| Tag | Content |
|---|
EnhancerAtlas ID | HS037-37770 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr8:26493400-26496250 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PAX5 | MA0014.3 | chr8:26495396-26495408 | AAGCGTGACCAG | + | 6.11 |
|
| | Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
| SE_00237 | chr8:26492392-26501692 | Adipose_Nuclei | | SE_03143 | chr8:26492054-26494168 | Brain_Angular_Gyrus | | SE_03143 | chr8:26494488-26500819 | Brain_Angular_Gyrus | | SE_03863 | chr8:26478564-26501810 | Brain_Anterior_Caudate | | SE_04776 | chr8:26478354-26502050 | Brain_Cingulate_Gyrus | | SE_05786 | chr8:26478645-26502176 | Brain_Hippocampus_Middle | | SE_06684 | chr8:26478162-26501773 | Brain_Hippocampus_Middle_150 | | SE_07727 | chr8:26478421-26494315 | Brain_Inferior_Temporal_Lobe | | SE_07727 | chr8:26494359-26501859 | Brain_Inferior_Temporal_Lobe | | SE_08783 | chr8:26495044-26495694 | Brain_Mid_Frontal_Lobe | | SE_09397 | chr8:26492262-26494282 | CD14 | | SE_09397 | chr8:26495825-26496893 | CD14 | | SE_32944 | chr8:26492987-26494437 | H1 | | SE_32944 | chr8:26494753-26496295 | H1 | | SE_40698 | chr8:26491949-26494435 | Left_Ventricle | | SE_40698 | chr8:26494438-26501799 | Left_Ventricle | | SE_42132 | chr8:26491963-26501899 | Lung | | SE_44172 | chr8:26491139-26494411 | NHDF-Ad | | SE_44172 | chr8:26494419-26501513 | NHDF-Ad | | SE_44989 | chr8:26494574-26497177 | NHLF | | SE_45747 | chr8:26492658-26501543 | Osteoblasts | | SE_48590 | chr8:26494610-26501568 | Right_Atrium | | SE_51461 | chr8:26494684-26500378 | Skeletal_Muscle | | SE_55993 | chr8:26492281-26501980 | u87 | | SE_65620 | chr8:26493963-26494630 | Pancreatic_islets | | SE_65620 | chr8:26495668-26496305 | Pancreatic_islets | | SE_67760 | chr8:26492281-26501980 | u87 | | SE_69104 | chr8:26491957-26494696 | H9 | | SE_69104 | chr8:26494823-26496923 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 26493428 | 26493565 | | chr8 | 26494825 | 26495200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I026634 | chr8 | 26491560 | 26501188 |
|
Enhancer Sequence | ATGGCTTGGT TTCTACTTCC CTGCATCATG CAATCCACAT GGATCAAGGT GGGCTGTGGG 60
ATTTTTTTCA CTGGCGGGTG ACTTGCTGCA AGCCCTGGAA CAAATTGCTC AATGATGACT 120
GAGTCATCTT GTCCCAGAGA TGATGACTTC CAGACGGACC CAGCGACTCC TGGCCCTGGT 180
TCTTTGGAGT GCTCCTGGGG CCTCTGTCCT TAGGCTACAC ATCAAATGGT TGCTGCCTTT 240
CTGTCTTCTC CTGGCACCTT GAAGGAATTG CCTTTTAGAA ATAAGAAAGC ATTCACCTAA 300
AATAATGTAA CCTACTCAGA ATGAGCTTTG AGTTGTTTTC TAGGAGATAT TGTGGATGAC 360
GATGGAATCG GTGGCCTTGG GCCACCCAGA CACGCATTTG CAAGAAGGCA GCGCATTTGT 420
GGGAATCAGC CTCTGTACAG AAGGCCGGCC ACAGCACTGC TGCCCCCACG TAGTGTGGGG 480
ATGGTTGGCA TAGTGTCTGA AAGGGGGAAA GAATGAGACG GCTTATTTTC TGTATTTTAC 540
TACTGCGCTG TACCTAGATG ATGATGATAC GTGAGTTAGG CTAACATTTC AACGTAATTT 600
