| Tag | Content |
|---|
EnhancerAtlas ID | HS048-16776 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr17:73412730-73414080 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr17:73412980-73412993 | AAATTAATTAAAT | + | 6.07 |
| | | 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 |
| GH17I075416 | chr17 | 73412795 | 73413902 |
| Enhancer Sequence | CCAAGGTGGG AGGATGACCT GAAGTCAGAA GTTTGTGACC AGCCGGCCAA CATGATAAAA 60
CCCTGTCTCT ACTAAAATTA CAAAAAAAAT TAGCCAGGCA TAGTGGTACA TGCCTATAAT 120
CCCAGCTACT CAGGAGGCTG AGGCAGGAGA ATCACTTGAA CCCAGCAGGC GGAGGTTGCA 180
GCAGTGAGCC AAGATCGCGC CACTGCACTC CAGCCTGGGC GGTAGAGGGA GACTCTACCT 240
CAAAATAAAT AAATTAATTA AATAAAATAA AGAAAAAAAG AGGCCAGGCA TGGTGGCTCT 300
CACCTGTAAT TCCAGCAGTT TGGGAGGCCC AGGTGGGCGG ATTGCCTGAG GTTGGGAGTT 360
CAAGATCAGC CTGGCCAGCG TGGTGAAACC CTGTCTCTAC TACAAATAAA ATAATTAGCC 420
CAGCGTGGTG GCAGGTGCCT GTAATCCCAG CTACTCAGGA AGCTGAGGCA GGAGAATTGC 480
TTGAACCCGG GAGTCAGAGG TTGCAGTGAG CTGAGATCGT GCCATTACAC TCCATCCTGG 540
GCAACAGAAG GAGACTCTGT CTCAAAATAG AAAAAAAAAA AACTTCAGAT AAGCAAATGG 600
ACTCTGGTCC TGACAGCTCC CTGTAGCGAT GCCAGGGTCA GTTCAGAGGA GCCTGGCCTT 660
TCTCCTTTCC TTGTGTTTCA GTTTCCACAT CTCTTTTTCC TTAGCACACA CTCTGCCCGT 720
TAAGGAGATG AAGTCAGTTC CATTTTGGCC ATGAGCTAAA ATGCAAGTGA TGCATCCAAA 780
GGGTGGAAAT TTCCTCTGTG TTCCTACGCC TACAAGAAAG AAGCATTAGC AACTTTAGCA 840
ACTTAATACT AGGAAGTCTC TCCAACGTTG GTTTTTATAA AATTAAAAAT ATTTCAGGCC 900
AGAAGCGGTG GCTCACGCCT GTAATCCCAG CAATTTGGGA GGCTGAAGTG GGAGGATTGC 960
TTGAGGCCAA GAGTTCCAGA CCAACCTAGG CAACCTAGCA AGGCCCTTGT CTCTACAAAA 1020
ATTCAAAAAA ATTAGCCGGG TATGGTGGCA TGCACCTGTG GTCCCAGCTA CTCAGGAGAC 1080
TGAGGTGGGA GTATTGCTTA AGCCTGGGAG GTTAAGGCTG CAGTGAACTG TGATCATGGC 1140
ACTGCCTGGG TGACAGATCA AGACCCTGTC TCAAAAATAA ATAAATAAAT AAATAAATAA 1200
AAATTTCAGT AGCCATGCAT GGTGGCACAT GCCTGTAGTC CCAGCTACTC AGGAGGCTGA 1260
AGTGGGAGGA TCACTTGAGT CCAGGAGTTC AAGGCTGCAG TGTGCTATGA TCATGCCTGT 1320
GAACAACCAT TGCACTCCAG CCTGGGTAAC 1350
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