Tag | Content |
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EnhancerAtlas ID | HS180-04635 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:224255910-224256730 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:224256123-224256138 | CCTGTCCTTGACCTC | - | 6.16 | TCF3 | MA0522.2 | chr1:224256157-224256167 | AACACCTGCT | + | 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 |
GH01I224067 | chr1 | 224254881 | 224256038 |
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Enhancer Sequence | ACTCTACCAA GAATCTGATC CCCTCTCTAA GCAGATAATT ACAGTGACAA GTGACTTTCA 60 AGTTTATGCC CATATATACT CCTAGACTTC TGATGTGCCC CAGAAGGACG TTACCATTCA 120 TGTTCTGAGT GCTGGCCTCT GGGCCTGACC CTGTCTGCCT GGATTTGGAA CTTTGCCTTT 180 CCTTAACTTG TGACTTGCCC CCCTAGATTC CAGCCTGTCC TTGACCTCTG GCAACAGCAA 240 ACTCGTTAAC ACCTGCTCCG CATGCATAAA TCCTTGCCTT CTGCCCAATT CTTAATTCTG 300 ATTTTTGGAC TTCTGGACCA GGCTAATCCT TACAGTCTGG GGAGAATGAA AACATTGTTA 360 GACTGAAATA GCTAAGCCCA GAGTTTATGA TTAATGAGGA CAGACAGGCC AAGGAGTCAG 420 TAACCATACA AATGTTCACA AATGATTTGC CATAAGGCCT TAGATTTTAC ATATTATATA 480 TATGAGGTTC ATATGTTATA GCCAGTGTCA GGACACTAAC AAGTGAAAGA CTTTTCAAAC 540 CCAGGTCAGG GAACTCAAAG CATAGCCCTC AAAACGTACC TCAGATCATA GGGCAAATAT 600 ATGCAGACAT ATGTAGTCAC TGTTGCTGAG CTGAAAGTGT CACCCGTGCC CTGAGGACAC 660 GTTTGGTATC TATTTAAGAC CTGAGCATTG AGAGGCTGTA AGAGGTGCAT AAATTCTGGG 720 AAAGTCTTCA TCCTTTACAA ACACAAATGC ATTGTATGTA AAATTACATG CATTTCTTTG 780 AGGAAACTCT CACTATAAAT GTTCAAATAT GGTAGGGGCT 820
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