| Tag | Content |
|---|
EnhancerAtlas ID | HS095-00415 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:19756140-19757590 |
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 | AGCACATGGC TTATCTGCCA GGACTTTTAC ATAACATTTT TTAGGTGCTA GAGGGTCCTT 60
TCTGCCTGGA TTTTTCCCTC ACTTGACACA GGTTTTCCAT TCAGGCTGCC AGGAGTCTCT 120
AGAAAGGTAG GCGGAGTGTT ATGTCAGTTT CCAAGTCATT AAGCACCCAC AAAGGAGGGC 180
AGGCTTGCAC AGCACTCACT CCACACAACC GCCCCTGCCC TGAGTACGAC GGAGCACATG 240
GCTTCCCTAA AGCCACAAGG AGAAGAGAGG CAGGGACAGT GAGAGCTGAA GGAATTCCAC 300
ATGTGTCCAT GGAAGATCAC CTTCCCTTTG TTTTCCTGCA CTCTAGTAAC TCCCTCATGC 360
AGCTTGCTTT CTGAAGCCCT CTGCTCCATT TCCCCAGCCC AGGACAGCAT CAAGAAATAT 420
TTCCACCATC TCATCTATTT GAACCTTCTC CCTATTTACT GGTGCTCCCA ACCCCATCTG 480
AGGCCATCGA AACCAGACAA CTGTGGCAGC ACTAGCAGAG TCCCCAAACT ACCCTGACAC 540
CCTCCCTGGC AAGGAAAATT TCCACGCGCC TCTCCCTGGC ATATTTATTC CAGAGGAAAA 600
CTTAGCAACC TACACACTAC ACACAGGCTC TGTGTCAAAC TCTACAACAG CCATCAGTTG 660
ATCTTTCCCT TACACATCCC TCCAGGAAGT GAAATATCCG AAATGAGTCA TACTCAGGAG 720
TCGGAGCTAT ACTTCCACTG TAGTTTTTTT GGATAACCAA TTCACTGTTT ACACTCCAAA 780
ACCTCTAATT GCTGAACACA GAACAGTTCC TTTGCAGAGA TCAAAGCTTA CCTGGTGAAC 840
CTGGCGAAAT GACAAAAATT CTCCAAAAGG AGTTAGCCAT CCAGAGTGCC AGAGGAGGGT 900
GGCTGTACAA GCACATTTTA ATTGGCAAAG CAGAGTCGCT GCCCAGCAAG GAAGAGTATG 960
CAGGGGTTTA TTCTGCTGCT CTTCTATTTC CCCTTTAAGG CATATATCTC TTACCCCTGC 1020
ACCCACCAAC TTTAGTCACT CCTAGCACAC AGCTGGCGGC CGCCCACCCG CACCCGCACC 1080
TGCACCCGCA CCTCAGAGAG CTTGCTGATC CCTGAGCCGT GCACTGAAGC TTCCAAGCAG 1140
CTCTACCTAA AGGCAAGCAC TGCCTGCTTT TTACAACATA TACAATGGGC TAACCTGATG 1200
CACAGAAAAA CCCTGGGTCA CATGACAACC AACAAACTCA TTGCTCAGGA TGGCTCTCCG 1260
CCACGTTTCT CAGGCACTGT GCTTGGCTCT GCTGGCCAAC TGAGTGAGCT GGAGCATTTT 1320
CTCTTGGGTG TGCATACCCC TCCACCTGTC CAACTTTAAA ACACAGAATC AACAGGGATG 1380
TTACACTAAA GGGGACCCTA GAAACCATAT AAACGGTGGA AAATTGAGGC CTGGACTGAC 1440
CCATAACAAA 1450
|
