| Tag | Content |
|---|
EnhancerAtlas ID | HS183-10455 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr7:100876190-100877550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr7:100877123-100877138 | TGAACTCCTGACCTC | - | 6.22 | | SP2 | MA0516.2 | chr7:100876540-100876557 | CCAAATCCCGCCCACCC | + | 6.29 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28156 | chr7:100874742-100876791 | Fetal_Intestine | | SE_28156 | chr7:100876976-100884675 | Fetal_Intestine | | SE_52423 | chr7:100874627-100885461 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GATACCTGGG GACCGGAGGA CGACCCCAGT CCAGTCCAGG GGGAGGGATA GTGGGGGAGG 60
GGGCTTAGGG GAGAGGCAGG CAGGGGCTGC CCAGAGTAGG ACGGGGGCAC CAAGTCCCAG 120
AGCAGCAATT TCACTCAATT CCTTTCTCCC CACCCCAGTT TATAAGCCTT CCTCCTTCCT 180
GGGGTCAACT TCTCAGGGTA GCCCTTAGGC CCCAAGTCCA GCCCACCCAG CTCATCTCAC 240
ACTACCTCAA CCTCCTCCTG CCTCTTCTCT CTTTGGTCCC AGATCTACCT AGTTCATGCC 300
CACCTCTAGG GCCTTCATCC CATCATCTCC TCACCCAGAT GGAGCCCCAT CCAAATCCCG 360
CCCACCCTTG AAACCTTGAA AACCCAGCTG GGCCATGGGA GTCCAGGGTC GTCCTTTCCT 420
GAAGCCAGGC AGACCCCCGG GCTAGCACCA CCCTACTCAC TGGGGGCTTG TCCTCTTGCA 480
AGCCACCTGA CCTTTCTGGG CCTGTTTTAC CTCTGGAAAA CAAGCAATAC CCACCCTACC 540
TCAAAGGCTT ATTGTGAGGC AATGGGTACA GAAATGTTCT GCAAATTGAA AAGCAATGGC 600
CAGATGGCAT TGTTTTTGTT TTTTGCTGAG ACGGGTTCTC ACTATGCTGC CCAGGCTAGT 660
CTGGAACTCC TGGGCTCAAG GCAGTTCTCC TGCCTTGGCC ATTTTTTTTT TGACAGTCTC 720
ACTCTTTCAC CCAGGCTGGA ATGCAGTGGC ACAATCTTGG CTTACTACAA CTTCTGCCTC 780
CCAGGTTCAG GTGATTCTCC TGCCTCAGCC TCCAAGTCAG TGGGACTACA GGTGCCTGCC 840
ACCACGCCTG GCTAATTTTT TTTTTTTTTT TTTTTTTTTT TTTTTGGTAT TTTTAGTAGA 900
GACAGGGTTT CACCATGTTG GCCAGGCTGG TTTTGAACTC CTGACCTCAA GTAATCCACC 960
CACCTCAGCC TACCAAAGTG CTGGGATTAC AGGCATGAGC CACCATGCCC CGTGGTATGG 1020
CACTGTGGAC GTGCACTGTG TGTGTGCGCC ATAGCGTGCA CCCTAACTCT GCTCCCCAGC 1080
TAGGATGTAA GCTCCCGGAG GCAGCCGCTC ACTCTTATCT TCGAAGTCCC TCCCACACCT 1140
GGCCGTGGCC AGCCCCTACT GGGAGCTCAA GAAACACTGC CGATGGGCTG ATTTGCAGCC 1200
AGGAGATCTG GGGAGTACAG ATGAGGCAGG GGTGAGCAGG TGTCCATGCA GCAGGGTAGG 1260
GGAGGTGAGC ATGAGGAGTG GGAATTGGAG AGGAGATTAG ATGAGGACAA AGCAGCCTGA 1320
AGTCTGCGGT TGAGGGGGAC CCCCGCCCCA TCACCTTCCC 1360
|
