| Tag | Content |
|---|
EnhancerAtlas ID | HS051-28064 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr9:139456910-139459960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ETV6 | MA0645.1 | chr9:139457031-139457041 | CACTTCCGCT | - | 6.02 | | FOXP1 | MA0481.2 | chr9:139458142-139458154 | TTCTGTTTACTC | - | 6.27 | | Foxo1 | MA0480.1 | chr9:139459148-139459159 | AGTAAACAGGA | - | 6.32 | | PLAG1 | MA0163.1 | chr9:139458206-139458220 | CCCCTGAGGGCCCC | - | 6.37 | | Stat4 | MA0518.1 | chr9:139458969-139458983 | CTTCCAGGAAGGGG | + | 6.29 | | Znf423 | MA0116.1 | chr9:139457042-139457057 | TGCACCTTGGGTGCC | - | 6.01 |
|
| | Number of super-enhancer constituents: 18 | ID | Coordinate | Tissue/cell |
| SE_00323 | chr9:139457382-139461772 | Adipose_Nuclei | | SE_01312 | chr9:139458411-139460038 | Adrenal_Gland | | SE_05830 | chr9:139458173-139464804 | Brain_Hippocampus_Middle | | SE_06959 | chr9:139458825-139459693 | Brain_Hippocampus_Middle_150 | | SE_09731 | chr9:139456952-139460358 | CD14 | | SE_24688 | chr9:139457477-139458162 | Colon_Crypt_3 | | SE_24688 | chr9:139458276-139459609 | Colon_Crypt_3 | | SE_26827 | chr9:139458656-139461719 | Esophagus | | SE_30179 | chr9:139458759-139461453 | Fetal_Muscle | | SE_32032 | chr9:139458622-139461702 | Gastric | | SE_42178 | chr9:139457479-139461790 | Lung | | SE_48804 | chr9:139458191-139461746 | Right_Atrium | | SE_50167 | chr9:139458324-139461740 | Sigmoid_Colon | | SE_52818 | chr9:139458544-139460044 | Small_Intestine | | SE_54755 | chr9:139459149-139461701 | Stomach_Smooth_Muscle | | SE_65497 | chr9:139457797-139458714 | Pancreatic_islets | | SE_65497 | chr9:139458727-139459623 | Pancreatic_islets | | SE_68678 | chr9:139458119-139459941 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr9 | 139458466 | 139459800 | | chr9 | 139457385 | 139457887 | | chr9 | 139459100 | 139459353 | | chr9 | 139457647 | 139457762 | | chr9 | 139458570 | 139458737 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH09I136562 | chr9 | 139457253 | 139457623 | | GH09I136563 | chr9 | 139457641 | 139468347 |
|
Enhancer Sequence | CAGAATCACT GGGGAAGCCC GAGGAGAGCT CAGGAGTTGA AATTCAGCCC GTGGAACCGG 60
GATCCTTGAT CCTCATATCC ACCTGGTCTC TGCCTGAAGC TGGGTGACCT CAGGCAGGTG 120
ACACTTCCGC TCTGCACCTT GGGTGCCCTT CTGTGGAATG GACTCACTTT TGGCACCTGT 180
GAGGGGATGA GGTGGGCTCA GTGGGCACTT GGTGCTTGGC CCTGGGCCTG GCTTGTGGTC 240
AGCACTTTCA GTGGACAGCT GTGGTTTGGG GACCCACTGT TCCCCTAACC ATCTGCCCAC 300
GTGTTTGGAC TTCTGGGCCC AGGCTGCCTG GAACAGGGGG GCCTAGGACC TGTGCAGACC 360
CTATCTTCCA GGGGAGTTGC CGACCTGGGG GACATGAGCC ATCTTTGCCA CACCGTGGGA 420
AGGGATTACC AGGGAGGGAG CCCACATCAG GGTCAGGGAG CCCAAAGAGG GACAGACACA 480
AAGTCCAGGC AGCATTGCCG GAGCCCTGGA TCCAGCCACG CCAGGAGCTG CTGTGATTCT 540
GCAAGCGTTC ACTGCTTACA AGGCAACTGA ACAGTCATCT TCCCCTTTTG ACCTCCAGCG 600
ACCACCCCTC AAGATCACTG GGAAACTGAG GCCTGAGAGG GAAGGACAGC ATTGAAGGTT 660
