| Tag | Content |
|---|
EnhancerAtlas ID | HS050-69918 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:114110970-114112440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr9:114112242-114112253 | ATATTTACTTA | - | 6.14 | | STAT1 | MA0137.3 | chr9:114111448-114111459 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chr9:114111448-114111459 | TTTCCCAGAAA | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 4 | ID | Chromosome | Start | End |
| GH09I111348 | chr9 | 114111018 | 114111516 | | GH09I111350 | chr9 | 114111620 | 114111657 | | GH09I111351 | chr9 | 114111661 | 114111810 | | GH09I111349 | chr9 | 114112161 | 114112310 |
|
Enhancer Sequence | AGTGAGACTC CATCTCAAAA AAAATAATAA TAATTTATTG TCTAATATTA GGAGTTACAT 60
GTAAAAAGAA TACCTAAAAG AACACCTCCA ATTTTGTATC TTTCATGATG GAATTATGTG 120
AGCATAAACA TACAGAGGGG TCATGGAGGT GACAATCTAT AGGTCACATC TGGCAGACTC 180
CCAAATTAAC TGCCTGGGGA AAGTCTATAA GTCTTTGTGG CCTACATCCT GTTCCCTGAG 240
TAAAGAATCT TATCGTGAGT TCCTCCAACT GTTGACATAC TGATTAATAC ATAACCTATT 300
GACATTGCAA AGAACACTGA TTTGTTTCTG AATCATGCAA TTTTACTGCT TGTCCTGCAC 360
ATAGAACATT TTAGCCTGTA CGTTGTAATC TGTAGCCAAT GATTGCAAAC TCTTTATTGT 420
AATCACCAAT GAAAAAAGAT AACTCCCATA TAAGGAGTCC CTCTCCCTAC TCCTGAACTT 480
TCCCAGAAAA GCCTTTCAAG TTGTAGCTGA CTCCGGAACA CGGCCAACTT TGACAGTGTG 540
CCTCCCCAAG TTGGTCCTTA CATTTGACTT CCAATAAACC TTTATCAAAT TATTTCTGCC 600
TCAATCTCCT TAATTTTTGG TTGGCAGAGG CTTCTCTCCA GATCACCCCC CACCAAAAAA 660
AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA TCCCAAGCAT ACACTGGAAA TAAAGGTGAA 720
CAAGGAAGTT TCCAGAGCCT TATTTTCTAA ACACGGAACT TCTAGCTTAG CACATTTTTG 780
CGTTTGAAAG TTGTTTTGAT TGTCAAGACA GATGAAAGCA TAAACTTATT TATGAGATAA 840
GACTTCAAGC GTAGGCGGTA CTGACATCAT AAATGGGTTT AATGCCATAT TAAGTAAGTT 900
GAAATTAGTT CTGGGACAAT GGAGAACTGT TTTAAATAAC ATAGAGATAT AATTTGGTTT 960
ATGACCAAAT CAAGATGTAG AATATTCTTG AATCAAGAAG TTCCCTCATG CCCATTTACA 1020
GTCAATTATC TCCCCTGACC CCATGCCCCC AACTACAGAC CTGACTTCTG TCACTATAGT 1080
TTTTCCTTAT CCAGAATTTC ACATAAATAG AACTATGTAT AGTATGCAGT CACTCTACTT 1140
AGCAAGATGT TTTATGTTTA TGTAGTCATT TCTTTTGTTG CTGAGTAGTA TTCCACTGTG 1200
TAGATTTACA ACTGTTGATA TACTTACCAA TCGATAGACA TTTGGATGGT TTTCAGTTTT 1260
GACCTATAAT GAATATTTAC TTACGAGTCT TTGTGCAAAC ATAGATTTCC ACTTGTCTTA 1320
GGTAAATACA CCGGTGTAAA ATTTATGGGT CATAGTACAA GTGTATGCTT AACTTCGTAT 1380
GATATGTCAA ACTGTTTCTC AAAGATGCTG TCCTATTTTG CTATCCCATT AGCGATATAA 1440
GAATTCCTGT TGCTCCACAT CTGTGTGAAT 1470
|
