Tag | Content |
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EnhancerAtlas ID | HS082-24258 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr3:121716100-121718320 |
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) |
HNF4G | MA0484.1 | chr3:121717804-121717819 | TGACCTTTGGTCTCC | - | 6.2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 121716322 | 121718192 | chr3 | 121716830 | 121717448 | chr3 | 121717719 | 121718002 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I121997 | chr3 | 121716249 | 121718446 |
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Enhancer Sequence | ACCAGTCCTC CCTGATTTGA CTGACCAGTC ATTTCTGGGA CATCCTCAGG TGTTTCCTAG 60 AATCTGATGC CCCTTTGAAC TCTTGTCATT TTAGCTTTAG GAAACTACCA GCAGATGCTT 120 CTGGGTCCCA ACCAGGCAAT TGACCTCAAA TAGCCCTCCT CCCAATAGGG CTTTCCTTCT 180 TGACCTCTCA AACATGCATT CCCTCCTCTA TAGCAGCAGG TTAAACATTC CCCACCTCTT 240 AGGTCTTCCC CTGCCTGTGA ACTTTCTGCT GATGACTTCA TCTCTATTGA TGAAGAGGAA 300 CCAGCCCTGA ACGTGGAGCC AAGAAACCTA GGTTTAGTCC AGGGCCCACT GCTAACAGGC 360 TGTAACAAGT AATTGTGGAA AAATCTCCCT CGACTTCACT TCCCTCAGCT GTGAGGCAGA 420 AGGAGATGGG GCAGGAGAGA TCAGAGAGTC TCACTGTGGC TGTGGCCTAC TGCTGGGCAT 480 GCCTGGAGGT TCTCCAGTAA GGAGGGCCAG TAACTGCTCT AGGGATGAAA GCCGTTTCTC 540 CAGTTCTTAG GGAAAAAATA CGTTTCCATT TCAAAAATGT CTATCTTTAA GTCCTACAGA 600 GGGCTGTTTA CCACTATTAG GTGAACTATC AAGGGTTACT AAAATTTGGT CTTATTTTCA 660 TTTTTCTCCT CTCTAATCCT TTTTTAACTC TCACTAGAAA GTGGGAGCAG GTTGGGGAGG 720 TGGGATGTGA TCAAAGAAGT TCAAGAATCA CTGACATGTT TCTTGAAGCT TCCTTCTGCA 780 TCTAGAATTT TGATTTGCTG AAATCGAGTC AGGCAGATGT GAGCTCCCTC AGCTTCCTCC 840 CTTACATCTT AATCATCCTC CACATTTTAA TGACTTCCTT TCTGTCTTCA GAGGCCAGGC 900 TGCTTCCCTT TCCCTTCCGC TCCCTTTCTA AGGCCAGTTC TTTCCTTGTA GGGCTGAGGC 960 CACTCCTACC AGCTTCATCA CTCATCAGTG ACCTCACTTC TTAATGCTTC ACTTTACTCA 1020 TTTGATATTA ACCTTGGTTC TTTGCTTATA AACATGTTTA GGATTACCTT ATTCTACAAA 1080 CACCAACAAT AACTCCTTAC TCCTCTAACC AAAGAGCTTT CTTTAATAAC TCATGCCCTT 1140 CCATGCAATT CTTCTTGTCA ACAAACTTCT CAGGACAGTC TACCCCAGTG ACTCACTTTG 1200 AAAGTGACCT CATCGGCCCA AGTTCAGGGA TCTTTGTAAT CTACATTTCT TGATTTTACT 1260 AGTTTTTTAA AATGAACCTA ATCCCTCAGG AGAAACAACT CTCCCGCAGA ACCTCCATTT 1320 ATTAGTTTAC TAATAAGTGG TGCACTTATC ATTTGTGTTA GCTTTGTCCC CAGTCTTGCC 1380 TGCTTTTAGT GCCCCACGAA CCTAGGGAGT CTAAGCAGGC ATCTTGGGCG GGTTTTTCTT 1440 ATCTCATCCT GCATATTATT ACTCCAGTGA CAGTGATTTC TCCATGGCCT CCTCCCTAAG 1500 ATCCCTGAAA GGTAGGGGGC CCCACAGTCC AATGCTGCAT CCTCCACGAC TTTTCCCCTC 1560 CTACGGTGTC TTAGCCAATC CCACAGTGAT CCACCTACAG AGGCTGTGGC AGTCTCTGCT 1620 GTAGGAATGC AGACTCTCAC AAGTCAGATG AACATGGATT CAACTCTGCA AAACCACTGC 1680 TACTTCCTAG CTGTGGGGCT TTTCTGACCT TTGGTCTCCC ATCTTTTAAA AGAGATGACT 1740 TCTGCCTTCT AGGGTGGTTG TGAGGATTCA GTGAGGAAAC GTATGCAAGG GGACTACACA 1800 TCAGACATCC AATAAAAGTT AGTTCTCTTT TCCTGTAAGA CAGCAACCTC AGAGCACAGG 1860 CCTGAAACCA GACTCAGGCC ACCGACTTTC TTCACATTGT AGATCAGGTT TTGTTTCTAT 1920 CTTAATAGGT CATTCATTAT TTTTCCCTTA AAAAATTTCC TTTCAAATGG ATCAAACTGA 1980 TAAAGGTGGT TATCTCTGGG TACTCAGATG AGTCATTACA TTTTCCTGAA TTTCTCAAAT 2040 TTCCTACAAT ATAGTACTTT ATTTAGATCA TCTGGAAGAG GAAATGTTAT TGAAAATAGA 2100 AGCCAAAAAA AATTAAAAAC CTTCTATTTA AAGCAGTTGG TGCTATTCCA TCTATTTGAC 2160 CAAGAAAATA ACTTTATAGA ATAATTTTGT ATTATTTTGC CTTTACCATG TATTCTGTAG 2220
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