GTCCAGGAGG TTAGAGCAGA CGGGAGGAGA GCCCCGGCCT CCAGGTCTCC TTCCCACGGG 720
AGCCCGCTGG CTGGGTGTGT GGGCCGCCTG CCTGAGCCGC TGCTGTGGGA ACCACCCGCT 780
TCCTGAGCTC CCCTGAGCCC CCGCCCGCTG CCAAGCCAGC CTGGGAAAGC CCCTGTGGCG 840
GTGAGCTCGG GGCTCAGAGC AGACCCTTGA CCCAAAGCCT GTCACAGCAG ACGCCGCATC 900
CTCCCCTTTC CTCCCAGCCC GCGTGGCTAG GCTGGGGTCT GCCCTGCTAG CGGCCTCTGG 960
CCTGGAGCCT TCTCCTGCCT AGGCCCAGCA GTGGGCCCCC CACCAGCATG GACCCTTCTG 1020
TAGTCCCTGC GCCCACCTCC TCAGTCCAGA GCCAGCTGGG GCAGGCTGGC CGCACAGCAC 1080
ATTGAGGAGA GGCTGTTGGC TCTATCGGGA AATGGCGACC CGATGTCCTC CCACATGCTG 1140
AGCTGCACCC ACCCTGCCAG CAGGTGCTTC GGGAGACTCA GAGGTTCCTG GTGGGGTCAG 1200
AGGCACCTAG GACCCCAGGG CCAGGCCCTC GTTTCTGTTT ACTCCTGGAA GAAGAGAGTT 1260
CTTGTCCTCC CTGGCAGGAG CTGGGCTTCA ACAAGTCCCC TGAGGGCCCC TGGACCCTGG 1320
CAGTCCCTGC GCTGAGCCAG GAGCCGCTGC GGACCAACCA GACCAGGGTC TGACACCTGC 1380
CGGGCTGAGT CTGGTTTCTG TTTCTCAGGT CACAGAGGGG TTTGGTGGCT GGCGTGGGGG 1440
CCATGGAGCT GGGTTCTCAG GCGACTCTGC TGCGTCCACA CTGTTCCCTC AGTCAGCTCC 1500
ATGTTCTCAC CTGTACAGTG GGGCTATGGT GAGACACGCA GCGGGTGGCT GATCAGGTGC 1560
GCTCAGCATG AGGCCAGCAG GCAAGACCCC TGCCCAGAAA GCTGTGGGGC CACCTGCCCA 1620
CCCGACAGGG CCTGGACCAT GCCCTCCATG CGAGAGCGAA CTGCCCAAAG CAGCTGCCCC 1680
GGGACAAATC TCCCCCTCCC TGGCCCCGTC ATACCCCAGG CCCTGGGATT TCCAGAGGCC 1740
CACGGGCTTG TGGCTCAGAG CTTGGGAAGT GCTCAAGGGG AGGGGCCCAG GACTAGGCAG 1800
AAGGGCAGGA TTGGGGACAG GGCCGTGGGA CTCCTATAGT GACCGCAGGG AGGAGCAGCC 1860
CAGGTCACAG CAGAAGGGGC TGAGGAGGGG GGTTGTTGCA CGCTGAGGGT GGGTGTGAAC 1920
CTGACCAGGA GGCAGCTGCC AGCCTCACCT GGGAGGGGCG CCCTGCAGCC ACGCCTGGCA 1980
GGAGGTCCCT GGAGCCTGCC CGCAGCCTCC TGCCTTGCCC CAGAGGCTGC ATTGTCTCCC 2040
GCTGGAGAGG CAGGGAGGGC TTCCAGGAAG GGGCACAGCG GGCAGCACCC CAGGCCTGGA 2100
GCTAATGCGC TGGCTGCATG AAGGAGCCGG CCCCGACCAG CCCAGCTGCC TGCAGGCCGG 2160
GACCTGGGGG CCGAGGCCCA AAATGGAATC TGACAGCTAA GCCCAGCTCA ACCAGGTCAG 2220
GGCCCACCTC TGGGGTGCAG TAAACAGGAA AGTCCACAGG GGACCAGAGG CTGCCACGAG 2280
AAAGGAAAGG GCTGGGCCAG AGGGTTTCAC AAGATGTTTC AGATCAGCAG GAAATGGTGA 2340
CTTCTCACTG TCTGACTCCA CTGGCCTTAT TGAGCCAGCA CTGCGGCCAG CAACCGCGCT 2400
GGGTGTGTCT GTGAATTTCA AGGGAGCCCA CACGTGGGCG GCAGTCGCCC CGCTGGACTC 2460
CCAAGAGGAA GCCCCAGCTC CCAGCCTCAC CTCTCACCCC GTCCTAGTGA GGCCCTTCTG 2520
CGTGTGCGGT GATTCTGGAC CTGCCCAGGC TCCCGGCTGG AGCTGGGCAT GAGAAACTGA 2580
GGCCCAGCAG GGTCTGGGCT GACCCAAGGG TCCCCGCCTC CCATTGATGG GGCCCCACAA 2640
AGAAGCCCCA GGTGTCTCGG CAGGTCCCTG GCCCTTCTGA ATCATTCCCC AAAATGTAAA 2700
GCTGGCTTTG TGCATCTTCT AGCGTGAGAA CTGTTTGAAA TTGGGTGGGC CAGGCAGTGT 2760
GAGGCCCCGC AAGCGCAGTC CTGGGTTGGG TCAGCCATGC AGCGTGAGGC CCTGCAAGCG 2820
GAGTCCTGGG TGGACAGAGC ACCGCACTCC CGGCATCTGT GCACGGCCAT GCAGGCCCAG 2880
CTCCTTTCCG GAGAAGGTCC CGGCTCTGTA GAGGGGTCCT CGCTCTGTTC CAGATGGAGT 2940
CCAGATTCCT TCTGACGACC GTGTGTCCTA AGAGGCATAA AATGCTCGCA TTTTTGACCT 3000
AGTGATTCTC CTTCTGGGAG TTTATCCCGA GGAAATAGCA CGAAGCCAGA 3050
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