Tag | Content |
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EnhancerAtlas ID | HS191-18661 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr19:18589330-18590430 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:18590302-18590317 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_01013 | chr19:18588643-18590394 | Adrenal_Gland | SE_04099 | chr19:18588738-18590106 | Brain_Anterior_Caudate | SE_06012 | chr19:18587569-18592062 | Brain_Hippocampus_Middle | SE_09318 | chr19:18587289-18593113 | CD14 | SE_12155 | chr19:18588799-18590417 | CD3 | SE_15037 | chr19:18589123-18590617 | CD4_Memory_Primary_7pool | SE_17983 | chr19:18583928-18591813 | CD4p_CD25-_CD45ROp_Memory | SE_19379 | chr19:18587487-18590403 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20439 | chr19:18584612-18591598 | CD56 | SE_21047 | chr19:18588603-18591663 | CD8_Memory_7pool | SE_22689 | chr19:18583973-18591671 | CD8_primiary | SE_23893 | chr19:18589312-18590189 | Colon_Crypt_2 | SE_26168 | chr19:18588425-18592741 | Duodenum_Smooth_Muscle | SE_26932 | chr19:18588122-18592042 | Esophagus | SE_31681 | chr19:18588601-18590332 | Gastric | SE_41123 | chr19:18587807-18590387 | Left_Ventricle | SE_41560 | chr19:18589244-18590155 | LNCaP | SE_42344 | chr19:18587292-18590373 | Lung | SE_44495 | chr19:18587274-18592340 | NHDF-Ad | SE_46271 | chr19:18587413-18593123 | Osteoblasts | SE_47511 | chr19:18588888-18589813 | Pancreas | SE_47511 | chr19:18589872-18590274 | Pancreas | SE_48120 | chr19:18587362-18592202 | Psoas_Muscle | SE_48694 | chr19:18588545-18590349 | Right_Atrium | SE_50125 | chr19:18585873-18593035 | Sigmoid_Colon | SE_51145 | chr19:18587336-18592595 | Skeletal_Muscle | SE_52434 | chr19:18585882-18592848 | Small_Intestine | SE_53541 | chr19:18587934-18592552 | Spleen |
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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 |
GH19I018472 | chr19 | 18583787 | 18592442 |
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Enhancer Sequence | TTTCATTACC CAGCATGAGG TATGGAACTG GGAGCTCCTG AGATACAAAG TCACCCCCGC 60 TGCTGTACTT CAGGCCAGGG CCCCAGGTGG GAGCTGGGGA GCCTGGTAGG GCCGCCACAG 120 CTGGCCTGAC ACAGTCAGCA GGTCAGCTGG GTCTTCAAGG CCGGACAGGC AGGCACTGAG 180 CTGTGCCGAG GCTGGTGCTC CCCAGACCCA ACTGGACTTC AGACCCTGAC TCGGAGAACA 240 GACCTCAACA CAGCAGGGCA GTGATGCCTG CGCCCTGCGG TCACTTGGCC TGGGCGCCCA 300 CTGGGGCTAC TGAACACAGA CTGGGAGACT CCTGTAGGCA GCTCCCCCTC AATGAGGACA 360 CTCCTGTAAA GACAGCAATG CCTTTGGGAA AAGGGTCGAG GGTGCAGAGC CTGGGAGGCA 420 GTGAGAGTCC TCAATGCTGA GACAGAGGAA AGGGTGAGGA GGAACCTCTC CAGGGCCAGA 480 ATCCCCTGAT CCTCTCCCCT CCGGCAAAGA GCACTTCCGG GGATGAAGCA ACAGGAAGTG 540 GCTTACGAAA TCCACCTCCA GGCCGAGTGA CCAGTTTACA GGAAGTGTGG TGGGTGAATC 600 TTCCCCAGGG CACGAGGCAA TGTCTGGAGC CATTTCTGGT CCTCACCACT GAGGGCGGGG 660 ACAGTCCCCA CCATCTGGCT CGGGGGAGGC CAGGGATGCT GCTCAGCACA CTGCAGGCAA 720 CACAGAACCT CCTGCCCCAA ATGTCAAGCA GTGCAGGGGC TGAGAAGCCC TGGGCTGACC 780 CTGCCACGGG AAGCGACCAT CAGAGCAGAA AGCAGAAAAA TCTATGGGAA AAAAGACCTG 840 CTCCCTTCAA CAAATATAAA ATATAAATGG AAAAGTTACG GGTGAAGAAG AACGTATCTG 900 ATTGTTGGCC AGGCATGGTA CCTCACACCT GTAATCCCAG CATTTTGGGA GGCTGAGGCA 960 GGTGGACTGC TTGAGGTCAG GAGTTCAAGA CCAGCCTGAC CAACATGGTG AAACTCCATC 1020 TCTACTAAAA ATACAAAAAT TAGCCAGGCA TGGTGGCATA CGCCTATAAT CCTAGCTACT 1080 CGGGAGCCTG AGGCAGGAGA 1100
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