Tag | Content |
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EnhancerAtlas ID | HS116-02080 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:151960820-151963640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr1:151963075-151963085 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:151963075-151963085 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:151963075-151963085 | ATTTTCCATT | + | 6.02 | REST | MA0138.2 | chr1:151963182-151963203 | AAAGCTCTCCATGGTGCTTGC | - | 6.59 | TEAD1 | MA0090.2 | chr1:151962716-151962726 | CACATTCCAT | + | 6.02 | ZNF263 | MA0528.1 | chr1:151961795-151961816 | CTTCCCCTCCCCTCCTCCCCC | - | 7.84 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_00284 | chr1:151951696-151968835 | Adipose_Nuclei | SE_02826 | chr1:151960179-151963618 | Astrocytes | SE_09689 | chr1:151958965-151967354 | CD14 | SE_23217 | chr1:151961002-151967250 | Colon_Crypt_1 | SE_24041 | chr1:151961119-151961502 | Colon_Crypt_2 | SE_24041 | chr1:151961532-151962451 | Colon_Crypt_2 | SE_25129 | chr1:151961024-151962388 | Colon_Crypt_3 | SE_26790 | chr1:151960243-151968142 | Esophagus | SE_27992 | chr1:151959711-151968123 | Fetal_Intestine | SE_28908 | chr1:151959611-151968309 | Fetal_Intestine_Large | SE_33866 | chr1:151960207-151967313 | HCC1954 | SE_34778 | chr1:151959926-151968552 | HeLa | SE_35880 | chr1:151959933-151975921 | HMEC | SE_43050 | chr1:151960740-151967310 | Lung | SE_44654 | chr1:151960194-151968465 | NHDF-Ad | SE_45267 | chr1:151960456-151967435 | NHLF | SE_47215 | chr1:151938610-151969225 | Panc1 | SE_50609 | chr1:151960617-151968225 | Sigmoid_Colon | SE_52876 | chr1:151960623-151968189 | Small_Intestine | SE_56104 | chr1:151960357-151967571 | u87 | SE_57650 | chr1:151961137-151963029 | VACO_503 | SE_57650 | chr1:151963087-151963741 | VACO_503 | SE_58076 | chr1:151961586-151962069 | VACO_9m | SE_58076 | chr1:151962098-151962413 | VACO_9m | SE_58076 | chr1:151962967-151963306 | VACO_9m | SE_64176 | chr1:151960195-151967437 | HSMM | SE_64341 | chr1:151960135-151968569 | NHEK | SE_67706 | chr1:151960357-151967571 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr1 | 151960875 | 151961433 | chr1 | 151961675 | 151962369 | chr1 | 151962584 | 151962808 | chr1 | 151963069 | 151963635 |
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Enhancer Sequence | GCTTTGAGCT TAGATTGAAG GGCTGGCAAA TTCCTCTGCT GAAGAGCTCT AATGGGAACC 60 TGAGACATGC TTTGGTCTGG TTCCTATCTC TGAGAGATGC CTGTTCAACA CTGATTCTCA 120 AATGCTATCT TTTACAGAGG AGAAGGTGGA GTGGGTAAAC ATGAGGATTG AGCAATTAAC 180 ACTTAAGAAT TGTAAATTCT ACCCCTTAAT CTCCAGAAAA GTATGGGAAC CAGCAGGCCA 240 AAGAATGCTA TAAATCAGAA TCTGGCATGA GTCATCTGAA AGGCAGTTAG TTATCTTGGA 300 GAGAGCTGCA AATTAATGCT TCAAGGTCTG CTGTGAGATG AATTCCAGGG GAACCACACC 360 CTTTTCCTTC TCTTCTGACA CAGCTCAGAT CTGGCTCATC CCCCATCCCT CATATGGGTT 420 TCAGATGGCA GTGGGCTTAC AGAGAGTCTG