Tag | Content |
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EnhancerAtlas ID | HS050-01349 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:27353340-27354860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr1:27354844-27354854 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:27354844-27354854 | GGCACGTGCC | - | 6.02 | NFAT5 | MA0606.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | SP1 | MA0079.4 | chr1:27353734-27353749 | TAAGCCACGCCCCAC | + | 6.16 | SP4 | MA0685.1 | chr1:27353734-27353751 | TAAGCCACGCCCCACTC | + | 6.28 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 27353454 | 27354564 | chr1 | 27353661 | 27353962 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I027026 | chr1 | 27353011 | 27355170 |
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Enhancer Sequence | ACATCTCACT CACTCTGTCA CCCGGGCTGG AGTACAGTGG TGTGATCTCG GTTCACTGCA 60 ACCTCTCTCT CCCAAAATCC CAAATTTATA TATTCCAGTC CAGAGCTCTG TCTGGGACTC 120 CAGGCTCATT TATTTAATTT TAGTCAACAT CTCTACTTTC ATGTTTGTAG TCATCTCAAA 180 TTTTGCACGT TCAATGTTGA CTTCTCGAAC TGAAGTCCTA GCAAATGGCA AATTCCAGTT 240 CTTGGCCCCA AACTCTGAAG CCACTTTCCA CTCCTTTTTC TCTCACGCTG CACTTTCTCA 300 TTCGTCAGCA AGCCCTGTGG CTCTGCCTTC AGAACCCAAA CAGGCCCTGA CCACATCTTG 360 GCCCCACCTC CAGCTTACTG CCATCTCTGC GGTCTAAGCC ACGCCCCACT CTCCAGGATT 420 TTTGGAGCCT TTCTGCCGTC GTGCTTGTCG CCTACAGTGT TTTCATCCCA GCAAGCCAGT 480 GTGATCCTTT CTAAACACAA GTCAGATCAT GTCATTTTAA TGCCTCCTTC TCATTTGGAA 540 TACAAGCCGA AATCTCCTCC CACACCCCTT CCCTTATCGG GGGCAGCCAC ACTGGCCTCC 600 CTGATGTTCC TCAACCATGC CAGGCACGCT CCCACCTCAG GGCCTTGCGA CTGCTCTTCC 660 ATCTGCCTGG CACGGTCTCC TTTGATCCCC ACATGGCTGC TCTCTCAATT CCTCCAGGTC 720 GTCTTCTCCA TGTCTCCTGT TCTCAGGGAG GCCTTCTCTG ACTATCCAAT TAGAATGGCG 780 CCCTCGCTCC CCACACCTGC TAGCCTCTTC TCTATTTCCA AAGCACCTAA CACCATCTAC 840 CATGCTGCGT ATTTACCTAT TTATTGCCCC ATTTCCCGCC CCTGGAACCA AAGCTCCAGG 900 AGAGCAGGGA TTTTGTTTTC TATGTAATCC AGCACCTGGA AACCTGTGTG TGCTCAGTAA 960 ATATTCACGG GATGAGTGAA GGTGAGACAG GACTAACATG GGTCGCAGAA GAATGGAAAA 1020 TTCCAGGCAG CAGTTTCACA TGACTAGCAA AAGGAAGCTG TTGAAATAAC TGCAGAAGCT 1080 AGGGGCTCAT AAGACCCTGA ACAATCAGGG CATGGAGCAA GCTGGCTGAG ACCAACTGGA 1140 CACAGCATGG TGCTGGATTT GACCCAGGTT TCTCCTAGGA CCTCATTATA CGCTTATTAA 1200 CATACTAAAA ATCACACACC CACCAGCACC ACTATAGTTC CCATATTTGG TGTAAAAATG 1260 GGTGGCACCA CAGTTCCAAG AAATCTCCAC CTTTTTCCAG TAACTTTCAT AAATATTCCA 1320 CCCCTTGGTT AAAGAAACCT ATAAAAATAG AAACCACAGC TGGGCACAGT GGCTCACGCC 1380 TGTAATCCCA ACACTTTAGG AGGCCAAGGT GGGCAGATCA CATGAGATCA GGAGTTTGAG 1440 ACCAGCCTGG CCAATATGGT GAAACCCCGT TTCTACTAAA AATAAAAAAT TAGCCGGGCG 1500 TGGTGGCACG TGCCTGTAAT 1520
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