Tag | Content |
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EnhancerAtlas ID | HS048-11318 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr14:50854880-50857160 |
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 | chr14:50857040-50857055 | CCTGTCCTTGACCTC | - | 6.16 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 50854975 | 50855629 | chr14 | 50856767 | 50856981 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I050387 | chr14 | 50854342 | 50857012 |
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Enhancer Sequence | ACAGGCATGA GCCACTGCAG CTGGCTGAGG TTTTTACTGA GTGAGGAAAC ACTCCTTCAA 60 CTAATATTTG AAGAGCAGAA GCCCTTCCAA CTATGAAAGT TCTAATTAGA TTCTAATGCT 120 AGGGAGCATT TACATGGTAC TCTTAGCATT TAGTGGATGT GGCACTGCAC AGAGCACATT 180 CAGTTAAGCA CTTAATAAAT GCTTTGGATA ACAGGCAACC TTGACAGTCC TACTTCTTAA 240 AGCATGTGCC TGTCACCATG ATGGTAATGT GCCCAGCAGG ACTTCTGGTC TGCTCTTTGA 300 AGACAGTGAG CCTCTTGGGG GACTGTGTGA AGAGCTTTTG CCTCCAGCGC CTCCGTTGGC 360 CGTTGGCCAC AGCACTATGT TAAAATCCCA CCTTCTGCCC TTCTGTCTGT GCTTTCCTCT 420 TCTATGTTTA CTCCCTTTGA CCCTCTACTT TCCTGCTCTT GCATCCTTGA GGCTGCTTGA 480 CCGCTGTTAG ATGTTTGGCC CAAGAGCCCT CTGCCCTCCT CAGCAAAAAA TCAGCAAAGC 540 AATGCCAAAC AGGGACATAA ATCATAGCGA TAAGGCACGC CAGGCTCCAG GAAGCACCAG 600 AGCTTGCCCA AGGTCACTCC ACAGCTTCAA GCATGATCAG AAACTGAAGT TCCATAGCTG 660 GGTGTGGTGG CTCATGCCTG TAATCCCTGT ACTTAGGGAG GCCGAGGGAG GCGGATCATG 720 AGATCAGGAG TTTGAGACCA GCCCGGACAA CACAGTGAAA CCCTGTCTCT ACTGAAAATA 780 CAAAAATTAG CTGGGTGTGG TGGCACGCCC CTGTAGTCCT ATCTACTGGG GGAGGCTAAG 840 GCAGGATAAT CGCTTGAACC CAGGAGGCAG AGGTTGCAGT GAGCCGAGAT TGCGCTATTG 900 CACTCCAGCC TGGGCAGCAG AGTGAGACTG TCTTCAAAAA AAAAAAAAAA AAAAAAAAAA 960 AGAGAGAGAA AAGAAAACTG AAGTCTCTAA CTGTAGCTCC TGTCCCCATG CCCCTGTCCC 1020 TTCTATAAGG CTACTGATCA AAGGGGACAG CAGGGAAAAA AGGGATGCTC TGGACATTCT 1080 GCAGGTTACT ATTCACGATG AATTAAAATC AAATGAGAGC CTACTTCTGG CACCTAGGAT 1140 ACACTCAACA GTGCCACTCG CCCACACCCC ATGCACCTTT TTTCATTTCT CTCCCTCAAA 1200 GAGTCATTTT ACACATTTTT TCTAATCACT TACCAATGAA ATTTTAATAT CACAAATATA 1260 CTATATATCT GTATATGAAC CATATGTATA TCTGTGCTTT AAACAATAAA AAAGTTAGAT 1320 TTTTTTGCCA CCTGCCAAGA ACCAATTTTC ACCCTTTAGG AGTGACCTTG TTCTCATTAT 1380 GAATCTCTGC ATTACGTTGT GATATTTATA ATTAATTTTC AAATGGACAT TTCCCCTCAC 1440 ACTTATTCTC ATCTTTGTAG GTGGCAAACC TACAAAGGTT TGTACAAAGG TTTAGAAGGC 1500 TATTTTAGCC TTCTAAAATA GTCCATAGGG TTATGGAATG AGATATGGAA AGAACGGCTG 1560 TTCAGCTACA ATCTGCACTC AGGCCTCCAC AGAAGCCACA AATCTCACAG CTAAGGCCCT 1620 GCGGGAGAAC GGGCAGTATA AATTCTGACG ACCAGTCATT GGGAGACTTC AGAGTATGGT 1680 GTTTGGTATA AAGTGATGGA TGGTTCTGGT ATGGGGAAAC CACATGGCAT GAACTTGGGG 1740 ACAGACAGAA CTGTGTCTGC ATTCCAGCTT ACTGACCGGG AGGCCTTGGC AAATCATTAA 1800 CCATACTGAA TCCATTTGTA AAATGGGATA ACAATATCTA CCTTCTAAGG TTGTTATTAG 1860 TGTAACGATA TCTACCTTCT AAGGTTGTTA TTAGTGTAAT TTGTGCATCC TAAGTAACAA 1920 TGATACTTGG CAGTTTGTCC AAATTTACTA GGTCCCTTGC CCCTACCTGC CACATAGCAG 1980 TAGATGATTC CTTCTCTTTG TCTCACTTGT TTTTCTTGTT TTCTGGAGGG AGACATGTCA 2040 TAGACAATGT CCCAGCTGCT GCTTTCAGCC CTTGACCAAT GCTGGTCTAA TATATTTTAA 2100 CGCCCCCATA CCACCTGCCA TAGGTAGAAC GTCTGCCCAG GGATCCCACA GTGACACTGT 2160 CCTGTCCTTG ACCTCCAACT CCGCTAGGAG CATCTACTTT TTCTGCCACT GCTGGCAGAA 2220 ATTCTTTCTT TCCTCTTCTT ACCATTTTCA TTCCACAGAG AGAAGGTTCA GCAGCATAGG 2280
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