Tag | Content |
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EnhancerAtlas ID | HS082-02200 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:159567190-159568660 |
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) |
RORA | MA0071.1 | chr1:159567589-159567599 | TGACCTTGAT | - | 6.02 |
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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 |
GH01I159596 | chr1 | 159566407 | 159569121 |
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Enhancer Sequence | TCCTAACTAC CACCAACTGA AAATTATACA TATAAAAGCT TTAAACAAAG TCTCTTGAGG 60 CTCTCAAGGG AGTTTACATT ACAGTATAGT TCAGCAAACA ATTTTAAATC AAATAGTACA 120 CCTCTTTATT CTTAGAATTC CCTCTGCCAA AAAAGAAATC AGCTACTTTT TTTTAAATTC 180 AAGGTCCAAC TTTCTGTTGT GTTGCTGATT CTCTTCTCTC TTTTTCCAAC GACTTCCACT 240 TCTCTCTCTA GTTTACATGT CTCCAAACCT TAAGCCTCTG TTAATACTTT CACAATAAGT 300 CAATTTTGCC AACGGTTTGC CTCCCCTAGA CCATCTAGGC TGGGCCCAGA ACACCTCATC 360 TTCACTCCCA CTGAAGTGTT CCTGAAGGTC AGCTCTCACT GACCTTGATT CTGCTCCCCT 420 ACACTGTCAC CAGAAGCTAT CCACCTATGG TTCTAATTCA GTAAGTCCAA CTCTCTCACC 480 CCCTTTTTTT GTCTCAGCTG TGTGGGCTTT CCCAGGATGG CATGCAATGG GACCCCTGTG 540 CCATGCATAT TGTAAAGGAA AATGCCTCCC TCCATGCGCT ACAAAACAGC ACATTTATGA 600 TGGCACTTTG AAAAGATATG GGTTGTGGTG TCACATATTG ACAATTCCTT GGCCAGAGGC 660 TTAACAGTGC CAGCAGTGCC AGAAGATTAA GAAGACAGCA AAAACAGAAA AGGGAGAAGA 720 TGGTGAAGTA GTTATATAAC ATGAGCGAGA ATGCTCCTGA TTACAAAGCA GAGAAATTGA 780 CTTTTTTTCT TAGTGTTTTC TATAGTCATT GCTCTATCCC TGTTCTAGAA TTCAAGTCAT 840 GATAAGAATT TCTTCACGTT GACTTCCTGC ATTGCTTTCA GACATTGCAA TTAAAGAATG 900 CGAAGAAAGA ACCTCACAGA GGTAACAGAG TTTGTTTTCC TGGGATTCTC CAGATTCCAC 960 AAACATCACA TCACTCTCTT TGTGGTTTTT CTCATCCTGT ACACATTAAC TGTGGCTGGC 1020 AATGCCATCA TCATGACCAT CATCTGCATT GACCGTCACC TCCACACTCC CATGTACTTC 1080 TTCCTGAGCA TGCTGGCTAG CTCAAAGACA GTGTACACAC TGTTCATCAT TCCACAGATG 1140 CTCTCCAGCT TCGTAACCCA GACCCAGCCA ATCTCCCTAG CAGGTTGTAC CACCCAAACG 1200 TTCTTCTTTG TTACCTTGGC CATCAACAAT TGCTTCTTGC TCACAGTGAT GGGCTATGAC 1260 CACTATATGG CCATCTGCAA TCCCTTGAGA TACAGGGTCA TTACGAGCAA GAAGGTGTGT 1320 GTCCAGCTGG TGTGTGGAGC CTTTAGCATT GGCCTGGCCA TGGCAGCTGT CCAGGTAACA 1380 TCCATATTTA CCTTACCTTT TTGTCACACG GTGGTTGGTC ATTTCTTCTG TGACATCCTC 1440 CCTGTCATGA AACTCTCCTG TATTAATACC 1470
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