Tag | Content |
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EnhancerAtlas ID | HS081-01213 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:151960770-151963230 |
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_24041 | chr1:151962505-151962780 | 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_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 | 151960819 | 151962444 | chr1 | 151960875 | 151961433 | chr1 | 151961675 | 151962369 | chr1 | 151962584 | 151962808 |
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Enhancer Sequence | GAGACTGTAA TATAGCACTA AAAAATAAAA ATAAATAATC ACAAGAATAG GCTTTGAGCT 60 TAGATTGAAG GGCTGGCAAA TTCCTCTGCT GAAGAGCTCT AATGGGAACC TGAGACATGC 120 TTTGGTCTGG TTCCTATCTC TGAGAGATGC CTGTTCAACA CTGATTCTCA AATGCTATCT 180 TTTACAGAGG AGAAGGTGGA GTGGGTAAAC ATGAGGATTG AGCAATTAAC ACTTAAGAAT 240 TGTAAATTCT ACCCCTTAAT CTCCAGAAAA GTATGGGAAC CAGCAGGCCA AAGAATGCTA 300 TAAATCAGAA TCTGGCATGA GTCATCTGAA AGGCAGTTAG TTATCTTGGA GAGAGCTGCA 360 AATTAATGCT TCAAGGTCTG CTGTGAGATG AATTCCAGGG GAACCACACC CTTTTCCTTC 420 TCTTCTGACA CAGCTCAGAT CTGGCTCATC CCCCATCCCT CATATGGGTT TCAGATGGCA 480 GTGGGCTTAC AGAGAGTCTG CCTTGCCTGG ACTGGTACTC CAAGTCCAGC AATTTAAGAG 540 AACTGAACTG GGCGAGTCAC CTCTGGGAGA AGGACGTGGG ATCCCACCCC AGTTCTTAAA 600 TAACTCAGGA AAGGAGTCAG ACACCACAGA GGTTTAAAAA TACCTGTGCT CAAGTTCAGA 660 GCAGCAGAGC ACTTCAGGAT CAATTCCCAA AGATCCCAGA AATTGGAACT GGGTGGGGTA 720 CCTAGTTTAC TTTTTTCAGA TGACAGGACA GAAGGAAAGT GCAGAATTAA GAAAGGGAAT 780 GCAGCAGGGT AAGGACCTCT AAATTTTAAA AAGGCTAATT TTAGGAGGTT CTAAGAAATA 840 CAAGTTGTCA GCTGAGGAAA TCCTGGCCAC CCTTGAGTAT CTTCTTCAGG AGAGCAAGGT 900 GAGTCTACCT CACACTGTGT GAGTGCTTAG GTCTGAAGTC ACTCAGTCGC ATGCCTCTCT 960 TGCCCACAGC CATTACGAAG TGACGGAGCT TCCTTCTCTG AAGTTACATC CTTCTCCCAC 1020 TTGGTCTTCC CCTCCCCTCC TCCCCCAGCG GTTTTATTCA GTGGATGGAT TGTGAATATT 1080 GCAGCCAGCT GACTCCCTGT GTGTCCAGTA GGCCTTCTGC AATAAGGATG CAGAGGAGGG 1140 AGTAGCCAGG AGGTGAAAAT AGCATTGAAA ATCAGTGGAG AAGCCCTTGT CTCCTCAGCA 1200 ACCAGTACCC CAAAGGGCAC TGACCAGGGC CACAGCAAGG AACTCTGTTT TGGGGAAGGA 1260 GTTGCACACT GGCTTTAAAA TAAGACAAAG GAAAGGGGGA AATGTTGTGA TTAAAACTCT 1320 GTTCTCTTGG CTAGAGGATG AATCATGTAA CTCTTGTCTG AGTGCAGCCA ATGGTTGCCC 1380 AACTGAGTCA GCCCTGCCTG GCCCTCCGTT CTTGGGTGGG GCTTGCCTGG GCAGGGCTGT 1440 CTGCAGCACT GCTAGCTGCC AAAACTGAAG TTCTTCAGGG ACTTCAATCT GGCATTTCCA 1500 CCCTCACGTA GCCACTCTGC AAGCTCTATT CCTGGACAGA TGTGGGCTTC CTGCATCCTG 1560 GTTAGACACA TTTTGACAGG AGGGCCTTGG GGCTGGGGCT GAGGGGCTGC AGTGTCCTCT 1620 CTATCCCCAA TAACGTACTC TTGCACCTGA AACATTCAAT TTCATTTAAT TGTTTACTTG 1680 TCTGCCTGAG ATTTAAGCTT CTCTTGATTA AGAACTACAA ATTATTCTGC TTTTATTCAT 1740 GGAGCACTAT ATAACTGTTA TGTGCATAAA TGAACCACAC AATCCCTTGG GCAGTAGCTG 1800 AGGTGCAGGT GTGATTACCC AGGACTAGGC TGAAAGCCTT GTAGCTCAGA GCTCAGGAGG 1860 ACGATGTGAG AGCTGGGAAG GGCCAGGAAA GGGGCCCCAA AAGTGTTCAA CTATGAACGG 1920 AACAGTAGAT AGAGTACACA GGAGTGCACA TTCCATACGC AAAAGGAAAA ATATGTGTCC 1980 TGCTAAACAG GTCTAGTCAG AATGACATGA CTGTGCTCCT TCTCTTCTAA CACTTGCTAT 2040 TTTCTCGTGT TTCATTCATC CCATCTTCTA CTTTTTGCTT TTCTAGTGCT GCTATCTCAC 2100 TGCTGAGCTC CACAGGATAA TAACAGCCTT GCTGTCCACT CACCTTTTAT TGAAGTATTC 2160 TAATCTGATG CCTATACATG CCCTCTACAT GTTTGTCTGA GCAACAGGTC TTAAGAAGGG 2220 AGGCGGAGAC ATCTTTCTCT GCATAGTTTT CTCTATGGAA AACAATTCTG GACTCCACAA 2280 ATTTAGTTAC CTTAGGAGGA ATTCAATTTT CCATTTTTGG TTCTCCCTCC CTGAGCACCT 2340 ACTTTGAATG TCCCAGACAT GGTGTTAGGC ATGAGGGTGT TCACACACAC ATACACACAT 2400 GCACACACAC ACAAAGCTCT CCATGGTGCT TGCCTTTGAG GAGTTCACCA GCTAATGGAA 2460
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