Tag | Content |
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EnhancerAtlas ID | HS091-48228 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr9:111651670-111653480 |
Target genes | |
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) |
ZNF263 | MA0528.1 | chr9:111653158-111653179 | TCTCCCCACTCTCCTTCCTTC | - | 6.07 |
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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 |
GH09I108883 | chr9 | 111644654 | 111652743 |
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Enhancer Sequence | TTCCTGTAGA GACAATAAGC AGCAGTTGAC TACAAAGTTA AACAGATACT TTAGCTCAAG 60 TGCTTCTTTA ATATGTCTTT ATTATGTATG AAACTATGTA CTTTCTGAAT TTCTGTGAGG 120 GAATAGGTAT ATACACCACA GAGTCCTATC TTAAATGGCA GCTAGAATCT AAATTTAGCA 180 CAGGAATTGA AAATCATATA CAGCCAAAAT TAGCCTTGAA AGATGCTTCC AAAGCATGTA 240 TATGGGAAAA TGACCTGGTA TCTCTCACTA AACCACTTCG TCCCTTAACA GTAAGAGACC 300 ACTATTTCTT TGGTTGAGCA CTAGATGGAG GTAGCTGACT TATGTTTGAG TCATGCAGTG 360 TCTTTAGATC CTAGAATCAC TCTCAGCCCA ATTGAGATAA ACCACAATGA GAGGCACAGA 420 GAACCCAAGG CTTTCGAAGG AGCTGGTAGA TTCCGGTCTC TCATTGCATG CTCACTCCAG 480 TGCATATATC ACTAAAAAAA GTAGGTAAAA TCACCTCCAC TATTTAAATA GTTACCTTTC 540 TTTTGCTCTC TTGTGTAAAC TGCCTACGTT AAATGTACAC ACAGAGTGAC TCCAGTGTGT 600 AACATTTCTC AAACATCTTT GACCACTGCC CTCCCCACCT ACTTTTGCTA AACATCTGAG 660 AAAAACTAGA AATACTCCCT CATAAGACAT GGGAAATAGC AAGCTAAGAG CTGTAAAGAA 720 TAGAAGAGAT CCAAGAACAG AGATAGAAGG TATAAACAAC CAATATCATA AATTTCTAAA 780 GCAGAAAGGA ACAATGGAGA CCGAACGAAT AACTAAAAGG CCTGAAATAA GGAATTCTCG 840 ACATTTGTAA AAAGAGGCCA GCATGGAAAC GGAGGGATTT GGGAAAGGCT AATAACCAGA 900 AAAAGAAAAG TGATAATCCC ATACACTGGT ATAATCCCAA GAAAAAAAGA ATACTGCAAA 960 TGACAAAGAA GGACTGGTAC ATAAATTTAA CAAAATTTAA CAGGATAGAG TTTGGAATTT 1020 TTTTAGGACT GCTTTTTATT TTTTTCTTTG AGATCTCAAC AATATTTACA AGTTAGGGAA 1080 AAAAATATAC CAGTCATTGC TTTACTTCAA GCACTGCTGA GATGACCAGA GCTTCTGCTC 1140 ATCTCTTTTC ATAGGTGTCC TTACCCTTTC CTCCACTCTG GTACTAGAGC CCCTGGTACC 1200 AGCCTCGCCT CTGGTTCGGG CAACCCTTGT CCCTGACGCA GCTAAACTGC CTTTGCTTTC 1260 AGAATGCTTC GACATTTGGC CTTTTATTTT CCCCACCTCA TTCCTGGCTA TTCCAACAAC 1320 CTACTGTCTA TAACAGAATG GACCCATCCA AAAATTCATC TTTACCTTCT TACAGGGCAC 1380 AGCCCATCCA GCTACATGGC GTGGCCGAGA TGGAATAGAA GGTGATAGTT TAACTTCCAT 1440 CCAGGTCATT TCCAACTTAA AGGTAAATGT TTTACCATGA TTCTAACTTC TCCCCACTCT 1500 CCTTCCTTCC CCACAGCTGT GGAGATAACC CAGCTACAAC CATCTGCCTA AAAGGTTGCA 1560 GAGCCACACA ACGGAAGGGC CTATAAATCC CTATGGGAGA GAGAAATAAA CTTCTTTCCA 1620 TATTGGGCCA CTGCATTCTG GGACTCTTGC TGTAGTAGCT TATCCTTTAA AGCATTCTAA 1680 ATTAATTTTT ATCAGTGAGA ACAAGACTGT CTCAGAGTAT TCTGCCCTAA ATTTATTTGC 1740 AAAATTACCA AACAAAAGAA ATAAATTTTT TAAAACCTTT GTAGATGTAA ACATATAAAT 1800 GATTGTACTT 1810
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