Tag | Content |
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EnhancerAtlas ID | HS098-33959 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr20:2295080-2296730 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr20:2295404-2295415 | TTAATCCTCTT | - | 6.14 |
| | 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 |
GH20I002313 | chr20 | 2293918 | 2296806 |
| Enhancer Sequence | GTAATCCCAG GACTTTGGGA GGCTAAGGCA GAGAATCACT TGAGCCCAGG AGTGTGAGAC 60 CAGCCTGGAC AACATAGTGA GACCTCATCT ACACATACAC ACACACACAC ACACACACAC 120 ACACACACAC ACACACAGGA GCCAGGCATC GTGACACATG CCTGTAGTCC CAGCTACTTG 180 GGAGGCTGAG CTGGGGGAAT TGCATGAGTC CGTTAGTTGC AGGCTGCAGT GATCTGTGAT 240 TGCGCCACTG CACTTCAGCC TGGGTGACAC AGCAAAAGCC TATCTCCAAA AAAAAAGGCG 300 AAAAGTCAAA GTGAATTCTT TACTTTAATC CTCTTAAACT AAGTAATTAC CCAGAAATCC 360 TGTAACCTTT ATTTATTTAT TTCTATGTTT CATGGTTTAG GCATTTCTTG ATCTCTTGAC 420 TTTTGAGTTG GATATGTCCA TGCTAATGAG CTAGTTACTT GGTTAAAAAT GTGAACAACT 480 TCTCAGCTGC ATGATAAATA TCCGGGGTGC ATCTGAGAGG GCTTTTGGAA AGAGCTGAGT 540 CTTAGACTGA GCCTGGCAAG AAAGGAGTAA GGTGGGCCCA GGGAACTTAG TAGCCGAGGG 600 AGAGTATGGA GAGGAAGTGA GCCTGGAACA GAATCTTGAA ACCAAATGGC CTGGAAGAGG 660 TGGGATTAAA GCCCTGGTGA CTTAGAAGGC TGAGTCTCTT TGGCCTAGGA GAGAGTGGGT 720 GAGGCCAGCG GCTCCTGCAG CTGCTGACTC ACTCGCACCC CAGGGCCAAA CCACTTTATC 780 GTGGAGCCAA TTTCCTCAGC TGCACCTCCC AGATGCTCTA TTCAGACCTC CCAGCTGGGC 840 TGGGCCATGA ACTAATTATG GCCTGTGCGG AGCTTTGAAG TGCTCAGCTT TCAGCCAGAG 900 ATGACCGTGC TGATAGCCAC TTTGGAGGCT GGAGCACCAG TGACTCAGGA GATGGGGAAG 960 GGCTGCGCAA CCTTCCATCT CTAAGGAGGC CCTGTCTTGC CTGACTCTGC CATGACAGCC 1020 CAGGACCTCC TGGAAGGGGT GCAGAACTCA CTACTGCACT GAGGGCCTGG CAAGGCTGGG 1080 CATGGCCTGT CCTGGGCAAG GATCCCTCTG TGTCCAGACT GTCCATTCTC ATAGGCCTTG 1140 CCACTTACAG GCACTCCAAG GAGAAGGGGT AGGACACACA GGCTGGAGGA GCCTTCAGAG 1200 ATCCTGGTCC AGCCTCTCAT TGCACAGTTC AGATAAACGA CAGCCAAAGT TTCATAAACC 1260 CTGACCCTTG ACTACAAAAG ACACCTCAGA GCACCTTTGT CCTAACTTTC CCTTGAAAAT 1320 TCCCTTCCCT ATTGGAAGGT GAAGAACTAA GGCCTAGAGA GGTGAACAGA CCTTTGTGCA 1380 ATCATCAAGT TGGCAAGTGG CAAGGTGGGG CTTGTAACCT CAGTGTCTCC TTCTCTCTTT 1440 TAACTTTTAT TATGGAAAAG TTCAGACCTA CATAAAAGTA GAGAGAAAAG CATAATGAAC 1500 TCCTGTGTCT GCATCACAAG CTTCAGCAAT TACCTCTTCA AGGCTGGTGT CATTTCATCT 1560 GCGACCCTCT CTTTCACAGA TGATTTGATA AATCTTAGAC ATTACACATT TGTCATAATT 1620 TCACCTGTAA ATATTTCCAA GTGTGTCCCT 1650
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