| Tag | Content |
|---|
EnhancerAtlas ID | HS184-27378 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr7:12130350-12131270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr7:12130862-12130878 | ACTGGACTCTGAACCC | - | 6.16 | | IRF2 | MA0051.1 | chr7:12130931-12130949 | TGAAAGCGAAACCTGTAT | + | 6.11 |
|
| | 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 |
| GH07I012090 | chr7 | 12130451 | 12131231 |
|
Enhancer Sequence | TGTGAGTATG AAGAGGGCAC TGAAGTACCT GGAAGTGCAC AGCACCAATG AGGAACATGC 60
CTTTGCCAGC AGAGTCAGAC GGGCATTTGT AACTGTGCTG CGGGAGGTGC ATGCCCAGTT 120
CCTGCAGGAT GCCAGGCAGG GAGGAGGCTC CTCTGCTGCG GGCTCACCCT GTGATCCATC 180
AGAAGGCAGA ACATGAGCAG CCAATGGGAC CCCAGGGGAG AGCCCAGGGC CCCCCCACAG 240
TGGTGGAACA CAGCTCTTAT AGTGCTTATA CCCCCACTGA GTTGCAGGAG TTAAGCAAGT 300
AATCTCGGCA GTCATGTGCA GACTTAGTGT AAGTCACATG GGAGAAGGAC ATTGCTGCGC 360
AACCCAGTCC TGCCCAAGCA TTCCAGTTCA CAGACTGCCT GCTGCAGTTA GGTGGAAGTG 420
TAAAGCCTTT TCTGTTTGAT AAGAGACTGA CCAAGATGCC TGGCTTAGGG GGGCACTGGA 480
TGACCAAAGA CCATATGTGG ACTTGGCAAT CTACTGGACT CTGAACCCGG ATAAGTTTCT 540
GGGCAGAGCT GCAGTTATTG ATGGTTATGA AGACTGGTCA GTGAAAGCGA AACCTGTATC 600
TTTGCATCTT GGTATCTGCT GCTTGGTTTT CCGCTCATGA ACTGTGTATG TCTCTCCCAT 660
GCCTGAGGAC ATTCTGGCTG GGGATGTTTT ACACGGCTTG GCAGCTGTAC CATCTGTCAC 720
AGACTTGCTG GACTGCTTAA CAATGGAACT GGGATTCTTG TCCAGAGAAC CAGGAATAGT 780
TTGCCTTCAT TGGAGGGTGA CAATGGACTT TCACAGTGTT GCTACAGGGC AATATGCATA 840
GCCCCACTCT ATGTCATAGT CTTGTTGATG ATGTTATGTT AACTTCTGAT TCTCTTGCAG 900
ATTTAAAAGT GGCAACGCCC 920
|
