| Tag | Content |
|---|
EnhancerAtlas ID | HS046-00405 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr1:19755820-19757600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox3 | MA0514.1 | chr1:19756464-19756474 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
| SE_00361 | chr1:19746887-19757387 | Adipose_Nuclei | | SE_01631 | chr1:19755843-19757681 | Aorta | | SE_02919 | chr1:19755911-19756933 | Bladder | | SE_04046 | chr1:19756053-19757455 | Brain_Anterior_Caudate | | SE_05833 | chr1:19750586-19757279 | Brain_Hippocampus_Middle | | SE_09593 | chr1:19755451-19756990 | CD14 | | SE_18410 | chr1:19754667-19757430 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19269 | chr1:19755104-19757108 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_23237 | chr1:19755928-19757811 | Colon_Crypt_1 | | SE_25786 | chr1:19750802-19758037 | Duodenum_Smooth_Muscle | | SE_26537 | chr1:19754835-19758103 | Esophagus | | SE_28668 | chr1:19755603-19757198 | Fetal_Intestine_Large | | SE_29645 | chr1:19755678-19757560 | Fetal_Muscle | | SE_31164 | chr1:19754803-19757992 | Fetal_Thymus | | SE_31447 | chr1:19755938-19757724 | Gastric | | SE_41031 | chr1:19755895-19757535 | Left_Ventricle | | SE_42185 | chr1:19755689-19757735 | Lung | | SE_45110 | chr1:19755943-19756940 | NHLF | | SE_45720 | chr1:19751083-19757454 | Osteoblasts | | SE_46635 | chr1:19755894-19756886 | Ovary | | SE_47234 | chr1:19755677-19758314 | Panc1 | | SE_48688 | chr1:19755923-19757600 | Right_Atrium | | SE_50058 | chr1:19755847-19757828 | Sigmoid_Colon | | SE_51211 | chr1:19755657-19757588 | Skeletal_Muscle | | SE_52345 | chr1:19754876-19757871 | Small_Intestine | | SE_54550 | chr1:19750611-19758089 | Stomach_Smooth_Muscle | | SE_56083 | chr1:19755047-19757873 | u87 | | SE_65446 | chr1:19755872-19757833 | Pancreatic_islets | | SE_67779 | chr1:19755047-19757873 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 19756629 | 19757043 | | chr1 | 19756200 | 19757454 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I019422 | chr1 | 19749273 | 19757876 |
|
Enhancer Sequence | ATAACTTGGG GTCCAGAGTC ACAGCCCACA AATAGTTTGT AAGTACCTTG ACACTATATG 60
AAGATTACTT CTTCCTTTTC TTGAAGAAGT TCAAGACTCT AAAGGCAGAG ATACGATATA 120
CTAATAATTC CTACTTTCCC ATACAACCTG CATAAGCAAG TCACCACCTC ATCCCTTGGA 180
ACCTCAGTCT TCTTTAAAAC CTGGGTCCGA CGGTACTGTC TACCTCACGG GCCACTGGGA 240
ATGAGGTACC ACGTCTGGGC CATAAGGGCA CCGCCCACAG AGCATCCTCC ATAAAGGGTA 300
GGAACTCTCC CAGAGAGTAA AGCACATGGC TTATCTGCCA GGACTTTTAC ATAACATTTT 360
TTAGGTGCTA GAGGGTCCTT TCTGCCTGGA TTTTTCCCTC ACTTGACACA GGTTTTCCAT 420
TCAGGCTGCC AGGAGTCTCT AGAAAGGTAG GCGGAGTGTT ATGTCAGTTT CCAAGTCATT 480
AAGCACCCAC AAAGGAGGGC AGGCTTGCAC AGCACTCACT CCACACAACC GCCCCTGCCC 540
TGAGTACGAC GGAGCACATG GCTTCCCTAA AGCCACAAGG AGAAGAGAGG CAGGGACAGT 600
GAGAGCTGAA GGAATTCCAC ATGTGTCCAT GGAAGATCAC CTTCCCTTTG TTTTCCTGCA 660
CTCTAGTAAC TCCCTCATGC AGCTTGCTTT CTGAAGCCCT CTGCTCCATT TCCCCAGCCC 720
AGGACAGCAT CAAGAAATAT TTCCACCATC TCATCTATTT GAACCTTCTC CCTATTTACT 780
GGTGCTCCCA ACCCCATCTG AGGCCATCGA AACCAGACAA CTGTGGCAGC ACTAGCAGAG 840
TCCCCAAACT ACCCTGACAC CCTCCCTGGC AAGGAAAATT TCCACGCGCC TCTCCCTGGC 900
ATATTTATTC CAGAGGAAAA CTTAGCAACC TACACACTAC ACACAGGCTC TGTGTCAAAC 960
TCTACAACAG CCATCAGTTG ATCTTTCCCT TACACATCCC TCCAGGAAGT GAAATATCCG 1020
AAATGAGTCA TACTCAGGAG TCGGAGCTAT ACTTCCACTG TAGTTTTTTT GGATAACCAA 1080
TTCACTGTTT ACACTCCAAA ACCTCTAATT GCTGAACACA GAACAGTTCC TTTGCAGAGA 1140
TCAAAGCTTA CCTGGTGAAC CTGGCGAAAT GACAAAAATT CTCCAAAAGG AGTTAGCCAT 1200
CCAGAGTGCC AGAGGAGGGT GGCTGTACAA GCACATTTTA ATTGGCAAAG CAGAGTCGCT 1260
GCCCAGCAAG GAAGAGTATG CAGGGGTTTA TTCTGCTGCT CTTCTATTTC CCCTTTAAGG 1320
CATATATCTC TTACCCCTGC ACCCACCAAC TTTAGTCACT CCTAGCACAC AGCTGGCGGC 1380
CGCCCACCCG CACCCGCACC TGCACCCGCA CCTCAGAGAG CTTGCTGATC CCTGAGCCGT 1440
GCACTGAAGC TTCCAAGCAG CTCTACCTAA AGGCAAGCAC TGCCTGCTTT TTACAACATA 1500
TACAATGGGC TAACCTGATG CACAGAAAAA CCCTGGGTCA CATGACAACC AACAAACTCA 1560
TTGCTCAGGA TGGCTCTCCG CCACGTTTCT CAGGCACTGT GCTTGGCTCT GCTGGCCAAC 1620
TGAGTGAGCT GGAGCATTTT CTCTTGGGTG TGCATACCCC TCCACCTGTC CAACTTTAAA 1680
ACACAGAATC AACAGGGATG TTACACTAAA GGGGACCCTA GAAACCATAT AAACGGTGGA 1740
AAATTGAGGC CTGGACTGAC CCATAACAAA TGAGACATCA 1780
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