| Tag | Content |
|---|
EnhancerAtlas ID | HS176-42854 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr9:131673390-131675260 |
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 | GGAGGGAGGT GGCCCCTGGA ATGCCCTGTC TGTCCTCCTG GGCCCCAGGA CAGGACACAC 60
CTTCTCCAGC ATCACTCAGA CTAGATGCTT CAGGCCCTCC AGATGCCTGC TGGCTTGGAA 120
GCCTTCCTCC CCTCTTCCCC AGGGCTCCCT TACTGCAGAG CAACCTGCAA CCCACATGTA 180
TCAGGGATTT TGACAAGTCC TTATCTCCGG CCACCCCATA TTATGACTTG AGCACAGTGG 240
GAGAGTGGAC CAGGGCAGGG TTTTCTCTTG TAGTTTCGGG ACAGGCCCAC TGAATAGGAA 300
AACTGGAGTC CCCTGGGGAG AAGCCACATT TGGGAAGCAC AGAACAAACC CAGCCCTTCT 360
TTAATCTGTG GAGGGGGAGA CCCTGTGGCT TCCCCATAGC ACAGTGCTGC CCTTGATAAG 420
CTGGGACTTC CTCACAGCTC CTGCCATTCC TGCCCTGTCC CGGGTGCTGT GCTGGGGCTG 480
TCCTCCTGGT TGGGGGAGGG TTCAAGCCTC CAGCCTGGCT CCCCATCCTG TCCCCCACCC 540
CCAGCTCCTC CCGCCAAGCT TGCCTGTTAG TGTCATGCCT GCTGGCTGAG GTCACCCCTC 600
AGGAAAGGAG CTGGCGGCAA GCACGCTGTC CCAGAGGAAG GAGACCCTCT GGACACCCTG 660
TTTAGCACAT GGCTTAATCA CATCCTGTCC CCACCCCCTG GAACACCAGA GCCTTAATAG 720
GGAAAACAGT TCACTTGGGC CAACCCCAGG CAGGCCCCTC ATTCTGAGTG GGAGGCCTGA 780
GCCCCTCTTC CTCCTCACTC GGGCTTGATG GCTCCTTCTC AGCCACCTTG GCCAGTGGTG 840
ACCAGGAGGG GTGGGCGTGG CCTGCCCACG CCCTTGCGTG CTGTTTCTCC AGATTTATAC 900
TCTTGCTAAT GAAAGCCTTG ACAAGACAGT ATTCATTCGT TCACTCGTTT ACTGATGTGT 960
GCAAATTGTT ATGTTTTGTT TGTTTGTTTT TTTGGTAGAG ACAGGGTCTC ACTGTGTTTT 1020
CTAGGCTGGT CTTTAAACTC CTGGCCTCAA AGCCTCCCAC CTTGGCCGCC CAAAGTGCTG 1080
GTATTACAGG CATGAGCCAC TTCGCCTGGC CTTTGTGCAG ATGTTTTTTG AGCACTTCTA 1140
GAATCCAGCT ATGGAGCAAG GCGCCGGGGA CATGGGGATG AAGAAGGCCA AGTAACGAGG 1200
CAGTTAGCAC AGTGCGTAGG CGCTCTGCTG GAGCACCAGG TCCCTGGGAA CACAGAGGAA 1260
CAGGCCCCTG AAGAACGAGG AGGAGGAAGC CAGGTGGAGG GGAAAGGGAC AGTCCAGGAG 1320
GTTCTGGTGG GGAGGAGCAG TGAGATGGGC TGCCCAGGAA TGTGGGCATC CTGGAGAGCA 1380
GAGGTGGGGC TATGGGGGGG GGTGTGGATG GCAGGGGGGT CCTGTCCTAC ACCTCAGTTT 1440
CAATTGTCTC TTCATTTGTT TAACAGCCGA TCCCTTGCCA GCCCATAGGC TCTGATGACT 1500
AAGACCTAGC TCTTTTGTTC AAGCAAGTGT TTACCGAATT CCTAGTGATT GAGTGGGTGA 1560
AGGAATGAGC TGACTTGCAG CGTGAGGTTC CTCTTGCGGT AGTGTGTGGG GTGGGGTGAG 1620
TGAGAGGTGG GAGGTGGAAG AGAGCTGTTA AGAGACCACG ATTAGCCATC AGGTGAGGCC 1680
ACGGGGCCTG GCGTGGCCAA GGCAGGTAGG GATGGAGAGA CATGGACGGA TCTGGGAGAC 1740
GCTGGAGGGG GAATTCAAAG GGACGGGAGT TGATGGTGGG GGTGGTCTGA GTGACTTGAG 1800
CTTTTTTTTG TGGATTGTTG AGACTGGAGG AAGCACAGGT TTTCAGAGGC CAAGGTGTGT 1860
CTCATGTCAG 1870
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