| Tag | Content |
|---|
EnhancerAtlas ID | HS130-00677 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr1:44046950-44049140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr1:44048046-44048064 | AGCAGGCCCAGGCATGCT | - | 6.03 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_05962 | chr1:44045982-44048063 | Brain_Hippocampus_Middle | | SE_23829 | chr1:44046994-44048030 | Colon_Crypt_2 | | SE_23829 | chr1:44048164-44048638 | Colon_Crypt_2 | | SE_26649 | chr1:44045820-44048922 | Esophagus | | SE_27645 | chr1:44047195-44049958 | Fetal_Intestine | | SE_28595 | chr1:44047280-44048969 | Fetal_Intestine_Large | | SE_33537 | chr1:44045757-44056755 | H2171 | | SE_52524 | chr1:44047044-44048792 | Small_Intestine | | SE_65452 | chr1:44047303-44047936 | Pancreatic_islets | | SE_65452 | chr1:44048025-44048999 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 44047816 | 44048271 | | chr1 | 44047550 | 44048400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043581 | chr1 | 44046992 | 44049104 |
|
Enhancer Sequence | TACGGGGGTT CCTTTAGTTC CAGCCCCACT TGCCAGGGAC TCCAAAACAG CCAAACCTGA 60
CTTCTGTTGT CTCTCTCACA CACACATACG ACGTTCCTCT AGGCCCTGAT GTCTCAGGAC 120
CGTTTCTAAG CTCTGTCCCC AGGACCTGCC TCATGTAGAC CCTAATTGAA TCTACACCAC 180
CCTGCTTTGC CAAGAGCAAC CTGCCCCATA GGCCCTACTG TCCTACTGAC AGGACTTAGG 240
CACACCTGAA AGGCCCTGCT CCCTGGGTGC CTTGCCTCTG GTGCCCCCAC TGCTCGTCAT 300
CTCATGGTTG GCAAAACCCC TGCCTTCTGC CCTCAGCAGT ACTAGGGGCC CTTCAGCCCC 360
AGCGCCTGGG GACAGCCTGT ACTGGGCTGA CCACCAGCTC TGCATCCTGA GCCCTGCTTG 420
TGGGTGGATG GCCGTGGAGG AGTCCCCAGT GCCAGCCTGC TTTCTGGCCT GCACCCCGTC 480
CCATCTCCCA GCAGAGAGGC TTCGAGGTTT CCTCCCACAG CAGGCTCCTG AGCCTCAGAC 540
GGCTTGATGT GGGCTCTAGC CCTGAACTTC TCAGCCGCAG CACTGTTGAC ATTTTGGGCT 600
GGACGATTCT TAGTTGTGAG GGGCCATCCT GTGCATTGGA GGGTGTTTAG CAGCATCTCT 660
AGCTCACTAG ATGCCAGTGG CACCCCTCAG TCAAAACAAA CGTTGCAACG TGTCACCTGG 720
GGGAAATTAC TGATGGCTTC CCACTGCCAT TGTCTCCACC CATCTGACTC TCTTCACCTG 780
TGTCCACTGG CCGCAAGGCT TCGTCTCCTC ATCAGACTTG GCTTCGGTGT CTACCTCACA 840
TCTCCCTTCT GTCCCCCAAA TTCTCAGGGC TCCCAGTGTC GCTCTCTGAG GCCACGCGAC 900
TGCTACATTT AATGGGACAG TACACGTGAA GCACCAGGCA CATTGCCAGG CACACAGGAA 960
GCACTTGCTA GTCAGTAGCC TCTGCAGCTA GCACTCGGCT ACTAGTCAGT AGCCTCTCGG 1020
ATAGCACTGT GGGGGGATGT GTCATCCAGT TACATCTGAC TTTGTTCACA GTTGCCTGCA 1080
GCTCCACCCA CAGTCTAGCA GGCCCAGGCA TGCTGGGTGG GCCAGAGCCT TTCTCCTTCA 1140
CCACCTGACT CTCCCTGAGT GACTCATTCT CTCCTTCCAT CTACAGCTCT CTGGGTGTAC 1200
AGCTGCTGGG GCCAGGGTGG AGCCCTGCCC TCCTCAGAGC CTGGCCTACC TGTGCCAGGA 1260
CTACCAGCCT TCCCCCTTTC TCTAGGGACC TGGCTGCGGG CCACAGCTGT CTAAAACAGG 1320
GACAGTGCCT TTTTCCCCAC AGGTGCCCAG ACATGCTCCT TACACCGGTG GTGTGTGTGG 1380
GGGTGGCTTC TAGTGGCTCC TGTACCTTGG CAGGTTTGTG GGCTGGGTGG GCCTTGACCC 1440
CAGAGCCCGG TCCACAGGGT CTGTCTGAGC TGTGGGGTGC GTGTGAGGCA TGGGGGCCTG 1500
CCTGTGCCCC ATTTTCACCT GCCCCGGCCC CACCCTCGGC CTCCCTGGCG CCTGCTGGCG 1560
GGCCTCAGCC CTGTCCACCA TGTCCTCCAT GAGTCCTGAG TCTTTTGTGA GTGATGTGGT 1620
TCGTGTGCAC CTGTGTGCAT GTGTGTGTGC GAGGGGGCAC AGGAGTCTCG TCTCGTCTCC 1680
GTGCTGTGTG GGCAGATGAA GGTTGGCCTG TTTTTACTCT CTCTGTGTTT CTCCTTGTCT 1740
TTTTTTTATT CCCTCCTCAT CTTCATCGCA CTCTGCCATC AACCCAAACT CTCATCTCTC 1800
AGATCAGCGA GAAGGTTGGT CCTTTTCACT TCTTATCCAT CTACAGTTCG CCCATCGATG 1860
GGACACGCCT GTCAGTAGGG CCCAGCGGGC TCGGTCAGCT CCCTCAGGCT CACTGCGCCG 1920
TGCCTGCCTG CCAGTCTCTG TTGTTTGGGC CGGCGGGCAG GCAGGACCAG GGATGGGTGG 1980
GCAGACCCCT GACCTGCATG TTCCTGCTGC TTGGGTCCCT GGTGCACCAC GTGTCTGCAT 2040
GTCCCCTTAG CCTGGTTCCC CTGCAAGGGT GGTGGGGTGG GCATGCTGCA TGGCATGAAA 2100
CTGTACCCCA CCTTTGCACC CAGGCCGGGC CAGCTGTCTG ATCCAGGCGG TGCTCAGGAA 2160
TGGTTGTGGG GGGCTGTGGT CAGAGAGAGG 2190
|
