EnhancerAtlas ID | HS118-15575 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr5:156937970-156940440 |
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 | CTTGGTAATC TTCAGGGTTT TGTCCAAACC AGAGATCCTG AAATTCTATA CCCAAGATCT 60 GACTCGACCT CCTCGAGGCT AGAGCTACAT CTAATCTTTA TGATCTGGCA TTTTTCACCT 120 CATACAAATA TAAGCAGGAG GAGGGTTTTC TTTAAAGCTA AACCACTGGA AGGTGTGGAT 180 ACAACGGGTT CTTTGATGGG TCCACCCTAC AAATACTGAG CCAGTGACTT AATAAAAAGC 240 CCCATGTATG GAGAGGACAT AATGAGCAGG AGATACCATC TTTATCCAAA ATTGGTAGGT 300 ACTGCCCCAG CTGAAAAGAA TAATCATAGC ACCAACATTT TTCCACCACT TTTTACGTAC 360 TAGGCACTGA GGCTTAGAGA AGTTAAGGAA CTTGCCCAAA GTCTCAGCAA GAAGATGGTG 420 GAGCCAGGAT GAAGGCCCAA ATTACAACCT CAGAGCCTAT TTGTGACCCT TTACTACTTC 480 AGTGCTGCAG TACCTACACA TCCAGATAAT CCACTCGCTC CAAGAAACGC TGGTCAAGAT 540 GGGCTCCAGA TTCAGTGAAA TATCAGTTTA TTTCAACAGA AATTTTGATT TTTCTGTTTT 600 GTGCCAGTTC AATCGTTACA GAAAATAAAA GGTTCAGATT CCAATTTGAA TTTGCTTTAC 660 TAGGGAGCTT TTGAAGGAAG TAAACTTGGC TTTTTTTCAC AGTTACAGAA AAACATTTTG 720 GATTGGGTTC ATGACTCAGC ACGAGTCCAA TTCATTCCAG TTTTAGTTCA ACAATAGTTC 780 AGTTCAAGTA GCTAGGTCAG CAAGCTCCAG AGAAGTGGGC GTGGCTTCCC TTACCCGCCA 840 GGAGTGACTA ACACCAGCCG CGAGGAGAGA GCCAAGACGG CTGCACAGGA TGCATGGGCC 900 ACCCAGGCTT AGGGCTTTCA GTAAGGACTG GGGCTTGCTG GTGCCTCTCT TCTCCCTTCA 960 CTTGTCACCA GCGCCCTTGG TTCCATCACA TACCCCACAG AGGGGATACC CAGCCAAGTC 1020 CGAACCTGCC AGGTCTCCAA ACAATAGATG TCACATGGGG GAAAGCAGAG TCAGCCTCCC 1080 ATATTCTCCC CAGGGAAACA AGCTTCCCTT GTTTTCCCAG ATGTCAAATG TTTGGGTTGT 1140 AGGATTATTT AAATGTTATT CTTGAGTGAG TCAGGAGCTA GAGGGAGGAC TGGACTGTGT 1200 CCCTAGAGTC TGTCCTTCCA GGAAATGCCA GTGTTTGACT TTCACCTGTC ACTGACCACT 1260 GACCTTTGTT TCCAGAGCCA TCTAGGGCAG AAAAAAACCA TGGGCATGGA AACTGCCATC 1320 TGATGACTTC AGAACTAATA CATTTGCCTA TTAATCCCTA AAACATATTT TAAGTGATCT 1380 CCTATATTCT CTAGTGTTTA GGAAAAAATG ATTTTCCCTT TAGACCTGGA ATTCATGAAT 1440 CCCTAGCAGG CCCAAAGTTA AGCTTCATCA ATGTTATGAG TATTCTAAAA TTGTGCAATA 1500 AACGTTACCA GATTCTCAAA GAGACTTTTG ATCCCAAACA CATGAAAAAC TACTTTTAAA 1560 AACTATATAC TACTAGCCTA CCAAGAGGCT ACTGTCATTC TAGGTTACCT ATTCTGCATT 1620 TTGTACTATA ACAAATATCT TCTTTCATAT ACACAATGTA CTTCCAAGTC CCAGACCAGC 1680 CCGTTCTAGT AAAATTCAAA AATGTAGGTA TTTCCGAAGA GCATCTTGTA AAAGGTCCTG 1740 ACCTAGGAAA GTTAACCACT GCACATCCTT CCTAAGAGAC AAGACATAAT TTTAGGATAA 1800 CTTTACAGAT GGAGACTTTA TAGATTAGCC CCAAGCAACC CACTTCTCAG ACAATCCGCT 1860 TCTCAAGCAA CCCACTTCTC AAACAGCCCA CTTCTCAACT TTTAAGGCTG TGTGTCTTTC 1920 CCACCCTGAC CTACCTCAAT TCCCTCCTAA GTCAGAGAAT CCCTGGGCTT TGTATCTGGA 1980 AGGAACCTTA AAGAACCTTA AAGGATTCTT AAACTGGGCT CTTCCATGCC CCAAGCTGCT 2040 CGGGAGCCAC TGCAGGGGTA AGAGGAAGGG GTCAGAAGGA CAGTGTTCTG GGTCCTCACC 2100 CCAGCTCCCA CTTAGAGCAG TCTGTTTTCA TCTAACTTTT ATAGTAGATA TTGGCATAAG 2160 ATTTCATTTT TTAAAATTCC ACCAGGAAAA TAAAAATAAC AAAAAAAAAC CACACATTGA 2220 TTTACGACAG CCTTTCTATT TATAAGCTGA AAACAGAACA AAAGAAAAAA AAATGCAACA 2280 CAAAGAAAAT GAGTTACTTG CCTAAGGGTA CGTAGTTCAG GGCTCTGTCA TGACCGCCCT 2340 GGGCCTCTAT GGCACTGCTC ATTCCCTTTC AGAAGATGGC TGGGGCAGCC AATCCAGCAG 2400 AAGGCAGCTC CAGTGCCCTT GGAAGTGCTG GCACCTGGCA CCTTTCCCAC AAAGTACACA 2460 CCTGGTCTCA 2470
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