| Tag | Content |
|---|
EnhancerAtlas ID | HS050-09511 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr10:100108750-100110150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chr10:100109307-100109320 | GCACATCTGGATT | - | 6.62 | | ZNF263 | MA0528.1 | chr10:100109557-100109578 | AGGGGAGGAGGAAGTAGAAAA | + | 6.17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 100109052 | 100109819 | | chr10 | 100109446 | 100109785 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I098348 | chr10 | 100108682 | 100110157 |
|
Enhancer Sequence | CTCTGGACAG TGGCCTTGAA GTCCCCATTT GCTTATCAGT TACCTTTTGG GTTGGCATAA 60
GAGTGTTCGT CTCTCAGCAA TACCAGCCTC TCCCGTGTCT CCAGGATTCA CATCCCAGAG 120
CTTCTTGTGC TTTTCTCCAC GGAATTTTGG GATCACAGCT AAAAGAATCA ACCAGTCTGT 180
TGGAACATTT AAGTTTTCCT GCCCTCCTGG TATCTGCAGA CGTAGGTAAC AATTCCATGT 240
GCAAAACTTT CAAGTAATGA TGAATCCGCT GGGGCCATAA CTCACACCCT GAGGCCACCC 300
CGGAAGGATG GCTGGAGGTA CCCCACTGAG GAGTCATCCC GCCCACTAGT ACCACGAGTC 360
ACGCCCTCTC ATTAGATCAA ATCAGAGGCA GGGAGAGATT TACAGCTTAT CTCAAAACAT 420
CTGGACCGGC AATGTCGATT CCAGACCAAC AGCAGGAGAG GGTACTTGGG GACCACATTA 480
CAAGCCTTGC TTCTGAAGAG CAGCTGCCCT GAATGTTCAC CTCGAACACT TCTCAGCACG 540
CTGCCTCCTC AGAGTGTGCA CATCTGGATT TGAAACTAAA AGCAAGAACT ATGCATTTTT 600
CTTGCTGTTG AAATATGGCT CCCTGGGGAC CCAGCAGGTC GGGCCAACAC AGACACTTCC 660
TGCATCCTGA CCTCAGACAA GCCCACATTC TCTAGGATAA CTGAAGGGAA CGCTTCCAAG 720
TCTGCAAGCT GCCGTCAACT AAGATCTCAG GCATCCTCAC TTCGTGCCGA GAGGAGGCTC 780
TTAAACATCA CTGCCTGGGC TGAGCTTAGG GGAGGAGGAA GTAGAAAATG TGATTAACAT 840
GTAACCATAA AATGTTGCAG CCATAAAAAA AGAGAGAAGT TATGCGTAAG TTATGGCTGC 900
GTGAATGGCC ACATCAAGCC ATTTCCAAAA GCCCATCTCA CTAAACAGCA GTTATCTTGC 960
TCCTCAAGTG GAAACCGCTT TGAGACATTT CAAAATTAGT GATTTTCTGC CAGCAGCTAC 1020
ACTGACTGCA CCAGAGATCC TGACCACAGT CCTTGCTAGA GTCTCAAACA GACTTGCATT 1080
TGACTTTTTC TATTTTTTAT TTTTTTTGAG ACAGAGTCTC ACTCTGTCAC CCAGGCTGGA 1140
GTGCAGTGGT GTGATCTCAG TTCACTGAAT CCTCTGTCTC CTGGGTTCAA GCGATTCTCC 1200
TGCCTCAGCC TCCTGAGTAG CTGGGACTAC AGGCACCTGT CACCATGCCC AGGTAATTTT 1260
TGTATTTTTA GTAGAGGCCG GGTTTCACCA TGTTGGCCAG GCTGGTCTCA AACTTCTGAC 1320
CTCAAATGAC CCACCCACCT CGCCCTCCCA AAGTGCTGGG ATTACAAGTG TGAGCCACTG 1380
CACCAGGCCA AACAGACTTG 1400
|
