| Tag | Content |
|---|
EnhancerAtlas ID | HS140-01699 |
Organism | Homo sapiens |
Tissue/cell | Namalwa |
Coordinate | chr2:97711470-97712660 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr2:97712245-97712255 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr2:97712245-97712255 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr2:97712245-97712255 | AATGGAAAAT | - | 6.02 | | ZNF263 | MA0528.1 | chr2:97711955-97711976 | GAGGGAGGAGAATGGGGTGGG | + | 6.08 | | ZNF263 | MA0528.1 | chr2:97711958-97711979 | GGAGGAGAATGGGGTGGGAGG | + | 6.92 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATCAATTAAA AAACGTAAGA AGCCAATCCT GCATGCTTAA TCCAATATGT ATTAAAAAAT 60
AAGAATCATC ATATGTTTAC GGAATCTTAA CCTTGCTAAG GAGAAGTGAG AAATGCACCT 120
GGGAAATTCT AAGAAACAAG AAATCTAAGA GAGAAGACAA AGAGAAAAGG GAATTTATCC 180
TACTCATGCA GCACAGATTT TATCTCTATT GGTTTCTCTC TAAACAGAGA CAATCTTTAA 240
GTCATTTTGC CCTCAAGAGA GGCTCCCAGC ATCCCCTTGG CTCTTTCCAC CCCACTGCAC 300
CCATCAGGGG ATTTGCATAT TGTCCCCTAG GGAGGACCTT CCATTGTGAG TCTGAGATAA 360
AAGCTCAGCT CTAACCTTGC CTTGACTGAT CAGGACTCCT CAGTGCACCT TCTCGCAATG 420
AGGCTCCCTG CTCAGCTCCT GGGGCTGCTA ATGCTCTGGG TCCCTGGTAA GGACAGCAGG 480
GAGATGAGGG AGGAGAATGG GGTGGGAGGG TGAGCTCTGG GGGCCCAATG CCTCCCATGT 540
GTGTTCAGTC CACGTGTTAG ATGTGCAGGT CTTGTTCTGC AGCATGAGGC ATATGATGTA 600
CTGATCTCTG AGAGGGAGGA AGATTTTAGA AGGAAGGATA TGTGCCCTGA AGAAACGCAA 660
GTCTTAGAAA GAGGATGATG GTATGGGAGA CCACTTTGTG CCTTGCATCT GTTGAGTTCT 720
TTTTGAAATT GGATATTCTT GAAATTGCAA AGAAATTATA CAGGCTGAAA TAATAAATGG 780
AAAATTATGA GCATAACGCA TAATATTTGT ACATAACTTT GCCCTTTTCT GTCATCATTC 840
CAGGATCTAG TGGGGACATT CTGTTGACCC AGACTCCACT GTCCCTGTCC ATCACCCCCG 900
GAGAGCCGGC CTCCATCTCC TGCAGGTCTA GTCGGAGCCT CCTGCATAGT AATGGAAACA 960
CCTATTTACA TTGATAGCTG CAGAAGCTAG GCCAGCCTCC ACAGTGTCTA ATCTACACGG 1020
TTTCCAACCG GTTTTCTGGG GTCCCAGACA GGTTCAGTGG CAGTGGGTCA GGCATTGATT 1080
TCACACTGAA AATCAGCCCG GTGGAGGCTG AGGATGTTGG GGTTTATATT ACTGCATGCA 1140
AGCTACACAC TGGCCCCCCA CAGTGCTACA TCCTGGAACA GAAACCTCTC 1190
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