| Tag | Content |
|---|
EnhancerAtlas ID | HS034-20793 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr3:46204410-46205560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr3:46204896-46204907 | CTGAGTCATCC | - | 6.32 | | FOSL2 | MA0478.1 | chr3:46205159-46205170 | CTGAGTCATCC | - | 6.32 | | JUNB | MA0490.1 | chr3:46204896-46204907 | CTGAGTCATCC | - | 6.14 | | JUNB | MA0490.1 | chr3:46205159-46205170 | CTGAGTCATCC | - | 6.14 | | NFE2L1 | MA0089.2 | chr3:46205155-46205170 | ACGGCTGAGTCATCC | - | 6.09 | | NFE2L1 | MA0089.2 | chr3:46204892-46204907 | ATGGCTGAGTCATCC | - | 6.36 |
|
| | 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 |
| GH03I046161 | chr3 | 46203463 | 46206226 |
|
Enhancer Sequence | CTGTCCCAGG AAGACAACAG AAAATTGTCA GCCATAGAAC ACTGGTAGGG GTGACCAGAG 60
ACCCTGGCTG GGAGGTCCTG CCCAGCAAGG AGGAATGGGT CAGGGTTCCA TTTAAAGAAG 120
CAGTCTGGTC ATGCCTTGGC AAAGCAGCCA TACTGTGCTG GGGTGTTGCC TCCTCCCCAG 180
TCTGTTTGGA CTCTCCAAAG CTCACAGGCT GGAATACCCG AGTGACCCAA ACAGCAAAGG 240
TGGCAGCCTG CCCCTCCTAG TGGTCACTCT GTCCTAGGGA GAAATTTGAA CTCTGTCAGC 300
CATAGGATAT GAGTTGGGGT GGCTGAAGGT CCTGGATGGG AGGTCCTGCC CAGTGAGGAG 360
GAATGGATCA GGGTCCCGCT TAAAGAAGCA GTCTGGCCAC AATTTGGTAA ACCAGCTGTG 420
GTATGCTGGG AGATCCCTTT CTTGTCTGGT CAGTTTGTAC TCTCCAAAGC CCACAGGTTG 480
GAATGGCTGA GTCATCCAAA CAACACAGGT GGTGGCCTGC CCCTCCCCGC AGGCACTCTG 540
TCCCAGGGAG AAATCAGAAC TCTTTAGAAT ATGGGTGAGG GTGGCTGGAG GCCCCGGATG 600
GGAAGTCCAG CCCAGTGAGC AGGAGTGGAT CAGGGTCCCA CTTAAAGAAG GAGTCTGCCC 660
ACATTTTGGT AAAGCAGCTG TGTTGTGCTG GGCGAATCCC TTTCTTGTCT GGTTCATTTG 720
GACCCTCCAA AGCCCACAGG CTGGAACGGC TGAGTCATCC AAACAAAAAA GGTGGCAGCC 780
CATCCCTCCC CCAGGAGCTC TACCCTGTCT CAAGTAGGTG CTACCCTGTT GCTGGTGGCT 840
GGCTGGAATT CCAAGCCAGT TGATCTTATC CTGTGAGGTC CCTTGGAAGT GGGGCCCACA 900
GACTGACGCT GCTCTGCTTC CTGGATTCAG CCCTCTTCCT AAGGGTATGT ATGGACCTCT 960
TGTCTTGCTT AAGTTGTAGT CATGTTTGCC AAAGATCCCA GAGTAGATTA TGTAAAGCTC 1020
CTGGGCCTCT GTGCATGCCT AAGCAGCTGC TCTGCTGTGA CTCCACACAG CTCTGTGTGT 1080
CAGACCCAAG GCCCTGGTGG AGTGGGTTCA TGAGGGGGAT CTCCTGATCT GAGGGTTGCA 1140
AAAATCTGTG 1150
|
