| Tag | Content |
|---|
EnhancerAtlas ID | HS054-00639 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr1:205262460-205264970 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:205263880-205263891 | GGATGACTCAT | + | 6.62 | | IRF2 | MA0051.1 | chr1:205263976-205263994 | GGAAAGAGAAAGGAAAAG | + | 6.03 | | JUN(var.2) | MA0489.1 | chr1:205263882-205263896 | ATGACTCATCCCCC | - | 6.22 | | JUNB | MA0490.1 | chr1:205263880-205263891 | GGATGACTCAT | + | 6.62 | | PRDM1 | MA0508.2 | chr1:205262631-205262641 | GTGAAAGTGA | - | 6.02 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_02431 | chr1:205262567-205264599 | Astrocytes | | SE_05801 | chr1:205262462-205264469 | Brain_Hippocampus_Middle | | SE_11085 | chr1:205262547-205264187 | CD20 | | SE_26974 | chr1:205262635-205264492 | Esophagus | | SE_29391 | chr1:205262567-205264765 | Fetal_Intestine_Large | | SE_32765 | chr1:205262511-205264574 | H1 | | SE_38936 | chr1:205262243-205265794 | IMR90 | | SE_46173 | chr1:205262329-205265260 | Osteoblasts | | SE_50327 | chr1:205262518-205264578 | Sigmoid_Colon | | SE_52983 | chr1:205262582-205264598 | Small_Intestine | | SE_54130 | chr1:205262477-205264677 | Spleen | | SE_55645 | chr1:205263252-205263684 | Thymus | | SE_56704 | chr1:205262588-205264656 | u87 | | SE_56704 | chr1:205264714-205265918 | u87 | | SE_58462 | chr1:205242169-205295027 | Ly1 | | SE_58967 | chr1:205242236-205295022 | Ly3 | | SE_60263 | chr1:205242326-205284722 | Ly4 | | SE_60576 | chr1:205242267-205294889 | DHL6 | | SE_61365 | chr1:205242037-205294994 | HBL1 | | SE_61423 | chr1:205183427-205322469 | Toledo | | SE_62465 | chr1:205242393-205294944 | Tonsil | | SE_65493 | chr1:205262566-205265065 | Pancreatic_islets | | SE_68815 | chr1:205262515-205265189 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 205262860 | 205263030 | | chr1 | 205262798 | 205264485 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I205293 | chr1 | 205262232 | 205274585 |
|
Enhancer Sequence | CCCCTTTATA AGGGGCTGGG GCCAGGAAAG CGGGTGGAGG CCCTTTATTA AACATTTATT 60
GAGTACCTGT TCTCACTCCT TAGGTTTTCT CCAGTGATGT ATTGCTTAAA AAGCATGTTC 120
ATGTGTTGTC TCATTTAATC CTTGCAGTAA TGTGATGGGT GTGAGCTGAC TGTGAAAGTG 180
ACTCTCTAAG TCATTGCAAT GCACTCTGTG GGAAGAATGT GCTAGCCCAG CAAGGCTGTC 240
TTTGTGATGT CCGATGTGTA CGTGCGTGGG GAGGCGCTCC CAAAAGCTGC GCTGGGGCAG 300
GGTGTCCTGA ACGGCGTTAC CAGATGTATC TTGACAAAGA GGTTGGCACC ACCATGAAGA 360
CCAATTCAAC CAGCTCTCCT AGCCCAGCTT CCATGCTCTT CAAGGAGACT TCCCACTGAA 420
