| Tag | Content |
|---|
EnhancerAtlas ID | HS050-06062 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:225864790-225865830 |
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 |
|
| | 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 | GTGGGGGGTG CAGATGGTGG TAGCAGAGGA GCCCCGCACA CCTTAGACGT TCTGAGCTGG 60
AACAGTGAAA GAGCCTCAGC AACGAGGACC AAGAGCCTGC CACATCAGGG TAAATGAAAG 120
GAATACATGT TTCAAAAACA AAAATGTTTT AAAAATTTGC AGCTTGGGTT CTTAAAGAAA 180
GAAGTTGCAG TTACCTGGAA GATTCATCAA AATTCACCAA TACCGAGAAG TTTTTTCTCC 240
ACCCCCAGTG CTAGACAAAG GAGGTGTGAT TTGTCCAACG CTCGCAGCCA TTTGAGCCAC 300
CCCACACGGA GGCGAGCCTC GCTAGCGCCT CGGTTACAGC CTTTCCCGCA AGGCTTCATT 360
CAGTCGCGCC GGCTCCGGGG ATGCTGCCTT CTCTCGGGCC GGTGCTTCGG CCCTCCAGAC 420
TGGGCCCGGA CTGACCCCCG CAGCAGCCCA GCCTCTCCGG AGGGCTGGAG GGGGCAGGCG 480
CAGCCACAGC CGCGCTCCGA GGGTTGGGGC CCTGGGGCCT TCCCGGGAGC CGCCACCGGC 540
CCTTAGGGAG AGAATTGATG GACTCGTTGA AATCACAAGT TGCACACGTT ACTTTTCACT 600
CCACCTGCTC ATCGAAAGGG AATCCCTTGT TTCTCCTTTC TTTCCCTCTG GGTGACAAAC 660
CATTTAATAT GCGTAGCGCT TAGTATTTTA AGTGCTCGAC GACCACTTAA GGCTGGTCCC 720
AGGGCGATCA TCAGAAACAG AGAGATACAA CCCCATTTGG AGTTGGGTGA CTTTCTTAGA 780
GCAAGCAGTT TTGAAGGATT TGCGGGGGCG TGGAGCGGGG AGGTGGGAAA TAACCAGCTT 840
TGCCGCACAA AAGGTAAATG CCAGCCTGAT GGCTTGAGGG GAGAGAGGGC GCCAAAGTGA 900
GCTTCCGTAA GGCTTATAAA GGCTTGGGAA GTTCTGGTCA AACTAACGAG CAGTTGATTC 960
CACCTAGGAT CCCTTAGGTC AACCTGTGGA CAGCACCCCC TTAGGGGAAG TTTCTGGAGT 1020
CCTTAGCCCC TTGGATCAGA 1040
|
