Tag | Content |
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EnhancerAtlas ID | HS167-01261 |
Organism | Homo sapiens |
Tissue/cell | Retina |
Coordinate | chr1:36668660-36671710 |
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 | Zfx | MA0146.2 | chr1:36671681-36671695 | GAGGCCGAGGCGGG | - | 6.01 |
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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 | AACCAACATG ATTGGTCAGG CTGATATTGA ATTCCTGACC TCAAGTGGTC TGCCCGCCTC 60 AGCCTCCCAA AAGGAATGGA ATCTTAAAAA AAAAAAAAAC AGTGATGGGA ACAGGATCTC 120 ACTATGTTGC CCAGGCTGGT CTTGAACTCC TCCTGACTGA ACCTCCCAAA CTGCTGGGAT 180 TACAGGTATG AGCCACCATG CCTGGCCAAA AGTCCCTCAA CTTTCTGTTT TAAAAATTGC 240 CACCAGACTT TTCTGCAATG TCACCTGAAG GGTTCCTGGT CTCACACAAT GCCCACCCCT 300 AAAACACAGC AGCCTAGGCC ACCACGTTCT GCCAGGCGAG GTGTGTGGTA GGAAGAGGGC 360 AGGCAGCTCT GGCCTCAGGC ACAAAGGGCT GAGTCCTGGG TCCTGGGGAC AGGCACTGGC 420 AATTGAATCT GGACACTGAG CACTGGGTCC TAACACAAGA AATCATTTCC TGGCTCAGGG 480 CAGTGATCTC TGGGTCCTAA AAACTAGGAC CAGAGCAGAG ACCATAGGTC CCTTATCTCT 540 GGGCGGAGGG TGCTGGGCTA AGTGGCAGTC ACCCAAGGCA GGGCCAGGGG TAAGGAGATG 600 CCCAGCCCCC AGTTGTTTTG TAACAGCTGC TGGACTGGGC TGGAGGGGAA ATTTAAGGAA 660 CCAGGGGGTG AGGTAAGGAG GAAGAGGTCA GTGGGCAGGG CAAGGCCACT CGGGCATGCT 720 GGATTGGTCC CAGGCCCTGG AGGGCGAGAG AAAGACAGTG GCTGGATCTC TAGGGCTCTC 780 ATTGGCAGAC ACTGGGGCCC CAGGAACTAG GGCAAGAAGA GTGGTGAGGA TAGCAGGGAG 840 TGTGTGCTAC CCCCTACCCC CAACCCCCCT CTTTGTACCC TCCCCCCTTT GTCAACCTCC 900 TGGCTCCGCT CCCAGGCCGA GGCAGCTGGA GTGATTAGTG TGGGTGAAGG AGTACAAATG 960 CCAAAGGCTT GTCTCACGTC TCAGAACACA GGGATCCAGC CAGAGTGGAT GGCACAACTG 1020 AGTGAGAAAT GGAGACCGAG AGATAAACAG AAATAAACAG GGACAACACC AAAGAGATAG 1080 AGGAGAGAAG CAGGGCGGGA GACAAAAGAA GAGACCAAAG GCCCACACAG AGCAAGGGGG 1140 TTGTGGGGAG GGAGGGTTCA GTAGCTACAG GGCAGGCTGA CCTTTTCCTG TCTCTTCTCT 1200 GACCCCGTCC TGTCTGAGTT CCCCTCCGCT GTGTCCCTAT CCCAGGCTTT CTCAACCTCA 1260 GCACTGTTGA CATTTGGGGC AGGATAATCT TGGATGGTGG GGGTGGGTGG GTGGGTGGGG 1320 GGTGTTCTGT GCCCTGTAGG ATGTTTAGCA GCCTCCTTGG CCCTTATCCA CCACATGCCA 1380 