Tag | Content |
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EnhancerAtlas ID | HS047-17689 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:45226690-45227940 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr19:45226881-45226902 | GAAGGAGGAGTAGGAGAGATG | + | 6.2 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09606 | chr19:45225026-45227473 | CD14 | SE_23197 | chr19:45226609-45227960 | Colon_Crypt_1 | SE_23877 | chr19:45226698-45227829 | Colon_Crypt_2 | SE_26699 | chr19:45226534-45229277 | Esophagus | SE_31568 | chr19:45227174-45229356 | Gastric | SE_34750 | chr19:45226424-45229782 | HeLa | SE_47531 | chr19:45227242-45227666 | Pancreas | SE_53360 | chr19:45226521-45227795 | Spleen | SE_56197 | chr19:45227061-45227913 | u87 | SE_62704 | chr19:45221152-45271677 | Tonsil | SE_65330 | chr19:45226619-45230111 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I044721 | chr19 | 45225041 | 45229949 |
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Enhancer Sequence | GCCCTGGCAA ACTCTTTAGC TTGGCATTCA TTCATTCATT CATTCATTCA CTCATTCATT 60 CCATAAACAT TCCCTGGAGT GCATTGTCAG TGTCAGGCCC CAGGGGAACA CAGCAGTGAC 120 CACGACAGCC CCACCAGACC ATGACCCTGA CCAGGGGGCT CACGAGGGCG GAGACATCTA 180 CTCCAAGACC TGAAGGAGGA GTAGGAGAGA TGCTGGGGAA GAGGCAGGGA AGGGTGTTCC 240 TGGCAGAGGG AACAGCCTGT GCGAAGGCCT GAAGGTAAGT TTTGCATATG ACACCTTTGA 300 GAAACTACTT ATTGTTCAAC TGAAGCATAG GGTTGTTCAG AAGAAGCCAG CCTTGTGGCC 360 GGGTGTGGAC TTCCTCCCAG GGCACCAGGG AGCCACTGCA GAGTTGTGAG CAAGGGACAG 420 ACAGAGGTAG GCTTGTACTT CCAAGAGACT CCCCCAGCTG CCACATGCAG GGTGAATGGA 480 ATGATGCACA GAATCCAGTT TCAGGGGTAG TTTGGTACTT GGACCCAGGT CCCAGGGAGA 540 GAGTCCAAGG AGCCCTTCTC TGGTCTTCCA AGGAGCTGCT CTCCCCAAGC TCCGGATGGA 600 AGGCGTGCCC ATGGCAACCG CTAGGTGGTG CCCGTACACC ACCAGCCAGG TCTTTTTTTG 660 CCAAAAGTAG ATCAGGCCCA GAGCTGGGCA GAACTGCCCC TGGGTCAGGA GAGCAAATCG 720 TCTCTGTCTT TTGGTCCTGG CTCCCTGGCC AGGCATCCTG GGGCCATTTG ACTCCCAGGC 780 TCAGGAAGGA GCTGGCTGAG CTGCAGTGAG TATGTTCTTC GTCTCTTTCC TCACCTTGGA 840 ATCTCAGACG GGAGCACCCT GGCTCCCACT TCAGACAGGA AGATTCTTAC CTCCCTCATC 900 AGACTAGCAG GCTCTTTGTC TCCCCACCAG TTTGAGGGGC TCCCCATTTC TATCATTCAT 960 TTGGAAGCTC ATCAGCTCTC CCAGAAGGCA TGGGAGCCCT TCAACACCCC CATCAGACTA 1020 GGACTACCCA TCTCCCCCAT CAAATTAGAA CTGCATTGTC TCACACATCA AAGTATCACT 1080 CCTGGCCAGG TGCAGTGGCT CCCGCCTGTA ATCCAAGCAC TTTGGGAGGC CGAGGCAGGA 1140 GGATCACCTG AGGTCAGAAA TTCAAGACAA ACCTGGCCAA CACGGTGAAA CCCGGTCTCT 1200 ACTAAAAATA ACAAATTAGC CAGGCGTGGT GGTGTGCGTC TGTAATCCCA 1250
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