| Tag | Content |
|---|
EnhancerAtlas ID | HS193-36841 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr9:131673460-131675490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr9:131673511-131673529 | CCTTCCTCCCCTCTTCCC | - | 6.24 | | Foxd3 | MA0041.1 | chr9:131674367-131674379 | GTTTGTTTGTTT | + | 6.32 | | KLF14 | MA0740.1 | chr9:131674238-131674252 | GGGTGGGCGTGGCC | - | 6.69 | | Klf12 | MA0742.1 | chr9:131674237-131674252 | GGGGTGGGCGTGGCC | - | 6.15 | | REST | MA0138.2 | chr9:131673840-131673861 | TGCCCTGTCCCGGGTGCTGTG | - | 6.28 | | RREB1 | MA0073.1 | chr9:131674986-131675006 | CGGTAGTGTGTGGGGTGGGG | - | 6.13 | | SP1 | MA0079.4 | chr9:131674239-131674254 | GGTGGGCGTGGCCTG | - | 7.44 | | SP3 | MA0746.2 | chr9:131674239-131674252 | GGTGGGCGTGGCC | - | 7.52 | | SP4 | MA0685.1 | chr9:131674237-131674254 | GGGGTGGGCGTGGCCTG | - | 7.15 | | SP8 | MA0747.1 | chr9:131674239-131674251 | GGTGGGCGTGGC | - | 6.62 | | ZNF263 | MA0528.1 | chr9:131673920-131673941 | TCCCCCACCCCCAGCTCCTCC | - | 6.72 |
|
| | Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
| SE_01786 | chr9:131670844-131677719 | Aorta | | SE_02982 | chr9:131673318-131674904 | Bladder | | SE_03426 | chr9:131673447-131673893 | Brain_Angular_Gyrus | | SE_03426 | chr9:131674081-131674559 | Brain_Angular_Gyrus | | SE_07249 | chr9:131672970-131676358 | Brain_Hippocampus_Middle_150 | | SE_15043 | chr9:131674459-131677196 | CD4_Memory_Primary_7pool | | SE_26602 | chr9:131672946-131677452 | Esophagus | | SE_31756 | chr9:131673115-131677345 | Gastric | | SE_36103 | chr9:131673104-131676522 | HMEC | | SE_38626 | chr9:131672733-131677091 | HUVEC | | SE_40990 | chr9:131670925-131677482 | Left_Ventricle | | SE_42380 | chr9:131670371-131677535 | Lung | | SE_48867 | chr9:131672896-131676330 | Right_Atrium | | SE_65947 | chr9:131673076-131674381 | Pancreatic_islets | | SE_65947 | chr9:131674506-131675933 | Pancreatic_islets | | SE_68883 | chr9:131672842-131676445 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I128909 | chr9 | 131671741 | 131677288 |
|
Enhancer Sequence | ATCACTCAGA CTAGATGCTT CAGGCCCTCC AGATGCCTGC TGGCTTGGAA GCCTTCCTCC 60
CCTCTTCCCC AGGGCTCCCT TACTGCAGAG CAACCTGCAA CCCACATGTA TCAGGGATTT 120
TGACAAGTCC TTATCTCCGG CCACCCCATA TTATGACTTG AGCACAGTGG GAGAGTGGAC 180
