Tag | Content |
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EnhancerAtlas ID | HS094-00725 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr1:36668440-36671280 |
Target genes | Number: 20 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr1:36669828-36669843 | AGGGCAGGCTGACCT | - | 7.55 | NKX2-5 | MA0063.2 | chr1:36668699-36668709 | CTCAAGTGGT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:36671235-36671250 | GAGGTCAGGAGTTCA | + | 6.22 | RREB1 | MA0073.1 | chr1:36669953-36669973 | ATGGTGGGGGTGGGTGGGTG | - | 6.09 | RREB1 | MA0073.1 | chr1:36669965-36669985 | GGTGGGTGGGTGGGGGGTGT | - | 6.55 | RREB1 | MA0073.1 | chr1:36669957-36669977 | TGGGGGTGGGTGGGTGGGTG | - | 7.58 | RREB1 | MA0073.1 | chr1:36669961-36669981 | GGTGGGTGGGTGGGTGGGGG | - | 8.79 | Tcf12 | MA0521.1 | chr1:36669281-36669292 | AACAGCTGCTG | + | 6.32 |
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| Number of super-enhancer constituents: 18 | ID | Coordinate | Tissue/cell |
SE_03303 | chr1:36668859-36669950 | Brain_Angular_Gyrus | SE_04066 | chr1:36668642-36670588 | Brain_Anterior_Caudate | SE_05024 | chr1:36668499-36670996 | Brain_Cingulate_Gyrus | SE_05887 | chr1:36668484-36671079 | Brain_Hippocampus_Middle | SE_06862 | chr1:36668431-36670706 | Brain_Hippocampus_Middle_150 | SE_07920 | chr1:36668568-36670940 | Brain_Inferior_Temporal_Lobe | SE_26652 | chr1:36668722-36670470 | Esophagus | SE_31707 | chr1:36668687-36670477 | Gastric | SE_37181 | chr1:36668315-36671203 | HSMMtube | SE_42156 | chr1:36668410-36670672 | Lung | SE_42156 | chr1:36670696-36671441 | Lung | SE_48111 | chr1:36668314-36670674 | Psoas_Muscle | SE_48599 | chr1:36668452-36670657 | Right_Atrium | SE_48599 | chr1:36670712-36671339 | Right_Atrium | SE_49470 | chr1:36668484-36670597 | Right_Ventricle | SE_49470 | chr1:36670844-36671269 | Right_Ventricle | SE_54589 | chr1:36668333-36671420 | Stomach_Smooth_Muscle | SE_65351 | chr1:36668762-36670397 | Pancreatic_islets |
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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: 2 | ID | Chromosome | Start | End |
GH01I036202 | chr1 | 36668509 | 36670600 | GH01I036205 | chr1 | 36670697 | 36671441 |
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Enhancer Sequence | AAAGTGCTGG GATTACAACA CTTTTTTTTT TTTTTTTTTT TTTTTTTGAG ACGGAGTCTC 60 ACTCTGTCGC CTAGGCTACA GTGCAGTCGC GCGATCTTGG CTCACTGCAA CCTGCTCCTC 120 CCGGCTTCAA GCGATTCTCC TTGAATCGCT TCCCAAGTAG CTGGGATTAC AGGCGCCTGC 180 CACCATGTCT GCTAATTTTT GTATTTTTAG TAGAGACTAA AACCAACATG ATTGGTCAGG 240 CTGATATTGA ATTCCTGACC TCAAGTGGTC TGCCCGCCTC AGCCTCCCAA AAGGAATGGA 300 ATCTTAAAAA AAAAAAAAAC AGTGATGGGA ACAGGATCTC ACTATGTTGC CCAGGCTGGT 360 CTTGAACTCC TCCTGACTGA ACCTCCCAAA CTGCTGGGAT TACAGGTATG AGCCACCATG 420 CCTGGCCAAA AGTCCCTCAA CTTTCTGTTT TAAAAATTGC CACCAGACTT TTCTGCAATG 480 TCACCTGAAG GGTTCCTGGT