| Tag | Content |
|---|
EnhancerAtlas ID | HS146-00174 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr1:19756150-19757590 |
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 | TTATCTGCCA GGACTTTTAC ATAACATTTT TTAGGTGCTA GAGGGTCCTT TCTGCCTGGA 60
TTTTTCCCTC ACTTGACACA GGTTTTCCAT TCAGGCTGCC AGGAGTCTCT AGAAAGGTAG 120
GCGGAGTGTT ATGTCAGTTT CCAAGTCATT AAGCACCCAC AAAGGAGGGC AGGCTTGCAC 180
AGCACTCACT CCACACAACC GCCCCTGCCC TGAGTACGAC GGAGCACATG GCTTCCCTAA 240
AGCCACAAGG AGAAGAGAGG CAGGGACAGT GAGAGCTGAA GGAATTCCAC ATGTGTCCAT 300
GGAAGATCAC CTTCCCTTTG TTTTCCTGCA CTCTAGTAAC TCCCTCATGC AGCTTGCTTT 360
CTGAAGCCCT CTGCTCCATT TCCCCAGCCC AGGACAGCAT CAAGAAATAT TTCCACCATC 420
TCATCTATTT GAACCTTCTC CCTATTTACT GGTGCTCCCA ACCCCATCTG AGGCCATCGA 480
AACCAGACAA CTGTGGCAGC ACTAGCAGAG TCCCCAAACT ACCCTGACAC CCTCCCTGGC 540
AAGGAAAATT TCCACGCGCC TCTCCCTGGC ATATTTATTC CAGAGGAAAA CTTAGCAACC 600
TACACACTAC ACACAGGCTC TGTGTCAAAC TCTACAACAG CCATCAGTTG ATCTTTCCCT 660
TACACATCCC TCCAGGAAGT GAAATATCCG AAATGAGTCA TACTCAGGAG TCGGAGCTAT 720
ACTTCCACTG TAGTTTTTTT GGATAACCAA TTCACTGTTT ACACTCCAAA ACCTCTAATT 780
GCTGAACACA GAACAGTTCC TTTGCAGAGA TCAAAGCTTA CCTGGTGAAC CTGGCGAAAT 840
GACAAAAATT CTCCAAAAGG AGTTAGCCAT CCAGAGTGCC AGAGGAGGGT GGCTGTACAA 900
GCACATTTTA ATTGGCAAAG CAGAGTCGCT GCCCAGCAAG GAAGAGTATG CAGGGGTTTA 960
TTCTGCTGCT CTTCTATTTC CCCTTTAAGG CATATATCTC TTACCCCTGC ACCCACCAAC 1020
TTTAGTCACT CCTAGCACAC AGCTGGCGGC CGCCCACCCG CACCCGCACC TGCACCCGCA 1080
CCTCAGAGAG CTTGCTGATC CCTGAGCCGT GCACTGAAGC TTCCAAGCAG CTCTACCTAA 1140
AGGCAAGCAC TGCCTGCTTT TTACAACATA TACAATGGGC TAACCTGATG CACAGAAAAA 1200
CCCTGGGTCA CATGACAACC AACAAACTCA TTGCTCAGGA TGGCTCTCCG CCACGTTTCT 1260
CAGGCACTGT GCTTGGCTCT GCTGGCCAAC TGAGTGAGCT GGAGCATTTT CTCTTGGGTG 1320
TGCATACCCC TCCACCTGTC CAACTTTAAA ACACAGAATC AACAGGGATG TTACACTAAA 1380
GGGGACCCTA GAAACCATAT AAACGGTGGA AAATTGAGGC CTGGACTGAC CCATAACAAA 1440
|
