| Tag | Content |
|---|
EnhancerAtlas ID | HS002-00135 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:19755970-19757460 |
Target genes | |
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 | CATAAGCAAG TCACCACCTC ATCCCTTGGA ACCTCAGTCT TCTTTAAAAC CTGGGTCCGA 60
CGGTACTGTC TACCTCACGG GCCACTGGGA ATGAGGTACC ACGTCTGGGC CATAAGGGCA 120
CCGCCCACAG AGCATCCTCC ATAAAGGGTA GGAACTCTCC CAGAGAGTAA AGCACATGGC 180
TTATCTGCCA GGACTTTTAC ATAACATTTT TTAGGTGCTA GAGGGTCCTT TCTGCCTGGA 240
TTTTTCCCTC ACTTGACACA GGTTTTCCAT TCAGGCTGCC AGGAGTCTCT AGAAAGGTAG 300
GCGGAGTGTT ATGTCAGTTT CCAAGTCATT AAGCACCCAC AAAGGAGGGC AGGCTTGCAC 360
AGCACTCACT CCACACAACC GCCCCTGCCC TGAGTACGAC GGAGCACATG GCTTCCCTAA 420
AGCCACAAGG AGAAGAGAGG CAGGGACAGT GAGAGCTGAA GGAATTCCAC ATGTGTCCAT 480
GGAAGATCAC CTTCCCTTTG TTTTCCTGCA CTCTAGTAAC TCCCTCATGC AGCTTGCTTT 540
CTGAAGCCCT CTGCTCCATT TCCCCAGCCC AGGACAGCAT CAAGAAATAT TTCCACCATC 600
TCATCTATTT GAACCTTCTC CCTATTTACT GGTGCTCCCA ACCCCATCTG AGGCCATCGA 660
AACCAGACAA CTGTGGCAGC ACTAGCAGAG TCCCCAAACT ACCCTGACAC CCTCCCTGGC 720
AAGGAAAATT TCCACGCGCC TCTCCCTGGC ATATTTATTC CAGAGGAAAA CTTAGCAACC 780
TACACACTAC ACACAGGCTC TGTGTCAAAC TCTACAACAG CCATCAGTTG ATCTTTCCCT 840
TACACATCCC TCCAGGAAGT GAAATATCCG AAATGAGTCA TACTCAGGAG TCGGAGCTAT 900
ACTTCCACTG TAGTTTTTTT GGATAACCAA TTCACTGTTT ACACTCCAAA ACCTCTAATT 960
GCTGAACACA GAACAGTTCC TTTGCAGAGA TCAAAGCTTA CCTGGTGAAC CTGGCGAAAT 1020
GACAAAAATT CTCCAAAAGG AGTTAGCCAT CCAGAGTGCC AGAGGAGGGT GGCTGTACAA 1080
GCACATTTTA ATTGGCAAAG CAGAGTCGCT GCCCAGCAAG GAAGAGTATG CAGGGGTTTA 1140
TTCTGCTGCT CTTCTATTTC CCCTTTAAGG CATATATCTC TTACCCCTGC ACCCACCAAC 1200
TTTAGTCACT CCTAGCACAC AGCTGGCGGC CGCCCACCCG CACCCGCACC TGCACCCGCA 1260
CCTCAGAGAG CTTGCTGATC CCTGAGCCGT GCACTGAAGC TTCCAAGCAG CTCTACCTAA 1320
AGGCAAGCAC TGCCTGCTTT TTACAACATA TACAATGGGC TAACCTGATG CACAGAAAAA 1380
CCCTGGGTCA CATGACAACC AACAAACTCA TTGCTCAGGA TGGCTCTCCG CCACGTTTCT 1440
CAGGCACTGT GCTTGGCTCT GCTGGCCAAC TGAGTGAGCT GGAGCATTTT 1490
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