| Tag | Content |
|---|
EnhancerAtlas ID | HS129-00476 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:19755850-19757730 |
Target genes | | Number: 14 | 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: 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 | AATAGTTTGT AAGTACCTTG ACACTATATG AAGATTACTT CTTCCTTTTC TTGAAGAAGT 60
TCAAGACTCT AAAGGCAGAG ATACGATATA CTAATAATTC CTACTTTCCC ATACAACCTG 120
CATAAGCAAG TCACCACCTC ATCCCTTGGA ACCTCAGTCT TCTTTAAAAC CTGGGTCCGA 180
CGGTACTGTC TACCTCACGG GCCACTGGGA ATGAGGTACC ACGTCTGGGC CATAAGGGCA 240
CCGCCCACAG AGCATCCTCC ATAAAGGGTA GGAACTCTCC CAGAGAGTAA AGCACATGGC 300
TTATCTGCCA GGACTTTTAC ATAACATTTT TTAGGTGCTA GAGGGTCCTT TCTGCCTGGA 360
TTTTTCCCTC ACTTGACACA GGTTTTCCAT TCAGGCTGCC AGGAGTCTCT AGAAAGGTAG 420
GCGGAGTGTT ATGTCAGTTT CCAAGTCATT AAGCACCCAC AAAGGAGGGC AGGCTTGCAC 480
AGCACTCACT CCACACAACC GCCCCTGCCC TGAGTACGAC GGAGCACATG GCTTCCCTAA 540
AGCCACAAGG AGAAGAGAGG CAGGGACAGT GAGAGCTGAA GGAATTCCAC ATGTGTCCAT 600
GGAAGATCAC CTTCCCTTTG TTTTCCTGCA CTCTAGTAAC TCCCTCATGC AGCTTGCTTT 660
CTGAAGCCCT CTGCTCCATT TCCCCAGCCC AGGACAGCAT CAAGAAATAT TTCCACCATC 720
TCATCTATTT GAACCTTCTC CCTATTTACT GGTGCTCCCA ACCCCATCTG AGGCCATCGA 780
AACCAGACAA CTGTGGCAGC ACTAGCAGAG TCCCCAAACT ACCCTGACAC CCTCCCTGGC 840
AAGGAAAATT TCCACGCGCC TCTCCCTGGC ATATTTATTC CAGAGGAAAA CTTAGCAACC 900
TACACACTAC ACACAGGCTC TGTGTCAAAC TCTACAACAG CCATCAGTTG ATCTTTCCCT 960
TACACATCCC TCCAGGAAGT GAAATATCCG AAATGAGTCA TACTCAGGAG TCGGAGCTAT 1020
ACTTCCACTG TAGTTTTTTT GGATAACCAA TTCACTGTTT ACACTCCAAA ACCTCTAATT 1080
GCTGAACACA GAACAGTTCC TTTGCAGAGA TCAAAGCTTA CCTGGTGAAC CTGGCGAAAT 1140
GACAAAAATT CTCCAAAAGG AGTTAGCCAT CCAGAGTGCC AGAGGAGGGT GGCTGTACAA 1200
GCACATTTTA ATTGGCAAAG CAGAGTCGCT GCCCAGCAAG GAAGAGTATG CAGGGGTTTA 1260
TTCTGCTGCT CTTCTATTTC CCCTTTAAGG CATATATCTC TTACCCCTGC ACCCACCAAC 1320
TTTAGTCACT CCTAGCACAC AGCTGGCGGC CGCCCACCCG CACCCGCACC TGCACCCGCA 1380
CCTCAGAGAG CTTGCTGATC CCTGAGCCGT GCACTGAAGC TTCCAAGCAG CTCTACCTAA 1440
AGGCAAGCAC TGCCTGCTTT TTACAACATA TACAATGGGC TAACCTGATG CACAGAAAAA 1500
CCCTGGGTCA CATGACAACC AACAAACTCA TTGCTCAGGA TGGCTCTCCG CCACGTTTCT 1560
CAGGCACTGT GCTTGGCTCT GCTGGCCAAC TGAGTGAGCT GGAGCATTTT CTCTTGGGTG 1620
TGCATACCCC TCCACCTGTC CAACTTTAAA ACACAGAATC AACAGGGATG TTACACTAAA 1680
GGGGACCCTA GAAACCATAT AAACGGTGGA AAATTGAGGC CTGGACTGAC CCATAACAAA 1740
TGAGACATCA CATAATGGCA AATGAACCAT GACCAGAAAA CAAATCTCTT TAGTACACAG 1800
TTTAGCGCTT CTGCTTATAC AGGTTGAACA GCCCTAACCC AAAAATCCAA ATCCCAAACT 1860
TTTTGAGCGA AGACATGAGG 1880
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