| Tag | Content |
|---|
EnhancerAtlas ID | HS050-03888 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:118250790-118253150 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr1:118251056-118251066 | GCTAATCCCC | + | 6.02 | | PLAG1 | MA0163.1 | chr1:118251748-118251762 | CCGCCTTGGGCCCC | - | 6.39 | | REL | MA0101.1 | chr1:118251683-118251693 | GGAAATCCCC | - | 6.02 |
|
| | 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 |
| GH01I117708 | chr1 | 118250679 | 118251611 |
|
Enhancer Sequence | GGAAAAGTTG GTCACCCTGC TCAGAGGGTT TGTTCTGGTC ACCCAAGTCA CCTGGAAGGA 60
GAAACAGGGC ATCTGAGTGT CTTGGAATGA TCCCTGGGCT GGGGCCAGGA CACCCGGGTT 120
TAAGTCCCAG CTCTGTCCCA CACCAGCCTT GTAATTCTGA GGAAGTTGTG TCTCTAGCCT 180
CCCTATATTG ACAACATTTG CTTAGTTTCT ATATTCTGTA TGCTCTGGAA ATTGGGGCTT 240
CGATCCTAGA GAGATTTCTA GGGCTAGCTA ATCCCCAGAG TAAGCAAATG GCTCCCCGTG 300
GAGCATGCTT TTGATATGCA AACCAGCCAA TCCAGAGCCT GCACCCCCAA CCCTCTCCTT 360
TATCAAACGC TCACACACCA ATGCAATATC TCCCCTGCCC TAAACCACCC CAGGGCCAAG 420
TCCTGGACAA CTAGGGATCA CGCCTATAGC CCAGAACCTA CTGAAATTAT CCAAACTACC 480
CAAAGCTGAA CTTACTCAGC ATAGTTGCAG TACCTTGCCC ATTCCTTCCC ACAGGAACCC 540
CAGTAAAGGC CCTGAGCCAT GCATACTCTC CTCTCCCCTC CCCACTTCTG CCTCCTGACC 600
GACCCAGCGC TTCCTGGGGT GGCCTGCGTG GCACGCCGTA CCTCCTGTTC TAGAGGCCTG 660
TGAGTATAAA CTTTTTCCTC CCTGACAATC ATTTCCATTT CTTACCATGC CTGATTAAAA 720
CAAACTCCAG GTCCATTTTA TCACACTCCT CCCTGCCGTT ATTGGCCCTC CTGCCTCACG 780
GGGTTGTTGC GAGGGCCTAA TAAGATAATG TTTATAAAAA TGCTTTGTCA GCTTTCAAGG 840
ATAAGGTATT TTTATGATCA TTCCTTTCTG CATCATTTAG GTTTGAAAAT GCTGGAAATC 900
CCCACAGGGT CCTGATGAGG ATGCAGGGAG ACTGTTCTTA GGAGGCTGAT CCAGGTCACC 960
GCCTTGGGCC CCTCTCCACT GTGAGCAATC CGTCTGCCAG GCAGTAGTGG CCAAGGCCCA 1020
TTTGGACAGC AGCCTCCTGG ACTCCTGGTC TGGCCGCCTC TTCTCCAGCT TGCACCTCCT 1080
TTTCCTTTCA CTGGGGGAAC AAACACATTT AGAGTTTAGA GGAATGGAAC TACTCCATGA 1140
AATGCTTGTC TGCAGGAGAA AAGCTTCCCA TTCCTTTGGA GAGCATGCAT GCCACAAAGC 1200
AGGTCTCCCC AAAGTATTCC TCCAAGAAAA ACATATGGGA GCTGTTAAAG TCAAGAGGCC 1260
AGCACACTGG GTGGGACCCT CCTCATAAAA GCAGGAGCCT GCATCCTCTC TTCTAAATCT 1320
CTTCCTGGAA AAGATCCTCT TTTCTTCCAG CTGAGGGCTG TTTATTCTGG TTTACCTCCC 1380
GGCTGTGTGG TTCACATCCA TGCGGCCAAC ACAAAGGCAG TGTACGACCC GTGACTACCT 1440
CTCAGGCACC CAGGCTGTGA AATAAAGTTT TGAGCAGGCT GTGGGCAGTT ATGTGGTTCT 1500
GTGGCTTCAG TGAGTGCTAA GTGGGCATGA CAGTAGCTCG AAGGGCCTTG GGATAGAGGT 1560
GCCAGAGAAA ACACAGGATG CCTGAATATT GCACAGGACA TACTTATACA CAAAAGTATT 1620
TGCTATGTAT CTGAAATTCA AATTTAACTG GGCTTCCTGC ATTTTTGTTT GCTAAATCTG 1680
GTAACCCTAA CTTAGGAGCC CATTTCTGAA TCTATTTTTT TACTTCCCGC ATAGAACAGG 1740
CCCATGTCCT TCATTTCCTG TGGAGATTTC TGGGTCTAGT CTTTTGTTCC TGTCCCCTGC 1800
TGCATGGGTC ATAGACTCCC AGGCATCACC AGGTGGGCTC CAGAAGTAAC TTGCTCTGAG 1860
GTCTATAACT AATTAGGTCT CTACTTAATG GGCAGATGAA AGAGCTCAGT GTGGGATTGG 1920
AGGGTGATCA AACTGGCGAA TCTTGCAAAG CCTTGAAGAG AACACTTGTA CACACAGAAC 1980
ACATGAGTGT GGGTGGGTTA AGTGATGTCC AGGGCCTTGG GCAGGCAGTG GCCTGCTGCT 2040
GTGTTGCTGG AGGGGAAGGG TTAGACACCA GCCCTTCTGC AACACATCTT TGGCTTTGGG 2100
GTCTTGACAA CTGCCATGTG GAGCCTCCAG TATTAATTGT ATCCAGGAAT TTGCAAGGGC 2160
CCTGGAAAAA AGGTGTCAGG GTTACAACCT CTTTTTCTAG ACTTCCGCAA TAATTAAGGC 2220
TTGTGTGAAC TAGGTGGCCT TGGTGAAGTC CTGACAATAG AAAAGGCAGT GAGGGACCCC 2280
AAGAGGAAAC ACTGCACAAA GAAGGAGGTG GGAAGGAGCA GAGCTCATGA AGGAGAGTGC 2340
CTCTCCTAGG CACAGTGTGC 2360
|
