| Tag | Content |
|---|
EnhancerAtlas ID | HS047-17604 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:41827230-41828490 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr19:41827779-41827791 | TGCCTTAGGGCA | + | 6.04 | | TFAP2C | MA0524.2 | chr19:41827779-41827791 | TGCCTTAGGGCA | - | 6.32 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_01266 | chr19:41827473-41832460 | Adrenal_Gland | | SE_01941 | chr19:41826114-41834937 | Aorta | | SE_02341 | chr19:41827299-41835217 | Astrocytes | | SE_06609 | chr19:41827940-41835020 | Brain_Hippocampus_Middle | | SE_10928 | chr19:41826548-41839191 | CD20 | | SE_12871 | chr19:41828331-41830463 | CD34_Primary_RO01480 | | SE_13335 | chr19:41827590-41831869 | CD34_Primary_RO01536 | | SE_14717 | chr19:41828274-41835424 | CD4_Memory_Primary_7pool | | SE_17526 | chr19:41828356-41835571 | CD4p_CD25-_CD45RAp_Naive | | SE_20013 | chr19:41827344-41835576 | CD56 | | SE_20919 | chr19:41828272-41831918 | CD8_Memory_7pool | | SE_22408 | chr19:41827603-41828479 | CD8_primiary | | SE_26210 | chr19:41827478-41831409 | Duodenum_Smooth_Muscle | | SE_27131 | chr19:41827046-41832712 | Esophagus | | SE_31885 | chr19:41826804-41832672 | Gastric | | SE_37091 | chr19:41826651-41835398 | HSMMtube | | SE_38093 | chr19:41826925-41835502 | HUVEC | | SE_40475 | chr19:41828286-41832867 | K562 | | SE_41125 | chr19:41824878-41835177 | Left_Ventricle | | SE_44313 | chr19:41826974-41833634 | NHDF-Ad | | SE_44950 | chr19:41827136-41832669 | NHLF | | SE_45824 | chr19:41826675-41835471 | Osteoblasts | | SE_48776 | chr19:41825187-41832669 | Right_Atrium | | SE_50262 | chr19:41826769-41835431 | Sigmoid_Colon | | SE_52575 | chr19:41827074-41832699 | Small_Intestine | | SE_54849 | chr19:41827115-41832913 | Stomach_Smooth_Muscle | | SE_62666 | chr19:41801738-41841748 | Tonsil | | SE_65513 | chr19:41827124-41830643 | Pancreatic_islets |
|
| | 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 |
| GH19I041321 | chr19 | 41827009 | 41835422 |
|
Enhancer Sequence | TGGACCATGG GGACCCTCAT TCAGCAGGCA TCACTGCTGT TCCCAAGCCA GGGCCCAGGA 60
GGAAATTGGG GGTGGCAGGG ACCACAGTGT GTTGCCTCGG GAGGGCAGCA GTGGCCCCGA 120
CGTGTCCCCC ATCCGTGCAT TCAGTTGGCA TGTGCTGAGC ATCTGTGATG TCCACAGGCT 180
CTGGGGATAA GGCGGGGACC AAAACCAACG AAAGGCTTCC CTGCCTGAAA AGGGGTCCCA 240
CTCTAGTGAG GAAGATCTAG AATTTTCTAG CACTTCATGG TGATGGGGCC ATGAGGAAAA 300
GTGAAGCAGT GGGAGGGGAG TGACAGGGTG GCTAGGGAAG GCCTCTCTGA GGGGCTGACA 360
GCAAAGGCCT GCAGGAAGTG GGAGGAGCAT TCCTGGCAGA GGCCATAGTA GGTGCCAGAG 420
CCCCCAGCAG CACCAAGGGG CAGAAGGGGC TGGAGCAGTC GCAAGGGGTC GCAAGGGGGT 480
AGGAGATCTC TGAGTGGCCA AATCAAGCTA GGCTTGGCAA CCCAAGTGCG TGCTGCTGGG 540
TTTACTTGCT GCCTTAGGGC ATGGGCAGCT GTCCTGCCTG TGGTCAGCTC TGGCTAATCC 600
CGGCCTCTAT CCACTGGAGG GCAGTAGCAA GCCCCCAGTG ATGACGTCAA AATGTCAAAA 660
TGCCGTGGGG GCAAAATTAC CCCCAAGTGG TTCTTTGTTG AGAGCCACTG CCTGCTTGAG 720
AATGTAAGCC CATGTGTCGC CACATTTTAC AGCTTTTTAA GAAAAACTAG AGCTTTGGGG 780
TTTTTTTTAG ACAGGGTCTC CTTTGTCACC CAGGCTGGAA TGTGGTGGTT TGATCATAGC 840
TCACCGCAGC CTTGACCTCC TGGCCTGAAG TGAGCCTCCC GCCTCAGCCA ACTGAGTAAG 900
CTGGGACTAC AGGTGCTCAC CACCACGCCT GGCTACTTTT TCAATTTTTT TGTAGAGACA 960
GGGTCTCCCT TTGTTGCCCA GGGCTCCAAC TGCTGGGCTC AAGCCATCTT CCTGCCTTGG 1020
CCTCCCATAG TGCTGGGATT GCAGGCATGA GCCACCATGC CCAGCCCAGA GTTTTTGTGC 1080
AAACTCTGAT TTGGAAAATG TTCCCTTGAG TTTTAAACCC TGAGAGTTTT AAACACTATC 1140
TCCCTTGGGA GGGTCAGCTC TGACGGCTGC CAGCACATGG CCTTTGACAT CAGGGTGCCC 1200
CAGGCCTTTG ACCTGGGCAT CCGAGGGTCC CAGGGAGACC CAGTCCTTGA CAGCCTCCTC 1260
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