| Tag | Content |
|---|
EnhancerAtlas ID | HS007-12183 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr4:782320-783720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF3 | MA0522.2 | chr4:783660-783670 | AGCAGGTGTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41845 | chr4:781551-787921 | LNCaP |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 783401 | 783527 | | chr4 | 782851 | 783048 |
|
Enhancer Sequence | GGAACGTTCT CCGCACAACA GGGGCGACAC CCAGAGGGCC CTGCAGGCCC AGAACAAAGC 60
CCTGACCCTG TGGGGCAGCA AGAGCAGATT GGTTCTCGTC CTAGCCATCC ACAGCGGGAA 120
GGGCAGCAGC TCCAGGCACG GAAGTGGAGG GAGCATGTGC TCTTCGTCCT GTGGGGCCAG 180
GGGTGTGCTG GGGAGAGCGA TGCCACTGGA AGCTAGGTCC GGCCAGAGAG CCTCCCTCCA 240
GCCAGGGGTG TGGGGGTCTG TGCATGTGGC GGCAACATGT GTATCCAGCC CAGGAGGCTG 300
TGCTGCCCAC AGCAAAAGCA CTCAGGAACA TGTGTGTGCT CAGAGGAGCA TGCCTGTAAC 360
GGCGGAACAT GAGTTGTGTG AGCAAAGGAA CCTCCCAGGT CAGGGGAGTG ACCCTTGGGG 420
CTTGTGGGAC CCTGTCTGCA AACGGTGTGG GATCCTTCCT TCTGGGCCCA GGAAGGAGAC 480
CCCAGGCCCT GCCACCAGGT TGTGGGACAC TCGGAGCTTG GCCTGAAGTG CCAGTTGCTG 540
CAGTGAGGCT CCAGGTCATT CTGAGGCTGA GGTCACGCCG GACTTGGCCT GAGGGCCAGG 600
GTCACTCTGC CGGGAAAACA GGCTCCGGGG CTGGGCTGCA CACCAGAGCC TGGCTTCCAC 660
GTGGTCTGGC TGAGACCCAG TTCTGAGGCG TCTGCTCCAG AGACAAACGC CCAGGCACAC 720
CCAGCCCCAG GCCCACCGTG ATGCTGGGCA GCAGCTCTCC AGGAAGTAAC ACCTGAGGAT 780
GGGAGTGGCT GCTGGGGGCG CCCAGGAGGC CCTGACACGT CTGAGGTGAG ACCCTGAACC 840
CTGAAAACAC GGTATTCGTG AGAAAAAAGG GCAGTGGGTG CTAATCAATG CTGAGAACCA 900
ACAATAGGAA TGATAGGACC AAACAGCCAG CATTCAGCAA CCAGGTGGAC ACCTCCTAGC 960
CGCTGTGGGA GCTGCGGGGG GTAGGGGGAT GCAATGTATT GAGGGAGCCT AGTGGGCCCT 1020
CAGAAGGCCC GTGCAGGAAG GCCCAGGTGT GGGCTGCCCA ACATGGGTGG CTGGAAGCTT 1080
ATGCAGGACA AGGGCGGGTC AGTGCGCGGA GCACAGCGGG GCAGTCTCCC TCCTGCTCCC 1140
TGGGCCCGGG CCTGTCCAGA TGGCTGCCTG ACAGGAGGTG CAGGCGCGCT GCTCCTCTGG 1200
GAACTGCCTA GGGGGCTGGA CACTCCAAAA GGACCCAGTC CCCATCTGCA CAGAGGCCTT 1260
GGACAGGGCA GCTCAGCGTC TCTTCTCTAA CCAACCCCCA AGATGCCGGG GGGTGCCACG 1320
GCCCAGAGGA GGCTGGAGGC AGCAGGTGTT CTGATCAGGT GGCCACGCCT GAGGGCAGGG 1380
TTCCCCCACC CCAACAGGTG 1400
|
