| Tag | Content |
|---|
EnhancerAtlas ID | HS178-19537 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr5:150001190-150004180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr5:150001743-150001754 | TTCTTATCTCT | + | 6.32 | | Gata1 | MA0035.3 | chr5:150001743-150001754 | TTCTTATCTCT | + | 6.32 | | ZNF263 | MA0528.1 | chr5:150002338-150002359 | CCCCCTCCACTCCCCTGCTCC | - | 6.41 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_00123 | chr5:150000621-150011231 | Adipose_Nuclei | | SE_00895 | chr5:150002893-150008036 | Adrenal_Gland | | SE_01549 | chr5:150000855-150008263 | Aorta | | SE_04527 | chr5:150000872-150002956 | Brain_Anterior_Caudate | | SE_04527 | chr5:150003014-150004186 | Brain_Anterior_Caudate | | SE_06402 | chr5:150002382-150004325 | Brain_Hippocampus_Middle | | SE_08263 | chr5:150000684-150004189 | Brain_Inferior_Temporal_Lobe | | SE_23666 | chr5:150003534-150004189 | Colon_Crypt_1 | | SE_26296 | chr5:150003263-150004159 | Duodenum_Smooth_Muscle | | SE_27146 | chr5:150003356-150007113 | Esophagus | | SE_29818 | chr5:150003404-150008087 | Fetal_Muscle | | SE_31661 | chr5:150001822-150008147 | Gastric | | SE_40596 | chr5:150000663-150013521 | Left_Ventricle | | SE_42134 | chr5:150000692-150008117 | Lung | | SE_47583 | chr5:150002962-150003373 | Pancreas | | SE_47583 | chr5:150003453-150004178 | Pancreas | | SE_48061 | chr5:150002676-150013526 | Psoas_Muscle | | SE_48556 | chr5:150000708-150008294 | Right_Atrium | | SE_50806 | chr5:150001825-150008100 | Sigmoid_Colon | | SE_51080 | chr5:150002321-150013846 | Skeletal_Muscle | | SE_52506 | chr5:150002802-150004184 | Small_Intestine | | SE_53523 | chr5:150003411-150007829 | Spleen | | SE_55733 | chr5:150000674-150008204 | u87 | | SE_65294 | chr5:149997055-150010504 | Pancreatic_islets | | SE_67470 | chr5:150000674-150008204 | u87 |
|
| | 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 |
| GH05I150621 | chr5 | 150001179 | 150002674 |
|
Enhancer Sequence | TTGTACCTGC CTCTCTAGAG GGCTCACAGG CAGGTTTAAG TATGAGCCAC TATATCTTCT 60
GCTTTGGGCA CTGCAGATAC CTTTGTTTGG GGTCAGTGGG TACCAGTGCC ATTTCTCCAA 120
GGCCTGAGTA CCAGCTGAGC AGGGCAACAC AGGGCCCTGT GGGCAGGCTA GAGGGATAGA 180
GGGTACAGAG AGATGCCATC AGCTGCTGCC AATTTGGGAA AATAGATCTG GGGAGGAAAG 240
GGTAGTGTAG AGCTCATGAT CAGGCCTCAG CCAACACTAG GGCCCCCAGC TCACCAAGAC 300
AGCCCCATGC TAAGCTGCCC TCCCCAAAGT CTCAGCTGGT CATAACTGGT AGCGTTTCTT 360
GAGATTGTTG TGCAGATGGA GACTCTGAGT GCCAGAGATG GCAAGTGACT TGTCCAAACT 420
CACACAGTAA GTTGGTGGCA AAGCTAGGGC TGGAACCCAG GGCTTATGCC TCCCAGTTCA 480
GCTGCCCAGC ACTGTGCTAA ATGCGCCATA TGGAGTATTT AATCCTATAA ACAATCCTGT 540
GAAGTTCATA CTTTTCTTAT CTCTGTTTTA CAGATGAGGA AACTAAGGCA TAAGGAATTT 600
AAGTGAATTG TCAAAGTCTC ACAGCCTGTG GGTGGAGGAG CTGAGATTTG AACCCCAGGA 660
