Tag | Content |
---|
EnhancerAtlas ID | HS184-13801 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:48981070-48983150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr17:48981187-48981201 | AGTCCCTGGGGAAG | - | 6 | FOXH1 | MA0479.1 | chr17:48982978-48982989 | TCCAATCCACA | + | 6.62 | Foxd3 | MA0041.1 | chr17:48981168-48981180 | AAACAAACAAAC | - | 6.32 | SNAI2 | MA0745.2 | chr17:48982947-48982957 | TGCACCTGTT | - | 6.02 |
|
| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_02991 | chr17:48980818-48981364 | Bladder | SE_02991 | chr17:48981621-48983308 | Bladder | SE_04178 | chr17:48981233-48983332 | Brain_Anterior_Caudate | SE_05235 | chr17:48980897-48982005 | Brain_Cingulate_Gyrus | SE_06067 | chr17:48981497-48983596 | Brain_Hippocampus_Middle | SE_07466 | chr17:48981344-48983162 | Brain_Hippocampus_Middle_150 | SE_08899 | chr17:48982381-48982593 | Brain_Mid_Frontal_Lobe | SE_12167 | chr17:48980692-48983336 | CD3 | SE_19619 | chr17:48979853-48984374 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23191 | chr17:48981481-48983372 | Colon_Crypt_1 | SE_23784 | chr17:48981620-48983342 | Colon_Crypt_2 | SE_24830 | chr17:48981426-48983406 | Colon_Crypt_3 | SE_26011 | chr17:48979932-48984292 | Duodenum_Smooth_Muscle | SE_26691 | chr17:48979620-48983743 | Esophagus | SE_27621 | chr17:48979817-48984219 | Fetal_Intestine | SE_28540 | chr17:48979724-48984381 | Fetal_Intestine_Large | SE_29967 | chr17:48979940-48983528 | Fetal_Muscle | SE_31399 | chr17:48980105-48984402 | Gastric | SE_36690 | chr17:48980078-48983446 | HMEC | SE_41117 | chr17:48980937-48983480 | Left_Ventricle | SE_42844 | chr17:48981354-48983454 | Lung | SE_47468 | chr17:48980975-48981325 | Pancreas | SE_47468 | chr17:48981487-48983527 | Pancreas | SE_49193 | chr17:48981509-48983050 | Right_Atrium | SE_49713 | chr17:48981753-48983169 | Right_Ventricle | SE_50311 | chr17:48981438-48983399 | Sigmoid_Colon | SE_52502 | chr17:48981399-48983501 | Small_Intestine | SE_54412 | chr17:48981548-48983164 | Spleen | SE_54634 | chr17:48978631-48984793 | Stomach_Smooth_Muscle | SE_59738 | chr17:48979175-49044314 | Ly4 | SE_65373 | chr17:48981580-48984477 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 48982200 | 48982800 | chr17 | 48982000 | 48982200 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I050902 | chr17 | 48979760 | 48984332 |
|
