| Tag | Content |
|---|
EnhancerAtlas ID | HS050-37180 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:74967520-74968670 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr2:74968403-74968414 | AGCCTCAGGCA | + | 6.32 |
| | | 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 |
| GH02I074739 | chr2 | 74966347 | 74969939 |
| Enhancer Sequence | ACCACTTGGC TGGCAGCCTG GAATATAGAG GGGCAATCTT CTCAATGGGT TGTCAGGGCT 60
ACCACATTTT GGACTTGCTG CCAGGAGACC CAGGTTCAAG TCCCCACTCT GCTGCTATCT 120
CACATTGTGA CCTTGAGTGG TCACTAATCT CTCACTAGAT ACTGGGCCTC GGTAGCCTCG 180
TCTGTTAAAG GGGATGACTC AACTTGGGTA AGTCTAAAGT TTTCTCAGCT TTAAAACGCA 240
GGGATTCCAT GTGTCACCTC TCCCAGGAAT ATTTGTATCT GTGGAATGAA AGACCTTTTG 300
CTGCTGTCTC AGAGAAGTAT TTATGCAGGT CAGGGGTCCT TTCCCAATGC GTTGGACTCA 360
TCCATCTGGA GGAGCTCTTC TACCGAAGGG CACTACCTTC TCACCAGGCT GTGGCAGCAG 420
AGGGGTTAAA CAGCATGCCC TGCCCTGCTC CAGGCAGAAG GGTTGTAGGA CTTAATCACG 480
TTTCAGCTTG GCTGTCGGGC TGTGAGTCAC GGTTGCACTG CGATTATGTA AGCACGCAGG 540
AATAGGTGGC ATGACATATA TGCTGCCAGC AGCCACGGGC CTCGCCCTTC CGAGTCACCA 600
CTACTTTTTA AGCCTTTTTT TGGATACAAG TTTCTTTGGG TTCATCTTTG GAATGGAAAT 660
GGAAGCATGA TTGCAGAATA GGCAGAACAG GAATTATCCA TCAATCAGAG AGAACCCAGC 720
CCTTTAAGAG AAGCTGGAAT TAGAATATGG AATTCCTGAG CCTTGAGCTG GCATAGCCGA 780
GCCCTGGTTT ATGCTCTTCC TGCCTCCCTC CTTTTTTCCC TCCTGCCTGT GTGCTCCACT 840
TCCTCTCCTG AGACTCCCCC AAGGTAGCAT CACTCCCACC AGGAGCCTCA GGCAGGAAAA 900
ATAAGGCCCA GAGAAGGGAC TGTCCCTGGG GACGTGCACT GAGTGTGTGT GAGGGTGCGG 960
GGCAGGAATA GGAGTGCCAG GAGTCTACCT CTGGAGCAAT GCCTCCCACA GTATTTCTGT 1020
AGGGGAAAGG ATAGAAACTC ACTTCTTGGG TTCCTCCAAT CACCATGCAC ATGTCAGTCC 1080
TTCAGCTATA AATGCAAAGG AAAGCCAGAA CTGAGATTTG AGCTTTCTCA CCATCTCCAT 1140
GGTCAGATAT 1150
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