| Tag | Content |
|---|
EnhancerAtlas ID | HS106-01296 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chr2:162094840-162096210 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr2:162096076-162096091 | TGACCTCCTGACCCC | - | 6.57 | | Sox6 | MA0515.1 | chr2:162095267-162095277 | AAAACAATGG | - | 6.02 | | ZNF263 | MA0528.1 | chr2:162095359-162095380 | CTCCTCCGCGCTCCCTCCTCC | - | 6 | | ZNF263 | MA0528.1 | chr2:162095345-162095366 | TCCTCCCGGCCTCCCTCCTCC | - | 7.26 |
|
| | 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 |
| GH02I161237 | chr2 | 162093712 | 162096390 |
|
Enhancer Sequence | TCTCTCGGCG TGGAAGCAGT GTTTCCCGCA AAACTGCCAG CCCGCCCCCC GCTCACGCAC 60
AGACACCCAA TTTCCCATAT ACAGATAAAT GCACACATGT ATACGCGAAA GGTTAACTCG 120
GCGGAGGACT CGCCCAAATA AGCACCGGGA TTGCATTTAA AATAATAATA ATAAATAAAT 180
AAATAAACTA GGAAGGAAAG CGGGGGGAGG GAAGCAGAAG TCGGGAAGAA AAGAGAAAAG 240
CAGCAGGCTG ATTACGAGGT GTCAAAACTG CCAGGAGCAA GAAGGTGATA GCAATCAGGG 300
GTGAGAAGAG TGCGGCATTC GTGCGGGGCA ACTAATTATC CGTCTCATTT GAGAAGAGCA 360
GCATTTGAGG CAGCAGCGTT CGCCTGCTGA ACGGTGACAG ATTGGCGCGG AGGAGAGGGG 420
AGGTGTTAAA ACAATGGAGC CGGGCGCGCG AGCGCTGCTG CATGCTAATC AGCCCTCCCT 480
CCGCCTGCCT GCCGCGCTCC CTCCTTCCTC CCGGCCTCCC TCCTCCGCGC TCCCTCCTCC 540
CGCCTGCGGC GCTCCCTCCT TTCCAGCGGG CCCCGCGCCG CCGCCGCCAC CCGCTTCCTG 600
CTCCCTCGCT TTCCCGCGCG TCCTTCCCGC CGCTGGCGAG TGGAACCCAG CCACCGCCAC 660
CGAGTCCCTA GCGGGCCAGG AGCCCCCGCG CGGCCCCCAG CGCCGGCCCG GTGGAGTGCA 720
GCCCCGCGCG GGCTCGCCCG AGGGCTCGGC CTGCGCCGCG CGCCCACTCC CCGGGGCGGT 780
GGGGCGAGGA CCCGCGCTCC GGGATCCACG TACTGGGGAA GCGGCCGAAG AGCCTGCGTT 840
CTCACGCCCA CTCGCTGTCT GGTGAATCGA CCGCGTCGGC CAGCGAGCGC GACTGGGAGT 900
CCAGGCGAAT TCAGAAAGGG CTAGGGCCAG CCAGGGGTGA AAAGAGTGAC AGGGCCACAA 960
AGGCCAAGAA GGGCTCCAGG ACTGAGCGCA GATCTCCTGC CCTGCCCGAG CGTGGCCGCC 1020
ACCCCGAGGC CTCCAGCCGC CCCCAACCCG CCCTGCAGTG GCCGCGCCCC GCTGGCCTGC 1080
GGCGAGTCGG CGAGGTCAGC GCCCCCCGCC ACGCCTCGCG CGCTGCGGCT CTTAGACCCC 1140
TGGAGCCCCT TTTTTGCCAG AGCTACCGGT CCACGGTTTA AATGATCGCA GCGAAGATAC 1200
ATAAAGGGCC TTAGCATTAG CTGTGCTTCC AAGGCCTGAC CTCCTGACCC CAAGACTAGA 1260
TTAAGGGGCC GTCTGGGCCT CGAGAGTTCC CTCGAAAGAC CGTCGCGGGG AGAGAAGGGC 1320
CTGGAAAGAA GCGGGCCGCG CTCCCCCCTG CCGCGAAGAC TGTGGGGCAG 1370
|
