| Tag | Content |
|---|
EnhancerAtlas ID | HS098-39981 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:129248460-129249710 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr3:129249371-129249391 | ACACAACACACACACACACA | + | 6.19 | | ZNF263 | MA0528.1 | chr3:129249548-129249569 | TCTGCCCCTTCCCCCTCCTCC | - | 6.07 | | ZNF263 | MA0528.1 | chr3:129248685-129248706 | GAGGCAGGGAGAGGGGAAGAG | + | 6.12 |
|
| | 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 |
| GH03I129530 | chr3 | 129248844 | 129249644 |
|
Enhancer Sequence | GCAATGGGCT CGGTCCCCTC TGGCATCCTC TGCCTCCCCT CTCAGCCCCT GTCCTCAGGT 60
GCCCCTCCAG CCTCCCTGCC GCGTTCCAAG TCTCCTGGTG TTGAGAACCG CAAGCAGCCG 120
CTCTGAAGCA GTTCCTTTTT GCTTTAGAAT AATGTCTTGC ATTTAACAGG AAAACAGATG 180
GGGTGCTGCA GGGATAACAG ATCCCACTTA ACAGAGAGGA AAACTGAGGC AGGGAGAGGG 240
GAAGAGACTC ATTTAGGGAT GTGGCCAGGC AGCAACAAGA GCCTAGGTCT CCTGGCTGTG 300
ATCCAGGAAT ATCTCTGCTG AGATGCAGGA GGAGACGCTA GAAGCAGCCA TTGCAAAGCT 360
GGGTGACGGG GAGAGCTTAC CGCCAGCCAC AAGCGTCTCT CTGCCAGCCT TGCCCTGTCT 420
CCCCCATGTC CAGGCTGCTG CCTCGGTCCC ATTCTCAGGG AATCTCTGGC CATTGTTGGG 480
TGTTTGTTGC ATTCAATAAT CACAGATCAC TCAGTTCTGG CCAGAAGGTG GGTGTGCCAC 540
TTACGGGTGG TTGTTCTCTG CAGGGTCAGT CCCAGTTTAC AAATATTGTC CCTTTCACTG 600
TTAGGAATGT CCCAGTTTGG TTGATTAACT ATATGGCCAC TCTCCCTATG GAACTTCATG 660
GGGTGGTGAG CAGGACAGAT GTCTGAATTC CATCATTTCC TTCTTCTTCC TCTGGGCAAA 720
ACATTGCACA TTGCTTCATG GCTCCTAGGA GAGGCCCCCA CATGTCCGGG TTATTTCATT 780
TCCCGAGAAG GGAGAGGGAG GAAGGACTGC CAATTCTGGG TTTCCACCAC CTCTGCATTC 840
CTTCCCAACA AGGAACTCTG CCCCACATTA GGATGCATTC TTCTGCTAAA CACACACACA 900
CACACACACA CACACAACAC ACACACACAC ACACACACAC ACACACACAC AAAACTCCCT 960
ACCGGGTTCC CAGTTCAATC CTGACCCCCT GATCTGATTC GTGTCCCTTA TGGGCCCAGA 1020
GCGCTAAGCA AATAACTTCC CCCATTCCCT GGAATTTCTT TGCCCAGCTC TCCTCAGCGT 1080
GTGGTCCCTC TGCCCCTTCC CCCTCCTCCC AGCACCAAGC TCTCTCCTTC CCCAAGGCCT 1140
CCTCAAATCC CTCTCCCACT CCTGGTTGCC TTCCTAGCTA CCCTCTCCCT GTCTAGGGGG 1200
GAGTGCACCC TCCTTAGGCA GTGGGGTCTG TGCTGACCGC CTGCTGACTG 1250
|
