| Tag | Content |
|---|
EnhancerAtlas ID | HS105-50024 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr20:36808390-36809630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr20:36808997-36809012 | TGAACTCCTGACCTC | - | 6.22 | | ZNF263 | MA0528.1 | chr20:36809304-36809325 | CATCCCTCTCTCTGCTCCTCC | - | 6.19 | | ZNF263 | MA0528.1 | chr20:36809307-36809328 | CCCTCTCTCTGCTCCTCCCCT | - | 6.24 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 36808423 | 36808713 | | chr20 | 36809238 | 36809499 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I038180 | chr20 | 36808508 | 36810321 |
|
Enhancer Sequence | GTATGGCCTG CAGAACCCTG AGCCAATTAA ACCTCTTTTC TTTATAAATT ACCCAGCTTC 60
AGACATTCCT TTATAGCAAC GTAAGAACAG CCTAACAGAC ATGCAAACAG ACTTGTCTGT 120
GCACACAGGG GTAAAGTTAC AGAAGTGAGG AATGGTGTAG AGAATTCACA GGAAGAAGGA 180
GTCGAACGGT ATGGCTGGGG TTTTGGGGGT ACTTGGAAGG AATGTCAAGG CTGGAGTGGT 240
TAGTGGGGCT CGGACAACAA ACGTCTCTGT CTACCAGGCT CAGTTTAGGA CACGGGAAGC 300
CATGGGAAAG TTTAAAGCAG GGAAGTGGCA TAGTCAAGGC TGCATTCTGG GAAGATAGTG 360
CTGGAATTGT TTATCATGGA ATTTTAGATT TTTTTTTTTT TTTTTTTTTT TGAGGCAGAG 420
TCTTGCTCTA TTGCCCAGGC TGGAGTGCAA TGGTGCAATC TCGGCTCACT GCAACCTCTG 480
CCTCCTAGGT TCGAGCCATT CTCCTTCCTC AGCCTCCTGA GTAGCTGGGA CTACAGGTCT 540
GCGCCACCAC GCCCAGCCAA TTATTTTGTA TTTTTAGTAC ATTTCACCAT ATTGGCCAGG 600
CTGGTCTTGA ACTCCTGACC TCATGTGATC CACCCACCTT GACCTCCCAA AGTGCTGGGA 660
TTACAGGTGT GAGCCACCAT GCCTGGCCAG AATTTTAGAT CTTGAATTTA GTGATTATCA 720
TCATCCCTGG GCCCTTTTTA AAAGAAGAGC AAATTGAGGC CAGAAAGGGA AATGGCACCC 780
ACCGTTCATC AGGGACAGAA GCATTTGCTC CCACCTTGGT CTGTGTAGGT GGGGCTGAGC 840
CTGAGGCTGG AGTATGTTTG CAGATCCTGT GGGGTGAGCT GTTCCCAGTG GGACCAGTTC 900
CCAGTTCTCT GTGACATCCC TCTCTCTGCT CCTCCCCTTC GGACCTGCCC TGCAGGCTCC 960
AAATATCGTG GTTGATATGG AAACTCTCCT GTTACACATT CCTTTTCCAG TTGTGTGACC 1020
CTGGCAGTGT CCTTCCTCTC TGGAGCTTCG GTTTCCCCAT CTGTCTAATG GGAGTGATAA 1080
ATGGAGTGAT GGCTGGCACT GATTATCAAG CACTCGGGCA TCTCCTCCAA TTCTCCCAAA 1140
GGCCCCAAGG AAGAAGAGGG TCTGCCATTA TCAGTGCCCT GTCCACCGGC AGAAAGTGTG 1200
AGGCAGAGCT CGTTGTGGAA AGCAAGGCTC ATAATTTACC 1240
|
