| Tag | Content |
|---|
EnhancerAtlas ID | HS105-83697 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr9:133735280-133738140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr9:133737578-133737589 | TAATTTAATCA | + | 6.62 | | ZBTB18 | MA0698.1 | chr9:133737176-133737189 | AGTCCAGATGTTT | + | 6.11 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_00366 | chr9:133732453-133737837 | Adipose_Nuclei | | SE_01968 | chr9:133735264-133736834 | Aorta | | SE_01968 | chr9:133736842-133737530 | Aorta | | SE_02272 | chr9:133731761-133738408 | Astrocytes | | SE_04314 | chr9:133735429-133736608 | Brain_Anterior_Caudate | | SE_04314 | chr9:133737790-133738866 | Brain_Anterior_Caudate | | SE_05130 | chr9:133735408-133737102 | Brain_Cingulate_Gyrus | | SE_05130 | chr9:133737149-133739531 | Brain_Cingulate_Gyrus | | SE_06032 | chr9:133732733-133739645 | Brain_Hippocampus_Middle | | SE_07346 | chr9:133737573-133738657 | Brain_Hippocampus_Middle_150 | | SE_08183 | chr9:133735434-133736911 | Brain_Inferior_Temporal_Lobe | | SE_08183 | chr9:133737148-133739623 | Brain_Inferior_Temporal_Lobe | | SE_25919 | chr9:133732719-133738593 | Duodenum_Smooth_Muscle | | SE_29704 | chr9:133735386-133737343 | Fetal_Muscle | | SE_37162 | chr9:133731973-133739075 | HSMMtube | | SE_38276 | chr9:133732453-133738344 | HUVEC | | SE_39095 | chr9:133735366-133737532 | IMR90 | | SE_44222 | chr9:133731804-133739249 | NHDF-Ad | | SE_44804 | chr9:133735203-133737735 | NHLF | | SE_45626 | chr9:133731609-133743483 | Osteoblasts | | SE_51003 | chr9:133735260-133736786 | Sigmoid_Colon | | SE_51821 | chr9:133735177-133737678 | Skeletal_Muscle_Myoblast | | SE_54734 | chr9:133732881-133739101 | Stomach_Smooth_Muscle | | SE_55903 | chr9:133735211-133738601 | u87 | | SE_63600 | chr9:133735208-133738875 | HSMM | | SE_67557 | chr9:133735211-133738601 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr9 | 133735372 | 133735672 | | chr9 | 133736245 | 133736518 | | chr9 | 133735759 | 133736780 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I130856 | chr9 | 133732030 | 133739419 |
|
Enhancer Sequence | TGGTTTCGAA CGCCTGACCT CGTGATCTGC CCTCCTTGGC CTCCCAAAGT GCTGGGATTA 60
CAGGCGTGAG CCACTGCTCC TGGCAAAATG CTGTTTCTAA GCGTTTCTTT GACAAGTCCC 120
ATCCTTCAGG TTCATGCATG ATTAGGGAGA GGCAGCAGCC CTGACTGAGC ACCTGAGTGT 180
TCATGGAACC AGGTGCATAG CGTAATGACA TGCCATTCAT GACACTACTT TCTTCCCTGA 240
ACATGCCATG AATTCCTGAT GATTACACAG TTCCCCAACA AGTGCTGCTC AAAACCTGGA 300
ACTAATCAGA AGGAAGCACC AGCCTTGACT GTTAGTGGGA CACGGGGAAG ATGGCTGTGA 360
ACCAAATATG CGGTGCCTTT GGGGGAGAAT GGTTTTAGTA TTTAGTAAGT GTCAGTATGT 420
AAGTTTTATG TTGAAAAATG AACTAAGTCA CAACAAGGTC TATAAATTTA ATTATTGAAA 480
AGGATAAAGT TGGGCCATTC AGTGAAACCT CCTGTAACTG AAGTCTCTAA CACAGTAGCC 540
