| Tag | Content |
|---|
EnhancerAtlas ID | HS129-19022 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr2:11837020-11838720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr2:11837834-11837845 | CTGAGTCATCC | - | 6.32 | | JUNB | MA0490.1 | chr2:11837834-11837845 | CTGAGTCATCC | - | 6.14 | | MSC | MA0665.1 | chr2:11838600-11838610 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr2:11838600-11838610 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr2:11838600-11838610 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr2:11838600-11838610 | AACAGCTGTT | - | 6.02 | | PLAG1 | MA0163.1 | chr2:11837532-11837546 | CCCCCGTGGGCCAC | - | 6.55 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_46853 | chr2:11836621-11839146 | Ovary | | SE_48242 | chr2:11834961-11841451 | Psoas_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I011696 | chr2 | 11836394 | 11839998 |
|
Enhancer Sequence | CCAGGTGTGC CTCCCCTGGC CGCACCTCCT CTGTGCTCCT GCGTCTCTCT GTTCTTCTTT 60
AGAGTGGTTC TGCACGTCAG CAGCATCTGT GGTGTGGGCC TGGGACCCTT CAGAACAGGG 120
GCTCCTGCCC AGCCTCTGGG TCCCCCACCT GTGGCCCAGG GAAGGCTCTT TGTTCCTCAG 180
CCCCAAGCTG TATCTGGTGA GAACAGATGC GTAGTCCCGG AGCTCAAGTT CTGGGAAGGG 240
CAGTGCCCTT TTCTGTGGGG CCCTGGGCTT GTTCTGCATT GTTTCTAAGA GGAGCTGCCA 300
CTCAAATAGG CAGCCCTGCA ATCGGAGGGC TGCGTGCTCC CCCTGATCAG CCCCCAGCTG 360
CTTCTGGATA CAACCGCACT ACCCAGATGC TTCCTGGCCT CGCCCAGCTC TTGTGCTCCT 420
GGCAGCCCTG AGCTCTGTCT TTGCTCCAGG CTGGAACAGC AAGCAAGCAG CTCCTGGTGG 480
CCTGTGGCCA GTGCAGGAGG AACAGGAAGC AGCCCCCGTG GGCCACTGTG GGGCTGCACC 540
AGGAGCTGTG CTCGGCTCCT GCTTCTCCCT GGTTTGGCCT AGAAGCTGGA AGTCTGCCCG 600
AATCTGTGCG TCGTGTCTTG GGAATTCATC CCTTCCTCCC TAGCACTTGG GTGCCCAGTG 660
CTTGCTGAAC CGTGGTGACC TGCTGACTCC TTCCCTTGCC TGCCACTGGT AGTGACCTGG 720
CCTGGGGACA GGGAAAGGAC GCCCATTCAT TGGCAGGGTG AGTGGAGAAG TGCTTGGTGG 780
GCTGGTTTTG CAGCCACTGA AAACCTGAAT CACACTGAGT CATCCTGTTG GCCTTGCTGG 840
TGTGTGAGTG CTGGCAGAGT CTGGGTACCA AATGCCCCGG GCCTTGTGTC CTTCCCCATT 900
TACAACCCCC TCCTCCCCAT CTCACCAGGC CAGGGAACAA GCCCTACCGC ACATTACATG 960
GAAGCGAGTG TGCTCAGAAA TGCAGGTTCT CCCGAGGGGC AGCCCTCAGT CACAAGCCAG 1020
ACTAGTCACG CACCCCCGGC TGTGGGTGGC TTCCTGACCC AGAAGTGCCC AGTTTTGCCT 1080
ACAGTCCTGG TGGAGCCGGT GGTGGTCAGA GAGTTTCACT GTCTCCAGCG CTGTGTTGTC 1140
GTTTCTGTCA AGCGATGGGC CCATTTCTGT CTAGAGCCCC TCTCTCAGGT CCTGATCCTG 1200
CTGGGATGTT GGTGTCTGTG ACCCAGAATA GCTCAGTCAG GGGTGTGCGG GGCGGCTCCG 1260
GTGGCCATCC TCACTTGACG TCATGGCAAG CCCTGACTCA GGCTGTCTGT TCTCCCCTGG 1320
CCGGGCCCAG ATGAGCCGCA CGTGGCCCTC ATTCCTGACA GCTTTGCTGC AGGTTGCAGC 1380
TGTCTCAGGA GACCAGATGC TTTGGGAGAA GGCACTGGAT GTACTTGAAG TCAAGGGGCT 1440
GTGTCCGAGT TCTGTATTTA AAAATCCTCT TTAGAGTCAA GGCTTCTGTG ACTGGCTGCC 1500
ACGTCCTACG CCTCTTCCGG GAAACGTAGG AACAGCACAC AGTAGCAGGG ACAACACCAC 1560
GTGGCTCCAA CAGTTTCAGA AACAGCTGTT TCTTCATGTT CCTGGTGCTA TTTCTGCAGA 1620
AGAACCCACT CACGTGTGAG CTGGTGGATC AGGCCCAGGT TGTTAAAAGC TGGTCTTCTA 1680
GATTGCCCGA CACCATGCCT 1700
|
