Tag | Content |
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EnhancerAtlas ID | HS045-00434 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:10821140-10823520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:10821482-10821500 | CTTTCCTTCCCCACTTCC | - | 6.44 | KLF4 | MA0039.3 | chr1:10821537-10821548 | AGAGGGTGTGG | - | 6.02 | Klf12 | MA0742.1 | chr1:10823046-10823061 | ATAAAGGGTGTGGCC | - | 6.06 | Klf1 | MA0493.1 | chr1:10823050-10823061 | AGGGTGTGGCC | - | 6.32 | NR2C2 | MA0504.1 | chr1:10821254-10821269 | CAGGGTGAAAGGTCA | + | 6.47 | Nr2f6 | MA0677.1 | chr1:10821255-10821269 | AGGGTGAAAGGTCA | + | 6.38 | RARA(var.2) | MA0730.1 | chr1:10821391-10821408 | TGACCCCTGGGTGGCCT | - | 6.3 | Rxra | MA0512.2 | chr1:10821255-10821269 | AGGGTGAAAGGTCA | + | 6.63 | SCRT1 | MA0743.1 | chr1:10821429-10821444 | AATCAACAGGTGTCT | + | 6.57 | SCRT2 | MA0744.1 | chr1:10821429-10821442 | AATCAACAGGTGT | + | 6.11 | SOX10 | MA0442.2 | chr1:10822447-10822458 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr1:10822448-10822458 | CCTTTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr1:10823091-10823112 | TCCCCATTCCTGCCATCCTCC | - | 6.09 | ZNF263 | MA0528.1 | chr1:10823063-10823084 | GCCTCCTCCTCCTTTTCCCCC | - | 6.28 | Znf423 | MA0116.1 | chr1:10821391-10821406 | TGACCCCTGGGTGGC | - | 6.17 |
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| Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
SE_23090 | chr1:10818611-10823631 | Colon_Crypt_1 | SE_23754 | chr1:10818629-10823664 | Colon_Crypt_2 | SE_24724 | chr1:10818599-10823675 | Colon_Crypt_3 | SE_26723 | chr1:10821621-10823254 | Esophagus | SE_31374 | chr1:10818597-10824019 | Gastric | SE_40607 | chr1:10820904-10826781 | Left_Ventricle | SE_41555 | chr1:10820455-10821564 | LNCaP | SE_41555 | chr1:10821708-10822458 | LNCaP | SE_41555 | chr1:10822496-10823699 | LNCaP | SE_42099 | chr1:10820091-10823559 | Lung | SE_48119 | chr1:10820700-10826466 | Psoas_Muscle | SE_48591 | chr1:10821093-10823671 | Right_Atrium | SE_50332 | chr1:10818515-10823452 | Sigmoid_Colon | SE_52397 | chr1:10818536-10827620 | Small_Intestine | SE_59918 | chr1:10814600-10857062 | Ly4 | SE_65281 | chr1:10821705-10822832 | 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: 1 | ID | Chromosome | Start | End |
GH01I010758 | chr1 | 10818662 | 10823159 |
