| Tag | Content |
|---|
EnhancerAtlas ID | HS187-01873 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:172814220-172815700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr1:172814444-172814455 | CCTTCCCGCCC | - | 6.62 | | NR2C2 | MA0504.1 | chr1:172815179-172815194 | TGACCTCTGACCCTA | - | 7.05 | | Nr2f6 | MA0677.1 | chr1:172815179-172815193 | TGACCTCTGACCCT | - | 6.93 | | Rxra | MA0512.2 | chr1:172815179-172815193 | TGACCTCTGACCCT | - | 6.73 |
|
| | 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 |
| GH01I172845 | chr1 | 172814541 | 172814940 |
|
Enhancer Sequence | TCAGTCCAAA TTAGGCTAGA GATTTTTTTA AAGTATATAT TTAGTCCTGT TTCCTTTCAT 60
TTCCCAAAAC AAATGTATTA TAGGTGTCCC TGTCAATTTT CCTCACCCCT TGCACAGATG 120
CGTGCATGCT CACACACCCT AAGCAATAAT TCCCACTCTA GAGCCTTTGC TCCTGGTGTT 180
TTTCCACCTA AAAGACCCTC TTCTCCCTCT GCACTCATCT ACATCCTTCC CGCCCTTCAA 240
ATCTTAAGTC GTATTTGAAG CCCTAGAATC ATAAAGCTGT TGCCTGTACT ATTATCTTTG 300
CTTTATATTT TTCCTCATTC CAGGGAACTC CTCCAGTCCC CTGAAATGAA GACAGTGTGC 360
TCCAGCTGAC TGTGCCCTGG GGACTGTGTC CCTGCTAGCT TCTGATCAAA TACTCACACC 420
CTGCATAGGT CCCTGGCTGT CCTCACCCAG GGCAATCCCC CTGGCCTGGA GCTGACGTGG 480
CTTTGAACTC CCACGCAGAG CTGCTCTTCT GCCCTACTTC TGGATTTTAC TGTAACTTGC 540
TTAGCAGTCA GAGGTGCTGA AGTTGCAGAA AGGCCCTGTG GGTTTGCTTT TGATAGTGTT 600
CAAATTGTTT CCAAAACTGT TTAGCATTTC CTGCTCTTAA CAGGCTCCTT GAGCTCAGCT 660
TTTGCCATTG TCTGTCCTCC CTGGGCTCCT TTTCCTTATT TTTTATTCCC CATTTTGACT 720
TTCCCCATTC CATTTCTTTG TTTCTCTTAG GTCATTGATT CATTGCAATC ACCCAAATCT 780
CCCCTGCCTT TCTTCCCTTT TTTTTTTTTT TTTTTTTTGG TCACTATCAC GTTTTTCTCT 840
CTGGCATCGT GACTGGCATT GTCCCTTATT TCTACTATTG AAGTAATAAG TTTTTAGGGA 900
AAACAGTTTC AAGCAATTTA GCAGAATTTT TGATTTCAGA CTGACCCTGA CTTCAAATCT 960
GACCTCTGAC CCTAGTTTAA CCTTTGGTGA ATTACTTCCA CTGTTTTGAG TCTCAGCTTT 1020
ATCCTCTCTT ACAGAGGCAC CATAAATTCT GACTTGCACA AATTGGGAGG ATACATGAGA 1080
TCATTTATAG GCAGTGTTTG ATGTCACAGT AAATAATATT CCTCATCCAA TCTATTTCCT 1140
GCCTTCTCAT GAAGAAGTGA CTCCATTTTG GTGCTGATTG TTAGATTTCC ACTCATTCAT 1200
TTATTCAATC AATATCTGCC CATTTATTGT GTGACAGGCA CTGAGGTAGC ATTGGAAACA 1260
CAGTGATAAA ATGTGCTAGA CCAGGGATCC CCAAGGCCCG GCCATGGCCG GGGCACCAGT 1320
CTGTAGCCTG TTAGGAACTG GGCCACTCAA TAGGAGGTGA GCAGTGGTGA GTATTCCCGC 1380
ATTAGATTCT CATAGGAGCA TGAACCCTAC CATGAACTGT ATGCGAGAGA TCTGGGTTGC 1440
GCTTTCCTTA TGAGAATCTA ACAAAAAGGT TGGGGATCAC 1480
|
