Tag | Content |
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EnhancerAtlas ID | HS091-16779 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:23703650-23706040 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr16:23705308-23705320 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr16:23705312-23705324 | GTTTGTTTGTTT | + | 6.32 | LHX6 | MA0658.1 | chr16:23705187-23705197 | ACTAATTAGC | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr16:23704258-23704273 | TGAACTTTTGGCCTC | - | 6.12 | RARA | MA0729.1 | chr16:23704255-23704273 | TCTTGAACTTTTGGCCTC | - | 6.5 | Stat4 | MA0518.1 | chr16:23703690-23703704 | CTTCCAGGAAGTCA | + | 6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 23703779 | 23704048 | chr16 | 23704090 | 23704209 |
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Enhancer Sequence | GTCTGGAGCC AGAGAGATGG GCATGAGAAG GAAATCTCTG CTTCCAGGAA GTCAGCCTGG 60 CTAAATTCTC CCATGGGCTG ATAGAGCTGC CAGGGGTTTG GCTCAGACTG GAACTCAAGA 120 TGCTTCCTGG GCAGCATCTC CTTGGCTCTA GATCCCTCCC CTCTACACTA CTATAGGGGG 180 CCCATGGTTT TCATCCAAAA CCTTTGCCCT TACTGAGCTA GTTCAGGTTT CCAAGCTTCA 240 TTCCTGCAGG GTATAGGGTT ACATAAGTGG GTGCCATACA TGAGGCAATA AGGCAATCAG 300 GAGGACTGTG GTGACCTGGC ATGGGTTTTT TCTGCAGGGG CAGCTGGTCC TTAGCTTCAA 360 CCGGTTGTCA CCAGGGGACT CTCCAGGGTG GCAGAGCTGA TTTTGTTTTT TTTTTTGTTG 420 GGGCTTTGCT CATGTTGCCC AGGCTAGAGT GCAGTGGCGC AACCACAGCT CACTGTAACC 480 TCAAACTCCT GGGCTCAAGC AATCTACCTC GGCCTGAGTA GGTGGGACTA CAGGCATGTG 540 CCACCATGCC TGACCAATTT TTAAATTGTT TGTAGAGATG GGTCTTCTTA TGTTACCCAG 600 CCCGATCTTG AACTTTTGGC CTCAAGCGAT TCTGATTTTT TTTTTTTTTA AAGAAAATCC 660 AGAAATCCAA ATTTTATGTG GAATTTCTCA AATGTTAAAA TATTGGGCCA GGCATGTGGC 720 TGACACCTTG TAATCCCAGC ACTTTGGGAG GCCAGGAGTT CAAGACCAGC GTGGGCAACA 780 TGGTGAGACC CTGCCTCTAC AAAAAAATAC AAAAATTAGC TGGGTGCCAT GTTGTGTGCC 840 TGTAGTCCCA GCTACTTGGG AGGCTGAGGT GAGAGGATCC CTTGAGCCCA GGAGTTTAAG 900 GCTGCAGTAA GCTGTGATGG TATGACTGCA CTCCATGACA GAGCAAGACC CTGTCTCAAA 960 AATATATATA TATAGGGCCA AGCACAGTGG CTCATGCCTA TAATCTCAGC ACTTTGGGAG 1020 GCCGAGGTAG GTGAATCACC TGAGGGCTGG GAGTTCGAGA CCAGCCTGGC CAACATGGCA 1080 TAAACCCCAT CTCTACTAAA AATACAAAAA TTAACTGGGC ATGGTGGCAC CTGCCTATAG 1140 TCCCAGCTAC TAGGGAGGCT GAGGCAGGAG AATCACTTGA ACCCAGGAGG TGGAGGTTGC 1200 AGTGAGCTGA GATCATGTCA CTGCACTCCA GCTTGGGCAA CAAGAGCGAA ACTCCATCTC 1260 AAAAAAAAAA AAATATATAT ATATATAGGC CACTAATTTA AATATAAACT GTATAGTCTC 1320 ATGACATCAT GCATTTAGTC CTTGAGCCCT GCTCACCACT TTGAGCTTTC TCTCAACTTT 1380 AGGAGTGGGG GCAGCCTTCC CTGGTGACTG TCCTTTTGTG TGATTGGCAT CCATTTCTCT 1440 GGCTTCAACT TCCGCCCACA CACTGTGACT CAAAATCCGT AATTCAGGGG TCCCAAACGC 1500 AAGTGTCTGT GTGGGTCAGA CGCTGCTCTG TGTATCAACT AATTAGCTCA TCTGATGCCC 1560 TCCAAAACCT TCGATACCAG TGGTTCTGGA ACTTGGCTCC ACATAAAAAT GACCCAGGCA 1620 ATTAGGTAAA AATCACGGGG TGTGGGGCCT GGGGTTTTGT TTGTTTGTTT GTTTTTTGTT 1680 TTTTGAGAGA AAGAGTCTCA CTCTGTTGTC CAGGCTAGAG TGCAGTAGTG TGATCTTGAC 1740 TCTGGAACTT CCACCTCCCA GGCTCAAGCG ATCCTCCCAC CTCAGCCTCC CAAGTAGCTG 1800 GGACCACAGA TGCACACACC CACACCGGCT AAATTGTGTG TGCTTTTGGT AGAGACGAGG 1860 TCTCCCTAGG TTACCCAGGC TGGTCTCGAA CTCCTGAGCT CAAGCAATCT GCCTGCCTCG 1920 GCCTCTCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCA CCCGGCAATG GGCATTCTTT 1980 TTTTAAGTTG CGCAGTGGTT GTGAAGCACA GTGAAGATTA CAAACCATTT TCTAGCTCAG 2040 GGTTTCCCAA CCTCAGCACA ACTGGCATTT TGTTAGTTCT TTGTGTTGGG TGTTGTCCTG 2100 TCCTGTAAGA CATTTAGCAG CATTTCCAGC AGATGCCAGT AGCCCCTCCC TCCCAAGTCA 2160 TGGCAGTCAA AAATGTCTCC AGACATTGCC TAATGTCCCC TGGGTGGCAA AACAGTCCTG 2220 ATACTGCTGT AGAAGGAGGG ACAAATTATC CCTTCTTTAA GGGAAACAAG CTTGGAGGAG 2280 CAGCTCAAAG TCACACAGCA AGTGTCATGG AGTCTCCTCA GGAGGGGAAC TGGGACAGGG 2340 ACGGATTCCT GCAGCCTGGG GCAGCTGTGT GCCTGGAGGA CTTGGTGGAT 2390
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