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Enhancer Sequence | AATGGCTACG CAGTTGTTGT ACCTAATAAA AGAAGCAAAC AGGTAGAAAC AATACTAGGC 60 CAATCAGGTG CCTCCCCAGG TAACACAGAA GGATCACACC CAAGGCTGGG CACCCAGGGT 120 GAAAGGTCAG GCCTGAAAAT GGATCAAGCC AATACTGGAA ACAGATCAAA CCCATGCAAC 180 CAAACCAACC CTGGGCTCCC CAACGCCTGC TCCCTCCAGA CTTTCCCTGC GCCAGCTCCC 240 AGCTGCTCCC CTGACCCCTG GGTGGCCTTC TGGGAGCCTC TATAAAAGGA ATCAACAGGT 300 GTCTCTGCAG CGACCCAGGA TAGTGAATTT AATTTCTTCT GGCTTTCCTT CCCCACTTCC 360 ATTCTGGTAC TGTGGGACTC AATTTCATAA AAAGAAAAGA GGGTGTGGGC CCTTGCCCTG 420 AAAGGGGGCT GCTGAGATTC AGTTGCGATA GGTGTTGGGA CAAAAAAAAA AGTAGCCAAA 480 GAAAGTTGGT GCCCTGCTAC CGGCAACCTT TGTGTCAATT TAAACAAATA TTGTGGTGTT 540 TCCATGGTGA TTCCTGTTTT GAATATCCAC TACACTCACT TTTTAAAGGG CTTTTCCTGT 600 TTGCGTTTCA ACTTCAAACC TGTAAATATT TTCAGCATTT TTAGAAAAAA GGAGCTCATG 660 CGCGTGCAAA CACAAACACA CAACCCGATC TCGGCGTACG ACCTCCCAGC CCTGGAAGCC 720 CGGCCTCGTG GATGTGAGAA TGGGGTGCTG AGAACCCAGA GGGGGTGCTC GGTCCGCTCT 780 CCTGCCCACC CTGCCTGCGG AGCTGGCATC AGGAAGATTG CCACTGAAAT CCCGGCCCTT 840 TCCTTCCCCC TTTGCGGGAA GATTGCAGCA GCCACAGCAG CTCTGCGTTC CTGAAGCGTG 900 TGAGCGGGCT GGGCCCTGCC TCCTTAGTGT GGCATGGTGT GGGCAGCTGC CCTGCAGGTT 960 CTCCAACTTG GCCCGGCCCT CAGAGTCCCC GGAGGCCTTG CAGGAGTGCA CGAACCCCTC 1020 CCCTCCTGCC TCCCAAGGTT GGACCTGAGT GCGAGGGGGA GTTGGCTCTT TGAAGGTGAG 1080 AGCTTCAGCA TCAGCTCTGC CCTACCTCGG CTGGGGCAAT GCCACCGAGA CCAGCTCCCT 1140 GGGGGAGGCC ATCAGGGGTG GACAGCATCC ACTGTCCAAG GCTTGGATCA GCCCAGCTCC 1200 CATCCCACCC CTCGGCGCCA CACAGGGTTA ACAGCGGGTT TCCTGGTTTC CATGGATTCC 1260 TGCCAGGCCC CTAATGTGAG TTTCGTGTGA TTTGGGGGAA GTGGATTTCC TTTGTTTTCC 1320 AGTTTGGGAA TATTTTTTTC TTTAAAAAAG AGGAAAAAAC ACTTTAATGG AAACTTCAGG 1380 GCCACTGGGA GACTCACTCC TCTGGGCTCT GAAACTCCCC TGCCTGTTAG TCCAGAATCC 1440 CCCAAAGCCC TGGGCAGCCC GTCCACCCAC AAAACTCCCC TGGGCTAGAA GAAGGCATGC 1500 CTTGGACCAC CTACACTCCT ACTCCAAGAA TCTCCATCTG CTGGGGGTCT CCACTCCAAT 1560 ATCCCATCAG AACGAACCCA CCTAAAAGCC AGCATCTTAC ACAGGAGGCT GACATGCCCC 1620 TCTTCCAGCT TTGTAAAACA GACATGTACA TTCCCCAGAA AAAAGGTTAA GGGAAACACA 1680 TCTACCTCCC CAACTCCAGG CAAGGCGCTG GCAAGACCAG GGGCTGACCA CAGGCCAACG 1740 GTGAACACTC TCGGTGTTTC ATGTCCTTGG CTCAGAGGAG GTTCCAGCTA TGGAAGGAAA 1800 GGGGGCTCCA GGCCCTGGTG GGACGCTCGT TGGGCTTCTT CCAGCGGAAA GTGGGGCCTG 1860 CCCAGGGCAG AGGATGCTTT TCAGCTTTGG CAGCAAGAAC AACTGAATAA AGGGTGTGGC 1920 CAGGCCTCCT CCTCCTTTTC CCCCACGGTC TTCCCCATTC CTGCCATCCT CCAAGCCTGC 1980 CAGGGCGTGG CCTTGCTCCA GGATTGTCCC CAACCAAGTG GCCTGACCCA CTTACCAAAC 2040 CAGGGCACAG GCCGCGGGGC CTTCCATAAA CTGAGGCTTT CCCACAGCCC AGGCCCCGGG 2100 GGCCATGGAT CCCGGTCAGA AAGTGCAGAG CGCAGAGGCC GGGTCTCTGT GACCAGCGGC 2160 TCCATGGTGA AGAAGTGAGA AGCTGAGTGA GCGTGCTTAC AGAAATCACA ACGGGCTGAG 2220 AACCAGGAGA CGTGGGTCCG AGTCCCACTT CTGTCCCCGA AACCTCCATG GGCCCTTAGA 2280 CAAGCCTGCT AATCTCCCTA GGTTCCGTCC CCTCACCAGC CAGACGGAGA CGATGCCTAA 2340 GACTTCCCTC CTACCTTGCA GGCTGCGCGG AGGATGGACA 2380
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