| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00537 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:19755510-19757890 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
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: 30 | 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 | chr1:19754772-19755839 | Sigmoid_Colon | | 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 | ATCTCTCTAA AATGTATTAC CTGCTCTACA TTTTTACACA ATGCAAATGA TCACAGGACA 60
ATGCAATGAA CACAGCTAAA CCATTTCTCA TTAGCCTAAG GACAGTGTAT GAGTAGCCAC 120
TCTTGGAACA GCACCCTGTG TCTGCTTTTT ACATTTATCT GCTTCTTCTG CCAGGCTGTC 180
AGCTACACTT CCTCAACTAA TATGTTGCTT CTAATCTGCT ATGAGGTTGA GAACCCAGAA 240
AATTAGAAAT CTGCTCTCAT TTCAAACAAA AAAAAAAAAG AAACTCTGAG AGAAGGAATA 300
AATCAGGTTG ATAACTTGGG GTCCAGAGTC ACAGCCCACA AATAGTTTGT AAGTACCTTG 360
ACACTATATG AAGATTACTT CTTCCTTTTC TTGAAGAAGT TCAAGACTCT AAAGGCAGAG 420
ATACGATATA CTAATAATTC CTACTTTCCC ATACAACCTG CATAAGCAAG TCACCACCTC 480
ATCCCTTGGA ACCTCAGTCT TCTTTAAAAC CTGGGTCCGA CGGTACTGTC TACCTCACGG 540
GCCACTGGGA ATGAGGTACC ACGTCTGGGC CATAAGGGCA CCGCCCACAG AGCATCCTCC 600
ATAAAGGGTA GGAACTCTCC CAGAGAGTAA AGCACATGGC TTATCTGCCA GGACTTTTAC 660
ATAACATTTT TTAGGTGCTA GAGGGTCCTT TCTGCCTGGA TTTTTCCCTC ACTTGACACA 720
GGTTTTCCAT TCAGGCTGCC AGGAGTCTCT AGAAAGGTAG GCGGAGTGTT ATGTCAGTTT 780
CCAAGTCATT AAGCACCCAC AAAGGAGGGC AGGCTTGCAC AGCACTCACT CCACACAACC 840
GCCCCTGCCC TGAGTACGAC GGAGCACATG GCTTCCCTAA AGCCACAAGG AGAAGAGAGG 900
CAGGGACAGT GAGAGCTGAA GGAATTCCAC ATGTGTCCAT GGAAGATCAC CTTCCCTTTG 960
TTTTCCTGCA CTCTAGTAAC TCCCTCATGC AGCTTGCTTT CTGAAGCCCT CTGCTCCATT 1020
TCCCCAGCCC AGGACAGCAT CAAGAAATAT TTCCACCATC TCATCTATTT GAACCTTCTC 1080
CCTATTTACT GGTGCTCCCA ACCCCATCTG AGGCCATCGA AACCAGACAA CTGTGGCAGC 1140
ACTAGCAGAG TCCCCAAACT ACCCTGACAC CCTCCCTGGC AAGGAAAATT TCCACGCGCC 1200
TCTCCCTGGC ATATTTATTC CAGAGGAAAA CTTAGCAACC TACACACTAC ACACAGGCTC 1260
TGTGTCAAAC TCTACAACAG CCATCAGTTG ATCTTTCCCT TACACATCCC TCCAGGAAGT 1320
GAAATATCCG AAATGAGTCA TACTCAGGAG TCGGAGCTAT ACTTCCACTG TAGTTTTTTT 1380
GGATAACCAA TTCACTGTTT ACACTCCAAA ACCTCTAATT GCTGAACACA GAACAGTTCC 1440
TTTGCAGAGA TCAAAGCTTA CCTGGTGAAC CTGGCGAAAT GACAAAAATT CTCCAAAAGG 1500
AGTTAGCCAT CCAGAGTGCC AGAGGAGGGT GGCTGTACAA GCACATTTTA ATTGGCAAAG 1560
CAGAGTCGCT GCCCAGCAAG GAAGAGTATG CAGGGGTTTA TTCTGCTGCT CTTCTATTTC 1620
CCCTTTAAGG CATATATCTC TTACCCCTGC ACCCACCAAC TTTAGTCACT CCTAGCACAC 1680
AGCTGGCGGC CGCCCACCCG CACCCGCACC TGCACCCGCA CCTCAGAGAG CTTGCTGATC 1740
CCTGAGCCGT GCACTGAAGC TTCCAAGCAG CTCTACCTAA AGGCAAGCAC TGCCTGCTTT 1800
TTACAACATA TACAATGGGC TAACCTGATG CACAGAAAAA CCCTGGGTCA CATGACAACC 1860
AACAAACTCA TTGCTCAGGA TGGCTCTCCG CCACGTTTCT CAGGCACTGT GCTTGGCTCT 1920
GCTGGCCAAC TGAGTGAGCT GGAGCATTTT CTCTTGGGTG TGCATACCCC TCCACCTGTC 1980
CAACTTTAAA ACACAGAATC AACAGGGATG TTACACTAAA GGGGACCCTA GAAACCATAT 2040
AAACGGTGGA AAATTGAGGC CTGGACTGAC CCATAACAAA TGAGACATCA CATAATGGCA 2100
AATGAACCAT GACCAGAAAA CAAATCTCTT TAGTACACAG TTTAGCGCTT CTGCTTATAC 2160
AGGTTGAACA GCCCTAACCC AAAAATCCAA ATCCCAAACT TTTTGAGCGA AGACATGAGG 2220
CTCCAACGAG CATATCAGAC TTTCGGATTA GGAATGGTCA ACCAGTAAGT TCTGCAAATA 2280
TTCAAAATCT GAAAAGAATC CAAAGAAGTC TCAAATCCAA AATGCTTCTG GTCCCAAGCA 2340
TTTCGGATAA GAAACCTGTA GTTTAATCAT CAGTCAAAAT 2380
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