| Tag | Content |
|---|
EnhancerAtlas ID | HS139-28591 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:43332230-43335210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr2:43333307-43333318 | AACAGCTGCAG | + | 6.02 | | NR2F1 | MA0017.2 | chr2:43334978-43334991 | CAGGGGTCAAGAG | + | 6.04 | | SPI1 | MA0080.4 | chr2:43333276-43333290 | CACTTCCCCTTTTG | - | 6.41 | | SPIB | MA0081.2 | chr2:43333276-43333288 | CACTTCCCCTTT | - | 6.07 | | Tcf12 | MA0521.1 | chr2:43333307-43333318 | AACAGCTGCAG | + | 6.62 | | ZBTB18 | MA0698.1 | chr2:43332401-43332414 | TGTCCAGATGTTT | + | 6.07 | | ZNF263 | MA0528.1 | chr2:43333023-43333044 | CTCTTTTCCCTCCCCACCTCC | - | 6.14 | | ZNF263 | MA0528.1 | chr2:43333171-43333192 | TCCTCCTCCTCCTCTAGCTCC | - | 6.55 | | ZNF263 | MA0528.1 | chr2:43333026-43333047 | TTTTCCCTCCCCACCTCCCCC | - | 6.69 | | ZNF263 | MA0528.1 | chr2:43333165-43333186 | TGTCCCTCCTCCTCCTCCTCT | - | 7.52 |
|
| | Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
| SE_01697 | chr2:43332753-43335255 | Aorta | | SE_04239 | chr2:43331196-43335343 | Brain_Anterior_Caudate | | SE_06096 | chr2:43331316-43337950 | Brain_Hippocampus_Middle | | SE_09287 | chr2:43330985-43338582 | CD14 | | SE_25333 | chr2:43331341-43335102 | DND41 | | SE_26129 | chr2:43332097-43338251 | Duodenum_Smooth_Muscle | | SE_27532 | chr2:43332666-43335248 | Esophagus | | SE_29578 | chr2:43332536-43334974 | Fetal_Muscle | | SE_36112 | chr2:43332213-43333814 | HMEC | | SE_37723 | chr2:43332329-43334538 | HSMMtube | | SE_38910 | chr2:43331932-43335128 | IMR90 | | SE_42533 | chr2:43331715-43335313 | Lung | | SE_48821 | chr2:43331891-43335282 | Right_Atrium | | SE_50539 | chr2:43331753-43335309 | Sigmoid_Colon | | SE_53008 | chr2:43331834-43335297 | Small_Intestine | | SE_53913 | chr2:43331902-43337194 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 43332767 | 43333000 | | chr2 | 43334400 | 43335196 | | chr2 | 43333846 | 43334697 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I043104 | chr2 | 43331740 | 43338502 |
|
Enhancer Sequence | GGCATGGGGA TCTTCAGTCA GGCTCTCTGA GGTCTTCCAG CCTCCAACCC CTGGGCTAGG 60
AGCCTTGTGT AGCAATCTTC CTGTTGCTAC CATGGAGACC TGAGCCCCAG GTCAGCCCTG 120
GGAAGGGTTG GGTGCATTCC TGGCCATAGG GATGGTGCAT TTCATTCAGG CTGTCCAGAT 180
GTTTATGTCC CCCCCAAATT AATATGTTGA AATCTTCACC CCTAAAGTGA TGAAGGTAGG 240
AGTCGGGCCT TTGGGAGGTG ATTAGGTCCT GGGGGTGGAG CCCTCATGAA TAGGATTAGT 300
GCCCTTATAT TATGCCCTGA GACAGACCCC TAACCCCTTC TGCCATGTGA GGTTAGAGTA 360
AGAAGTCACC ATTTATGAGG AGATCGCCCT CACCAGACAC TGAATCTGCC GGCCCCGTGA 420
TCTTGGACTT CCAGCCTCCA GAACTGTGAG AAACAAATGT CTGCAGTTTA CAAGCCATCC 480
AGTCTATGAT ATTAAATGTC TGCTGTTTAT AAGCCATCCA GTCCATGATA TTTTGTTATC 540
GTAGCCTAAA TGGACTCAGA TATCAGATAT ATTTCTGTAT AGCTTGGGGG AAGGAAGAGT 600
TCCTCCTCTC ACATCCCCTT CTGTGGGCTG GACTATGTTG AGAAAACCTC CACGTTTCCA 660
