Tag | Content |
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EnhancerAtlas ID | HS051-14382 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:45226740-45227820 |
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 | CTCATTCATT CCATAAACAT TCCCTGGAGT GCATTGTCAG TGTCAGGCCC CAGGGGAACA 60 CAGCAGTGAC CACGACAGCC CCACCAGACC ATGACCCTGA CCAGGGGGCT CACGAGGGCG 120 GAGACATCTA CTCCAAGACC TGAAGGAGGA GTAGGAGAGA TGCTGGGGAA GAGGCAGGGA 180 AGGGTGTTCC TGGCAGAGGG AACAGCCTGT GCGAAGGCCT GAAGGTAAGT TTTGCATATG 240 ACACCTTTGA GAAACTACTT ATTGTTCAAC TGAAGCATAG GGTTGTTCAG AAGAAGCCAG 300 CCTTGTGGCC GGGTGTGGAC TTCCTCCCAG GGCACCAGGG AGCCACTGCA GAGTTGTGAG 360 CAAGGGACAG ACAGAGGTAG GCTTGTACTT CCAAGAGACT CCCCCAGCTG CCACATGCAG 420 GGTGAATGGA ATGATGCACA GAATCCAGTT TCAGGGGTAG TTTGGTACTT GGACCCAGGT 480 CCCAGGGAGA GAGTCCAAGG AGCCCTTCTC TGGTCTTCCA AGGAGCTGCT CTCCCCAAGC 540 TCCGGATGGA AGGCGTGCCC ATGGCAACCG CTAGGTGGTG CCCGTACACC ACCAGCCAGG 600 TCTTTTTTTG CCAAAAGTAG ATCAGGCCCA GAGCTGGGCA GAACTGCCCC TGGGTCAGGA 660 GAGCAAATCG TCTCTGTCTT TTGGTCCTGG CTCCCTGGCC AGGCATCCTG GGGCCATTTG 720 ACTCCCAGGC TCAGGAAGGA GCTGGCTGAG CTGCAGTGAG TATGTTCTTC GTCTCTTTCC 780 TCACCTTGGA ATCTCAGACG GGAGCACCCT GGCTCCCACT TCAGACAGGA AGATTCTTAC 840 CTCCCTCATC AGACTAGCAG GCTCTTTGTC TCCCCACCAG TTTGAGGGGC TCCCCATTTC 900 TATCATTCAT TTGGAAGCTC ATCAGCTCTC CCAGAAGGCA TGGGAGCCCT TCAACACCCC 960 CATCAGACTA GGACTACCCA TCTCCCCCAT CAAATTAGAA CTGCATTGTC TCACACATCA 1020 AAGTATCACT CCTGGCCAGG TGCAGTGGCT CCCGCCTGTA ATCCAAGCAC TTTGGGAGGC 1080
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