| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00099 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:2118890-2120350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:2118961-2118976 | TGAACTCCTGACCTC | - | 6.22 | | Zfx | MA0146.2 | chr1:2120204-2120218 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH01I002188 | chr1 | 2120278 | 2122904 |
|
Enhancer Sequence | CTGCCCCACG CCCGGCTAAT TTTTGTATTT TTAGTAGAGA CGGGGTTTCA CCATGTTTGC 60
CAGGCTGGTC TTGAACTCCT GACCTCAGGT GATCCACCTG CCTCAGCCTC CCAAAGTTCT 120
GGGATTACAG GCGTGAGCTA CCGCGCCCGG CCTGAAGCCA TTTTCTTAAG TAGGCATATA 180
TCAGGGCAGT TTTAGGCTCC CAGCAAAATG AGCAGAAGGT GCAGCCAAGT CCCCATGCCC 240
CTGCCCTGCC CGTCCTGCCC TGCCCAGCCT CCCCCACCAC AGGACACGCT GCTCACAGCT 300
GCTGGGCCTG CCCTTGTCGT CGCCCCACGC CCAGAGTTCC CGCCCAGCTC GCCCAGGGCA 360
CCGTCAGTCC CGTGGGTGTG GACAGGCACG TGACAGTGTG GATTCACCAC TGTGGGGCCA 420
TGCAGAGGAG CCCATGCCCC GGAGACCTCC TGTGCTCCGC CTGTGCCTTC CTAGCCCCTG 480
CACTCTCTTG ATGTTTTTGG TCCTCACGGT GTTGCCTTTT CCAGAACCCC CTAGGGTTGG 540
AATCACAGTG TGTAGCATTT TCTTTCCCTT AGTGATCTGC ATTTATGGCT CCGTGTTTTT 600
TGCGGCCTAT CTGAGGCCAT GATTGAAAGG AAAATACAGA CGTCTGGGTG TTCACACCAC 660
GTCTGCCCCC AGATCTGTTC CCTCAGCCAC CACAAACGGG GGTCAGAGCT GAGCCCGCAA 720
AGCCCGGCTC TCCAGAACCT GGGGGCTGAA CAGCAGTGGA CAGGAAGCTC CCTGAAGACG 780
CTGCTTTCTG TGCTCCACTC ACACTGTGAG CCCAGGCAGA CGGTGGCTGA CGGATCTGGG 840
TGAACCAGAT GCCCACTGCT GCTGTCCTTC CCCAGAAACT CCGGATTTCA GGAGAAGCTG 900
CCTCAAAACC CCTGGCGAAT GATGAGGCCC TGGAGCCCCC GGAGAGTCTC AGCTCCCGCA 960
GCCCTAACAA ACGACCACAG ACCTGGGGCT TCAACCAGAC TCTCTCGGCT CCAGAGGACG 1020
GCCCTCTTCT GGCCTGTGTC CCCCACGGTA GAAGGAGCAA GGGAACTCCC CAGGGTCTCC 1080
ATTATGGGGC ACTAATCCCA TCGAGAGGCG CCGCCCCGAC CTCCTGTCCT GGCAGAGTTC 1140
TTGCCTTGTG GTGAGGATTT CAACCTAGGG ATTGGGGAGT TACAGGCCCG CAGCACACGG 1200
TGGCAGGAGC CTTTCCTTTT CATAACTAGC TGCAGCTGCA AGTTCATTTT GGGGAATTAA 1260
AACACCACCG ATGGTGGAGC GCGGTGGCTC ACGCCTGTAA TCCCAGCACT TCGGGAGGCC 1320
GAGGCGGGCG GATCACGAGG TCAGGAGATC AAGACCATCC TGGCTAACAC GGTGAAACCC 1380
CGTTTCTACT GAAAACACAA AAAATTAGCC GGGCGTGGTG GCGGGCGCCT GTAGTCCCAG 1440
CTACTCGGGA GGCTGAGGCA 1460
|
