| Tag | Content |
|---|
EnhancerAtlas ID | HS182-09278 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:29145440-29146610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr17:29146078-29146092 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_63101 | chr17:29132825-29152846 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 29145769 | 29146007 | | chr17 | 29145734 | 29145800 |
|
Enhancer Sequence | TAAAAGGAGC AATAATGGCT TTCTTTTCTT TTCCTTTTTT TTTTTTTTTT GAGACAGTTT 60
CACTCCTGTT GCCCAGGCTG GAGTGCAGTG GCATGATCTC GGCTCACCGC AACCTCCGTC 120
TCCTGGGTTC AAGCAATTCT CTTGCCTCAG CCTCCCGAGT AGCTAAGATT ACAGGCGCCC 180
ACCACCACAC CCGGCTAATT TTTGTATTTT TAGTAAAGAT AGGTTTTCAT CGTATGGGTC 240
AGGCTTGTCT CAAACTCCTG ACCTCAGGTG ATCCGCCCGC CTCAGCCTCC CAAAATGCTG 300
GGATTACAGG TGTGAGCCAC CACGCCTGGC CAACAGCTTT CTTTTCTTTG CTAAGCTACT 360
GAGACTTCCT GTCTTGGTTT TTTGAAATAA CTTTTGAGTG TTTTTTTTTT TTTGAGACAG 420
TCTTCTTCTG TTGCTGAGGC TGGAGTGCAG TGGTGCCATC TTGGCTCACT GCAACCTCCA 480
TCTCCCAGGT ATAAGCAATT CTCCTGCCTC AGCCTCCAGA GTAGCTGGAA TTACAGGTGC 540
ATTCCACCAC ACCTGGCTAA TTTTTTTTAC ATTTTTAGTA GAGACAGAGT TTTGCCATGT 600
TGAAGGCTGG TCTCAAACTC CTGATCTCAT GTGATCCACC CGCCTCGGCC TCCCAAAGTG 660
CTGGGATTAC AGGCGTGAGC CACTGAGCCC AGCCACCAAC TAGTATCTTA ATTAGGTACC 720
AGGATCTTAC CATTTGCTCT TGAAGGAGCA GAGACTTGCT TTTGTCAGTG TCCTGAGAAA 780
TACTGAATCA GAATACCAAA AGGTACATGA AAGCCAACAT AGTCATTTTA TAGAGTGAAC 840
TACAACACAC AGACTAAAAT ACTGGCATTT CTCACTGTAG ACACCTCCAG TACCTCAACT 900
AATTCCCCTT TGATAATGTA CCAAGATGAA GTTTTTGGAC TTACAAAGAT TAAAGACCAG 960
GCCCTGACTT TGGCATTGTC ATCAAGGTGG TGCCACTCTG TGAGGCCTGA GTGGCCAGCT 1020
GACATCACTA CGTGACATTT TGATCAGTTA TCTCTACTTA CGTTTTTGTT TTTGAGATGG 1080
AGTCTCGCTC TGTCGCCCAG GCTGGAGTGC AGTGGTGTGA TCTTGGCTCA CTGCAACCTC 1140
CGCCTGCCCG GCTCAAGCAA TTCTCCTGGC 1170
|
