| Tag | Content |
|---|
EnhancerAtlas ID | HS099-13167 | Organism | Homo sapiens | Tissue/cell | HSMMtube | Coordinate | chr2:225349800-225350880 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr2:225350836-225350850 | AAAGATCAAAGGTA | + | 6.46 |
| | | 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 |
| GH02I224483 | chr2 | 225348493 | 225351270 |
| Enhancer Sequence | GCCCAAATAC TACGCTTTGC CCACAGTTTT TGCAACCCGC AGACCAGGAG ATTCCCTTGT 60
GTGCCTACAC CACCAGGACC CTGGGTTTCT AGCACAAAAC TGGTCGGCTG TTTGGGCAGA 120
TACCAACTTA GCTGTAGGAG TTTTTTTTCA TATCCCAGTG GCAGCCGGAA CCCCAGCGAG 180
AGAGAACCGT CCACTCCCCT GGAAAGGGGG CTGAAGCCAG GGAGCCAAGT GGTCTTACTC 240
AGTGGGTCCC ACCCCGACAG ATCCCAGCAA GCAAGCTAAG ATCCACTGGG TTGAAATTCT 300
CACTGCCAGC ACAGCAGTCT GAAGTCAACC TGGGACACTC AAGCTTGGTG GGGGGAGGGG 360
CGTCCACCAT TCCTGAGGCT TGAGTAGGCG GTTTTCCCCT CACAGTGTAA ACAAGGCCTC 420
CAGGAAGTTC GAACTGGGCG GGTGGCAAAG CTGCTGTGGC CAAACTGCCT CTCTAGATTC 480
CTCTTGACTG GGCAGGGCAT CTCGGAAAGA AAGGCAGCAG CCTGAGTCAC GGGCTTGTAA 540
ATAAAACTCC CATCTCCCTG GGACAGAGCA CCTGGGAAGA AGGCAGCTAT GGGCCCAGCT 600
TCAGCAGAAT TAAATGTTCT TGCCTGCTGG CTCTGAAGAG AGCAGTGGAT CCCACAGCGC 660
AGCACTCCAG CTCTGCGAAG GGACAGACTG CCTCCTCAAG TGGGTCCGTG TCCCCCATGC 720
CTCCCTGACA GGAGACACCT CCCAGCAGGG GTCAACAGAC ACCTCATACA GGAGAGCTCC 780
GGCTGGCATC TGGCAGGTGC CCCTCTGGGA CAAAGCTTCC AGAGGAAGGA GCAGGCAGCA 840
ATCTTTGCTG TTCTGCAGCC TCCACTGGTG ATACGTAGGT GAACAGGGTC TGGAGTGGAC 900
CTCCAGCAAA CTGCAGCAGA CCTGCAGAAG AGAGGCCTGA TTGTTAGAAG GAAAACTAAC 960
AAACAGAAAG CAATAACATT CAACATCAAC GAAAAGAATG CCCATGCAAA AACCCCATCC 1020
AGAGGTCATC AGCATCAAAG ATCAAAGGTA GATAAATCCA TGAAGATGAG GAAAACCCAG 1080
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