| Tag | Content |
|---|
EnhancerAtlas ID | HS012-14168 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr16:70491210-70492070 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr16:70491989-70492000 | AAATCACAGCA | + | 6.62 | | Nr5a2 | MA0505.1 | chr16:70491368-70491383 | GCTGGCCTTGAACTC | - | 8.25 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_28634 | chr16:70489731-70492040 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 70491717 | 70492024 | | chr16 | 70491309 | 70491670 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I070457 | chr16 | 70491481 | 70491630 |
|
Enhancer Sequence | GCAGTGGCGT GATCTTGGCT CACTGCAGCC TCCGTCTCCT GGGTTCAAGT GATTCTCCTG 60
CCTCAGCCTC CTGAGTAGCT GGGACTACAA GCGCGCATCA CTACACCCGG CTAATTTTTG 120
TACTTTTAAA AGAGATGGGG TTTTGGCATG TTGGCCAGGC TGGCCTTGAA CTCCTGAACT 180
CAAGTGATCT GCCCACTTTG GCCTCCCGAA GTGCTGGGAT TCCGGATGTG AGCTACCACA 240
TCTGGCCATT TCAAGGGTTT CTTTCTTTCT TTCTTTCTTT CTTTTTTCCT CAGACAGGGT 300
CTGGCTTTGT TACCCAGGGT GGAATGTATT GGTGCCAGTT TACTGCAACC TCTGCCCCCA 360
GGGCTGAAAC AATGCTTCCG CCTCAGCCTC CTGAGTAGCT GTGACTATAG GCACATTCAC 420
TGTGCCTGGC TAATTTTTGT ATGTGTGTGG TTTTTTGTTT TTTTTTTTTT GGTAGAGATG 480
GGGTTTGCCA TGTTGCTCAG GCTGGTCTCA AACTCCTGGG CTCAAGCCAT CCGCCTGTCT 540
TGGCCTCCCA AAGTGCTGGA ATTACAGGTG TGAACCACTG CACCTGGCCT CTTGCTGTCT 600
TTCAGTGCCT TTGCTTGGGA CCAGATATCA TTATCACTAT CACCTGAATA AGGATCCAAA 660
AGACCCAGGT GTGTTGCAAC TTTGACTATA GCGTCTCCTG GCCTCTGTGA AGTGGAGATA 720
ATAGGAGATA ATAATACTTA TCTTGCAGGG TCTAAGGGTG TTGTCAAGAT AAAAAAAAAA 780
AATCACAGCA CCTTAACTGT GGTCCAGAGT GCTCAGTCCT AGTGGCTATT ATTAATTTTT 840
TTTCTTTCTT TCTTTCTTTT 860
|