CTTCCGAATA CCCTTGTGTG AAACTGCCAC AGGCAGTGAA TGTGCTCATC AGCAAACCCA 480
AGTATCTGGT TGGTTTGACA GGGGTTTTGT TATTCATTAG AAATGAATGA ATTGGCATGT 540
TGGCTGAATC CATTCCTCTC CTAGAGCTCA GTGAGTCTGC TCCTGAGCCT CCTAGCCTGT 600
TGATAAGCAA GGTTTCTGAG CAGCAAAGTG AGGCTGCTCA CTTTGGCAAA CAGGTCTTCA 660
GGTGAGCCCG GCCACCATGT GAGGCCCTGT TGGCAGGCCA GGCTCTCCCC AGGCCCCACC 720
TGGCCTCACC AATGGCTCTT GGATTCACAG AGGACTGCAC ATTGGACTGG GAGACAGGGC 780
AAGCCAGGGG TCCCTTAGCA GAGAAGGGAT CCCTGCCAGT AACTAGCCTG CTGTGAGTAT 840
GAAGTTGCCA CTTACCAAGG ACCCTCCTGA TGGACACAAC AAAGGCGATG GGTGATTGCT 900
GCCAGGGCTC ATAAAGAGGT GATTCAGAAT CTAGCTGGGG GAACTTTGAA AGGTCATTGC 960
ACCTTGACCC TAGCTTCCAG GCGGGACATG TGGTGAGTTC TGCTGCAATG GCTGGGTGCC 1020
CTCACAGGCC AGAGCTCAGG TTAATGCAGC TCAGAGCTCG AATTCTGATC ACAGGAAGAG 1080
AATGGTGAGG AGGATGGAGG CAGGGGTGCT GGCTGGGCCC AGAACACCAA AGGCAGAGCT 1140
GAACACTTCC ACTGGGAAGT GGGGGTTTTG GCCTCTTGGG CTGGGAAATT CCTGGCCGGC 1200
ACTGTCTGTT TATCAGGGAA GCTGAGTCAG ACTGAAACGT ATCTCCTAAA AAGCTCTGCT 1260
ATTTCTAGGA TTCCATCCGG TCAAAGCCAG CCTCCTCTTC CCTGGGGAAT TCCTTTGAGG 1320
GTGGAGAGAT AGAGGGGACA GACTGGCCTT TTCCTAGACA TGGAAACCTG AAATCTGAGT 1380
TTTTGCCCAT TTATGGACCT GAAATCCCCT CCCCCACCTA GGATGACTCA TCCCCCAGCT 1440
TGACCCAACT GCCCCTAGAG AGGGGAAAGG GTGAAACTGA GATGGTGGGA TTAGCTCAGG 1500
GAGGGGGTTG GAGGCTGGAA AGAGAAAGGA AAAGACAACT GAAAAGGATG GGGAATTCCT 1560
TTGCAAAGAG ATGGTGAGGA GAGGATTTCA GAGCCAAAAA GAGGCAGAAT GAGAAAGAGA 1620
GAAAGATTTT CATCCCAGAG GGAAGCTGCA TGCCTGGCAG AGTAAAAATC TTCCAGGTTA 1680
AGGTAGGTTC AGGCCCTCAC CTTGAGTAAA TTCTGGAACT TTAGTGTGAT CAGAGCCACT 1740
TGCCGTGCTT GTGAAAATGC AGAGATTCCC GTGCCCTCCC TGGGCTGTGA TCCGCTTCCA 1800
GGCTCCTTCA GGGATCTGAA GTAGGAAGTT CTGAAACACA GAAAGAGGAT TGACTGGGAA 1860
TCCTTCTCCC AACCTGGGGC CTCTGCTGTA TAAAGCGACT CACAACCCCT CTGCAGGTGC 1920
CAATGTCAGA GGCAGAGCCC TGGTCCAAGG GTGACGTTTC TAACATTCTT ATAAAAATCT 1980
GTGAAAGACT TTGGCCAGGC CCAGTGGCTC AAGCCTGTGA TCCCAGCACT TTAGGAGGCT 2040
GAGGCAGGTG GATCTCTTGA GGTGAGGAGT TCGAGACCAG CCTGGCCAAC ATGGCAAAAC 2100
CCGTCTCTAC TAAAAATACA AAAAAATTAG CTGGGTGTGG TGGCATGCAC CTGTAGTCCC 2160
AGCTACTGGA GGAGCAGGGG GGCGCTGAGG TGGAGGATCG CTTGTGCTCA GGAGGTCGAG 2220
GCTGCAGTAA GCTGAGATTG CACCATTGTA CTCCAGCCTG GGCCACAGAG TGAGATCCTG 2280
TGTCAAAAAA AAAAAAGACT TTTTATCGGA TGGAGAAAGC CAGTCCCCAC CAGGCCAAAT 2340
ATGCCTCCTC ATTGCAGCAC TGCCCACCTC CCCACATAAT CATATCAGAG AAGCTTTGGA 2400
AAGAACTGCT TTCCTAGTCA ATACAATCCT AGGATCTTTA CAGCCAGAAG GGACTTCTTC 2460
AGGTATCATC TGGCGGGATT TTTCACCTGA AGCAGAAATT CCTTCTAGCA 2510
|
