| Tag | Content |
|---|
EnhancerAtlas ID | HS154-13601 | Organism | Homo sapiens | Tissue/cell | Osteoblast | Coordinate | chr20:2294800-2296590 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr20:2295404-2295415 | TTAATCCTCTT | - | 6.14 | | Foxd3 | MA0041.1 | chr20:2294815-2294827 | AAACAAACAAAC | - | 6.32 |
| | | 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 | GTAAGACCCT ATCTCAAACA AACAAACAAA AATTAGCCAA GCATGGTGGT ACATACCTGT 60
ATTCCCAGCT ACTCAGGAGG CTGAGGCAGG GGGATTACTT GAACCCAGGA GCTTGAGGTT 120
ACAGTCAGCT ATGATGGCAC CACTGCACTC AGGCCTGGGT TATAGAGCAA GACCCTGTTT 180
CCAAAAATAT TCATCCAGAA TATCTAAACC TAGATCAACC TGCTCAAAAG TTGTAAGTTA 240
AGATGCAAAA AGTCGTGATC AGGCACAGTG GTTCACACCT GTAATCCCAG GACTTTGGGA 300
GGCTAAGGCA GAGAATCACT TGAGCCCAGG AGTGTGAGAC CAGCCTGGAC AACATAGTGA 360
GACCTCATCT ACACATACAC ACACACACAC ACACACACAC ACACACACAC ACACACAGGA 420
GCCAGGCATC GTGACACATG CCTGTAGTCC CAGCTACTTG GGAGGCTGAG CTGGGGGAAT 480
TGCATGAGTC CGTTAGTTGC AGGCTGCAGT GATCTGTGAT TGCGCCACTG CACTTCAGCC 540
TGGGTGACAC AGCAAAAGCC TATCTCCAAA AAAAAAGGCG AAAAGTCAAA GTGAATTCTT 600
TACTTTAATC CTCTTAAACT AAGTAATTAC CCAGAAATCC TGTAACCTTT ATTTATTTAT 660
TTCTATGTTT CATGGTTTAG GCATTTCTTG ATCTCTTGAC TTTTGAGTTG GATATGTCCA 720
TGCTAATGAG CTAGTTACTT GGTTAAAAAT GTGAACAACT TCTCAGCTGC ATGATAAATA 780
TCCGGGGTGC ATCTGAGAGG GCTTTTGGAA AGAGCTGAGT CTTAGACTGA GCCTGGCAAG 840
AAAGGAGTAA GGTGGGCCCA GGGAACTTAG TAGCCGAGGG AGAGTATGGA GAGGAAGTGA 900
GCCTGGAACA GAATCTTGAA ACCAAATGGC CTGGAAGAGG TGGGATTAAA GCCCTGGTGA 960
CTTAGAAGGC TGAGTCTCTT TGGCCTAGGA GAGAGTGGGT GAGGCCAGCG GCTCCTGCAG 1020
CTGCTGACTC ACTCGCACCC CAGGGCCAAA CCACTTTATC GTGGAGCCAA TTTCCTCAGC 1080
TGCACCTCCC AGATGCTCTA TTCAGACCTC CCAGCTGGGC TGGGCCATGA ACTAATTATG 1140
GCCTGTGCGG AGCTTTGAAG TGCTCAGCTT TCAGCCAGAG ATGACCGTGC TGATAGCCAC 1200
TTTGGAGGCT GGAGCACCAG TGACTCAGGA GATGGGGAAG GGCTGCGCAA CCTTCCATCT 1260
CTAAGGAGGC CCTGTCTTGC CTGACTCTGC CATGACAGCC CAGGACCTCC TGGAAGGGGT 1320
GCAGAACTCA CTACTGCACT GAGGGCCTGG CAAGGCTGGG CATGGCCTGT CCTGGGCAAG 1380
GATCCCTCTG TGTCCAGACT GTCCATTCTC ATAGGCCTTG CCACTTACAG GCACTCCAAG 1440
GAGAAGGGGT AGGACACACA GGCTGGAGGA GCCTTCAGAG ATCCTGGTCC AGCCTCTCAT 1500
TGCACAGTTC AGATAAACGA CAGCCAAAGT TTCATAAACC CTGACCCTTG ACTACAAAAG 1560
ACACCTCAGA GCACCTTTGT CCTAACTTTC CCTTGAAAAT TCCCTTCCCT ATTGGAAGGT 1620
GAAGAACTAA GGCCTAGAGA GGTGAACAGA CCTTTGTGCA ATCATCAAGT TGGCAAGTGG 1680
CAAGGTGGGG CTTGTAACCT CAGTGTCTCC TTCTCTCTTT TAACTTTTAT TATGGAAAAG 1740
TTCAGACCTA CATAAAAGTA GAGAGAAAAG CATAATGAAC TCCTGTGTCT 1790
|
| |
|
|
|
