Tag | Content |
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EnhancerAtlas ID | HS165-06669 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr18:46310420-46313080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr18:46311519-46311537 | CTTTCCTTCCTTCCTTCC | - | 10.53 | EWSR1-FLI1 | MA0149.1 | chr18:46311499-46311517 | TTGTCCTTCCTTCCTTCT | - | 6.19 | EWSR1-FLI1 | MA0149.1 | chr18:46311547-46311565 | CCCTCCTTCCTTCCCTCT | - | 6.84 | EWSR1-FLI1 | MA0149.1 | chr18:46311543-46311561 | TTTTCCCTCCTTCCTTCC | - | 7.52 | EWSR1-FLI1 | MA0149.1 | chr18:46311511-46311529 | CCTTCTTTCTTTCCTTCC | - | 7.69 | EWSR1-FLI1 | MA0149.1 | chr18:46311503-46311521 | CCTTCCTTCCTTCTTTCT | - | 7.85 | EWSR1-FLI1 | MA0149.1 | chr18:46311507-46311525 | CCTTCCTTCTTTCTTTCC | - | 7.87 | EWSR1-FLI1 | MA0149.1 | chr18:46311523-46311541 | CCTTCCTTCCTTCCTCTC | - | 8.32 | EWSR1-FLI1 | MA0149.1 | chr18:46311515-46311533 | CTTTCTTTCCTTCCTTCC | - | 8.46 | IRF8 | MA0652.1 | chr18:46311640-46311654 | TCCAAACCGAAACT | + | 6.19 | Stat6 | MA0520.1 | chr18:46311322-46311337 | TAGTTCCTGAGAAGC | + | 6.11 | ZNF263 | MA0528.1 | chr18:46311515-46311536 | CTTTCTTTCCTTCCTTCCTTC | - | 6.03 | ZNF263 | MA0528.1 | chr18:46311519-46311540 | CTTTCCTTCCTTCCTTCCTCT | - | 6.14 | ZNF263 | MA0528.1 | chr18:46311539-46311560 | TCTCTTTTCCCTCCTTCCTTC | - | 6.28 | ZNF263 | MA0528.1 | chr18:46311511-46311532 | CCTTCTTTCTTTCCTTCCTTC | - | 6.44 | ZNF263 | MA0528.1 | chr18:46311535-46311556 | CCTCTCTCTTTTCCCTCCTTC | - | 7.14 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_01683 | chr18:46304671-46311446 | Aorta | SE_05932 | chr18:46301923-46312490 | Brain_Hippocampus_Middle | SE_05932 | chr18:46312613-46315031 | Brain_Hippocampus_Middle | SE_27873 | chr18:46312286-46315809 | Fetal_Intestine | SE_37828 | chr18:46312562-46315221 | HSMMtube | SE_42484 | chr18:46302671-46311530 | Lung | SE_48564 | chr18:46302481-46311501 | Right_Atrium |
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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 |
GH18I048783 | chr18 | 46310332 | 46312838 | GH18I048786 | chr18 | 46312957 | 46315644 |
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Enhancer Sequence | CTGTGTTCCA GGCAGCGAGA TGGTGGAAAA ATGGAAAAGG AGGTCCCCTC TCCTGCCATT 60 GGGCATCTCC TAATCTGGTG GGGAATGCAG ACAGTACCCA GTAACTCCAG ACCAGCATGC 120 TAGGTGCTGT CATCGCGGCA CACCCAGACG GCCCCGAGCA TCGAGAGGAG AGAGAACTCA 180 CATGAGGGTG TCTCACAGAG AGAGGAACAC AGGCCTGAGT CCCAGCACCT GGGCTGGGGG 240 TGCCAAACAA AGAAACGTGC AGAAGGGCAT TGTCTAGGCG AATACAGGAG CATGAGCAGA 300 GGCAAGAAGC AGACAAGAAT CATGTACAGC AAAAGAAGGG GTTGTTCCCG AGTATAGTGT 360 GCACTGGGGG CTGAGGTGGG AGGAGAGAGT GTGGGCCAGA ACCAGCTTGG GAGGGGCACT 420 GTTTGCCCTA