Tag | Content |
---|
EnhancerAtlas ID | HS092-32558 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr5:156937380-156940440 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| 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 |
|
| 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 |
|
Enhancer Sequence | CTGAGGCAGG AGAATCACTT GAACCCGGGA GGCAGGGGTT GCGGTGAGCC AAGATTGTGC 60 CATTGCACTC CAGCCTGGGC CACGGGCGAA ACTCCGTCTC AAAAAAAAAT AAAAATAAAA 120 TAAAGCCATC GCCATCATCC AGTGTTAGAA TATTTTCATC ACATCGGTGA GATCCCTCAT 180 GTCTATTGAT AGTCATTTCC CATTCTCACC CTCAGCCCAG GCAACCGTGC ATCTACTTTG 240 TTTCTATTCT GCCTTTTCTG GACATTTGTT TTACAATATG TGGTTTTGTG TGTCTGGCTT 300 CTCTCACTTA CCATAATGTT TTTGAGATGT ATCCATGTGT TAGAGTGTAT TCGTTTATGA 360 TTTCTCTTTA TTGCTGAATA ATATTCTTTC GTATGGATAT ACCAAATTAT ATTAATACAT 420 GGATATTTTA TTATAAAATG TCTCCCACTC ATTTTGGAAG TAAATGAGTA TAAATGACAT 480 AAAAGTGCAC AGATATGCTT ACTCTTCAAA TTTTCTTCCC CATCCCTGGA TAGTCTCAGG 540 TTTTGTCAAG GATGGAATAA GCAGGTTGCA AGCAATAGAC TACAGACGTT CTTGGTAATC 600 TTCAGGGTTT TGTCCAAACC AGAGATCCTG AAATTCTATA CCCAAGATCT GACTCGACCT 660 CCTCGAGGCT AGAGCTACAT CTAATCTTTA TGATCTGGCA TTTTTCACCT CATACAAATA 720 TAAGCAGGAG GAGGGTTTTC TTTAAAGCTA AACCACTGGA AGGTGTGGAT ACAACGGGTT 780 CTTTGATGGG TCCACCCTAC AAATACTGAG CCAGTGACTT AATAAAAAGC CCCATGTATG 840 GAGAGGACAT AATGAGCAGG AGATACCATC TTTATCCAAA ATTGGTAGGT ACTGCCCCAG 900 CTGAAAAGAA TAATCATAGC ACCAACATTT TTCCACCACT TTTTACGTAC TAGGCACTGA 960 GGCTTAGAGA AGTTAAGGAA CTTGCCCAAA GTCTCAGCAA GAAGATGGTG GAGCCAGGAT 1020 GAAGGCCCAA ATTACAACCT CAGAGCCTAT TTGTGACCCT TTACTACTTC AGTGCTGCAG 1080 TACCTACACA TCCAGATAAT CCACTCGCTC CAAGAAACGC TGGTCAAGAT GGGCTCCAGA 1140 TTCAGTGAAA TATCAGTTTA TTTCAACAGA AATTTTGATT TTTCTGTTTT GTGCCAGTTC 1200 AATCGTTACA GAAAATAAAA GGTTCAGATT CCAATTTGAA TTTGCTTTAC TAGGGAGCTT 1260 TTGAAGGAAG TAAACTTGGC TTTTTTTCAC AGTTACAGAA AAACATTTTG GATTGGGTTC 1320 ATGACTCAGC ACGAGTCCAA TTCATTCCAG TTTTAGTTCA ACAATAGTTC AGTTCAAGTA 1380 GCTAGGTCAG CAAGCTCCAG AGAAGTGGGC GTGGCTTCCC TTACCCGCCA GGAGTGACTA 1440 ACACCAGCCG CGAGGAGAGA GCCAAGACGG CTGCACAGGA TGCATGGGCC ACCCAGGCTT 1500 AGGGCTTTCA GTAAGGACTG GGGCTTGCTG GTGCCTCTCT TCTCCCTTCA CTTGTCACCA 1560 GCGCCCTTGG TTCCATCACA TACCCCACAG AGGGGATACC CAGCCAAGTC CGAACCTGCC 1620 AGGTCTCCAA ACAATAGATG TCACATGGGG GAAAGCAGAG TCAGCCTCCC ATATTCTCCC 1680 CAGGGAAACA AGCTTCCCTT GTTTTCCCAG ATGTCAAATG TTTGGGTTGT AGGATTATTT 1740 AAATGTTATT CTTGAGTGAG TCAGGAGCTA GAGGGAGGAC TGGACTGTGT CCCTAGAGTC 1800 TGTCCTTCCA GGAAATGCCA GTGTTTGACT TTCACCTGTC ACTGACCACT GACCTTTGTT 1860 TCCAGAGCCA TCTAGGGCAG AAAAAAACCA TGGGCATGGA AACTGCCATC TGATGACTTC 1920 AGAACTAATA CATTTGCCTA TTAATCCCTA AAACATATTT TAAGTGATCT CCTATATTCT 1980 CTAGTGTTTA GGAAAAAATG ATTTTCCCTT TAGACCTGGA ATTCATGAAT CCCTAGCAGG 2040 CCCAAAGTTA AGCTTCATCA ATGTTATGAG TATTCTAAAA TTGTGCAATA AACGTTACCA 2100 GATTCTCAAA GAGACTTTTG ATCCCAAACA CATGAAAAAC TACTTTTAAA AACTATATAC 2160 TACTAGCCTA CCAAGAGGCT ACTGTCATTC TAGGTTACCT ATTCTGCATT TTGTACTATA 2220 ACAAATATCT TCTTTCATAT ACACAATGTA CTTCCAAGTC CCAGACCAGC CCGTTCTAGT 2280 AAAATTCAAA AATGTAGGTA TTTCCGAAGA GCATCTTGTA AAAGGTCCTG ACCTAGGAAA 2340 GTTAACCACT GCACATCCTT CCTAAGAGAC AAGACATAAT TTTAGGATAA CTTTACAGAT 2400 GGAGACTTTA TAGATTAGCC CCAAGCAACC CACTTCTCAG ACAATCCGCT TCTCAAGCAA 2460 CCCACTTCTC AAACAGCCCA CTTCTCAACT TTTAAGGCTG TGTGTCTTTC CCACCCTGAC 2520 CTACCTCAAT TCCCTCCTAA GTCAGAGAAT CCCTGGGCTT TGTATCTGGA AGGAACCTTA 2580 AAGAACCTTA AAGGATTCTT AAACTGGGCT CTTCCATGCC CCAAGCTGCT CGGGAGCCAC 2640 TGCAGGGGTA AGAGGAAGGG GTCAGAAGGA CAGTGTTCTG GGTCCTCACC CCAGCTCCCA 2700 CTTAGAGCAG TCTGTTTTCA TCTAACTTTT ATAGTAGATA TTGGCATAAG ATTTCATTTT 2760 TTAAAATTCC ACCAGGAAAA TAAAAATAAC AAAAAAAAAC CACACATTGA TTTACGACAG 2820 CCTTTCTATT TATAAGCTGA AAACAGAACA AAAGAAAAAA AAATGCAACA CAAAGAAAAT 2880 GAGTTACTTG CCTAAGGGTA CGTAGTTCAG GGCTCTGTCA TGACCGCCCT GGGCCTCTAT 2940 GGCACTGCTC ATTCCCTTTC AGAAGATGGC TGGGGCAGCC AATCCAGCAG AAGGCAGCTC 3000 CAGTGCCCTT GGAAGTGCTG GCACCTGGCA CCTTTCCCAC AAAGTACACA CCTGGTCTCA 3060
|