Tag | Content |
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EnhancerAtlas ID | HS191-03077 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr1:201986940-201988630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr1:201988332-201988343 | AGCCACACCCA | + | 6.14 | NR2C2 | MA0504.1 | chr1:201987451-201987466 | TGCCCTCTCACCCCT | - | 6.45 | NR2C2 | MA0504.1 | chr1:201987162-201987177 | TGACCTTTGCCCTGC | - | 6.4 | Nr2f6 | MA0677.1 | chr1:201987162-201987176 | TGACCTTTGCCCTG | - | 6.45 | RARA(var.2) | MA0730.1 | chr1:201987749-201987766 | AGGTCAGAGGGAGGTCA | + | 6.41 | REST | MA0138.2 | chr1:201988024-201988045 | CTCAGCACCTTGCACAGCGCC | + | 7.87 | Rxra | MA0512.2 | chr1:201987162-201987176 | TGACCTTTGCCCTG | - | 6.09 | Zfx | MA0146.2 | chr1:201988564-201988578 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_23058 | chr1:201986872-201988608 | Colon_Crypt_1 | SE_23723 | chr1:201986912-201988613 | Colon_Crypt_2 | SE_24689 | chr1:201986888-201988638 | Colon_Crypt_3 | SE_25977 | chr1:201976074-201988947 | Duodenum_Smooth_Muscle | SE_26730 | chr1:201985712-201988797 | Esophagus | SE_27624 | chr1:201975812-201989193 | Fetal_Intestine | SE_28545 | chr1:201974530-201989440 | Fetal_Intestine_Large | SE_31432 | chr1:201983938-201989177 | Gastric | SE_33417 | chr1:201986876-201989229 | H2171 | SE_33792 | chr1:201978127-201990221 | HCC1954 | SE_34304 | chr1:201974676-201989923 | HCT-116 | SE_34741 | chr1:201985668-201989981 | HeLa | SE_41626 | chr1:201986861-201988608 | LNCaP | SE_43434 | chr1:201986862-201988630 | MCF-7 | SE_47796 | chr1:201986886-201988593 | Pancreas | SE_50066 | chr1:201978058-201988672 | Sigmoid_Colon | SE_52354 | chr1:201976011-201988714 | Small_Intestine | SE_56834 | chr1:201986879-201988600 | VACO_400 | SE_57376 | chr1:201986910-201988595 | VACO_503 | SE_57945 | chr1:201986912-201988581 | VACO_9m | SE_65333 | chr1:201986253-201989108 | Pancreatic_islets | SE_67013 | chr1:201986876-201989229 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 201987200 | 201988600 | chr1 | 201987611 | 201988279 |
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Enhancer Sequence | TCAAAAAAAA GAAGAGAGGT GACCCAGTGT GGCCTGAAGT CACCTAGCCA AGAAGTGGGG 60 GAGGGGCCTC TAGAGCCCGG GACATGCTTG TTCAGCCTCC CTTGACTCCC AGCCTCTTCA 120 GCTTCTAAAG GAGATCCTAG CAGGGAGGAG GGCTGGGAAT ATGGCGCTCA GCCCCTTCAC 180 CCTCTTCTGG AGGGCTGGGG GCAGGTGCTG CCCGCTGCGT GCTGACCTTT GCCCTGCCAT 240 TTGCAGTTTA TGAGGCGCTT TCCTCATCCC ATTATCTCAT TTGATCCGCC CCACAGCTCG 300 CTGAGGAGAC CAGGTGTCCC CATTTTACTG ACAAGGCTAG TGGTGGGCTG AAGTCACTGA 360 CTGGGTGAGA GCGGGGCCAG CTCACAGCAT GCCTGCCTCC ACGCTGCAGC TCAGTGAGAC 420 CACCTGGGCA GGTGGCCTCT GCAGGGCAGC GCCTGGGACA GCCTGGAAGA CGGCAGCTCT 480 GGGAGGGACG CCTTTCTCCC CAACAGTTCT CTGCCCTCTC ACCCCTCAGG ATGCTGCAGA 540 GTCCTGGCAC GGGCCCCTGG GCTGGCCTCC GTGCTGCCCT CTCTGTCGGG CACCAGTCAC 600 CCTTACCCCG ACTCTCACCA GCCCAGGGGC CTCCTAGCAG GAGACGGCCC GGTCTCTCGC 660 CCACCAGAGT CTGCATCCCC TCAGGTGTGT CCTGGGCTGG GGAGTGGGGG TGGGGAGGAA 720 GCCACAGGGC CGGGCTGTTT ATATCCCGCC CTGCCGGAGC TGCTGGTCAC CTCTTATCTG 780 CTTCTGTGGG ATTGGGTGTG TCGCTGAGCA GGTCAGAGGG AGGTCACCCC TCCCGTCGTG 840 TTTGGGTGTG CCTGAGGAGG GGCTGGGGTT GGCCCCCTGG GACAGTTCCT GGCTTATCCC 900 ACAGCCCCAC CTGTCCCACC AATTCTGGGG AAGTCTGGCT TCTCCTGGGG GAAGTGGGTG 960 AAGGGGTTGC ATTTCTGAGG AGTCTGGTTT CAATCTGCTC TCTCTCTCTG CTGTTGTCTG 1020 TTTACACATC TCTCTCTCTC GCCGGGCTGT GAGCACCTCT GGGCAAGTGC TGGGGCTTAC 1080 TCACCTCAGC ACCTTGCACA GCGCCTGGCA CAGAGGAGGT GCTCGATAAA TATTTGCTAA 1140 ATGGCCCCGT GACTCTCCCT GCCCTGGCCA CTACCTCCCC CACACACCAC ACACATTCAT 1200 ACACACTCAT GGGAACCAAA GTCACACACA CTCACACTCA CAAAGATAAA TATTCACAAG 1260 CCCTCACTCA CATGCCCCTG CACGCACTGC AGACGCTGCC TGCTCTCACA CACTCGCATG 1320 GACCGTATTC ACAACCTCAC ACACTTGCAC ACACCAGCGC ACGCAACACA CTCCCACCTC 1380 ACAGTCTCAC ATAGCCACAC CCAGGCCTGC CTGCACGACT CACCTCCTCC CTCGGGGTCC 1440 TTCTATGAAG CATTTCCTGA CCTCCTCTTT GGCCCTTTTC CCCCACCAGA TGGGTTCAGC 1500 CCTTGCCTCC AGTCAGGACA GGCCTGGTAA TTTGCAGAGC CCAGTGCAAA GTGAAAGCCT 1560 GGGCCCTTGT TAAAGAATTA TTAGGCTGGG CGCAGTGGCT CATGCCAGTA ATCCCACACT 1620 TTGGGAGGCC GAGGCGGGTG GATCGCCTGA GGTCAGGAGT TTGAGACCAG CCTGACCAAC 1680 ATGGCGAAAC 1690
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