Tag | Content |
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EnhancerAtlas ID | HS017-21359 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr21:40211660-40213250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr21:40212398-40212408 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr21:40212398-40212408 | GGCACGTGCC | - | 6.02 | MEF2C | MA0497.1 | chr21:40212426-40212441 | TTTTATTTTTAGTAT | - | 6.12 | Nr2f6(var.2) | MA0728.1 | chr21:40212485-40212500 | TGAACTCCTGACCTC | - | 6.22 | Nr5a2 | MA0505.1 | chr21:40212582-40212597 | GCTGGCCTTGAGCTG | - | 6.62 | REL | MA0101.1 | chr21:40212202-40212212 | GGGGATTTCC | + | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_26886 | chr21:40211585-40212348 | Esophagus | SE_28570 | chr21:40210940-40212412 | Fetal_Intestine_Large | SE_34978 | chr21:40209649-40213598 | HeLa | SE_36155 | chr21:40210493-40213751 | HMEC | SE_50186 | chr21:40211703-40212366 | Sigmoid_Colon | SE_52374 | chr21:40211703-40212315 | Small_Intestine | SE_64260 | chr21:40210447-40214043 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 40211972 | 40212276 | chr21 | 40212954 | 40213097 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I038837 | chr21 | 40209875 | 40213675 |
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Enhancer Sequence | TTCTAAAGTT TGTATGATGC AACGTTCTTG TGAATTATAG ACAAATGATT CATCTGTTTG 60 ACTCAGATTC AAGGACATTT TTTGTGGTGA AGTAAGGCAC TGAGTCTCAA GATATAATGT 120 AAAGATATGG AGTTGCTATG CCAGGAAAAG AACTATAGAA AGGGCAGCTA GGAAGTCAAT 180 GCAATAGTCA GCACACCTCT GGGGCCCTCC CTGGGAGCCT CTGATTCCAT TACTCTTGGG 240 TGGGCCCTGG ACATCTATAT TTTCTCCAAG TTCCATTCAT GATTCTAATG CTCAGCAAAG 300 CTGGGGAACC ACTGCAATAA GGCATGATCT TGAGAGTTAT GGCGCAGAGA CATGCATCTG 360 CCTCTGACTC AGCACAAGGG GCACCCCGCT TCTCACGTCT CATGACTGCA TGGTGTACAG 420 TGTGGTCAGT TCAGCCTTTA TGTCTAACCT CTGTCCTTCT CCACCCTGTG GGGTGCCGCT 480 GACCTGTGGG GTGTTGACCA CAAACAGATT CCTACCCCAT GTTTCTTGGG GGTTCATCCC 540 ATGGGGATTT CCAGAAGGAG ACTGGAGTTT CACTCTCCTG CCTCCCCTGA TCCCTGCTTT 600 TTTTTTTTTT TTTTGAGACA GGGTCTCACT CTAACACTCA GGCTGGAGTG CCGTGGTATG 660 ATCTCGGCTG ACTAGCAACC TCCACCTCCT GGGTTCAAGC GATTCTTCTG CTTCAGCTTC 720 CCGAGCTGCT GAACTAAAGG CACGTGCCAC CACGCCTGGC TAATTTTTTT ATTTTTAGTA 780 TATTTTAGTA GAGACGGAAT TTCACCGTGT TGGCCAGCCT GGTCTTGAAC TCCTGACCTC 840 AAGTGATCTG CCCGCCTTGG CCTCCTAAAG TGCTAAGATT CCAGACGTGA GCCACCGGGC 900 TCTCCTGCCT CCCTTTTGAC CAGCTGGCCT TGAGCTGGCT GTGTCCGTGG GCCTGAGGCT 960 ATGCTCCTCT CAAAGGCTGA CTCTCCATGG CTCTCCTTGT GGTTCCACTA ACTAGTGCCT 1020 ACCCTTGTCC CTCGAGGCTT AGAAGGTGCT GAAGCTGAAC TGCAGGGAGC CCCAGGTTAC 1080 TGCCTGTATT CATTACCTGT GTCTGCTGTA AGAAATTTCC ACACACTCAT TCACTTAAAA 1140 CAACATATAT TTATTATCTT ACATTTCTAG AGGACAAGAG TCCAGAAATA GTCCCACTGG 1200 GCTAACGTCA AGGGCTAGTG CCCTCTGGAG CTCCTAGAGT CAGCCTGCAT TCCCAGGCTT 1260 ATGGCCCCTT CCACCATCCT GAGAGCCAGC AGTGTGGCAC CTTCAACTCT CTCTCTGCCC 1320 ACCCTCCGCT TTCATCATCA CTCATCTCTG ACTGTGAGGA TCCTGCTTCC CTCTTTCGAG 1380 GAACCCTGTG ACTACATGGG TGATCCATGA CAGTCTGCCC ATCTCCAGAT CCTCAGTCAC 1440 CCTGCAAAGT CTCTTTTGCC GAGTAAGGCA GCATGTTCAC AGGTTCTGGG GAGCAGGAGG 1500 TGGACCTCTT GGGGGTCATT ATTGCGTGTA CCGCACCTTG CTTTCTACTT TGCAGTTTCC 1560 TACGCCCACA CCTTTGTGAA CAGCCCCGTG 1590
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