| Tag | Content |
|---|
EnhancerAtlas ID | HS052-03319 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:205262270-205265280 |
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 | GTGCTGTTAA CATCCATCCT GTAGGTGTTA GTTTATGGCC CCAACTTTAT TATAAGTAAA 60
TTCCTTGAAG GAGGGGACGT GCCTCAATTG CTTCTGTATT TTCCATGGCA CCTAGAACAA 120
TAGTAAGGTC TTAATAAATG TTGATGTGTT TATTAGGGAA TGGGTTTTCA CTTGATTTAA 180
CTATCAAGTT CCCCTTTATA AGGGGCTGGG GCCAGGAAAG CGGGTGGAGG CCCTTTATTA 240
AACATTTATT GAGTACCTGT TCTCACTCCT TAGGTTTTCT CCAGTGATGT ATTGCTTAAA 300
AAGCATGTTC ATGTGTTGTC TCATTTAATC CTTGCAGTAA TGTGATGGGT GTGAGCTGAC 360
TGTGAAAGTG ACTCTCTAAG TCATTGCAAT GCACTCTGTG GGAAGAATGT GCTAGCCCAG 420
CAAGGCTGTC TTTGTGATGT CCGATGTGTA CGTGCGTGGG GAGGCGCTCC CAAAAGCTGC 480
GCTGGGGCAG GGTGTCCTGA ACGGCGTTAC CAGATGTATC TTGACAAAGA GGTTGGCACC 540
ACCATGAAGA CCAATTCAAC CAGCTCTCCT AGCCCAGCTT CCATGCTCTT CAAGGAGACT 600
TCCCACTGAA CTTCCGAATA CCCTTGTGTG AAACTGCCAC AGGCAGTGAA TGTGCTCATC 660
AGCAAACCCA AGTATCTGGT TGGTTTGACA GGGGTTTTGT TATTCATTAG AAATGAATGA 720
ATTGGCATGT TGGCTGAATC CATTCCTCTC CTAGAGCTCA GTGAGTCTGC TCCTGAGCCT 780
CCTAGCCTGT TGATAAGCAA GGTTTCTGAG CAGCAAAGTG AGGCTGCTCA CTTTGGCAAA 840
CAGGTCTTCA GGTGAGCCCG GCCACCATGT GAGGCCCTGT TGGCAGGCCA GGCTCTCCCC 900
AGGCCCCACC TGGCCTCACC AATGGCTCTT GGATTCACAG AGGACTGCAC ATTGGACTGG 960
GAGACAGGGC AAGCCAGGGG TCCCTTAGCA GAGAAGGGAT CCCTGCCAGT AACTAGCCTG 1020
CTGTGAGTAT GAAGTTGCCA CTTACCAAGG ACCCTCCTGA TGGACACAAC AAAGGCGATG 1080
GGTGATTGCT GCCAGGGCTC ATAAAGAGGT GATTCAGAAT CTAGCTGGGG GAACTTTGAA 1140
AGGTCATTGC ACCTTGACCC TAGCTTCCAG GCGGGACATG TGGTGAGTTC TGCTGCAATG 1200
GCTGGGTGCC CTCACAGGCC AGAGCTCAGG TTAATGCAGC TCAGAGCTCG AATTCTGATC 1260
ACAGGAAGAG AATGGTGAGG AGGATGGAGG CAGGGGTGCT GGCTGGGCCC AGAACACCAA 1320
AGGCAGAGCT GAACACTTCC ACTGGGAAGT GGGGGTTTTG GCCTCTTGGG CTGGGAAATT 1380
CCTGGCCGGC ACTGTCTGTT TATCAGGGAA GCTGAGTCAG ACTGAAACGT ATCTCCTAAA 1440
AAGCTCTGCT ATTTCTAGGA TTCCATCCGG TCAAAGCCAG CCTCCTCTTC CCTGGGGAAT 1500
TCCTTTGAGG GTGGAGAGAT AGAGGGGACA GACTGGCCTT TTCCTAGACA TGGAAACCTG 1560
AAATCTGAGT TTTTGCCCAT TTATGGACCT GAAATCCCCT CCCCCACCTA GGATGACTCA 1620
TCCCCCAGCT TGACCCAACT GCCCCTAGAG AGGGGAAAGG GTGAAACTGA GATGGTGGGA 1680
TTAGCTCAGG GAGGGGGTTG GAGGCTGGAA AGAGAAAGGA AAAGACAACT GAAAAGGATG 1740
GGGAATTCCT TTGCAAAGAG ATGGTGAGGA GAGGATTTCA GAGCCAAAAA GAGGCAGAAT 1800
GAGAAAGAGA GAAAGATTTT CATCCCAGAG GGAAGCTGCA TGCCTGGCAG AGTAAAAATC 1860
TTCCAGGTTA AGGTAGGTTC AGGCCCTCAC CTTGAGTAAA TTCTGGAACT TTAGTGTGAT 1920
CAGAGCCACT TGCCGTGCTT GTGAAAATGC AGAGATTCCC GTGCCCTCCC TGGGCTGTGA 1980
TCCGCTTCCA GGCTCCTTCA GGGATCTGAA GTAGGAAGTT CTGAAACACA GAAAGAGGAT 2040
TGACTGGGAA TCCTTCTCCC AACCTGGGGC CTCTGCTGTA TAAAGCGACT CACAACCCCT 2100
CTGCAGGTGC CAATGTCAGA GGCAGAGCCC TGGTCCAAGG GTGACGTTTC TAACATTCTT 2160
ATAAAAATCT GTGAAAGACT TTGGCCAGGC CCAGTGGCTC AAGCCTGTGA TCCCAGCACT 2220
TTAGGAGGCT GAGGCAGGTG GATCTCTTGA GGTGAGGAGT TCGAGACCAG CCTGGCCAAC 2280
ATGGCAAAAC CCGTCTCTAC TAAAAATACA AAAAAATTAG CTGGGTGTGG TGGCATGCAC 2340
CTGTAGTCCC AGCTACTGGA GGAGCAGGGG GGCGCTGAGG TGGAGGATCG CTTGTGCTCA 2400
GGAGGTCGAG GCTGCAGTAA GCTGAGATTG CACCATTGTA CTCCAGCCTG GGCCACAGAG 2460
TGAGATCCTG TGTCAAAAAA AAAAAAGACT TTTTATCGGA TGGAGAAAGC CAGTCCCCAC 2520
CAGGCCAAAT ATGCCTCCTC ATTGCAGCAC TGCCCACCTC CCCACATAAT CATATCAGAG 2580
AAGCTTTGGA AAGAACTGCT TTCCTAGTCA ATACAATCCT AGGATCTTTA CAGCCAGAAG 2640
GGACTTCTTC AGGTATCATC TGGCGGGATT TTTCACCTGA AGCAGAAATT CCTTCTAGCA 2700
ACAACCCCCA CATCTCTATC TCCAACCCAA ATCTCTCAAA CTCCAGGCTC CTCATACCAC 2760
TTATCTTTGC CTGGAGGCCT AAGTGCCTCT GACTTCACCT CACACCTCCT CCATCTGCAA 2820
GTCTTCCCCG ACCCAGCTAA TGGACACTCT ACCCTCCAAG TTTCTCAGGC CAGAGACCAT 2880
GGAGTGATTC TTGGTTTCTC TCTTTCTTTC ATACCCTACA TCTAATCCAT CAGGAAAGCC 2940
TGTTGGCTCT AGCTTCAGAA TATGTCAGAA ATCTGACAAC TTGTCATTTC TTTACTACTG 3000
ACTCCAGTCC 3010
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