Tag | Content |
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EnhancerAtlas ID | HS118-05722 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr14:36899240-36900690 |
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) |
NFIL3 | MA0025.1 | chr14:36900628-36900639 | TTATGTAACAT | + | 6.32 |
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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: 2 | ID | Chromosome | Start | End |
GH14I036429 | chr14 | 36899021 | 36899801 | GH14I036430 | chr14 | 36900081 | 36900110 |
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Enhancer Sequence | GAGATAAGAG ATGCAGATAA ATTATTTTGA TACAGTAGAA AAAAGAAGTA GAGAAAAGGA 60 GTCACAGTGT TATATCAATT TAGAAGAAGG AGAAATTATC TTATGCAAAG ACACTCGTGA 120 AGTGCTTAAT GCTAAGTACT AAGCCTTATG GATATCCAAG CATACAACAC TTGTAGTACC 180 TATGCTCAAT GGTTATTCAC CTCAAACTTA TGGGAACTGT GGTAGGTCTC AAACAACATG 240 TGGAATTTAG ATACAAATAC AGGATGCAGA TGGGGGTGGG AAAGGCATTC TGATTAATGG 300 AGCCCAGGAA GAATAGCATG GAGATGGGAA TACTTCCCAG CGGCTTTCGC AGGTGAAAAT 360 GCAGGAATGC AGAGCTGTCG AATTTAGCTG GCATGGAAGG AGCATTGAAG GAGAAGAGTG 420 AAAAATGAGC TCCAACAGTG GTTTGGAGCC AGTTTGTGGA AGATCCAGAA TGCTAAGGAA 480 TGGGCTGGCA CGGGCAATGT GTTCCTCATA GTTTGAACTC TGAATTTCTT GTCACACACA 540 AAAATAAAGG AGGACAGGTA GTGGGTACTA GTTTCAGTCT GTGAGTTATA TTCACTATTT 600 CAGAAAGTTT AAAACATTAG TCTTTTTTTT GCTTTTGGTT AGAATTACGT ATCACCTTTT 660 CCTTAGGGAA ACTGGTTAGA TCATGTTGGG AAGAAGTTTG GCTTGACCGT TGCTGGCTTC 720 ATAGTCATTT GTGGGATGGG ATTGGGACAC CTGGCTGTGT TATCCTATCA ACAGGCTAGC 780 AGTCACTGCA GAGCATTTCA CAAGAAATAG CTCATTGCTT TTTCACATTG TAGGTTAATT 840 ATTTTACATG ATTGTGCAAC TCTGATAGCC ATTGGTTATT CACGAAAACT TGACTCGATA 900 TTTAAGTGGA AAGTATGCCA ACACTTACTA AATGCTGTTT GTTTGGTACA TAGCTTTCAG 960 AACATGGTGT CCACAGGCAG TGTGGATGTT GTCCAGGGAA GTGAGCGAAA GAGGTCCTTA 1020 GTGGAAAAAA GATTAGGTAA CACTAATATG TGCCCTGCTA TGGGGACATT TCATAAAGAA 1080 ACCTTTTAAC TTAAATTGAT TGCTTTTAGT TTAAGAGTAA TAATGAAAGA TATTGATCCT 1140 TTATTGTAAG TCTTGTTGGA CCTAGATGAG GCATAAGTTA TAAATAACAA TGTCCAATAT 1200 GTCTGATTTT TTAGTTGTTA CATAGTTTTG GTATCTTAGG GGAGAAAATA GAGAGGAAAC 1260 AGTTTTCTTG CTTTTGATTT TGATCTATGA ACAATTTCTT AGAGTCACTA ACCTGATAGA 1320 ATTACTTTTC AAGCTATTGA AACTTTCAAA GGTCATAAAT ATGTAACACT AGGGGATTAA 1380 CTGATATATT ATGTAACATC TGTAATGGGA ATACGATATA GCCATTAAAG ATGATTTTGT 1440 AAAACATTTA 1450
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