| Tag | Content |
|---|
EnhancerAtlas ID | HS158-00803 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:19613660-19614980 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:19614861-19614881 | GGGGTGGGGGCGGTGGGGGG | - | 6.8 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_31682 | chr1:19609376-19616092 | Gastric | | SE_52842 | chr1:19611041-19616161 | Small_Intestine |
|
| | 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 |
| GH01I019287 | chr1 | 19613987 | 19615092 |
|
Enhancer Sequence | GGTGTGGTGC TACTGTAGTA GTCCCAGCTA CTCAGGAGAC TGAGGTGGGA GGATGGCTTG 60
AGCCCTGAGA GGTCAAAGCT GCAATGAGCC CTATCGCACC ACTCCACTCC AGCCTGGGCA 120
AAAAAGCAAG ACCCTGTCTC AAAAAAAAAA AAAAAATCAG AAATATGGTT AGAGCTCTCA 180
CTGAGTGGCA GCCGGGTGAT CTAGAAAGAG CGTGGCACTG GGATGCACGC ACAGGCCAGG 240
TTCGTTCTGG ATCTACCATG TGGTGAATCA GAGGAGAAAT AAGACTCCAC TCAGACACTC 300
AGTGGAAGGA GGCAAATGGT GCTAATACTA AGAACAAACA AACAGCTAAC ATTTCCCAGC 360
CCTCACTATG TGCCTGCCAG GCATCGGCCT AAGCACTGCA AATGGCATCA GACTGAGGGC 420
GGCTCCTCCT GCCCCTATAC ACACATCCTC CCCTCCGGCC ACACCTGCCT CCTCCAGCAC 480
CCGCGGCATT GCCAAAACAC ATTTGCCTTT CCACACCCAT GCCCACTGCC CTGACGCCCT 540
TGCCCCTTGT ACTCTTCCTG GCAAACTCCT ATCCATTCTT TCTTCACGGG GTCCCTCCCA 600
GGAAGGGGTC ACTCTGGGCT CCCCAGCCAT CTCTAGAACT GGAGCTTCCT GGAGTGGGTT 660
AGTGTCCATT TCTCTCCAAT AGCCTCCGAC AGAGCCTCCC ACAGAGAGGG CAGTGAGACT 720
CTGTACCACC CCAATCCCTC ATCCCCCTGA GGGAGCTGCC AAGGCTTCCG GGCACTGCCA 780
CCCTTGTGAG GTGCCCTTGT GAGTACCACA AGGTACTCAG AGCAAAGTCC GGGGCCCCGA 840
GCAGGCTGGC ATGTGCAAAG GAGGAAGCAG ATAGTGTGCT GGGTCCAAAC TCTGATTTTG 900
GACTGTGCCA GGGAGTGCCA GGCGGTAAGA ACAGAATTTC TGCAGATCAG GCCCGTCAAG 960
GGCACCTGGA GGGCACAGGT GGGGACAGGA GCTGCACAAT GCCAGATCCC AGTGTTTTTT 1020
GTGCTCCAGA GAGGGGCTAG CCAAGTCATT CCAGGCAAGA CCAAGTCATC CAGGCGTCAG 1080
TGAGGGTGCT GGCTACCTCC CGGAAGAGAA GAGAGACGAA CAGAAGAGAA GACGAGAGAA 1140
AAGTTGTCCG GAGCTAGACG TGCCTAAGGA GCCTGGTGTT CCCAAGGCTG CGAGGTGAAC 1200
AGGGGTGGGG GCGGTGGGGG GGACAAAACT TTGGGTGCTG CCCCGGGGCC AGGGAGAGCG 1260
GGGCGGTACA CGGCTGTGGA CAGGCTCAGC TCTGCACCGT GCAGGGGGAG GATCAGGGGC 1320
|
