| Tag | Content |
|---|
EnhancerAtlas ID | HS091-39545 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:156937450-156940440 |
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 | CAGCCTGGGC CACGGGCGAA ACTCCGTCTC AAAAAAAAAT AAAAATAAAA TAAAGCCATC 60
GCCATCATCC AGTGTTAGAA TATTTTCATC ACATCGGTGA GATCCCTCAT GTCTATTGAT 120
AGTCATTTCC CATTCTCACC CTCAGCCCAG GCAACCGTGC ATCTACTTTG TTTCTATTCT 180
GCCTTTTCTG GACATTTGTT TTACAATATG TGGTTTTGTG TGTCTGGCTT CTCTCACTTA 240
CCATAATGTT TTTGAGATGT ATCCATGTGT TAGAGTGTAT TCGTTTATGA TTTCTCTTTA 300
TTGCTGAATA ATATTCTTTC GTATGGATAT ACCAAATTAT ATTAATACAT GGATATTTTA 360
TTATAAAATG TCTCCCACTC ATTTTGGAAG TAAATGAGTA TAAATGACAT AAAAGTGCAC 420
AGATATGCTT ACTCTTCAAA TTTTCTTCCC CATCCCTGGA TAGTCTCAGG TTTTGTCAAG 480
GATGGAATAA GCAGGTTGCA AGCAATAGAC TACAGACGTT CTTGGTAATC TTCAGGGTTT 540
TGTCCAAACC AGAGATCCTG AAATTCTATA CCCAAGATCT GACTCGACCT CCTCGAGGCT 600
AGAGCTACAT CTAATCTTTA TGATCTGGCA TTTTTCACCT CATACAAATA TAAGCAGGAG 660
GAGGGTTTTC TTTAAAGCTA AACCACTGGA AGGTGTGGAT ACAACGGGTT CTTTGATGGG 720
TCCACCCTAC AAATACTGAG CCAGTGACTT AATAAAAAGC CCCATGTATG GAGAGGACAT 780
AATGAGCAGG AGATACCATC TTTATCCAAA ATTGGTAGGT ACTGCCCCAG CTGAAAAGAA 840
TAATCATAGC ACCAACATTT TTCCACCACT TTTTACGTAC TAGGCACTGA GGCTTAGAGA 900
AGTTAAGGAA CTTGCCCAAA GTCTCAGCAA GAAGATGGTG GAGCCAGGAT GAAGGCCCAA 960
ATTACAACCT CAGAGCCTAT TTGTGACCCT TTACTACTTC AGTGCTGCAG TACCTACACA 1020
TCCAGATAAT CCACTCGCTC CAAGAAACGC TGGTCAAGAT GGGCTCCAGA TTCAGTGAAA 1080
TATCAGTTTA TTTCAACAGA AATTTTGATT TTTCTGTTTT GTGCCAGTTC AATCGTTACA 1140
GAAAATAAAA GGTTCAGATT CCAATTTGAA TTTGCTTTAC TAGGGAGCTT TTGAAGGAAG 1200
TAAACTTGGC TTTTTTTCAC AGTTACAGAA AAACATTTTG GATTGGGTTC ATGACTCAGC 1260
ACGAGTCCAA TTCATTCCAG TTTTAGTTCA ACAATAGTTC AGTTCAAGTA GCTAGGTCAG 1320
CAAGCTCCAG AGAAGTGGGC GTGGCTTCCC TTACCCGCCA GGAGTGACTA ACACCAGCCG 1380
CGAGGAGAGA GCCAAGACGG CTGCACAGGA TGCATGGGCC ACCCAGGCTT AGGGCTTTCA 1440
GTAAGGACTG GGGCTTGCTG GTGCCTCTCT TCTCCCTTCA CTTGTCACCA GCGCCCTTGG 1500
TTCCATCACA TACCCCACAG AGGGGATACC CAGCCAAGTC CGAACCTGCC AGGTCTCCAA 1560
ACAATAGATG TCACATGGGG GAAAGCAGAG TCAGCCTCCC ATATTCTCCC CAGGGAAACA 1620
AGCTTCCCTT GTTTTCCCAG ATGTCAAATG TTTGGGTTGT AGGATTATTT AAATGTTATT 1680
CTTGAGTGAG TCAGGAGCTA GAGGGAGGAC TGGACTGTGT CCCTAGAGTC TGTCCTTCCA 1740
GGAAATGCCA GTGTTTGACT TTCACCTGTC ACTGACCACT GACCTTTGTT TCCAGAGCCA 1800
TCTAGGGCAG AAAAAAACCA TGGGCATGGA AACTGCCATC TGATGACTTC AGAACTAATA 1860
CATTTGCCTA TTAATCCCTA AAACATATTT TAAGTGATCT CCTATATTCT CTAGTGTTTA 1920
GGAAAAAATG ATTTTCCCTT TAGACCTGGA ATTCATGAAT CCCTAGCAGG CCCAAAGTTA 1980
AGCTTCATCA ATGTTATGAG TATTCTAAAA TTGTGCAATA AACGTTACCA GATTCTCAAA 2040
GAGACTTTTG ATCCCAAACA CATGAAAAAC TACTTTTAAA AACTATATAC TACTAGCCTA 2100
CCAAGAGGCT ACTGTCATTC TAGGTTACCT ATTCTGCATT TTGTACTATA ACAAATATCT 2160
TCTTTCATAT ACACAATGTA CTTCCAAGTC CCAGACCAGC CCGTTCTAGT AAAATTCAAA 2220
AATGTAGGTA TTTCCGAAGA GCATCTTGTA AAAGGTCCTG ACCTAGGAAA GTTAACCACT 2280
GCACATCCTT CCTAAGAGAC AAGACATAAT TTTAGGATAA CTTTACAGAT GGAGACTTTA 2340
TAGATTAGCC CCAAGCAACC CACTTCTCAG ACAATCCGCT TCTCAAGCAA CCCACTTCTC 2400
AAACAGCCCA CTTCTCAACT TTTAAGGCTG TGTGTCTTTC CCACCCTGAC CTACCTCAAT 2460
TCCCTCCTAA GTCAGAGAAT CCCTGGGCTT TGTATCTGGA AGGAACCTTA AAGAACCTTA 2520
AAGGATTCTT AAACTGGGCT CTTCCATGCC CCAAGCTGCT CGGGAGCCAC TGCAGGGGTA 2580
AGAGGAAGGG GTCAGAAGGA CAGTGTTCTG GGTCCTCACC CCAGCTCCCA CTTAGAGCAG 2640
TCTGTTTTCA TCTAACTTTT ATAGTAGATA TTGGCATAAG ATTTCATTTT TTAAAATTCC 2700
ACCAGGAAAA TAAAAATAAC AAAAAAAAAC CACACATTGA TTTACGACAG CCTTTCTATT 2760
TATAAGCTGA AAACAGAACA AAAGAAAAAA AAATGCAACA CAAAGAAAAT GAGTTACTTG 2820
CCTAAGGGTA CGTAGTTCAG GGCTCTGTCA TGACCGCCCT GGGCCTCTAT GGCACTGCTC 2880
ATTCCCTTTC AGAAGATGGC TGGGGCAGCC AATCCAGCAG AAGGCAGCTC CAGTGCCCTT 2940
GGAAGTGCTG GCACCTGGCA CCTTTCCCAC AAAGTACACA CCTGGTCTCA 2990
|