CCTGGTCGGA GGGACCATAC CCTTTGGTCT CTGGGGCACC ACCAAAGGTT 480 TGTAAGGATG GAGGTGATGT CTCCTGGTTG GCATCTTTGG CTCTCTCTCT GCAGCAGGAT 540 GGAGGAGGGC AGGATAAGGA CCCTGGGAGG AGCAAAGCAC CCCACTGGGG GTGTCCTATT 600 GGAGCCTCCT GGGAGAGCCA GGAGAGGTGT GGGCAGCCTC AACTCTGTGG CAGTGGGGCC 660 TAAGGGTCAG GGGATGATCC ATGAGTGGTC AGCAAAAAGA GAGAGACAGA GAGAGAGGTG 720 GGGGGACTAC CTGTAGAGCA GTTAACATGC ATCAGCACCA CAAGCAGGAG GACCGCTGGG 780 CAGAGAAACA TGTATGCACA TTCATGCACG TGTACATGTG AATAACTCCT CTCACACATG 840 CTGGAGGAAA CCCTCGCTGT CATCCACACT CCCAGGAATG GCCACATTAG ACATCTTCCC 900 CCTAGTTCCT GAGAAGCAAA CCCGGGAGAG CCCAGCCCTC AGCCTTGCTG CATGCGTGAG 960 CATGGAGTTT TGCACTCTGG CCAGTTTTGC CTCTAGTTCT TTGTTTCTGG AAAAAACAGG 1020 CACTAGGGTG AATTTCTTTT CTCTTTTCCT ACCATCCCAT CTTCCTTCTT CCTTCTCTTT 1080 TGTCCTTCCT TCCTTCTTTC TTTCCTTCCT TCCTTCCTCT CTCTTTTCCC TCCTTCCTTC 1140 CCTCTCTTTC TTTCATGAAG AAAAGCTCAC AGAAAGGCAG AAGGAACCAC AGTCTATTGA 1200 CGTTTCTGAC TCTTAGAGGC TCCAAACCGA AACTCAGCTG TGGTTGCTCT AAGTGGCTAC 1260 AAAATTAGAA AAATAATTTG CAGAAATGAA ACCTGACTTG GGATGCCGTT TCACAAAATA 1320 GGCTAGATGG CCTTGATGTG TCATGAGGCT CCCACCACTG CGGCCTGCAC TGCTGGAGGA 1380 ACTCCTCACA TCTCAGGCTG GGGAGCATTT CCACCCCTGC AGTCAGGCAT CCTACAGAAA 1440 CCTGCCCCCT GCCTACCTGA AGACAGTTCA CAGTTTCCTC TGAAATGGGC GGAAGAGCTG 1500 GACCCAGCCA CAAGACCATC AAGGAAAGCA AAAGGCTTTC AAAAGTGAGA CTCCCCAGAG 1560 ACCAAACCCA GGGGAAGGGA TCTGGGGATT CTTAACAGAC TCCCTGGGAG TCCAAACCAG 1620 GCTGTGAGCT TGGCTTTGCC ATGAACTAGC TCTGACCTCC GTGCCTTTGG TAAACAGTAT 1680 CAACAGCTGC CATTTACCAA ATTTCTATGG GGTACCTTGC TTGGCTGCAC CTGGGGAGAT 1740 TTGGAAAATG CCAATGCCCA GGCTATGCCC CAAGCAAATT GTGTCACCAT CTTATGGGTA 1800 GGACCCCCGC ATCAACATTG TTTAAAGCTT CCCGAGTGAG CCCAACATGC AGCCACAGCT 1860 GAGAACCACT GCCCCCACCC ATTTGGCTGG AGACTTACGT AGGTTCATCC TCACAGCAAC 1920 CCCGCCAGGG TTTATGAATA AGGAAGCTGA GGCTAGGAGA GTTTGAATCA CTCATCCGAG 1980 ATCCTTGAGG TTCTCCCTCA TCCCAAAGCC CATCATTCTT CCTCCTTTGC AGGGCTGGAT 2040 ATACCTGTAC AGACCCCGCA CAGCATCAGT GAGTGATCCA ACCAGCCAGC TGAAGGAGCT 2100 CAGAGAGCAC TGCAGGGAGA CAGGGGAGGT GCCGGCGGAG CAGTCTGCCT GTTCCTGGCG 2160 TTTGGGAGGG GGTGCAAGCC TCAGGCCTGT TTTTCAGCCT CCCTCCCAAG TCACGATTGG 2220 TCCCTAGTCC TGGGGATCCA GGCTGTCTGG GTCAGTTTGA ACCTGAGCCT CACTCAGCAG 2280 ATGCTCTTAG TGTCTAAGCC CAGCGGTGGG CACTGTCAAG AGCCTGGACT CAGGAGCCGC 2340 ATTCCTGCCT AGGTTCAAAT CCCAGCTCCA CTACTTATAA GCTGTGTGCC TTTGCAAAGT 2400 GAGTGATCTT TCTGTATGTC AGTTTCTTCA TCTGCATGAT GGGGTGACGT TAGAGTTGTT 2460 AGGAGTACTA AATGAGACAG TGCATATCAG GATTGAAAGC AGTTCCTGGA ACATAGAAAA 2520 CAAGAAAATC CCAGGCACTC TAAGGATTAC GACTGTGAAC GTGCAGTTCA TTGCTGAGCA 2580 GAAACTCGAT GGAACATGGG CCTGAATCAG TCAAGGTGAT AAGTTTAAGT CAATGTTTGC 2640 CCTTTGGCCT TGCCTGTTCT 2660
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