| Tag | Content |
|---|
EnhancerAtlas ID | HS158-14474 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr12:120890260-120891640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr12:120891346-120891361 | AGTCAATCATTAATT | - | 6.72 | | HNF1B | MA0153.2 | chr12:120891347-120891360 | GTCAATCATTAAT | + | 6.34 | | MEOX1 | MA0661.1 | chr12:120890814-120890824 | GTTAATTAGC | - | 6.02 | | PLAG1 | MA0163.1 | chr12:120890742-120890756 | CCCCCTTCGGCCTC | - | 6.33 |
|
| | 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 |
| GH12I120452 | chr12 | 120890670 | 120891614 |
|
Enhancer Sequence | TATGAACCAA AAACTTCAAA CTCTTAGGCT CAAGCCATCC TCCTGTCTCA GCCTCTCAAG 60
TAGCTGGGAC TACAGGTGTG TACCCCTATG GCCAGCTAAT TTTTTTCTTT GTTACTTTTT 120
TTTTGGTGGA GACAGGATCT TGCTGTGTTG CCCAAGCTGG TCTCGAACTC CTGGGCTCAA 180
GTGATCCTCC TGCCTCGGCC TCCCAAAGTG CTGGCATTAT AGGCATGAGC CATCATGCCT 240
GGCCTGAATC CAGAACTTTT TTTTTCTCAT TCTGTTGCCC AGGCTGCAGT GCAGTGGCGC 300
AATCTTGGCT CACTGCAGAC TCCACCTCCT GAACTCAAGT GATCCTCCCA CCTCAGCCTC 360
CCGAGTAGCT GAGACTATAG GCACACGCCA CCACCCCTGG CTAACTTTTG TATTTTTTAG 420
GGGAGATGGG GTCTCACCAT GTTTCCCAGG CTGGTCTTGA ACTCCTGGGC TCAAACAATT 480
CACCCCCTTC GGCCTCCTGA AGTGTTGGGA ATATAGATGT GAGCCACCTT GCCTGGCTCA 540
GAACTTTTAA CCAAGTTAAT TAGCCCCCAT TCCAGTCTGC ATCAAACTAG AAATAAAGTA 600
GGAGGAAGGG AGAAGGCTTT TAGATGGAAG TAGAGGGGTC CACAAGAAGC TATTCCTTCC 660
AGCCAGATAG CAGAAAAGAA GCTCAAAGAA AGAAAAGCAG TGGGAGAACG GTCCCATCAG 720
TGAGTCCAAG GGCTGACAGA ATCACAAATG GAGCCACTTT GTCCTCCCTG TTGCCACAGC 780
ACTTTCCAAT GCCACCGTAG CAGCATTTCT CACAGTTACT TAAGTTATTG TTCCTGAGTT 840
TTAACCAGCA GGGACTTCTA GTTTACAACT GAAGTCTTTC TCAACCAGGG TTCCTCAGCC 900
AAACCAGAAC ACAGAAAGAT TCAAGTGACT TTTTTTCAGT TCTCCCAAGG ACAGTATATG 960
ACAAATGTTA GCTTAAACAC ACAGGAGATA AGTTAACTTA TCATCAGAAT GGGTGTCTTG 1020
GGGTATGTAG GCTAACTTAT CTTACAGAAC CCTGATTGGG AAAGACAGGT GGTGAGGTAG 1080
AAGTTTAGTC AATCATTAAT TGATCTGAAA AGCTCATCTG GTCCTGTTCA GTGTTTTATA 1140
TAATTCTGAG GTCCAAGAAA GTGAAGCAAC TCACCAAGTG AGAGGTATGC TTGCTGTACC 1200
ACTGTCACAG AGACCGTGGG TTCAGGAGCC TGTAATTAAT AAAGCTAGGT ATGGTGGTGC 1260
ACACCTGTAA TCCCAGCTGC TTGGGAAGCT AAGGTGGGAG GATCACTTGA GCCCAGAAGT 1320
TTGAGACCAG CCTAGGCAAC ACAGCAAGAC CCTGTCTCAA AAAAAAAAAG TAAAACAACA 1380
|
