| Tag | Content |
|---|
EnhancerAtlas ID | HS042-03941 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:225864680-225865890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr1:225865588-225865602 | TTTGCGGGGGCGTG | - | 6.46 | | EGR3 | MA0732.1 | chr1:225865588-225865603 | TTTGCGGGGGCGTGG | - | 6.51 | | EGR4 | MA0733.1 | chr1:225865587-225865603 | ATTTGCGGGGGCGTGG | - | 6.57 | | RREB1 | MA0073.1 | chr1:225864769-225864789 | GGGAGGGGGGTGGTGGGGAG | - | 6.25 |
|
| | 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 |
| GH01I225677 | chr1 | 225864946 | 225865926 |
|
Enhancer Sequence | GGCCCTATAC AAATTAAAGA CAGCAAAATA GGCCTCAAGA GGTAGCGATG GGTGCGATAG 60
CAGAGCGAGC CGGCGCCTAC AAACAGGTGG GGAGGGGGGT GGTGGGGAGA GTGGGGGGTG 120
CAGATGGTGG TAGCAGAGGA GCCCCGCACA CCTTAGACGT TCTGAGCTGG AACAGTGAAA 180
GAGCCTCAGC AACGAGGACC AAGAGCCTGC CACATCAGGG TAAATGAAAG GAATACATGT 240
TTCAAAAACA AAAATGTTTT AAAAATTTGC AGCTTGGGTT CTTAAAGAAA GAAGTTGCAG 300
TTACCTGGAA GATTCATCAA AATTCACCAA TACCGAGAAG TTTTTTCTCC ACCCCCAGTG 360
CTAGACAAAG GAGGTGTGAT TTGTCCAACG CTCGCAGCCA TTTGAGCCAC CCCACACGGA 420
GGCGAGCCTC GCTAGCGCCT CGGTTACAGC CTTTCCCGCA AGGCTTCATT CAGTCGCGCC 480
GGCTCCGGGG ATGCTGCCTT CTCTCGGGCC GGTGCTTCGG CCCTCCAGAC TGGGCCCGGA 540
CTGACCCCCG CAGCAGCCCA GCCTCTCCGG AGGGCTGGAG GGGGCAGGCG CAGCCACAGC 600
CGCGCTCCGA GGGTTGGGGC CCTGGGGCCT TCCCGGGAGC CGCCACCGGC CCTTAGGGAG 660
AGAATTGATG GACTCGTTGA AATCACAAGT TGCACACGTT ACTTTTCACT CCACCTGCTC 720
ATCGAAAGGG AATCCCTTGT TTCTCCTTTC TTTCCCTCTG GGTGACAAAC CATTTAATAT 780
GCGTAGCGCT TAGTATTTTA AGTGCTCGAC GACCACTTAA GGCTGGTCCC AGGGCGATCA 840
TCAGAAACAG AGAGATACAA CCCCATTTGG AGTTGGGTGA CTTTCTTAGA GCAAGCAGTT 900
TTGAAGGATT TGCGGGGGCG TGGAGCGGGG AGGTGGGAAA TAACCAGCTT TGCCGCACAA 960
AAGGTAAATG CCAGCCTGAT GGCTTGAGGG GAGAGAGGGC GCCAAAGTGA GCTTCCGTAA 1020
GGCTTATAAA GGCTTGGGAA GTTCTGGTCA AACTAACGAG CAGTTGATTC CACCTAGGAT 1080
CCCTTAGGTC AACCTGTGGA CAGCACCCCC TTAGGGGAAG TTTCTGGAGT CCTTAGCCCC 1140
TTGGATCAGA GCAGTTTTGC CTTTGTTAGT TTTAAATTCT GAATACACTT GTCTTTGAAA 1200
AACCATAAGC 1210
|
