| Tag | Content |
|---|
EnhancerAtlas ID | HS176-15478 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr16:72281470-72282830 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr16:72282045-72282056 | AAGCCATAAAA | + | 6.62 | | FOS | MA0476.1 | chr16:72281959-72281970 | AATGAGTCAGA | - | 6.32 | | Gfi1b | MA0483.1 | chr16:72281930-72281941 | AGCTGTGATTT | - | 6.14 | | NFIC | MA0161.2 | chr16:72281909-72281920 | TCTGCCAAGTA | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I072247 | chr16 | 72281321 | 72282189 |
|
Enhancer Sequence | GAAATAGGAT TCAGTGACAA GGTGCAATGT GGCTTGTGAA ATATTAGTTT TGGACAATCA 60
CAAATCAGGA TCCAAGGGTA TGTTAAATTA TTCGGCATTC TTGACCTCAT TATTAAGTGA 120
CTTCATATGG GTTTTTGCTC ATATTCATAT AATCTTGGGA TACAAAGAGC TTAATTTTTG 180
TTTCCTTTCC CCAGCCATTT CCCTTTTTAT GTATCAGAGA TTTTATGTAT ATCTCTTTAT 240
TTTTATCCTG TTTAATTTTA GAATTTAAAG GGCAATGGCT ATGTTTTTGT TTGGGGAACA 300
CACAAGGAGG ACACTTACTC ATATGATGAC ACATATCAGA AACATGAATA TTAGTTAGAA 360
ATTTGGTTTG CAGATTTTTC TTTGCTAACA CACTACTTCA GGTAACAGAA CAATTTTTCC 420
AACCAAACAT CTGCCTCGGT CTGCCAAGTA TCGAACAGAA AGCTGTGATT TGTAACACAT 480
GGTCTTATAA ATGAGTCAGA ACTTCAAGGC CAAGTCGGCT TCTGGAAGTG TTCTAAAGTG 540
ATAGCAACAA TATTATTTTC CAAAATAATG GGAGAAAGCC ATAAAAACAC TCCAGGAAGA 600
TCGTGTACCA AAGATGTTTG TTGATTTTGT TTTGTTCCAA AGTTGTTTGG AACAATGATT 660
AGTTGGCGCT GACAGGATTT CTACAACTAG GAAGTGTGTT GGACACTTAA AACTTTAAAT 720
CAGTGTTCCA GTAAGTTCTA AAGAACTTTA ACCAATTGAA CAATTATCCT AAGAATATGA 780
CTACCAGCTG TCGCTTAAAC TTACAAGTTA AAACACTTTA TATCATTGGG GCAAAGCAAT 840
GATATGGACC TGGGATAGGA AAATTACCAG AGAATGTGAC TGAATCAGTG AATATCTGCC 900
AAAAAAAAAT CTCTTTGAGA TGAACAAAAG AAATTAGGTA GTATTAGGCT ACTCATAGGA 960
CAACTGGCCA GAGCACAGTT TCTTCTTTGA GATTTGTGTG TTTTATAATT TTGTTAATGA 1020
TTCAGACCAA AACAAATACT TTGAAAGTAG AAACACATAA TTCCATTTCA GCATATCCCA 1080
ACCAGATGGG ATCAGAACAG GTGTGATCAT TTTAGAGTGT TCTTCTCCAT AAATCAACTT 1140
CTGGTTCATT CCAGAGTGGG GCTGTCAGCT TTTAGGCGCC CAATGAAGTT GAGAATTTTC 1200
AGCAAACTAA ACACAGCCAT TAAAATAATG TTTGAATTAG TTTTAATCAC AGTGACCTAG 1260
ATTCTCATGC TCCCCAGGAC CTCACTGTAT CTCTTCCATG TGTGAGATCC ATGGGAGGGC 1320
TGCACATGGG GAAGACTCAC CGAGTGCAGA GCAGGAAGAA 1360
|