AATGGGGGAA TCAAATGAGC CCAAGAAGAA ATTCTGCGTA AACTAGGACT TAGGGGAGCC 600
CTTAGCATTC CACTTTGGAG TGAAGGAACC CGATCCGCCA GTTGGGGAAC GCTCCTTTGA 660
GGCCCATGTG CTTCCTGCTC CGACGGGAGA GAGGGATAAT GAGACTTGCT CCCAGGTGCC 720
CTGCCCTGGA GCCCAGCAGG CCACACGGGC TCTTTGACTC TGTACTGTGC CAGTGATTTC 780
CAAGATGGGA GTGGTGCTCT GATTGCAGGA ATGTCTTCTT GGAATGGCTT TTCTCACTTC 840
TCTAGAGTCC TTGGTAGGGA GCACATCATC AGCTGAGCTA ACGTGAGAAC AGGGGTTGGA 900
GCACTTGCCA CCGGCAGTGA AGTAATCGGA CAGCTGACAG TCTTTTCCAG AGGGTCGGGG 960
ATTGGGAGCT GACCCCAGGT CCCGCTCCGT TTTCTTTGTG TGCAGCACTT GTGTTGGTGA 1020
CCAGCAGTGA AGAGAGTGCG TGGACGTCAC CGTGTGGTTA TGAAGCTAAC GGCAGCCCTC 1080
AGCGGTGCCG ACTTCCGCTC CCCGACACAT TCCTGTGTGC ACGTTCGTGG GTCTGAGCGT 1140
GACTCATGGT GTGTGTCCCT AGAGCAGTTC ACTCAGAGGC TTCTCTTCCG TGCTCTCAAG 1200
AATAAAAGCA GGGCCGCCAC ATCCTGATAA GTCTTGCCAT TCAGCGGTCC TGTCTTGCAG 1260
AGGGATAAGC CAGTGTCCCC AGGCCACAGT CCTTACACCT TGAGCAAGTT CCCCAGAGTG 1320
AAGCAATCTT TCTAGACAAG TTTTGCGTTT CTCAGAATTT TATTTTAGTG ATATTGTTAC 1380
CAAAAGATTG TAACCCCAAA ATGTGTGCCT TTGGCTTGCC TGTTTTAGGA ATTCACTTGT 1440
GTTATCTCCC CAAGCAAAAC AAAAGAAAGA GAAACCTTCC TGTTGACGAA TCCTTTTTAC 1500
CTTCTTGAGA GTTGTCAATG GGACTAACTT GTATATTTCT TTGCTACCTT CTTTTAAAAA 1560
CATTTTTCTT ATTTACTATT ACAGACGTAT AGTAATGGTG CCTGACATAA CCCACAGCCA 1620
AAGGCCTTGG CCTTGCTGTG TGTATTTCAG GCTTTTTCTT CCCTTTTCTT TTTTTTTAAG 1680
TAATAAGATA TTACAGTTAT AGCTGAAGCC TGATCCTGTT CCCTTTTCTC CCTCTCGTCC 1740
CAAGCATCAC CACTGTCCCA AATCTGCTCC TTCTTCCCAC ATCTTTGCAG TTTGGGCAAG 1800
TCTTCTGAAT GCCTAGTCAT GATTTTAAGT CTTCTTTCCA CCTTCAGTGA TGGTTGGCTA 1860
CCCTGAGCAA GCCAGTAGAT TCAGTTATGT GCCTGGAGTC CAGATGTTTT ATGTGGATTT 1920
TTCATGTGGA ATTGTTTTTG GTAAGGAAGT ATTCCCTTGC CACACCAATG AAAAGAGAAG 1980
AAAACAGGTA GCTGGCACCC ACTGCATTGT TGCTTTCTGC CAGCCTGCTC CTTCTCCTTC 2040
CTCTCCAGCT CTGTTGTGTC CAGATGCAAA CTCTACATGC AGGGTTTGAC CCTAGGTCCT 2100
CACCTGCTGT AGCTCTCACA CGGGGACCGA ATGCTCTTGT GTCGTAAATC CTTCCTTTTG 2160
CTTCCTCGTG TTGGATGTGT TTAGTGGTTT TCATCTTCTG GTCACTATTT CATTCTAGGT 2220
TTATCCCCTT TAAATTATAA ATTAAATGAA TTCTTCGCTT TTCCTACCAG CAACTACCCA 2280
CCAAGTTCTA CCATGTGTTA ATTTAATCAA CAGTTATTTA TTGAGTACTT ATTACATGTT 2340
GATTTCCTGT TCTCAACATT GGAATGAAGA CAGCTTAGGG TTCTGCTTTC ATGAAGCTTG 2400
CATGCTCTTA GGTGGAGACA GACAGTAATT AAGCAGATAA ACAGGAAATT ATGAGCTAGT 2460
AGTGGGTCCA TTGCTGAGAA GTAAGACAGG TGGTAGGATG ACCCGTGCCG TGTGATGACT 2520
TTAGATTGGG TGGTTGGGGA AGACTTCACG GACCTTAAAA CTGGCCTTGG AACGGGAAGC 2580
GAGAACTGGG CACGGAAGAT GAGGGAGTGG GAGATTTCAG GCAGAGGGAG CAGCAGCAGG 2640
TACAGAGGCC CTGAGGCCTT TTATTGTGTC TTTTTGCTTG AGCGAGTAAC TTAGAGCACA 2700
CGTAGAGAAA GACAGCAGAA GTGATCTTCT AAACACTCTG TCCTGTGTGG AGAGCTCCTT 2760
ATGTGAGATT TTGCTGTGTA GTGAATTAAG GCTCAGCCAA ACTGGCTCAC GTGAGCTCTT 2820
TGAGCTTGCC TGTCTCTGTG GGCTGAAGGC TGTTCCCTGT 2860
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