| Tag | Content |
|---|
EnhancerAtlas ID | HS105-38535 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:4425230-4426740 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr19:4426477-4426489 | GTTTGTTTGTTT | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr19:4426689-4426704 | TGAACTACTGACCTC | - | 6.07 | | Nr2f6(var.2) | MA0728.1 | chr19:4425469-4425484 | TGAACTCCTGACCTC | - | 6.22 | | RARA | MA0729.1 | chr19:4426686-4426704 | TCTTGAACTACTGACCTC | - | 6.1 | | Zfx | MA0146.2 | chr19:4426408-4426422 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH19I004425 | chr19 | 4425407 | 4426227 |
|
Enhancer Sequence | TCTCTCTTTT TTTACAAAAA TTATTTATTT ATTTAGAGAC GGAGTATTGC TCTGTCACCC 60
ATGCTGGAGA GCAGTGGCGC TATCTCTCGG CTCACTCTAA CCTTTGTCTC CCGGGTTCAA 120
GCAATTCTTC TACCTCAGCC TCCCGAGTAG CTGGGATTAC AGGTGCCTGC CACCACTCCC 180
AGCTAATTTT TTGTGTTTTT AGTAGAGACG GGGTTTCACC ATATTGGCCA GGCTGGTCTT 240
GAACTCCTGA CCTCAGATGA TCTGCCCATC TCAGCCTCCC TAATTTTATT TTTAGTAGAG 300
ACTGGGTCTC ACTGTGTTGC CAGGGCTGGT CTCGACCTCC TGGTCTCAAG CATTTCTCTC 360
GCTTTGGCCA CCCACCGTGC TAGGATCACA GGCATGAGCC ACAGAGCCTG CCACTATCTC 420
AACCTCTTTG CCCCTCAGTG GTGTAGGGGG GGTCCCTGCA CATGCTTCTC TGCACACATG 480
CATTCCTCTG GGACAGCCAA GTAAGCATGA GTTCACCTCT AGGACAAAAT AGCATATTGC 540
TGAAGCATCA TGAGCCATGG CCAGAGTGCG TGCCAGATGG GAAACTCAGA TGTACATTCC 600
CGGCGATGTG TGGAAATTTC CTCCCCATTC TCTGCTATCA CTGCAATTTT TATGGGATTA 660
ATTTTCTTTT AACTTTGCCA GTCTGATGGA TTTTTAAAAA TTGACATTGT TTTACTTTCC 720
ATTTTTACTT GACTCTTGGT GCAGTTGAGC ATCTTTTTCT GTTCGTTTGC CATTTTAGTT 780
CTTCTATGAC TTGCCAATTC CTATTTTTTT ACCTATTTTT CTACAGGATT TTCTTTTTTT 840
TTCTTTGCCT GATCTGTAAG TTTTTTTTAA CATAGTCTAG TATTTCATTC TCCGTGATAT 900
TTCGTCTCAG CCTGTTACCT CTTTGTTTAC AGTCTTTTTT TTTTTTTTTT TTGAGACACA 960
GTTTCACTCT GTTGCTGAGG CTGGAGTGCA GTGGTGCCAT CTCGGCTCAC TGCAAGCTCC 1020
ACCTCCTGGG TTCACACCAT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG ACTACAAGCG 1080
CCCGCCACCA TGCCCCGCTA ATTTTTTGTA TTTTTAGTAG AGACGGGGTT TGCACCGTGT 1140
TGGCCAGGAT GGTCTCGATC TCCTGACCTT GTGATCCGCC CGCCTCGGCC TCCCAAAGGG 1200
CTGGGATTAC AGGTGTGAGC CACCGTGCCC GGCCTTTGTT GTTTTTTGTT TGTTTGTTTT 1260
GAGACAAAGT TTCGCTCATT GCCCAGGCTG GAGTGCAGTG GCATGATCTC AGCTCACCAC 1320
AACCTCTGCC TCCTGCGTTC AAATGATTCT CTTGCCTCAG CCTCCCGAGT AGCTGAGATT 1380
ACAGGCATGT GCTGCCACGC CCAGCTAATT TTGTATTTTT AGTAGAGACG GGGTTTTTCC 1440
ATGTTGGTCA GGCTTGTCTT GAACTACTGA CCTCAGGTGA TCCGCCTACC TCGGCCTCCC 1500
AAAGTGCTGG 1510
|
