Tag | Content |
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EnhancerAtlas ID | HS048-17620 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr18:43659960-43660880 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr18:43660271-43660284 | CAAAGGTCAAGTG | + | 6.92 | ZNF263 | MA0528.1 | chr18:43659989-43660010 | TGTTCTCCCTCCTCCTCCTTA | - | 6.23 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I046080 | chr18 | 43660265 | 43660736 |
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Enhancer Sequence | TATTTACAAG ACATGATGAA TTGGTCTTTT GTTCTCCCTC CTCCTCCTTA CTCCTAGGTT 60 AGGTAAGTTA TTGATGGAGT CCTTTTGTGT CTTACTCATC TTTGAATCCT TTTTAGTGTT 120 CATCTCATAG GTAATGCTCA ATTAATAGCT GAACTAAGTA CTACTTCAGA TATGCTTATC 180 TTAATATTCT TGCAATCATA GATTATAGAG CTGAGACGCT AAGAACTTTC AGGAGAGCAA 240 AAAAGACAAG ACCTTACAGT TAACAAATAG TTTTTAAAAT ACAAGTCTGA AATCCATAAA 300 ACTTCACATT TCAAAGGTCA AGTGCCTTCT CAAATGTTCA CCACCCCCAG TGATAAGATA 360 AATGCACACA GACACAATTT TATGACAGCC ATTTTGTTGC CACACAGAAG GGCCACTTGG 420 GCAGTGTATT TAGGCCTGCC TGGTTAAAAA CAGCCAGGTG CCTATGAGGT CTCCTATGTC 480 ATTAGTCTGT AAGTACTTAG TAAAAAGCAG TATTTGAATC TCATGGTTCA TTGCTGTAAC 540 AGAAAGGGCT GGACTCTATA GCTCAGCAAA AACACCAGGG AAAGGACTAT ACAGTTTTAG 600 GGGAGATCTT GAAGTCTTCT AGCACAACTT TTTTTAAGAG TCAGGGTCTC TGTCACCTAG 660 GCTGGAGTGC AGTGGCGTGA TCATAGCTGA CTGCAGCCTG TTTCAAACTC CTGGGCTCAA 720 GTGATCGTCC CAAAGTGCTG AGATTACAGG CGTAAGCCAC TGCGCCTGGG CTATCATATT 780 CTTTAAAAAT ATCACATATT TTTAAATGTG ATATTTAAAA ATCACATTTT TAAATATCAC 840 TGTGCCTGGC GTGGGCCAGG CACAGTGGCT CACGCCTGTA ATCCCAGCAC TTTAGGAGGT 900 CGAGGCACGT GGATCATCTA 920
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