Tag | Content |
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EnhancerAtlas ID | HS094-43551 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr9:114822300-114825210 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EN2 | MA0642.1 | chr9:114823243-114823253 | CCCAATTAGC | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr9:114824758-114824773 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr9:114822763-114822778 | TGAACTCCTGACCTC | - | 6.22 | TP53 | MA0106.3 | chr9:114824577-114824595 | GACATGTCCTAACATGCA | - | 6.22 | TP53 | MA0106.3 | chr9:114824577-114824595 | GACATGTCCTAACATGCA | + | 6.24 | TP63 | MA0525.2 | chr9:114824577-114824595 | GACATGTCCTAACATGCA | + | 6.75 | TP63 | MA0525.2 | chr9:114824577-114824595 | GACATGTCCTAACATGCA | - | 7.34 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_02843 | chr9:114821302-114822743 | Astrocytes | SE_02843 | chr9:114822752-114824648 | Astrocytes | SE_28204 | chr9:114819961-114824713 | Fetal_Intestine | SE_29159 | chr9:114819796-114824755 | Fetal_Intestine_Large | SE_30746 | chr9:114822664-114824824 | Fetal_Muscle | SE_36599 | chr9:114821040-114824796 | HMEC | SE_37072 | chr9:114820182-114826053 | HSMMtube | SE_38312 | chr9:114820486-114825049 | HUVEC | SE_38966 | chr9:114821262-114824800 | IMR90 | SE_40486 | chr9:114821053-114823986 | K562 | SE_44179 | chr9:114819976-114826304 | NHDF-Ad | SE_44994 | chr9:114821042-114824806 | NHLF | SE_45614 | chr9:114820116-114826322 | Osteoblasts | SE_51720 | chr9:114821228-114824972 | Skeletal_Muscle_Myoblast | SE_55723 | chr9:114821209-114824815 | u87 | SE_55723 | chr9:114824914-114825758 | u87 | SE_58816 | chr9:114652459-114841988 | Ly3 | SE_60959 | chr9:114735912-114841786 | HBL1 | SE_62263 | chr9:114654503-114840084 | Tonsil | SE_63509 | chr9:114821214-114824972 | HSMM | SE_67537 | chr9:114821209-114824815 | u87 | SE_67537 | chr9:114824914-114825758 | u87 |
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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 |
GH09I112057 | chr9 | 114820116 | 114826107 |
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Enhancer Sequence | TCAGCGTGAA ATATAATTAG GGTAATTTCC AAAACTCATT AGGCCATGTA ATTCTATTTT 60 ACCAGTAAAT TTGAACTTCC TGCTTCACAT GTCAAACGCC CTATCTCCTG CTTCCTAAGA 120 GCCCATGAAT CACTAGGTTA AGAAGAGGGA GCCCTCCTCC ACAGTGGGTG TTGGATATGG 180 AAAGTCTCCC CCCACCAGGT TCCCAAACAT CCTAGGTATC CTCAGGGCCC TGATTTTCTT 240 TCTTTTCTTT TCTTTTTTAA GAAGGGAGTC TTGCTCTGCT GCCCAGGCTG GAGTGCAGTG 300 GTGTGATCTC AGCTCACTGC AACCTTTACC TCCCAGGTTC AAGCGATTCT TCTGCTTCAG 360 CCTCCTGAGT AGCCAAGACT ACAGGCACTC GCCACTATGC CCGGTTAATT TTTTTTGTAT 420 TTTTAGTAGA GATGGTGTTC CACCATGTTG GCCAGGCTGG TCTTGAACTC CTGACCTCTT 480 TAGCTGGGGG AAGTTGTTGC ACGTATCACT GCCCTGTGTG CCCACCTCTG CCTCCCAATG 540 GGCTGGGATT ACAGGCGTAA GCCACTGTGC CTGGCCCAGG GTCCTGATTT