TGGATAGAGA CCTTGTCTAA AGTTTACTTC ATATTCAAAC CTGTCCAAAT GAGAAGACGG 660
AGGGGTCCTA CATGTCCCAG ACTTTAGTTG GGGGAGGTGG AGTCGTGGGC CAGCCCTGCC 720
GCAGGCCTCC TCCTCTCTGT CCCTCAGGGT TCTTCTCAGG TGGAGTTGCG GAGCTGGAGT 780
GTGTTGTTGC GGTGCCCAGT TTGGACCTAT TACCCCAACT CAGTGCCTGG TAGCCCCCGT 840
TGTTGTTTTT TTTAATTTAT TTTATTTTAT TTTTGAGATG GAGTCTCACT CTGTCGCCCA 900
GGCAGGCGTG CAGTGGTGCC ATCTCAGCTC ACTGCAGTCT CCGCCTCCTG GACTCAAGCG 960
ATTCTCCCGC CTCAGCCTCC TTAGTTGCTG GGATTACAGG CGCCCCCCCA TCACACCCAT 1020
CTAATTTTTA TATTTTTAGT AGAGACGGGG TTTCACCATG TTGACCAGGC TGGTCTGGAA 1080
CTCCTGACCT CAGGTGATCT GCCCGCCTCG GTCTCCCAAA ATACTGGGAT TACAGGCATG 1140
AGCCACTGCA CCTGGCCACC CCTATTGTCT TTATAACCTT GACACACTGT GTGTCTTATG 1200
GGGTGAGCAG TAGGAGGGGA CTTTAGTCTG TTCCCTTCCA GAGCCTTCTG AGTGTGAGTC 1260
CAAATGTGCC CACACCATGG TTCCCAGGAT GGCATTTGCA TTCAAACTGT TACCCATTAA 1320
TCTGTGAAAG CCTGAGCTTT AGACAAACCT GAGCTGCCAG AAAGGAATTT CCAGTGCATT 1380
CAGGTGCTAA TGAGCAGGAA TGAGAAGTCC TAGCTAACTT CCTAGGCTCT TAGGCTCTTT 1440
CCCATCTTGC TGGAACTTCC TAGCAACTTT GGGAGGCAGC CCTGGCAGGA ATTTTTATAT 1500
TTTGTTTTAC TTTGCAGCTG AGTAAACTGA AGCTCAGAGC TCATGTATAG TGGAATTGGG 1560
GCTTGACTGT CAGGCATCTA ACTTGAGGCC ACAAATATCC GTGTAAATGT TTGACTGACT 1620
TACCTTCATG CTTTGAGATT ATTTTAATAC GGTGATGCTT GTGACCTGTG TCTGTTGGGG 1680
CTTAGTTCCT TAAGAATCCT GATTGAAACA GTGGCCTGAC ACCCAGCAGA GATATGGGTA 1740
ATGTACACAC AAGGATTCCC AAATGACCAA GAAGGAAAGC TCTGTAAGGG AGTATTAATT 1800
GTTTGCCTCC AGGATCAGTA TTCATTCTTG GATCAAACCC CAGCTCCACT GTACACCAGC 1860
CACGTGATGC TGGGTGCTTC CTCATCATCT CCACATGTCC TTTTGCCATC TGCAAGGGGA 1920
GGATAGTAAC CATGACTCAT CTCACAGGGT GATGATGATG TGTACATGAG ATATTGCAGG 1980
TAAAGATGGA GATGAGAAGC GTGACCAGTT ATTGTGACTA CAGGATGAAG GGGCTGGTCT 2040
AACCTTGAGC TTGCGAGGAA AGCAGAGTAA AGATGCCTGC TGACCCTGGA CAAGGGTTTT 2100
CTGCTCAGAA TTGTTTGTCC ACTTCAGGTG GGTTCTTCTG GCCCCCTGAG GCAAGTGTGT 2160
GCACTGCCAC AGCCCCCTTT CTGATGCTGC ATTTCTTCCT CTGTGAATGG AGAGATTCTG 2220
AATTCATTGA ATGCATTTTC ATGATGTGAT ACTTTAGGCC TGCGTACCAG GAAAATAAAT 2280
GGTCCCAACC ACAGTTAGCT CCTCGACTTG CAGGGGAAGG ATGCTGAGTG GAAAGTCACA 2340
TTGGGAGGTA GTCGGGGCTA CAAAAGGGGT ACAAGTCAGG AGAGGTTGAG CCCAGAAGGG 2400
AGTCTCAGAG AGGTCAGGCT GCGTAAGCAG ACTCGAAATT TTGCTATAAA TGTGAGCTTT 2460
GAAAAATGAT AATCCTGCCC TGGGAGGAGT AGTAATGTCT CCTTCTCTTA GTGATCCACA 2520
TGAACCTCCC CAGCCAAGAC CTGCTGGTCC AGAATCTAAG ACAAGAGAAG TTCGGGGAAG 2580
TGAGGATATG AGGTGAAACG AATGAGAACT GTTTTCACGT GCCTGCTTGA GCCAGCACGA 2640
CTGCATCCTG CCTTCCCTGA GAGACACGCT GAGAGACACG CTGCTTCCAT CAGCCGCTCT 2700
GTGGCTGTTC AGCAGGATGG CGTGTTCAGC CGGGGAGTGG TGTGTCATCA ACCCAATTTG 2760
GCAGCTGAGG CAATGAACAC AGAGCCAGGA CCAGACGACC TGGGGGCATT TTTACTCTTG 2820
AAAAGAACTT AGACATTGAT CAACTTAATA 2850
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