Enhancer Sequence | GGCAGGAGAA TGTTTTCTGG TGAAGCAAAG AACCGCCCCC ACAACCAAAG CACCACACAA 60 ACTTACGAAA AAAACAAACA ACAACAACAA CACCAAAAAA ACAAACAAAC CCTGCTCAGT 120 CCCTGGGGAA GAGAAAAGGC CAGGATATGG AACAGGGAGG GAAGGGCTGC ATTCAAAATC 180 CCGTCCTACC CATACATTGT AAAATGGTAC AACCACTTTA GGAAACAGTT GGGTGGTTTC 240 TTTAAAAGTG AAACATACAC TTACCATGTG ACCCAGCAAT CCCTCTTCTA GTTACTAATG 300 CGAGAGAAAT GAACACATGC ATCCACATGA TGATTTATAT ACAAATGTTC ATAACTGCTT 360 TACTCATAAT AGCTGCCAAC TGGAAACAAC CCAGATGTCC AAACACAGGT GAATGGCTAC 420 ACAAACTATA ACATATCCAT ATAATGGAAT ATATTACTCT GCAATAACAA GGAAAGAACT 480 ATGATAGACG CAACAATATG AACGAATCTT GAAATCATTA GGCTGAGGGG GAAAAGTCAG 540 AGGTAAGAGT AGAGTAGAAA CTGTATGGTA ACGTATACAA AACATGCAAA TCTGATCTGT 600 CATGACAGAA AGCAGATTGG TGCTTGCCTG GGGCCAGGGA AGGGGCATGA CTGACTCAGA 660 AGGGGCCACA GGGAACCTTT CAGGGTAACG GAAATGTTCT CTACTTTGGT TATTGTGGTA 720 GGTATGCAAA CATACAACAG TGCACCTAAA ATGGGCACAT TTTGTTGTGC GTAAGTTAGA 780 CCTCAACAAA GTTGACTTAA GAAATAATTC CTTCCCGAGA GCCTGGCCTA CGAGGTGCGG 840 GCAAGCAGAG AGGCCTCCCT CAAGGCACTG GCGATACTGC CAAGCTGGAA AAACGGCTCG 900 CTGGCAGCCT GGAAAAGGCC GTTCTCTGGC TCTTGATCCT TAAAAGGCTG GAATTTCTGG 960 CTGAACAAGA AGGCCTGGGC CCAGTCCCCA GGGGGCAGCT TCTCCTCAGC TCTGGGCAGG 1020 GTGCCCGGCC ACCCCTCACA CAGGTGCTGG CTTGCTGCCC AAACACAGGA CCAGGGGGCC 1080 TGGGCAGGCC CCCACAGCCC TGCTGGGGGA AGAGGAGGAG ACCAGCCCGT AGCCAGCCCA 1140 GCCTCAGCCC CAGCAGCCTG TGGCTGGCAG GGCCTCTGCC TACACAGCAA GCTCTCAGAG 1200 TGGGGGGATG GGAGCAGCGC CCAGGCACCC ACCCAGCTCC CCCAACCCAG AGTGTCACCG 1260 GGGACCTTTA CCCTGAATGG GGATGGTTTT AACAGCCCCT AGAGAGGGTC AGGGCATCTG 1320 TGACAGGACA GGGTCTGAGC CCCGGACTTT CACCTCTCAG CCCAGTGCCC TTTTCCCCGC 1380 AGCAGCCTAA GCTCCCAGTG ATTCTCTGGG GGAGGGATTT CTGATGGGGC TGGTTCTAAA 1440 GAAAAGCTCT CCAGGGCAGG GCCTGTGAAA CCCAAGGACT GACTGCTGCG GGGGCTGGAT 1500 AGCCTTTGGG GACAGAGGAG GGGAGAGGGT GGCAGAACCT AAACAGCTGC GGCCGCTGCT 1560 TTGTCCAAGG GCAACCCAGC CTCCCAGGTG TGGCCATCAC CTCTGCCTCT GACCTGAGTC 1620 TCAGACCAGA GCCAGCTGAG GCCTGGGTGC TCCCTTCAGC CCCTTCTGGT TCTGCAATTC 1680 AAGGCCCAGT TAACCCCCTG TGGGGTCATA GAGAAGCTTG CAGAGGGTGA AGCCTGGGAC 1740 CTGATTCTGC TCACCCTGGA CTCTGGCCCA GCCAGTGCCT TCTGGCAACA GGGACCCTCT 1800 GGGGTCCCAG GAGCCCTGGA ACCTCCTCTG CTCCCTCTGG CTCTGTCTCC TGCCCCACCC 1860 CCTTCCCTGT TGCCACCTGC ACCTGTTTTT CCAGCCTTGC TCAATCTCTC CAATCCACAG 1920 GCTGTTTGTT CCCAGGGGTC GCCTCCCCTT ATCTCCCAGG CAGCTGTTGG CCATGGCCTG 1980 AAGGTACAGA ATTCATTGTT AACTCTTCAG CTTCCCTCAC ACACTCCACC CCCAAAAACC 2040 ATAGCAGCAA AGAGCACCAG GGAGGGCCCA GGTTTGGGGT 2080
|