TTGGCACTCC CCCAACTCCT CTGCTCTTGT GACAATCCAA ACTGCCTCCA GATATTGCCG 1440 GATGTTTCCT GGGAAGGGAT TGCTCCTGAC TGAGAACTGT CCCCAGGTAG GTTCATGTTC 1500 TTGAGAAGAG GCTACCCCAG GGTGTCTGGC TGGTTCTCCC TTCGGCCCGT GTGCACAGGG 1560 CCCCCTGGCT CTAGCATGGC TTAAGTTGCC CTAAGTCAGA AGCCGGGGAA ACTAGGAGAG 1620 CCACTGAGAC TGAAGAGCAG TCTAGGTACA GCAGTAACGA AGTCCCTGCC CTCATGGAGC 1680 TTCTGTTCTT ATTCCACCCA AAAGGCATCC CAGGTGTGTT TTGGGATGTG CTAGGGGTGT 1740 TTCATGAGTG GGTGTGCACT CTCGTCTCTA AGGGAGGAAG AAGAGATGGG CCCCCAAGTA 1800 TGTCTGGACA AGATACAGGT AACAAATATG CATTTTATTC CATGATGCTT AGATGTAAGA 1860 AATGTCCCAT TTATCCAGGC ATGGTGGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCT 1920 GAAGCGGGCG GATCACGAGG TCAGGAGATT GAGACCATCC TGGCCAACAT GGTGAAACTC 1980 CGTCTCTACT AAAAATACCA AGAAATTAGC CAGGCGTGGT GGCGGGCACC TGTAGTCCCA 2040 GCTACTCGGG AGGCTGAGGC AGGAGAATGG CATGAACCCG GGAGGCGGTG CTTGCAGTGA 2100 GCCGAGATCG CGCCACTGCA CTCCAGCCTG GGCAACAGAG CAAGACTCTG TCTCAAAAAA 2160 AAAAAAAAGA ATTGTCCCAT ATATTTAATT CTCTAAACCA GATGATCTGC TCCAAAAACC 2220 CCCTGCCAGG CTGGCTGGTG AGAAATTCAA TCACAGTCAT GTTTTGGGAA TCTCTACCCA 2280 GTGGTGTGCT GGTGAATGTT TACAAATGGT TTGGGGTGCA TTAGGGAGGG ACTTGATTTG 2340 TCACATTTGC CAACTTCCAT GATGTAAACA CTCCCACCAT GGCCAATTTC AAGCTGCCAA 2400 CATAATGTCA GTGCAGGTGG AGCAGGGAGG AGTGAGCAAT GGCACACTGT CACACAGGGT 2460 ATTCACCCGG CAGATGCCAA CAACTTTAAA AGGATTGATA ATAGTAAACT GGGCCAGGTG 2520 TGGTGGCTCA TGCCTGTAAT CCCAGCACTG GGAGGCTGAG GTGGGTAGAT CATCTGAGGT 2580 CAGGAGTTCA AGACCAGCCT GGCCAACATG GCAAAACCCT GTCTCTACTA AGAATACAAA 2640 AATTAGCTGG GTGTGGTGGC ACAAGCCTGT AATTTCAGCT ACTCAGGAGG CTGAGGCTGA 2700 AGAATTGCTT GAACCTGGGA GATGGAGGTT GCAGTGAGCC CAGATGGTAC CACTGCACTC 2760 CATCCTGGGC GACAGAGTAA GACTCTGTCT CAAAAAAAAA AAAAAAAAAA TTAGCCAGAT 2820 GTGGTGGCAC ATGCCTGTAA TCCCACTTAC TCGAGAGGCT GAGGCAGAAT TGCTTGAACT 2880 CGGGAGGCAG AGGTTGCACT GGGCTGAGAT GGCACCACTG CACTCCAGCC GGGACAACAG 2940 AGCGAGACTC TGTCTCAAAA AAAAAAAAAA AAAAAAAAAG GCCAGGCTTG GTGGCTCATG 3000 CCTGTAATCC CAGCACTTTG GGAGGCCGAG GCGGGTGGAT CACGAGGTCA 3050
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