| Tag | Content |
|---|
EnhancerAtlas ID | HS054-01181 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr10:104614830-104617010 |
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 | chr10:104615508-104615520 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr10:104615512-104615524 | GTTTGTTTGTTT | + | 6.32 | | NFE2L1 | MA0089.2 | chr10:104616707-104616722 | ACTGCTGTGTCATCC | - | 6.21 | | Nfe2l2 | MA0150.2 | chr10:104616709-104616724 | TGCTGTGTCATCCTA | - | 6.17 | | Nr2f6(var.2) | MA0728.1 | chr10:104615133-104615148 | CGAACTCTTGACCTC | - | 6.24 |
|
| | 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 |
| GH10I102855 | chr10 | 104615042 | 104616510 |
|
Enhancer Sequence | ATTTTATATA TGCTAGACAC TGTTGTCTTT TATGGAGTTT AATTCATGAA GTCTTTAGAA 60
TGACTAATTG AAGGAAGTAC TTTTCCTTTT TTTTTTTTTT TTTTGAGACG GAGTCTAGCT 120
CTGTCGCCAG GCTGGAGTGT AGTGGTGTGA TCTTGGCTCA CTGCAACTTC CGCCTCCTGG 180
GTTCAAGTGA TTCTCCCGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGC ACGCACCACC 240
ACACCTGGCT ATTTTTGTAT TCTTAGTAGA GATGAGGTTT CACCATGTTG GCCAGGCTGG 300
TCTCGAACTC TTGACCTCAT GATCTGCCTG CATCAGCCTT CCAAAGTGCT GGGATTACAG 360
GCGTGAGCCA CCGCTCCTGG CAGCATTGCT TCTTGAGCAG TCTCCACATA GCTATTTTGT 420
TTGATTAGCT GAGAATTTCA TGTGTAAAAA ACTCATTCCA CAGTATTCAT TTAACAAATA 480
CTTATTGGGT GTCTGCTATG TGCCAGGAAC TGCTCTAGGT ACACGGAATA AACAAAACTA 540
AATCCCTCTA CTTGGGAAGT TTACATTTTA GTGAAGAGAC AGACGATAAA CAAGTGAAAC 600
AGAAAAAAAT CAGGTGGTGG TAAATCCTGT GAAGCAAAAT TAATCTGGGA ATAGAGAGTG 660
ATGAAAGGGT TAATCTTTGT TTGTTTGTTT GTTTTGAGAC AGAGGAGGAG TCCCACTAGC 720
TCTGTCACCC AGGCTAAAGT GCAGTGGCCC GATCTCGGGC TCACTGCAAC CTCTGCCTCC 780
TGGGTTCAAG CGATTCTCCT GCCTCAGCCT CCTGAGTAGC TGGGATTATA GGCGCCTGCC 840
ACCACACCCA GCTAATTTTT GTGTTTTTAG TAGAGATGGG GTTTCACCAT GTTGGCCAGG 900
CTGGTCTCAA ACTCCTGACC TCAAGTGATC CTTCCCGCTT TGGCCCCCTA AAGTGCTGGG 960
ATTACAGGCA TGAGCCACCA CACCCGGTCG AAAGGGTTAA TCTTAAACAG ATGATCAGGG 1020
AAGGGGTCTC TGGGGAGAGA GCCTGTGAGG AGAAACACAC TGACATTTGC CCACAGCATA 1080
ATGAGTGGTT ATGACTCATA GGCTTGTCTC TTGCATGCCT GCGCTTCTCC TCCTCCATTT 1140
GAGTTGTGTG CTTAGTGAGG GTCCATTGTG TTTTTTTCTA AACATCATGT GTCTGTGGGC 1200
TGGGCGCAGT GGCTCATGCC TGTAATCCTA ACACTTTGGG AGGCCGAGGC AGGATTGCTT 1260
AAGCCCAGGG GTTCGAGACC AGCCTGGGCC ACATAGTGAT ATCTTGTCTC TGTAAAAAAA 1320
GGAAAAAAAA AAAGAATGAA AACAATTTTT TAAATGTGTG TATGGCACTT ATGCTTACAG 1380
TTGCAACTAC GTAATTTAAT GAAATAATAC GAAAAATGAA ATATGAGTAC CAAAAAAGAG 1440
GGTTGCTATT GCTATGAAAA CTAAGTTGAA AATCAGAAAC ACTTGTTGAA GATGAGTAGC 1500
TAAGACAAAT TGTTATTGAG TTAATTATGA ACAAGTTAAT GGTAAAAGCC TAGGAGAAAA 1560
ATTTATAGAA ATCTAAAAAG ATTCTGTAGT GAAGATTGTT TTACAGGTGT ATTCAAGATG 1620
TTCTTCCATT TTAAAGAAAG CAAAACTAGA AATCTCAGAT GGTATGTTAT GTGTCTGGTC 1680
TGTTTATGTA GGAAAGTGAT GCAGAATGCC AATGAATATA TCAAGGAAAA GCCTTGGCTT 1740
TACATTACAA CAGCCCCTGC CTTCAAGGCA ACCACAACTC CCATTGAGTC TGTTTTCTAA 1800
ATGTCTCACA AATCCTTTGT TTCTTTTTTT CTTGGCTACT TCTGTGTTTC AGGCCATCCT 1860
CATTCCTTGC TTAGAGTACT GCTGTGTCAT CCTAACCAAT CTCTCTGCCT CATTCCCCAC 1920
TCTAGTCCAC CTGCTTACCA CATTTCTAAA ACAGAAAAAT GGATCATGCC ATTTTTCTCT 1980
AGAATTACAC ACAAAGATGA ATTCTAAACC CTAACTTTTA AGTCTCAGAT TAGAAGTCAC 2040
TTCTTTTAGG GACCTTTCCT GAACACCTAC CCCTGTAATC AGTTAGACAC TCCTGCCCCA 2100
CTACATGCTC CCGGAGCAGC CAATGCTTCC CCATCAGCAC TTACCATAAG GTGATGTAAG 2160
TGCCTATGTT CCCTTTGTAA 2180
|
