| Tag | Content |
|---|
EnhancerAtlas ID | HS104-00659 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:19755830-19757650 |
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 | GTCCAGAGTC ACAGCCCACA AATAGTTTGT AAGTACCTTG ACACTATATG AAGATTACTT 60
CTTCCTTTTC TTGAAGAAGT TCAAGACTCT AAAGGCAGAG ATACGATATA CTAATAATTC 120
CTACTTTCCC ATACAACCTG CATAAGCAAG TCACCACCTC ATCCCTTGGA ACCTCAGTCT 180
TCTTTAAAAC CTGGGTCCGA CGGTACTGTC TACCTCACGG GCCACTGGGA ATGAGGTACC 240
ACGTCTGGGC CATAAGGGCA CCGCCCACAG AGCATCCTCC ATAAAGGGTA GGAACTCTCC 300
CAGAGAGTAA AGCACATGGC TTATCTGCCA GGACTTTTAC ATAACATTTT TTAGGTGCTA 360
GAGGGTCCTT TCTGCCTGGA TTTTTCCCTC ACTTGACACA GGTTTTCCAT TCAGGCTGCC 420
AGGAGTCTCT AGAAAGGTAG GCGGAGTGTT ATGTCAGTTT CCAAGTCATT AAGCACCCAC 480
AAAGGAGGGC AGGCTTGCAC AGCACTCACT CCACACAACC GCCCCTGCCC TGAGTACGAC 540
GGAGCACATG GCTTCCCTAA AGCCACAAGG AGAAGAGAGG CAGGGACAGT GAGAGCTGAA 600
GGAATTCCAC ATGTGTCCAT GGAAGATCAC CTTCCCTTTG TTTTCCTGCA CTCTAGTAAC 660
TCCCTCATGC AGCTTGCTTT CTGAAGCCCT CTGCTCCATT TCCCCAGCCC AGGACAGCAT 720
CAAGAAATAT TTCCACCATC TCATCTATTT GAACCTTCTC CCTATTTACT GGTGCTCCCA 780
ACCCCATCTG AGGCCATCGA AACCAGACAA CTGTGGCAGC ACTAGCAGAG TCCCCAAACT 840
ACCCTGACAC CCTCCCTGGC AAGGAAAATT TCCACGCGCC TCTCCCTGGC ATATTTATTC 900
CAGAGGAAAA CTTAGCAACC TACACACTAC ACACAGGCTC TGTGTCAAAC TCTACAACAG 960
CCATCAGTTG ATCTTTCCCT TACACATCCC TCCAGGAAGT GAAATATCCG AAATGAGTCA 1020
TACTCAGGAG TCGGAGCTAT ACTTCCACTG TAGTTTTTTT GGATAACCAA TTCACTGTTT 1080
ACACTCCAAA ACCTCTAATT GCTGAACACA GAACAGTTCC TTTGCAGAGA TCAAAGCTTA 1140
CCTGGTGAAC CTGGCGAAAT GACAAAAATT CTCCAAAAGG AGTTAGCCAT CCAGAGTGCC 1200
AGAGGAGGGT GGCTGTACAA GCACATTTTA ATTGGCAAAG CAGAGTCGCT GCCCAGCAAG 1260
GAAGAGTATG CAGGGGTTTA TTCTGCTGCT CTTCTATTTC CCCTTTAAGG CATATATCTC 1320
TTACCCCTGC ACCCACCAAC TTTAGTCACT CCTAGCACAC AGCTGGCGGC CGCCCACCCG 1380
CACCCGCACC TGCACCCGCA CCTCAGAGAG CTTGCTGATC CCTGAGCCGT GCACTGAAGC 1440
TTCCAAGCAG CTCTACCTAA AGGCAAGCAC TGCCTGCTTT TTACAACATA TACAATGGGC 1500
TAACCTGATG CACAGAAAAA CCCTGGGTCA CATGACAACC AACAAACTCA TTGCTCAGGA 1560
TGGCTCTCCG CCACGTTTCT CAGGCACTGT GCTTGGCTCT GCTGGCCAAC TGAGTGAGCT 1620
GGAGCATTTT CTCTTGGGTG TGCATACCCC TCCACCTGTC CAACTTTAAA ACACAGAATC 1680
AACAGGGATG TTACACTAAA GGGGACCCTA GAAACCATAT AAACGGTGGA AAATTGAGGC 1740
CTGGACTGAC CCATAACAAA TGAGACATCA CATAATGGCA AATGAACCAT GACCAGAAAA 1800
CAAATCTCTT TAGTACACAG 1820
|
