| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04876 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:178597860-178599290 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr1:178597950-178597963 | AATATGATGTCAT | + | 6.41 | | STAT3 | MA0144.2 | chr1:178598646-178598657 | TTTCTGGGAAG | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 178598791 | 178598883 | | chr1 | 178598955 | 178599085 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I178628 | chr1 | 178597541 | 178600136 |
|
Enhancer Sequence | TGAAATCCAA GTAAAGCAAG AGTGGGACAG AGGCCTTGCA AGGAAAAACT CAGCTACTAC 60
AGCCCAAGCC ATGCCAGTGT CTATGACCAG AATATGATGT CATCCACCAC ACTTCCTTCA 120
CCTGTCCAGG CTCACTGCCT GTAAATGGCA GGTGAAAATG GAAACCTATT CTGAAGCCAT 180
GCCCTTGTCA TTGTTAAATG ATATGCTGAC TAGCAAAACC AAAATTTCTT GGAATTATAT 240
TTTCCCTCTC TAATCTTCCT TTGCAGTTAA AGAAGCTATA GCCATGCAAT TAAGCACTAG 300
CCCACAGAAA CACACCACTA AACCACTTTC GGCTTTATCT CATCAAGTTA CAATAGTAAT 360
GGAAATGAAA CCTGCTATAT TCAACACAAA CTTGAGTACA CTGCACAAGT GGATAAAAGC 420
TAATGAAGAA AGCAAAGCTA ATATGTCAAG TCACATTTTT TCTTGAATGT GAAGGGTTTG 480
GTTTTTTGTT TTTCTTTTAA AGAAAGTGAC TTTCTTACTT TCAGCTCACA GATATTTCCT 540
TAACTGACCT CTAATTCACA GATGCAACCC CCTGGCAGTC AGGCCTATGC TAAAACGGCT 600
TCATCCCCTG ACCTCAGTGA GTGATCTCAC AGTAATCCCT TCCAGGGATT AGTCTGGGCC 660
AAACTCCCAT CTCAGTGTGG GCCAAATTCC TAACTGGAGA TGCAGTGAAT TCTTCTGAAA 720
TTTGCTGCCC AGCATCTCCT CCTCTTCTGA AACTGCCCCC CGCCTCCCCA TCAAGTCACA 780
GTGCAGTTTC TGGGAAGACC TGCTTCTTAG GACTGACCTC TCAGGCCGTG TTTGATTGGT 840
CCGGAGGGAC TGGGCCTCAG AAACTGACCA GACCTTAAGG CCTGTGGGCA GCACCCAGTG 900
CTGCCTCTCT TCTCTCAGCT TTTCTTTTTC CCTCTGCAGA CTGGCTCTTT CTGTTGCTCA 960
GTCCATGTGG CAGAAGATGG CAGTGCAGAA ATTTGTCTCT CCAAAGTTAG AACTCTTGTT 1020
TGCAAGCAAC AAGGTGTCAC AGAAACCAAC AGCAGGATTG CAGATGGGCC TCAGGCACAA 1080
GAAGAGCCAG GGACTTGAAT GAGAATGTGG GCAAGAGTCT CATATGGTCA CTTTTCCCTA 1140
TCTCTTTTTA CTTATCTTAT CAGTCATCTC TCACTGCAGA TTGGTTCTCT TTCCAACCCC 1200
CAAACTAAAT AATGGCCACG GCCAATAGTT CCTAACATCT CCTGGAGATA CAACTCTCCA 1260
GTTCAAGAGA GCACCTATAC TGGATTGGAA TCTTAGTCCA ATTCTAAATT CCTGGGGAAC 1320
CCTTTGGTTG TGTCTGTACA GGATGTTGTT GGCTTTTTAG GCACAGCAAG TCATGCTCTG 1380
CAGAACTCTC CCATCCCTGG CAGGACATTT CACGTAGTGG CCCCTGTCCA 1430
|
