| Tag | Content |
|---|
EnhancerAtlas ID | HS102-00943 | Organism | Homo sapiens | Tissue/cell | HuCCT1 | Coordinate | chr1:54480840-54483040 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:54481546-54481561 | TGAACTCCTGACCTC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 54481793 | 54482552 | | chr1 | 54480902 | 54481047 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I054015 | chr1 | 54481563 | 54483001 |
| Enhancer Sequence | CAATCTAGTT CACTGCACCC TATAAGTCCT AGGCTCAAGC AGTCCTCCTG CCTCAACCTC 60
CCAAAATGCT GGGACAACAG GCGTGCACCA CTGTGTCTGG CCTGTTATTG CTTATTGAGG 120
ACTTACCATG TGCCGAGCCT TATTCTAAGC ACTATGGAGA TAGCAGTGAT AGGGGACGTC 180
CCTGCTCTTG TAGAACTGTA CTTTAATTCT CCTTTAATTC TCCCCTGCTT ACAAAATAAT 240
AAAAGAAGGC TTTACTGAGG ACCTCCTGGG TGCCCTGCTG TGCAGCTTGC CCTGGTCCTT 300
GCCCTCTGCA GCTTGTTATT GCACTTAGAA GGCAAGGCAT GGACATGCCT GAAGGGGTGT 360
GGGAGCTACT GACGTGCCCA GGCCACAGGT ACCTCAGAGA AAGGGGCAGG AGCAGGTGTG 420
ATTCATCCCT GTGACCCCAG GGCCCAGCCC AGAGCCAGGC ACGTGGTGGG GGCTTTTGTT 480
TTTTTTGTTT TTTTTGTTTT TTTTTTGAGG CGGAGTCTTG CTCTATTGCC CAGGCTGAAG 540
TGCAGTTGCA TGATCTCAAC TCACTGCAAC CTCTGCCTTC TGGGTTCAAG CGATTCTCCT 600
GCCTCAGCCT CCCGAGTAGC TGGGATGACA GGCGCCCGCC ACCATGCCTG GCTAATTTTT 660
GTATTTTTAG TAGAGACGGG TTTCACCATG TTGGCCAGGC TGGTCTTGAA CTCCTGACCT 720
CAGGTGATCC GCCCACCTTG GCCTCCCGAA GTGCTGGGAT TACAGGTGTG AGCCACCACA 780
CCGGCCTGGG GCTTTGTGAA CACTCTGTGA ATATGCCGAC CTGGGGGTCC AGGAGGCAAG 840
AGAAGGCCCC CAGTATGGGT CAGTCCAGGT TATTTCCAAT CCATTCACAT TTCTGATGCA 900
GTGTCCTCAG AAGCAGAATG GGATTTCCAC AGGCAGGTAA GGGGAGGGTG CAAAGAGAGG 960
GCATTCCAGG CAGAGGGCGT GGCAGGAGTA AAGGCCCAGT GGTTGCAGGT GGGGGAGCAC 1020
AAATGGCCTG GGGTGGTGGG ACTCCAAGAT GGATGTGTAT TGGGAGGGGA GACAATAGCA 1080
GGAGAGGCAG CATAAATCTA AAACCTGTCA TCCCTACAGC CCTAGTTGGT GGCTCCTTGG 1140
CCATCAGCAA ACAGGGTAAA CTCAGGTAAC CAGGGAGGCA GCGTGACTCT GGGCAGGGAG 1200
AGGTGTCCTG ATCAGCCAAG CAGCTCCTCA AATATTTGTG CAGCACAGAC CATGCACAAG 1260
GTGGGGCCAT GGGAGAACCC GCAGAACCAA GGCTCCTGCC CAGGTGAAGC TGTTGCACTT 1320
CAAAGCCAGA AAGCCCTTAG GTGCCAGTCC TCTCCCTGTA CCGATGAGGA AAAGGAGGTG 1380
ATTCTTTCCA CAACCCCGCC CATCATGAGT CAGGACTTAG AAATAAACAA ACACCAGCTC 1440
GGAGCAACAA AAGCCCTGGG GCTTTGTAAC CAGAGAGACC TCAGTTCACA TTTGAACCCT 1500
GGCCCTCCAA CCTCCCTGCT GTGTGACCTT GGCCTGGTTA CTCAACCTCT CTTAGTTTCA 1560
GCTGTCTCAT CTGTTATTGC CCCATAACAG GGCCCCTGTC TCAGAGCTGT CCTGAGGATT 1620
AAAGAGATCA TGCAGTGCCA GGCACCTAAC TGGGGATGGA TTCTTTATAG CTGGTATTTT 1680
AATCTACCTC TCTGAGTGTG TTTCGTCATT GATCAAATGT GGGCCAAGCC AGGGCATATG 1740
CAAAGCTCAG TACATGTGTG TTTCTTCCTT CTTCTATTTT CAGAAGGGTA AAGAGGACTG 1800
TCCTGGTCAC ACCATGGGCC AGTGGCACAT AGTAGGGCTA AATAAATGTG TCACTTTATC 1860
CATCAGAGTT AAAGAGAATT GCCCAGGTCA CCCACTGAGT CAAGAATTTG ACGCTGGTGC 1920
TCTTTTCTCT GTGTTACAGG TGGGCACTGT ATGCAGTTTG GTGCCTGTGA GGTAGGCAGC 1980
ACACAGTAGG TGCTTAATGA ATGCATGTGC ATGGAGAGAA TGAATAACCC TATTAAGCAA 2040
GTGACTGTCA GCATGGCTGG CCAGGAAGCT GGGAGCAGAC AACGTTAACA TGGAGGCAGA 2100
GGTCTGAGGG ACAGTGGGAG CCTTGAACCC TCCTCATGTC TCTATCGCCA ACTGCCAGCT 2160
TCAAGGGAGC CCCACAGGGC ACTGGCCCCA GGCCCTCCAG 2200
|
| |
|
|
|
