Tag | Content |
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EnhancerAtlas ID | HS076-04580 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr1:175220850-175222320 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr1:175221576-175221592 | ATTGGACTTTGACTTT | - | 6.16 | ONECUT1 | MA0679.1 | chr1:175221419-175221433 | AAGAAATCAATATT | + | 6.07 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGACCAGAG AGAGGGAAGA TCAATGGATT ACTTAGGAAT CCTGTGTGAC TGAAAGTCCT 60 TAATGAAGCA TCCCTTATAC TACAAAGGAA CAGAAGGAGT CAGAGCCCTG TCAGCCCTCC 120 ATCAGTTCCC TCTCAGTCTC CTAGCTTCGT TTGAAGAACA TATTGTCACT ATGATCCTTG 180 ACATTCCTCC TTAGTCACTT AGTTTCTCTA AAATGCAAAG ACAGAAAAGG AGTTCATTTG 240 TAAACCCATT ATAGAGCGTT CTGAAAAGCC ATTCAGATGT TGACTTATAG ACATCCTAGT 300 CTTTGGTTTA AGGCCAGGCA CCAGGAGTAG AGGATCCACA ACACAGGTCT CAGGCTTGTC 360 TGAGAACCTG GGAGGGGAAG AAAAACGTGA GGAGGACACA GAAAGATAAA CACTCTAAAT 420 GCCTTCAAAA CCAGAAATCT TCCCTATTGC ATTTATTCAT TGAAACATTG ACTTCAGGTT 480 CATGGCAATA ATATTTAGTA ATCATTGGAT ATTAAGTAAA AATTCTATGG GGTTTATAAA 540 GGCAGCATTG TGATTCAATG TAAAAAAGGA AGAAATCAAT ATTAGGCAGG TTGAGACCAT 600 CCAGCTAGTT AGTGTTGGAG GTAGAACTCA GCCAGCTAGT GTTGGAAGAG ATCTCATGTC 660 TCTTCATCCC ATCAGTGGGG CTCCCTCTAC AGTGTTATGT ACCTAGCACC ACATGTATTT 720 AAATATATTG GACTTTGACT TTTCTCAAAT ACTCCACTAA CCTTTTGTAT TCATTATGAT 780 TATACATTTA CAAGATGCTT TGTTTCATTA TTTGATAGCA AAATGTTGTA ACAAGTAAAT 840 GGTTTCCCAT ATTGGTGGGA GTGACAGTCG TTGTTGGTTG TCAATCCCAG AACATTTACT 900 CTTTCTTCTT CGCTGACACA TTTTATTTGT CTTCCTCTGA GAATCTGCTT TCTTCAGCAG 960 GGGCTGAGAT CTTCTTAGCC TTAGGGCACT GAATCTTAAT TGATCTAAGC TAGTTAATAT 1020 AGTTTCACTT GCCAAATGAC TGTTGAACTG AGAGCATATG GTGAAACTGT GGCCAATCAG 1080 TCATGAAAGG AGGTTGCTTA TGCTTTCAAA AAGGCACACA TTACAGAGAT ATTCCCTTTT 1140 CTTCCTCTGG ACTTTGCCTA CTACAGGTGA TGCCTGGAAC TTGGAACCAT GAGAATATAT 1200 TTAATACAAT GTGAATAGTA GAGAAGAAAA AGGGAAAGGA CCTGGGTTCT TGATGATGTT 1260 ACTGAGGCAC CGAATCAACC AAATGCAGGA CTGCTCTTCC CTCAGATTTT ATCTGGGGTT 1320 TCTTTTTTTA GCAGCCAAAA GCATCCCAAC AAATACAGAG TGACGGAGAT TCACTCTGCC 1380 ATAACTGGCA TCGAACAACC AGAGTTGAAA TCTCAACTGT ATCACCAACT AGCTTTGTAA 1440 CCTTGAATGA GTTATTTTCT TTCCAAGAGC 1470
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