TCATAAAGTC 600 TTGGCTCACT TTCAGCCAAG GGCTTTCTAC AAAAGAGATA AAGTAAAACC CACAGGGCAA 660 TAAGTTGTCA CCACCAGTAA ACATTTATTA AGCATCCACT GCCTATGGGG AACACCTGTA 720 ACAACAAACT TGCCGGGAGA CTTGAAGACA TCCCTACATC ATAGCCACAG GTAAGAAAGT 780 AAATGTTGCA GCACCTCCAT GCGGTCCATA AGTACATCTT TAAATCCCTC TCATCTTTCC 840 ATGCAGGTGG TGGTGGTCAA GAGCAAGGTC GAGGCTCACC TGTGCCCATT TGGTTCCGTA 900 CATTGCTCAC TAGAGGCATC ATCGACAGAG TATGAATCAG CTCCCCAATT AGCCTGACCG 960 TAATCACCTG TGTTGCTTGA TTATTATACA AATTCCCCGA CCTCATACCG ACCTACTGAA 1020 TCGAAATCTC TAGGAGTAGA TTCTGGGAAT CTGTATCGCT GGTAAAGCTC CCAGGTGATT 1080 CCTATAATCT GGCAATGTGG GAGACACGAG CATTAAGGGA ACCCAGCAAC AGGCTCCATC 1140 CTCTGCCTAA CATCAGCAAC CTCAGCAGAG ACTTGGTCCC AGGGACCTTG CTCCATTATG 1200 TACCCCAAGA CACTGTCCCT AAATGGTGCA CAAAGCAGAC TCAGGCCTGT CTCACACACT 1260 GGCAAAGCTG CTGCCCCCCA GCTCAAACCA GGTAGTCAGG CTTAGGAAAA CCACCCTGCC 1320 TGCTGGTAAT TAGCCATGTG ATGTTAAAGA AGCAGCTGTG GCTGTTTGGA ATATGACTGT 1380 TCTGGAAGGA CTTTTCTCCT CTTTTTCACC ACCACACTCC CTCGAATGAC TCACAGTTCT 1440 CCACTTCCTG TTTTGGAGGC GCTGGCCGGC ATATAGCCAC AAGGGTAAGC TGTCATTTGG 1500 CTTTTCTTTT GCATTATGTC ATTATTTGAC ATAAATATCA CATTTGTTCT TGCAAATGCT 1560 CTCAGGAAGT GACATCACAA CTTCTGTTCT CTTTATAATG ACAGAATTAC AATGCCTTCT 1620 GGTAACTTGT CAAGAATCAG AACAATTTAT ACAATGTCCA TCCCTGGAAA GATCTTTGCA 1680 CATTTACTGA ACTTAAATGA ATATAAAAGC AGGAAAACCC TAAGTTTTAT TATAAATGGA 1740 TATACAGATA ATATCGCCAG ACTTTCTTTT TTGTAATTTT ATAATATCTC ACTTTTTTTT 1800 TTTTAACCTT GATTTTACCG AAGGGTCAGC AGAGACAAAG GCAATGTTGG TGAGGCCATG 1860 TACATTTTCA TCTCCTTGAG CTGGTACTGT GAGCAAGCTG TTCATCTCTC CACGCCAACC 1920 TCAATCTTCC TCTCTAAAAA AGGGACTGAT GCTACTTTCC TAATCCTGCC ATGACCTTTG 1980 CAAATAAAAC ACTTAACTGA ACACACTGTA GTCCTCCAAC TGAGGTAAAT TAATTCCATC 2040 CTAATGCCAT CTGGAATCCC AGAAGCAGTC ATTAATTATA CAGTGTCTTG CCTGTAACTC 2100 AATACATGAA AAGACAAAAA GATTTACCTA AATGATCTTT TCAGAAACCA CTGCACACCC 2160 CCCAAGATCA ACCTTACATA AAGGGCAACA TATTCTGCCT TTGGGAAATG AAACGATGCC 2220 CCTGACCCAC CATCCATAAA GGATGTACTA TGAGACATGA GTGCAAAGGA CAATCCTGAC 2280 ATGTCCTAAC ATGCAACCGA CGTTTACCCA GGGACCAAAG GAATGGATGT AATTTCTTGA 2340 GCTAAACTGC CCAAATGCTT GTATATAGGG TCCTTTAGAA GTCTCTCTAT GTGGCCGGGT 2400 GTGGTGGTTC AAGCCTGTAA TCCTAGCACT TTGGGAGGTT GAGGCTGGTG GATCACCTGA 2460 GGTCAGGAGT TCAAGACCAG CCTGACCAAC ATGGCAAAAC CTCGTCTCAA CTAAAAATAC 2520 AAAAATTAGC CAGGTGTGGT GGTGCACACC TATAATCCCA GCTACTCAGG AGGCAGTGGA 2580 AGGAGAATCA CTTGCACCCA GCAGGTGGAG GTTGCAGTGA GCTGAGATCG CAACACTGTA 2640 CTCCGGCCTG TATGATGGGA GTGACACTCC ATCTCAAAAA AATAAAAAAT AAAATTTAAA 2700 TTTTAAAAAA AAGAAGTCTC TCTCACCATT AGAAAGGATG CTGGTTGGGA TTAAAGGCCA 2760 GTCTGTACCC AAGGAAACAA AAGAGGCCCC AACTGCATTG TTCTAACCAC CCAAGTGCAG 2820 CCACCAACAC AGAAGTCTTC TCCTCACCAA AATCAAAGTT TCCAAAACAC TCCATGGGGA 2880 TCACTGGGCA ACCGTGGAGA AAGGACAGCT 2910
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