| Tag | Content |
|---|
EnhancerAtlas ID | HS156-11697 |
Organism | Homo sapiens |
Tissue/cell | P493-6 |
Coordinate | chr9:6067920-6070250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr9:6069037-6069058 | ATTCACTTTCTCTTTCCTATA | + | 6.42 | | IRF1 | MA0050.2 | chr9:6069031-6069052 | TCTTACATTCACTTTCTCTTT | + | 7.07 |
|
| | 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 |
| GH09I006068 | chr9 | 6068472 | 6070025 |
|
Enhancer Sequence | AATGCTTTCA GTTGCAAGTA ACAGAACATC CAACTTAAAG GAAAGGGGCA AGCTTGCAGG 60
AAAGGATCTT TAAGTCATCT ACATTTGGGT ATAAATGACA GCCACAGAGT ATTTACCCTT 120
TTTGGGACGT AATTTTATCA GGAGACCAAA GCTTTTAGCT AAAAACATAA ATTTCAAACA 180
TTAGGACAGT CATTTTACAG AAACAAAATA AATAATTTCA AAGAAACTAT TACCTTCTTA 240
AAGACTAGAC TGCGATTGTG AACCCCTGAA GTATCCACAG ATCCTGAAGA GTGCCCAGCT 300
GTCTTGACAA GGAAACGGAG AGTCAAGAAG TTTAGTGAGG TCAACAAGAA TCCTGCAGCA 360
TCTCATCTTC CAGATCTGCA GCAGCCTGTG TTGCAGTCCT ACTAAGCTGA AGGCTTAACC 420
ATGTCTGCCA GTTCAGGGTA CGGAACCCTG GTTACTATTT ACTTTCCTTC TTTCTTCCTA 480
TAGTGGATAT TCTCCTTCAG TGGCCACACA ACATCAAAGA TTCGCCTTCA TTTTTGTATT 540
TTCTACATTG TGTGTACTAC CTTCTCAATG TAGAAGCCAG AAAACTTACA CATGCTCAGA 600
TTCCTGTGTA GTTATAGTGC AATCATGTGA CCTATTTTCT ATGAATCATA TGTATCCACA 660
TGAGACCAGG ATTTCTTCAA GGGCAGTGTG ACGAGATAGT CACAGACAGC GGGAGTGATC 720
TTCTGGTACT TTATCCTGAG CATTATAGAT GTTTAATGAC AATGACAGTG ACATTCCCCC 780
AAAAGCACCC GCACCCCCGC CTTACCCAAA GTGTGGTCTG GGCACTGGGT TTGGCTATGT 840
GGCCTCAGAG TCTGGCCTCT GATCCTCCCA GAGAATCTGT GAGCTATCAG TTATTGTTTA 900
ATGAATCTCT CCACCTTATT TTTTTCTTAG ACTAGCTAGA AAGGATTCTG TTGTTTGCAG 960
GCTAACAATA TACTCCTGAA AGGCAAATAC AGTCAGTAAA GGCCCATATC AGCCAAATCC 1020
CACCTTACAT GTATTAGTAT ATTCTGAATT TTTCACTCAT TAATATCCTG ACTTCTGCTT 1080
TAAATCTATA GCCTTAACCT TGCACCACAT GTCTTACATT CACTTTCTCT TTCCTATAAG 1140
GAAGTGGTGC TAACTGAATG ACATGGGTGT CAGCAGAACA TGCTGTGGCT TCACAACAAT 1200
GGTTTGTAAT ATTATGAGAT AGCTTTGTTC CTTTTCCTTT TTGTTTCTGA TCTGTTTTTG 1260
TTTTTCAGGG AGATGAAATT GCTAAGGTAA TCTTCAAAGG CAAGGCATCA AAATGGTCCT 1320
TTTTTTTTTT TTTTTTTTTT TTTTGAGACA AGTTCTTGCT CTGTTACCCA GGTTGGAGTG 1380
CAGTGATGTG ATCATAGCAT AATAATGCAG CCTCAGCCTG CTGGGCTCAA GTGATCCTCC 1440
CACCTCAGCC TCCCAAGAGC TAGGACTACA TGTGTGCGCT AATTTTTTAA TTTTTATTTT 1500
TGTAGAGTTG GGGGGGTCTT GTTATGTTGT CCAGGCTCAT ATAAAATCTT AGCCACTAGA 1560
AATACCATTT ATGGCCAAAA CCACATATCA AGGACTTGAC CGCCCTTTCC CTACATGGGT 1620
GTTTCCCTGA ACTGTTTTTT TTTGCTGTTG TTGTTTTGGA GACAGAGTCT CTGTTGCCCA 1680
GGCTGGAGTG CAGTGGCACA ATCACGGCTC ACTGCAACTT CCACCTCCTG GGCTGAAGCC 1740
GTTCTCCTGC CTCAGCCTCC CGAGTAACTG GGATTACAGG CCCGTGCCAC CACACCCAGC 1800
TAAATTTTGT GTTTTTTTTG TAGGGATGGG GTTTCACCAT GCTGCCCAGG CTGCTCTCGA 1860
ACTCCTGAGC TCAAGTGATC CACCTGCCTC AGCCTCCCAA AGTGCTAGGA TCATAGGTAT 1920
GAGCAACCAT GCCCGGCCCT GAACTGTTCT TAACCTTCAA AATAGCGAAC AACGACCACT 1980
TCTAGCCTGA CACCCAGTCC ACAGGGAGAC TCATGACTGT CTGCTCTCTT ATTACTTAAC 2040
AGCGATTGAT TTTGAGATTG GGCAATGTTA TGGGGATTGA CTTATTGAGA ATATTTTCTG 2100
ACGTTTTCTT TTTTTGGAAC TGCTTTAGAA GTGATAATGT GAACATTCTC CAATGACACA 2160
TGCTTTTGCT GCTGCAATTA TACAAGCGCA AACAACTGTT GCACTTGGAT GTGCCCAGGA 2220
CCTACAGTCT TCCTCTTTGT GCATGATATG TGGGAGCTCA GGCATGGAGA AAAATATCAG 2280
AAAATCAAAG TTCTGATGGG CTTTGAGAGG GCCAGGTTAA TATACTTTTA 2330
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