| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04865 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:178026390-178027840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr1:178026521-178026532 | AATTTAATTAA | + | 6.32 | | ZNF263 | MA0528.1 | chr1:178027360-178027381 | GAAGGAGAGAGAGGAGGAAAG | + | 7.5 | | ZNF740 | MA0753.2 | chr1:178027027-178027040 | TTGCCCCCCCCAC | + | 6.59 |
|
| | 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 |
| GH01I178055 | chr1 | 178024137 | 178028240 |
|
Enhancer Sequence | CACACATCAA AATGTAAAAC TCTTAATCAG GCCTCTCGTC CTTATCTACA TGTTAGCTGA 60
GAAGCAGGTG ATGGCAGTAA ACTTTAATGA CCAGAGGAAG TGTAATACTA ATGCAGCCGT 120
TTAAACCTCC CAATTTAATT AAAGTCTAGT TCCGCGCTTG CTGCTTGCCT GGAGAATAGT 180
CAAAGGAGCA CTTTTTTTTT TAAACCACTA ACTCCACCCT CAGGCCAATC CCAAAGCAGC 240
CTGCACTATA TCCTCATTTC CTAAAATGGA AGCCGAATGT ATGGAGAACA GGCCTTGGAG 300
GGACACAGGT TCCTCAATTC CGGCCTCTGT GACAGGGAGG TCTCCCGCCC AGTTTCCTTT 360
CCTTCAGAGT GAGGAAGAGT CTGTGTGCAG GGGCTGGAGC CTCTGGACAC AAAAATAGAA 420
TATTCGAGCG TTTGGATTTT CCTTTCCTGA CAGTGAACTT ACTCAGGAAG AGGCATTTAA 480
GCAAGATTTT TTTTCCTCTG TTTTTCAAAA AACACGTTTA ATGGGAGGAA CAAAACTGTT 540
GAGAGAAGAT TTTTCAGCCC CATCTTCTTT GGCCCCAAAC AGGCCAAGGT GAGGCAGTCT 600
TTTTCTTCCT TAATTGCCCT TTTTGCTTGC AATCACATTG CCCCCCCCAC ATGCCTCCCC 660
CCAGCATGCT TCTAGACGCC TTTGCAAGGC CCCCCACCAA GTCTTCAAAG CACCACCATG 720
TCTTTGATTG TTGGGCTCAT AACTGAGACT TCCCACACAG TGGTATGAAG CGACATATGA 780
TTCAAGCATC CTCATTCCAG AAATATTATT AGTCTCAGGA AAAAAAAAAT AGGGGCCTGC 840
TCTGTGTCTG TCACCTGAAA TAAACTCCCT GTTCCTCTCC TACTGCTTCT CAGATACTCA 900
ATTCTAAAGA TTATTCCAGC TTATTTTGCC ACCCCCAAGG TTTCTAACCC CAGCCCCCCA 960
GCTAGTGACT GAAGGAGAGA GAGGAGGAAA GGGGCCCTCT GAAGTTGGCC ACCTCAGGGT 1020
ATATGAAGCA CGTGCTTGTC ACGTGGAGAA AAAATGTGCT GGGCTAACCT CTGAGACTCC 1080
CTAGAGAATC CAGAGTTTGT GTCTCTTTGC AGAGCTCAGA ACAGCCTGTA TGTTCTCCTC 1140
TCCCTGTTGT GCGCCTGGCG CTTCCCCAGT GAGATATCTC CTGCAAAAGC TTTTCCTGTA 1200
AGGGGTGGGG AGCTTTTGTT CTCTGGGAAA TATGGTGAAG CTAATTAAGA GCATTGTCCT 1260
GTGAGGGGGG GAAGGCGGAG GGCTTTCCGA GATGGTGGTT TTCACCAGGG GTAAGTGAGG 1320
GCTGCTGAGA TCTCTCTGTC CTGCTGGGTC AACCGTTTTA GGGGGAGATT GTGATGAAGC 1380
CCAATAACAT AAAAATAGAT ACGTGAAGTA TAATCTCTCC CTCCCTCCCT CTCTCTTTCT 1440
CTCTCTCTTT 1450
|