GCACCTCTCA CCATCTCCCT GCACCCCTTT AGAGGAAACC CCTTCCTGGG CCTTCAGGGC 720
ATGGCTGGGC ATGCTCCCAG CACACTTCAT GTTTGCTTCC AACCTAAGAA AGGCCAGGCT 780
TCCCAGCTGG GAGCTCTTTT CCCTCCCCAC CTCCCCCTTT CTTGTCTGTC TGCCTCCCTT 840
TCACACTCCC CTATCTCCAT CCCCTCAAAC CCAAGAGTTT CCACAGTGAC AACATGTGGG 900
CCCCAAATCA AACCCCTGTC CACAGGTCCT GCCTGTGTCC CTCCTCCTCC TCCTCTAGCT 960
CCCCAGCCTG GCCACCCTTG TCAGCCCCAC CCTCACTCCC ACACCCCCAC CATTCCTCCT 1020
TGTGGACAAC TTTCTAAATG CAGCCACACT TCCCCTTTTG AGCCACAGGG CCTATAAAAC 1080
AGCTGCAGAC AGTCAGCGGC ACTGCAAAAG TCCTCTTGCC AAGTTTGGCT GAGACCAATA 1140
CCCTCTAACT CTAGCCATTG CTTCCCCACT ACCAGGCACT GAGAGAACAG GCTCCTTTTC 1200
GAGTAAACAG TGGGGAGACA TCATGTTCCC AACATTCTAA ACTAAAGAGG ACTCACTGAG 1260
GGGCCCAGCC AGTGGGAGGA GGCAGCCCAA AGCCTAGCCT GGCTTCCCAC ACCCCCAACC 1320
CTGCCAGTGC CCTGTGAGAC CCTGACTACT CCACCCCCTC CAGTCTTCTG TTTTGCAGGA 1380
TGAGGGGTAG CTTGGTTGGT TTCCTGGCCC TTTCTGAGTC TAAAACTCCA CAAATCTGTC 1440
ACTTCTCCTT AGGGTGCTCC TGCCCAGTGC CTGGAGAGGG AAGGGGCTTT GCTGAGAGAC 1500
ATGCTGCCAC CTGAGGGTTG TCCAGACACG AACTCAGTCC CCCACCTGCC TTCTGTGCTC 1560
TTTCTGCAAC ACTCTGGCCT CAGTGAAACA GTAGCTCTCA GTCCTGGCCA CATAGCAGAA 1620
TCACCCAGGG AGATTTTACA ACATCTCAAT CCCCAGCCAC ACTCCAGACC CATGAAATCT 1680
GAATCGTGGG TTGGGGCCTG GAAATCAGTC TGTTTGGAAA GTTACCCAGG TGATTCTGCT 1740
AAGCGGTCAG GGTTGAGAAC CACGGTGGGA AAGGCTTCCA GGAAGTAAAG ATGAAGCTAT 1800
AAGCCAGAGG TGATACATTT CCGTCCCACA TTCTCCGCTG AGAAGGATCT TGAGGCTGGT 1860
AGGAAGAGAT CTGGGATGAA CTAGGCATGT CTGTCAGGGA TGGGTAGGGA GTGGCTGTGG 1920
CCTGAACTAG GTATTTGTCC TCGGGCTTTG GTGGCTCAGA GGTCCTGCCC TGAGGATGCA 1980
GGAGAGGACC AGCCTCCAGG CACTGGCTCA TTGGCCGGCT TGCTTCCTCC CAAACCTCCC 2040
ACCTCCCAAG TCTCATTATG GCCCTTGAAG TCAGACAGCC CCAGGGCTAC CGTCCAGGAA 2100
CTGGAAACCA ACCTCAGCCA GAGCCAAGAG GCCCCAGGTC AGCCCCAGCC CTCCAAGGGC 2160
TTTGTGTAGA TTGAAAAAAG GAAAATAGAG AAGGGAAACC AAAGCAGGGC AGAATGCAGT 2220
GAAGGAGAAA AAGACAAGAG AAAGGGGAAG GACCCTGAGG TCAGAGAGTC ATGTGAATGG 2280
CATTTAGGGA ACAAAACCTG GCTCCTCTCC ATCCATCATC CCCTGGGCCG GGAGAGAAGC 2340
ACTCTTCTGC CAGGGTCCAG GGCACAGAGA TCCAGGCCAG AAAATCCAGA TCCAGAAATC 2400
TGCCCAACCA TGTGTCTGTG AGCACCATGC AGAGCCAACA GAGGAGCCTC CTCGCACAGA 2460
CACCCTCAGA TCCCCACCTC TTCTTCTCAC CAGAGCCACA GCCTCCTGTT GGACATTTAA 2520
GCGAAATCAC TTGGTCATTC CTCAACCAAA AAAAAAAAAG AAAAAAAAAA ACACATTAAA 2580
TCCAGTTCCC AAGACACTTG GCATCACATC AGGGTGACCT GGGTGATGCT GCTGTCGAGC 2640
TGCATGACCT GGAGTGAGCC ACCTCCCTTC CCTGCCCGGG CCTCAGGGCC TGACCTTGCC 2700
TGCCTGCCTG CGAAGTCATA TTTGAATGGA AGGGACACTG CTGTAGCCCA GGGGTCAAGA 2760
GCCTGGGCTC TGGAGACAGA GGCCTGGACC TGGCTCACCA CTTACTAGCT GTGTGAGCAT 2820
GGGCAGCTAT GGCTGTGAAC TTCTGCTTCC TCATCTGTAA GGCAAGAGTT AGCAGACTGA 2880
TGACAGAAAA GGAGAAGAAA ACACAGGCCA CACCAATGTG GGACTCATAT TTAGAAAACA 2940
CAAGGACTGG CCAGGTACGG TGGCTCATGC CCTGTAATCC 2980
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