| Tag | Content |
|---|
EnhancerAtlas ID | HS101-01607 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:54481530-54483040 |
Target genes | |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I054015 | chr1 | 54481563 | 54483001 |
|
Enhancer Sequence | TTGGCCAGGC TGGTCTTGAA CTCCTGACCT CAGGTGATCC GCCCACCTTG GCCTCCCGAA 60
GTGCTGGGAT TACAGGTGTG AGCCACCACA CCGGCCTGGG GCTTTGTGAA CACTCTGTGA 120
ATATGCCGAC CTGGGGGTCC AGGAGGCAAG AGAAGGCCCC CAGTATGGGT CAGTCCAGGT 180
TATTTCCAAT CCATTCACAT TTCTGATGCA GTGTCCTCAG AAGCAGAATG GGATTTCCAC 240
AGGCAGGTAA GGGGAGGGTG CAAAGAGAGG GCATTCCAGG CAGAGGGCGT GGCAGGAGTA 300
AAGGCCCAGT GGTTGCAGGT GGGGGAGCAC AAATGGCCTG GGGTGGTGGG ACTCCAAGAT 360
GGATGTGTAT TGGGAGGGGA GACAATAGCA GGAGAGGCAG CATAAATCTA AAACCTGTCA 420
TCCCTACAGC CCTAGTTGGT GGCTCCTTGG CCATCAGCAA ACAGGGTAAA CTCAGGTAAC 480
CAGGGAGGCA GCGTGACTCT GGGCAGGGAG AGGTGTCCTG ATCAGCCAAG CAGCTCCTCA 540
AATATTTGTG CAGCACAGAC CATGCACAAG GTGGGGCCAT GGGAGAACCC GCAGAACCAA 600
GGCTCCTGCC CAGGTGAAGC TGTTGCACTT CAAAGCCAGA AAGCCCTTAG GTGCCAGTCC 660
TCTCCCTGTA CCGATGAGGA AAAGGAGGTG ATTCTTTCCA CAACCCCGCC CATCATGAGT 720
CAGGACTTAG AAATAAACAA ACACCAGCTC GGAGCAACAA AAGCCCTGGG GCTTTGTAAC 780
CAGAGAGACC TCAGTTCACA TTTGAACCCT GGCCCTCCAA CCTCCCTGCT GTGTGACCTT 840
GGCCTGGTTA CTCAACCTCT CTTAGTTTCA GCTGTCTCAT CTGTTATTGC CCCATAACAG 900
GGCCCCTGTC TCAGAGCTGT CCTGAGGATT AAAGAGATCA TGCAGTGCCA GGCACCTAAC 960
TGGGGATGGA TTCTTTATAG CTGGTATTTT AATCTACCTC TCTGAGTGTG TTTCGTCATT 1020
GATCAAATGT GGGCCAAGCC AGGGCATATG CAAAGCTCAG TACATGTGTG TTTCTTCCTT 1080
CTTCTATTTT CAGAAGGGTA AAGAGGACTG TCCTGGTCAC ACCATGGGCC AGTGGCACAT 1140
AGTAGGGCTA AATAAATGTG TCACTTTATC CATCAGAGTT AAAGAGAATT GCCCAGGTCA 1200
CCCACTGAGT CAAGAATTTG ACGCTGGTGC TCTTTTCTCT GTGTTACAGG TGGGCACTGT 1260
ATGCAGTTTG GTGCCTGTGA GGTAGGCAGC ACACAGTAGG TGCTTAATGA ATGCATGTGC 1320
ATGGAGAGAA TGAATAACCC TATTAAGCAA GTGACTGTCA GCATGGCTGG CCAGGAAGCT 1380
GGGAGCAGAC AACGTTAACA TGGAGGCAGA GGTCTGAGGG ACAGTGGGAG CCTTGAACCC 1440
TCCTCATGTC TCTATCGCCA ACTGCCAGCT TCAAGGGAGC CCCACAGGGC ACTGGCCCCA 1500
GGCCCTCCAG 1510
|
