| Tag | Content |
|---|
EnhancerAtlas ID | HS184-21225 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:149986320-149987150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr3:149987060-149987075 | AGAGGTCAGAGTTCA | + | 6.08 | | Hnf4a | MA0114.3 | chr3:149987061-149987077 | GAGGTCAGAGTTCACT | + | 6 | | JUN | MA0488.1 | chr3:149986715-149986728 | ATGACATCATTCA | - | 6.41 | | JUND(var.2) | MA0492.1 | chr3:149986714-149986729 | GATGACATCATTCAC | - | 6.49 | | NR2C2 | MA0504.1 | chr3:149987060-149987075 | AGAGGTCAGAGTTCA | + | 7.03 | | Rxra | MA0512.2 | chr3:149987061-149987075 | GAGGTCAGAGTTCA | + | 6.1 |
|
| | 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 |
| GH03I150268 | chr3 | 149985816 | 149990342 |
|
Enhancer Sequence | CAGAGAGGAA TCCAATCTTC TGTAAGCTCT AGAAACGCGT TAATATTTTT CTTATACCAC 60
CTAGTCAAAT ATCTTTTTTC CCAGACAGGT TCTGCTTTGT GGAAATGAGC TGCAAAGACC 120
TGCCAATTCA ACTCTCAATG ATAAACAAAG CCTACTTGTC TTAAAATTTT GTCAAGGCAG 180
AATTTTACCT GTCAATTTCA TTTCAAATTG TACAGACTGC CCTATGTTTG CAGGAAAAAA 240
CCCAGCTTGT TAACAGTAGG ACCCAAATAC TAAACTTACA AAGGTAGTCC AAGAGGAAGC 300
ACCCACGACA AACAGAAACT TCCAAAACCT AACACAATGT GGACATGCAC ATCACACTCA 360
GATCTTTGCC TTCACTAAAA AAAGTAAACA GTGTGATGAC ATCATTCACA GCCAATTAAA 420
GCACAGCCCC ATGGCAAAGG AAGTGCTGGG AGATCCTTCT GCAAGTAAGC ATAAGAGTGA 480
ACATGCAATA TGTTTGATAA GCTGTCCTAG TACATGTCCA GGGGCTCTAA GCTGTATTTA 540
CAAAATAGCA TTTGTTGCTG CTTCAAAAAC AGCTGAGGGT GGCCAGCAAT ATATCACATT 600
CCACAAGAGG AGCAATTGCG GTGATGGACA CAGGATGACC AGGAACAACC TTTGTTCGTC 660
GTTCCATCAC ATGGTTCAAT AATAAATATT ACTACTCATC CAGTGTACAC ATAGGATGTG 720
GTGAGGCAAA ACCCTCTCCC AGAGGTCAGA GTTCACTCCC TTTTCCAGGC AGATCCCTTA 780
ATCAAATTTA TTGTCTTTAC TTTGGGGAAA CACAATTTTC CCATCAAGTA 830
|
