| Tag | Content |
|---|
EnhancerAtlas ID | HS053-19377 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr19:19096660-19098100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GCM1 | MA0646.1 | chr19:19097402-19097413 | CATGCGGGTGC | + | 6.02 | | Nr5a2 | MA0505.1 | chr19:19096775-19096790 | GCTGGCCTTGAATTC | - | 7.03 | | Sox3 | MA0514.1 | chr19:19097301-19097311 | CCTTTGTTTT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I018984 | chr19 | 19095611 | 19097008 | | GH19I018986 | chr19 | 19097211 | 19098008 |
|
Enhancer Sequence | AAGTGATCCT TCCTCCTCAG CCTCCCAAGT AGGTGGGACT ACAGGCATGT GCCACCATGC 60
CCGGCTAGGG TTTCTTTTTT TTTTAATAGA GATGGGGTCT TGTTACGTTG CCCAGGCTGG 120
CCTTGAATTC CTGGCCTCAA GCAGTGCTCT TTCCTCTCCC TCCTAAAGTG CTGGGATTGC 180
AGGTGTGAGC CACCACGCCC AGCTTGGAAC ATCTTTATTT TAAGATGAGC ATGCTGGGGC 240
CTCAGGGAGT GAAGTGAATT TTCCAAAGTC ACTCGTTGTG ACCAGGACAC TGGAGTCAAG 300
GCCCTTTCAT CATGTCATGG GGTCTAGGTA AGGACTCAGG AAACTTCATT TATTTATTTA 360
TAGATAGAGT TTTGCTTTTG TAGCCCAGGC TGGAGTACAG TGGTGCGATC TCGGCTCACT 420
GCAACCCCCG CCTCCTGGAT TCACGCGATT CTCCTGCTTC GGCCTCCGGA ATAGCTGGGA 480
TTACAGGCAT GCACCACCAC ACCCAGCTAA TTTTTGCATT TTTAGTAGAG ACGAGGTTTC 540
ACCATGTTGG CCAGGCTGGT CTCGAACTCC TGACCTCAGG TGATCTGCCT GCCTCGGCCT 600
CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCACGCCTG GCCTTTGTTT TAAGGAGGAG 660
GAGTCAGCCA ATGGGATGCC TCAAGGACTG GGTCCACTGA CACAGAACAA TGGAAACAGA 720
TCAGCGATGT CTGAGTTCAC AGCATGCGGG TGCTGCTCCT AAGAACCCTT CTGTAGATGC 780
TACTGTTCTC CCCATTTGCA AATGAGGAAG CTGACACTCA GAGATGTGGA TCACCCGCCC 840
CAGGTTACAC AGCACAGAGA GGACATGTTA GGACTGAGGA TTCAAATTCT TAAGGTTTGC 900
TTTCCTCCTG GCAAAAGCAA GTCATGAAGG CGTGGAAGCT GAAATCTCGA GGCTAACGCT 960
CCCCTTTTCA CACCTGGCCA CAAGCTGCAA GAACTGGGAG TTGGTGCTCC CATGAGTCCA 1020
ACCTGAGGAT TCGCTGGAGA AAAATTCAGC CAAGAAAAGC TCAGCTCGTG AGGTCCCCCT 1080
CCTGGGCTGT GAAGGAAGCG GATAGTGCCA GTCATTACAG AGCCGCAATT CCTGAGTGTT 1140
AAAGTTCTCA GGGCCATGAG TATGGACTTC GTGGGAAATA GAAGCACCGT GTAGACCTAT 1200
GCATGTGTGT ATGTCTGTGT GCATACGTGT GCATGTCTCT GTGTATGTAT GTGCATGTGT 1260
GCACGCATTC GCACATGGCG TTGCACAGGG TGTGTCCATG TGTACGCAAG TGTGTGTATA 1320
TAGGGAGCTT CTAAATCAGA TGAAACCAAC TGGAAATCCG GATACTGATG TTTAGAATTC 1380
AAGCTCTGGA GTCAGACTGC CCCAGGCCTC AGTTTTTCCA TTGGGAAATG GGCTGATCCT 1440
|