CCTTGCCTGG ACTGGTACTC CAAGTCCAGC 480 AATTTAAGAG AACTGAACTG GGCGAGTCAC CTCTGGGAGA AGGACGTGGG ATCCCACCCC 540 AGTTCTTAAA TAACTCAGGA AAGGAGTCAG ACACCACAGA GGTTTAAAAA TACCTGTGCT 600 CAAGTTCAGA GCAGCAGAGC ACTTCAGGAT CAATTCCCAA AGATCCCAGA AATTGGAACT 660 GGGTGGGGTA CCTAGTTTAC TTTTTTCAGA TGACAGGACA GAAGGAAAGT GCAGAATTAA 720 GAAAGGGAAT GCAGCAGGGT AAGGACCTCT AAATTTTAAA AAGGCTAATT TTAGGAGGTT 780 CTAAGAAATA CAAGTTGTCA GCTGAGGAAA TCCTGGCCAC CCTTGAGTAT CTTCTTCAGG 840 AGAGCAAGGT GAGTCTACCT CACACTGTGT GAGTGCTTAG GTCTGAAGTC ACTCAGTCGC 900 ATGCCTCTCT TGCCCACAGC CATTACGAAG TGACGGAGCT TCCTTCTCTG AAGTTACATC 960 CTTCTCCCAC TTGGTCTTCC CCTCCCCTCC TCCCCCAGCG GTTTTATTCA GTGGATGGAT 1020 TGTGAATATT GCAGCCAGCT GACTCCCTGT GTGTCCAGTA GGCCTTCTGC AATAAGGATG 1080 CAGAGGAGGG AGTAGCCAGG AGGTGAAAAT AGCATTGAAA ATCAGTGGAG AAGCCCTTGT 1140 CTCCTCAGCA ACCAGTACCC CAAAGGGCAC TGACCAGGGC CACAGCAAGG AACTCTGTTT 1200 TGGGGAAGGA GTTGCACACT GGCTTTAAAA TAAGACAAAG GAAAGGGGGA AATGTTGTGA 1260 TTAAAACTCT GTTCTCTTGG CTAGAGGATG AATCATGTAA CTCTTGTCTG AGTGCAGCCA 1320 ATGGTTGCCC AACTGAGTCA GCCCTGCCTG GCCCTCCGTT CTTGGGTGGG GCTTGCCTGG 1380 GCAGGGCTGT CTGCAGCACT GCTAGCTGCC AAAACTGAAG TTCTTCAGGG ACTTCAATCT 1440 GGCATTTCCA CCCTCACGTA GCCACTCTGC AAGCTCTATT CCTGGACAGA TGTGGGCTTC 1500 CTGCATCCTG GTTAGACACA TTTTGACAGG AGGGCCTTGG GGCTGGGGCT GAGGGGCTGC 1560 AGTGTCCTCT CTATCCCCAA TAACGTACTC TTGCACCTGA AACATTCAAT TTCATTTAAT 1620 TGTTTACTTG TCTGCCTGAG ATTTAAGCTT CTCTTGATTA AGAACTACAA ATTATTCTGC 1680 TTTTATTCAT GGAGCACTAT ATAACTGTTA TGTGCATAAA TGAACCACAC AATCCCTTGG 1740 GCAGTAGCTG AGGTGCAGGT GTGATTACCC AGGACTAGGC TGAAAGCCTT GTAGCTCAGA 1800 GCTCAGGAGG ACGATGTGAG AGCTGGGAAG GGCCAGGAAA GGGGCCCCAA AAGTGTTCAA 1860 CTATGAACGG AACAGTAGAT AGAGTACACA GGAGTGCACA TTCCATACGC AAAAGGAAAA 1920 ATATGTGTCC TGCTAAACAG GTCTAGTCAG AATGACATGA CTGTGCTCCT TCTCTTCTAA 1980 CACTTGCTAT TTTCTCGTGT TTCATTCATC CCATCTTCTA CTTTTTGCTT TTCTAGTGCT 2040 GCTATCTCAC TGCTGAGCTC CACAGGATAA TAACAGCCTT GCTGTCCACT CACCTTTTAT 2100 TGAAGTATTC TAATCTGATG CCTATACATG CCCTCTACAT GTTTGTCTGA GCAACAGGTC 2160 TTAAGAAGGG AGGCGGAGAC ATCTTTCTCT GCATAGTTTT CTCTATGGAA AACAATTCTG 2220 GACTCCACAA ATTTAGTTAC CTTAGGAGGA ATTCAATTTT CCATTTTTGG TTCTCCCTCC 2280 CTGAGCACCT ACTTTGAATG TCCCAGACAT GGTGTTAGGC ATGAGGGTGT TCACACACAC 2340 ATACACACAT GCACACACAC ACAAAGCTCT CCATGGTGCT TGCCTTTGAG GAGTTCACCA 2400 GCTAATGGAA TACTATTAAA GCATTTGGCC TGAATTCTAG TTATTTGTGT TTCTGTTTCT 2460 TTCCTCACTA GGTTGCAGGT TTTTTGAGCA GGGTCCCAAT AGCCAGTGCC CCAGCCCTCA 2520 TAGAGCCTGC TCGATGAATT GTTAAGAAAT TGATAATGAT GTATTTTGGT TGTCCTGCGA 2580 GTAGCAGACA AGCAGGAGTC CTCCTCAGAA AAGTGTCTGC TCCTGAAAAA TCTCAAATGT 2640 TTGCTTTGGA CCTATGCCCA GATCCCGGCT GCAGTTTCAA AGAGGACACT TCTGCAGAGT 2700 GAGTCGGACT TGCTTTGCTC CTCTGTGTCT TGTCCATACC CTAGTTTTCT TACAGCCCAC 2760 CCAGAAAATA AACGGCAGGG TGTCAGTAAA AACAAACATC TGTTATTTAA AATATGTTTG 2820
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