| Tag | Content |
|---|
EnhancerAtlas ID | HS102-22607 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr9:34157800-34159590 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr9:34158550-34158561 | TTTGTTTACTT | - | 6.62 | | KLF5 | MA0599.1 | chr9:34158632-34158642 | GCCCCGCCCC | + | 6.02 | | Nfe2l2 | MA0150.2 | chr9:34158539-34158554 | AGCTGAGTCATTTTG | - | 6.13 | | Nr5a2 | MA0505.1 | chr9:34158892-34158907 | CTTGACCTTGGACTT | - | 6.29 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 34158190 | 34158272 | | chr9 | 34158294 | 34159108 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I034157 | chr9 | 34157931 | 34159519 |
|
Enhancer Sequence | TTTTTAAATA CATTTAACAG AAGGATAATG TATGGAATAT GCCAGCTCCT TCAAATATAT 60
AAGAAAAAAG GAAACAACCC AGTGGTAAAA TGGGCAGAGG ATAATAACAA GCAATTCACA 120
AATGGTCAAT AAACACAAGA AATATACAGC ATAAGGAAAT ACAAATTAAA ATCCAATGAA 180
AAACCATTCA TTGGCTTGGT AGGATGGCTC ACGCTTGTAA CCCTGTGCTT TGGGAGGTCA 240
AGGTGGGAGG ATCACTTGAA TTCAGGAGTT TGAGGCCAGC CTGGGCAACA TAGCAAGATC 300
CCTGTCTCTA CAAAAAACTA AAAAATTAGC TGGGCATGGT GGTGCATGCC TGTAGTCACA 360
GCTACTCTGG AGGCTGAGGC AGAAGGATCA CTTAAGTCCC AGAATTTGAG GCTGCAGAAA 420
GTTATGATTG GGCCAGTACA CACCAGCCTC AGCGACAGAG CAAGACTCTG TCTCTCTCTC 480
TCTTTTTTTT TTTTTAGCAA AATCAAAAAA ATTTTAAATG TCGGCAAGAA TACAGCAAAA 540
CAGCTACCTT CATACACTTT GGTTCCAGTG TAAAGAAATC TGTTTGACAC GCAATTTGGA 600
GAAATGGGGA AGCTGTGGTG AATGGGAATT CATGGCCCTG GACCTACAAA AAGCCTGCAT 660
TCCTGCCAGT ATGGCTACTT TGTTCATGTG CGCACTGTGC CTGCTCTGGG GGGGTTAATG 720
ACACAGGCTA TCATCAACTA GCTGAGTCAT TTTGTTTACT TGGCTGTTCA GTGCCTCTTA 780
TGTGGTGCAT TCTCTCTGGT ATGCCTTAAC ATGTTGTTAC GAACTGAATT GTGCCCCGCC 840
CCTCCAAGTT CTTATGTTGA AGTCCTAACC ACCCCACTTA CCTCAGAATG TGACTGTATT 900
TGGAGAAAGG GCCTTTAAGT AGGTGATTAA AGATCCTAAT GCAATCTGAC TGGAGGCCTT 960
ATAAGGAAGA AATCTGGACA CACAGAGATA CCAGAGACGT GAGTGCACAG AGAAAAGGCA 1020
TAGAGTTGAG GATACAGTGA GAAGGCGAAA GCTAAGGAGA GAGGCCTGAG AAGAAACCAA 1080
ACCTCCTGAC ACCTTGACCT TGGACTTCTG GCCTCCAGAA CTGTGAGAAA ATAGATTTAC 1140
ATTGTTTAAT CCATCCAGTC TATAGTATTT TGTTATGGCA ACCCTAGCAA ACAAATACAC 1200
ATGTGATACA AAGATCTTCA TACTCATGCC CCTTCCTATA TGTTCACTTG GAATTCTTTG 1260
TCCTTAGATC TCCTTATTCC CAATGTTTCC AGTCTTTCTC ATTCAAGGCC TCTAACCAAC 1320
CAACCAGTCA CTCACCACTA TCCATGATTC TGAATATATC CTAACCTCAG GCTACTTTTA 1380
TTCACCAAAA TTAGATGGTG CATTTGCCAA AGCTTCCCAG TTAGGAGGAT TGCTTCTTAA 1440
CACCTTGTCT TTCAGGGTCC TCACTATGTC CTATTTTCTG CTTGCGTTTT CTCACCCACC 1500
GAGCCAACCT CCTCTGTTAG CTGGCCACAA GAGCATATAT GGCAATAGAT ATAAGCTAAG 1560
AGGTGCTAAG GTAAGAGCAG TAGATGACTG GGGGCTCGTG CCACCTGCAG CTTATACACT 1620
TTAGCTGTAT TTGTGTCTGC TCCTGAATGT ACCACTTCTG CATTGCGACA GATTGCTGCT 1680
GGCCCATCCA CCTTATGATG TGGTGAGTCT GAGAAACAAA ACTTTTTTTT TTTTTTGAGA 1740
CAGAATCTCA CTCTGTTGCC CAGGCTGGAG TGCAATGGTG CAATCTTGGC 1790
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