CAGGGCAGGG TTTTCTCTTG TAGTTTCGGG ACAGGCCCAC TGAATAGGAA AACTGGAGTC 240
CCCTGGGGAG AAGCCACATT TGGGAAGCAC AGAACAAACC CAGCCCTTCT TTAATCTGTG 300
GAGGGGGAGA CCCTGTGGCT TCCCCATAGC ACAGTGCTGC CCTTGATAAG CTGGGACTTC 360
CTCACAGCTC CTGCCATTCC TGCCCTGTCC CGGGTGCTGT GCTGGGGCTG TCCTCCTGGT 420
TGGGGGAGGG TTCAAGCCTC CAGCCTGGCT CCCCATCCTG TCCCCCACCC CCAGCTCCTC 480
CCGCCAAGCT TGCCTGTTAG TGTCATGCCT GCTGGCTGAG GTCACCCCTC AGGAAAGGAG 540
CTGGCGGCAA GCACGCTGTC CCAGAGGAAG GAGACCCTCT GGACACCCTG TTTAGCACAT 600
GGCTTAATCA CATCCTGTCC CCACCCCCTG GAACACCAGA GCCTTAATAG GGAAAACAGT 660
TCACTTGGGC CAACCCCAGG CAGGCCCCTC ATTCTGAGTG GGAGGCCTGA GCCCCTCTTC 720
CTCCTCACTC GGGCTTGATG GCTCCTTCTC AGCCACCTTG GCCAGTGGTG ACCAGGAGGG 780
GTGGGCGTGG CCTGCCCACG CCCTTGCGTG CTGTTTCTCC AGATTTATAC TCTTGCTAAT 840
GAAAGCCTTG ACAAGACAGT ATTCATTCGT TCACTCGTTT ACTGATGTGT GCAAATTGTT 900
ATGTTTTGTT TGTTTGTTTT TTTGGTAGAG ACAGGGTCTC ACTGTGTTTT CTAGGCTGGT 960
CTTTAAACTC CTGGCCTCAA AGCCTCCCAC CTTGGCCGCC CAAAGTGCTG GTATTACAGG 1020
CATGAGCCAC TTCGCCTGGC CTTTGTGCAG ATGTTTTTTG AGCACTTCTA GAATCCAGCT 1080
ATGGAGCAAG GCGCCGGGGA CATGGGGATG AAGAAGGCCA AGTAACGAGG CAGTTAGCAC 1140
AGTGCGTAGG CGCTCTGCTG GAGCACCAGG TCCCTGGGAA CACAGAGGAA CAGGCCCCTG 1200
AAGAACGAGG AGGAGGAAGC CAGGTGGAGG GGAAAGGGAC AGTCCAGGAG GTTCTGGTGG 1260
GGAGGAGCAG TGAGATGGGC TGCCCAGGAA TGTGGGCATC CTGGAGAGCA GAGGTGGGGC 1320
TATGGGGGGG GGTGTGGATG GCAGGGGGGT CCTGTCCTAC ACCTCAGTTT CAATTGTCTC 1380
TTCATTTGTT TAACAGCCGA TCCCTTGCCA GCCCATAGGC TCTGATGACT AAGACCTAGC 1440
TCTTTTGTTC AAGCAAGTGT TTACCGAATT CCTAGTGATT GAGTGGGTGA AGGAATGAGC 1500
TGACTTGCAG CGTGAGGTTC CTCTTGCGGT AGTGTGTGGG GTGGGGTGAG TGAGAGGTGG 1560
GAGGTGGAAG AGAGCTGTTA AGAGACCACG ATTAGCCATC AGGTGAGGCC ACGGGGCCTG 1620
GCGTGGCCAA GGCAGGTAGG GATGGAGAGA CATGGACGGA TCTGGGAGAC GCTGGAGGGG 1680
GAATTCAAAG GGACGGGAGT TGATGGTGGG GGTGGTCTGA GTGACTTGAG CTTTTTTTTG 1740
TGGATTGTTG AGACTGGAGG AAGCACAGGT TTTCAGAGGC CAAGGTGTGT CTCATGTCAG 1800
GTGTCTGGGG CTCTGGGATG TCCAAGGGAC CATCTTGAAT CCACCTGAAG CCCAAGGAGT 1860
CACCCTTTCC AGGCTCATGG GTGAAGATGG GTCCTTGACT TGCTCACTGT GGAGAGCAGA 1920
GAGGGAGAAG GACAGGAGTC TGCAGAAGAG GAGGGCGAGG CCAGAGCGTG GGGCACATGG 1980
GGCCTGGGGA GTTGGCTGGA TTAGGAACTG GTGACTTTGG CCAGAGAGTT 2030
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