| Tag | Content |
|---|
EnhancerAtlas ID | HS111-00483 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr1:205262570-205264940 |
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: 22 | 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_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 | AAGCATGTTC ATGTGTTGTC TCATTTAATC CTTGCAGTAA TGTGATGGGT GTGAGCTGAC 60
TGTGAAAGTG ACTCTCTAAG TCATTGCAAT GCACTCTGTG GGAAGAATGT GCTAGCCCAG 120
CAAGGCTGTC TTTGTGATGT CCGATGTGTA CGTGCGTGGG GAGGCGCTCC CAAAAGCTGC 180
GCTGGGGCAG GGTGTCCTGA ACGGCGTTAC CAGATGTATC TTGACAAAGA GGTTGGCACC 240
ACCATGAAGA CCAATTCAAC CAGCTCTCCT AGCCCAGCTT CCATGCTCTT CAAGGAGACT 300
TCCCACTGAA CTTCCGAATA CCCTTGTGTG AAACTGCCAC AGGCAGTGAA TGTGCTCATC 360
AGCAAACCCA AGTATCTGGT TGGTTTGACA GGGGTTTTGT TATTCATTAG AAATGAATGA 420
ATTGGCATGT TGGCTGAATC CATTCCTCTC CTAGAGCTCA GTGAGTCTGC TCCTGAGCCT 480
CCTAGCCTGT TGATAAGCAA GGTTTCTGAG CAGCAAAGTG AGGCTGCTCA CTTTGGCAAA 540
CAGGTCTTCA GGTGAGCCCG GCCACCATGT GAGGCCCTGT TGGCAGGCCA GGCTCTCCCC 600
AGGCCCCACC TGGCCTCACC AATGGCTCTT GGATTCACAG AGGACTGCAC ATTGGACTGG 660
GAGACAGGGC AAGCCAGGGG TCCCTTAGCA GAGAAGGGAT CCCTGCCAGT AACTAGCCTG 720
CTGTGAGTAT GAAGTTGCCA CTTACCAAGG ACCCTCCTGA TGGACACAAC AAAGGCGATG 780
GGTGATTGCT GCCAGGGCTC ATAAAGAGGT GATTCAGAAT CTAGCTGGGG GAACTTTGAA 840
AGGTCATTGC ACCTTGACCC TAGCTTCCAG GCGGGACATG TGGTGAGTTC TGCTGCAATG 900
GCTGGGTGCC CTCACAGGCC AGAGCTCAGG TTAATGCAGC TCAGAGCTCG AATTCTGATC 960
ACAGGAAGAG AATGGTGAGG AGGATGGAGG CAGGGGTGCT GGCTGGGCCC AGAACACCAA 1020
AGGCAGAGCT GAACACTTCC ACTGGGAAGT GGGGGTTTTG GCCTCTTGGG CTGGGAAATT 1080
CCTGGCCGGC ACTGTCTGTT TATCAGGGAA GCTGAGTCAG ACTGAAACGT ATCTCCTAAA 1140
AAGCTCTGCT ATTTCTAGGA TTCCATCCGG TCAAAGCCAG CCTCCTCTTC CCTGGGGAAT 1200
TCCTTTGAGG GTGGAGAGAT AGAGGGGACA GACTGGCCTT TTCCTAGACA TGGAAACCTG 1260
AAATCTGAGT TTTTGCCCAT TTATGGACCT GAAATCCCCT CCCCCACCTA GGATGACTCA 1320
TCCCCCAGCT TGACCCAACT GCCCCTAGAG AGGGGAAAGG GTGAAACTGA GATGGTGGGA 1380
TTAGCTCAGG GAGGGGGTTG GAGGCTGGAA AGAGAAAGGA AAAGACAACT GAAAAGGATG 1440
GGGAATTCCT TTGCAAAGAG ATGGTGAGGA GAGGATTTCA GAGCCAAAAA GAGGCAGAAT 1500
GAGAAAGAGA GAAAGATTTT CATCCCAGAG GGAAGCTGCA TGCCTGGCAG AGTAAAAATC 1560
TTCCAGGTTA AGGTAGGTTC AGGCCCTCAC CTTGAGTAAA TTCTGGAACT TTAGTGTGAT 1620
CAGAGCCACT TGCCGTGCTT GTGAAAATGC AGAGATTCCC GTGCCCTCCC TGGGCTGTGA 1680
TCCGCTTCCA GGCTCCTTCA GGGATCTGAA GTAGGAAGTT CTGAAACACA GAAAGAGGAT 1740
TGACTGGGAA TCCTTCTCCC AACCTGGGGC CTCTGCTGTA TAAAGCGACT CACAACCCCT 1800
CTGCAGGTGC CAATGTCAGA GGCAGAGCCC TGGTCCAAGG GTGACGTTTC TAACATTCTT 1860
ATAAAAATCT GTGAAAGACT TTGGCCAGGC CCAGTGGCTC AAGCCTGTGA TCCCAGCACT 1920
TTAGGAGGCT GAGGCAGGTG GATCTCTTGA GGTGAGGAGT TCGAGACCAG CCTGGCCAAC 1980
ATGGCAAAAC CCGTCTCTAC TAAAAATACA AAAAAATTAG CTGGGTGTGG TGGCATGCAC 2040
CTGTAGTCCC AGCTACTGGA GGAGCAGGGG GGCGCTGAGG TGGAGGATCG CTTGTGCTCA 2100
GGAGGTCGAG GCTGCAGTAA GCTGAGATTG CACCATTGTA CTCCAGCCTG GGCCACAGAG 2160
TGAGATCCTG TGTCAAAAAA AAAAAAGACT TTTTATCGGA TGGAGAAAGC CAGTCCCCAC 2220
CAGGCCAAAT ATGCCTCCTC ATTGCAGCAC TGCCCACCTC CCCACATAAT CATATCAGAG 2280
AAGCTTTGGA AAGAACTGCT TTCCTAGTCA ATACAATCCT AGGATCTTTA CAGCCAGAAG 2340
GGACTTCTTC AGGTATCATC TGGCGGGATT 2370
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