| Tag | Content |
|---|
EnhancerAtlas ID | HS047-02908 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:205262400-205265240 |
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 | TTAATAAATG TTGATGTGTT TATTAGGGAA TGGGTTTTCA CTTGATTTAA CTATCAAGTT 60
CCCCTTTATA AGGGGCTGGG GCCAGGAAAG CGGGTGGAGG CCCTTTATTA AACATTTATT 120
GAGTACCTGT TCTCACTCCT TAGGTTTTCT CCAGTGATGT ATTGCTTAAA AAGCATGTTC 180
ATGTGTTGTC TCATTTAATC CTTGCAGTAA TGTGATGGGT GTGAGCTGAC TGTGAAAGTG 240
ACTCTCTAAG TCATTGCAAT GCACTCTGTG GGAAGAATGT GCTAGCCCAG CAAGGCTGTC 300
TTTGTGATGT CCGATGTGTA CGTGCGTGGG GAGGCGCTCC CAAAAGCTGC GCTGGGGCAG 360
GGTGTCCTGA ACGGCGTTAC CAGATGTATC TTGACAAAGA GGTTGGCACC ACCATGAAGA 420
CCAATTCAAC CAGCTCTCCT AGCCCAGCTT CCATGCTCTT CAAGGAGACT TCCCACTGAA 480
CTTCCGAATA CCCTTGTGTG AAACTGCCAC AGGCAGTGAA TGTGCTCATC AGCAAACCCA 540
AGTATCTGGT TGGTTTGACA GGGGTTTTGT TATTCATTAG AAATGAATGA ATTGGCATGT 600
TGGCTGAATC CATTCCTCTC CTAGAGCTCA GTGAGTCTGC TCCTGAGCCT CCTAGCCTGT 660
TGATAAGCAA GGTTTCTGAG CAGCAAAGTG AGGCTGCTCA CTTTGGCAAA CAGGTCTTCA 720
GGTGAGCCCG GCCACCATGT GAGGCCCTGT TGGCAGGCCA GGCTCTCCCC AGGCCCCACC 780
TGGCCTCACC AATGGCTCTT GGATTCACAG AGGACTGCAC ATTGGACTGG GAGACAGGGC 840
AAGCCAGGGG TCCCTTAGCA GAGAAGGGAT CCCTGCCAGT AACTAGCCTG CTGTGAGTAT 900
GAAGTTGCCA CTTACCAAGG ACCCTCCTGA TGGACACAAC AAAGGCGATG GGTGATTGCT 960
GCCAGGGCTC ATAAAGAGGT GATTCAGAAT CTAGCTGGGG GAACTTTGAA AGGTCATTGC 1020
ACCTTGACCC TAGCTTCCAG GCGGGACATG TGGTGAGTTC TGCTGCAATG GCTGGGTGCC 1080
CTCACAGGCC AGAGCTCAGG TTAATGCAGC TCAGAGCTCG AATTCTGATC ACAGGAAGAG 1140
AATGGTGAGG AGGATGGAGG CAGGGGTGCT GGCTGGGCCC AGAACACCAA AGGCAGAGCT 1200
GAACACTTCC ACTGGGAAGT GGGGGTTTTG GCCTCTTGGG CTGGGAAATT CCTGGCCGGC 1260
ACTGTCTGTT TATCAGGGAA GCTGAGTCAG ACTGAAACGT ATCTCCTAAA AAGCTCTGCT 1320
ATTTCTAGGA TTCCATCCGG TCAAAGCCAG CCTCCTCTTC CCTGGGGAAT TCCTTTGAGG 1380
GTGGAGAGAT AGAGGGGACA GACTGGCCTT TTCCTAGACA TGGAAACCTG AAATCTGAGT 1440
TTTTGCCCAT TTATGGACCT GAAATCCCCT CCCCCACCTA GGATGACTCA TCCCCCAGCT 1500
TGACCCAACT GCCCCTAGAG AGGGGAAAGG GTGAAACTGA GATGGTGGGA TTAGCTCAGG 1560
GAGGGGGTTG GAGGCTGGAA AGAGAAAGGA AAAGACAACT GAAAAGGATG GGGAATTCCT 1620
TTGCAAAGAG ATGGTGAGGA GAGGATTTCA GAGCCAAAAA GAGGCAGAAT GAGAAAGAGA 1680
GAAAGATTTT CATCCCAGAG GGAAGCTGCA TGCCTGGCAG AGTAAAAATC TTCCAGGTTA 1740
AGGTAGGTTC AGGCCCTCAC CTTGAGTAAA TTCTGGAACT TTAGTGTGAT CAGAGCCACT 1800
TGCCGTGCTT GTGAAAATGC AGAGATTCCC GTGCCCTCCC TGGGCTGTGA TCCGCTTCCA 1860
GGCTCCTTCA GGGATCTGAA GTAGGAAGTT CTGAAACACA GAAAGAGGAT TGACTGGGAA 1920
TCCTTCTCCC AACCTGGGGC CTCTGCTGTA TAAAGCGACT CACAACCCCT CTGCAGGTGC 1980
CAATGTCAGA GGCAGAGCCC TGGTCCAAGG GTGACGTTTC TAACATTCTT ATAAAAATCT 2040
GTGAAAGACT TTGGCCAGGC CCAGTGGCTC AAGCCTGTGA TCCCAGCACT TTAGGAGGCT 2100
GAGGCAGGTG GATCTCTTGA GGTGAGGAGT TCGAGACCAG CCTGGCCAAC ATGGCAAAAC 2160
CCGTCTCTAC TAAAAATACA AAAAAATTAG CTGGGTGTGG TGGCATGCAC CTGTAGTCCC 2220
AGCTACTGGA GGAGCAGGGG GGCGCTGAGG TGGAGGATCG CTTGTGCTCA GGAGGTCGAG 2280
GCTGCAGTAA GCTGAGATTG CACCATTGTA CTCCAGCCTG GGCCACAGAG TGAGATCCTG 2340
TGTCAAAAAA AAAAAAGACT TTTTATCGGA TGGAGAAAGC CAGTCCCCAC CAGGCCAAAT 2400
ATGCCTCCTC ATTGCAGCAC TGCCCACCTC CCCACATAAT CATATCAGAG AAGCTTTGGA 2460
AAGAACTGCT TTCCTAGTCA ATACAATCCT AGGATCTTTA CAGCCAGAAG GGACTTCTTC 2520
AGGTATCATC TGGCGGGATT TTTCACCTGA AGCAGAAATT CCTTCTAGCA ACAACCCCCA 2580
CATCTCTATC TCCAACCCAA ATCTCTCAAA CTCCAGGCTC CTCATACCAC TTATCTTTGC 2640
CTGGAGGCCT AAGTGCCTCT GACTTCACCT CACACCTCCT CCATCTGCAA GTCTTCCCCG 2700
ACCCAGCTAA TGGACACTCT ACCCTCCAAG TTTCTCAGGC CAGAGACCAT GGAGTGATTC 2760
TTGGTTTCTC TCTTTCTTTC ATACCCTACA TCTAATCCAT CAGGAAAGCC TGTTGGCTCT 2820
AGCTTCAGAA TATGTCAGAA 2840
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