| Tag | Content |
|---|
EnhancerAtlas ID | HS050-70050 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:116903770-116905070 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr9:116904399-116904415 | TCTTATGTAAACAGAG | + | 6.23 | | FOXP1 | MA0481.2 | chr9:116904403-116904415 | ATGTAAACAGAG | + | 6.32 | | FOXP2 | MA0593.1 | chr9:116904403-116904414 | ATGTAAACAGA | + | 6.02 | | ZNF263 | MA0528.1 | chr9:116903874-116903895 | TTCTCCTCTCCTGACTCCTCC | - | 6.64 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH09I114140 | chr9 | 116902964 | 116904012 | | GH09I114141 | chr9 | 116904141 | 116904410 |
|
Enhancer Sequence | TAAGGATGAG AAAAACACCT GCCCCCTCGT CCTGGGATGA GAAGGACCCC TAATGTGTGC 60
ATAGAGCTTG GCAGATGAGA GATGCTCACT GCTTCTTCAC TTCCTTCTCC TCTCCTGACT 120
CCTCCAAATG AGATGAGTGT CTTTGAGTGG AAGAATTTCC CTTTAGAGAC ATTCAACTCC 180
CCTGTGGACA CTGGCTGGAG AAGTGGATGA GTGGTAGGGG GAGAGACCCT GGGAGCTTCT 240
GTGATGGACA GGCTCGGAGA GCAGAGGACA AGGCCAGCTC AGAGAAGGAC AAAAATGACT 300
GCATCTGCCA AATCCCACCT CTATTTTTGG TGTTTACAGG CACTAGTGCT GGAAAGGGGC 360
CCATCTTCGA AATTCCTTTT CTTTGCATAG AGTGGTTAAG ATCATGGGCT CTAGAATCAG 420
ATGGTTCTAG GTTAGTGTTT CAGTTCCATT AGTTACCAGC TGTGAGACCT TGGGCAGGTT 480
GCCAGCTTCT CTGCTACTCA TCTGTAAAAG AAGCAGAATA ATGTCTACAT CTGAGGATTT 540
TGTGAGTAAT CAATGAGCTA ATATGTGCAA AGCTCTTTAC AGGAGACCCG GCAGATATCA 600
AGTGCTTAAA AAACAGATGC CACGGCCAAT CTTATGTAAA CAGAGCCTCT TAACGTCCAC 660
GCCCATGCAG ACCAGAGTCC AGTGAGATGT CTGCAAAGCC CATGATTCCA CATCTCCAGA 720
CAATCTCTTT TTTGGTGGTC TTCAGAGTGA GGCAGTGACC ACACACAGAA ACAAGTCCTG 780
GTATCCTCAG ACGGCAGCTG ACCCATCAAA TTTGACACTT GGAAGCCATC CTGAAGTTTC 840
TAGTGCTTGG ATCTCCTTTC CATTGCCCTT GCCAAATGGA AATCTCCTAG GACTCATCCA 900
GAGGCAGGAG CTCTGAGGCC TGGGGGCTCA GGGATGGCTG CCTCTCTGCG ACTTCTCACC 960
CCTGGTCCTG GTGGAGTCTC CACTTTCCAG ACTCATTTTC CCTTCATTGT TTCCCCAGGC 1020
TGGAGGCGTC TGCAGATCAG CCCTGGTCAA AATGCCCAGC ACAGGAGCTG GCTTCCATAG 1080
GTCAGGGGCA GAGTAATCTT TGCTGAACTG GAAGAGCTAA AACTCAAAAA CTAACACCTG 1140
TCCCTGGTTA ATAGCCAAGG ATGACTTTCA TCAGTGTGTC TTATTTTGTG GGCAAAGAAA 1200
CTGGGTGATT GGTTCATCCA TCTGCTCATC CACTTCCTCA CTGGACAATA GTTACTAAGC 1260
ACCTACTGTG TGCCAAGTCC TAGGAACACA AAAATGGATT 1300
|