GGTCTGGGCC CATGCTTTTA ACCACCCTCT CTACTGCCTG TCTCCATGGT GATGAGGCAG 720
CAGGCTGTGT TCTTCCACCC ACCTGGGGCT GGGAAAAGGT TGTTCAGGCT CTGGGAGTTG 780
TTGGAAGATT TTGCCAAGCC AAATTCCCTC CCACTCGGAT GCTCTGGGGG AAACCTGGGT 840
ACTCACCGCT GATGCCTCCC TGCCTTTGCT GGTGGCCACT TGTTATTGGA GGCTGGAGGT 900
GTGTAGCAGA TTTAGAGCCA CTTCCAACTC TAGTGGACAC TGTTCTGAGC CTCTGGGGTG 960
GGGAGGGGTG TGGGTCTGTG TTGTCAGATG AGTCCTGCCA CTGGACATGT CTGTTTTGTT 1020
CAGGCAGAGG GACCTGTGTG CGTGTTAACA GCTGACAGTG GTCACTGGGC CCAGAACAAG 1080
GCTCCTGCTC CTCAGGCTGT GACAGAGAGG GCAGATGGAG CAGGAGCCTG GGCAGGAAGC 1140
TGCCTACTCC CCCTCCACTC CCCTGCTCCA CAGTGATTGT AACAGGAGGG TGATGGTGAG 1200
GAGCACTGCT CACAGGTTCA CATACACCTC ACCATGCACT CACACATACA TGCTTTCACA 1260
TCCATCCGTA AACACACATG TATCTACACA TGATGTATAG ATGCCATGTT CTCATGCAAA 1320
CCATCACACA TATGCACTCA CACAACTGCA CACACATGGA GGCCCTCAGA CACACATCCA 1380
TGCATGGGGT ACACACTGGC ACATACCTTC CTGAAGGCCC CCTCACCCAT GCACAGCTGC 1440
CACATGTGAA CACGTCTCAG ATTTGCTTAC AGAGCTGCAG TTGCATCTGA AAACATATAA 1500
GCAGACATAG GCACACTTTC TCACACAAAC ACACATATTC CCTCTCATAG ATACAGGTGA 1560
AAAGCATGTT CTTTTCTCCA TTTCCTTTTG CTACACACCT ACACTTTGAA ATCTTTCACA 1620
CATTCTCTCC TACAGACCTA GCCACTCTTG CACACCCACT GTCACACACC TACGTACAGA 1680
CCGAATCACT TTCTCTCCTT TCTTTTCCAC ATCTCTTTCT CTTTCATACC ACCCACACAG 1740
CAATCCTAGC CTCTCTCTCT CTTTTCCTCT CACCCACACA CAGCTTCCTG GTTTCCCACA 1800
GGCTGGGCTG CAGCCACTTC CCTAGAGCAG GCACTCTCAG GGTTAGCGAT ACCCCAACCT 1860
GGTGGGGGTC CCAGGATCCC ACCCCCACCC CTCACTCTCC CAACCTGCCC TCTACCCTGG 1920
GTACAAGATG ATGAGAGCAG AGCAGCCACA CGATCAGAGG AATTCTCTGA AGCCCATGAG 1980
GCCAGGAGGA GAAATGGGAA CTGCCAGGGA GGGTTCCTGC ATTCTGAGTC TCCCCAGTGT 2040
GAACAGGGGA CATCCCAAAC CCAGGCCACC TGCAGGTCTG TGTTTCACAG GCCCTTGTGT 2100
GGGGTGGGCT TACGCTAGCA CATTCCTAAC TTCCTTTAGC AGAAATCTAA ACACACAACT 2160
CTTGATGCAA AAGACAGATG AAAGTGGAAC CACCCTGGTC AAGGGGGTGG GGAACCCGGG 2220
GAAACTTCGG TGAAAACCTA GACCAGCATT TCTCCAACCG TGGTTCTGTT TCAAAATTGC 2280
TGGGGCTGTG GAGGGTACTT GCCATCAGTC CTGTGCCAAG CCCACCAGCT CGTGCCCTCA 2340
ATGGGAGTGG TGCTGGAATG TGGGTATCTG GACTTTTAAC AGCATCCCAC GTGACTCTGA 2400
TGTACATGGC CACTGCCATG GGGCTTCGCA CGCTCAATCT GAATGGCATT TTGCTCAGTG 2460
AAAGGTGGGG AGCTGAGCCC CAGAGCTGCC ATACAGCACC CTGCCTTGTT GCTGACCCAC 2520
TGGTGAAGTC AGGGGATGGC AGCAGGTGGG TGGGGACATG GTCACCCTTC TCAGTGCCCA 2580
TTTGCCTAAG TTCTACCAAG AGAGACAGTT ATTCTAGTTA CTGGGGCTGA GACATAGCGG 2640
GGAAGATGGG CCTGAGCACC CAGGTCTGAA AGGAGAGCCA GGAAGAGGTA GGGTGGGAGG 2700
TGGTACCAGT TATGGGGACA GAATCACAAA GGCAGATTTC AAAGTGGGTA GTGGGTGGGT 2760
TAGAGAAAAG AAAAGGGGAC ACAAAGAAAC TGTCTCCCTC CTAGCCGAAG GAGATAGGAG 2820
GATTTTAGGA CAGACCGACC GACCTAGCGA TACAGAAAAT GATAAGGAAA CGGAGAGACA 2880
GACAACCAGG CAGCAGAGAG TGAGGCACAG CGAGAGGAAA GAGAGGTGCC CCCGCCTGGA 2940
GATGGGAGGC TGAGCGGGTG GAGGAGGGAG TCGCACCCCC AGGGCTGGGC 2990
|
