| Tag | Content |
|---|
EnhancerAtlas ID | HS042-30262 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr22:35919100-35920200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr22:35919911-35919924 | TGCATTTGCATAA | + | 6.29 | | Pou2f3 | MA0627.1 | chr22:35919910-35919926 | TTGCATTTGCATAACA | - | 6.44 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 35919585 | 35919671 | | chr22 | 35919689 | 35919852 | | chr22 | 35919751 | 35919972 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I035523 | chr22 | 35919751 | 35919972 |
|
Enhancer Sequence | GGGTCTGAGG GAGGACACAG GCAGGTAAGC AGGCAGCGAG GATGGTGGGT GCAGAGTGCC 60
GTGCTGGGAA CAGTTTGCCG GGGGTTCGCG TGGATCCCTG AAAAGGCTCG TTCCAGCTTA 120
GGAAATGTTA GCCTGACCAG GTGGAAAGCT CACCCCTGCT CGCCATCTGC TGAAGAAGGG 180
TCACGTACAT GCCACCTGGC TTTCTGCGGG GAGATAGCAT CTGGAAGGCA GAGAAAGCTC 240
CTCTGGGTGG GGAGAAGTTT CACTGGGCAC CATCATGATT TATTCAGCAG CGTCAGACAC 300
CTGCACCCTG GGGCCAGCGC CGGCCTTGGT GGTTCTCCAG GATTCGTTCT GGGTGCACAC 360
ACCTGTCTCT TCCTACACCC GGGGAATGGG GGGTGGGGGA CAGAGGCCAG TCCAGAGGCA 420
GCAGCCTCTC CCACCCTTAG CCTGGGTAGG GGGAGGAAGC AGTCCTGGCC AGAGCCCCAG 480
ACTCACAGCG GATGTGGCCA GCTCACCTGG TGGCAAGAGG GAGCCAGAAA CGTCCTTGGG 540
GCCCTGAGTC CCAGTGCCAG GACTGTTCCC TGCAAGATTT CTCCTCCTAG GCTCACCACG 600
AGATTCAGTA TCCTGTGAAG CCTTCTCCTA ATAACCCCAG GCAGAACTCA CTGCTACCAG 660
CACCTGGCAG GCTCCCTTTG TGTGGATTGT GTGTGCACAC ACGTGCACGT GATGTGTTTA 720
CAAACTAGAT GTGGGCCGTT TTGATACCTC CAAGCTAGGA TTATGTTAAC ACTGTCTGAG 780
TAATATAAAT CATCACGGAT TAAAAACAGC TTGCATTTGC ATAACATGTC GTACTTCTCC 840
AGATGCTGCT CACATCTTCA TTTTCTGCAT CGGTCTCACC AGGATCCTGA GAGGAGGAGA 900
GGGCGGGTAT TAGATGTCCC CAAGAAGTGA AAAAAGAAGT GTCACCGGCA TTAAAGACTG 960
AGCAAGGAGG CGTCAAATCT CCTTGACCCC ATGCTCACAG CACAGCTGGA GGAGACAGAG 1020
GTCTCGCCTT CACCGAGCTT AGCGGTATGA CATGTTTCTC CAGGCCAGCC TTGCAGTTTT 1080
TAACACCACT GTTTAAATGA 1100
|