CTCACACAAT GCCCACCCCT AAAACACAGC AGCCTAGGCC 540 ACCACGTTCT GCCAGGCGAG GTGTGTGGTA GGAAGAGGGC AGGCAGCTCT GGCCTCAGGC 600 ACAAAGGGCT GAGTCCTGGG TCCTGGGGAC AGGCACTGGC AATTGAATCT GGACACTGAG 660 CACTGGGTCC TAACACAAGA AATCATTTCC TGGCTCAGGG CAGTGATCTC TGGGTCCTAA 720 AAACTAGGAC CAGAGCAGAG ACCATAGGTC CCTTATCTCT GGGCGGAGGG TGCTGGGCTA 780 AGTGGCAGTC ACCCAAGGCA GGGCCAGGGG TAAGGAGATG CCCAGCCCCC AGTTGTTTTG 840 TAACAGCTGC TGGACTGGGC TGGAGGGGAA ATTTAAGGAA CCAGGGGGTG AGGTAAGGAG 900 GAAGAGGTCA GTGGGCAGGG CAAGGCCACT CGGGCATGCT GGATTGGTCC CAGGCCCTGG 960 AGGGCGAGAG AAAGACAGTG GCTGGATCTC TAGGGCTCTC ATTGGCAGAC ACTGGGGCCC 1020 CAGGAACTAG GGCAAGAAGA GTGGTGAGGA TAGCAGGGAG TGTGTGCTAC CCCCTACCCC 1080 CAACCCCCCT CTTTGTACCC TCCCCCCTTT GTCAACCTCC TGGCTCCGCT CCCAGGCCGA 1140 GGCAGCTGGA GTGATTAGTG TGGGTGAAGG AGTACAAATG CCAAAGGCTT GTCTCACGTC 1200 TCAGAACACA GGGATCCAGC CAGAGTGGAT GGCACAACTG AGTGAGAAAT GGAGACCGAG 1260 AGATAAACAG AAATAAACAG GGACAACACC AAAGAGATAG AGGAGAGAAG CAGGGCGGGA 1320 GACAAAAGAA GAGACCAAAG GCCCACACAG AGCAAGGGGG TTGTGGGGAG GGAGGGTTCA 1380 GTAGCTACAG GGCAGGCTGA CCTTTTCCTG TCTCTTCTCT GACCCCGTCC TGTCTGAGTT 1440 CCCCTCCGCT GTGTCCCTAT CCCAGGCTTT CTCAACCTCA GCACTGTTGA CATTTGGGGC 1500 AGGATAATCT TGGATGGTGG GGGTGGGTGG GTGGGTGGGG GGTGTTCTGT GCCCTGTAGG 1560 ATGTTTAGCA GCCTCCTTGG CCCTTATCCA CCACATGCCA TTGGCACTCC CCCAACTCCT 1620 CTGCTCTTGT GACAATCCAA ACTGCCTCCA GATATTGCCG GATGTTTCCT GGGAAGGGAT 1680 TGCTCCTGAC TGAGAACTGT CCCCAGGTAG GTTCATGTTC TTGAGAAGAG GCTACCCCAG 1740 GGTGTCTGGC TGGTTCTCCC TTCGGCCCGT GTGCACAGGG CCCCCTGGCT CTAGCATGGC 1800 TTAAGTTGCC CTAAGTCAGA AGCCGGGGAA ACTAGGAGAG CCACTGAGAC TGAAGAGCAG 1860 TCTAGGTACA GCAGTAACGA AGTCCCTGCC CTCATGGAGC TTCTGTTCTT ATTCCACCCA 1920 AAAGGCATCC CAGGTGTGTT TTGGGATGTG CTAGGGGTGT TTCATGAGTG GGTGTGCACT 1980 CTCGTCTCTA AGGGAGGAAG AAGAGATGGG CCCCCAAGTA TGTCTGGACA AGATACAGGT 2040 AACAAATATG CATTTTATTC CATGATGCTT AGATGTAAGA AATGTCCCAT TTATCCAGGC 2100 ATGGTGGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCT GAAGCGGGCG GATCACGAGG 2160 TCAGGAGATT GAGACCATCC TGGCCAACAT GGTGAAACTC CGTCTCTACT AAAAATACCA 2220 AGAAATTAGC CAGGCGTGGT GGCGGGCACC TGTAGTCCCA GCTACTCGGG AGGCTGAGGC 2280 AGGAGAATGG CATGAACCCG GGAGGCGGTG CTTGCAGTGA GCCGAGATCG CGCCACTGCA 2340 CTCCAGCCTG GGCAACAGAG CAAGACTCTG TCTCAAAAAA AAAAAAAAGA ATTGTCCCAT 2400 ATATTTAATT CTCTAAACCA GATGATCTGC TCCAAAAACC CCCTGCCAGG CTGGCTGGTG 2460 AGAAATTCAA TCACAGTCAT GTTTTGGGAA TCTCTACCCA GTGGTGTGCT GGTGAATGTT 2520 TACAAATGGT TTGGGGTGCA TTAGGGAGGG ACTTGATTTG TCACATTTGC CAACTTCCAT 2580 GATGTAAACA CTCCCACCAT GGCCAATTTC AAGCTGCCAA CATAATGTCA GTGCAGGTGG 2640 AGCAGGGAGG AGTGAGCAAT GGCACACTGT CACACAGGGT ATTCACCCGG CAGATGCCAA 2700 CAACTTTAAA AGGATTGATA ATAGTAAACT GGGCCAGGTG TGGTGGCTCA TGCCTGTAAT 2760 CCCAGCACTG GGAGGCTGAG GTGGGTAGAT CATCTGAGGT CAGGAGTTCA AGACCAGCCT 2820 GGCCAACATG GCAAAACCCT 2840
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