Tag | Content |
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EnhancerAtlas ID | HS048-02913 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:183512650-183513480 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr1:183512684-183512696 | TTCTGTTTACCT | - | 6.14 | NFAT5 | MA0606.1 | chr1:183513334-183513344 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:183513334-183513344 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:183513334-183513344 | ATTTTCCATT | + | 6.02 |
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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 |
GH01I183543 | chr1 | 183512841 | 183512990 |
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Enhancer Sequence | GGATCCGAGT TTTAGAGATA ATGAGTCCAG CATTTTCTGT TTACCTTTCC TCCATTCTCT 60 GTAACTGCTC ACAATAAGGT CCAGACTGAA AATACAATCT CCTTTTTTGG TTTCTCATCC 120 ATCTCAAATC ACCTATAAAT GATTAAAGAA AGAAAGAGTA AACATATCAC CACACTCTGT 180 ACCTCGTCCT GGGTTTTCTA TAAATGCTAC TCATGTTCCC TCATTTTGCT CAACTTTGAG 240 CAGTGCATAT GACATCTACT CTCTGGCTCC ATCTATAGGA TCTCAGGGCC TGTTCCTTAC 300 TGCTGAAAGT ATCCTTATTT ATTCTGAAGG GTGGTAAAGT TGCAGGGTGG AAGGTGGATG 360 CCTGACTGCA CATATGGCTA CCCAGATGAA ATCAAACTGA GGGCCAAAAT AACTCACCTA 420 TGGGTTAATA GTCATTATTA GTTCATAATT CATGTATGTC GTTTAATGAA TTAGAGTATA 480 GAGAACCCTG GGCCCCAGAA CAAGCAACTT AAAGTCATAG ACAAGTTTTT TTCAACTTGT 540 TAGCATCAGG CATCTCATTT GTAAAACAAA TGGGCTCTAA GGTCCTTTAC ATTTTTGGAT 600 TTTTGTGATC ATGGGAAAGC AAAATAATTA GTAAAACTAA GATAGTAAAA TTATCTTTTA 660 TTGGCTATTA AATAATTTGC TTTGATTTTC CATTTTTAAC TTAGGTGAAT TTAAATATCT 720 TCAGCATGTA CTTTTTGATC TAATGAGGTT TTAAATACTT TCTTAGGAGT AGGGTCTTCT 780 TTCTAGCACA TTTGAGTTTC AATTTATTAT AGATAGTTTT GCTTCTATTG 830
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